STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT This investigation was made with United States government support awarded by the following agencies : USDA Grant Number : 96-35500-3172 BACKGROUND OF THE INVENTION Within the United States, ongoing research is directed toward developing alternative energy sources to reduce our dependence on foreign oil and nonrenewable energy. The use of ethanol as a fuel has become increasingly prevalent in recent years.

The current domestic use of ethanol in transportation fuels is about 1. 2 billion gallons almually. In the U. S., the majority of ethanol is obtained from the fermentation of cornstarch. Projections made by the Department of Energy indicate that by the year 2020, annual ethanol usage in fuels will have increased dramatically to an estimated 20 billion gallons. This greatly exceeds what can be economically produced from cornstarch.

In order to meet the increased demand for ethanol, it will be necessary to ferment sugars from other biomass. Biomass refers to materials such as agricultural wastes, corn hulls, corncobs, cellulosic materials and the like. Biomass from most of these sources contains xylose at a concentration of up to about 25-30% of the total dry weight. The D-xylose content of hardwood species and herbaceous angiosperms is about 17% and 31% of the total dry weight, respectively. Because agricultural residues, pulping wastes, and fast-growing hardwood species have a high xylose content, the potential economic and ecologic benefits of converting xylose in these renewable materials are significant. In order for biomass conversion to be economically feasible, a practical, large-scale use must be found for xylose.

Biomass conversion employs microorganisms that serve as biocatalysts to convert cellulosic materials into usable end products such as ethanol. Efficient biomass conversion in large-scale industrial applications requires a microorganism that can tolerate high sugar and ethanol concentrations, and which is able to ferment multiple sugars simultaneously.

The pentoses D-xylose and L-arabinose are among the most difficult sugars in biomass to metabolize. Bacteria can ferment pentoses to ethanol and other co-products, and bacteria with improved ethanol production from pentose sugars have been genetically engineered. However, these bacteria are sensitive to low pH and high concentrations of ethanol, their use in fermentations is associated with co-product formation, and the level of ethanol produced remains too low to make the use of these bacteria in large-scale ethanol production be economically feasible.

In general, industrial producers of ethanol strongly favor the use of yeast as biocatalysts, because yeast fermentations are relatively resistant to contamination, are relatively insensitive to low pH and ethanol, and are easier to handle in large-scale processing. Many different yeast species use xylose respiratively, but only a few species use xylose fermentatively. Fermentation of xylose to ethanol by wild type xylose-fermenting yeast species occurs slowly and results in low yields, relative to fermentation rates and ethanol yields that are obtained with conventional yeasts in glucose fermentations. In order to improve the cost effectiveness of xylose fermentation, it is necessary to increase the rate of fermentation and the ethanol yields obtained.

The most commonly used yeast in industrial applications is Saccharonzyces cerevisiae. Although S. cerevisiae is unable to grow on or ferment xylose, it was reported that homogenates of S. cerevisiae could readily ferment D-ribulose-5- phosphate to ethanol, and that it could also convert D-xylulose-5-phosphate to a lesser extent (Dickens, 1938). Efforts to create strains of S. cerevisiae with enhanced xylose fermentation by introducing genes capable of converting xylose to metabolites fermentable by S. cerevisiae have been largely unsuccessful (Ueng et al., 1985 ; Chan et al., 1989 ; Amore et al., 1989 ; Sarthy et al., 1987 ; Toivari et al., 1996).

Pichia stipitis is a yeast species that is able to ferment xylose to produce ethanol. In P. stipitis, fermentative and respirative metabolism co-exist to support cell growth and the conversion of sugar to ethanol (Ligthelm, 1988). P. stipitis differs

significantly from the glucose-fermenting yeast S. cerevisiae in its ability to produce ethanol from xylose. It is known that P. stiptis requires a well-controlled low level of oxygen to reach maximum rate of ethanol production. In 1996, Passoth et al. first observed a peculiar pattern of respiration in P. stipitis. After the cells of P. stipitis were transferred from aerobic to oxygen-limited conditions, no decrease in the respiration capacity was observed. In addition, there was no increase in the respirative quotient (C02 production/02 consumption), and no change in the level of a key respiratory enzyme, pyruvate dehydrogenase. Moreover, respiratory activity was not repressed in the presence of fermentable sugars or low oxygen tension. In a survey of alternative pathways present in Crabtree-positive and-negative species, Jeppsson et al. (1995) reported that P. stipitis has an alternative respiratory pathway that is resistant to cyanide or antimycin A, but is sensitive to salicyl hydroxymate (SHAM). The pathway is believed to include a SHAM-sensitive terminal oxidase (STO). Jeppsson et al. hypothesized that the STO pathway would serve as a redox sink to avoid the accumulation of xylitol in P. stipitis.

Although STO respiration was discovered 70 years ago (Keilin, 1929), the physiological roles and the functional components of this pathway remain unclear.

STO respiration has been widely reported from higher plants (for review, Douce and Neuburger, 1989 ; Vanlerberghe and McIntosh, 1997), fungi (Lambowitz and Slayman, 1971 ; Downie and Garland, 1973), and yeasts (Lloyd and Edwards, 1977). The STO pathway branches from the conventional cytochrome pathway at the level of ubiquinone, just before cytochrome b (Seidow, 1980 ; Storey, 1976), where electrons are directly donated to Sto to reduce molecular oxygen to water. Sto is unable to translocate protons (Moore and Rich, 1985), thus it by-passes two out of the three energy-generating sites in plants. Therefore, it is considered as an energy-wasting pathway. Most of the current information concerning biochemical and regulatory aspects of the pathway has been obtained from the studies in plant Sto proteins.

Because this protein is tightly associated with the mitochondrial inner membrane, no pure forms have been obtained as yet for characterization studies of the metal center and kinetics. Moreover, the plant Sto proteins lose activity when they are solublized.

These difficulties have hindered progress in understanding the physiological roles of the STO pathway.

Research involving the identification and characterization of STO protein and its role in P. stipitis was undertaken in our laboratory. The information that resulted from these efforts has allowed us to develop genetically engineered, xylose-fermenting yeast strains with enhanced ethanol production from xylose.

BRIEF SUMMARY OF THE INVENTION One aspect of the present invention is an isolated polynucleotide comprising a sequence encoding the Pichia stipitis SHAM-sensitive terminal oxidase of SEQ ID NO : 26. Preferably, the isolated polynucleotide of the present invention is an isolated DNA molecule comprising the sequence of SEQ ID NO : 25.

In another aspect, the present invention includes a vector comprising a polynucleotide comprising a sequence encoding Pichia stipitis SHAM-sensitive terminal oxidase, SEQ ID NO : 26.

The present invention provides a genetic construct comprising a sequence encoding the Pichia stipitis SHAM-sensitive terminal oxidase of SEQ ID NO : 26 operably connected to a promoter functional in yeast.

The present invention provides a xylose-fermenting mutant of a yeast or fungal species, the mutant having reduced SHAM-sensitive terminal oxidase relative to the levels of SHAM-sensitive terminal oxidase in the parent strain from which the mutant was derived, wherein the species is selected from the group consisting of Pichia stipitis, Group I species and Group II species, wherein Group I species natively comprise a cytochrome pathway and a SHAM-sensitive pathway, and wherein Group II species natively comprise a cytochrome pathway, an antimycin A-and SHAM-insensitive pathway, and a SHAM-sensitive pathway. Preferably, the mutant yeast strain is a P. stipitis mutant.

In one embodiment, the mutant xylose-fermenting yeast is a P. stipitis SHAM- sensitive terminal oxidase disruptant. Preferably, the P. stipitis SHAM-sensitive terminal oxidase disruptant is derived from FPL-UC7 (NRRL 21448). More preferably still, the P. stipitis SHAM-sensitive terminal oxidase disruptant is FPL-Shi 31 (NRRL Y-30230).

In an alternative embodiment, the mutant xylose-fermenting yeast comprises a construct expressing SHAM-sensitive terminal oxidase antisense mRNA.

A further aspect of the invention is a method for producing ethanol from the fermentation of xylose comprising the steps of culturing a mutant of xylose-fermenting yeast in a xylose-containing medium under suitable conditions for a period of time sufficient to allow fermentation of xylose to ethanol, the mutant yeast having reduced SHAM-sensitive terminal oxidase relative to the wild type parental strain from which the mutant is derived.

The present invention includes a recombinant yeast comprising a sequence encoding the Pichia stipitis SHAM-sensitive terminal oxidase of SEQ ID NO : 26, the coding sequence operably connected to a promoter functional in yeast, the yeast belonging to a species selected from the group consisting of Saccharomyces cerevisiae, Saccharomyces carlsbergensis, Sacclzaojnyces byanus, Sacclzaromyces delbrueckii, Saccharomyces diastaticus, Saccharomyces sake, Saccharomyces thermotolerans, Saccharomyces ut-warum and Group III species, wherein the recombinant yeast expresses SHAM-sensitive terminal oxidase and wherein expression of the SHAM- sensitive terminal oxidase is correlated with cyanide-resistant respiration, the yeast species natively comprising an antimycin A-insensitive pathway and a cytochrome pathway.

It is an advantage that the mutant xylose-fermenting yeast of the present invention ferments xylose at an increased rate, relative to the parent strain having wild- type levels of SHAM-sensitive terminal oxidase.

Other advantages and features of the present invention will become apparent upon review of the specification.

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS Fig. 1 shows the phylogenetic relationship of PsSto to Sto proteins from seven other yeast and fungi.

Fig. 2 is a schematic representation of the PsSto disruption cassette ; open box represents PsSto sequence and hatched box represents the PsURA3 gene.

Fig. 3A shows the construction of a PsSTOl expression cassette having a Saccharomyces cerevisiae promoter and terminator sequence.

Fig. 3B and 3C compare the respiration rate of S. cerevisiae expressing PsSTOl (solid) and S. cerevisiae lacking PsSTOl (hatched) without inhibitor (Fig. 3B) and in the presence of 1 mM KCN (Fig. 3C).

Fig. 4 compares the cell growth (a), ethanol production (), and xylose utilization (-) of PsSto disruptant FPL-Shi31 (Fig. 4A) and the cell growth (Cl), ethanol production (a), and xylose utilization (O) of FPL-UC7.

DETAILED DESCRIPTION OF THE INVENTION Pichia stipitis is a crabtree-negative yeast with oxidative and fermentative metabolism coexisting, which include a cytochrome pathway and a cyanide or antimycin A resistant, SHAM-sensitive pathway. We previously discovered that disruption of the cytochrome pathway in P. stipitis results in increased xylose fermentation (U. S. Application Serial No. 09/274, 642, which is incorporated by reference in its entirety).

As reported herein, we have identified, cloned and sequenced a coding sequence for SHAM-sensitive terminal oxidase from P. stipitis. The gene is designated PsSTOl for Pichia stipitis SHAM-sensitive terminal oxidase. Using the PsST01 coding sequence, a disruption and an expression vector were developed.

The disruption cassette was used to create a mutant of Pichia stipitis in FPL- UC7, which contains the PsSTOl gene and has wild type levels of PsSto. The PSSTOI disruptant mutant of Pichia stipitis was characterized as described in detail in the Examples. Briefly, the mutant grown on xylose showed faster xylose utilization, exhibited higher volume production of ethanol, and had reduced cell growth relative to the parent strain from which the mutant was derived. Faster xylose utilization, increased ethanol production, and reduced cell growth are all desirable properties for a yeast used in industrial fermentations.

A genetic construct comprising the PsSTOl gene operably connected to a promoter functional in yeast was introduced into Saccharomyces cerevisiae and expression of PsSto protein was obtained. It if of interest to note that the respiration rate of transformed S. cerevisiae increased relative to that of a control yeast.

Respiration was resistant to KCN, which suggests the expression of PsST01 can impart functional SHAM-sensitive respiration in S. cerevisiae.

To date, efforts to enhance xylose fermentation to ethanol by S. cerevisiae by introducing into the yeast xylose fermenting enzymes (e. g., xylose reductase or xylitol dehydrogenase) have proven ineffective. At low oxygen levels, recombinant S. cerevisiae with a wild type cytochrome respiratory system converts xylose into xylitol.

Instead of being converted to ethanol, xylitol accumulates because of the cofactor imbalance of the first two step enzymes in the engineered xylose pathway. In addition, S. cerevisiae does have transhydrogenases to use NADPH to regenerate NAD+. We hypothesized that by introducing the Sto protein into S. cerevisiae, it may be possible to confer cyanide resistant respiration to promote regeneration of NAD+ in S. cerevisiae.

We have transformed S. cerevisiae with a Pst01 gene under control of a constitutive ScGAPDH promoter and found that transformants have increased respiration that is resistant to cyanide. Any promoter that is functional in yeast may be used in place of the ScGAPDH promoter to allow expression of a heterologous PsSTO gene in yeast. It is reasonably expected that S. cerevisiae mutants expressing Sto proteins with the combination of xylose reductase and xylitol dehydrogenase will have enhanced ethanol production from biomass. Therefore, the S. cerevisiae mutants of the present invention will make good targets for developing genetically engineered yeast with heterologous enzymes involved in xylose fermentation.

It is expected that other commercially important yeast that are closely related to S. cerevisiae may also be genetically engineered to express Sto proteins. Suitable yeast species include, but are not limited to, Saccharomyces carlsbergensis, Saccharoayces <BR> <BR> <BR> <BR> byanus, Saccharomyces delbrueckii, Saccharomyces diastaticus, Saccharorayces sake, Saccharomyces thermotolerayas, and Saccharomyces urvarum.

The present invention provides a mutant xylose-fermenting yeast strain that is characterized by reduced expression of a functional SHAM-sensitive terminal oxidase.

The mutant yeast of the present invention has been found to ferment xylose to produce ethanol at a higher rate than the parent strain, which has wild-type levels of SHAM- sensitive terminal oxidase.

Preferably, the mutant yeast strains of the present invention have volumetric ethanol production rates that are about 20% or more higher than that of the corresponding parent strain having wild type levels of SHAM-sensitive terminal oxidase.

In a preferred embodiment, the mutant yeast of the present invention is a SHAM-sensitive terminal oxidase disruptant mutant. By a"SHAM-sensitive terminal oxidase disruptant mutant,"it is meant a mutant in which a part or all of the functional SHAM-sensitive terminal oxidase gene natively present in the parent strain is removed

or replaced with DNA, the expression of which does not result in an expression product having SHAM-sensitive terminal oxidase activity.

In an alternative embodiment, expression of SHAM-sensitive terminal oxidase may be down-regulated through the use of an anti-sense construct in which part or all of the antisense strand coding for the SHAM-sensitive terminal oxidase is expressed under the regulation of a promoter that responds to diminished oxygen. In this embodiment, the antisense mRNA for SHAM-sensitive terminal oxidase is expressed under oxygen limiting conditions, and thereby inhibits translation of SHAM-sensitive terminal oxidase transcript. Using the sequence information disclosed herein, one of ordinary skill in the art could construct a vector expressing antisense RNA.

By"wild-type yeast,"it is meant a xylose-fermenting yeast strain with normal or wild-type levels of functional SHAM-sensitive terminal oxidase from which the mutant strain of the present invention is derived. In certain cases, the"wild-type yeast" as defined herein may include mutagenized yeast. For example, the P. stipitis strain FPL-UC7, from which the PsST01 disruptant FPL-Shi31 was developed, is itself a mutated yeast strain. However, FPL-UC7 is also a wild-type yeast, as defined herein, because it is a xylose-fermenting yeast with normal levels of functional SHAM- sensitive terminal oxidase used to develop a mutant yeast strain of the present invention.

As described in detail in the Examples, a disruption cassette comprising a 1. 4- kb PsURA3 fragment inserted into the PsST01 gene was introduced by site-specific integration into the genome of P. stipitis FPL-UC7 (Lu, et al. 1998b), a ura3 auxotroph.

A resultant disruptant strain, designated FPL-Shi31, was obtained and characterized as detailed below. The P. stipitis strain FPL-Shi31 was deposited at the ARS Patent Culture Collection in Peoria, IL on October 20, 1999 under the Budapest Treaty and was assigned accession number NRRL Y-30230. It is reasonably expected that similar stol-lN disruptants of P. stipitis may be obtained using a disruption cassette comprising larger or smaller portions of the 5'and 3'regions of the PsST01 gene or its flanking regions.

In addition to FPL-Shi31, other stol-A disruptant mutants can readily be obtained using FPL-UC7 (NRRL Y-21448) or P. stipitis FPL-PLU20 (Lu et al., 1998 ; Cho and Jeffries, 1999), as the progenitor. The P. stipitis strain FPR-PLU20 was

deposited at the ARS Patent Culture Collection in Peoria, IL on March 30, 1998 under the Budapest Treaty and was assigned accession number NRRL Y-21970.

Several yeast and fungal species in addition to P. stipitis are known to employ more than one respiratory pathway. These species can be assigned to one of four groups : Group I (a cytochrome pathway and SHAM sensitive pathway) ; Group II (a cytochrome pathway, an antimycin A-and SHAM-insensitive pathway, and a SHAM- sensitive pathway) ; Group III (an antimycin A-insensitive pathway and a cytochrome pathway) ; and Group IV (cytochrome c pathway). Group I includes Pichia stipitis, Hansenula anomala, Hansenula California, Schwayaniomyces castellii, Aspegillus niger, and Neurospora crassa. Group II includes Hansenula saturnus and Endomycopsis capsularis. Group III includes Schizosaccharoynyces pombe, Candida utilis, Candida parapilosis, and Kluyveromyces lactis. Group IV includes Hansenula glucozyma.

It is anticipated that a mutant having reduced expression of functional SHAM- sensitive terminal oxidase may be easily obtained from any member of Group I or II yeast using standard molecular biology techniques and the teachings set forth herein.

For example, one wishing to obtain such a mutant could isolate the STO gene from the target species, construct a disruption cassette having a selectable marker such as UM3, transform a sensitive strain (e. g., a ura3 auxotrophic strain) with the cassette, and select for putative transformants on selection medium (e. g., medium lacking uracil). Putative disruptants may be confirmed by PCR amplification as described in the Examples.

It is reasonably expected that, in addition to expressing SHAM-sensitive terminal oxidase in S. cerevisiae, expression of SHAM-sensitive terminal oxidase and cyanide-resistant respiration may be achieved by introducing a heterologous SHAM- sensitive terminal oxidase gene operably connected to a promoter expressible in yeast into Saccharomyces carlsbergensis, Saccharomyces byanus, Saccharomyces delbrueckii, Saccharomyces diastaticus, Saccharoinyces sake, Saccharoiiiyces t7aermotolerans, and Saccharoonyces urvarum or Group III yeast using the teachings of the present invention and standard molecular biological techniques.

In another aspect, the present invention provides a method of fermenting xylose in a xylose-containing material to produce ethanol using the mutant yeast of the invention as a biocatalyst. Preferably, the mutant yeast is recovered after the xylose in the medium is fermented to ethanol and used in subsequent fermentations.

By"xylose-containing material,"it is meant any medium comprising xylose, whether liquid or solid. Suitable xylose-containing materials include, but are not limited to, hydrolysates of polysaccharide or lignocellulosic biomass such as corn hulls, wood, paper, agricultural by-products, 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 oligosaccharides.

Hydrolysates may be produced by enzymatic or acid hydrolysis of the polysaccharide- containing material, or by an other suitable means.

Preferably, the mutant yeast strain is able to grow under conditions similar to those found in industrial sources of xylose. The method of the present invention would be most economical when the xylose-containing material can be inoculated with the mutant yeast 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. Passaging of the yeast selects for yeast that are better able to grow in the presence of sulfite or phenolic inhibitors.

It is expected that mutant yeast strains of the present invention may be further manipulated to achieve other desirable characteristics, or even higher specific ethanol yields. For example, selection of mutant yeast strains by passaging the mutant yeast strains of the present invention on medium containing hydrolysate may result in improved yeast with enhanced fermentation rates.

The sequence of the deduced amino acid sequence of the putative protein encoded by the Pichia stipitis ST01 gene is provided in SEQ ID NO : 26. The sequence of the STOl gene isolated from Pichia stipitis is shown in SEQ ID NO : 25. It is understood that the sequence encoding the STO to be expressed or used in the construction of a disruption cassette can have a sequence with minor variations, substitutions, additions or deletions relative to the sequence isolated from P. stipitis shown in SEQ ID N : 25.

With respect to expression of the STO gene, it is well understood among those of ordinary skill in the art that certain changes in nucleic acid sequence make little or no difference to the overall function of the protein or peptide encoded by the sequence.

Due to the degeneracy of the genetic code, particularly in the third position of codons, changes in the nucleic acid sequence may not result in a different amino acid being specified by that codon. Changes that result in an amino acid substitution may have little or no effect on the three dimensional structure or function of the encoded protein or peptide. In addition, changes that result in insertions or deletions of amino acids may also be acceptable.

Similarly, slight variations in the sequence of the STO gene are expected to be suitable for the use of the STO gene in the development of a disruptant mutant. It is important that there is a sufficiently high degree of complementarity between the STO gene used in constructing the disruption cassette and that of the target host so as to permit efficient, site specific recombination to occur.

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

EXAMPLES I. Methods and Materials.

A. Microbial strains and maintenance Microbial strains used in this study are listed in Table 1. P. stipitis strains were maintained or cultivated in YNB minimal medium containing 1. 7 g L-1 yeast nitrogen base without amino acids (YNB ; Difco), 5 g L-1 ammonium sulfate, and 20 g L-l glucose. For yeast transformations, yeast host strains were grown in YPD medium consisting of yeast extract, 10 gL-l, peptone, 20 gL-l, and glucose, 20 g*L-l. For cultivation of ura3 and leu2 auxotrophs, media were supplemented with 20 mgL~l of uridine or leucine, respectively. For other growth or fermentation experiments, yeast strains were normally grown in YNBUP medium containing 1. 7 gel-l yeast nitrogen base without amino acids, 2. 27 gel-l urea, 6. 56 gel-l peptone, and sugar (2-4%). Yeast strains were cultivated at 30°C. E. coli was cultivated at 37°C in Luria-Bertani medium supplemented with 100 mg L-l ampicillin or kanamycin when required.

B. Enzymes, primers and chemicals Restriction enzymes, DNA modification enzymes and molecular reagents were obtained from New England Biolabs, Promega, Strategene and Roche Biochemicals.

Reaction conditions were as recommended by the suppliers. All general chemicals were purchased from Sigma and Fisher. All DNA preps were performed using Qiaprep Spin Table 1 Microbial strains<BR> Strain Genotype (NRRL number) Reference or source<BR> P. stipitis<BR> CBS 6054 Wid-type (NRRL Y-1145) Centraalbureau voor Schimmelcultures<BR> (Delft, The Netherlands)<BR> FPL-UC7 ura3-3 (NRRL Y-21448) Lu et al., 1998<BR> FPL-Shi21 cyc1::ura3 (NRRL Y-21971) Shi et al., 1999<BR> FPL-Shi31 sto1::ura3 (NRRL Y-30230) This work<BR> FPL-Shi41 sto1::ura3 This work<BR> FPL-PLU5 ura3-3, leu2# Lu, et al., 1998<BR> S. cerevisiae<BR> 679α MATαtrp1-1 Dr. Culbertson (Univ. of Wisconsin, Madison, WI)<BR> 679α(pNQ32) Contains expression cassette of PsSTO1 this work<BR> 679α(pYPR2831) Contains empty vctor without PsSTO1 This work<BR> B06748 MATα can1-100 cyc1-783 cycl1::lacZ) cyc7::CYH2+cyh2 Holzschu et al., 1989<BR> his3-#1 leu2-3 112, trp1-289 ura3-52<BR> B06748(pNQ32) Contains expression cassette of PsSTO1 This work<BR> B06748(pYPR2831) Contains empty vector without PsSTO1 This work<BR> Escherichia coli<BR> DH5α F recA1 endA1 hsdR17(rK-,mK+)supE44 thi-1 gyrA relA1 Life Technologies<BR> TOP10 F mcrA #(mrrhsdRMS-mcrBC) # 80lacZ#M15 #lacX74 recA Invitrogen<BR> deoR araD139 #(ara-leu)7697 gal# galKrpsL (StrR) endA1 nupG

columns from Qiagen. Zymolyase 20T was purchased from ICN while Novozyme234 was purchased from Sigma. Oligo primers were synthesized by Sigma-Genosys. The oligonucleotides used in this study are listed in Table 2 ; vectors are listed in Table 3.

C. DNA sequencing Sequencing of all DNA clones was performed by using a 371 ABI automated sequencer (Perkin-Elmer). DNA sequence analysis was conducted by using the Genetics Computer Group sequence analysis software package and DNAMAN (Lynnon BioSoft). Phylogenetic trees were drawn according to the neighbor-joining method (Kimura, 1983).

D. Genome walking to clone the alternative oxidase Two highly conserved regions of the six fungal alternative oxdiases : IFLES (I/V) AGVPGMV (SEQ ID NO : 27 and SEQ ID NO : 28, respectively) and HRFVGYLEEEAV (SEQ ID NO : 29), were selected to design two degenerate oligos.

Primer 1 and 2 (SEQ ID NO : 1 and SEQ ID NO : 2, respectively) were used to amplify a 293-bp region of Pst01 from P. stipitis wild-type CBS 6054 by Pfu DNA polymerase (Strategene). The PCR reaction was carried out at 95°C for 5 min as the initial cycle, followed by 36 cycles of 95°C for 60 s, 55°C for 60 s and 72°C for 90 s.

The final extension time was 15 min at 72°C. One pL PCR products were directly cloned into the PCR2. 1-TOPO vector (Invitrogen) to create pNQ28. The 293-bp fragment was sequenced and compared to the consensus of the fungal alternative oxidase genes. This region became the starting point for genome walking to clone the entire gene.

The Universal Genome Walker Kit (Clonetech) was used to clone Pst01.

One ug of genome DNA from wild-type CBS 6054 was used to construct five individual linear fragment libraries by 5 blunt-end enzymes supplied in the kit. The blunt-ended linear fragments were ligated to the adapters provided by the manufacturer.

Gene-specific primers were designed based on the sequence of the 293-bp amplified region to allow"walking"in each direction. The two adapter specific primers (3 and 4) were supplied by the manufacturer. For the 3'end walking, primers 3 and 5 (SEQ ID NO : 3 and SEQ ID NO : 5, respectively) were used to amplify the primary PCR products, while primers 4 and 6 (SEQ ID NO : 4 and SEQ ID NO : 6, respectively) were used for the secondary PCR using the first round of PCR products as templates. For the 5'end walking, primers 3 and 7 (SEQ ID NO : 3 and SEQ ID NO : 7, respectively) were Table 2 Oligonucleotides Template Primer number and sequence CBS 6054 1 : 5ATITTCCTYGAATCYRTYGCYGGIGTYCCWGG-3' genomic DNA 2 : 5'ACRGCYTCYTCYTCIARGTADCCRACGAATCTGTG-3' 3 : 5'-GTAATACGACTATAGGGC-3' (APl) Linear fragment 4 : 5'-ACTATAGGGCACGCGTGGT-3' (AP2) libraries of CBS 6054 5 : 5'-CCGTTGCTTCCTTCATCAGACACTTGCAT-3' 6 : 5'-GGTGTATTCTGCAACTTGTTCTTCTTGT-3' 7 : 5'AAGAATGCAAGTGTCTGATGARGAAGGAAGCAA-3' 8 : 5'-GAACAAGAAGAACAAGTTGCAGAATACAC-3' PsSTOl (3 kb) 9 : 5'-GGCTCGTCTTTACGTCTTCGCATCTCAT-3' 10 : 5'-GCATGTGAAGACTTGAACGGGTTGACTT-3' PsURA3 (1. 4 kb) 11 : 5'-CCATCGATGGGAGCCGTTGTCTGAGAAG-3' 12 : 5'-CCATCGATGGAATAGGCCTCTGCTTGT-3' PsSTO1 coding region 13 : 5'-ATGCTTCTGTGCAGACTACAAGAGCC-3' (1. lkb) 14 : 5'-TTACAATTTCAATTCTTCCTTCTCCC-3' PsLEU2 (1. 6 kb) 15 : 5'-GGCATGACTAACCAAAGTGAA-3' 16 : 5'-CGTTCGCTCTTGTGAGAGCATT-3' PsCYCl 5'flanking region 17 : 5'-CGGGATCCGAGCTGTCTCATGTCCCTTACAA-3' (1 kb) 18 : 5'-CGGGATCCACCTGGGATGTACTTCTTTGGGTT-3' PsCYCl 3'flanking region 19 : 5'-CCGCTCGAGCCAGCATAGAGTGAACGAAACCAC-3' (0. 8 kb) 20 : 5'-CCGCTCGAGCAGGGAGCTTTAGACCAGCATGGT-3' PsCYCl coding region 21 : 5'-ATGCCAGCTCCATTCGAAAGGG-3' (0. 3 kb) 22 : 5'-TTACTTGGTGGCGGAAGCCAAG-3' PsSTO1 coding region 23 : 5'-CCGCTCGAGCGGATGCTTCTGTGCAGACTACA-3' (1. 1 kb) 24 : 5'-CCGCTCGAGCGGTTACAA'ITTCAATTCTTCCTTC-3' Table 3 Vectors and plasmids<BR> Plasmid Relevant characteristics Reference<BR> PCR2.1 TOPO Cloning vector Invitrogen<BR> PCR Blunt II-TOPO Cloning vector Invitrogen<BR> pNQ28 Contains the 293 bp PsSTO1 Thiw work<BR> pNO30 Contains full length (3.0 kb) PsSTO1 this work<BR> pNQ31 Contains the psSTO1 disruption cassette This work<BR> pYPR2831 Contains ScGAPD promoter and terminator Horiuchi et al., 1990<BR> pNO32 Cotains the expression cassette of PsSTO1 in pYPR2831 This work<BR> pNQ35 Contains 0.9 kb PsACT1 gene This work<BR> pNQ38 Contains RT-PCR products of PsSTO1 This work<BR> pNQ37 Contains PsLEU2 cassette This work<BR> pNQ39 Contains PsLEU2 cassette fused to PsCYC1 5' flanking region This work<BR> pNQ41 Contains PsCYC1 disruption cassette using PsLEU2 This work

used for the primary PCR, while primers 4 and 8 (SEQ ID NO : 4 and SEQ ID NO : 8, respectively) were used for the second round. The Advantage PCR kit (Clontech) was used in all the PCR reactions for waLking. The PCR conditions were as recommended by the manufacturer's manual. The secondary PCR products were directly cloned into the PCR2. 1-TOPO vector for DNA sequencing. After obtaining the sequences, primers 9 and 10 (SEQ ID NO : 9 and SEQ ID NO : 10, respectively) were used to amplify a 3-kb PsSTOl fragment by using Pfu DNA polymerase (Strategene). This fragment, which contained 1 kb of each flanking region and the coding region, was cloned into the PCR- BluntII-TOPO vector (Invitrogen) as pNQ30. This 3-kb clone was fully sequenced as the final deposited data.

E. Isolation of mRNA and RT-PCR Cells of CBS 6054 grown under fully aerobic conditions (OD600<2) on YNB- xylose (2%) were used to isolate total RNA. Under this condition, no ethanol was formed (Shi et al., 1999). mRNA was extracted using a Dynabeads mRNA Direct Kit (Dynal). 100 gL cells were mixed with 1 mL lysis buffer and Dynabead Oligo (dT) 25 for 5 min. The mRNA was separated by a Magnetic Separation Stand (Promega) and washed twice with the washing buffer. The mRNA was eluted at 65 °C and stored at- 80°C for future uses. Reverse transcription PCR (RT-PCR) was performed by using a Super Script One-Step RT-PCR System (Life Technologies). The reaction volume was 50 zip containing 0. 3 ßg m : RNA, 0. 2 uM each primer, 25 uL 2X reaction mix, 1 uL Super Script RT/Taq DNA polymerase mix. cDNA was synthesized at 50°C for 3 min and denatured at 94°C for 2 min. The nRT-PCR was carried out by running a program consisting of 40 cycles : 94°C for 15 s, 55°C for 30 s and 72°C for 80 s. The final RT- PCR reaction was terminated with 1 cycle of 72°C for 10 min. The primers for RT-PCR of PsSTOl were SEQ ID NO : 11 and SEQ ID NO : 12.

F. Construction of the single stol-knockout stain A one-step gene replacement method was employed to disrupt the PsSTOl gene in FPL-UC7 (Lu et al., 1998). A 1. 4-kb PsURA3 fragment was amplified from pVY2 (Yang et al., 1994) using Pfu DNA polymerase by primers 13 and 14, (SEQ ID NO : 13 and SEQ ID NO : 14, respectively) with a ClaI site at each end. The PCR conditions were the same as described in Shi and Jeffries (1998). This fragment was

digested with ClaI, and sub-cloned into the CM site of the PsSTOl coding region in pNQ30 to create pNQ31.

G. Yeast transformation The disruption cassette was liberated from pNQ31 by NdeI and EcoRI, and used to transform FPL-UC7. This cassette was also used to transform another P. stipitis host, PLUS, which has two selectable markers (Lu et al., 1998). REMI transformation (SYnchez et al., 1998) was carried out by using the EZ-transformation kit (BiolOl).

Putative stol-A colonies from FPL-UC7 or FPL-PLU5 were picked after 2-3 days on YNB-glucose (2%) minimum medium without uridine.

H. Screening of putative stol-A disruptants Two aL of the yeast cells were lysed by using a Yeast Whole Cell Lysis Kit (BiolOl) at 37°C for 1 h. The resulting lysate was mixed with 200 uM dNTPs, 10 uM each primer, 10X PCR buffer, 1. 5 mM MgCl2 to 99 tiL volume, and heated at 95°C for 15 min. Five units of Taq DNA polymerase (Roche) were added to the mixture, and the PCR reaction was run with 40 cycles of : 95°C for 1 min, 50°C for 1 min And 72°C for 1 min. The PCR reaction was terminated with 4 min of final extension at 72°C. Primers 11 and 12 (SEQ ID NO : 11 and SEQ ID NO : 12) were used to screen the putative disruptants. The single knockout strain from FPL-UC7 was named FPL-Shi31while the single knockout from FPL-PLU5 was named FPL-Shi41.

1. Construction of a double knockout (stol-A, cycl-A) strain In order to obtain a double knockout strain using FPL-Shi41, a new PyCrC7 disruption cassette was constructed. A PsLEU2 cassette was amplified by primers 15 and 16 (SEQ ID NO : 15 and SEQ ID NO : 16, respectively), and the fragment was sub cloned in the BluntII-TOPO vector to make pNQ37. A l-kob 5'flanking region of PsCYCl was amplified by primers 17 and 18 (SEQ ID NO : 17 and SEQ ID NO : 18, respectively) with a BamHI site at each end. This fragment was cut with BamHI and cloned into the BamHI site of pNQ37 to create pNQ39. A 0. 8-kb 3'flanking region of PsCYC1 was amplified by primers 19 and 20 (SEQ ID NO : 19 and SEQ ID NO : 20, respectively) with a XhoI site at each end. This fragment was cut with XhoI and cloned into the X7iol site of pNQ39 as pNQ41. The resultant disruption cassette was linearized by NdeI and Ncol, and used to transform FPL-Shi41. The putative double knockout colonies were selected on YNB-glucose minimum medium without uridine and leucine.

The putative disruptant colonies were screened by colony PCR using primers 21 and 22 (SEQ ID NO : 21 and SEQ ID NO : 22, respectively).

J. Mitochondrial isolation and protein analysis P. stipitis cells were grown overnight in 25 mL sugar-limited medium (yeast extract, 3 g*L-t, malt extract, 3 g L-1, xylose, g I. ;') in a 125-mL baffled flask (Guvinden, 1995). The flask was shaken at 160 rpm at 30°C. The next day, 15 mL of the overnight culture was used to inoculate 500-inL fresh medium in a 2-L baffled flask. The culture was shaken at 160 rpm at 30°C for 24 h. Mitochondria from P. stipitis were isolated mechanically as described by (Luttik et al., 1998) or by the sucrose gradient ultra centrifugation method (Defontaine et al., 1991 ; Querol and Barrio, 1990). For the mechanical method, 20 mg Zymolase 20T was used in 35 mL of buffer A containing 25 mM potassium phosphate, 1 mM MgCl2, 1 mM EDTA (pH 7. 5).

For the sucrose gradient method, the cells harvested from of one liter cultures. The cells were treated with 0. 5 mg'L' Novozyme 234 in 5 mL of solution A containing 0. 5 M sorbitol, 10 mM Tris-HCl (pH 7. 5). Mitochondrial protein was released by using glass beads in a cell disruption buffer containing 100 mM sodium phosphate, 1 mM EDTA and 5 mM ß-mercaptolethanol (Ciriacy, 1975). After vortexing three times for 1-min in a glass tube, the mixture was transferred to a new microfuge tube. The tube was spun down at 16, 000 g for 2 min and the top layer was transferred to a new microfuge tube. Protein concentration was determined by the BCA protein assay system (Pierce). Fifteen ug mitochondrial protein was loaded on a 10-20% Tris-HCl reducing SDS-PAGE gradient gel (Biorad). After electrophoresis (40 min at 200 volts), the protein was transferred to a nylon membrane (Schleicher & Schuell). The blot was first hybridized with 1 : 100 dilution of a mouse monoclonal antibody raised against the Sto of Sauromatum guttatum (Elthon et al., 1989), then the blot was cross-reacted with an anti-mouse secondary antibody conjugated with an alkaline phosphatase at a 1 : 5000 dilution (Promega). The color was developed by the NBT/BCIP system (Promega).

K. Expression of PsST01 in S. cerevisiae To express the PsST01 gene in S. cerevisiae, the coding region was amplified using Pfu DNA polymerase from CBS 6054 genomic DNA. Primers 23 and 24 (SEQ ID NO : 23 and SEQ ID NO : 24, respectively) were used, which contained a SoI site at each end. The PCR conditions were described in Shi and Jeffries (1998). The amplified fragment was digested with Show, and cloned into the SalI site of an

expression vector, pYPR2831 (Horiuchi et al., 1990) by using a Rapid DNA Ligation Kit (Roche). Thus, the PsST01 was driven by the constitutive glyceraldehyde phosphate dehydrogenase (GAPDH) promoter from S. cerevisiae, and terminated with the GAPDH tenninator. The resultant clone was named as pNQ32, and 5 ug of the plamid DNA was used to transform two S. cerevisiae strains, 679a a gift from Dr.

Michael Culbertson, University of Wisconsin, Madison, WI) and B06748 (Holzschu et al., 1989). The empty vector without the PsST01 was also used to transform as the control. Yeast transformation was carried out by using the EZ-transfonnation Kit (BiolOl). Necessary amino acids were added when required for the growth of the control strains.

L. Analysis of the S. cerevisiae transformed with PsST01 Primers 13 and 14 (SEQ ID NO : 13 and SEQ ID NO : 14) were used to confirm the transformants carrying the PsST01 expression cassette. Transfonnants carrying the expression cassette were used for subsequent studies. For the 679a transformants bearing the pNQ32or pYPR2831 plasmid, cells were grown in 500 mL fresh YNBUP medium containing 8% glucose. The cells were grown in 1-L flask and the flask was shaken at 30°C at 140 rpm for 2 days. The cells were harvested and washed twice with 20 mM potassium phosphate buffer (pH 7. 0) containing 5 mM magnesium chloride, and resuspended in 4. 5 mL of the same buffer. Oxygen uptake rates were measured as described above and the assay substrate was 5mM ethanol.

For the B06748 transformants bearing the pNQ32 or pYPR2831 plasmid, a fermentation study was carried out instead of measuring respiration. The strains were first grown in 50 mL fresh YNBUP medium containing 2% glucose for three days at 30°C. The cells were shaken at 140 rpm in a 125-mL Erlenmeyer flask. The cells were harvested and washed with sterile water twice. Then the 3-day-grown cells were cultivated in fresh YNBUP medium at 30°C in a 125-mL Erlenmeyer flask that was shaken at 140 rpm.

M. Dry weight determination and HPLC analysis Cells were spun down at 16, 000 g for 5 min, washed with water for three times, and desiccated in a 105°C oven overnight. At least 2 to 3 replicate samples were used to determine dry weight. One optical density (OD) unit at B=600 nm corresponds to 0. 22 g FPL-UC7 and FPL-Shi31 cells (dry weight) per liter, or 0. 2 g FPL-Shi21 cells (dry weight) per liter. For analyzing fermentation end products, samples were drawn

daily and the samples were spun at 16, 000 g for 5 min. The supernatant solution was diluted 5 fold and subjected to high performance liquid chromatography (HPLC) analysis by using an ICSep-ION-300 column (CETAC Technologies). The column was operating at 60°C with a 0. 4 mL/min flow rate using 0. 008 M sulfuric acid as the solvent. Glucose, xylose, xylitol and ethanol are eluted at 16. 3 min, 17. 5 min, 22. 8 min and 34. 8 min, respectively.

N. Cytochrome spectra studies Strains of P. stipitis were grown in yeast extract medium containing 2% xylose, glucose or ethanol as the sole carbon source. The yeast cells were grown on the surface of a plate for three days as thin"lines"and examined by a spectroscope as described by Sherman et al. (1974). Low temperature (-196°C) spectro-photometric recordings of the FPL-UC7 and FPL-Shi31 were performed with whole cells. The strains were grown on 1% yeast extract, 2% peptone, and 2% xylose at 30°C for three days. The absorption spectra were recorded as previously described (Hickey et al., 1991).

O. Aerobic growth studies P. stipitis cells were grown in 25 mL YNBUP medium containing either 2% glucose or 2% xylose in a 125-mL baffled flask. The flask was shaken at 140 rpm at 30°C for 3 days. The cells were harvested and washed with sterile water twice. The culture was then used to inoculate a 25 mL fresh YNBUP medium containing either 2% glycerol or 2% ethanol in a 125-mL baffled flask. The flask was shaken at 140 rpm at 30°C. The starting cell density was 0. 05 g L-1. Samples were taken every 4 h to monitor growth by measuring the optical density at B=600.

P. Shake-flask fermentation trial Strains of FPL-Shi31, and FPL-UC7 were grown for 2 days under oxygen- limited conditions (Shi et al., 1999) in YNBUP medium containing 2% glucose or xylose. Cells were harvested and washed twice with sterile water. Cells were then used to inoculate 50 mL fresh YNBUP medium containing 8. 4% xylose or 9. 4% glucose in a 125-mL Erlenmeyer flask. The starting cell density was approximately 0. 9 g L-1. The cultures were then grown at 20°C with shaking at 100 rpm. Samples were drawn daily and analyzed by HPLC as described above.

Q. Respiration measurement P. stipitis strains were grown overnight in YNBUP-xylose (2%) medium under aerobic conditions. Then half of the overnight-grown cells were transferred to 25 mL

fresh medium to grow for 16 h to mid-log phase under the same conditions. The cells were harvested and washed in an assay buffer containing 20 mM potassium phosphate (pH7. 0) and 5 mM magnesium chloride. The cells were resuspended in 500 tL of the same buffer for assays. Oxygen uptake was measured by using a Clark type of electrode (Yellow Spring Instrument). The assay was performed in an assay buffer containing 20 mM potassium phosphate, 5 mM magnesium chloride, plus xylose or glucose (2%) as the substrate at 30°C. The assay buffer was saturated with air before the experiment. Ten to fifty tL of cells were injected into the assay chamber and the total reaction volume was 2 mL. Antimycin A, SHAM or rotenone was dissolved in dimethyl fonnamide while potassium cyanide was dissolved in water. Inhibitor solution was injected into the chamber after adding the cells.

R. Oxygen utilization kinetic studies P. stipitis strains were grown under aerobic conditions in 25 mL of YNBUP medium in a 125-mL baffled flask containing 2% xylose. The cells were shaken at 140 rpm at 30°C for overnight. No ethanol was formed under this growth condition. Half of the overnight cultures were then used to inoculate 25 mL of the same medium and the cells were cultivated under the same conditions for 12 h. The cells were harvested and washed twice with 20 mM potassium phosphate buffer (pH 7. 0) plus 5 mM magnesium chloride, and resuspended in 1. 2 mL of the same buffer. Half of the cells were used for dry weight determination while the other half was used for oxygen uptake measurements. Oxygen consumption curves were obtained by injecting cells in an assay buffer containing 20 mM potassium phosphate, 5 mM magnesium chloride, plus 2% xylose as the substrate at 30°C. The oxygraphic curve was recorded from 100% to 0% of air. Thirty to sixty gL of cells were used in the measurements. The assay buffer was saturated with air before the experiment. The dissolved oxygen concentration at 30°C is 237 uM. The data were plotted using the Origin program (Microcal Software).

II. Results A. Cloning of the PsST01 gene To clone PsST01 from P. stipitis, we aligned the available fungal Sto protein sequences, and found that they are highly conserved in two regions IFLES (I/V) AGVPGMV and HRFVGYLEEEAV. The first region contains a putative ubiquinol binding site (Berthold, 1998 ; Andersson and Nordlund, 1999) while the

second region contains a highly conserved ion-binding motif (Vanlerberghe and McIntosh, 1997). Even though these two segments are highly conserved, the organisms and their codon usage may have diverged significantly. We first developed a codon usage table for P. stipitis using 19 cloned genes (obtained by using database : http ://www. dna. affrc. gojp/-nkainura/). We then amplified a 293-bp region, which is located in the center of PsSTOl from wild-type genomic DNA of CBS 6054. This segment displayed 70% similarity at the DNA level with the STO genes from two other yeast species, Pichia anomala and Candida albicans. It was then used as the starting point for genome walking to clone the entire PsSTOl gene.

For the walking strategy, five linear fragment libraries were constructed as described in Methods. For the 5'end walking, two overlapping PsST01 fragments (1. 7 Icb and 4 kb) were obtained from the PvuII and the StuI libraries. For the 3'end walking, five different lengths of overlapping PsSTOl fragments were obtained from the five libraries. Sequencing of all the fragments allowed the merging of the coding region of 1071 bp, and about 1. 0 kb each for the 5'and 3'flanking regions.

B. The biochemical properties of the PsSto protein The open reading frame of PsSTOl encodes for 357 amino acids. The deduced molecular weight for the predicted protein is about 41, 326 daltons. It has a calculated pI of 9. 1. These values are comparable to values reported for Sto proteins from other yeast and fungi (Huk and Kang, 1999 ; Sajoko et al., 1993). A hydrophobicity plot of the PsSto protein revealed two trans-membrane helices that are similar to all reported Sto proteins. A deduced cleavage site for the signal peptide is predicted at the 27th amino acid after the methione start codon.

C. Putative 5'cis-acting elements A search in the 5'untranslated region (UTR) for cis-acting elements revealed two putative TATA boxes at-86 to 79,-194 to-187. Other putative binding sites included a 25-bp AT segment of mitochondrial control region (-158 to-133), a common transcriptional activator responding to stress signals, AP-1 (-689 to-683), an Adh-UAS2 sequence (-666 to-659), a heat shock factor (hsp70) and a nitrogen- regulatory element (-756 to-743). These observations indicated that the PsST01 gene could be regulated by various environmental signals.

D. PsST01 does not contain introns Because introns are found in several fungal STO genes, we decided to examine whether PsST01 contains introns. RT-PCR was performed on wild-type CBS 6054 cells grown on YNB-xylose under fully aerobic conditions. A single 1. l-kob band of RT-PCR product, which was similar in size to the genomic PCR product of PsSTOl, was observed. Complete sequencing of the cloned RT-PCR products revealed that there was no intron present in the PsST01 gene.

E. Phylogenetic studies of the fungal Sto proteins A phylogenetic tree drawn using eight Sto proteins from yeast and filamentous fungi showed that they broke into two separate branches (Fig. 1). PsSto showed 53% identity to these yeast and fungal counterparts. However, PsST01 displayed 33% identity to three other yeast STO genes at the DNA level, and 64% identity at the amino acid level. The PsSto is most closely related to the Sto of P. anomala.

F. Construction of a stol-A mutant in P. stipitis Disrupting the STOI gene in P. stipitis had two purposes. First, we needed to ensure that the cloned sequence encodes for Sto. Second, we hoped to obtain a mutant with the STO pathway impaired, so the electrons only go through the cytochrome c oxidase. This mutant would be used to compare with the cytochrome c disruptant obtained earlier to elucidate the physiological roles of alternative respiration in P. stipitis. To do that, a one-step gene replacement was employed by inserting the PsURA3 gene in the middle of the PsST01 coding region in FPL-UC7 (Fig. 2). The putative disruptants of stol-A were screened by colony PCR. They all showed a single 2. 4-kb band, which corresponded to the size of the coding region of PsST01 plus the inserted PsURA3 gene. The parental strain, FPL-UC7, only showed a 1. l-kob coding region band.

A double mutant (cycl-lS, stol-A) was attempted in a P. stipitis host strain, FPL-PLU5 (Lu et al., 1998) which has two selectable markers. However, the putative double knockout colonies were small as pinpoints. They were not viable after being transferred onto selective medium without uridine and leucine. We therefore concluded that at least one of the respiratory pathways must be present to support cell growth under the conditions we used for cell cultivation.

G. Respiratory inhibitor studies One stol-A strain, was named FPL-Shi31, and it was confirmed by measuring respiration in the presence of inhibitor antimycin A or SHAM. SHAM blocks Sto probably by interfering with the ubiquinol binding site (Berthold, 1998). Upon adding 4 mM SHAM to the stol-4 cells pre-grown on YNB-xylose (2%), the respiration trace did not show any change. This suggested that the SHAM-sensitive respiration in this mutant was totally impaired due to the loss of the structural gene. On the other hand, when 10 uM antimycin A, an inhibitor that blocks electron transfer from the cytochrome bcl complex to cytochrome c, was added to the cells of the stol-t mutant, respiration dropped to zero. This observation indicated that the mutant was unable to sustain any respiration when the CYT pathway was blocked. Conversely, FPL-Shi21 (cycl-A) displayed insensitivity to antimycin A and respiration was completely blocked by SHAM.

H. No other Sto isoforms were induced in the stol-A strain To determine whether there were any isoforms of Sto present in the stol-S mutant (FPL-Shi31), we isolated mitochondrial proteins from four strains of P. stipitis.

A monoclonal antibody raised against Sto from Savromatum guttatum (voodo lily) was used to cross-react with the PsSto. In the samples from CBS 6054, FPL-UC7 and FPL- Shi21, only a single 39 kd band was observed, which corresponded to the size of mature Sto proteins from other yeasts. However, this band was missing from the FPL- Shi31 sample in which the PsST01 was disrupted. This result indicated that no isoforms of Sto are induced in FPL-Shi31. Thus, the Sto in Pstipitis FPL-UC7 is encoded by a single gene, which is similar to the cases reported in P. anomala (Sakajo et al., 1993) and the rice-blast fungus, Magnaporthe grisea (Yukioka et al., 1998).

These results also confirmed that we had obtained a mutant in which the STO respiration was totally blocked. Therefore, cytochrome c oxidase is the only functional terminal oxidase in the stol-A mutant.

I. Cytochrome spectra study in the stol-A strain Because the components of the STO pathway in P. stipitis were unclear, we decided to examine the cytochrome contents in the stol-S mutant to see if any changes occurred in the stol-A mutant. Cells of the stol-0 mutant and the parental strain were cultivated in three media. In the initial studies, the cytochome b, c, cl, and aa3 from

the mutant appeared to be at normal levels under spectro-microscopic examinations.

Subsequent low temperature recordings of both the mutant and parent cells grown on xylose medium was also performed. Cytochromes b, c, and cl from the mutant showed no significant differences from those observed in the parental strain. This indicated that deletion of PsST01 in P. stipitis does not alter the levels of cytochromes b, c, and cl in the cell. The a-a3 peak in the mutant was slightly higher than the parent. The small increase in aa3 suggested that the deletion of Sto might affect the level of the remaining cytochrome c oxidase (aa3). We therefore concluded that the STO pathway does not contain cytochromes as functional components.

J. Introducing PsST01 in S. cerevisiae strains We expressed PsST01 in S. cerevisiae for two purposes. First, we wanted to determine whether PsSto could confer cyanide-resistant respiration in a Crabtree- positive yeast, S. cerevisiae, which does not have the STO pathway. Second, we wanted to examine how PsSto functioned in a Crabtree-positive physiological background. The PsST01 gene was introduced into two different S. cerevisiae strains, 679a and B06748. 679a is a strain that has normal respiration capacity (Culbertson, personal communication). By expressing PsST01 in this strain, we could evaluate the effect on its respiration capacity after getting an additional terminal oxidase. Both oxidases would accept electrons from the rotenone-insensitive NADH dehydrogenases.

On the other hand, B06748 is a cytochrome c null mutant (Holzschu et al., 1987) due to the deletion of the 6*cCYC7 and ScCYC7, which encode the two isoforms of the cytochrome c. As previously reported, deleting cytochrome c in S. cerevisiae and other yeasts can lead to simultaneous disappearance of cytochrome aa3 (Cox) (Bottorff et al., 1991 ; Pearce, 1995 ; Shi et al., 1999). Therefore, it is unable to accept electrons from the cytochrome respiratory chain. Therefore, B06748 is a slow grower and uses fermentation to generate energy. In this genetic background, we could evaluate the effect of using Sto as the only terminal oxidase in a Crabtree-positive yeast. A constitutive ScGAPDH promoter was used to drive the PsST01 gene in both strains (Fig 3. 11A).

Genomic PCR was used to confirm that the transformants bear either the pNQ32 plasmid or the empty vector, pYPR2831, in 679a or B06748 (data not shown).

For the 679a transformants, we measured oxygen consumption rates from the cells grown aerobically in the presence of glucose. Oxygen uptake experiments showed that

the respiration rate from 679a (pNQ32) is 63% higher than that recorded from the control. This indicated that introduced Sto contributed to the increased respiratory capacity in transformed strain. Our observations resembled the reports on the functional expression of Sto of Candida albicans in S. cerevisiae (Huh and Kang, 1999) and Sto of S. guttatum in Schizosaccharomyces pombe (1996). Because the Sto is resistant to cyanide, an inhibitor that blocks the activity of the cytochrome c oxidase, we also measured the respiration rate in the presence of 1 mM KCN. Upon adding KCN to the cells, the 679a (pNQ32) strain containing PsST01 was able to show about 4-fold higher cyanide-resistant respiration than the control. We observed a similar result when 10 jim antimycin A was used as the inhibitor (data not shown).

For the B06748 transformants, a respiro-fermentation trial was conducted under oxygen-limited conditions instead of the respiration consumption measurements. The growth condition used was to induce the respiration from the introduced PsSto. In the trial, the transformed strain containing PsST01 showed no significant difference in cell growth from the control strain (Fig. 3A). This indicated that Sto is not phosphorylating.

However, the transformed strain bearing PsST01 showed a slower glucose utilization rate (Fig. 3B) and a lower ethanol production rate (Fig 3C) than the control strain.

These observations suggested that the introduced PsSto could support electron transport as a terminal oxidase in the B06748 background. Taken all the data in this section together, we concluded that introducing PsST01 in S. cerevisiae could impart a functional cyanide-resistant pathway.

K. Aerobic growth results The stol-S mutant (FPL-Shi31) was then tested for its growth capacities on non-fermentative carbon sources. The parental strain, FPL-UC7 and the cycl-A mutant (FPL-Shi21) were used as the controls. The stol-S mutant showed no significant difference from the parent when it was cultivated on glycerol as a carbon source.

However, it showed higher cell density in the ethanol medium than the parent indicating that this strain could oxidize ethanol more quickly than the parental strain.

Conversely, the cycl-A mutant (FPL-Shi21) showed no growth during the 16 h experiment on glycerol and ethanol, which matched the previous observations (Shi et al., 1999).

L. Shake-flask respiro-fermentation results To evaluate the effects of losing the STO pathway to the respiro-fermentative capacity of the mutant, the stol-S strain was tested for its growth and ethanol production rates in medium containing 8. 4% xylose or 9. 4% glucose. In xylose medium, the growth of mutant showed no significant difference from the parent in the first five days. The mutant stopped growing after day 5 while the parent continued to grown until the end of the trial. However, the volumetric ethanol production rate from the stol-A strain on xylose was approximately 20% higher than that from the parent.

The mutant also appeared to use xylose faster than the parent (Fig. 4A and 4B). The mutant did not accumulate any significant amounts of polyols. Interestingly, the mutant did not exhibit significant differences in cell yield, ethanol production rate or sugar utilization rate from the parental strain when grown on glucose. In a separate trial to test the ethanol re-oxidation rate of the stol-A strain and the cycl-A strain, cells from the two strains were grown in YP medium containing 2% xylose. Both strains consumed all the sugars in 36 h. They then began to use the ethanol to support growth.

The ethanol re-assimilation rate for the stol-S strain was faster than the cycl-A strain and the parent.

M. Respiration rate of stol-A strain To test whether the deletion of Sto in stol-S strain would affect its respiratory capacity, oxygen consumption rates of the mutant grown in xylose and glucose media were measured. Respiration rates from the parental and the cycl-A strains were also measured for comparison. For xylose-grown cells, respiration rate was measured using 2% xylose as the assay substrate. The xylose-grown grown cells of the stol-A mutant showed approximately 21% higher respiration rate than the parent. However, the cycl- A mutant showed twofold higher respiration rate than the parent. For glucose-grown cells, respiration rate was measured using 2% glucose as the assay substrate. The glucose-grown cells of the stol-A mutant did not show significant difference in the oxygen consumption rate to the parent. The cycl-lS mutant displayed threefold higher respiration rate than the parent. These results suggested that losing one respiratory pathway could affect the activity of the other system. This effect is more dramatic in the cycl-A mutant, which loses the major energy-generating CYT pathway.

N. Measurement of the oxygen utilization kinetics Due to our primary interest in understanding the oxygen requirement for xylose utilization in P. stipitis, we compared the oxygen affinity constants of the Sto and Cox.

In this study, we created two P. stipitis mutants, cycl-A (FPL-Shi21) and stol-S (FPL- Shi31), each of which has a single functional terminal oxidase. These mutants were obtained from the same genetic background, so other factors were similar. Oxygen affinity of Sto and Cox were studied using xylose as the substrate.

In physiological studies, the Km (02) values can be calculated from the non- linear region of an oxygraphic curve. This occurs between the linear region, in which oxygen saturates the uptake system, and 0% oxygen where oxygen consumption stops.

This can be measured at whole cell level (Rice and Hempfling, 1978 ; Dubreucq et al., 1990). In this non-linear region, oxygen uptake rates (V) at different oxygen concentrations (S) can be deduced. By using V as a function of the oxygen concentration at which the tangent is drawn, the Km value can be deduced from a double-reciprocal plot of oxygen uptake rates against oxygen concentrations. Vmax measured, in this case, is the oxygen consumption rate of each pathway, which corresponds to its theoretical maximum capacity. The deduced 1/Km value reflects the affinity of the oxidase to oxygen. In this experiment, the affinity constant represents the affinity of the oxidase as the electron donor with regard to oxygen, which is used as the electron acceptor.

Xylose-grown cells of FPL-Shi21 and FPL-Shi31 were used in this study. The deduced Km and Vmax values were obtained. Under our growth condition, the deduced Km of Cox was 1. 6-fold higher than that of Sto indicating Sto has higher affinity to oxygen than Cox. The Km of PsSto is in line with those reported before from plant mitochondria (0. 5-2 juM. Ribas-Carbo et al., 1994 0. P. stipitis employs different proton-translocating sites during xylose or glucose metabolism Because certain Crabtree-negative yeasts contain different NADH oxidation systems, we decided to test if the rotenone-sensitive or the rotenone-insensitive NADH dehydrogenases are present in P. stipitis. This study is very important because it will provide information on the first component of the respiratory systems in P. stipitis.

This information can also aid in understanding the functional organization of the STO pathway. The NADH dehydrogenase complex I (Complex I or Site I) is sensitive to

rotenone while the internal and external NADH dehydrogenases are resistant to it. The internal or the external NADH dehydrogenase can be distinguished by their different temperature dependency (Marx and Brinkman, 1978).

In the first trial, we measured respiration from aerobically xylose-or glucose- grown cells of wild-type CBS 6054 P. stipitis in the presence of rotenone. When 0. 1 mM rotenone was injected to the glucose-grown cells of CBS 6054, the cells died and floated in the chamber within 1 minute of injection. This indicated that these cells were sensitive to rotenone and could not sustain any respiration. Conversely, when 0. 1 mM rotenone was injected to the xylose-grown cells of CBS 6054, respiration was sustained and the rate was similar to that detected from the untreated cells (Table 4). Rotenone- insensitive NADH dehydrogenases are present in the xylose-grown cells, which enables the cells to by-pass Site I. A subsequent trial was performed on the xylose-and glucose-grown cells in four P. stipitis strains. Xylose-grown cells of wild type CBS 6054 and the parental strain, FPL-UC7, displayed insensitivity to rotenone. However, the xylose-grown cells of the stol-A and the cycl-A mutants were rotenone-sensitive.

On the other hand, the glucose-grown cells of the four strains were rotenone-sensitive (Table 5). These results implied that there might be a fundamental difference in numbers of proton-translocating sites present in cells during xylose and glucose metabolism.

The present invention is not limited to the exemplified embodiments, but is intended to encompass all such modifications and variations as come within the scope of the following claims.

Table 4 Oxygen consumption rates of cells of P. stipitis wild-type CBS 6054 in the presence<BR> or absence of 0.1 mM rotenone.<BR> <P>Glucose-grown cells Xylose-grown cells<BR> µM#mg-1#h-1<BR> -rotenone +rotenone -rotenone +rotenone<BR> 2.9~0.1 NDa 4.5~0.2 4.6~0.2<BR> NDa: not detected Table 5 Rotenone sensitivity experimnt on four P. stipitis strains in the presence of 0.1 mM rotenone<BR> Strains<BR> Wild-type CBS6054 FPL-UC7 (ura3-3) FPL-Shi31 (sto1-#) FPL-Shi21 (cyc1-#)<BR> Xylose-grown cells + + - -<BR> Glucose-grown cells - - - -<BR> +:Cells sustained rotenone-insensitive respiration<BR> -:Cells could not sustain rotenone-insensitive respiration

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