Media and culture conditions

Yeast strains in this study were grown in YPD or synthetic medium (0.67% Difco yeast nitrogen base without amino acids) supplemented with complete amino acids and filter sterilized D-glucose (2%), D-xylose (2%), xylitol (2%) or xylulose (0.5%)

Plasmid construction

Plasmids and oligonucleotides used in this study are listed in Tables 1 and 2. For complementation studies all genes were cloned into the integration plasmid CIpACT1-CYC, which contains the Candida albicans ACT1 promoter, CYC1 terminator and RPS1 gene, to allow the cloned in gene of interest to be integrated at the RPS1 locus [18] and expressed under the control of the ACT1 promoter. Integration is targeted to RPS1 by linearizing the plasmid with either a StuI or NcoI digest. However a fraction of integrations were also found at ACT1. All plasmids used in this study were linearized with StuI for integration with the exception of pDH271, which was linearized with NcoI. All constructs were sequenced to confirm integrity.

The open reading frames of the S. stipitis (Ss.) genes XYL1 and XYL2 were amplified by PCR from Ss. (CBS 6054) genomic DNA using primers ODH326/328 and ODH322/323 respectively. The products were cloned into the SmaI/NheI linearized vector CIpACT1-CYC to give rise to pDH271 and pDH270 respectively. ODH328 was designed to mutate the NcoI site in the XYL1 gene so the plasmid could later be linearized with NcoI for integrating at RPS1. The S. cerevisiae (Sc.) SOR1 and XYL2 coding regions were PCR amplified from S. cerevisiae (BY4743) genomic DNA with ODH352/353 and ODH354/355 respectively and the products cloned to the MluI/SalI sites of CIp-ACT1-CYC to produce pDH279 and pDH280. The coding region for the ScGRE3 gene, which contains 5 CTG/Leu codons, was amplified by PCR from S. cerevisiae (BY4743) genomic DNA with primers p648/649 and cloned at the MluI/NheI sites of the vector CIpACT1-CYC to produce plasmid Plate 393. For the “candidized” version, the coding region for the ScGRE3 gene, with the addition of flanking MluI and NheI restriction sites, was synthesized (GenScript, New Jersey) with each of the 5 CTG/Leu codons changed for TTG/Leu codons and the synthetic gene cloned in vector pUC57 to produce plasmid Plate 395. Plasmid Plate 395 was then digested with MluI and NheI; the 1-kb fragment for the “candidized” ScGRE3 coding region was gel-purified and cloned in vector CIpACT1-CYC to produce plasmid Plate 396.

The open reading frames of 4 xylose isomerase genes were also synthesized by GenScript: XYLA from Piromyces sp. (CAB76571), Orpinomyces sp. (ACA65427) designated OrpXI, TTHXYLA from Thermus thermophilus (BAA14301) and Clostridium cellulolyticum (YP_002507697) designated as CcelXI. TTHXYLA and CcelXI were codon optimized for Candida albicans. The start codon for TTHXYLA was changed from GTG to ATG and SalI and NheI sites were added 5’ and 3’ respectively. XhoI and SpeI sites were added 5’- and 3’-end respectively to XYLA, OrpXI and CcelXI. The synthesized genes were supplied in the vector pUC57 at the EcoRV site.

To clone these genes into the integrating plasmid, the XYLA, OrpXI and CcelXI genes were each cut out from pUC57 with an XhoI digestion, blunt-ended, and subsequently digested with SpeI. These genes were then cloned into the CIpACT1-CYC plasmid at the SmaI/NheI sites to give rise to pDH275, pDH276 and pDH278 respectively. pDH277 was constructed similarly, except that the TTHXYLA gene was moved out of the pUC57-based construct with a SalI digestion, blunt-ended and followed by an NheI digestion. Cloning in this way removed an out-of-frame ATG between the SmaI and SalI site of the vector.

Strain construction and manipulation

All strains used in this study are listed in Table 3. All C. albicans strain constructions, transformations, and subsequent manipulations were carried out using standard procedures [19,20]. Candida deletion strains were all constructed in strain SN148 using PCR-based gene targeting [21]. To construct the gre3-9 and xyl2-16 deletion strains, two runs of PCR using 80-mers were performed on plasmids pGEM-HIS1 or pRSARG4∆SpeI, and the PCR products were used to replace the entire targeted ORF of either GRE3 or XYL2 at one allele marked with HIS1 and the second allele with ARG4. To construct the Candida gre3/xyl2-3 double deletion mutant, XYL2 was deleted in the gre3-9 strain. PCR products generated from plasmids pSN40 or pSFS2A were used to replace the entire targeted ORF at one allele with LEU2 and the second allele with SAT1. The SAT1-FLP cassette [22] was then looped out to leave behind only the FRT sequence.

All strains used for complementation analyses were created by chromosomally integrating the desired genes at either the RPS1 or the ACT1 locus. Specifically, the C. albicans gre3-9 strain was transformed with the plasmid pDH271 carrying the SsXYL1 gene to create strain CDH120. Transformation of strain xyl2-16 with pDH270 carrying SsXYL2 gave rise to strain CDH116, and pDH279 carrying ScSOR1 created the strain CDH139. The complementation of the Candida gre3/xyl2-3 double deletion strain was carried out with the S. stipitis XYL1 and XYL2 homologs. The xyl2 complementation was done first with plasmid pDH270 linearized with StuI, and integration at RPS1 was confirmed by PCR (with primers p565/p544). The resulting strain, named CA220, was grown in liquid synthetic medium with xylitol, then selected on a 5-fluoroorotic acid (5-FOA) plate containing xylitol as the sole carbon source to “recycle” the URA auxotrophic marker and retain the xylitol dehydrogenase function to give rise to the ura^- strain CA227. Transformation of CA227 with NcoI linearized pDH271 (SsXYL1) followed by selection on 2% xylitol-uridine plates gave rise to strains CA242 and CA243.

Complementation of the gre3-9 strain with ScGRE3 was carried out with StuI linearized Plate 393 to produce strain CA247, and with StuI linearized Plate 396 to produce strains CA255 and CA256. Transformation of the gre3-9/xyl2-16 double deletion strain with pDH275, pDH276, pDH277 or pDH278 constructs harboring the heterologous xylose isomerases created strains CDH128 (Piromyces), CDH129 (Orpinomyces), CDH130 (Thermus thermophilus) and CDH131 (Clostridium cellulolyticum) respectively. The single deletion strains gre3-9 and xyl2-16 were also transformed with the Piromyces isomerase plasmid pDH275 to create strains CDH140 and CDH141.

Growth curves

Overnight cell cultures were grown in synthetic complete medium containing dextrose (2%). Cells were washed once with sterile water before diluting to an OD_600nm of 0.2 in 5-10 ml of synthetic complete medium containing xylose (2%), xylitol (2%) or xylulose (0.5%). Cells were grown aerobically at 30°C with shaking, and the OD_600nm was taken at intervals for up to two weeks.

Microarrays analysis

The strain BY4743 of S. cerevisiae was used for transcription profiling in xylose medium. A 10-ml starter culture in 2% raffinose (to minimize glucose repression effect) was grown for about 2 days and used to inoculate a 400-ml culture in 2% raffinose. This culture was grown to an OD₆₀₀ of approximately 0.75 - 0.8 (24-34 hr). The cells were then washed twice with sterile water. The cell pellet was resuspended in 8 ml of synthetic medium without sugar (S), and 2 ml was used to inoculate 100 ml cultures, either without sugar (S), with xylose (SX) or with dextrose (SD) for the reference. These cultures were incubated until an increase in OD₆₀₀ was observed for the culture with dextrose (1.5 - 2 hr); there was no increase in the OD₆₀₀ for the culture in xylose medium.

The Candida albicans strain SC5314 was used for microarray in xylose medium.

Starter cultures in xylose and in dextrose media were grown overnight and used to inoculate the xylose and dextrose subcultures, respectively, and these were grown to an OD₆₀₀ of approximately 0.8.

Cells were disrupted with glass beads in the FastPrep-24 instrument (MP Biomedicals). RNA was extracted with the RNeasy kit (QIAGEN cat. 74104), and 20 µg of total RNA was used for the cDNA synthesis with either cyanine-3 or cyanine-5 dyes. Probe synthesis, microarray hybridizations, washings and analyses were as described [23,24]. S. cerevisiae microarrays (Y6.4k7, 6240 ORFs) were obtained from the University Health Network Microarray Centre (http://www.microarrays.ca, Toronto, Canada). C. albicans microarrays (double-spotted 6,394 intragenic 70-mer oligonucleotides) were obtained from the Biotechnology Research Institute microarray facility center (http://www.nrc cnrc.gc.ca/eng/services/bri/microarray.html, Montreal, Canada). The data sets for these array experiments are provided as excel files as supplementary S2, and the full data sets have been registered at NCBI with the GEO accession number GSE50476.

S. cerevisiae, S. stipitis and C. albicans share conserved xylose metabolic enzymes but have different capacities for metabolizing xylose

The baker’s or brewer’s yeast S. cerevisiae, the fungal pathogen C. albicans, and the pentose-sugar fermenting yeast S. stipitis (formerly Pichia stipitis) are related ascomycetes, with C. albicans and S. stipitis in a lineage that uses the codon CTG to encode serine, unlike S. cerevisiae, which, consistent with the universal genetic code, uses CTG to encode leucine. These ascomycetes have distinct ecological niches; S. cerevisiae is almost a domesticated organism primarily associated with human brewing and baking, C. albicans is a human commensal colonizing mucosal surfaces and the gastrointestinal system, while S. stipitis inhabits the guts of some insects. These niches all provide efficient access to the hexose sugar glucose, but only the guts of wood-eating insects provide high levels of pentose sugars such as xylose for possible metabolism.

Although each of these organisms has different access to xylose as a potential carbon source, they all encode the enzymatic capacity to direct xylose into the pentose phosphate pathway. In fungi in general, the metabolism of xylose involves its transformation to xylulose through a two-step process, the first the reduction of xylose to xylitol by the action of a xylose reductase (XR), and the second the production of xylulose from xylitol by the action of a xylitol dehydrogenase (XDH) (Figure 1A). Sequence analysis indicates that all three species have genes that are predicted to encode these functions, and these genes are conserved (Figure S1). The GRE3 genes of C. albicans and S. cerevisiae, and the XYL1 gene of S. stipitis, are highly related sequences encoding predicted xylose reductase activity. The XYL2 genes of S. stipitis and C. albicans, as well as the XYL2, SOR1 and SOR2 genes of S. cerevisiae are also closely related genes encoding putative dehydrogenases. The SOR1 and SOR2 genes, although annotated as sorbitol dehydrogenases, are more similar to the C. albicans and S. stipitis XYL2 genes than is the yeast gene designated XYL2. Intriguingly however, although the species have similar genomic potential for xylose utilization, they actually have very different growth behaviors on this sugar. As shown in Figure 1B, while strains of each organism were able to grow in medium containing xylulose as the sole carbon source, the S. cerevisiae strain was not able to grow when the carbon source was the related pentose sugar xylose. Overall, Candida grows better than the others in both xylose and xylulose, while S. cerevisiae grows slowly in xylulose, and S. stipitis grows well in both xylose and xylulose, but reaches a plateau after 1 day of incubation in both sugars.

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Figure 1. Xylose entry to the PPP pathway and xylose metabolizing capacities of different ascomycetes.

A) The schematic presentation of conserved genes encoding enzymatic activities for the xylose entry into the PPP pathway in ascomycetes. C. a for Candida albicans, S. c for Saccharomyces cerevisiae, and S. s for Schefferomyces stipitis. B) Growth of C. albicans (SC5314), S. stipitis (CBS6054) and S. cerevisiae (BY4741) in SC with 2% xylose or 0.5% xylulose. Strains were grown aerobically at 30°C and the optical density measured over a period of six days, n=3.

https://doi.org/10.1371/journal.pone.0080733.g001

Transcription profiling of cellular response to xylose

Previous work has established that in response to growth in xylose, S. stipitis induces the genes for XR and XDH, as well as for some sugar transporters [25,26]. We have examined the response of both C. albicans and S. cerevisiae to incubation with xylose as the sole carbon source. As shown in Figure 2A, C. albicans generates a robust signal when shifted from growth in glucose to xylose. 175 genes have at least a 2-fold transcription increase in xylose when compared to cells in glucose, of which 44 genes with more than a 5-fold induction in xylose are listed in the table. The induced genes include those that are critical for xylose metabolism such as GRE3 (30 fold) and XYL2 (7 fold), as well as the xylulose kinase XKS1 (5 fold). Some genes encoding sugar transporters, including HGT2, HGT12, HXT5, HGT9 and HGT17, are also strongly induced. This shows that C. albicans is capable of shifting its metabolic constitution to exploit xylose as a carbon source. In contrast, S. cerevisiae has no cell growth under these conditions, has a very modest response to the shift from glucose to xylose. This response is quite similar to that seen when shifting yeast cells from glucose medium to a medium containing no sugar source (Figure 2B). This behavior is consistent with the inability of S. cerevisiae to grow on xylose as the sole carbon source, although S. cerevisiae is capable of transporting xylose [27]. The data sets for the C. albicans and S. cerevisiae transcriptional profiling results are presented as Figure S2.

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Figure 2. Transcription profile of C. albicans and S. cerevisiae in xylose

A) From microarray experiments with C. albicans grown in xylose, 175 genes have at least a 2-fold transcription increase in xylose when compared to cells in dextrose. The 44 genes with more than a 5-fold induction in xylose (SX) are shown with their corresponding value. Data for S. cerevisiae is shown for comparison, and in gray-shade if no reciprocal best-hit ortholog is found. B) Transcription modulation of the S. cerevisiae sugar transporters in xylose. The data from the microarray experiments in xylose (SX) and in no-sugar condition (S) is shown for 18 members of the sugar transporter family, relative to cells in dextrose. HXT5 and HXT2 are likely induced due to the absence of dextrose (glucose). HXT6, HXT7 and HXT4 are induced specifically by the presence of xylose. HXT4, HXT1 and HXT3 show a transcriptional reduction only for the no-sugar condition (S), likely due to the absence of sugar. A summary for the transporters description from SGD is reported in the ‘SGD description’ column.

https://doi.org/10.1371/journal.pone.0080733.g002

GRE3 and XYL2 are necessary for xylose metabolism in C. albicans

To examine whether GRE3 and XYL2, encoding potential xylose reductase (XR) and xylitol dehydrogenase (XDH) activities respectively, are solely responsible for the metabolism of xylose in C. albicans, we created disruption mutants of both genes. The two alleles of either GRE3 or XYL2 were replaced by HIS1 and ARG4 in strain SN148 [28]. A double mutant, gre3 xyl2, was created by replacing the two alleles of XYL2 with the LEU2 and SAT1 markers in a strain already deleted for GRE3. All the resulting strains were unable to grow on xylose as a sole carbon source, while as expected the gre3 mutant strain was able to grow on xylitol (Figure S3). This confirms that in C. albicans the oxido-reductase activities encoded by the GRE3 and XYL2 genes are solely necessary for the metabolism of xylose.

Complementation of gre3 and xyl2 mutants

We asked whether the corresponding XR and XDH genes of S. stipitis were capable of complementing the C. albicans gre3 and xyl2 deletions. Because both C. albicans and S. stipitis belong to the CUG clade, there was no need to modify the S. stipitis genes prior to introducing them into the C. albicans mutants. The S. stipitis XYL1 gene integrated at the RPS1 locus of C. albicans was capable of supporting robust growth of the gre3 strain within two to three days in xylose medium (Figure 3A). As well, integration of the S. stipitis XYL2 gene in the C. albicans xyl2 strain complemented the deletion strains growth defect within one day in both xylitol or xylose medium (Figure 3B). We also tested the S. stipitis XR-XDH modular unit in the Candida gre3/xyl2 double deletion mutant in xylose metabolism. Integration of S. stipitis XYL1 and XYL2 into the gre3/xyl2 strain allowed the transformed Candida mutant to grow in medium using xylose as the sole carbon source, indicating that the XR-XDH module from S. stipitis is functional in C. albicans (Figure 3C). However, we noticed that these Candida cells showed a lag time of approximately 48 h when grown in medium with xylose compared to medium with xylitol as a carbon source. This lag was not observed with wild-type C. albicans cells, suggesting that the S. stipitis XR-XDH module may not be perfectly coupled to the other parts of the xylose metabolic pathway of C. albicans.

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Figure 3. The xylose reductase and xylitol dehydrogenase genes from S. stipitis complement C. albicans deletion mutants of the equivalent genes.

(A) S. stipitis XYL1 (CDH120), and (B) S. stipitis XYL2 (CDH116) complement the C. albicans gre3 and xyl2 deletion mutants respectively. (C) The S. stipitis XYL1-XYL2 module (CA242) complements the C. albicans gre3 xyl2 double deletion mutant. Strains were grown aerobically at 30°C in SC with 2% xylose (SX) or 2% xylitol (ST). The optical density was measured over a period of up to 14 days, n=3.

https://doi.org/10.1371/journal.pone.0080733.g003

Similarly, we investigated the ability of the S. cerevisiae homologs to complement the C. albicans mutants. Because ScGRE3 contained 5 CTG codons that would encode leucine in S. cerevisiae but serine in C. albicans we used a synthetic gene with the 5 CTG codons switched to TTG to assess complementation. As shown in Figure 4A, integration of the candidized ScGRE3 gene at RPS1 [18] could complement the gre3 mutation. The CTG codon unmodified ScGRE3 gene was not able to complement when introduced at the same site (data not shown), suggesting the change of one or more leucine residues to serines compromised the enzymatic function. We also assessed the ability of SOR1 and ScXYL2 to complement the xyl2 mutant of C. albicans. The SOR1 gene contained no CTG codons, and when integrated at RPS1 was capable of complementing the xyl2 mutant for growth on xylitol within one day, however complementation of growth in xylose took several days (Figure 4B) The ScXYL2 gene contained 4 CTG codons, and was not capable of complementing the function (data not shown). This could represent problems caused by the leucine/serine discrepancy, or could simply reflect the point that the SOR1 gene is more similar to the C. albicans gene than is ScXYL2. Nonetheless, the observation that ScGRE3 and SOR1 can complement the Candida gre3 and xyl2 mutants shows that S. cerevisiae has XR and XDH enzymatic capacity for the crucial xylose-xylulose conversion steps of xylose metabolism.

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Figure 4. The xylose reductase and xylitol dehydrogenase genes from S. cerevisiae complement C. albicans deletion mutants of the equivalent genes.

(A) S. cerevisiae GRE3 (CA255), and (B) S. cerevisiae SOR1 (CDH139) complement the C. albicans gre3 and xyl2 deletion mutants respectively. Strains were grown aerobically at 30°C in 2% xylose (SX) or 2% xylitol (ST). The optical density was measured over a period of 14 days, n=3.

https://doi.org/10.1371/journal.pone.0080733.g004

When we tested XR-XDH as a modular unit from S. cerevisiae for its capacity to complement the Candida gre3/xyl2 double deletion mutant in xylose. We found the S. cerevisiae XR-XDH module (GRE3-SOR1) showed a clear, but relatively weak ability to support the growth of the C. albicans double mutant on xylose medium. Significant cell growth takes about two weeks (data not shown), which is much slower growth compared to the more rapid growth conferred by either ScGRE3 or ScSOR1 when complementing a gre3 or xyl2 single mutation of C. albicans. These results, along with those from S. stipitis, may suggest that the proper coupling of all the steps in the metabolic pathway is as important as the enzyme activities per se in each step.

Fungal xylose isomerases enable a Candida gre3/xyl2 double mutant to metabolize xylose

We further assessed whether alternate enzymatic activities could function in the xylose utilization pathway of C. albicans. Because the role of XR and XDH is to transform xylose to xylulose, we asked whether expression of a heterologous xylose isomerase could complement the gre3 xyl2 double mutant. Xylose isomerases exist in bacteria, in plants, as well as in some fungi, however, ascomycete fungi like yeast and C. albicans do not have endogenous xylose isomerases. Sequence analysis with phylogenic clustering of 17 xylose isomerases indicate that there are two classes of this enzyme, one represented by the enzyme from Piromyces, and the other from that of Thermus thermophilus as shown in the alignment (Figure S4). Genes corresponding to the XI from fungi (Piromyces sp. and Orpinomyces sp.), and bacteria (Thermus thermophilus and Clostridium cellulolyticum) were synthesized and introduced into the gre3 xyl2 double mutant strain. Piromyces and Orpinomyces have the same codon usage as C. albicans, and thus required no CUG codon modification. Thermus and Clostridium have standard codon usage, so the xylose isomerase genes from these organisms were synthesized with CUG codon modification to reflect C. albicans codon usage. As shown in Figure 5, the isomerase from Piromyces allowed growth of the double mutant in xylose medium within one to two days indicating that the activity of the XI provides effective xylose-xylulose conversion. The same effect was observed with the Orpinomyces XI (data not shown). On the other hand the bacterial isomerases were not able to support the growth of the double the mutant in xylose medium; this could represent a problem with protein production, although the genes were codon optimized for expression in C. albicans, or a problem in enzyme function in situ. The Piromyces isomerase was also able to allow growth of the C. albicans gre3 single deletion mutant in 3-4 days (Figure 5); however, it could not complement the growth of the xyl2 single deletion mutant under the same conditions (data not shown), suggesting an inhibiting effect of accumulating xylitol on XI in xyl2 mutant.

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Figure 5. The xylose isomerase gene XYLA from Piromyces sp. complements a double gre3/xyl2 deletion or single gre3 deletion in C. albicans.

Growth analysis in synthetic medium (SC) with 2% xylose as the sole carbon source for C. albicans strains: gre3-9 (gre3 deletion), gre3/xyl2-3 (gre3 xyl2 double deletion), CDH128 (gre3/xyl2-3 with the integrated Pir.XYLA) and CDH140 (gre3-9 with the integrated Pir. XYLA). The optical density was measured over a period of 6 days, n=3.

https://doi.org/10.1371/journal.pone.0080733.g005