A xylose-fermenting yeast hybridized by intergeneric fusion between Saccharomyces cerevisiae and Candida intermediamutants for ethanol production
© Kahar and Tanaka; licensee Chemistry Central Ltd 2014
Received: 17 December 2013
Accepted: 7 August 2014
Published: 22 August 2014
Bioethanol production from lignocellulosic biomass, in particular xylose, is currently of great concern, given the abundance of this sugar in the world, because Saccharomyces cerevisiae, which is widely used for bioethanol production, is unable to naturally ferment xylose. The aim of this study was to obtain a novel yeast capable of stably producing ethanol from biomass containing xylose by protoplast fusion between S. cerevisiae and xylose-utilizing yeast.
We describe a novel xylose-fermenting yeast strain, FSC1, developed for ethanol production by intergeneric hybridization between S. cerevisiae and Candida intermedia mutants by using a protoplast fusion technique. The characteristics of the FSC1 strain are reported with respect to xylose fermentation, morphology, gene, and protein expression. Mutation of the parental strains prior to protoplast fusion endowed the FSC1 strain with the ability to convert xylose to ethanol. Microscopic analysis confirmed that the parental and FSC1 strains produced spores in the potassium acetate medium. The FSC1 strain is uninucleate diploid, has a stable metabolism, and expresses proteins at a higher level than the parental strains. We found that FSC1 strain could stably achieve an ethanol yield of 0.38 g/g-substrate in fermentation of a mixture of glucose and xylose. In addition, the fermentation ability of FSC1was improved by successive chemical mutation, resulting in a higher ethanol yield of 0.42 g/g-substrate, corresponding to 82% theoretical yield.
The mutation-fusion technique we have described here is very useful for the development of intergeneric hybrids capable of xylose fermentation, and the FSC strains generated using this technique have the potential for industrial use in ethanol production from lignocellulosic biomass.
KeywordsXylose fermentation Intergeneric hybridization Mutation and fusion Saccharomyces cerevisiae Candida intermedia
With the increasing appreciation of the problem of global warming, bioethanol has recently gained increasing attention as a renewable and carbon-neutral energy source. Bioethanol production through the fermentation of lignocellulosic biomass, in particular xylose, is currently of great concern, given the abundance of this sugar in wood and herbs. Given that Saccharomyces cerevisiae, which is widely used for bioethanol production, is unable to naturally ferment xylose, there is increasing investigation of its metabolic alteration to endow it with the ability to ferment xylose.
In general, fungal xylose fermentation initially requires two sequential reactions, namely, the conversion of xylose to xylitol, catalyzed by xylose reductase (XR), and the conversion of xylitol to xylulose, catalyzed by xylitol dehydrogenase (XDH). In a reaction catalyzed by xylulokinase (XK), xylulose is then phosphorylated to xylulose-5-phosphate before entering the pentose phosphate pathway (PPP). While S. cerevisiae is unable to ferment xylose because of the lack of XDH activity in the presence of glucose, it possesses the XYL2 gene, encoding XDH , as well as the homologous gene XKS1, encoding XK –, and GRE3, encoding aldose reductase, which is closely related to XR . In addition, the ability of S. cerevisiae to take up xylose through hexose transporter, and its aldose reductase activity, can be enhanced by chemical mutation and intensive screening on the basis of 2-deoxyglucose (DOG) tolerance .
The metabolic alteration of the yeast for ethanol production has been attempted through mutation, fusion, and recombination. Improvements in yeast metabolism have been reported by mutation and fusion between S. cerevisiae and Zygosaccharomyces fermentati, S. cerevisiae and Pichia stipitis, Kluyveromyces marxianus TS8-1 and TS87-8 , and S. cerevisiae and Candida shehatae. During culture passages, however, some fusants were dissociated into segregants resembling the parental strains , and fusant offspring are almost completely sterile mainly because of the inability of the chromosomes of the partner genomes to pair or to recombine . More recently, several attempts have been made to transfer specific genes for xylose utilization to S. cerevisiae by construction of recombinant strains (reviewed by Matsushika et al., ref ). The recombinants are expected to be practically applied for ethanol production from lignocellulose by overcoming such problems as redox imbalance in the initial step of xylose fermentation and reverse flux in glycolysis .
The xylose transporter of yeast Candida intermedia PYCC 4715, which grows equally well in xylose and glucose and has a high xylose transport capacity , has been functionally expressed in recombinant S. cerevisiae to increase its xylose uptake . From these studies, we think that cell fusion between Saccharomyces and Candida strains may yield a strain which can take up and utilize xylose, as well as glucose, for ethanol production. Since cell fusion allows the transfer of complete segments of genomic DNA from parental yeasts, a fusant rich in genetic information could be obtained by protoplast fusion and stabilized by routine mutation and screening techniques. C. intermedia is nonpathogenic and safe for use. Consequently, C. intermedia has potential as a cell fusion partner with S. cerevisiae for the transfer of genes for xylose fermentation.
The aim of this study was to obtain a novel yeast capable of stably producing ethanol from biomass containing xylose by harnessing recent progress in intergeneric hybridization techniques with proteomic analysis. We developed a novel xylose-fermenting strain by intergeneric protoplast fusion between S. cerevisiae and C. intermedia strains altered, in advance, by mutation. The fusant obtained was subsequently characterized with respect to xylose fermentation, ethanol yield, morphology, and gene and protein expression.
Mutation of wild-type strains and fermentation by mutants
The mutant M2 strain improved in xylose uptake had been selected from diverse mutant colonies of S. cerevisiae grown on medium containing DOG as described in a previous study . Since the M2 strain lacks the XDH activity, C. intermedia was used as a donor of xdh gene in cell fusion of this study. C. intermedia can originally take and metabolize xylose into ethanol, but its ability of ethanol production is not high. Therefore, it is important to use the C. intermedia mutant that has no ability for taking xylose upon the fermentation. As described in the Methods, C. intermedia was mutated using ethyl methane sulfonate (EMS) to obtain a strain in which xylose uptake was strongly suppressed, but which contained the xdh gene. DOG was used for screening DOG-sensitive mutants to surely repress the growth of parental m11 in regeneration of fused protoplast cells. We finally selected a mutant m11 strain considered to have the potential to endow the fusant with the ability to metabolize xylose when hybridized with the M2 strain by protoplast fusion, as described in the following hybridization.
Hybridization between S. cerevisiae M2 and C. intermediam11 by protoplast fusion
A target strain that first appeared was selected from three colonies formed in MMXDOG medium and named FSC1, as a fusant between S. cerevisiae M2 and C. intermedia m11. Brilliant Green staining and SEM observation confirmed that the FSC1 strain produced spores in KAc medium (Figure 2b, d and f).
Metabolism by xylose-fermenting fusant FSC1
Fermentation characteristics of FSC strains determined by batch fermentation in YMGX medium at 30°C under microaerobic condition
(g g-cells−1 h−1)
(g L−1 h−1)
Stability of metabolism is also concern for strains altered by mutation and fusion. As shown in Figure 5c, the FSC1 strain showed a high stability in both ethanol production and xylose consumption over 14 generations.
Requirements of S. cerevisae M2, C. intermedia m11 and FSC1 strains on amino acids in MMG medium at 30°C
Growth (+, grow; −, not grow)
S. c. M2
C. i. m11
Enriched with amino acids
Mutation is often used to generate improved yeast strains . We tried to improve the fermentation ability of the FSC1 strain by mutating twice using EMS in the manner described for the parental strains in Methods. The FSC1 mutant obtained showed 0.42 g/g-substrate in ethanol yield, 10% higher than by the FSC1 strain, as shown in Table 1. A xylose consumption rate was also 6 times higher, improved from 0.18 to 1.07 g/g-cell.h.
mRNA and total protein expression
With regard to total protein expression analyzed by two-dimensional polyacrylamide gel electrophoresis (2D-PAGE), most of the protein spots detected in the M2 and m11 strains were present at higher levels in the FSC1 strain (Figure 6b). Based on a search using Mascot, two of the proteins were considered to match to XR (score = 72, required score > 43, p < 0.05) and glyceraldehyde-3-phosphate dehydrogenase (TDH) (score = 130, required score > 59, p < 0.05).
Here, intergeneric hybridization between the S. cerevisiae M2 and C. intermedia m11 strains was conducted by protoplast fusion. The resulting xylose-fermenting FSC1 strain was characterized in terms of xylose metabolism, protein expression and ethanol yield.
Fusants are generally less stable in metabolism because of the loss of non-homologous genes and chromosomes in chromosome segregations. To overcome this problem, we used haploid cells formed under suppression of mating by exogenous α factor in the M2 strain , anticipating a similar effect in the m11 strain, and performed electrofusion to attain more stable uninucleate polyploids  after chemical fusion using polyethylene glycol (PEG). Exogenous α factor inhibits mating when present in excess , though it is reported that prior activation of cells by α factor induces nuclear fusion . In addition, we employed C. intermedia as a donator of the genes for xylose fermentation on the basis of a study reporting that genes and proteins necessary for xylose fermentation from C. intermedia can be functionally expressed in recombinant S. cerevisiae.
The FSC1 strain possesses high and stable rates of xylose fermentation and ethanol production from a substrate containing glucose and xylose. We consider that the mutation of the parental strains enabled their fusion to transfer genes for xylose fermentation of C. intermedia and for ethanol production of S. cerevisiae. Since the FSC1 strain was apparently uninucleate (Figure 4d), we confirmed that our mutation-fusion technique resulted in nuclear fusion of protoplasts, which is desirable since homocaryons are metabolically more stable than heterocaryons. Since the FSC1 strain produces spores in KAc medium for sporulation (Figure 2b, d and f), we believe that the FSC1 strain is diploid, resulting from fusion between M2 and m11 haploids. This is not contradictory to previous studies reporting that several Candida species have MTL loci with two idiomorphs, namely a and α, which are mating type-like loci similar to MATa and MATα of S. cerevisiae, although Candida is a large and heterogeneous taxon.
All genes necessary for xylose metabolism xr, xdh, and xk (xks1) were expressed at a higher level in FSC1 than in the parental strains (Figure 6a). Moreover, the level of total protein expression in FSC1 was also higher than a simple summation of the parental strains when the same amount of crude cell extracts were loaded on gel (Figure 6b), most likely due to the activation in FSC1 of numerous metabolic pathways during fermentation. RT-PCR and matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF/TOF) analysis indicated that XR derived from C. intermedia m11, and TDH from S. cerevisiae M2, were both expressed in FSC1. Since TDH is required for glycolysis and, by extension, cell viability , the expression of TDH in the FSC1 strain is important to convert xylose to ethanol via glycolysis. These results indicate that the FSC1 strain is an intergeneric hybrid between S. cerevisiae M2 and C. intermedia m11, a fact supported by the observation that normal mating of the parental strains did not occur (Figure 3d).
The metabolic properties of the FSC1 strain indicate that it maintains the redox balance required for fermentation inside the cell. Redox imbalance, which is thought to be caused by coenzyme specificity differences between heterogenic XR (with NADPH) and XDH (with NAD+) enzymes, is a major cause of xylitol accumulation inside and outside the cell, resulting in the reduction of ethanol yield –. Since cell fusion allows the transfer of complete segments of genomic DNA from parental cells, a fusant will be rich in genetic information. We suggest that the higher expression of proteins in the FSC1 strain is not caused simply by the activation of metabolic pathways (PPP) for xylose fermentation, but by the presence of overall metabolic (glycolysis and PPP) regulation to maintain the redox balance for fermentation inside the cell. This is a key point behind the improved xylose utilization, which was supposed from the protein level.
Although fermentation was conducted under microaerobic conditions, undesirable byproducts as glycerol and acetate were not produced. As summarized in Table 1, the ethanol yield and production rate of the FSC1 strain were 0.38 g/g-substrate, corresponding to 75% theoretical yield, and 0.33 g/L · h in fermentation of the mixture of glucose and xylose, respectively. In addition, the fermentation ability of FSC1was further improved by successive mutation, achieving a higher ethanol yield (0.42 g/g-substrate). The ethanol yields of the FSC strains are comparable to 0.34 g/g-substrate of engineered strains of the recombinant S. cerevisiae TMB3400, generated by introducing the gene for xylose transporter from C. intermedia, in a mixture of xylose and glucose, and 0.05-0.46 g/g-substrate in fermentation of xylose as a sole carbon source by various recombinant S. cerevisiae strains . Although the xylose consumption rate (1.07 g/g-cell. h, i.e., 7.1 mmol/g-cell. h) of FSC1 mutant was lower than those with previous reports such as the recombinant S. cerevisiae TMB3400 , the substrate was completely consumed within 30 h, shorter than a normal reaction time 48 h in ethanol fermentation for practical use. We believe that the mutation-fusion technique developed in this study is applicable for metabolic alteration of ethanol producing yeasts as a diverse method from recombination.
We developed a novel xylose-fermenting yeast strain, FSC1, for ethanol production by intergeneric hybridization between Saccharomyces cerevisiae and Candida intermedia mutants by using a protoplast fusion technique. The fermentation ability of the FSC1 strain was further improved by chemical mutation. The mutation-fusion technique we have described is useful for the development of an intergeneric fusant capable of xylose fermentation. The FSC strains obtained by this technique hold the potential for ethanol production from globally abundant lignocellulosic biomass.
Strains and cultivation media
Wild-type yeast strains S. cerevisiae NBRC 2114 and C. intermedia NBRC 10601 were obtained from the NITE Biological Resource Center (NBRC) at the National Institute of Technology and Evaluation (NITE) in Tsukuba, Japan. C. intermedia NBRC 1060 was originally designated as a K. cellobiovorus strain that was reported to be capable of producing ethanol from xylose in 1984 , but was later classified as a neotype of C. intermedia (Ciferri & Ashford) Langeron et Guerra . S. cerevisiae is taxonomically classified into Saccharomycetaceae in family and C. intermedia NRRL Y-981 belongs to the Metschnikowia clade . Because S. cerevisiae and C. intermedia belong to different taxonomical families, experiments on cell fusion were conducted taking the containment measures confirmed by the competent minister under the Act on the Conservation and Sustainable Use of Biological Diversity through Regulations on the Use of Living Modified Organisms (Act No. 97 of 2003, Japan).
The cultivation media were YM medium and minimal medium (MM). YM medium containing 5 g/L Bacto peptone, 3 g/L Bacto yeast extract, and 3 g/L Bacto malt extract was supplemented with the following carbon sources: 10 g/L glucose (YMG liquid); 10 g/L glucose with 20 g/L Bacto agar (YMG); 10 g/L xylose and 5 g/L DOG with 20 g/L Bacto agar (YMXDOG); and 10 g/L fructose and appropriate amounts of DOG with 20 g/L Bacto agar (YMFDOG). MM agar containing 1.7 g/L yeast nitrogen base (without amino acids) with 5 g/L ammonium sulfate and 20 g/L Bacto agar was also prepared with carbon sources of 10 g/L xylose and 5 g/L DOG (MMXDOG). DOG was used for screening DOG-sensitive or DOG-tolerant mutants. MMXDOG and YMXDOG were used for screening the target strain in protoplast fusion. In fermentation tests, YM and MM liquid were supplemented with carbon sources of glucose and xylose at 10 g/L each for seed preparation (YMGX) and at 20 g/L each for fermentation (MMGX). Minimal liquid medium supplemented with 10 g/L glucose (MMG) was also used for the evaluation of amino acid requirements for growth.
All chemicals used in this study were purchased from Sigma-Aldrich (St. Louis, MO, USA), except where mentioned otherwise.
Mutation and screening
To obtain a variety of species of different phenotypes for screening target mutants, S. cerevisiae and C. intermedia strains were individually mutated using EMS (Wako Pure Chemicals, Ltd., Osaka, Japan) as described in our previous study . The strain was grown at 30°C for 6 h in 50 mL of YM medium in 1 L of distilled water. Next, a 1-mL aliquot of the cell suspension was transferred to a 1.5-mL tube. After centrifugation, the cell pellets were washed twice with cold 0.1 M sodium phosphate buffer (pH 7.0), then suspended in 1 mL of the same buffer. EMS (30 μL, purity ≥ 98%) was added to the suspension, giving a final volume of EMS at nearly 3% (v/v). The tube was incubated at 30°C on a roller shaker for 60 min. The reaction was stopped by adding 10% (w/v) sterile sodium thiosulfate solution at a final concentration of 1% (v/v), and the suspension was centrifuged at 5,000 × g for 1 min. After removal of the supernatant, 1 mL of 10% (w/v) sterile sodium thiosulfate solution was added to the pellet, and the suspension was mixed and incubated at room temperature for 15 min to completely terminate the reaction.
After mutation, the mutant cells were washed with 0.1 M sodium phosphate buffer (pH 7.0) three times, and 100-μL aliquots of the suspension were spread on YMFDOG containing 3 g/L DOG. Replica plates were also prepared on YMG, and the plates were incubated at 30°C for colony formation. To screen a DOG-tolerant mutant (named the M2 strain) from S. cerevisiae strain, colonies that appeared were replicated on YMFDOG containing 5 g/L DOG and then screened after incubation at 30°C for 3 days. To screen a DOG-sensitive mutant (named the m11 strain) from C. intermedia, colonies that were unable to grow on YMFDOG containing 3 g/L DOG, were selected from the replica plates. Growth of both mutant strains was evaluated on YMG.
Protoplast fusion and regeneration
Before protoplast fusion, M2 and m11 strains were separately plated onto agar medium containing 1 g/L Bacto yeast extract, 0.5 g/L glucose, 10 g/L KAc, and 20 g/L Bacto agar, and incubated for 24 h for sporulation. A lump of asci containing haploid spores in each strain was cultivated at 30°C for 2–4 h in YMG liquid medium containing 2 mg/L α factor to inhibit mating in M2 strain, with expectation of a similar effect in the m11 strain. Nuclear fusion of S. cerevisiae requires prior activation by α factor, leading to arrest in the G1 portion of the cell cycle, in conjugation , but exogenous α factor inhibits mating when present in excess . Haploid cells in early logarithmic growth phase (α cells) were collected by centrifugation at 5,000 × g for 10 min. Cell pellets were then treated with 20 mM Tris/HCl buffer (pH 7.5) containing 1% (v/v) β-mercaptoethanol and 10 mM ethylenediaminetetraacetic acid disodium salt (EDTA-2Na) for 10 min.
After centrifugation at 5,000 × g for 10 min, the cell pellets were suspended in 20 mM phosphate citrate buffer (pH 6.5) containing 0.6 M sorbitol, 0.6 M KCl, and 10 mM β-mercaptoethanol. Zymolyase 20-T (Takara Bio Inc., Shiga, Japan) was added into the mixture at a final density of 20 mU/mg-cell, and cell pellets were incubated at 30°C for 1 h to obtain protoplasts. Each protoplast was suspended for purification in equal amounts of 20 mM phosphate citrate buffer (pH 6.5) containing 30% (w/v) MgSO4 and 20 mM Tris–HCl buffer (pH 7.5) with 1 M Sorbitol and 0.1 M EDTA, and collected by centrifugation at 3,000 × g for 10 min. Protoplast fusion was carried out by mixing purified protoplasts of both strains at a 1:1 ratio in 1 mL fusion buffer containing 1.2 M sorbitol, 30% (w/v) PEG4000, 0.1 M calcium propionate, 10 mM Tris/HCl (pH 7.2), 1 g/L bovine serum albumin (BSA), and 15% (v/v) dimethyl sulfoxide (DMSO). The suspension was incubated at 30°C for 1 h to enable protoplast fusion, transferred to an electrophoresis apparatus, then exposed to direct current at 50 V for two seconds in triplicate to ensure complete protoplast fusion.
To screen for strains tolerant to DOG, fused protoplast cells were suspended in regeneration medium containing 1.2 M sorbitol, 5× YM (YM enriched with 5-fold additions of Bacto peptone, Bacto yeast extract, and Bacto malt extract), 2% glycerol, 0.6 M potassium chloride, 1 mg/mL colchicine and 5 g/L DOG, and incubated at 28°C for 6–8 h. Colchicine was used as a mitosis inhibitor  for fused protoplast cells, although it has been reported that colchicine does not bind with S. cerevisiae tubulin . Partially regenerated cells were collected by centrifugation at 3,000 × g for 10 min and suspended within 1.5% (w/v) soft agar containing 0.4 M calcium propionate, and then immediately layered onto MMXDOG containing 0.6 M potassium chloride, to allow the complete regeneration of fused protoplast cells.
Seed preparation and fermentation
Seed preparation for fermentation was performed in two steps. In the first step, a single colony of the yeast was inoculated into 100 mL of YMG liquid medium in a 500-mL flask after autoclaving at 122°C for 20 min, and then incubated at 30°C overnight on a shaker at 150 rpm. In the second step, 10 mL of the first seed were transferred in quadruplicate to 100 mL of YMGX liquid medium in a 500-mL flask, which was then incubated at 30°C for 24 h on a shaker at 150 rpm. After collecting and washing twice with sterile phosphate-buffered saline (PBS), cells were resuspended in PBS in a minimal volume (50 ml).
Fermentation was started by adding 50 mL of cell suspension containing 1.3–1.5 g-dried weight (DW) of cells to 950 mL of MMGX medium in a jar fermenter. 5 N NaOH was used to maintain pH 5 in the culture. To maintain microaerobic conditions, air was pumped through a sterilized membrane filter into the reactor to maintain 5% dissolved oxygen under the air-saturated condition. Levels of glucose, xylose, xylitol, glycerol, and ethanol in the culture medium were quantified by high performance liquid chromatography (HPLC) as described in the previous study . Stability of fermentation by fusant cells was confirmed in both ethanol production and xylose consumption over 14 generations. Generation in this context refers to the culture of glycerol stock cells obtained from one single colony appearing on appropriate cultivation agar YMGXDOG.
Gene and total protein expression analyses
Cells were harvested from the jar fermenter directly after depletion of the carbon sources, washed with cold sterile water twice and then freeze-dried. Freeze-dried cells (100 mg) were suspended in 250 μL Yeast protein extraction reagent (Y-PER) supplemented with 5 μL protease inhibitor (Wako Pure Chemicals, Ltd., Osaka, Japan), incubated for 60 min, then centrifuged at 14,000 × g for 10 min. To remove excess salts, the supernatant was passed through a desalting column Bio-Gel P-6 (BioRad Lab., Inc., Hercules, CA) buffered with 10 mM Tris/HCl (pH7.4), and the eluate was used as a protein mixture sample for total protein analyses.
To confirm the expression levels of genes related to xylose utilization (xr, xdh, and xk) and conversion of acetaldehyde to ethanol (adh1) in M2, m11, and fusant cells, RT-PCR analyses were performed. Cells were microaerobically cultivated for 18 h then collected by centrifugation at 5,000 × g for 10 min at 4°C. Collected cells were washed twice with cold sterile water and immediately freeze-dried. After mechanical disruption with a sample grinding kit (GE Healthcare, Inc., Uppsala, Sweden), total RNA was extracted from cells (30 mg-cell DW) using NucleoSpin RNA II (Macherey-Nagel GmbH & Co. KG, Düren, Germany). mRNA was purified from total RNA using Oligotex-dT30 < super > mRNA purification kit (Takara Bio, Inc.). PCR primers were designed on the basis of NCBI databases of genomic DNA from S. cerevisiae (Sc) and Candida species (Ci) as follows: (forward) 5′-CCATCCAGGCAGTACCACTT-3′ and (reverse) 5′-TACCATCCAACCAGGTCCAT-3′, for Sc-gre3 (Accession no. CR382125.1); (forward) 5′-GGCTCAATTAACAGGGTCCA-3′ and (reverse) 5′-ACAGGCATCTGCCTCCTCTA-3′, for Sc-xks1 (Accession no. NC_006041.1); (forward) 5′-AGGCCAACGAATTGTTGATCA-3′ and (reverse) 5′-GTGTCAACAACGTATCTACCA-3′, for Sc-adh1 (Accession no. NC_006042.1); (forward) 5′-CCTGCTGTTTTGCAAGTTGA-3′ and (reverse) 5′-CTCTTTGAGCGGACCATCTC-3′, for Ci-xr (Accession no. AF278715.1); (forward) 5′-AATGGTCTTGGGTCACGAATCC-3′ and (reverse) 5′-GCTCTGACCAAGTCGTAGGCTTC-3′, for Ci-xdh (Accession no. JN578088.1); (forward) 5′-GGATTCGACTTATCCACCCAACAA-3′ and (reverse) 5′-CCAGTACACGGATCCATGTTG-3′, for Ci-xk (Accession no. FM992691.1); (forward) 5′-CACTCACGATGGTTCATTCG-3′ and (reverse) 5′-AAGATGGTGCGACATTGG-3′, for Ci-adh1 (Accession no. KC236900.1). RT-PCR amplification of purified mRNA was carried out using a One Step PrimeScript RT-PCR Kit (Takara Bio, Inc.). RT-PCR gene products were separated electrophoretically in a 1% (w/v) TAE agarose gel and viewed using a UV transilluminator.
For total protein expression, the protein extract of each strain was analyzed by 2D-PAGE as previously reported . Isoelectric focusing (IEF) electrophoresis of desalted protein samples was performed using IPG ReadyStrip pH3-10 NL (BioRad Lab., Inc.) conditioned in Protean IEF system (BioRad Lab., Inc.). We prepared the crude cell extracts adjusted to 100 μg respectively from M2, m11 and FSC1 strains, under the same procedure. After treatment in an alkylation solution containing 100 mM iodoacetate, 6 M urea, 2% (w/v) sodium dodecyl sulfate (SDS) and 20% (v/v) glycerol in 0.375 M Tris/HCl (pH 8.8), the IPG strip was applied to a 15% non-gradient SDS-PAGE electrophoresis. Finally, the developed gel was stained using a sensitive colloidal Coomassie G-250 solution to observe significant changes of total protein expression.
Protein spots were identified by MALDI-TOF/TOF analyses. Spots were enzymatically digested in a manner similar to that previously described  using modified porcine trypsin (Promega Corp., Madison, WI). Gel pieces were washed with 50% (v/v) acetonitrile to remove SDS, salt, and stain. Washed and dehydrated spots were then vacuum-dried to remove solvent and rehydrated with trypsin (8–10 ng/μL) solution in 50 mM ammonium bicarbonate at pH 8.7 and incubated for 8–10 h at 37°C. The samples were analyzed using an Applied Biosystems 4700 proteomics analyzer with TOF/TOF ion optics (Genomine Inc. Pohang, Korea). Sequence tag searches were performed using Mascot search (http://www.matrixscience.com).
For microscopic observation of sporulation, each strain was sporulated using KAc agar containing 10 g/L KAc and 20 g/L Bacto agar for 7 days at 30°C in the manner described earlier. After incubation, spores were removed from the surface of the agar medium by washing with 0.05% Tween 80 in saline solution. The suspension was centrifuged at 3,000 × g for 10 min at 4°C. The supernatant was transferred into fresh tube and kept at 4°C until use. To confirm sporulation using the Wirtz-Conklin spore staining technique , the spores were strained with 5% brilliant (malachite) green (dye for staining spores) solution on a slide, heated with a Bunsen flame for 5 min and washed with MilliQ water, then counterstained with 0.5% safranin (dye for staining vegetative cells) solution for 1 min. Staining was conducted before and after swelling the cell by soaking in saline solution for a few days. After drying, the slide was observed under a light microscope. SEM observation was also performed to confirm the morphology of ascospores from each strain. The spores were fixed overnight at 4°C with 0.1% (vol./vol.-PBS buffer) glutaraldehyde, washed three times with PBS buffer, dehydrated in an ethanol series, then dried at room temperature. After coating with Pt-Pd using a sputter coater (Hitachi E102 Ion Sputter, Hitachi, Tokyo, Japan) for 2 min at DC20 mA, spore samples were observed with SEM (Hitachi S-4700 Type II, Hitachi, Tokyo, Japan) at 10 kV.
For microscopic observation of cell fusion, cells were harvested after 18 h cultivation under microaerobic conditions in YMG liquid medium. After washing with sterile 20 mM Tris/HCl (pH 8.0) twice, the cells were appropriately diluted in 20 mM Tris/HCl (pH 8.0) and placed on acid-washed slide glasses. For DAPI staining, fusant cells on glass slides were covered with DAPI mounting solution containing 2 mg/mL DAPI (Lonza, Basel, Switzerland), 0.2 M 1,4-diazabicyclo-2,2,2-octane and 90% (v/v) glycerol in 20 mM Tris/HCl (pH 8.0).
PK was a researcher of the Laboratory of Water Environment and Bioenergy at Meisei University, when the study was conducted from 2010–2012. ST is a professor of the laboratory and was a representative of the study.
Pentose phosphate pathway
Ethyl methane sulfonate
Scanning electron microscope
Reverse transcription polymerase chain reaction
Two-dimensional polyacrylamide gel electrophoresis
Matrix-assisted laser desorption/ionization time-of-flight/time-of-flight
High performance liquid chromatography
This research was financially supported by the Environment Research and Technology Development Fund (K22027, K2339, and K2411) from Ministry of the Environment, Japan. We thank Mr. Kazuo Taku and the staff of the Collaborative Research Center of Meisei University for their assistants on measurements and analyses.
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