The present invention is related to modified sterol acyltransferase enzymes with improved activity and/or specificity towards acylation of the vitamin D3 precursor 7-dehydrocholesterol (7-DHC) to be used in biotechnological production of vitamin D3. The invention further relates to a yeast strain expressing said modified enzymes and their use in a process for production of vitamin D3 or derivatives and/or metabolites thereof.

Vitamin D3 (also known as cholecalciferol or calciol) can be synthesized in the skin of mammals from provitamin D3 (also known as 7-dehydrocholesterol or 7- DHC) which is product of cholesterol biosynthesis upon exposure to UV light, whereby 7-DHC is photochemically converted into provitamin D3, which isomerizes at body temperature to the biologically active form vitamin D3. In the liver, vitamin D3 is converted to the biologically inactive 25-hydroxyvitamin D3 (also known as calcidiol, calcifediol, 25-hydroxycholecalciferol, 25-OH-D3 or HyD), which is the major circulating form of vitamin D3. Further hydroxylation occurs in the kidney.

For industrial production of vitamin D3, both chemical and biotechnological synthesis is (in principle) available. Chemical synthesis starts with cholesterol isolated from e.g. wool fat which is dehydrogenated into 7-DHC, an important intermediate in both chemical and biotechnological synthesis. Through exposure by UV-light and further purification/extraction steps 7-DHC is converted into vitamin D3. Modified yeast stains can be used for biosynthesis of 7-DHC, wherein acetyl-CoA is converted in a multi-step enzymatic process into 7-DHC. Said enzymatic conversion takes place in the endoplasmatic reticulum of the yeast. Excessive amounts of sterols, including 7-DHC and precursors thereof, not required in cellular membranes, are toxic to the yeast and are thus stored as steryl esters into intracellular organelles (so-called lipid bodies) from which they can be further isolated. The equilibrium between free sterols and those stored in the lipid bodies (mainly in the form of steryl esters) is triggered via the action of several proteins (enzymes), including action of sterol acyltransferases. In yeast, particularly Saccharomyces cerevisiae, ester formation of sterols is mainly carried out by the two sterol acyltransferases Arel p and Are2p.

Due to the unspecific action of said sterol acyltransferase enzymes, the steryl ester pool which is stored within the lipid bodies is relatively diverse, including but not limited to e.g. esters of ergosterol, zymosterol, lanosterol, lathosterol, cholesta-5,7,24(25)-trienol, or 7-DHC. Since only cholesta-5,7,24(25)-trienol, a precursor for 7-DHC, and not zymosterol can be used for vitamin D3 synthesis, there is a need for either selective storage of specific esters, such as e.g. esters of 7-DHC, into the lipid bodies and/or for increasing the turnover of

intermediates of 7-DHC produced by such a yeast strains which are further converted to vitamin D3 and/or derivatives or metabolites thereof. A particular metabolite which is also in focus of the present invention is 25-hydroxyvitamin D3.

Thus, it is an ongoing task to generate host cells, such as yeast capable of producing sterols, with high productivity/specificity for 7-DHC and/or reduced accumulation of side-products/intermediates including zymosterol, lanosterol or lathosterol, in particular esters of such intermediates stored in the lipid bodies.

Surprisingly, we now found that the specificity of the sterol acyltransferase activity in the host cell can be shifted towards 7-DHC via introduction of certain amino acid substitutions in the sequence of ARE2 and/or ARE1 which will lead to higher productivity and/or product ratio of the host cell towards 7-DHC as important intermediate in vitamin D3 production.

Thus, the present invention is directed to modified enzymes with sterol acyltransferase activity, i.e. modified sterol acyltransferases, particularly activity of sterol acyltransferase isoform Arel p and/or Are2p, comprising one of more amino acid substitution(s) at (a) position(s) corresponding to residues selected from 592 and/or 595 in the polypeptide according to SEQ ID NO: 1 , said modified enzyme has increased specificity towards 7-DHC over side- products/intermediates including zymosterol.

The polypeptide according to SEQ ID NO: 1 , showing ARE1 activity, including polynucleotides encoding such polypeptide according to SEQ ID NO: 1 , has been isolated from Saccharomyces cerevisiae. The polypeptide according to SEQ ID NO: 3, showing ARE2 activity, including polynucleotides encoding such

polynucleotide according to SEQ ID NO:3, has been isolated from Saccharomyces cerevisiae. The terms "sterol acyltransferase", "acyltransferase", "ARE", "enzyme having acyltransferase activity" or just "enzyme" are used interchangeably herein and refer to enzymes [EC 2.3.1.26], i.e. acyltransferases transferring fatty acyl groups from one molecule to another. Such transfer or enzymatic activity can be measured by means known to the skilled person. Sterol acyltransferases have been isolated from different origins, including mammals, yeast or plants. Both ARE1 and ARE2 are capable of acylating sterols such as e.g. zymosterol and/or 7- DHC to the respective esters. As used herein, a "modified" enzyme, i.e. modified acyltransferase, has a preferred activity and/or specificity towards esterification of 7-DHC compared to esterification of e.g. zymosterol and/or improved formation of total sterol esters, including e.g. 7-DHC or zymosterol. Preferred acyltransferase isoforms are Arel p or Are2p. A "non-modified" sterol

acyltransferase, particularly ARE1 and ARE2, as used herein refers to the respective endogenous enzymes not carrying one or more amino acid

substitution(s) as defined herein.

As used herein, a host cell carrying a modified sterol acyltransferase activity as defined herein, particularly ARE2 and/or ARE1 comprising one or more amino acid substitution(s) as defined herein, is referred to as "modified" host cell. The respective host cell carrying a non-modified sterol acyltransferase activity, i.e. encoding the wild-type ARE1 and/or ARE2 genes, is referred to as "non-modified" host cell.

As used herein, the terms "zymosterol", "lanosterol", "lathosterol","cholesta- 5,8,24(25)-trienol", "cholesta-5,7,24(25)-trienol", or "7-DHC" specifying vitamin D3 intermediates include both the free form and the ester form of said compounds. As used herein, a sterol mix contains 7-DHC and "side-products" or intermediates, including but not limited to zymosterol, lanosterol, lathosterol, cholesta-5,8,24(25)-trienol, or cholesta-5,7,24(25)-trienol.

As used herein, a "cholesterol-producing yeast" cannot produce ergosterol anymore but cholesterol products, including, but not limited to cholesta- 5,7,24(25)-trienol, cholesta-5,8,24(25)-trienol, cholesta-7,24(25)-dienol, 7-DHC or zymosterol. Particularly, this might be achieved via introduction of erg5erg6 double-knock out.

In one embodiment, the modified enzyme as defined herein, in particular modified ARE1 activity, comprises an amino acid substitution at a position corresponding to residue 592 in the polypeptide according to SEQ ID NO: 1 , preferably substitution of phenylalanine by leucine (F592L). Preferably, the enzyme having modified ARE1 activity is originated from Saccharomyces, such as S. cerevisiae. Using said modified ARE1 enzyme, the ratio 7-DHC to zymosterol in the sterol mix could be increased by at least about 15% compared to a strain expressing the non-modified endogenous ARE1 .

In one embodiment, the modified enzyme as defined herein, in particular modified ARE1 activity, comprises an amino acid substitution at a position corresponding to residue 595 in the polypeptide according to SEQ ID NO: 1 , preferably substitution of phenylalanine by leucine (G595D). Preferably, the enzyme having modified ARE1 activity is originated from Saccharomyces, such as S. cerevisiae. Using said modified ARE1 enzyme, the ratio 7-DHC to zymosterol in the sterol mix could be more than doubled, i.e. increased by at least about 55% compared to a strain expressing the non-modified endogenous ARE1 .

In a further embodiment, the modified enzyme as defined herein, in particular modified ARE2 activity, comprises an amino acid substitution at a position corresponding to residue 624 in the polypeptide according to SEQ ID NO:3, preferably substitution of phenylalanine by leucine (F624L). Preferably, the enzyme having modified ARE2 activity is originated from Saccharomyces, such as S. cerevisiae. Using said modified ARE2 enzyme, the ratio 7-DHC to zymosterol in the sterol mix could be increased by at least about 15% compared to a strain expressing the non-modified endogenous ARE2.

In a further embodiment, the modified enzyme as defined herein, in particular modified ARE2 activity, comprises an amino acid substitution at a position corresponding to residue 627 in the polypeptide according to SEQ ID NO: 3, preferably substitution of glycine by aspartic acid (G627D). Preferably, the enzyme having modified ARE2 activity is originated from Saccharomyces, such as S. cerevisiae. Using said modified ARE2 enzyme, the ratio 7-DHC to zymosterol in the sterol mix could be increased by at least about 15% compared to a strain expressing the non-modified endogenous ARE2.

The described amino acid substitution(s) at a position corresponding to residue F592L and/or G595D in SEQ ID NO: 1 might be combined with further

substitutions as defined herein, i.e. substitutions on one or more position(s) corresponding to amino acid residue(s) 624 and/or 627 in the polypeptide according to SEQ ID NO:3 and as described herein. Preferably, the amino acid substitution at a position corresponding to residue F592L in SEQ ID NO: 1 might be combined with further substitutions, such as amino acid substitutions at position(s) corresponding to G595D in SEQ ID NO: 1 and/or F624L in SEQ ID NO:3 and/or G627D in SEQ ID NO:3. A preferred modified enzyme is an enzyme having ARE1 activity and comprises at least an amino acid substitution at a position corresponding to G595D in SEQ ID NO: 1 , showing at least about 30, 35, 40, 45% higher 7-DHC titers, at least about 15, 20, 25, 30% less zymosterol in the sterol mix with a percentage of 7-DHC in the sterol mix of about 70-76%.

As used herein, the activity of ARE1 and/or ARE2 is modified. This might be achieved by, e.g. introducing (a) mutation(s) into the endogenous gene coding for ARE1 and/or ARE2, i.e. amino acid substitution(s) on one or more positions as described herein. The skilled person knows how to genetically manipulate a yeast cell resulting in modification of ARE1 and/or ARE2 activity. These genetic manipulations include, but are not limited to, e.g. gene replacement, gene amplification, gene disruption, transfection, transformation using plasmids, viruses, or other vectors.

The generation of a mutation into nucleic acids or amino acids, i.e. mutagenesis, may be performed in different ways, such as for instance by random or side- directed mutagenesis, physical damage caused by agents such as for instance radiation, chemical treatment, or insertion of a genetic element. The skilled person knows how to introduce mutations.

The present invention is particularly directed to the use of such modified ARE1 and/or ARE2 enzymes as defined herein in a process for production of 7-DHC, an intermediate for vitamin D3. Preferably, the modified enzymes of the present invention are introduced and/or expressed in a suitable host cell, such as yeast, preferably sterol-producing yeast, in particular cholesterol-producing yeast cell, such as selected from Saccharomyces cerevisiae, Schizosaccharomyces spp., Pichia spp., Klyuveromyces spp., Hansenula spp. or Yarrowia lipolytica, preferably S. cerevisiae. The modified host is used for production of 7-DHC, which might be further converted into vitamin D3 and/or 25-hydroxyvitamin D3.

A suitable host cell might be further modified to further increase production of 7-DHC, an important intermediate towards biosynthesis of vitamin D3, and/or reduce accumulation of side-products.

Thus, in one embodiment the invention is directed to a yeast strain having modified ARE1 and/or ARE2 activity and furthermore wherein ERG5 and ERG6 are inactivated. The yeast cell might be further modified via expression of a heterologous enzyme having C24-reductase activity, particularly selected from EC 1.3.1.72, such as a heterologous C24-reductase that is active on cholesta- 7,24-dienol, zymosterol, or trienol (e.g. cholesta-5,7,25-trienol), preferably a plant or vertebrate sterol A24-reductase, more preferably from vertebrate source, even more preferably from human, pig, dog, mouse, rat, horse, Danio rerio or any known source, as long as it can be expressed within said yeast cell. Most preferably, the sterol A24-reductase is selected from Danio rerio, rat or human. The sequences expressing said sterol A24-reductase enzymes are publicly available, including but not limited to Um ^' ProtKB/Swiss-Prot reference Q15392, Q60HC5, Q8VCH6, Q5BQE6, Q39085 or P93472 (see e.g. W02003064650). Using such a yeast strain, the percentage of 7-DHC present in the sterol mix is in the range of about 70 or more, preferably such as 75, 80, 88, 90, 95, 98% based on the total amount of sterols.

In another embodiment, the host cell according to the present invention might be further modified via introduction of homologs of endogenous enzymes involved in biosynthesis of 7-DHC, such as e.g. C5-sterol desaturase (ERG3) and/or C8-sterol isomerase (ERG2), resulting in increased specificity and/or productivity of 7-DHC with reduced accumulation of side-products or vitamin D3 intermediates, including but not limited to zymosterol, lanosterol and/or lathosterol. Preferably, the modified host cell as defined herein comprises a heterologous ERG2 and/or ERG3, wherein the ERG2 is preferably selected from Ustilago maydis (sequence derived from Um ^' ProtKB P32360), and/or wherein the ERG3 is preferably selected from Pichia pastoris (sequence derived from

Um ^' ProtKB C4QY87) or Schizosaccharomyces pombe (sequence derived from Um ^' ProtKB 094457). Strains comprising both ERG2 and ERG3 homologs together with the modified ARE1 and/or ARE2 as defined herein produce a sterol mix with over about 80% 7-DHC percentage and increased 7-DHC to cholesta-8-enol and/or lathosterol ratio by at least about 15 to 20%. Even more preferred is a modified strain as defined herein further comprising two or more copies of either ERG2 and/or ERG3 homologs as described above.

In a particular embodiment, the invention relates to a process for improving a host cell towards production of 7-DHC, wherein a modified host cell as defined herein, i.e. modified via introduction of one or more amino acid substitutions in sterol acyltransferases ARE1 and/or ARE2 as defined herein, in particular a cholesterol-producing yeast cell, preferably a yeast cell in which ERG5 and ERG6 are inactivated and wherein optionally a heterologous enzyme having C-24- reductase activity as defined herein is expressed, and/or wherein optionally homologs of endogenous ERG2 and/or ERG3 are expressed, wherein the host cell is improved such that the percentage of 7-DHC in the total amount of sterol produced by said host cell is increased from to about at least 70, 75, 80%, preferably 88, 90, 95, 98%, in particular wherein the ratio of 7-DHC to side- products including zymosterol and cholesta-8-enol is increased by at least about 5, 10, 15, 18, 20, 25% and as compared to a yeast strain expressing the non- modified, i.e. wild-type ARE1 and/or ARE2 activity.

In one aspect of the present invention, a host cell comprising modified ARE1 and/or ARE2 activity as defined herein is used in a process for production of vitamin D3 precursor 7-DHC. The modified host cell may be cultured in an aqueous medium supplemented with appropriate nutrients under aerobic or anaerobic conditions and as known by the skilled person for the respective cholesterol-producing host cells. Optionally, such cultivation is in the presence of proteins and/or co-factors involved in transfer of electrons, as known in the art. The cultivation/growth of the host cell may be conducted in batch, fed- batch, semi-continuous or continuous mode. Depending on the host cell, preferably, production of vitamin D3 and precursors thereof such as 7-DHC can vary, as it is known to the skilled person. Cultivation and isolation of 7-DHC and other intermediates in production of vitamin D3 is described in e.g.

WO201 1067144 or WO2017108799. The 7-DHC might be isolated and/or optionally further purified from the sterol mix and might be further converted to vitamin D3 and/or 25-hydroxyvitamin D3 using methods known in the art.

Using a host cell as described herein, the substrate-specificity of sterol acyltransferase activity could be shifted towards 7-DHC, leading to a percentage of at least about 70% 7-DHC in the total sterols produced by said host cell, with titers of up to about 10 g/l or more 7-DHC produced after about 100 h

fermentation under suitable culture conditions.

The terms "ARE1 " and "Arel p", "ARE2" and "Are2p", "ERG5" and "Erg5p", "ERG6" and "Erg6p" are used interchangeably herein and refer to a polypeptide encoded by the respective genes are1 , are2, erg5, and erg6. For the purpose of the present invention, the cholesterol-producing yeast cell is modified such that it does show modified activity of ARE1 and/or ARE2, e.g. carries a modification in either endogenous ARE1 , ARE2 or both, leading to modified specificity of ARE1 and/or ARE2, wherein said modification is achieved via introduction of one or more amino acid substitutions as defined herein.

Genes encoding ERG5, ERG6, ARE1 , ARE2, ERG2, ERG3, or sterol A24-reductase (ERG4), cultivation and genetic engineering of the yeast cell as used herein are known and described in e.g. US 7608421 . As used herein, the terms "C-24-reductase" or "A24-reductase" are used interchangeably herein. In yeast, this enzyme is encoded by erg4 and is active on the methyl-group of the carbon atom on position 24. Trienol, which does not exhibit such methyl-group on said position, is therefore not an acceptable substrate for the yeast ERG4.

The terms "C-8 sterol isomerase", "delta 8,7-isomerase", or "enzyme having C-8 sterol isomerase" are used interchangeably herein and refer to enzymes which are capable of catalyzing the conversion of cholesta-8-enol into cholesta-7-enol and/or zymosterol into cholesta-7,24-dienol. In yeast, this enzyme is encoded by erg2. A preferred ERG2 homolog to be used in a modified host cell according to the present invention is a polypeptide having at least about 41 %, such as e.g. at least 44, 45, 48, 49, 53, 56, 60, 70, 80, 90, 92, 95, 98 or up to 100% identity to SEQ ID NO:5 showing C-8 sterol isomerase activity and including polynucleotides encoding such polypeptide, obtainable from Ustilago maydis. Particularly, 1 or more copies, such as at least about 1 , 2, 3, 5, of said ERG2 homolog are expressed in a modified host cell as defined herein.

The terms "C-5 sterol desaturase", "enzyme having C-5 sterol desaturase are used interchangeably herein and refer to enzymes which are capable of catalyzing the conversion of cholesta-8-enol into cholesta-7,24-dienol and/or cholesta-7-enol into cholesta-5,7,24-trienol and/or 7-DHC. In yeast, this enzyme is encoded by erg3. A preferred ERG3 homolog to be used in a modified host cell according to the present invention is a polypeptide having at least about 45%, such as e.g. at least 50, 52, 60, 70, 80, 90, 92, 95, 98 or up to 100% identity to SEQ ID NO: 7 showing C-5 sterol desaturase activity and including polynucleotides encoding such polypeptide, obtainable from Pichia pastoris or Schizosaccharomyces pombe. Particularly, 1 or more copies, such as at least 1 , 2, 3, 5, of said ERG3 homolog are expressed in a modified host cell as defined herein.

The terms "sequence identity", "% identity" are used interchangeable herein. For the purpose of this invention, it is defined here that in order to determine the percentage of sequence identity of two amino acid sequences or of two nucleic acid sequences, the sequences are aligned for optimal comparison purposes. In order to optimize the alignment between the two sequences gaps may be introduced in any of the two sequences that are compared. Such alignment can be carried out over the full length of the sequences being compared.

Alternatively, the alignment may be carried out over a shorter length, for example over about 20, about 50, about 100 or more nucleic acids/bases or amino acids. The sequence identity is the percentage of identical matches between the two sequences over the reported aligned region. The percent sequence identity between two amino acid sequences or between two

nucleotide sequences may 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). Both amino acid sequences and nucleotide sequences can be aligned by the algorithm. 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, Longden and Bleasby, Trends in Genetics 16, (6) pp276-277,

http: //emboss.bioinformatics.nl/). For protein sequences EBLOSUM62 is used for the substitution matrix. For nucleotide sequence, EDNAFULL is used. The optional parameters used 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.

After alignment by the program NEEDLE as described above the percentage of sequence identity between a query sequence and a sequence of the invention is calculated as follows: number of corresponding positions in the alignment showing an identical amino acid or identical nucleotide in both sequences divided by the total length of the alignment after subtraction of the total number of gaps in the alignment. The identity as defined herein can be obtained from NEEDLE by using the NOBRIEF option and is labeled in the output of the program as "longest identity". If both amino acid sequences which are compared do not differ in any of their amino acids, they are identical or have 100% identity. With regards to enzymes originated from plants as defined herein, the skilled person is aware of the fact that plant-derived enzymes might contain a chloroplast targeting signal which is to be cleaved via specific enzymes, such as e.g. chloroplast processing enzymes (CPEs).

The ARE2 and ARE1 enzymes/homologs, as defined herein also encompass enzymes carrying amino acid substitution(s) which do not alter enzyme activity, i.e. which show the same properties with respect to the wild -type enzyme and catalyze acylation of sterols as defined herein. Such mutations are also called "silent mutations", which do not alter the (enzymatic) activity of the enzymes as described herein. As used herein, the term "specific activity" or "activity" with regards to enzymes means its catalytic activity, i.e. its ability to catalyze formation of a product from a given substrate. The specific activity defines the amount of substrate consumed and/or product produced in a given time period and per defined amount of protein at a defined temperature. Typically, specific activity is expressed in pmol substrate consumed or product formed per min per mg of protein. Typically, pmol/min is abbreviated by U (= unit). Therefore, the unit definitions for specific activity of pmol/min/(mg of protein) or U/(mg of protein) are used interchangeably throughout this document. An enzyme is active, if it performs its catalytic activity in vivo, i.e. within the host cell as defined herein or within a suitable (cell-free) system in the presence of a suitable substrate.

The skilled person knows how to measure enzyme activity, such as e.g. by HPLC.

With regards to the present invention, it is understood that organisms, such as e.g. microorganisms, fungi, algae or plants also include synonyms or basonyms of such species having the same physiological properties, as defined by the

International Code of Nomenclature of Prokaryotes or the International Code of Nomenclature for algae, fungi, and plants (Melbourne Code).

In particular, the present invention features the present embodiments:

(1 ) A modified enzyme having sterol acyltransferase activity comprising one of more amino acid substitution(s) at (a) position(s) corresponding to residues selected from 592 and/or 595 in the polypeptide according to SEQ ID NO: 1 , preferably substitution corresponding to F592L and/or G595D.

(2) A modified enzyme as defined herein and as of embodiment (1 ) catalyzing the esterification of sterols comprising 7-dehydrocholesterol (7-DHC) and zymosterol, wherein the ratio of 7-DHC to zymosterol in the sterol esters is increased by at least about 15% compared to the ratio of 7-DHC to zymosterol in the catalysis using the respective non-modified enzyme.

(3) A modified enzyme as defined herein and as of embodiment (1 ) or (2), wherein the amino acid substitution is selected from G595D.

(4) A host cell, preferably a yeast, more preferably a sterol-producing yeast, even more preferably a cholesterol-producing yeast, comprising a modified enzyme as defined herein and as of embodiments (1 ), (2), (3).

(5) A host cell as defined herein and as of embodiment (4) used for production of a sterol mix comprising 7-DHC and zymosterol, wherein the ratio of 7-DHC to zymosterol is increased by at least about 15% compared to a host cell wherein expressing a non-modified enzyme. (6) A host cell as defined herein and as of embodiment (4) or (5), wherein ERG5 and ERG6 are inactivated.

(7) A host cell according as defined herein and as of embodiment (4), (5), (6), wherein the cell expresses a heterologous enzyme selected from EC 1.3.1.72 having sterol A24-reductase activity, preferably wherein the heterologous enzyme is originated from plant or vertebrate, more preferably originated from human, pig, dog, mouse, rat, horse or Danio rerio.

(8) A host cell as defined herein and as of embodiments (4), (5), (6), (7), wherein the host cell is selected from the group consisting of Saccharomyces, Schizosaccharomyces, Pichia, Kluyveromyces, Hansenula, and Yarrowia, preferably selected from Saccharomyces cerevisiae, Schizosaccharomyces spp., Pichia spp., Kluyveromyces spp. , Hansenula spp. or Yarrowia lipolytica.

(9) A process for reducing the percentage of zymosterol in a sterol mix comprising zymosterol and 7-DHC comprising cultivating a host cell as defined herein and as of embodiments (4), (5), (6), (7), (8) under suitable conditions and optionally isolating and/or purifying the 7-DHC from the sterol mix.

(10) A process for increasing the percentage of 7-DHC in a sterol mix comprising 7-DHC and zymosterol comprising cultivating a host cell as defined herein and as of embodiments (4), (5), (6), (7), (8) under suitable conditions and optionally isolating and/or purifying the 7-DHC from the sterol mix.

(11 ) A process for production of 7-DHC comprising enzymatic conversion of acetyl-CoA into a sterol mix comprising zymosterol and 7-DHC with a host cell as defined herein and as of embodiments (4), (5), (6), (7), (8), (9), (10), wherein the percentage of 7-DHC in the sterol mix is at least about 70%.

(12) A process as defined herein and as of embodiment (11 ), wherein the 7-DHC is further converted into vitamin D3.

(13) A process as defined herein and as of embodiment (11 ) or (12), wherein the 7-DHC is further converted into 25-hydroxyvitamin D3.

(14) Use of a modified enzyme as defined herein and as of embodiments (1 ),

(2), (3) or a host cell as defined herein and as of embodiments (4), (5), (6), (7), (8), (9), (10), in a process for production of 7-DHC, wherein the 7-DHC is isolated from a sterol mix comprising zymosterol and 7-DHC, and wherein the ratio of 7- DHC to zymosterol is increased by at least about 15% compared to a process using the respective non-modified enzyme and host cell, respectively.

The following examples are illustrative only and are not intended to limit the scope of the invention in any way. Examples

Example 1 : General methods, strains and plasmids

All basic molecular biology and DNA manipulation procedures described herein were generally performed according to Sambrook et al. (1989. Molecular

Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory Press: New York) or Ausubel et al. (1998. Current Protocols in Molecular Biology. Wiley: New York). Genotyps of the used S. cerevisiae strains and plasmids are listed in Table 1 and 2. Saccharomyces cerevisiae 7-DHC producing strain Y2140 was constructed starting from a wildtype CEN.PK background strain. Into this wildtype strain an erg5 disruption cassette was transformed that contained a codon-optimized gene for a sterol 24-reductase from zebrafish flanked by a PGK1 promoter and a CYC1 terminator in combination with TRP1 . Subsequently, an erg6 disruption cassette was transformed that contained the gene for a sterol 24-reductase from rat flanked by a TDH3 promoter and a PGK1 terminator in combination with LEU2. All mentioned strains are ALATa, and harbor an overexpressed copy of the truncated constitutively active HMG-CoA reductase gene (tHMG1 ).

Table 1 : Saccharomyces cerevisiae strains.

Table 2: plasmids used for construction of ARE mutations. "Seer" means

Saccharomyces cerevisiae.

Example 2: Construction of ARE1 -WT plasmid pHyD459

WT S. cerevisiae ARE1 was synthesized by DNA2.0, incorporating an Xbal site at the 5’ end (TCTAGAACAAAatg... ) and a Pstl site at the 3’end. This was cloned into an erg4A: :Hyg ^R deletion plasmid using unique Xbal and Pstl sites. LEU2 was subsequently used to replace the HygR moiety via a Kpnl-Agel cloning.

Example 3: Cloning of ARE1 mutant genes

S. cerevisiae ARE1 mutant variant pMB7584 (F592L) was generated by ligating a BsrG I -Bsal -cleaved PCR product generated from ARE1 (oligos according to SEQ ID NO: 16 & 17) with a double-stranded oligo derived by annealing SEQ ID NO: 19 and 20 into BsrG I -Pstl -cleaved pHyD459. Similarly, S. cerevisiae ARE1 mutant variant pMB7585 (G595D) was generated by ligating a BsrG I -Bsal -cleaved PCR product generated from ARE1 (oligos according to SEQ ID NO: 16 & 18) with a double- stranded oligo derived by annealing SEQ ID NO:21 and 22 into BsrG I -Pstl -cleaved pHyD459. The oligos as well as further sequences used herein are listed in the sequence listing.

Example 3: Introduction of ARE1 WT and mutant genes into Saccharomyces cerevisiae

To the test the impact of the mutant ARE1 genes in 7-DHC production in comparison to the WT gene, strain Y2140 was transformed with three different constructs:

(1 ) a Sail fragment of plasmid pHyD459 which is an erg4 disruption construct harboring the WT ARE1 gene under the control of the PGK1 promoter and LEU2.on construct harboring the WT ARE1 gene under the control of the PGK1 promoter and LEU2;

(2) a Sail fragment of plasmid pMB7584 which is an erg4 disruption construct harboring the are1 F592L gene under the control of the PGK1 promoter and LEU2are1 F592L gene under the control of the PGK1 promoter and LEU2;

(3) a Sail fragment of plasmid pMB7585 which is an erg4 disruption construct harboring the are1 G595D gene under the control of the PGK1 promoter and LEU2are1 G595D gene under the control of the PGK1 promoter and LEU2.

Transformants were selected on (minimal media) at 30°C and screened for hygromycin sensitivity. Strains resulting from these transformations are listed in Table 1 above. These strains were subsequently assayed for their 7-DHC productivity and overall 7-DHC sterol purity as described in Example 4 below.

Example 4: HPLC analysis of sterols in ARE mutant strains

Strains to be tested were initially plated onto YPD agar and incubated for 48 hours at 30 °C. Two milliliters YPD pre-cultures were inoculated from these plates and grown on a roller wheel for 24 hours at 30°C. In a 24-well microtiter plate, 0.8mL of YPD + 10 g/L ethanol were inoculated from the preculture to a final OD ₆ OO of 0.5. Microtiter plates were grown at 30° C in a humidified environment and shaking at 800 rpm on a shaker with an orbit of 3mm. At 24 and 48 hours post-inoculation, 16 pi ethanol was added to each well as a feed. At 72 hours post-inoculation the cells were sampled for sterol content.

For extraction of sterols from the cultures eighty microliters of whole broth was pipetted into a 2-mL Precellys tube with glass beads. Eight hundred microliters of saponification solution (5% KOH in ethanol) was added, and samples were placed into a Precellys 24 Homogenizer and agitated at 6500 rpm for 3 cycles at 15 seconds per cycle. Sixty microliters of glacial acetic acid were then added and the tubes were centrifuged for 1 minute at top speed. The supernatant was assayed via HPLC for sterol content (see Table 3).

Table 3: ratios of 7-DHC to selected sterol intermediates in control and ARE1 and/or ARE2 mutant strains. "Lano-/latho" means a mix of lanosterol and lathostherol, "zym" means zymosterol. Numbers are in mg/ml of sterols.

As the result of a screen of various S. cerevisiae Are1 mutants, the inventors found a number of Are1 variants that, when expressed, produce 7-DHC with a higher overall productivity, less accumulation of sterol side products

(zymosterol, lathosterol, lanosterol, cholesta-8-enol, etc), or both.