Field

The present invention relates to a eukaryotic cell with increased production of fermentation product. In particular the invention relates to acetic acid, pentose and glucose converting eukaryotic cells with improved acetate conversion. The invention further relates to the processes wherein the cells produce fermentation products such as ethanol.

Background

Second generation bioethanol is produced from e.g. lignocellulosic fractions of plant biomass that is hydrolyzed into free monomeric sugars, such as hexoses and pentoses, for fermentation into ethanol. Apart from the sugar release during pretreatment and hydrolysis of the biomass, some toxic by-products are formed. For instance, furfural and HMF are two of these products. The quantities in which they are formed depend on several pretreatment parameters, such as temperature, pressure and pretreatment time. Lignocellulosic hydrolysates also contain high amounts of acetic acid, which is a potent inhibitor of the fermentative capacity of microorganisms, such as eukaryotic cells. Several different approaches have been reported that could help to reduce the inhibitory effect of acetic acid on the fermentation of the sugars in hydrolysates as well as (partly) solving redox balance issues upon deletion of the genes involved in glycerol production, e.g. by genetic engineering of eukaryotic cells. Acetic acid, along with other inhibitors, can be removed from hydrolysates through chemical or biological detoxification procedures. Additional detoxification steps after pre-treatment though are costly and/or cause a loss of fermentable substrate.

Under anaerobic conditions, Saccharomyces cerevisiae cannot naturally consume acetic acid. Furthermore, acetic acid tolerance seems to vary considerably between different strains. Past research has mainly been focused on the identification of potential gene candidates associated with increased tolerance and on the generation of strains with increased robustness through the use metabolic/evolutionary engineering approaches. However, the concept of generating detoxifying strains through the expression of heterologous enzymes has not been sufficiently explored.

Medina et al. 2010 describes expression of mhpF from E.coli, encoding for a NAD ⁺ -dependent acetylating acetaldehyde dehydrogenase, enabled anaerobic growth of a gpdIA gpd2A strain by coupling the reduction of acetate to acetaldehyde with NAD ⁺ regeneration This approach completely abolished the formation of glycerol and resulted in an increase of 13% of the ethanol yield on sugar, caused mainly by the minimization of carbon losses for production of glycerol and the reduction of acetic acid to ethanol. An important additional benefit of this strategy is that it enables the in situ detoxification of acetic acid by the yeast. However, the amount of acetic acid that can be reduced in this way is limited by the amount of NADH that is generated during anabolism, which is coupled to biomass formation. Therefore there is still a need to improve the conversion of acetate, pentose and/or hexose to fermentation product.

Summary

It is therefore an object of the present invention to provide for eukaryotic cells that are capable of producing ethanol from acetic acid or acetate while retaining their abilities of fermenting hexoses (glucose, fructose, galactose, etc.) as well as pentoses like xylose, as well as processes wherein these strains are used for the production of ethanol and/or other fermentation products.

Another object is to provide for cells, e.g. eukaryotic cells that are capable of producing ethanol from glycerol and/or glycerol and acetic acid while retaining their abilities of fermenting hexoses (glucose, fructose, galactose, etc.) as well as pentoses like xylose. Another object is to increase the production of fermentation product (yield, production rate or both). In an embodiment thereof the eukaryotic cell produces less glycerol.

Further, it is an object of the invention to provide a eukaryotic cell strain that can an-aerobically co-ferment acetate, pentose and glucose. It is an object of the present invention to provide a cost-effective method of producing ethanol by fermentation of pentose and/ or acetate.

It is another object of the present invention to provide a eukaryotic cell that is capable of fermenting pentose at a higher rate than can be achieved using strains currently known to the art.

It is another object to reduce the fermentation time. It is another object to increase the yield of the fermentation.

Other objects, features, and advantages of the invention will be apparent from review of the specification and claims.

One or more of these objects are attained according to the invention that provides a eukaryotic cell that is genetically modified comprising one or more heterologous gene encoding: a) D-glucose-6-phosphate dehydrogenase; b) 6-phosphogluconate dehydrogenase and/or c) glucose dehydrogenase, gluconolactonase and gluconate kinase, wherein a), b) and the glucose dehydrogenase in c) are NAD ⁺ dependent.

According to the invention the cytosolic NADH level in the eukaryotic cell may be increased. This can lead in one embodiment to an improved yield of glycerol, which is advantageous in the wine industry. It o may, in a second embodiment, result in increased reduction of acetate level and/or increased yield of fermentation product, e.g. ethanol, that is advantageous in the biofuel industry. In an third embodiment, in particular when both a) and b) are NAD ⁺ dependent, the NADH generated may be used in the production of any fermentation product in the eukaryotic cell, wherein NADH in the cytosol acts as reducing co-factor. In a third embodiment, the NADH generated may be used in the production of any fermentation product in the eukaryotic cell, wherein NADH in the cytosol acts as reducing co- factor. These advantages are detailed herein below.

In one embodiment of the invention, the eukaryotic cell comprises a gene encoding NAD ⁺ dependent D-glucose-6-phosphate dehydrogenase a) (in that embodiment the 6-phosphogluconate dehydrogenase may still be NADP+ dependent). In another embodiment of the invention, the eukaryotic cell comprises a gene encoding NAD ⁺ dependent 6-phosphogluconate dehydrogenase (b) (in that embodiment the D-glucose-6-phosphate dehydrogenase may still be NADP+ dependent). In one embodiment, the eukaryotic cell comprises a genes encoding for both (a) and (b), i.e. both NAD ⁺ dependent D-glucose-6-phosphate dehydrogenase (a) and NAD ⁺ dependent 6-phosphogluconate dehydrogenase (b). The embodiments a) and b) generate cytosolic NADH. In an embodiment the cell comprises c) glucose dehydrogenase, gluconolactonase and gluconate kinase. These three enzymes form another pathway from glucose to 6-phosphate -gluconate than that in which (a) or (b) is involved, but which also generates NADH, since glucose dehydrogenase in (c) is NAD+ dependent. Embodiment (c) may be combined with embodiments (a) and/or (b). Thus, in an embodiment the eukaryotic cell has a disruption of one or more native gene encoding D-glucose-6-phosphate dehydrogenase and/or native gene encoding 6-phosphogluconate dehydrogenase, wherein native is native in the eukaryotic cell.

In an embodiment D-glucose-6-phosphate dehydrogenase native in the eukaryotic cell is replaced by the NAD ⁺ dependent D-glucose-6-phosphate dehydrogenase and/or the 6- phosphogluconate dehydrogenase native in the eukaryotic cell is replaced by the NAD ⁺ dependent 6- phosphogluconate dehydrogenase. In that way the co-factor of these enzymes is advantageously modified. A change of co-factor dependency/specificity may be called herein "co-factor engineering".

The eukaryotic cells according to the invention, with heterologous gene(s) encoding:

a) D-glucose-6-phosphate dehydrogenase;

b) 6-phosphogluconate dehydrogenase; and/or

c) glucose dehydrogenase, gluconolactonase and gluconate kinase. wherein a) and b) and glucose dehydrogenase in c) are NAD ⁺ dependent, produces more glycerol than the native strain (having both NADP ⁺ dependent D-glucose-6-phosphate dehydrogenase and NADP ⁺ dependent 6-phosphogluconate dehydrogenase). The strains produced that way are advantageous for application in the wine industry, since more glycerol may improve the taste of wine and at the same time the amount of ethanol may be reduced which is also desirable in the wine industry. These treats are obtained according to the invention with minimal effect on the fermentation of the wine yeast and wine production process. Alternatively the strains according to the invention are advantageously used in the biofuel industry, e.g. the bioethanol fuel industry.

In an embodiment, the NADH generated may be used in the production of any fermentation product, wherein NADH in the cytosol acts as reducing co-factor. This allows the production of fermentation products that would otherwise not be produced by the eukaryotic cells because of lack of NADH in the cytosol. Or it improves the yield in case the production of such fermentation product is limited by NADH level in the cytosol. In this embodiment it is advantageous, that both (a) D-glucose-6- phosphate dehydrogenase and (b) 6-phosphogluconate dehydrogenase are NAD ⁺ dependent, or even (a), (b) and (c1 ) glucose dehydrogenase are NAD ⁺ dependent. These embodiments allow the NADH- levels in the cytosol to be higher. Thus (a), (b) and (c1 ) create flexibility: It is possible for the skilled person, for each fermentation product and substrate, to convert a flexible part of the substrate to CO2 and NADH in the cytosol, that is adapted to the need to produce the fermentation product in a high yield. In an embodiment the fermentation product that is a product that is more reduced than the substrate from which it is derived, for example glucose. Examples of suitable fermentation products that are more reduced than glucose is glycerol. The skilled person can determine the fermentation products which can be fermented that way. Such fermentation may be aerobic or anaerobic.

In an embodiment, the eukaryotic cell is genetically modified, comprising one or more heterologous gene encoding: a) D-glucose-6-phosphate dehydrogenase and/or

b) 6-phosphogluconate dehydrogenase; wherein a) and b) are NAD ⁺ dependent. In an embodiment of the invention, wherein the eukaryotic cell comprises:

d) one or more nucleotide sequence encoding a heterologous NAD+-dependent acetylating acetaldehyde dehydrogenase (E.C. 1 .2.1.10);

e) one or more nucleotide sequence encoding a homologous or heterologous acetyl-CoA synthetase (E.C. 6.2.1.1 ); and optionally

g) a modification that leads to reduction of glycerol 3-phosphate phosphohydrolase (E.C.

3.1.3.21 ) and/or glycerol 3-phosphate dehydrogenase (E.C. 1.1.1.8 or E.C. 1.1.5.3) activity, native in the eukaryotic cell, the advantages of such strains according to the invention are increased consumption of acetate and increased production of fermentation product, e.g. ethanol.

Therefore the invention further relates to a process for the fermentation of a substrate to produce a fermentation product with the above eukaryotic cell, wherein the fermentation time is reduced and /or the yield increased, with simultaneous increased fermentation product output, relative to the corresponding fermentation with wild-type (as defined herein) eukaryotic cell.

Brief description of the drawings

FIG. 1 shows in vitro specific enzymatic activities of cell free extracts from exponentially growing shake flask cultures, harvested at OD (Optical density is herein measured at 660nm, and abbreviated as "OD") = 4 to 5. Cultures were grown in synthetic medium supplemented with 20 g L glucose, pH 6, 30°C, 200 rpm. Indicated are: Glucose-6-phosphate dehydrogenase activity, NADP ⁺ dependent 6- phosphogluconate dehydrogenase activity, NAD ⁺ dependent 6-phosphogluconate dehydrogenase activity are given for four strains:IMX585 (white bars, left), IMX705 (light grey bars), IMX706 (middle grey bars) and IMX707 (dark grey bars, right). Data from independent duplicate experiments, error bars indicate mean deviations of the duplicates.

FIG. 2. Fermentation profiles of IMX585 (Fig. 2a, top), IMX705 (Fig. 2b, top), IMX899 (Fig. 2a, middle), IMX756 (Fig. 2b, middle). Glucose = filled circles, biomass = filled squares, glycerol = open squares, ethanol = open circles. Fermentations were performed in synthetic medium supplemented with 20 g L glucose. Batches performed at pH 5, sparging of 500 ml min ^-1 N2, 30°C. Biomass was calculated by converting OD values throughout the fermentation to biomass based on an OD to biomass conversion formula derived from plotting actual biomass samples against OD during mid-exponential phase.

Glycerol yield on glucose from anaerobic batch fermentations performed with IMX585, IMX705, IMX899, IMX756 (Fig. 2a, bottom). Ethanol yields on glucose from the same fermentations (Fig.2b, bottom). Calculation of ethanol yields was based on data corrected for evaporation. Data is presented as averages of independent duplicate experiments.

FIG. 3: Fermentation profiles of IMX585 (Fig. 3a, top), IMX888 (Fig. 3b, top) and IMX860 (Fig 3a, middle). Glucose = filled circles, biomass = filled squares, glycerol = open squares, ethanol = open circles, acetate = triangles. Fermentations were performed in synthetic medium supplemented with 20 g L glucose and 3 g L acetic acid. Batches performed at pH 5, sparging of 500 ml min ^-1 N2, 30°C. Biomass was calculated by converting OD values throughout the fermentation to biomass based on an OD to biomass conversion formula derived from plotting actual biomass samples against OD during mid- exponential phase.

Ratio of acetate consumed per glucose consumed in anaerobic batch fermentations performed with IMX585, IMX888 and IMX860 (Fig. 3a, bottom). Ratio of acetate consumed per biomass formed from the same fermentations (Fig. 3b, bottom). Data is presented as averages of independent duplicate experiments.

FIG. 4 shows ATP driven transhydrogenase-like cycle catalyzed by Acs1 p/Acs2p, EutEp and Ald6p.

Brief description of the sequence listing SEQ ID NO: 1 Synthetic codon optimized gndA expression cassette; SEQ ID NO: 2 GndA protein (Methylobacillus flagellates); SEQ ID NO: 3 Synthetic codon optimized gox1705 expression cassette SEQ ID NO: 4 Gox1705 protein (Gluconobacter oxydans 621 H) SEQ ID NO: 5 Synthetic codon optimized 6pgdh expression cassette

SEQ ID NO: 6 6pgdh protein WP_01 1089498.1 (Multispecies [Bradyrhizobium])

SEQ ID NO: 7 azf gene codon optimized

SEQ ID NO: 8 azf protein (ADEE03728.1, Haloferax volcanii)

SEQ ID NO: 9 eutE expression cassette SEQ ID NO: 10 Primer confirmation of GPD2 deletion (Primer code: 2015) SEQ ID NO: 1 1 Primer confirmation of GPD2 deletion (Primer code: 21 12) SEQ ID NO: 12 Primer confirmation of GND1 deletion (Primer code: 2123) SEQ ID NO: 13 Primer confirmation of GND1 deletion (Primer code: 2124) SEQ ID NO: 14 Primer confirmation of ALD6 deletion (Primer code: 2164) SEQ ID NO: 15 Primer confirmation of ALD6 deletion (Primer code: 2171 ) SEQ ID NO: 16 Primer confirmation of GPD1 deletion (Primer code: 4397) SEQ ID NO: 17 Primer confirmation of GPD1 deletion (Primer code: 4401 ) SEQ ID NO: 18 Primer for Amplication of pMEL1 1 backbone (Primer code: 5792) SEQ ID NO: 19 Primer for Amplication of pROS1 1 backbone (Primer code: 5793) SEQ ID NO: 20 Primer for Amplication of pMEL1 1 insert sequence (Primer code: 5979)

SEQ ID NO: 21 Primer for Amplication of pMEL1 1 backbone (Primer code: 5980)

SEQ ID NO: 22 Primer for Amplication of pROS1 1 insert sequence (GPD1 targeting) (Primer code: 6965)

SEQ ID NO: 23 Primer for Amplication of pROS1 1 insert sequence (GPD2 targeting) (Primer code: SEQ ID NO: 24 Primer for Repair oligonucleotide (GPD1 knockout) (Primer code: 6967)

SEQ ID NO: 25 Primer for Repair oligonucleotide (GPD1 knockout) (Primer code: 6968)

SEQ ID NO: 26 Primer for Amplification of pMEL1 1 insert (GND2 targeting) (Primer code: 7231 )

SEQ ID NO: 27 Primer for Confirmation of GND2 deletion (Primer code: 7258) SEQ ID NO: 28 Primer for Confirmation of GND2 deletion (Primer code: 7259)

SEQ ID NO: 29 Primer for Repair oligonucleotide (GND2 knockout) (Primer code: 7299)

SEQ ID NO: 30 Primer for Repair oligonucleotide (GND2 knockout) (Primer code: 7300)

SEQ ID NO: 31 Primer for Amplification of pMEL1 1 insert (GND1 targeting) (Primer code: 7365)

SEQ ID NO: 32 Primer for Amplification of integration cassette (gndA, 6pgdh, gox1705) (Primer code: 7380)

SEQ ID NO: 33 Primer for Amplification of integration cassette (gndA, 6pgdh, gox1705) (Primer code: 7381 )

SEQ ID NO: 34 Primer for Confirmation of gndA integration (Primer code:7441 ) SEQ ID NO: 35 Primer for Confirmation of gndA integration (Primer code: 7442) SEQ ID NO: 36 Primer for Confirmation of 6pgdh integration (Primer code: 7443) SEQ ID NO: 37 Primer for Confirmation of 6pgdh integration (Primer code: 7444) SEQ ID NO: 38 Primer for Confirmation of gox1705 integration (Primer code: 7445) SEQ ID NO: 39 Primer for Confirmation of gox1705 integration (Primer code: 7446) SEQ ID NO: 40 Primer for Repair oligonucleotide (ALD6 knockout) (Primer code: 7608) SEQ ID NO: 41 Repair oligonucleotide (ALD6 knockout) (Primer code: 7609)

SEQ ID NO: 42 Primer for Amplification of pMEL1 1 insert (ALD6 targeting) (Primer code: 7610) SEQ ID NO: 43 Primer for Amplification of integration cassette (eutE) (Primer code: 7991 ) SEQ ID NO: 44 Primer for Amplification of integration cassette (eutE) (Primer code: 7992) SEQ ID NO: 45 Primer for Confirmation of eutE integration (Primer code: 8337) SEQ ID NO: 46 Primer for Confirmation of eutE integration (Primer code: 8338) SEQ 10 NO: 47 Amino acid sequence of aldehyde oxidoreductase (Escherichia coli EutE); SEQ 10 NO: 48 Amino acid sequence of glycerol dehydrogenase of E.coli (Escherichia coli gldA).

SEQ ID NO: 49 Nucleotide sequence of codon optimized gnc!A (6-phosphogluconate dehydrogenase) (Methylobacillus flagellatus)

SEQ ID NO: 50 Nucleotide sequence of codon optimized gox1705 (6-phosphogluconate

dehydrogenase) (Gluconobacter oxydans)

SEQ ID NO: 51 Nucleotide sequence of codon optimized 6pgdh (B-phosphogluconate

dehydrogenase) (Bradyrhizobium sp.) SEQ ID NO: 52 Nucleotide sequence of codon optimized azf (glucose- 6-phosphate dehydrogenase) (Haloferax volcanii)

SEQ ID NO: 53 Nucleotide sequence codon optimized eutE (Acetylating acetaldehyde

dehydrogenase) (E. coli)

Detailed description Throughout the present specification and the accompanying claims, the words "comprise" and

"include" and variations such as "comprises", "comprising", "includes" and "including" are to be interpreted inclusively. That is, these words are intended to convey the possible inclusion of other elements or integers not specifically recited, where the context allows.

The articles "a" and "an" are used herein to refer to one or to more than one (i.e. to one or at least one) of the grammatical object of the article. By way of example, "an element" may mean one element or more than one element. By way of example, cell can herein be one cell, but refer also to a population of cells or a strain.

"Eukaryotic cell" is herein defined as any eukaryotic microorganism. Eukaryotes belong to the taxon Eukarya or Eukaryota. The defining feature that sets eukaryotic cells apart from prokaryotic cells (Bacteria and Archaea) is that they have membrane-bound organelles, especially the nucleus, which contains the genetic material, and is enclosed by the nuclear envelope. The presence of a nucleus gives eukaryotes their name, which comes from the Greek ευ (eu, "well") and κάρυον (karyon, "nut" or "kernel"). Eukaryotic cells also contain other membrane-bound organelles such as mitochondria and the Golgi apparatus. Many unicellular organisms are eukaryotes, such as protozoa and fungi. All multicellular organisms are eukaryotes. Unicellular eukaryotes consist of a single cell throughout their life cycle. Microbial eukaryotes can be either haploid or diploid. Preferably the eukaryotic cell is capable of anaerobic fermentation, more preferably anaerobic alcoholic fermentation. "NAD ⁺ dependent" is herein a protein specific characteristic described by the formula:

1 < KmNADP KmNAD ⁺ <∞ (infinity)

NAD ⁺ dependent is herein equivalent to NAD ⁺ specific, NAD ⁺ dependency is herein equivalent to NAD ⁺ specificity. In an embodiment K _m NADP ⁺ / K _m NADP ⁺ is between 1 and 1000, between 1 and 500, between 1 and 200, between 1 and 100, between 1 and 50, between 1 and 10, between 5 and 100, between 5 and 50, between 5 and 20 or between 5 and 10.

The Km's for the proteins (e.g. proteins a), b) and c1 ) in the claims) and is herein determined as protein specific, for NAD ⁺ and NADP ⁺ respectively, using know analysis techniques, calculations and protocols. These are described herein and for instance in Lodish et al., Molecular Cell Biology 6 ^th Edition, Ed. Freeman, pages 80 and 81 , e.g. Figure 3-22.

"Sequence identity"

Amino acid or nucleotide sequences are said to be homologous when exhibiting a certain level of similarity. Two sequences being homologous indicate a common evolutionary origin. Whether two homologous sequences are closely related or more distantly related is indicated by "percent identity" or "percent similarity", which is high or low respectively. Although disputed, to indicate "percent identity" or "percent similarity", "level of homology" or "percent homology" are frequently used interchangeably. A comparison of sequences and determination of percent identity between two sequences can be accomplished using a mathematical algorithm. The skilled person will be aware of the fact that several different computer programs are available to align two sequences and determine the homology between two sequences. An overview of sequence comparison In D. Sankoff and J. B. Kruskal, (ed.), Time warps, string edits and macromolecules: the theory and practice of sequence comparison, pp. 1-44 Addison Wesley). The percent identity between two amino acid sequences can be determined using the Needleman and Wunsch algorithm for the alignment of two sequences. (Needleman, S. B. and Wunsch, C. D. (1970) J. Mol. Biol. 48, 443-453). The algorithm aligns amino acid sequences as well as nucleotide sequences. The Needleman-Wunsch algorithm has been implemented in the computer program NEEDLE. For the purpose of this invention the NEEDLE program from the EMBOSS package was used (version 2.8.0 or higher, EMBOSS: The European Molecular Biology Open Software Suite (2000) Rice, P. LongdenJ. and Bleasby.A. Trends in Genetics 16, (6) pp276— 277, http://emboss.bioinformatics.nl/). For protein sequences, EBLOSUM62 is used for the substitution matrix. For nucleotide sequences, EDNAFULL is used. Other matrices can be specified. The optional parameters used for alignment of amino acid sequences are a gap-open penalty of 10 and a gap extension penalty of 0.5. The skilled person will appreciate that all these different parameters will yield slightly different results but that the overall percentage identity of two sequences is not significantly altered when using different algorithms.

Global Homology Definition The homology or identity is the percentage of identical matches between the two full sequences over the total aligned region including any gaps or extensions. The homology or identity between the two aligned sequences is calculated as follows: Number of corresponding positions in the alignment showing an identical amino acid in both sequences divided by the total length of the alignment including the gaps. The identity defined as herein can be obtained from NEEDLE and is labelled in the output of the program as "IDENTITY".

Longest Identity Definition

The homology or identity between the two aligned sequences is calculated as follows: Number of corresponding positions in the alignment showing an identical amino acid in both sequences divided by the total length of the alignment after subtraction of the total number of gaps in the alignment. The identity defined as herein can be obtained from NEEDLE by using the NOBRIEF option and is labelled in the output of the program as "longest-identity".

A variant of a nucleotide or amino acid sequence disclosed herein may also be defined as a nucleotide or amino acid sequence having one or several substitutions, insertions and/or deletions as compared to the nucleotide or amino acid sequence specifically disclosed herein (e.g. in de the sequence listing).

Optionally, in determining the degree of amino acid similarity, the skilled person may also take into account so-called "conservative" amino acid substitutions, as will be clear to the skilled person. Conservative amino acid substitutions refer to the interchangeability of residues having similar side chains. For example, a group of amino acids having aliphatic side chains is glycine, alanine, valine, leucine, and isoleucine; a group of amino acids having aliphatic-hydroxyl side chains is serine and threonine; a group of amino acids having amide-containing side chains is asparagine and glutamine; a group of amino acids having aromatic side chains is phenylalanine, tyrosine, and tryptophan; a group of amino acids having basic side chains is lysine, arginine, and histidine; and a group of amino acids having sulphur-containing side chains is cysteine and methionine. Preferred conservative amino acids substitution groups are: valine-leucine-isoleucine, phenylalanine-tyrosine, lysine-arginine, alanine- valine, and asparagine-glutamine. Substitutional variants of the amino acid sequence disclosed herein are those in which at least one residue in the disclosed sequences has been removed and a different residue inserted in its place. Preferably, the amino acid change is conservative. Preferred conservative substitutions for each of the naturally occurring amino acids are as follows: Ala to ser; Arg to lys; Asn to gin or his; Asp to glu; Cys to ser or ala; Gin to asn; Glu to asp; Gly to pro; His to asn or gin; lie to leu or val; Leu to ile or val; Lys to arg; gin or glu; Met to leu or ile; Phe to Met, leu or tyr; Ser to thr; Thr to ser; Trp to tyr; Tyr to trp or phe; and, Val to ile or leu.

Nucleotide sequences of the invention may also be defined by their capability to hybridise with parts of specific nucleotide sequences disclosed herein, respectively, under moderate, or preferably under stringent hybridisation conditions. Stringent hybridisation conditions are herein defined as conditions that allow a nucleic acid sequence of at least about 25, preferably about 50 nucleotides, 75 or 100 and most preferably of about 200 or more nucleotides, to hybridise at a temperature of about 65 ^° C in a solution comprising about 1 M salt, preferably 6 x SSC or any other solution having a comparable ionic strength, and washing at 65 ^° C in a solution comprising about 0.1 M salt, or less, preferably 0.2 x SSC or any other solution having a comparable ionic strength. Preferably, the hybridisation is performed overnight, i.e. at least for 10 hours and preferably washing is performed for at least one hour with at least two changes of the washing solution. These conditions will usually allow the specific hybridisation of sequences having about 90% or more sequence identity. Moderate conditions are herein defined as conditions that allow a nucleic acid sequences of at least 50 nucleotides, preferably of about 200 or more nucleotides, to hybridise at a temperature of about 45 ^° C in a solution comprising about 1 M salt, preferably 6 x SSC or any other solution having a comparable ionic strength, and washing at room temperature in a solution comprising about 1 M salt, preferably 6 x SSC or any other solution having a comparable ionic strength. Preferably, the hybridisation is performed overnight, i.e. at least for 10 hours, and preferably washing is performed for at least one hour with at least two changes of the washing solution. These conditions will usually allow the specific hybridisation of sequences having up to 50% sequence identity. The person skilled in the art will be able to modify these hybridisation conditions in order to specifically identify sequences varying in identity between 50% and 90%. A "nucleic acid construct" or "nucleic acid vector" is herein understood to mean a nucleic acid molecule designed by man resulting from the use of recombinant DNA technology. The term "nucleic acid construct" therefore does not include naturally occurring nucleic acid molecules although a nucleic acid construct may comprise (parts of) naturally occurring nucleic acid molecules. The terms "expression vector" or expression construct" refer to nucleotide sequences that are capable of affecting expression of a gene in host cells or host organisms compatible with such sequences. These expression vectors typically include at least suitable transcription regulatory sequences and optionally, 3' transcription termination signals. Additional factors necessary or helpful in effecting expression may also be present, such as expression enhancer elements. The expression vector will be introduced into a suitable host cell and be able to effect expression of the coding sequence in an in vitro cell culture of the host cell. The expression vector will be suitable for replication in the host cell or organism of the invention.

As used herein, the term "promoter" or "transcription regulatory sequence" refers to a nucleic acid fragment that functions to control the transcription of one or more coding sequences, and is located upstream with respect to the direction of transcription of the transcription initiation site of the coding sequence, and is structurally identified by the presence of a binding site for DNA-dependent RNA polymerase, transcription initiation sites and any other DNA sequences, including, but not limited to transcription factor binding sites, repressor and activator protein binding sites, and any other sequences of nucleotides known to one of skill in the art to act directly or indirectly to regulate the amount of transcription from the promoter. A "constitutive" promoter is a promoter that is continuously active under most physiological and developmental conditions. An "inducible" promoter is a promoter that is physiologically or developmentally regulated, e.g. by the application of a chemical inducer. The term "selectable marker" is a term familiar to one of ordinary skill in the art and is used herein to describe any genetic entity which, when expressed, can be used to select for a cell or cells containing the selectable marker. The term "reporter" may be used interchangeably with marker, although it is mainly used to refer to visible markers, such as green fluorescent protein (GFP). Selectable markers may be dominant or recessive or bidirectional. As used herein, the term "operably linked" refers to a linkage of polynucleotide elements in a functional relationship. A nucleic acid is "operably linked" when it is placed into a functional relationship with another nucleic acid sequence. For instance, a transcription regulatory sequence is operably linked to a coding sequence if it affects the transcription of the coding sequence. Operably linked means that the DNA sequences being linked are typically contiguous and, where necessary to join two protein encoding regions, contiguous and in reading frame.

The terms "protein" or "polypeptide" are used interchangeably and refer to molecules consisting of a chain of amino acids, without reference to a specific mode of action, size, 3-dimensional structure or origin.

Yeasts are herein defined as eukaryotic microorganisms and include all species of the subdivision Eumycotina that predominantly grow in unicellular form. Yeasts may either grow by budding of a unicellular thallus or may grow by fission of the organism. Preferred yeasts cells for use in the present invention belong to the genera Saccharomyces, Kluyveromyces, Candida, Pichia, Schizosaccharomyces, Hansenula, Kloeckera, Schwanniomyces, and Yarrowia. Preferably the yeast is capable of anaerobic fermentation, more preferably anaerobic alcoholic fermentation. "Fungi" (singular: fungus) are herein understood as heterotrophic eukaryotic microorganism that digest their food externally, absorbing nutrient molecules into their cells. Fungi are a separate kingdom of eukaryotic organisms and include yeasts, molds, and mushrooms. The terms fungi, fungus and fungal as used herein thus expressly includes yeasts as well as filamentous fungi.

The term "gene" means a DNA fragment comprising a region (transcribed region), which is transcribed into an RNA molecule (e.g. an mRNA) in a cell, operably linked to suitable regulatory regions (e.g. a promoter). A gene will usually comprise several operably linked fragments, such as a promoter, a 5' leader sequence, a coding region and a 3'nontranslated sequence (3'end) comprising a polyadenylation site. "Expression of a gene" refers to the process wherein a DNA region which is operably linked to appropriate regulatory regions, particularly a promoter, is transcribed into an RNA, which is biologically active, i.e. which is capable of being translated into a biologically active protein or peptide.

The term "homologous" when used to indicate the relation between a given (recombinant) nucleic acid or polypeptide molecule and a given host organism or host cell, is understood to mean that in nature the nucleic acid or polypeptide molecule is produced by a host cell or organisms of the same species, preferably of the same variety or strain. If homologous to a host cell, a nucleic acid sequence encoding a polypeptide will typically (but not necessarily) be operably linked to another (heterologous) promoter sequence and, if applicable, another (heterologous) secretory signal sequence and/or terminator sequence than in its natural environment. It is understood that the regulatory sequences, signal sequences, terminator sequences, etc. may also be homologous to the host cell. In this context, the use of only "homologous" sequence elements allows the construction of "self-cloned" genetically modified organisms (GMO's) (self-cloning is defined herein as in European Directive 98/81/EC Annex II). When used to indicate the relatedness of two nucleic acid sequences the term "homologous" means that one single-stranded nucleic acid sequence may hybridize to a complementary single-stranded nucleic acid sequence. The degree of hybridization may depend on a number of factors including the amount of identity between the sequences and the hybridization conditions such as temperature and salt concentration as discussed later.

The terms "heterologous" and "exogenous" when used with respect to a nucleic acid (DNA or RNA) or protein refers to a nucleic acid or protein that does not occur naturally as part of the organism, cell, genome or DNA or RNA sequence in which it is present, or that is found in a cell or location or locations in the genome or DNA or RNA sequence that differ from that in which it is found in nature. Heterologous and exogenous nucleic acids or proteins are not endogenous to the cell into which it is introduced, but have been obtained from another cell or synthetically or recombinantly produced. In an embodiment, a heterologous gene may replace a homologous gene, in particular a corresponding homologous gene (expression enzyme with same function, but herein with a different co-factor, i.e. NAD ⁺ dependent). Alternatively the homologous gene may be modified in the cell to become NAD ⁺ dependent, e.g. by one or more point mutations in the genome, e.g. with CRISPR CAS technology. Generally, though not necessarily, such nucleic acids encode proteins, i.e. exogenous proteins, that are not normally produced by the cell in which the DNA is transcribed or expressed. Similarly exogenous RNA encodes for proteins not normally expressed in the cell in which the exogenous RNA is present. Heterologous/exogenous nucleic acids and proteins may also be referred to as foreign nucleic acids or proteins. Any nucleic acid or protein that one of skill in the art would recognize as foreign to the cell in which it is expressed is herein encompassed by the term heterologous or exogenous nucleic acid or protein. The terms heterologous and exogenous also apply to non-natural combinations of nucleic acid or amino acid sequences, i.e. combinations where at least two of the combined sequences are foreign with respect to each other. The "specific activity" of an enzyme is herein understood to mean the amount of activity of a particular enzyme per amount of total host cell protein, usually expressed in units of enzyme activity per mg total host cell protein. In the context of the present invention, the specific activity of a particular enzyme may be increased or decreased as compared to the specific activity of that enzyme in an (otherwise identical) wild type host cell.

"Anaerobic conditions" or an anaerobic fermentation process is herein defined as conditions or a fermentation process run in the absence of oxygen or in which substantially no oxygen is consumed, preferably less than 5, 2.5 or 1 mmol/L/h, more preferably 0 mmol/L/h is consumed (i.e. oxygen consumption is not detectable), and wherein organic molecules serve as both electron donor and electron acceptors.

"Disruption" is herein understood to mean any disruption of activity, and includes, but is not limited to deletion, mutation, reduction of the affinity of the disrupted gene and expression of antisense RNA complementary to corresponding mRNA. Native in eukaryotic cell herein is understood as that the gene is present in the eukaryotic cell before the disruption. It includes the situation that the gene native in eukaryotic cell is present in a wild-type eukaryotic cell, a laboratory eukaryotic cell or an industrial eukaryotic cell. Eukaryotic cell may herein also be designated as eukaryotic cell strain or as part of eukaryotic cell strain.

By "wild-type" eukaryotic cell, it is meant a pentose-fermenting eukaryotic cell strain with normal levels of functional NADP+ dependent genes from which the eukaryotic cell of the present invention is derived. In certain cases, the "wild-type eukaryotic cell" as defined in this patent application, may include mutagenized eukaryotic cell.

Reaction equations herein are non-stoichiometric.

Certain embodiments of the invention are now described:

In an embodiment, the eukaryotic cell has a disruption of one or more native gene encoding D- glucose-6-phosphate dehydrogenase and/or native gene encoding 6-phosphogluconate dehydrogenase, wherein native is native in the eukaryotic cell. In an embodiment, in the eukaryotic cell, the D-glucose-6-phosphate dehydrogenase native in the eukaryotic cell is replaced by the heterologous D-glucose-6-phosphate dehydrogenase and/or wherein the 6-phosphogluconate dehydrogenase native in the eukaryotic cell is replaced by the heterologous 6-phosphogluconate dehydrogenase. In an embodiment, in the eukaryotic cell the native genes that are part of the pentose-phosphate-pathway that are NADP ⁺ dependent are disrupted or deleted. Examples of genes to be disrupted or deleted are GND1, GND2 and ZWF1. The heterologous genes NAD ⁺ dependent D-glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase may be prokaryotic genes or synthetic genes encoding prokaryotic enzymes. In an embodiment, the eukaryotic cell has heterologous genes are prokaryotic genes originating from Methylobacillus, Gluconobacter, Bradyrhizobium and Haloferax, e.g. : Methylobacillus flagellatus, Gluconobacter oxydans, Bradyrhizobium or Haloferax volcanii.

In an embodiment the eukaryotic cell is a yeast cell, e.g. a Saccharomyces cell, e.g. Saccharomyces cerevisiae cell. In an embodiment, in the eukaryotic cell, an acetaldehyde dehydrogenase-6 (ALD6) is disrupted. In an embodiment, the eukaryotic cell comprises a disruption of one or more of the genes gppl, gpp2, gpdl and gpd2 native in the eukaryotic cell.

The eukaryotic cell may comprise: h) one or more nucleotide sequence encoding a heterologous xylose isomerase (E.C. 5.3.1.5) and/or i) arabinose pathway genes, j) one or more nucleotide sequence encoding a heterologous glycerol dehydrogenase (E.C. 1.1.1.6); and k) one or more nucleotide sequence encoding a homologous or heterologous dihydroxyacetone kinase (E.C. 2.7.1.28 or E.C. 2.7.1.29). In an embodiment, the eukaryotic cell is a pentose and glucose fermenting eukaryotic cell that is capable of anaerobic simultaneous pentose and glucose consumption. In an embodiment, the substrate is a hydrolysate of lignocellulosic material, e.g. an enzymatic hydrolysate of lignocellulosic material wherein the hydrolysate comprises acetate. The acetate may be at acetate concentration of 0.3% (w/w) or more in the hydrolysate.

The various embodiments of the invention described herein may be cross-combined.

In an embodiment, the invention provides a eukaryotic cell that is genetically modified comprising:

3lucose-6-phosphate dehydrogenase and/or b) 6-phosphogluconate dehydrogenase; c) glucose dehydrogenase, gluconolactonase and gluconate kinase, wherein a) and b) and glucose dehydrogenase in c) are NAD+ dependent; d) one or more nucleotide sequence encoding a heterologous NAD+-dependent acetylating acetaldehyde dehydrogenase (E.C. 1 .2.1.10); e) one or more nucleotide sequence encoding a homologous or heterologous acetyl-CoA synthetase (E.C. 6.2.1.1 ); f) a disruption of one or more aldehyde dehydrogenase (E.C. 1.2.1.4) native in the eukaryotic cell g) a modification that leads to reduction of glycerol 3-phosphate phosphohydrolase and/or glycerol 3-phosphate dehydrogenase activity, compared to the eukaryotic cell without such modification; h) one or more nucleotide sequence encoding a heterologous xylose isomerase (E.C. 5.3.1.5); i) Arabinose pathway genes j) one or more nucleotide sequence encoding a heterologous glycerol dehydrogenase (E.C. 1.1.1.6); and/or k) one or more nucleotide sequence encoding a homologous or heterologous dihydroxyacetone kinase (E.C. 2.7.1 .28 or E.C. 2.7.1.29).

These features and other embodiments of the invention are hereafter described in more detail. a) D-glucose-6-phosphate dehydrogenase that is NAD* dependent

Native enzyme D-glucose-6-phosphate dehydrogenase (herein abbreviated as G6PDH or ZWF1) is an enzyme that is part of the oxidative part of the pentose-phosphate-pathway (PPP pathway). In eukaryotic cells, this enzyme is NADP ⁺ dependent: The reaction catalyzed by the native enzyme is:

D-glucose-6-phosphate + NADP ⁺ < ZWF1 > D-6-phospho-glucono-lactone + NADPH +H ⁺

(equation 1 )

The D-glucose-6-phosphate dehydrogenase that is NAD ⁺ dependent that is used according to the invention uses NAD ⁺ as cofactor. The reaction of the NAD ⁺ dependent G6PDH enzyme is:

D-glucose-6-phosphate + NAD ⁺ < azf > D-6-phospho-glucono-lactone + NADH +H ⁺

(equation 2)

In an embodiment, the NAD ⁺ dependent G6PDH (enzyme or gene) originates from a prokaryotic organism, "originates" is herein understood to include a) isolated from an organism or b) synthesized gene or protein based on information derived from a gene sequence or protein.

In an embodiment the G6PDH is a heterologous gene encodes a D-glucose-6-phosphate dehydrogenase having at least 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 98, or 99% identity to SEQ ID NO: 7. In an embodiment the gene encodes an enzyme that is a D-glucose-6-phosphate dehydrogenase having at least 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 98, or 99% identity to SEQ ID NO: 8. Suitable examples of the above G6PDH enzymes are given in table 1. Table 1 : Suitable G6PDH enzymes and identity to G6PDH WP 004044412.1

b) 6-phosphogluconate dehydrogenase

Native enzyme 6-phosphogluconate dehydrogenase (herein abbreviated as 6PGDH or GND1 or GND2) is an enzyme that is part of the oxidative part of the pentose-phosphate-pathway (PPP pathway In eukaryotic cells, this enzyme is NADP ⁺ dependent: The reaction catalyzed by the native enzyme is:

6-phosphogluconate + NADP ⁺ < GND1 or GND2-— >

Ribulose-5-phosphate + NADPH +H ⁺ + C0 ₂

(equation 3) The 6-phosphogluconate dehydrogenase that is NAD+ dependent that is used according to the invention uses NAD+ as cofactor. The reaction catalyzed by the NAD ⁺ dependent 6PGDH enzyme is:

6-phosphogluconate + NAD ⁺ < GND1 or GND2 (GndA) >

Ribulose-5-phosphate + NADH +H ⁺ + C0 ₂ (equation 4)

In an embodiment, the NAD+ dependent 6PGDH (enzyme or gene) originates from a prokaryotic organism, "originates" is herein understood to include a) isolated from an organism or b) synthesized based on information derived from an enzyme or gene.

In an embodiment the 6PGDH is a heterologous gene encodes a D-glucose-6-phosphate dehydrogenase having 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 98, or 99% identity to SEQ ID NO: 1 . In an embodiment the gene encodes an enzyme that is a D-glucose-6-phosphate dehydrogenase having 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 98, or 99% identity to SEQ ID NO: 2. Suitable examples of the above 6PGDH enzymes are given in table 2.

In an embodiment the 6PGDH is a heterologous gene encodes a D-glucose-6-phosphate dehydrogenase having 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 98, or 99% identity to SEQ ID NO: 3. In an embodiment the gene encodes an enzyme that is a D-glucose-6-phosphate dehydrogenase having 6050, 55, 60, 65, 70, 75, 80, 85, 90, 95, 98, or 99% identity to SEQ ID NO: 4. Suitable examples of the above 6PGDH enzymes are given in table 3.

In an embodiment the 6PGDH is a heterologous gene encodes a D-glucose-6-phosphate dehydrogenase having 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 98, or 99% identity to SEQ ID NO: 5. In an embodiment the gene encodes an enzyme that is a D-glucose-6-phosphate dehydrogenase having 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 98, or 99% identity to SEQ ID NO: 6. Suitable examples of the above 6PGDH enzymes are given in table 4.

In an embodiment, the heterologous 6PGDH enzymes or genes are prokaryotic genes originating from an organism chosen from the genus list: Methylobacillus, Gluconobacter, Bradyrhizobium and Haloferax. In an embodiment, the 6PGDH enzymes or genes are prokaryotic genes originating from an organism chosen from the species list: Methylobacillus flagellatus, Gluconobacter oxydans, Bradyrhizobium and Haloferax volcanii. Examples of suitable 6PGDH proteins are given in tables 2, 3 and 4.

Table 2: Suitable 6PGDH enzymes and identity to AAF34407.1 6-phosphoqluconate dehydrogenase {Methylobacillus flagellates 6PGDH) Protein Identity (%) Accession

NAD-linked 6-phosphogluconate dehydrogenase 100 AAF34407.1 [Methylobacillus flagellatus] (gndA)

6-phosphogluconate dehydrogenase [Methylobacillus 90 WP_025869439.1 glycogenes]

6-phosphogluconate dehydrogenase [Methylovorus 82 WP_015829859.1 glucosotrophus]

6-phosphogluconate dehydrogenase [Methylovorus sp. 82 WP_013441936.1 MP688]

6-phosphogluconate dehydrogenase [Methylotenera 81 WP_047538584.1 versatilis]

6-phosphogluconate dehydrogenase [Methylophilus sp. 80 WP_029148659.1 5]

6-phosphogluconate dehydrogenase [Sulfuricella 75 WP_009206043.1 denitrificans]

6-phosphogluconate dehydrogenase [Candidatus 70 WP_046487838.1 Methylopumilus planktonicus]

6-phosphogluconate dehydrogenase [Thioalkalivibrio 66 WP_012637452.1 sulfidiphilus]

6-phosphogluconate dehydrogenase [Thermithiobacillus 60 WP_028989561.1 tepidarius]

6-phosphogluconate dehydrogenase [Deinococcus ficus] 58 WP_027462489.1 Table 3: Suitable 6PGDH proteins and identity to WP 011253227.1 ; 6-phosphoqluconate dehydrogenase (Gluconobacter oxydans 6PGDH1

Table 4: Suitable 6PGDH proteins and identity to WP 011089498.1 ; 6-phosphoqluconate dehydrogenase (Bradyrhizobium 6PGDH1

Protein Identity Accession

(%)

MULTISPECIES: 6-phosphogluconate dehydrogenase 100 WP_01 1089498.1

[Bradyrhizobium]

6-phosphogluconate dehydrogenase [Bradyrhizobium 98 WP_027546897.1 sp. WSM2254] Protein Identity Accession

(%)

6-phosphogluconate dehydrogenase [Bradyrhizobium 95 WP_02433941 1.1 japonicum]

6-phosphogluconate dehydrogenase [Bradyrhizobium 83 WP_028347094.1 elkanii]

6-phosphogluconate dehydrogenase 77 WP_01 1440787.1

[Rhodopseudomonas palustris]

6-phosphogluconate dehydrogenase [Microvirga lupini] 75 WP_036351036.1

6-phosphogluconate dehydrogenase (decarboxylating) 72 WP_002718635.1

[Afipia felis]

6-phosphogluconate dehydrogenase 71 WP_043757546.1

[Methylobacterium oryzae]

c) glucose dehydrogenase, gluconolactonase and gluconate kinase

In an embodiment the cell comprises glucose dehydrogenase, gluconolactonase and gluconate kinase. The introduction of these genes and the expression of the corresponding enzymes leads to the following reactions in the cell:

Glucose + NAD ⁺ < glucose dehydrogenase > gluconolactone + NADH

(equation 5), followed by:

Gluconolactone+ H2O < gluconolactonase > gluconate

(equation 6), followed by gluconate + ATP < gluconate kinase > 6-P-gluconate + ADP ⁺ + Pi

(equation 7) which completes the pathway from glucose to 6-P-gluconate.

These enzymes (designated as c1 ), c2) and c3) respectively are now described in more detail.

c1) NAD+ dependent glucose dehydrogenase (EC 1.1.1.118) is an enzyme that catalyzes the chemical reaction D-glucose + NAD ⁺ v~D-glucono-1 , 5-lactone + NADH (equation 8)

Thus, the two substrates of this enzyme are D-glucose and acceptor, whereas its two products are D-glucono-1 ,5-lactone and reduced acceptor. This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with other acceptors. The systematic name of this enzyme class is D-glucose:acceptor 1-oxidoreductase. Other names in common use include glucose dehydrogenase (Aspergillus), glucose dehydrogenase (decarboxylating), and D- glucose:(acceptor) 1-oxidoreductase. This enzyme participates in pentose phosphate pathway. It employs one cofactor, FAD. c2) Gluconolactonase (EC 3.1.1.17) is an enzyme that catalyzes the chemical reaction glucono-1 ,5-lactone + H2O D-gluconate (equation 9)

Thus, the two substrates of this enzyme are D-glucono-1 , 5-lactone and H2O, whereas its product is D-gluconate. This enzyme belongs to the family of hydrolases, specifically those acting on carboxylic ester bonds. The systematic name of this enzyme class is D-glucono-1 , 5-lactone lactonohydrolase. Other names in common use include lactonase, aldonolactonase, glucono-delta- lactonase, and gulonolactonase. This enzyme participates in the pentose phosphate pathway. c3) Gluconate kinase or gluconokinase (EC 2.7.1.12) is an enzyme that catalyzes the chemical reaction: ATP + D-gluconate v^ADP + 6-phospho-D-gluconate

(Equation 10)

Thus, the two substrates of this enzyme are ATP and D-gluconate, whereas its two products are ADP and 6-phospho-D-gluconate.

This enzyme belongs to the family of transferases, specifically those transferring phosphorus- containing groups (phosphotransferases) with an alcohol group as acceptor. The systematic name of this enzyme class is ATP:D-gluconate 6-phosphotransferase. Other names in common use include gluconokinase (phosphorylating), and gluconate kinase. This enzyme participates in pentose phosphate pathway. d) acetaldehyde dehydrogenase (acetylatinq) (EC 1.2.1.10). The cell of the invention may further comprise an exogenous gene coding for an enzyme with the ability to reduce acetylCoA into acetaldehyde, which gene confers to the cell the ability to convert acetylCoA (and/or acetic acid) into ethanol. An enzyme with the ability to reduce acetylCoA into acetaldehyde is herein understood as an enzyme which catalyzes the reaction (ACDH; EC 1 .2.1.10): acetaldehyde + NAD ⁺ + Coenzyme A acetyl-Coenzyme A + NADH + H ⁺ . (Equation 1 1 )

Thus, the enzyme catalyzes the conversion of acetylCoA into acetaldehyde (and vice versa) and is also referred to as an (acetylating NAD-dependent) acetaldehyde dehydrogenase or an acetyl-CoA reductase. The enzyme may be a bifunctional enzyme which further catalyzes the conversion of acetaldehyde into ethanol (and vice versa; see below). For convenience we shall refer herein to an enzyme having at least the ability to reduce acetylCoA into either acetaldehyde or ethanol as an "acetaldehyde dehydrogenase". It is further understood herein that the cell has endogenous alcohol dehydrogenase activities which allow the cell, being provided with acetaldehyde dehydrogenase activity, to complete the conversion of acetyl-CoA into ethanol. Further the cell has endogenous or exogenous acetyl-CoA synthetase, which allows the cell, being provided with acetaldehyde dehydrogenase activity, to complete the conversion of acetic acid (via acetyl-CoA) into ethanol.

The exogenous gene may encode for a monofunctional enzyme having only acetaldehyde dehydrogenase activity (i.e. an enzyme only having the ability to reduce acetylCoA into acetaldehyde) such as e.g. the acetaldehyde dehydrogenase encoded by the E.coli mhpF gene or E. coli EutE gene (the part coding for acetaldehyde dehydrogenase activity). Suitable examples of prokaryotes comprising monofunctional enzymes with acetaldehyde dehydrogenase activity are provided in Table 5. The amino acid sequences of these monofunctional enzymes are available in public databases and can be used by the skilled person to design codon- optimized nucleotide sequences coding for the corresponding monofunctional enzyme.

Table 5: Suitable enzymes with acetaldehyde dehydrogenase activity and identity to E.co// ^" mhpF

Organism Amino acid

identity (%)

Escherichia coli str. K12 substr. MG1655 100%

Shigella sonnei 100%

Escherichia coli IAI39 99%

Citrobacter youngae ATCC 29220 93% Organism Amino acid

identity (%)

Citrobacter sp. 30_2 92%

Klebsiella pneumoniae 342) 87%

Klebsiella variicola 87%

Pseudomonas putida 81 %

Ralstonia eutropha J MP 134 82%

Burkholderia sp. H160 81 %

Azotobacter vinelandii DJ 79%

Ralstonia metallidurans CH34 70%

Xanthobacter autotrophicus Py2 67%

Burkholderia cenocepacia J2315 68%

Frankia sp. EAN 1 pec 67%

Polaromonas sp. JS666 68%

Burkholderia phytofirmans PsJN 70%

Rhodococcus opacus B4 64%

In an embodiment, the cell comprises an exogenous gene coding for a bifunctional enzyme with acetaldehyde dehydrogenase and alcohol dehydrogenase activity, which gene confers to the cell the ability to convert acetylCoA into ethanol. The advantage of using a bifunctional enzyme with acetaldehyde dehydrogenase and alcohol dehydrogenase activities as opposed to separate enzymes for each of the acetaldehyde dehydrogenase and alcohol dehydrogenase activities, is that it allows for direct channeling of the intermediate between enzymes that catalyze consecutive reactions in a pathway offers the possibility of an efficient, exclusive, and protected means of metabolite delivery. Substrate channeling thus decreases transit time of intermediates, prevents loss of intermediates by diffusion, protects labile intermediates from solvent, and forestalls entrance of intermediates into competing metabolic pathways. The bifunctional enzyme therefore allows for a more efficient conversion of acetylCoA into ethanol as compared to the separate acetaldehyde dehydrogenase and alcohol dehydrogenase enzymes. A further advantage of using the bifunctional enzyme is that it may also be used in cells having little or no alcohol dehydrogenase activity under the condition used, such as e.g. anaerobic conditions and/or conditions of catabolite repression.

Bifunctional enzymes with acetaldehyde dehydrogenase and alcohol dehydrogenase activity are known in the art. The may be present in prokaryotes and protozoans, including e.g. the bifunctional enzymes encoded by the Escherichia coli adhE and Entamoeba histolytica ADH2 genes (see e.g. Bruchaus and Tannich, 1994, J. Biochem., 303: 743-748; Burdette and Zeikus, 1994, J. Biochem. 302: 163-170; Koo et al., 2005, Biotechnol. Lett. 27: 505-510; Yong et al., 1996, Proc Natl Acad Sci USA, 93: 6464-6469). Bifunctional enzymes with acetaldehyde dehydrogenase and alcohol dehydrogenase activity are larger proteins consisting of around 900 amino acids and they are bifunctional in that they exhibit both acetaldehyde dehydrogenase (ACDH; EC 1.2.1.10) and alcohol dehydrogenase activity (ADH; EC 1.1.1.1 ). The E. coli adhE and Entamoeba histolytica ADH2 show 45% amino acid identity. Suitable examples of bifunctional enzymes with acetaldehyde dehydrogenase and alcohol dehydrogenase activity and identity to E.coli adhE are given in table 6. Suitable examples of bifunctional enzymes with acetaldehyde dehydrogenase and alcohol dehydrogenase activity and identity to Entamoeba histolytica ADH2 are given in table 7.

Table 6: Suitable bifunctional enzymes with acetaldehyde dehydrogenase and alcohol dehydrogenase activity and identity to E.coli adhE

Organism Amino acid

identity (%)

Escherichia coli 0157:1-17 str. Sakai 100%

Shigella sonnei 100%

Shigella dysenteriae 1012 99%

Klebsiella pneumoniae 342 97%

Enterobacter sp. 638 94%

Yersinia pestis biovar Microtus str. 91001 90%

Serratia proteamaculans 568 90%

Pectobacterium carotovorum \NPP'\ 4 90%

Sodalis glossinidius str. 'morsitans' 87%

Erwinia tasmaniensis Et1 99 86% Organism Amino acid

identity (%)

Aeromonas hydrophila ATCC 7966 81 %

Vibrio vulnificus YJ016] 76%

Table 7: Suitable bifunctional enzymes with acetaldehyde dehydrogenase and alcohol dehydrogenase activity and identity to Entamoeba histolytica ADH2

Table 8: Suitable enzymes with acetaldehyde dehydrogenase and alcoholdehydroqenase activity and identity to E.coli EutE

Organism Amino acid identity (%)

Escherichia coli (EutE) 100%

Escherichia coli 01 '57. Ή7 99%

Shigella boydi 98%

Salmonella typhimurium 94% Organism Amino acid identity (%)

Salmonella enterica subsp. enterica 94%

serovar

Weltevreden

Salmonella choleraesuis 93%

Citrobacter youngae 93%

Klebsiella pneumoniae subsp. pneumoniae 92%

Yersinia intermedia 80%

Photobacterium profundum 59%

Bilophila wadsworthia 60%

Shewanelia benthica 58%

Thermincola potens 51 %

Acetonema longum 50%

For expression of the nucleotide sequence encoding the bifunctional enzyme having acetaldehyde dehydrogenase and alcohol dehydrogenase activities, or the enzyme having acetaldehyde dehydrogenase activity, the nucleotide sequence (to be expressed) is placed in an expression construct wherein it is operably linked to suitable expression regulatory regions/sequences to ensure expression of the enzyme upon transformation of the expression construct into the cell of the invention (see above). Suitable promoters for expression of the nucleotide sequence coding for the enzyme having the bifunctional enzyme having acetaldehyde dehydrogenase and alcohol dehydrogenase activities, or the enzyme having acetaldehyde dehydrogenase activity include promoters that are preferably insensitive to catabolite (glucose) repression, that are active under anaerobic conditions and/or that preferably do not require xylose or arabinose for induction. Examples of such promoters are given above.

Preferably, the nucleotide sequence encoding the bifunctional enzyme having acetaldehyde dehydrogenase and alcohol dehydrogenase activities, or the enzyme having acetaldehyde dehydrogenase activity is adapted to optimize its codon usage to that of the cell in question (as described above). e) acetyl-CoA synthetase (EC 6.2.1.1);

The cell of the invention may comprise a gene coding for an enzyme that has the specific activity of Acetyl-CoA synthetase. Acetyl-CoA synthetase or Acetate-CoA ligase is an enzyme (EC 6.2.1.1 ) involved in metabolism of carbon sugars. It is in the ligase class of enzymes, meaning that it catalyzes the formation of a new chemical bond between two large molecules.

The two molecules joined by acetyl-CoA synthetase are acetate and coenzyme A (CoA). The reaction with the substrates and products included is:

Acetate + CoA γ— Pyrophosphate + Acetyl-CoA (Equation 12) The Acs1 form and the Acs2 form of acetyl-CoA synthetase are encoded by the genes ACS1 and ACS2 respectively.

Suitable examples of enzymes with acetyl-CoA synthetase activity are provided in Table 9. Table 9: Suitable ACS's with identity to ACS2 protein of Saccharomyces cerevisiae.

f) disruption of one or more aldehyde dehydrogenase (E.C. 1.2.1.4) native in the eukaryotic cell. The enzyme that may be disrupted according to the invention is an aldehyde dehydrogenase aldehyde dehydrogenase (E.C:1.2.1.4) native in the eukaryotic cell.

In an embodiment the aldehyde dehydrogenase native in the eukaryotic cell is acetaldehyde dehydrogenase-6 (ALD6). ALD6 is herein any Mg2+ activated enzyme that catalyses the dehydrogenation of acetaldehyde into acetate, and vice-versa.

The reaction that is catalyzed by ALD6 is:

Acetaldehyde+ NAD7NADP ⁺ + H ₂ 0 <— -ALD6 > acetate + NAD/NADPH

(Equation 13)

The enzyme ALD6 in equation 13, generates NADPH and acetate. For that reason, in context of this invention, the disruption or deletion of ALD6 is a preferred embodiment.

A further advantage of deletion of ALD6 is apparent if the strain according to the invention comprises an acetylating acetaldehyde dehydrogenase (e.g., adhE or acdH) (see d) and WO2015028583 and WO2015028582)). Combination of acetylating acetaldehyde dehydrogenase and ALD6 in a eukaryotic cell according to the invention may lead to a futile cycle that consumes ATP. Deletion of ALD6 breaks the futile cycle, so that the ATP consumption by the futile cycle is avoided. In an embodiment of the invention the eukaryotic cell an ALD6 of Saccharomyces cerevisiae is deleted. This is illustrated in figure 4.

Suitable ALD6 nucleotide sequences for disruption with identity to the ALD6 nucleotide sequence of Saccharomyces cerevisiae in other eukaryotic cells are given in table 10.

Table 10: Suitable ALD6 nucleotide sequences for disruption occurring in different types of eukaryotic cell

Species and strain Accession % ID

number aldehyde dehydrogenase (NADP(+)) ALD6 NP_015264.1 100

[Saccharomyces cerevisiae S288c]

Ald6p [Saccharomyces cerevisiae AWRI796] EGA72659.1 99

Aldehyde dehydrogenase 6 CCD31406.1 97 Species and strain Accession % ID

number

[Saccharomyces cerevisiae x Saccharomyces kudriavzevii] hypothetical protein NDAI_0E02900 XP_003670350.1 80

[Naumovozyma dairenensis CBS 421] magnesium-activated aldehyde dehydrogenase BAP69922.1 74

[Kluyveromyces marxianus DMKU3-1042] aldehyde dehydrogenase (NAD+) XP_01 1273253.1 63

[Wickerhamomyces ciferrii] aldehyde dehydrogenase [Brettanomyces bruxellensis EIF46557.1 56

AWRI 1499] [Dekkera bruxellensis AWRI1499]

q) a modification that leads to reduction of glycerol 3-phosphate phosphohydrolase and/or glycerol 3-phosphate dehydrogenase activity

The eukaryotic cell further may further comprise a modification that leads to reduction of glycerol 3-phosphate phosphohydrolase and/or glycerol 3-phosphate dehydrogenase activity, compared to the eukaryotic cell without such modification.

In that embodiment, the cell may comprises a disruption of one or more endogenous nucleotide sequence encoding a glycerol 3-phosphate phosphohydrolase and/or encoding a glycerol 3-phosphate dehydrogenase gene. In such embodiment the enzymatic activity needed for the NADH-dependent glycerol synthesis is reduced or deleted. The reduction or deleted of this enzymatic activity can be achieved by modifying one or more genes encoding a NAD-dependent glycerol 3-phosphate dehydrogenase activity (GPD) or one or more genes encoding a glycerol phosphate phosphatase activity (GPP), such that the enzyme is expressed considerably less than in the wild-type or such that the gene encoded a polypeptide with reduced activity.

Such modifications can be carried out using commonly known biotechnological techniques, and may in particular include one or more knock-out mutations or site-directed mutagenesis of promoter regions or coding regions of the structural genes encoding GPD and/or GPP. Alternatively, eukaryotic cell strains that are defective in glycerol production may be obtained by random mutagenesis followed by selection of strains with reduced or absent activity of GPD and/or GPP. S. cerevisiae GPD1, GPD2, GPP1 and GPP2 genes are shown in WO201 1010923, and are disclosed in SEQ ID NO: 24-27 of that application.

Thus, in the cells of the invention, the specific glycerol 3-phosphate phosphohydrolase and/or encoding a glycerol 3-phosphate dehydrogenase gene may be reduced. In the cells of the invention, the specific glycerolphosphate dehydrogenase activity is preferably reduced by at least a factor 0.8, 0.5, 0.3, 0.1 , 0.05 or 0.01 as compared to a strain which is genetically identical except for the genetic modification causing the reduction in specific activity, preferably under anaerobic conditions. Glycerolphosphate dehydrogenase activity may be determined as described by Overkamp et al. (2002, Eukaryotic cell 19:509-520).

A preferred gene encoding a glycerolphosphate dehydrogenase whose activity is to be reduced or inactivated in the cell of the invention is the S. cerevisiae GPD1 as described by van den Berg and Steensma (1997, Eukaryotic cell 13:551-559), encoding the amino acid sequence GPD1 and orthologues thereof in other species.

Suitable examples of an enzyme with glycerolphosphate dehydrogenase activity belonging to the genus Saccharomyces, Naumovozyna, Candida Vanderwaltozyma and Zygosaccharomyces are provided in Table 1 1.

Table 11 : Suitable enzymes with glycerolphosphate dehydrogenase (GPD1) activity characterized by organism source and amino-acid identity to S. cervisiae glycerolphosphate dehydrogenase (GPD1)

However, in some strains e.g. of Saccharomyces, Candida and Zygosaccharomyces a second gene encoding a glycerolphosphate dehydrogenase is active, i.e. the GPD2, Another preferred gene encoding a glycerolphosphate dehydrogenase whose activity is to be reduced or inactivated in the cell of the invention therefore is an S. cerevisiae GPD2, encoding the amino acid sequence GPD2 and orthologues thereof in other species.

Suitable examples of organisms (hosts) comprising an enzyme with glycerolphosphate dehydrogenase activity belonging to the genus (Zygo)Saccharomyces and Candida are provided in Table 12.

Table 12: Suitable enzymes with glycerol phosphate dehydrogenase (GPD2) activity characterized by organism source and amino-acid identity to S. cervisiae glycerolphosphate dehydrogenase (GPD2)

In an embodiment, the cell is a eukaryotic cell wherein the genome of the eukaryotic cell comprises a mutation in at least one gene selected from the group of GPD1, GPD2, GPP1 and GPP2, which mutation may be a knock-out mutation, which knock-out mutation may be a complete deletion of at least one of said genes in comparison to the eukaryotic cell's corresponding wild-type eukaryotic cell gene.

h) Xylose isomerase (E.C. 5.3.1.5).

In an embodiment, the eukaryotic cell may comprise a xylose isomerase ((E.C. 5.3.1.5); xylA).

A "xylose isomerase" (E.C. 5.3.1 .5) is herein defined as an enzyme that catalyses the direct isomerisation of D-xylose into D-xylulose and/or vice versa. The enzyme is also known as a D-xylose ketoisomerase. A xylose isomerase herein may also be capable of catalysing the conversion between D-glucose and D-fructose (and accordingly may therefore be referred to as a glucose isomerase). Generally a xylose isomerase requires a bivalent cation, such as magnesium, manganese or cobalt as a cofactor. I) Arabinose pathway enzymes (L-arabinose isomerase (araA) , L-ribulokinase (araB), and L- ribulose-5-phosphate 4-epimerase (araD)) In an embodiment, the cell comprised genes that express enzymes of an L-arabinose fermentation pathway. EP 1 499 708 discloses the construction of a L-arabinose-fermenting strain by overexpression of the L-arabinose pathway. In the pathway,

the enzymes L-arabinose isomerase (araA) , L-ribulokinase (araB), and L-ribulose-5- phosphate 4-epimerase (araD) are involved converting L-arabinose to L-ribulose, Lribulose- 5-P, and D-xylulose-5-P, respectively. j) Glycerol dehydrogenase (EC 1.1.1.6)

A glycerol dehydrogenase is herein understood as an enzyme that catalyzes the chemical reaction (EC 1.1 .1.6): glycerol + NAD ⁺ glycerone + NADH + H ⁺ (Equation 14) Other names in common use include glycerin dehydrogenase, NAD ⁺ -linked glycerol dehydrogenase and glycerol:NAD+ 2-oxidoreductase. Preferably the genetic modification causes overexpression of a glycerol dehydrogenase, e.g. by overexpression of a nucleotide sequence encoding a glycerol dehydrogenase. The nucleotide sequence encoding the glycerol dehydrogenase may be endogenous to the cell or may be a glycerol dehydrogenase that is heterologous to the cell. Nucleotide sequences that may be used for overexpression of glycerol dehydrogenase in the cells of the invention are e.g. the glycerol dehydrogenase gene from S. cerevisiae (GCY1) as e.g. described by Oechsner et al. (1988, FEBS Lett. 238: 123-128) or Voss et al. (1997, Eukaryotic cell 13: 655-672).

k) one or more nucleotide sequence encoding a homologous or heterologous dihydroxyacetone kinase (E.C. 2.7.1.28 or E.C. 2.7.1.29)

A dihydroxyacetone kinase is herein understood as an enzyme that catalyzes one of the chemical reactions:

EC ADP + D-glyceraldehyde phosphate

M .29 ATP + glycerone <=> ADP + glycerone

O

phosphate HO. A .OH

(Equation 15)

Glycerone = dihydroxyacetone.

Other names in common use include glycerone kinase, ATP:glycerone phosphotransferase and

(phosphorylating) acetol kinase. It is understood that glycerone and dihydroxyacetone are the same molecule. Preferably the genetic modification causes overexpression of a dihydroxyacetone kinase, e.g. by overexpression of a nucleotide sequence encoding a dihydroxyacetone kinase. The nucleotide sequence encoding the dihydroxyacetone kinase may be endogenous to the cell or may be a dihydroxyacetone kinase that is heterologous to the cell. Nucleotide sequences that may be used for overexpression of dihydroxyacetone kinase in the cells of the invention are e.g. the dihydroxyacetone kinase genes from S. cerevisiae (DAK1) and (DAK2) as e.g. described by Molin et al. (2003, J. Biol. Chem. 278:1415-1423).

Suitable examples of enzymes with glycerol dehydrogenase activity are provided in Table 13. Table 13: Suitable GCY's with identity to GCY1 protein of Saccharomyces cerevisiae GCY1.

Suitable examples of enzymes with dihydroxy acetone kinase activity are provided in Table 14.

Table 14: Suitable DAK's with identity to DAK1 protein of Saccharomyces cerevisiae.

Description Identity (%) Accession number

Dak1 p [Saccharomyces cerevisiae S288c] 100 NP_013641 .1 dihydroxyacetone kinase [Saccharomyces cerevisiae 99 EDN64325.1 YJM789]

DAK1-like protein [Saccharomyces kudriavzevii IFO 1802] 95 EJT44075.1

ZYBA0S1 1-03576g1_1 [Zygosaccharomyces bailii CLIB 77 CDF91470.1 213] hypothetical protein [Kluyveromyces lactis NRRL Y-1 140] 70 XP_451751 .1 hypothetical protein [Candida glabrata CBS 138] 63 XP_449263.1

Dak2p [Saccharomyces cerevisiae S288c] 44 NP_1 16602.1 Other embodiments of the invention are now described in more detail.

The invention further relates to a eukaryotic cell as described herein in fermentation in the wine industry.

In another embodiment the invention relates to the use of the eukaryotic cell as described herein in fermentation in the biofuel industry.

Further the invention relates to a process for the fermentation of a substrate to produce a fermentation product with an eukaryotic as described herein, in the wine biofuel industry, wherein the acetate consumption is at least 10%, at least 20%, or at least 25% increased relative to the corresponding fermentation with wild-type eukaryotic cell. In an embodiment thereof, the ethanol yield is at least about 0.5 %, or at least 1 % higher than that of a process with the corresponding wild-type eukaryotic cell. In such process, preferably pentose and glucose are co-fermented. In such process a hydrolysate of lignocellulosic material may be fermented. The hydrolysate may be an enzymatic hydrolysate of lignocellulosic material. Such hydrolysate may comprise acetate. The acetate comprising hydrolysate may have an acetate concentration of 0.3% (w/w) or more. The eukaryotic cell may contain genes of a pentose metabolic pathway non-native to the eukaryotic cell and/or that allow the eukaryotic cell to convert pentose(s). In one embodiment, the eukaryotic cell may comprise one or two or more copies of one or more xylose isomerases and/or one or two or more copies of one or more xylose reductase and xylitol dehydrogenase genes, allowing the eukaryotic cell to convert xylose. In an embodiment thereof, these genes may be integrated into the eukaryotic cell genome. In another embodiment, the eukaryotic cell comprises the genes araA, araB and araD. It is then able to ferment arabinose. In one embodiment of the invention the eukaryotic cell comprises xy/A-gene, XYL1 gene and XYL2 gene and/or XKS7-gene, to allow the eukaryotic cell to ferment xylose; deletion of the aldose reductase (GRE3) gene; overexpression of PPP-genes, TALI, TKL1, RPE1 and RKI1 to allow the increase of the flux through the pentose phosphate path-way in the cell, and/or overexpression of GAL2 and/or deletion of GAL80. Thus though inclusion of the above genes, suitable pentose or other metabolic pathway(s) may be introduced in the eukaryotic cell that were non-native in the (wild type) eukaryotic cell. According to an embodiment, the following genes may be introduced in the eukaryotic cell by introduction into a host cell:

1 ) a set consisting of PPP-genes TALI, TKL1, RPE1 and RKI1, optionally under control of strong constitutive promoter;

2) a set consisting of a xy/A-gene under under control of strong constitutive promoter;

3) a set comprising a KS7-gene under control of strong constitutive promoter,

4) a set consisting of the genes araA, araB and araD under control of a strong constitutive promoter 5) deletion of an aldose reductase gene

The above cells may be constructed using known recombinant expression techniques. The co- factor modification may be effected before, simultaneous or after any of the modifications 1 )-5).

The eukaryotic cell according to the invention may be subjected to evolutionary engineering to improve its properties. Evolutionary engineering processes are known processes. Evolutionary engineering is a process wherein industrially relevant phenotypes of a microorganism, herein the eukaryotic cell, can be coupled to the specific growth rate and/or the affinity for a nutrient, by a process of rationally set-up natural selection. Evolutionary Engineering is for instance described in detail in Kuijper, M, et al, FEMS Eukaryotic cell Research 5(2005) 925-934, WO2008041840 and WO20091 12472. After the evolutionary engineering the resulting pentose fermenting eukaryotic cell is isolated. The isolation may be executed in any known manner, e.g. by separation of cells from a eukaryotic cell broth used in the evolutionary engineering, for instance by taking a cell sample or by filtration or centrifugation.

In an embodiment, the eukaryotic cell is marker-free. As used herein, the term "marker" refers to a gene encoding a trait or a phenotype which permits the selection of, or the screening for, a host cell containing the marker. Marker-free means that markers are essentially absent in the eukaryotic cell. Being marker-free is particularly advantageous when antibiotic markers have been used in construction of the eukaryotic cell and are removed thereafter. Removal of markers may be done using any suitable prior art technique, e.g. intramolecular recombination. In one embodiment, the industrial eukaryotic cell is constructed on the basis of an inhibitor tolerant host cell, wherein the construction is conducted as described hereinafter. Inhibitor tolerant host cells may be selected by screening strains for growth on inhibitors containing materials, such as illustrated in Kadar et al, Appl. Biochem. Biotechnol. (2007), Vol. 136-140, 847-858, wherein an inhibitor tolerant S. cerevisiae strain ATCC 26602 was selected. The eukaryotic cell further may comprise those enzymatic activities required for conversion of pyruvate to a desired fermentation product, such as ethanol, butanol (e.g. n-butanol, 2-butanol and isobutanol), lactic acid, 3 -hydroxy- propionic acid, acrylic acid, acetic acid, succinic acid, citric acid, fumaric acid, malic acid, itaconic acid, an amino acid, 1 ,3-propane-diol, ethylene, glycerol, a β-lactam antibiotic or a cephalosporin. In an embodiment, the eukaryotic cell is derived from an industrial eukaryotic cell. An industrial cell and industrial eukaryotic cell may be defined as follows. The living environments of (eukaryotic cell) cells in industrial processes are significantly different from that in the laboratory. Industrial eukaryotic cells must be able to perform well under multiple environmental conditions which may vary during the process. Such variations include change in nutrient sources, pH, ethanol concentration, temperature, oxygen concentration, etc., which together have potential impact on the cellular growth and ethanol production of Saccharomyces cerevisiae. Under adverse industrial conditions, the environmental tolerant strains should allow robust growth and production. Industrial eukaryotic cell strains are generally more robust towards these changes in environmental conditions which may occur in the applications they are used, such as in the baking industry, brewing industry, wine making and the biofuel ethanol industry. In one embodiment, the industrial eukaryotic cell is constructed on the basis of an industrial host cell, wherein the construction is conducted as described hereinafter. Examples of industrial eukaryotic cell (S. cerevisiae) are Ethanol Red® (Fermentis) Fermiol® (DSM) and Thermosacc® (Lallemand).

The eukaryotic cells according to the invention are preferably inhibitor tolerant, i.e. they can withstand common inhibitors at the level that they typically have with common pretreatment and hydrolysis conditions, so that the eukaryotic cells can find broad application, i.e. it has high applicability for different feedstock, different pretreatment methods and different hydrolysis conditions. In an embodiment the eukaryotic cell is inhibitor tolerant. Inhibitor tolerance is resistance to inhibiting compounds. The presence and level of inhibitory compounds in lignocellulose may vary widely with variation of feedstock, pretreatment method hydrolysis process. Examples of categories of inhibitors are carboxylic acids, furans and/or phenolic compounds. Examples of carboxylic acids are lactic acid, acetic acid or formic acid. Examples of furans are furfural and hydroxy- methylfurfural. Examples or phenolic compounds are vannilin, syringic acid, ferulic acid and coumaric acid. The typical amounts of inhibitors are for carboxylic acids: several grams per liter, up to 20 grams per liter or more, depending on the feedstock, the pretreatment and the hydrolysis conditions. For furans: several hundreds of milligrams per liter up to several grams per liter, depending on the feedstock, the pretreatment and the hydrolysis conditions. For phenolics: several tens of milligrams per liter, up to a gram per liter, depending on the feedstock, the pretreatment and the hydrolysis conditions.

In an embodiment, the eukaryotic cell is a cell that is naturally capable of alcoholic fermentation, preferably, anaerobic alcoholic fermentation. A eukaryotic cell preferably has a high tolerance to ethanol, a high tolerance to low pH (i.e. capable of growth at a pH lower than about 5, about 4, about 3, or about 2.5) and towards organic and/or a high tolerance to elevated temperatures.

Further the invention relates to a process for the fermentation of a substrate to produce a fermentation product with an eukaryotic cell as described herein, in the wine industry, wherein the glycerol yield is at least 5%, at least 10% or at least 10%, at least 20% or at least 30% higher than that of a process with the corresponding wild-type eukaryotic cell. In an embodiment of such process, the ethanol yield is not increased or decreased, compared to that of a process with the corresponding wild- type eukaryotic cell.

Any of the above characteristics or activities of a eukaryotic cell may be naturally present in the cell or may be introduced or modified by genetic modification. Recombinant expression

The eukaryotic cell is a recombinant cell. That is to say, a eukaryotic cell comprises, or is transformed with or is genetically modified with a nucleotide sequence that does not naturally occur in the cell in question. Techniques for the recombinant expression of enzymes in a cell, as well as for the additional genetic modifications of a eukaryotic cell are well known to those skilled in the art. Typically such techniques involve transformation of a cell with nucleic acid construct comprising the relevant sequence. Such methods are, for example, known from standard handbooks, such as Sambrook and Russel (2001 ) "Molecular Cloning: A Laboratory Manual (3rd edition), Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, or F. Ausubel ef a/., eds., "Current protocols in molecular biology", Green Publishing and Wiley Interscience, New York (1987). Methods for transformation and genetic modification of fungal host cells are known from e.g. EP-A- 0635 574, WO 98/46772, WO 99/60102, WO 00/37671 , WO90/14423, EP-A-0481008, EP-A-0635574 and US 6,265, 186.

Bioproducts production Over the years suggestions have been made for the introduction of various organisms for the production of bio-ethanol from crop sugars. In practice, however, all major bio-ethanol production processes have continued to use the eukaryotic cells of the genus Saccharomyces as ethanol producer. This is due to the many attractive features of Saccharomyces species for industrial processes, i. e. , a high acid-, ethanol-and osmo- tolerance, capability of anaerobic growth, and of course its high alcoholic fermentative capacity. Preferred eukaryotic cell species as host cells include S. cerevisiae, S. bulderi, S. barnetti, S. exiguus, S. uvarum, S. diastaticus, K. lactis, K. marxianus or K. fragilis.

A eukaryotic cell may be a cell suitable for the production of ethanol. A eukaryotic cell may, however, be suitable for the production of fermentation products other than ethanol

Such non-ethanolic fermentation products include in principle any bulk or fine chemical that is producible by a eukaryotic microorganism such as a eukaryotic cell or a filamentous fungus.

A preferred eukaryotic cell for production of non-ethanolic fermentation products is a host cell that contains a genetic modification that results in decreased alcohol dehydrogenase activity Liqnocellulose

Lignocellulose, which may be considered as a potential renewable feedstock, generally comprises the polysaccharides cellulose (glucans) and hemicelluloses (xylans, heteroxylans and xyloglucans). In addition, some hemicellulose may be present as glucomannans, for example in wood- derived feedstocks. The enzymatic hydrolysis of these polysaccharides to soluble sugars, including both monomers and multimers, for example glucose, cellobiose, xylose, arabinose, galactose, fructose, mannose, rhamnose, ribose, galacturonic acid, glucoronic acid and other hexoses and pentoses occurs under the action of different enzymes acting in concert.

In addition, pectins and other pectic substances such as arabinans may make up considerably proportion of the dry mass of typically cell walls from non-woody plant tissues (about a quarter to half of dry mass may be pectins).

Pretreatment

Before enzymatic treatment, the lignocellulosic material may be pretreated. The pretreatment may comprise exposing the lignocellulosic material to an acid, a base, a solvent, heat, a peroxide, ozone, mechanical shredding, grinding, milling or rapid depressurization, or a combination of any two or more thereof. This chemical pretreatment is often combined with heat-pretreatment, e.g. between 150-220 °C for 1 to 30 minutes.

Enzymatic hydrolysis

The pretreated material is commonly subjected to enzymatic hydrolysis to release sugars that may be fermented according to the invention. This may be executed with conventional methods, e.g. contacting with cellulases, for instance cellobiohydrolase(s), endoglucanase(s), beta-glucosidase(s) and optionally other enzymes, The conversion with the cellulases may be executed at ambient temperatures or at higher tempatures, at a reaction time to release sufficient amounts of sugar(s). The result of the enzymatic hydrolysis is hydrolyisis product comprising C5/C6 sugars, herein designated as the sugar composition.

The sugar composition

The sugar composition used according to the invention comprises glucose and one or more pentose, e.g. arabinose and/or xylose. Any sugar composition may be used in the invention that suffices those criteria. Optional sugars in the sugar composition are galactose and mannose. In a preferred embodiment, the sugar composition is a hydrolysate of one or more lignocellulosic material. Lignocelllulose herein includes hemicellulose and hemicellulose parts of biomass. Also lignocellulose includes lignocellulosic fractions of biomass. Suitable lignocellulosic materials may be found in the following list: orchard primings, chaparral, mill waste, urban wood waste, municipal waste, logging waste, forest thinnings, short-rotation woody crops, industrial waste, wheat straw, oat straw, rice straw, barley straw, rye straw, flax straw, soy hulls, rice hulls, rice straw, corn gluten feed, oat hulls, sugar cane, corn stover, corn stalks, corn cobs, corn husks, switch grass, miscanthus, sweet sorghum, canola stems, soybean stems, prairie grass, gamagrass, foxtail; sugar beet pulp, citrus fruit pulp, seed hulls, cellulosic animal wastes, lawn clippings, cotton, seaweed, trees, softwood, hardwood, poplar, pine, shrubs, grasses, wheat, wheat straw, sugar cane bagasse, corn, corn husks, corn hobs, corn kernel, fiber from kernels, products and by-products from wet or dry milling of grains, municipal solid waste, waste paper, yard waste, herbaceous material, agricultural residues, forestry residues, municipal solid waste, waste paper, pulp, paper mill residues, branches, bushes, canes, corn, corn husks, an energy crop, forest, a fruit, a flower, a grain, a grass, a herbaceous crop, a leaf, bark, a needle, a log, a root, a sapling, a shrub, switch grass, a tree, a vegetable, fruit peel, a vine, sugar beet pulp, wheat midlings, oat hulls, hard or soft wood, organic waste material generated from an agricultural process, forestry wood waste, or a combination of any two or more thereof.

An overview of some suitable sugar compositions derived from lignocellulose and the sugar composition of their hydrolysates is given in table 15. The listed lignocellu loses include: corn cobs, corn fiber, rice hulls, melon shells, sugar beet pulp, wheat straw, sugar cane bagasse, wood, grass and olive pressings.

Table 15: Overview of sugar compositions from lignocellulosic materials. Gal=galactose, Xyl=xylose, Ara=arabinose, Man=mannose, Glu=glutamate, Rham=rhamnose. The percentage galactose (% Gal) and literature source is given.

It is clear from table 15 that in these lignocelluloses a high amount of sugar is present in the form of glucose, xylose, arabinose and galactose. The conversion of glucose, xylose, arabinose and galactose to fermentation product is thus of great economic importance. Also mannose is present in some lignocellulose materials be it usually in lower amounts than the previously mentioned sugars. Advantageously therefore also mannose is converted by the eukaryotic cell. It is expected that eukaryotic cells of the present invention can be further manipulated to achieve other desirable characteristics, or even higher overall ethanol yields.

Selection of improved eukaryotic cells by passaging the eukaryotic cells on medium containing hydrolysate has resulted in improved eukaryotic cell with enhanced fermentation rates. Using the teachings of the present invention, one could readily such improved strains. By pentose-containing material, it is meant any medium comprising pentose, whether liquid or solid. Suitable pentose-containing materials include hydrolysates of polysaccharide or lignocellulosic biomass such as corn hulls, wood, paper, agricultural byproducts, and the like.

By a "hydrolysate" as used herein, it is meant a polysaccharide that has been depolymerized through the addition of water to form mono and oligosaccharide sugars. Hydrolysates may be produced by enzymatic or acid hydrolysis of the polysaccharide-containing material.

Preferably, the eukaryotic cell is able to grow under conditions similar to those found in industrial sources of pentose. The method of the present invention would be most economical when the pentose- containing material can be inoculated with the eukaryotic cell variant without excessive manipulation. By way of example, the pulping industry generates large amounts of cellulosic waste. Saccharification of the cellulose by acid hydrolysis yields hexoses and pentoses that can be used in fermentation reactions. However, the hydrolysate or sulfite liquor contains high concentrations of sulfite and phenolic inhibitors naturally present in the wood which inhibit or prevent the growth of most organisms. The examples below describe the fermentation of pentose in acid hydrolysates (or sulfite waste liquor) of hard woods and soft woods by the eukaryotic cells of the present invention. It is reasonably expected that eukaryotic cell strains capable of growing in sulfite waste liquor could grow be expected grow in virtually any other biomass hydrolysate.

Propagation

The invention further relates to a process for aerobic propagation of the acetate consuming eukaryotic cell, in particular aerobic propagation of the eukaryotic cell strain. Propagation is herein any process of eukaryotic cell growth that leads to increase of an initial eukaryotic cell population. Main purpose of propagation is to increase a eukaryotic cell population using the eukaryotic cell's natural reproduction capabilities as living organisms. There may be other reasons for propagation, for instance, in case dry eukaryotic cell is used, propagation is used to rehydrate and condition the eukaryotic cell, before it is grown. Fresh eukaryotic cell, whether active dried eukaryotic cell or wet cake may be added to start the propagation directly.

The conditions of propagation are critical for optimal eukaryotic cell production and subsequent fermentation, such as for example fermentation of lignocellulosic hydrolysate into ethanol. They include adequate carbon source, aeration, temperature and nutrient additions. Tank size for propagation and is normally between 2 percent and 5 percent of the (lignocellulosic hydrolysate to ethanol) fermentor size.

In the propagation the eukaryotic cell needs a source of carbon. The source of carbon may herein comprise glycerol, ethanol, acetate and/or sugars (C6 and C5 sugars). Other carbon sources may also be used. The carbon source is needed for cell wall biosynthesis and protein and energy production.

Propagation is an aerobic process, thus the propagation tank must be properly aerated to maintain a certain level of dissolved oxygen. Adequate aeration is commonly achieved by air inductors installed on the piping going into the propagation tank that pull air into the propagation mix as the tank fills and during recirculation. The capacity for the propagation mix to retain dissolved oxygen is a function of the amount of air added and the consistency of the mix, which is why water is often added at a ratio of between 50:50 to 90: 10 mash to water. "Thick" propagation mixes (80:20 mash-to-water ratio and higher) often require the addition of compressed air to make up for the lowered capacity for retaining dissolved oxygen. The amount of dissolved oxygen in the propagation mix is also a function of bubble size, so some ethanol plants add air through spargers that produce smaller bubbles compared to air inductors. Along with lower glucose, adequate aeration is important to promote aerobic respiration, which differs from the comparably anaerobic environment of fermentation. One sign of inadequate aeration or high glucose concentrations is increased ethanol production in the propagation tank.

Generally during propagation, eukaryotic cell requires a comfortable temperature for growth and metabolism, for instance the temperature in the propagation reactor is between 25-40 degrees Celcius. Generally lower temperatures result in slower metabolism and reduced reproduction, while higher temperatures can cause production of stress compounds and reduced reproduction. In an embodiment the propagation tanks are indoors and protected from the insult of high summer or low winter temperatures, so that maintaining optimum temperatures of between within the range of 30-35 degrees C is usually not a problem.

Further propagation may be conducted as propagation of eukaryotic cell is normally conducted. Fermentation

The invention relates to a process for the fermentation of a eukaryotic cell according to the invention, wherein there is an improved yield of glycerol, which is advantageous in the wine industry. It also may result in increased reduction of acetate level and/or increased yield of fermentation product, e.g. ethanol, which is advantageous in the biofuel industry.

In an embodiment, the eukaryotic cell according to the invention may be a pentose and glucose fermenting eukaryotic cell, including but not limited to such cells that are capable of anaerobic simultaneous pentose and glucose consumption. In an embodiment of the process the pentose- containing material comprises a hydrolysate of ligno-cellulosic material. The hydrolysate may be an enzymatic hydrolysate of ligno-cellulosic material.

The fermentation process may be an aerobic or an anaerobic fermentation process. An anaerobic fermentation process is herein defined as a fermentation process run in the absence of oxygen or in which substantially no oxygen is consumed, preferably less than about 5, about 2.5 or about 1 mmol/L/h, more preferably 0 mmol/L/h is consumed (i.e. oxygen consumption is not detectable), and wherein organic molecules serve as both electron donor and electron acceptors. In the absence of oxygen, NADH produced in glycolysis and biomass formation, cannot be oxidised by oxidative phosphorylation. To solve this problem many microorganisms use pyruvate or one of its derivatives as an electron and hydrogen acceptor thereby regenerating NAD ⁺ .

Thus, in a preferred anaerobic fermentation process pyruvate is used as an electron (and hydrogen acceptor) and is reduced to fermentation products such as ethanol, butanol, lactic acid, 3 - hydroxy-propionic acid, acrylic acid, acetic acid, succinic acid, malic acid, fumaric acid, an amino acid and ethylene.

The fermentation process is preferably run at a temperature that is optimal for the cell. Thus, for most eukaryotic cells or fungal host cells, the fermentation process is performed at a temperature which is less than about 50°C, less than about 42°C, or less than about 38°C. For eukaryotic cell or filamentous fungal host cells, the fermentation process is preferably performed at a temperature which is lower than about 35, about 33, about 30 or about 28°C and at a temperature which is higher than about 20, about 22, or about 25°C.

The ethanol yield on xylose and/or glucose in the process preferably is at least about 50, about 60, about 70, about 80, about 90, about 95 or about 98%. The ethanol yield is herein defined as a percentage of the theoretical maximum yield.

The invention also relates to a process for producing a fermentation product. The fermentation process according to the present invention may be run under aerobic and anaerobic conditions. In an embodiment, the process is carried out under micro-aerophilic or oxygen limited conditions.

An anaerobic fermentation process is herein defined as a fermentation process run in the absence of oxygen or in which substantially no oxygen is consumed, preferably less than about 5, about 2.5 or about 1 mmol/L/h, and wherein organic molecules serve as both electron donor and electron acceptors.

An oxygen-limited fermentation process is a process in which the oxygen consumption is limited by the oxygen transfer from the gas to the liquid. The degree of oxygen limitation is determined by the amount and composition of the ingoing gasflow as well as the actual mixing/mass transfer properties of the fermentation equipment used. Preferably, in a process under oxygen-limited conditions, the rate of oxygen consumption is at least about 5.5, more preferably at least about 6, such as at least 7 mmol/L/h. A process of the invention may comprise recovery of the fermentation product.

In a preferred process the cell ferments both the xylose and glucose, preferably simultaneously in which case preferably a cell is used which is insensitive to glucose repression to prevent diauxic growth. In addition to a source of xylose (and glucose) as carbon source, the fermentation medium will further comprise the appropriate ingredient required for growth of the cell. Compositions of fermentation media for growth of microorganisms such as eukaryotic cells are well known in the art

The fermentation processes may be carried out in batch, fed-batch or continuous mode. A separate hydrolysis and fermentation (SHF) process or a simultaneous saccharification and fermentation (SSF) process may also be applied. A combination of these fermentation process modes may also be possible for optimal productivity. These processes are described hereafter in more detail.

SSF mode

For Simultaneous Saccharification and Fermentation (SSF) mode, the reaction time for liquefaction/hydrolysis or presaccharification step is dependent on the time to realize a desired yield, i.e. cellulose to glucose conversion yield. Such yield is preferably as high as possible, preferably 60% or more, 65% or more, 70% or more, 75% or more 80% or more, 85% or more, 90% or more, 95% or more, 96% or more, 97% or more, 98% or more, 99% or more, even 99.5% or more or 99.9% or more.

According to the invention very high sugar concentrations in SHF mode and very high product concentrations (e.g. ethanol) in SSF mode are realized. In SHF operation the glucose concentration is 25g/L or more, 30 g/L or more, 35g/L or more, 40 g/L or more, 45 g/L or more, 50 g/L or more, 55 g/L or more, 60 g/L or more, 65 g/L or more, 70 g/L or more , 75 g/L or more, 80 g/L or more, 85 g/L or more, 90 g/L or more, 95 g/L or more, 100 g/L or more, 1 10 g/L or more, 120g/L or more or may e.g. be 25g/L-250 g/L, 30gl/L-200g/L, 40g/L-200 g/L, 50g/L-200g/L, 60g/L-200g/L, 70g/L-200g/L, 80g/L-200g/L, 90 g/L-200g/L.

Product concentration in SSF mode

In SSF operation, the product concentration (g/L) is dependent on the amount of glucose produced, but this is not visible since sugars are converted to product in the SSF, and product concentrations can be related to underlying glucose concentration by multiplication with the theoretical mamimum yield (Yps max in gr product per gram glucose)

The theoretical maximum yield (Yps max in gr product per gram glucose) of a fermentation product can be derived from textbook biochemistry. For ethanol, 1 mole of glucose (180 gr) yields according to normal glycolysis fermentation pathway in eukaryotic cell 2 moles of ethanol (=2x46 = 92 gr ethanol. The theoretical maximum yield of ethanol on glucose is therefore 92/180 = 0.51 1 gr ethanol/gr glucose.

For Butanol (MW 74 gr/mole) or iso butanol, the theoretical maximum yield is 1 mole of butanol per mole of glucose. So Yps max for (iso-)butanol = 74/180 = 0.41 1 gr (iso-)butanol/gr glucose. For lactic acid the fermentation yield for homolactic fermentation is 2 moles of lactic acid (MW

= 90 gr/mole) per mole of glucose. According to this stoichiometry, the Yps max = 1 gr lactic acid/gr glucose.

Similar calculation may be made for C5/C6 fermentations, in which in addition to glucose also pentoses are included e.g. xylose and/or arabinose. For other fermentation products a similar calculation may be made.

SSF mode

In SSF operation the product concentration is 25g * Yps g/L /L or more, 30 * Yps g/L or more, 35g * Yps /L or more, 40 * Yps g/L or more, 45 * Yps g/L or more, 50 * Yps g/L or more, 55 * Yps g/L or more, 60 * Yps g/L or more, 65 * Yps g/L or more, 70 * Yps g/L or more , 75 * Yps g/L or more, 80 * Yps g/L or more, 85 * Yps g/L or more, 90 * Yps g/L or more, 95 * Yps g/L or more, 100 * Yps g/L or more, 1 10 * Yps g/L or more, 120g/L * Yps or more or may e.g. be 25 * Yps g/L-250 * Yps g/L, 30 * Yps gl/L- 200 * Yps g/L, 40 * Yps g/L-200 * Yps g/L, 50 * Yps g/L-200 * Yps g/L, 60 * Yps g/L-200 * Yps g/L, 70 * Yps g/L-200 * Yps g/L, 80 * Yps g/L-200 * Yps g/L, 90 * Yps g/L , 80 * Yps g/L-200 * Yps g/L

Accordingly, the invention provides a method for the preparation of a fermentation product, which method comprises: a. degrading lignocellulose using a method as described herein; and b. fermenting the resulting material, thereby to prepare a fermentation product. Fermentation product

The fermentation product of the invention may be any useful product. In one embodiment, it is a product selected from the group consisting of ethanol, n-butanol, 2-butanol, isobutanol, lactic acid, 3- hydroxy-propionic acid, acrylic acid, acetic acid, succinic acid, fumaric acid, malic acid, itaconic acid, maleic acid, citric acid, adipic acid, an amino acid, such as lysine, methionine, tryptophan, threonine, and aspartic acid, 1 ,3-propane-diol, ethylene, glycerol, a β-lactam antibiotic and a cephalosporin, vitamins, pharmaceuticals, animal feed supplements, specialty chemicals, chemical feedstocks, plastics, solvents, fuels, including biofuels and biogas or organic polymers, and an industrial enzyme, such as a protease, a cellulase, an amylase, a glucanase, a lactase, a lipase, a lyase, an oxidoreductases, a transferase or a xylanase.

Recovery of the fermentation product

For the recovery of the fermentation product existing technologies are used. For different fermentation products different recovery processes are appropriate. Existing methods of recovering ethanol from aqueous mixtures commonly use fractionation and adsorption techniques. For example, a beer still can be used to process a fermented product, which contains ethanol in an aqueous mixture, to produce an enriched ethanol-containing mixture that is then subjected to fractionation (e.g., fractional distillation or other like techniques). Next, the fractions containing the highest concentrations of ethanol can be passed through an adsorber to remove most, if not all, of the remaining water from the ethanol. In an embodiment in addition to the recovery of fermentation product, the yeast may be recycled.

The following non-limiting examples are intended to be purely illustrative.

EXAMPLES

Example 1

1. Materials and Methods

1.1. Strains and maintenance All S. cerevisiae strains used in this appl. (Table 16) are based on the CEN.PK lineage (van

Dijken et al. 2000). Stock cultures of S. cerevisiae were propagated in synthetic medium (Verduyn et al. 1992), or YP medium (10 g L Bacto yeast extract, 20 g L Bacto peptone). 20 g L glucose was supplemented as carbon source in the above media. Stock cultures of E.coli DH5a were propagated in LB medium (10 g L ^~ Bacto tryptone, 5 g L ^~ Bacto yeast extract, 5 g L ^~ NaCI), supplemented with 100 μg ml ^-1 ampicillin or 50 μg ml ^-1 kanamycin. Frozen stocks of strains were stored at -80°C, after addition of 30% v/v glycerol to stationary phase cultures.

Table 16. S. cerevisiae strains used in this study.

Strain name Relevant Genotype Origin

CEN.PK1 13-7D MATa MAL2-8 ⁰ SUC2 P. Kotter

IMX585 MATa MAL2-8c SUC2 can1::cas9-natNT2 Maris et al. 2015

IMK643 MATa MAL2-8c SUC2 canl ::cas9-natNT2 gnd2A This appl.

MATa MAL2-8c SUC2 can1::cas9-natNT2 gnd2A

IMX705 This appl.

gnd1::gndA

IMX706 MATa MAL2-8c SUC2 canl ::cas9-natNT2 gnd2A This appl.

gnd1::6pgdh

IMX707 MATa MAL2-8c SUC2 can1::cas9-natNT2 gnd2A This appl.

gnd1:gox1705

IMX756 MATa MAL2-8c SUC2 can1::cas9-natNT2 gnd2A This appl.

gnd1::gndA ald6A

IMX817 MATa MAL2-8c SUC2 can1::cas9-natNT2 gnd2A This appl.

gnd1::gndA ald6A gpd2::eutE

IMX860 MATa MAL2-8c SUC2 can1::cas9-natNT2 gnd2A This appl.

gnd1::gndA ald6A gpd2::eutE gpdIA Strain name Relevant Genotype Origin

IMX883 MATa MAL2-8c SUC2 canl ::cas9-natNT2 gpd2::eutE This appl.

IMX888 MATa MAL2-8c SUC2 canl ::cas9-natNT2 gpd2::eutE This appl.

gpdIA

IMX899 MATa MAL2-8c SUC2 canl::cas9-natNT2 ald6A This appl.

1.2. Plasmid and cassette construction

Yeast genetic modifications were performed using the chimeric CRISPR/Cas9 genome editing system (DiCarlo et al. 2013). Plasmid pMEL1 1 (Mans et al. 2015) was used for single deletions of GND1, GND2 and ALD6. Plasmid pROS1 1 (Mans et al. 2015) was used for single deletions of GPD1 and GPD2. Unique CRISPR/Cas9 target sequences in each gene were identified based on the sequence list provided by (DiCarlo et al. 2013). Primers that are used herein are SEQ ID NO's 10-46, with their primer no.'s given. The plasmid backbone of pMEL1 1 and pROS1 1 were PCR amplified using primer combinations 5792-5980 and 5793-5793 respectively (Sigma-Aldrich). Plasmid insert sequences, expressing the 20 bp gRNA targeting sequence, were obtained by PCR with primer combinations 5979- 7365 for GND1, 5979-7231 for GND2 and 5979-7610 for ALD6 using pMEL1 1 as a template. Insert sequences expressing the gRNA sequences targeting GPD1 and GPD2 were obtained by PCR using primer combinations 6965-6965 and 6966-6966 respectively, with pROS1 1 as template. PCR amplifications for the construction of all plasmids and cassettes were performed using Phusion® Hot Start II High Fidelity DNA Polymerase (Thermo Scientific, Waltham, MA), according to the manufacturer's guidelines. In cases where plasmids were pre-assembled the Gibson Assembly® Cloning kit (New England Biolabs, MA) was used; reactions were performed according to the supplier's protocol (downscaled to 10 μΙ). The assembly was enabled by homologous sequences at the 5' and 3' ends of the generated PCR fragments. The assembly of the pMEL1 1 backbone and the insert sequences coding for the gRNAs targeting GND1 and GND2 yielded plasmids pUDR122 and pUDR123 respectively. In each case 1 μΙ of the Gibson Assembly Mix was used for electroporation of E. coli DH5a cells in a Gene PulserXcell Electroporation System (Biorad). Plasmids were re-isolated from E. coli cultures using a Sigma GenElute Plasmid kit (Sigma-Aldrich). Validation of the plasmids was performed by diagnostic PCR (Dreamtaq®, Thermo Scientific) or restriction analysis. A complete list of all plasmids used can be found in Table 17. The ALD6, GPD1 and GPD2 gRNA expressing plasmids were not pre- assembled; the backbone and insert fragments were transformed directly to yeast and the plasmids were assembled in vivo in each case.

Sequences of Methylobacillus flagellatus KT gndA (AF167580_1 ), Gluconobacter oxydans 621 H gox1705 (AAW61445.1 ) and Bradyrhizobium japonicum USDA 1 10 6pgdh were codon optimized based on the codon composition of highly expressed glycolytic genes. In the case of B. japonicum the sequence of 6pgdh was obtained by aligning its translated genomic sequence (NC_004463.1 ) with the other two proteins (45% and 57% similarity respectively). Yeast integration cassettes of the above genes were flanked by the promoter of TPI1 and the terminator of CYC1. The complete cassettes, including promoter, gene and terminator sequences, were synthesized by GeneArt GmbH (Regensburg, Germany) and delivered in pMK-RQ vectors (GeneArt). After cloning in E.coli the plasmids were re- isolated and used as templates for PCR amplification of the integration cassettes. The integration cassettes TPHp-gndA-CYCH, TPI1p-6pgdH-CYC1i and TPI1p-gox1705-CYC1i were obtained by PCR using primer combination 7380-7381 and plasmids pMK-RQ-gndA, pMK-RQ-6pgdH and pMK-RQ- gox1705 respectively as templates. For the gox1705 protein the K _m NADP+ is 440 μΜ and K _m NAD+ is 64 μΜ, so that the ratio K _m NADP+/ K _m NAD+ = 6.88. The gox1705 protein is NAD+ dependent.

A S. cerevisiae codon pair optimized et/iEwas obtained from pBOL199 by Xhol/Spel restriction cut and ligated in pAG426GPD-ccdB (Addgene, Cambridge, MA), yielding the multi-copy plasmid pUDE197. For integration cassette preparation a Sacl/Eagl cut pRS406 (Addgene, Cambridge, MA) was used as plasmid backbone and ligated with the cassette of TDH3p-eutE-CYC1t obtained by same restriction pattern from pUDE197, yielding plasmid pUDI076.

The integration cassette TDH3p-eutE-CYC1t was obtained using primer combination 7991- 7992 and plasmid pUDI076 as template. The above primers were designed to add 60 bp of DNA sequence on the 5' and 3' ends of the PCR products, corresponding to the sequences directly upstream and downstream of the open reading frame of the targeted loci in the genome of S. cerevisiae. The TPHp-gndA-CYCn, TPI1p-6pgdH-CYC1i and TPI1p-gox1705-CYC1i expressing cassettes were targeted to the locus of GND1 and the TDH3p-eutE-CYC1t cassette was targeted to the locus of GPD2.

Table 17. Plasmids used in this study.

Name Characteristics Origin pBOL199 Delivery vector, p42Q-TDH3p-eutE (Muller et al. 2010)

2 \\m ori, amdS, SNR52p-gRNA.CAN1 Ύ- pMEL1 1 (Mans et al. 2015)

SUP4i pROS1 1 AmdSYM-gRNA.CAN1-2mu-gRNA.ADE2 (Mans et al. 2015) pUDE197 2 μπι ori, p426-TDH3p-eutE-CYC1t This appl.

PUDI076 pRS406-TDH3p-eutE-CYC1t This appl. Name Characteristics Origin

2 [im ori, amdS, SNR52p-gRNA.GND2.Y- pUDR-122 This appl.

SUP4i

2 [im ori, amdS, SA/R52p-g RN A. GND 1.Y-

PUDR123 This appl.

SUP4i pMK-RQ-gndA Delivery vector, TPI1p-gndA-CYC1t GeneArt, Germany pMK-RQ-6pgdH Delivery vector, TPI1p-6pgdh-CYC1i GeneArt, Germany pMK-RQ-

Delivery vector, TPI1p-gox1705-CYC1i GeneArt, Germany

gox1705

1.3. Strain construction

Yeast transformations were performed using the lithium acetate method (Gietz and Woods, 2002). Selection of mutants was performed on synthetic medium agar plates (2% Bacto Agar, Difco) (Verduyn et al. 1992) supplemented with 20 g L glucose and with acetamide as the sole nitrogen source, as described in (Solis-Escalante et al. 2013). In each case, confirmation of successful integrations was performed by diagnostic PCR using primer combinations binding outside the targeted loci as well as inside the ORFs of the integrated cassettes. Plasmid recycling after each transformation was executed as described in (Solis-Escalante et al. 2013). Strain IMK643 was obtained by markerless CRISPR/Cas9 based knockout of GND2 by co- transformation of the gRNA expressing plasmid pUDR123 and the repair oligo nucleotides 7299-7300. The TPHp-gndA-CYCn, TPI1p-6pgdH-CYC1i and TPI1p-gox1705-CYC1i integration cassettes were transformed to IMK643, along with the gRNA expressing plasmid pUDR122, yielding strains IMX705, IMX706 and IMX707 respectively. Co-transformation of the pMEL1 1 backbone, the ALD6 targeting gRNA expressing plasmid insert and the repair oligo nucleotides 7608-7609 to strains IMX705 and IMX585 yielded strains IMX756 and IMX899 respectively, in which ALD6 was deleted without integration of a marker. Co-transformation of the pROS1 1 backbone, the GPD2 targeting gRNA expressing plasmid insert and the TDH3p-eutE-CYC1t integration cassette to strains IMX756 and IMX585 yielded strains IMX817 and IMX883 respectively. Markerless deletion of GPD1 in strains IMX817 and IMX883 was performed by co-transformation of the pROS1 1 backbone, the GPD1 targeting gRNA expressing plasmid insert and the repair oligo-nucleotides 6967-6968, yielding strains IMX860 and IMX888 respectively. 1.4. Cultivation and media

Aerobic shake flask cultivations were performed in 500 ml flasks containing 100 ml of synthetic minimal medium (Verduyn et al. 1992), supplemented with 20 g L glucose. The pH value was adjusted to 6 by addition of 2 M KOH before sterilisation by autoclaving at 120°C for 20 min. Glucose solutions were autoclaved separately at 1 10°C for 20 min and added to the sterile flasks. Vitamin solutions were filter sterilized and added to the sterile flasks separately. Cultures were grown at 30°C and 200 rpm. Initial pre-culture shake flasks were inoculated from frozen stocks in each case. After 8-12h, fresh pre- culture flasks were inoculated from the initial flasks. Cultures prepared this way were used in aerobic shake flask experiments or as inoculum for anaerobic fermentations. Bioreactors were inoculated to an OD value of 0.2-0.3 from exponentially growing pre-culture flasks. Anaerobic batch fermentations were performed in 2L Applikon bioreactors (Applikon, Schiedam, NL), with a 1 L working volume. All anaerobic batch fermentations were performed in synthetic minimal medium (20 g L glucose), prepared in the same way as the flask media. Anaerobic growth media were additionally supplemented with 0.2 g L sterile antifoam C (Sigma-Aldrich), ergosterol (10 mg L ) and Tween 80 (420 mg L ), added separately. Fermentations were performed at 30°C and stirred at 800 rpm. Nitrogen gas (<10 ppm oxygen) was used for sparging (0.5 L min ^-1 ). Fermentation pH was maintained at 5 by automated addition of 2M KOH. Bioreactors were equipped with Nonprene tubing and Viton O-rings to minimize oxygen diffusion in the medium. All fermentations were performed in duplicate.

1.5. Analytical methods Determination of optical density at 660 nm was done using a Libra S1 1 spectrophotometer

(Biochrom, Cambridge, UK). Off-gas analysis, dry weight measurements and HPLC analysis of culture supernatant, including corrections for ethanol evaporation, were performed as described in (Medina et al. 2010).

1.6. Enzymatic activity determination Preparation of cell free extracts for in vitro determination of enzymatic activities was executed as described previously (Kozak et al. 2014). Assays were performed at 30°C; enzymatic activity was measured by monitoring the reduction of NAD7NADP ⁺ (for 6PGDH) or oxidation of NADH at 340 nm (for EutE). The NADP ⁺ linked glucose- 6-phosphate dehydrogenase activity assay mix contained 50 mM Tris-HCI (pH 8.0), 5 mM of MgCI ₂ , 0.4 mM of NADP ⁺ and 50 or 100 μΙ of cell extract in a total volume of 1 ml. The reaction was started by addition of 5 mM of glucose-6-phosphate. The NAD ⁺ / NADP ⁺ linked 6-phosphogluconate dehydrogenase activity assay mixes contained 50 mM Tris-HCI (pH 8.0), 5 mM of MgCk, 0.4 mM of NAD ⁺ / NADP ⁺ respectively and 50 or 100 μΙ of cell extract in a total volume of 1 ml. Reactions were started by addition of 5 mM of 6-phosphogluconate. All assays were performed in duplicate and reaction rates were proportional to the amount of cell extract added. 1.7 Expression of a heterologous NAD* dependent 6-phosphogluconate dehydrogenase To change the co-factor specificity of 6-phosphogluconate dehydrogenase from NADP ⁺ to NAD ⁺ GND1 and GND2, encoding for the major and the minor isoform of the enzyme in S. cerevisiae respectively, were deleted. Heterologous genes encoding for NAD ⁺ dependent (M. flagellatus and B. japonicum) or NAD ⁺ preferring (G. oxydans) enzymes were codon optimized for expression in S. cerevisiae and integrated in the locus of GND1, under the control of the strong constitutive promoter of TPI1. Growth experiments performed in aerobic synthetic medium shake flasks (20 g L glucose) with the engineered strains did not indicate a significant effect of the overexpression of the heterologous genes on the maximum specific growth rate compared to the parental strain IMX585 (growth rate was app. 95% of the parental strain), with the exception of IMX706, expressing the enzyme from B. japonicum (Table 18).

Table 18. Average specific growth rates (μ) obtained in aerobic synthetic medium shake flasks (pH 6) containing 20 g L ¹ glucose (experiments performed in duplicate, mean deviations from duplicates are indicated), 30°C, 200 rpm.

To investigate functional expression of the heterologous 6-phosphogluconate dehydrogenase enzymes in S. cerevisiae enzymatic assays were performed in cell free extracts, prepared from exponentially growing aerobic shake flask cultures of the engineered strains (harvested at OD 4-5). Assays were performed for quantification of glucose-6-phosphate dehydrogenase activity, as well as NAD ⁺ and NADP ⁺ dependent 6-phosphogluconate dehydrogenase activities. Determination of glucose- 6-phosphate dehydrogenase activity was performed as a quality check of the cell free extracts, the enzymatic activity determinations demonstrated functional glucose-6-phosphate dehydrogenase and 6- phosphogluconate dehydrogenase in all generated strains (Figure 1 ). All engineered strains showed high NAD ⁺ and low residual NADP ⁺ dependent 6PGDH activities, in line with the expected functional expression of the heterologous enzymes and deletion of GND1 and GND2. Strain IMX705, expressing gndA from Methylobacillus flagellatus, showed the highest in vitro NAD ⁺ -dependent 6- phosphogluconate dehydrogenase activity (0.49 ± 0.1 μιηοΙ mg biomass ^"1 min ^~1 ). Furthermore, all engineered strains showed a significant increase in the ratio of NAD7NADP ⁺ linked 6-phosphogluconate dehydrogenase activities when compared to the control strain IMX585 (Table 18). In addition to the highest in vitro NAD ⁺ -dependent 6-phosphogluconate dehydrogenase activity, strain IMX705 also showed the highest ratio of all engineered strains (46 ± 10).

Table 18A. NAD7NADP ⁺ linked specific 6-phosphogluconate dehydrogenase activity ratios of cell free extracts from exponentially growing shake flask cultures, harvested at OD = 4 to 5. Cultures were grown in synthetic medium supplemented with 20 g L ¹ glucose, pH 6, 30°C, 200 rpm. Data from independent duplicate experiments, error bars indicate mean deviations of the duplicates.

The enzymatic assay results pointed towards the strain expressing gndA being the best performing strain; for this reason strain IMX705 was characterized further.

1.8 Anaerobic batch experiments Results from the enzymatic assays pointed towards a successful co-factor specificity change of

6-phosphogluconate dehydrogenase from NADP ⁺ to NAD ⁺ .

To investigate the effect of the co-factor specificity change of 6-phosphogluconate dehydrogenase on the anaerobic physiology of S. cerevisiae, anaerobic batch experiments were performed in bioreactors. Strains IMX585 (GND1 GND2) and IMX705 (gnd2A gnd1::gndA) were grown in synthetic medium supplemented with 20 g L glucose. The growth rate of the engineered strain IMX705 was similar to the reference strain (ca. 95% of IMX585 (Table 19)). In addition, sugar consumption profiles were comparable, with glucose being exhausted after ca. 12 hours (Figure 2). The anaerobic batch with strain IMX705 resulted in a 19.8% increased glycerol yield on glucose compared to IMX585 (Table 19). Additionally, the amount of glycerol formed per biomass in the fermentation with strain IMX705 was 24.1 % higher than the one with strain IMX585. In the anaerobic fermentations of strain IMX705, an increase of ca. 9% in the production of extracellular acetate per biomass formed was observed, compared to the reference strain IMX585 (Table 19). The increase in extracellular acetate could have been a result of up-regulation of the cytosolic NADP ⁺ -dependent aldehyde dehydrogenase which catalyses the reaction acetaldehyde + NADP ⁺ - acetate + NADPH + H ⁺ , encoded by ALD6. Along with the oxidative branch of the pentose phosphate pathway, Ald6p provides another major route for NADPH regeneration in the cytosol of the cells. It has been demonstrated that overexpression of ALD6 in a zwfIA strain results in increased growth rates on glucose; furthermore, zwfIA ald6A double mutants are not viable. Furthermore, in a scenario where the glycerol formation pathway in strain IMX705 has been replaced by the acetate reduction one, Ald6p can interfere with the generation of additional NADH in the cytosol by participating in a ATP driven transhydrogenase-like cycle in the cytosol (Figure 3). In this cycle, 1 mol acetate is converted to 1 mol acetyl-CoA via the reaction catalysed by Acs1 p and Acs2p, at the net expense of 2 mol ATP. The 1 mol acetyl-CoA is then reduced to 1 mol acetaldehyde via the reaction catalysed by acetylating acetaldehyde dehydrogenase, with a concomitant oxidation of 1 mol NADH to NAD ⁺ . The 1 mol acetaldehyde can then be oxidized back to 1 mol acetate via Ald6p, with a concomitant reduction of 1 mol of NADP ⁺ to NADPH. In this way both co-factors can be regenerated at the expense of ATP. Removal of the reaction catalysed by Ald6p prevents this potential cycle from taking place.

In wild type strains, the reaction catalysed by Ald6p is important for NADPH generation as well as the formation of acetate, which is a precursor of acetyl-CoA. In the ald6A strain IMX756, acetate can potentially be formed by the reactions catalysed by the cytosolic Ald2p and Ald3p or by the mitochondrial Ald4p and Ald5p isoforms. Ald2p and Ald3p are NAD ⁺ dependent and the formation of acetate required for growth through the reactions catalysed by these enzymes will likely result in additional formation of cytosolic NADH. Ald4p can utilize both NAD ⁺ and NADP ⁺ as cofactors. Nicotinamide cofactors cannot generally cross the inner mitochondrial membrane. In anaerobically grown cultures of S. cerevisiae, re- oxidation of NADH produced by acetate formation catalysed by Ald4p would require the transfer of reducing equivalents across the mitochondrial membrane. This could for example be accomplished via mitochondrial shuttle systems, such as the acetaldehyde-ethanol shuttle, which transfer reducing equivalents to cytosolic NAD ⁺ . The excess cytosolic NADH can then be re-oxidized via increased glycerol formation. In order to remove the alternative NADPH regeneration route catalysed by Ald6p, ALD6 was deleted in strain IMX705 yielding strain IMX756. We have found a deletion of ALD6 is potentially beneficial to the generation of an acetate consuming strain, as it can remove a potential ATP-driven transhydrogenase like reaction in the cytoplasm of the cells, created by Acs1 p / Acs2p, EutEp and Ald6p (Figure 4). To investigate the effect of Ald6p on the anaerobic physiology of wild type S. cerevisiae, ALD6 was also deleted in strain IMX585 yielding strain IMX899.

Strains IMX899 and IMX756 were characterized in anaerobic batch experiments, under the same conditions as the batches performed with strains IMX585 and IMX705. The growth rates of IMX899 and IMX756 were ca. 90% and 81 % of the growth rate of reference strain IMX585. Extracellular acetate formation was severely impacted in the early stages of the fermentations, and its concentration dropped to below detection levels in the later stages (data not shown) in fermentations with both strains. The anaerobic batch with strain IMX899 resulted in an increase of 1 % in the glycerol yield on glucose and of 5.3% in glycerol formed per biomass compared to the reference strain IMX585 (Table 19A), indicating a minor effect of the deletion in the generation of additional cytosolic NADH. However, the fermentation with strain IMX756, in which the deletion of ALD6 was combined with the overexpression of gndA and the deletions of GND1 and GND2, resulted in an increase of 39% in the glycerol yield on glucose and of 55% in glycerol formed per biomass formed compared to the reference strain IMX585 (Table 19A).

This study provides proof of principle that different heterologous, NAD ⁺ dependent 6- phosphogluconate dehydrogenases can be functionally expressed in S. cerevisiae. Furthermore, overexpression of gndA in a gndIA gnd2A strain resulted in an increase in glycerol formation per biomass formed, which points to an increase in cytosolic NADH formation per biomass formed. Further deletion of ALD6 in strain IMX705 showed a marked increase of the glycerol yield on glucose, as well as glycerol formation per biomass formed in anaerobic cultures of the mutant strain compared to the control. The engineering strategies caused only a minor decrease in the maximum specific growth rates of the mutant strains. This indicates that this strategy could be directly applied to industrial strains and potentially be used to increase acetic acid consumption in hydrolysates. Table 19. Maximum specific growth rates (μ), major product yields and ratios of glycerol and acetate formation per biomass formed. Data obtained from anaerobic batch fermentations performed in bioreactors, with strains IMX585, IMX705, IMX899 and IMX756. Fermentations were performed in synthetic medium supplemented with 20 g L ¹ glucose. Batches performed at pH 5, sparging of 500 ml min ¹ N ₂ , 30°C. Yields and ratios were calculated from data collected in the exponential growth phase, as the slopes of plots of the measured values. Calculation of ethanol yields was based on data corrected for evaporation. Data is presented as averages of independent duplicate experiments.

Strain IMX585 IMX705 IMX756 μ (h- ¹ ) 0.32 ± 0.00 0.30 ± 0.01 0.26 ± 0.01

Y glycerol/glucose (g/g) 0.106 ± 0.001 0.130 ± 0.002 0.144 ± 0.001

Y biomass/glucose (g/g) 0.094 ± 0.004 0.087 ± 0.002 0.083 ± 0.002

Y EtOH/glucose (g/g) 0.360 ± 0.01 0.368 ± 0.01 0.363 ± 0.02

Ratio glycerol formed/biomass

(g/g) 1.123 ± 0.04 1.394 ± 0.02 1.752 ± 0.05

Ratio acetate formed/biomass

(g/g) 0.090 ± 0.002 0.098 ± 0.001 Below detection limit

With taking ethanol evaporation into the calculation, with mmol instead of g for ratio calculations, and addition of data for IMX899, the data are given in table 19A:

Table 19A

Example 2

2.1 Co-factor specificity change of 6PGDH in combination with the acetate reducing

pathway

The combined change of the co-factor specificity of 6-phosphogluconate dehydrogenase from NADP ⁺ to NAD ⁺ and deletion of ALD6 in strain IMX756 resulted in a 37.7% increase in the glycerol yield on glucose compared to the control strain IMX585 in anaerobic batch fermentations. This result was in line with the estimated 40.5% increase in glycerol yield on glucose, in the scenario where excess NADH is generated in the cytosol based on the proposed strategy and the glycerol formation pathway is still intact. As the next step, the effect of the replacement of the glycerol formation pathway by the acetate reducing one on the amount of acetate that can be consumed by a strain with IMX756 as parental is investigated.

To replace the glycerol formation pathway by the acetate reduction one, GPD1 and GPD2 (encoding for glycerol-3-phosphate dehydrogenases) were deleted and eutE (encoded for E. coli acetylating acetaldehyde dehydrogenase) was overexpressed in strain IMX756, yielding strain IMX860. Furthermore, deletion of GPD1 and GPD2 and overexpression of eutE in IMX585 yielded the acetate reducing control strain IMX888.

In the acetate reducing strain IMX888 the 6-phosphogluconate dehydrogenase is NADP ⁺ dependent. Based on the theoretical analysis conducted herein, a consumption of 5.51 mmol acetate per gram biomass formed is expected for this strain, in anaerobic fermentations with glucose as the carbon source. In strain IMX860, in which the co-factor specificity is changed, a consumption of 8.75 mmol acetate per gram biomass formed is expected.

In this experiment, the effect of the engineering strategy proposed in this scenario in anaerobic acetate consumption is investigated. Strains IMX860 and IMX888 were grown in anaerobic fermentations in bioreactors, supplemented with 20 g L glucose and 3 g L acetic acid. Sparging, pH control as well as temperature were identical to the batches performed with strains IMX585, IMX705 and IMX756. Based on the theoretical analysis, an increase of 59% in acetate consumed per biomass formed is expected in strain IMX860 compared to IMX888. Furthermore, the engineering strategy in strain IMX860 should result in a theoretical increase of 3% in the ethanol yield on glucose compared to strain IMX888 and 22.4% compared to the wild type scenario. The results are given in Tables 20, 20A and 21. For Table 20A, calculation of acetate consumption increase on glucose and per biomass formed between strains IMX888 (using the Medina et al. 2010 strategy) and strain IMX860 (using the strategy in this example), the apparent consumption of the control strain IMX585 (which does not contain eutE) was subtracted from the calculated values. Table 20. Maximum specific growth rates, major product yields and ratios of acetate consumed on glucose consumed and biomass formed. Data obtained from anaerobic batch fermentations performed in bioreactors with strains IMX585, IMX888 and IMX860. Fermentations were performed in synthetic medium supplemented with 20 g L ¹ glucose and 3 g L ¹ acetic acid. Batches performed at pH 5, sparging of 500 ml min ¹ N ₂ , 30°C. Yields and ratios were calculated from data collected in the exponential growth phase. Calculation of ethanol yields was based on data corrected for evaporation. Data is presented as averages of independent duplicate experiments. Strain IMX585 IMX888 IMX860 μ (h- ¹ ) 0.28 ± 0.01 0.26 ± 0.01 0.20 ± 0.01

Y glycerol/glucose (g/g) 0.062 ± 0.000 N/D N/D

Y biomass/glucose (g/g) 0.076 ± 0.003 0.075 ± 0.000 0.077 ± 0.000

Y EtOH/glucose (g/g) 0.421 ± 0.001 0.460 ± 0.001 0.466 ± 0.002

Ratio acetate consumed/biomass

(g/g) 0.146 ± 0.006 0.424 ± 0.009 0.534 ± 0.002

Ratio acetate consumed/glucose (g/g) 0.009 ± 0.000 0.032 ± 0.000 0.41 ± 0.000

With taking ethanol evaporation into the calculation, and with mmol instead of g for ratio calculations and addition of glycerol/glucose (g g ^"1 ) data for IMX888 and IMX860, the data are given in table 20A.

Table 20A.

2.2. Co-factor specificity change of G6PDH on generation of additional cytosolic NADH and the acetate reducing pathway

Recently a NAD ⁺ dependent glucose-6-phosphate dehydrogenase, designated azf, has been characterized in the archaeon Haloferax volcanii (Pickl and Schonheit, 2015). In this example the effect of a co-factor change of glucose-6-phosphate dehydrogenase from NADP ⁺ to NAD ⁺ on the generation of additional cytosolic NADH per biomass formed, azf is overexpressed in a S. cerevisiae zwfIA background. Based on the theoretical analysis and the experiments conducted in this application, an identical theoretical impact as the co-factor change of 6-phosphogluconate dehydrogenase is expected.

The protein sequence of Azfp (ADE03728.1 ) from Haloferax volcanii DS2 is used to generate a yeast codon optimized version of azf, based on the composition of highly expressed glycolytic genes (Wiedemann and Boles, 2008). An overexpression cassette is synthesized, under the control of a strong constitutive glycolytic promoter and cloned in a plasmid. The plasmid is used as template to generate a PCR product in which the overexpression cassette is flanked by 60 bp homologous sequences to the direct upstream and downstream regions of ZWF1. The locus of ZWF1 is then deleted using the CRISPR/Cas9 system with the PCR product as the repair fragment, resulting in a zwf1..azf strain.

Determination of Azfp enzymatic activity in the zwflv.azf strain is performed as described previously (Pickl and Schonheit, 2015). Furthermore, the effect of the replacement of ZWF1 by azf on the aerobic maximum specific growth rate of the engineered strain is be investigated in an identical fashion to the way it was determined for strains IMX705, IMX706 and IMX707 in this application. The generated zwf1 : azf strain is characterized in anaerobic fermentations in bioreactors with

20 g L glucose as the carbon source and compared to its parental strain, as well as strain IMX705. The strain is expected to perform similarly to strain IMX705 in terms of glycerol yield on glucose and glycerol formation on biomass formed and have an increase of at least 22.6% on the glycerol yield on glucose compared to its parental, wild type strain. The zwf1 : azf strain is engineered further by deletion of GPD1 and GPD2 and introduction of eutE in the GPD2 locus, using the same steps as the case of the construction of strain IMX888. The relevant genotype of the resulting strain is gpdIA gpd2..eutE zwflv.azf.

In follow-up experiments, the effect of the engineering strategy proposed in this scenario on anaerobic acetate consumption is investigated. The gpdIA gpd2..eutE zwf1 : azf strain is grown in anaerobic fermentations in bioreactors, supplemented with 20 g L glucose and 3 g L acetic acid. Sparging, pH control as well as temperature is identical to the batches performed with strains IMX585, IMX705 and IMX756. Based on the theoretical analysis and similarly to strain IMX888, an increase of 59% in acetate consumed per biomass formed is expected in this strain compared to the acetate reducing strain IMX860, in which no co-factor change of glucose-6-phosphate dehydrogenase or 6- phosphogluconate dehydrogenase has been made.

2.2 Simultaneous co-factor specificity change of G6PDH and 6PGDH on generation of additional cytosolic NADH and the acetate reducing pathway

To investigate the effect of a simultaneous co-factor change of glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase from NADP ⁺ to NAD ⁺ on the generation of additional cytosolic NADH per biomass formed azfand gndA is overexpressed in a zwfIA gndIA gnd2A strain.

Generation of an azf overexpression cassette is performed as described previously in this application. Strain construction is performed identically to the one described for the zwf1v. azf strain. In this case, strain IMX705 is used as parental. The resulting relevant genotype of the generated strain is gnd2A gnd1::gndA zwf1..azf.

Determination of Azfp enzymatic activity in the zwflv.azf strain is performed as described previously (Pickl and Schonheit, 2015). Determination of GndAp enzymatic activity is performed as described in this application.

The generated gnd2A gnd1::gndA zwflv.azf strain is characterized in anaerobic fermentations in bioreactors with 20 g L glucose as the carbon source and compared to its parental strain IMX705, as well as strain IMX585 (no co-factor specificity change). In this scenario NADPH is mainly generated via the Ald6p catalysed reaction. The amount of additional NADH that is generated per biomass formed is determined by the flux of glucose through the oxidative part of the pentose phosphate pathway. In this scenario, assuming 100% specificity for NAD ⁺ , the flux through the oxidative part of the pentose phosphate is no longer coupled to NADPH generation. In a scenario where the enzymes preferably use NAD ⁺ , but also show activity towards NADP ⁺ , the flux through this pathway can still be correlated to NADPH provision. It is expected that the change of the co-factors of both glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase will result in an additional increase of formation of cytosolic NADH per biomass formed, when compared to the change of either co-factor alone.

The gnd2A gnd1::gndA zwflv.azf strain is engineered further by deletion of GPD1 and GPD2 and introduction of eutE in the GPD2 locus, using the same steps as the case of the construction of strain IMX888. The relevant genotype of the resulting strain is gpdIA gpd2::eutE gnd2A gnd1::gndA zwfl .azf.

In follow-up experiments, the effect of the engineering strategy proposed in this scenario in anaerobic acetate consumption is investigated. The gpdIA gpd2::eutE gnd2A gnd1::gndA zwflv.azf strain is grown in anaerobic fermentations in bioreactors, supplemented with 20 g L glucose and 3 g L acetic acid. Sparging, pH control as well as temperature is identical to the batches performed with strains IMX585, IMX705 and IMX756. An increased acetate consumption per biomass formed compared to strain IMX860 and the gpdIA gpd2veutE zwflv.azf \s expected in this case.

The advantages of strains according to the invention, as shown in the examples are summarized in table 21 ,

Table 21 Yield increase for ethanol and glycerol and acetate consumed with theoretically calculated values (between brackets), compared to wild-type strain and for acetate scenario (biofuel) and glycerol scenario (wine). Acetate scenario (bioethanol Glycerol scenario (wine)

fuel) compared to strain from compared to wild type strain Medina et al. 2010

Yield Ethanol on glucose 1.3% (3%) -0% (-4.5%)

Increase in %

Yield glycerol 38% (40.5%)

Increase in %

Acetate consumption (% 28% (59%)

increase (g acetate /g

biomass))

Biomass yield -13,2%(-1 1.5%)

From table 21 it is clear that substantial advantages may be obtained:

For application in biofuel industry 28% acetate consumption increase and 1.3% increase in ethanol yield is advantageous. For the application in the wine industry up to 38% increase of glycerol yield and same or lower ethanol production advantageous.

Based on the data and calculations of Tables 19A and 20A, like summary table 21 , is below summary table 21A:

Table 21A

From table 21 A it is clear that substantial advantages may be obtained:

For application in biofuel industry 44% acetate consumption increase per gram biomass formed and 3% increase in ethanol yield on glucose is advantageous.

For the application in the wine industry up to 39% increase of glycerol yield and same or lower ethanol production advantageous.

REFERENCES

Medina VG, Almering MJH, Van Maris AJA, Pronk JT. 2010. Elimination of glycerol production in anaerobic cultures of a Saccharomyces cerevisiae strain engineered to use acetic acid as an electron acceptor. Applied and Environmental Microbiology 76: 190-195. (Medina et al. 2010); van Dijken JP, Bauer J, Brambilla L, Duboc P, Francois JM, Gancedo C, Giuseppin MLF, Heijnen JJ, Hoare M, Lange HC, Madden EA, Niederberger P, Nielsen J, Parrou JL, Petit T, Porro D, Reuss M, van Riel N, Rizzi M, Steensma HY, Verrips CT, Vindel0v J, Pronk JT. 2000. An interlaboratory comparison of physiological and genetic properties of four Saccharomyces cerevisiae strains. Enzyme and Microbial Technology 26:706-714. (van Dijken et al. 2000); Verduyn C, Postma E, Scheffers WA, Van Dijken JP. 1992. Effect of benzoic acid on metabolic fluxes in yeasts: A continuous-culture study on the regulation of respiration and alcoholic fermentation. Yeast 8:501-517. (Verduyn et al. 1992);

Muller UM, Wu L, Raamsdonk LM, Winkler AA. Acetyl-coa producing enzymes in yeast. (Wiedemann and Boles, 2008); US 20100248233 A1 . Priority 30-9-2010. (Muller et al. 2010);

Gietz RD, Woods RA. 2002. Transformation of yeast by lithium acetate/single-stranded carrier DNA polyethylene glycol method. Methods in Enzymology 350:87-96. (Gietz and Woods, 2002);

Solis-Escalante D, Kuijpers NGA, Bongaerts N, Bolat I, Bosman L, Pronk JT, Daran JM, Daran- Lapujade P. 2013. amdSYM, a new dominant recyclable marker cassette for Saccharomyces cerevisiae. FEMS Yeast Res 13: 126-139. (Solis-Escalante et al. 2013);

DiCarlo JE, Norville JE, Mali P, Rios X, Aach J, Church GM. 2013. Genome engineering in

Saccharomyces cerevisiae using CRISPR-Cas systems. Nucleic Acids Research1-8. (DiCarlo et al. 2013);

Maris R, van Rossum HM, Wijsman M, Backx A, Kuijpers NG, van den Broek M, Daran-Lapujade P, Pronk JT, van Maris AJ, Daran JM. 2015. CRISPR/Cas9: a molecular Swiss army knife for simultaneous introduction of multiple genetic modifications in Saccharomyces cerevisiae. FEMS Yeast Research;15: fov004 (Maris et al. 2015);

Pickl et al. FEMS Biotechnology Letters, Volume 361 , Issue 1 , p. 76-83, December 2014:

Identification and characterization of 2-keto-3-deoxygluconate kinase and 2-keto-3-deoxygalactonate kinase in the haloarchaeon Haloferax volcanii (Pickl and Schonheid 2015).