Bulk Segregant Analysis by High-Throughput Sequencing Reveals a Novel Xylose Utilization Gene from Saccharomyces cerevisiae

doi:10.1371/journal.pgen.1000942

PLoS Genet. 2010 May; 6(5): e1000942.

Published online 2010 May 13. doi: 10.1371/journal.pgen.1000942

PMCID: PMC2869308

Copyright Wenger et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Bulk Segregant Analysis by High-Throughput Sequencing Reveals a Novel Xylose Utilization Gene from Saccharomyces cerevisiae

Jared W. Wenger, Katja Schwartz, and Gavin Sherlock^*

Department of Genetics, Stanford University, Stanford, California, United States of America

Zhenglong Gu, Editor

Cornell University, United States of America

* E-mail: sherlock/at/genome.stanford.edu

Conceived and designed the experiments: JWW KS GS. Performed the experiments: JWW KS. Analyzed the data: JWW KS. Wrote the paper: JWW GS.

Received November 25, 2009; Accepted April 8, 2010.

This article has been cited by other articles in PMC.

Abstract

Fermentation of xylose is a fundamental requirement for the efficient production of ethanol from lignocellulosic biomass sources. Although they aggressively ferment hexoses, it has long been thought that native Saccharomyces cerevisiae strains cannot grow fermentatively or non-fermentatively on xylose. Population surveys have uncovered a few naturally occurring strains that are weakly xylose-positive, and some S. cerevisiae have been genetically engineered to ferment xylose, but no strain, either natural or engineered, has yet been reported to ferment xylose as efficiently as glucose. Here, we used a medium-throughput screen to identify Saccharomyces strains that can increase in optical density when xylose is presented as the sole carbon source. We identified 38 strains that have this xylose utilization phenotype, including strains of S. cerevisiae, other sensu stricto members, and hybrids between them. All the S. cerevisiae xylose-utilizing strains we identified are wine yeasts, and for those that could produce meiotic progeny, the xylose phenotype segregates as a single gene trait. We mapped this gene by Bulk Segregant Analysis (BSA) using tiling microarrays and high-throughput sequencing. The gene is a putative xylitol dehydrogenase, which we name XDH1, and is located in the subtelomeric region of the right end of chromosome XV in a region not present in the S288c reference genome. We further characterized the xylose phenotype by performing gene expression microarrays and by genetically dissecting the endogenous Saccharomyces xylose pathway. We have demonstrated that natural S. cerevisiae yeasts are capable of utilizing xylose as the sole carbon source, characterized the genetic basis for this trait as well as the endogenous xylose utilization pathway, and demonstrated the feasibility of BSA using high-throughput sequencing.

Author Summary

Ethanol made from fermentation of lignocellulosic biomass by baker's yeast can be considered “carbon neutral” and is one alternative to fossil fuels for powering vehicles. One of the recognized requirements for cost-effective and energy-efficient cellulosic ethanol production is the need to convert the sugar xylose—a major component of cellulosic biomass—into ethanol; however, it has traditionally been thought that baker's yeast cannot ferment xylose. We sought to investigate this assumption by looking at close relatives of baker's yeast from around the world to see if any had an intrinsic ability to grow on xylose. We identified a number of yeasts, many of them used in winemaking, that grow very slowly on this sugar, and studied one in detail. We determined that in this particular yeast the ability to grow on xylose is due to the presence of a single gene, which we named XDH1. This gene is not present in the typical laboratory strains of baker's yeast, but appears to be very common in natural wine yeasts. This gene could be useful in continuing efforts to make yeasts that can efficiently ferment xylose to ethanol.

Introduction

It is clear that society has a responsibility to address the anthropogenic causes of climate change. Current estimates indicate that about 95% of the world's energy comes from burning fossil fuels [1], which is the leading contributor of carbon dioxide emissions. Combustion of liquid fossil fuels for transportation is responsible for a large fraction of these carbon dioxide emissions in the United States, second only to electricity generation (U.S. Environmental Protection Agency). For these reasons, creating “carbon neutral” liquid transportation fuels should be an important part of global efforts to reduce carbon emissions.

One solution already in widespread use is bioethanol fermented from sugar cane (Brazil) or cornstarch (U.S.) by various strains of Saccharomyces cerevisiae [2], which is used as a major component or additive to liquid transportation fuels. For bioethanol to become a sustainable, economically viable commodity, and not to compete with food sources, it is necessary to move away from sugar cane or corn biomass toward lignocellulosic biomass sources such as corn stover or other agricultural wastes, wood byproducts, or dedicated fuel crops such as Miscanthus or switchgrass [3]–[5]. However, there are technical challenges that must be overcome before this is possible. For sugar cane and corn biomass, the predominant sugars are glucose and/or fructose, both of which are readily fermented to ethanol by various S. cerevisiae yeast strains, usually wild isolates that are particularly suited for large-scale fermentations [6], [7]. However, in lignocellulosic biomass sources, the second most abundant carbohydrate after glucose is xylose, the major pentose of hemicellulose. There is as yet no known strain of Saccharomyces that is able to convert xylose to ethanol as efficiently as glucose. Because the mass proportion of hemicellulose ranges from 20–50% in common agricultural lignocellulosic biomasses, finding both a cost-effective and energy-efficient conversion of xylose to ethanol is a critical hurdle [8].

The budding yeast Saccharomyces cerevisiae is the microorganism of choice for industrial fermentations for a variety of reasons, mainly due to its high ethanol productivity both aerobically and anaerobically, its high ethanol and low pH tolerance, and its resistance to many of the harmful compounds in a typical biomass hydrolysate. Despite recent evidence that some natural S. cerevisiae can grow, albeit poorly, on xylose [9], it has generally been reported that both natural and laboratory S. cerevisiae strains do not ferment xylose [10]–[12] leading to the assumption that they cannot, without recourse to genetic engineering, be utilized for efficient conversion of lignocellulose to ethanol. While S. cerevisiae strains were shown to be able to ferment the xylose isomer xylulose and to possess genes putatively encoding enzymes capable of xylose reduction (GRE3, GCY1, YPR1, YDL124W, YJR096W), xylitol oxidation (XYL2, SOR1, SOR2), and xylulose phosphorylation (XKS1) (Figure 1), there have been a number of experimental observations indicating that S. cerevisiae could not ferment xylose [13]–[15]. Such observations include low levels of gene expression of the endogenous enzymes, poor transport of xylose, redox cofactor imbalances, and insufficient flux through the pentose phosphate shunt [16], [17]. Despite these issues being well characterized in laboratory strains of S. cerevisiae, little is known about natural variation within Saccharomyces yeasts as it relates to xylose utilization which, as has already been shown [9], is likely to be relevant to this phenotype.

Figure 1

Endogenous xylose pathway.

A significant amount of progress has been made over the last 30 years toward solving these problems, with much of the work focused on introducing foreign xylose pathway enzymes into S. cerevisiae: either the genes that code for xylose reductase [XR], xylitol dehydrogenase [XDH], or xylulokinase [XK] from the xylose-utilizing fungus Pichia stipitis [18]–[22], or genes coding for a xylose isomerase [XI] from other fungi and bacteria [23]–[28]. There have also been efforts to increase or adjust xylose pathway enzyme activities (XR, XK, XDH) [15], [29]–[33] and pentose phosphate flux [34], [35], reduce redox imbalances [36]–[41], and use directed evolution or random mutagenesis to increase xylose utilization [42]–[45]. Despite this large body of work, the fermentation of xylose to ethanol in these strains is still much slower than that of glucose, and there is still significant room for improvement in xylose fermentation, as well as co-fermentation of xylose and glucose, by S. cerevisiae for industrial scale applications.

As mentioned above, it has been determined that some natural strains of Saccharomyces cerevisiae are capable of growing on xylose, contrary to the notion that S. cerevisiae does not recognize this pentose as a usable carbon source [9]. It is also well characterized that there is abundant natural genetic and phenotypic variation within S. cerevisiae and closely related species [46]–[51]. In this work, we have screened a large number of wild, industrial and laboratory yeast strains to determine if other xylose-utilizing strains of Saccharomyces already exist in nature, and if so, to determine the genetic basis or bases for the phenotype. We screened 647 strains, and found a number of different Saccharomyces yeasts, predominantly wine yeasts, which are capable of utilizing xylose, albeit modestly. Through the application of high-throughput sequencing to Bulk Segregant Analysis [BSA] [52], we were able to identify the gene responsible for xylose utilization in a wine strain of S. cerevisiae, which encodes a novel putative xylitol dehydrogenase that we named XDH1. We observed that this gene is present in many different wine strains and is responsible for xylose utilization in these strains, however we have identified other strains in our screen that appear to have an independent genetic basis for their xylose utilization. We also carried out transcriptional profiling to characterize gene expression patterns during xylose utilization in wine strain derivatives and determined the contribution of native S. cerevisiae xylose pathway enzymes to the phenotype we observed. These data suggest that the putative enzyme encoded by XDH1 works in combination with the native xylose pathway to permit natural S. cerevisiae strains to recognize and utilize xylose.

Results

Screen for Xylose Utilization

To identify natural Saccharomyces species/strains that are able to utilize xylose, we screened each strain in our yeast collection for the ability, when placed in liquid medium with xylose as the sole carbon source, to increase in optical density [OD] after several days of incubation at 25°C. We measured the OD of 647 strains (Table S1) in a sealed 96-well plate format with constant, orbital shaking (see Materials and Methods). The collection largely comprises S. cerevisiae strains from various sources, including wine, brewing, baking, laboratory and clinical isolates, but it also contains other Saccharomyces sensu stricto yeasts and various hybrids between them. Of the 647 strains tested, we identified 38 strains that had some observable increase in OD (Table 1). These “xylose-positive” strains were predominantly (29/38) S. cerevisiae wine yeasts (although not all wine yeasts were xylose-positive), with the remainder being interspecific hybrids within the sensu stricto group. These xylose-positive hybrid strains generally reached higher OD in xylose media compared to the S. cerevisiae wine strains. Figure 2A shows a typical S. cerevisiae wine strain profile as well as the profile from one of the best hybrids, comparing growth in a xylose-containing medium to the same medium with no carbon source. While increase in OD does not provide evidence for fermentation of xylose to ethanol, or even of cell division, these data do show that there are natural Saccharomyces yeasts capable of utilizing xylose to accumulate biomass.

Table 1

“Xylose positive” strains.

Figure 2

Wine strains display a xylose-utilization phenotype controlled by a single gene.

To understand the genetic basis of this xylose utilization we chose to focus on the wine strains because many could be sporulated and crossed to a laboratory strain of S. cerevisiae, and we could thus determine the segregation pattern of the phenotype. Twenty-five of these xylose-positive S. cerevisiae strains could be sporulated and tetrads dissected (Table 1). Note that because the strains have a wild-type HO gene, the spore products obtained after tetrad dissection are actually fully homozygous diploids, due to self-mating of the haploid spore during its growth on the dissection plate. In 8/25 of the xylose-positive S. cerevisiae strains, all of the spore products were xylose-positive (e.g. Simi White, Figure 2B), while in 2/25 the trait segregated 2 xylose-positive: 2 xylose-negative (e.g. Lalvin AC, Figure 2C). In the remaining 15 strains, including three strains from which no xylose-positive spores were recovered, spore viability was so poor that no complete tetrads were obtained, and thus the segregation pattern(s) could not be identified. We then took xylose-positive spore products from all of the strains from which such spores could be obtained, and crossed them (see Materials and Methods) to a laboratory S. cerevisiae strain, S288c. We observed that all of the resulting diploids were xylose-positive, indicating that the phenotype is dominant (data not shown). The resulting strains were then sporulated, and in those strains where a segregation pattern could be established, the xylose-positive trait segregated to produce two positive and two negative spores, suggesting that a single gene was responsible for the xylose-positive trait (e.g. Simi White, Figure 2D). To determine if the same locus is responsible for xylose utilization in these various wine strains, we crossed xylose-positive spores between the various wine strains and determined the segregation pattern of the xylose phenotype in the progeny of these crosses. In all of the crosses that were performed, the xylose-positive phenotype segregated 4 [ratio]

0 in six tetrads (Figure 2E); this defines a cohort of at least 9 wine strains containing a single complementation group (locus) responsible for the phenotype (Figure 2F). These data indicate that a single, dominant locus is responsible for permitting xylose utilization in these S. cerevisiae strains and suggest that this mechanism of xylose utilization is common to all of the xylose-positive wine yeasts that we identified. These data also suggest that this locus may be identical by descent, consistent with evidence that wine strains are very closely related and have probably only diverged a few thousand years ago [46], [49], [50].

Identification of the Responsible Gene by Bulk Segregant Analysis

To determine the genomic location of the gene that permits xylose utilization we conducted BSA [53] using Affymetrix yeast tiling arrays. BSA works by taking advantage of DNA sequence polymorphisms between different strains and of the fact that it is relatively easy to pool large numbers of meiotic spore products (segregants) in yeast. Pooling segregants based on their phenotype allows the region of the genome responsible for the phenotype to be detected because DNA polymorphisms in regions unlinked to the responsible locus will segregate randomly and be “evened” out, while sequences or polymorphisms either directly responsible for the trait, or very closely linked to it, will be present in all positive segregants and absent in all negative segregants. In our case, the Simi White wine strain carrying the locus responsible for xylose utilization was crossed to a laboratory strain; the wine strain was previously estimated to carry DNA polymorphisms relative to the laboratory strain at a level of approximately .5% [54]. Spores from the Simi White/S288c diploid were screened for the xylose utilization phenotype and 39 positive spores were combined into one pool and 39 negative spores into another pool, and genomic DNA [gDNA] was isolated from each pool. We then hybridized the positive and negative gDNA pools to tiling microarrays (based on the S288c reference genome) with the expectation that regions of the genome derived from Simi White will hybridize less robustly to the array because of the DNA polymorphisms between Simi White and S288c. Log₂ ratios of probe intensities were calculated (negative/positive), and a peak was evident by visual inspection in the chromosome XV right subtelomeric region that corresponds to less robust hybridization to the microarray of the positive pool gDNA (Figure 3). We confirmed the localization of the xylose-positive trait to this region by linkage analysis using strains from the yeast deletion collection, showing that the xylose-positive trait co-segregated meiotically with PHR1 (YOR386W), YOR378W, and YOR365C (2). We cloned a 10 kilobase [kb] region of the genome distal to PHR1 (containing YOR389W, YOR390W, HSP33, YOR392W, ERR1, and PAU21) from haploid, xylose-positive segregants of Simi White (GSY2469) and Lalvin AC (GSY1362) and independently transformed an S288c-based laboratory strain (FY2) with the constructs, but neither the Simi White nor the Lalvin AC derived constructs conferred a xylose-positive phenotype (data not shown), suggesting that the responsible gene was not within this 10kb region. Because yeast telomeric regions are susceptible to amplifications, insertions and translocations [55], we instead considered the possibility that the trait of interest may lie in an insertion distal to the subtelomeric sequences present in the S288c reference genome.

Figure 3

Bulk Segregant Analysis by Affymetrix Yeast tiling microarrays.

To identify whether there is an insertion on chromosome XV that contains the gene responsible for the xylose utilization phenotype, we repeated BSA using Illumina high-throughput sequencing on the same Simi White gDNA pools, as well as four additional pools, containing 19 positives and 16 negatives derived from a Lalvin AC/S288c cross and 16 positives and 16 negatives from a SIHA Activ-Hefe 4/S288c cross. We chose BSA over sequencing individual isolates to enrich for sequences responsible for (or tightly linked to) the xylose-positive phenotype, as there are likely to be many other novel sequences in the wine strains that are not present in the S228c genome but are unrelated to the xylose phenotype. Simi White positive and negative pools were sequenced to approximately 50× coverage of the S288c genome (~17M mapped reads per pool), and the Lalvin AC and SIHA pools were sequenced to ~25× coverage (~8M mapped reads per pool) (Table S3). The 36 base pair sequence reads were aligned to the S288c reference genome using the software program MAQ [56].

To determine if any sequences were present in the positive pool that were not present in the negative pool, we performed de novo assembly of the reads that did not map to the S288c reference genome. Because de novo assembly with short sequence reads is challenging, it is important to have deep coverage and include only high quality sequence reads. To achieve this coverage and quality, we compiled all of the high-quality unmapped reads (where “high quality” reads were defined as those that did not contain any uncalled bases) from all three positive gDNA pools and used the software program Velvet [57] to perform the assembly. We then used MAQ to independently align the unmapped reads from all six gDNA pools (positive and negative) to the Velvet contigs created from the positive pools. We identified 9 individual contigs with a combined length of approximately 55kb that had no or very few reads map to them from the three negative pools. We designed primers that would amplify each of these 9 contigs and performed linkage analysis to confirm that these contigs are linked to the xylose-positive trait and yor365cΔ (Table S4). We then determined that there were approximately 28 open reading frames [ORFs] (>100 amino acids) within these 9 contigs and that a number of the ORFs are homologous to sugar metabolism genes, including a xylitol/sorbitol dehydrogenase homolog (Figure 4). The presence of a large insertion relative to the S288c reference genome containing these ORFs within the right sub-telomeric region of chromosome XV has independently been recently observed in the EC1118 wine strain genome sequence [54], [58]. The total size of the insertion is 65kb, indicating that de novo assembly identified most of the region. These data, combined with our observation that none of the previously annotated genes in the S288c reference genome distal to PHR1 were able to confer the xylose phenotype, strongly suggested that the xylose utilization trait resided in this telomeric insertion.

Figure 4

65kb insertion in subtelomeric region of chromosome XV.

Necessity and Sufficiency of Novel XDH Homolog

Of the ORFs within the chromosome XV insertion, the putative xylitol/sorbitol dehydrogenase was particularly interesting to us because it has homology to xylitol dehydrogenases from S. cerevisiae and other species (Figure S1), and we hypothesized that this gene was a likely candidate for the xylose utilization trait. We amplified this gene from both Simi White and Lalvin AC, along with approximately 400 bases of upstream and downstream sequences, and cloned it into the CEN/ARS vector pRS316 [59] to create pGS104 and pGS105. When either of these constructs were transformed into S288c, they were sufficient to permit xylose utilization in this previously non-xylose-utilizing laboratory strain (Figure 5A and data not shown). The phenotype is dependent on the presence of the plasmid containing the gene, as the xylose phenotype was lost when the transformants lost the plasmid (Figure 5A). These data show that this gene, which we have named XDH1, is sufficient to permit xylose utilization in an otherwise wild type, but xylose-negative strain.

Figure 5

Novel XDH homolog is sufficient and necessary for xylose utilization.

To show necessity of XDH1 for the phenotype, we created a deletion strain (xdh1Δ) and measured xylose utilization as before. Two Simi White derivatives (GSY2468/9) were transformed with a KanMX deletion cassette containing sequences (~400 bases) immediately up and downstream of XDH1. The deletion strains (GSY2472/1) were confirmed by PCR. Deletion of XDH1 completely abrogated the phenotype (Figure 5B). We crossed the deletion strain to another haploid derivative of Simi White and confirmed that the deletion always segregates in opposition to the xylose-positive phenotype in 9 tetrads tested (data not shown). These data prove that XDH1 is not only sufficient but also necessary for xylose utilization.

Having shown that XDH1 is responsible for xylose utilization in at least two S. cerevisiae wine strains (Simi White and Lalvin AC), and also considering our observation that all the other wine strains we were able to test appeared to be in the same complementation group, we sought to determine whether XDH1 is present in all of the xylose-positive S. cerevisiae strains and other Saccharomyces hybrids that we initially identified in our screen. To test for the presence of XDH1 in those strains, we performed colony PCR on all of the xylose-positive strains that were identified in the screen (Table 2). In 33/38 xylose-positive isolates, XDH1 was present. Interestingly, the 5 xylose-positive strains from which we could not amplify XDH1 were all recorded as being either S. bayanus or hybrids between S. bayanus and S. cerevisiae.

Table 2

Presence of XDH1 in xylose positive or negative strains.

Some of the positive strains from our screen were heterozygous for xylose utilization, because when sporulated, the trait segregated to produce two positive and two negative spores (or some number of each type in cases where there were not enough viable spores to determine a distinct segregation pattern) (Table 1). We performed colony PCR on some of these spores to test for the presence of XDH1 (Table 3). Among the meiotic progeny of these heterozygotes, every xylose-positive segregant contained this gene. In four cases (Lalvin AC, PDM, SIHA Activ-hefe 4, and WE14) the presence of XDH1 segregated with the xylose-positive spores, while the negative spores did not contain XDH1. Surprisingly, we found instances where some negative spores did contain the XDH1 gene. In one instance, one of the two negative spores contained XDH1, while the other negative spore did not (ATCC66283, note that the four spores not from the same tetrad). In the four other cases (Montrachet, BDX, Fermichamp, French White), all the negative spores tested positive by PCR for XDH1. We sequenced XDH1 and approximately 200 bases up and downstream of the ORF from all spores of two of these heterozygous tetrads (Fermichamp tetrad 1A–D, BDX tetrad 1A–D) and did not observe any DNA sequence polymorphisms between the xylose-positive and negative spores (data not shown). This suggests that there may be another locus that is epistatic to XDH1 in these strains. Overall, the ubiquity of XDH1 in the xylose-positive strains is consistent with the hypothesis that this gene is necessary for xylose utilization in natural S. cerevisiae strains.

Table 3

Presence of XDH1 in xylose positive progeny.

Genetic Dissection of Endogenous Xylose Pathway

As described above, there are genes encoding putative xylose pathway enzymes in the S288c reference genome, and it has previously been suggested that the major XR contributors are GRE3, YPR1, and YJR096W [14]. It has also been observed that co-over-expression of GRE3 and XYL2, which encodes a putative XDH, can confer a xylose-positive phenotype [14], [15]. To assess the contribution of these and the other endogenous xylose genes to our xylose phenotype, we deleted either singly or in various combinations these genes from a haploid, xylose-positive Simi White derivative (GSY2469) and assessed the growth phenotypes of the various deletion mutants (Figure 6).

Figure 6

Genetic dissection of the endogenous xylose pathway.

To test the contribution of each of the five putative xylose reductase genes, we introduced deletions of each of them individually in the XDH1 background. Only GRE3 significantly affected the phenotype, and none of the xylose reductase genes, when deleted individually, completely abrogated the phenotype (Figure 6, XR). We also tested sufficiency for each of the reductases by creating quadruple deletion mutants, leaving only one putative reductase gene intact (Figure 6, XR). The only two putative xylose reductases that alone contributed significantly to the ability to utilize xylose in our background were GRE3 and YPR1. The other three putative xylose reductases are insufficient by themselves to allow xylose utilization (YDL124W, GCY1, YJR096w). We also created a gre3Δ ypr1Δ double deletion in which the phenotype is almost completely removed (Figure 6, XR), though these data are not inconsistent with the other three putative xylose reductases contributing some residual XR activity. These data together suggest that both GRE3 and YPR1 are the major contributors to XR activity in a natural S. cerevisiae derivative.

Next, we tested the contribution of three putative xylitol dehydrogenases to the observed phenotype (Figure 6, XDH). Interestingly, when each potential XDH was deleted individually in the XDH1 background (sor1Δ, sor2Δ, xyl2Δ), the deletion mutants showed an improved xylose utilization phenotype relative to the positive control. Furthermore, when all three were deleted together (sor1Δ sor2Δ xyl2Δ), the phenotype was further enhanced (Figure 6, XDH). These data suggest that these putative xylitol dehydrogenases may actually be hampering the ability of this strain (and possibly all non-xylose utilizing S. cerevisiae strains) to utilize xylose, and thus are consistent with our newly identified Xdh1 protein being responsible for the presumptive xylitol dehydrogenase step of the canonical xylose utilization pathway.

Finally, we introduced an xks1Δ deletion into the XDH1 background, which encodes the putative xylulokinase, which is responsible for the phosphorylation of the fermentable metabolite xylulose to xylulose-5-phosphate [60], [61]. Deletion of XKS1 completely removed the ability of this strain to utilize xylose (Figure 6, XK), suggesting that the canonical pathway in this strain is responsible for metabolizing xylose and that XKS1 encodes the sole xylulokinase necessary for the xylose utilization phenotype we observe.

Transcriptional Profiling during Xylose Utilization

In addition to understanding how the endogenous xylose pathway genes contribute to the xylose phenotype, we sought to characterize how the presence or absence of xylose in the growth medium affected the S. cerevisiae transcriptional program over time, within the genomic context of presence or absence of the XDH1 gene. To do so, we measured mRNA levels in three pairs of sister spores from a Simi White strain that was backcrossed twice to S288c. Each pair of spores was from an independent tetrad, and contained one XDH1-containing spore (“positive”, GSY2465, 2466, 2469) and one spore that does not contain the XDH1 gene (“negative”, GSY2464, 2467, 2470). We pre-grew each of the six spores in YPD and used these cultures to inoculate minimal medium with or without 2% xylose as the sole carbon source (where the absence of xylose is the “no carbon” condition). Samples were taken from these cultures beginning immediately after inoculation (t

0) and continuing every 8 hours for 72 hours. We then assayed relative RNA abundance versus a pooled reference, containing equimolar amounts of each sample, using Agilent yeast catalog arrays. The gene expression measurements (Log₂(sample/reference)) were averaged among the three positive spores and the three negative spores at each time point.

To determine if the endogenous xylose pathway responds to the presence of xylose in the xylose-positive strain, we qualitatively compared the expression levels of all the putative xylose-pathway genes that are present in the S. cerevisiae S288c genome (Figure 7). In positive spores the putative xylose reductase genes are up-regulated compared to the reference only in the presence of xylose, while in the negative spores the xylose reductase genes are repressed under all conditions; the only exception is YDL124W, which appears to be up-regulated vs. the reference in all spore types and all growth conditions. The pattern of expression for the putative XDH XYL2 is similar to that of the xylose reductase genes; it is highly expressed across the time course in the positive strain in the presence of xylose, but is repressed over the time course in the positive strain in the no carbon medium and in both the xylose and no carbon media in the negative strain.

Figure 7

Endogenous xylose pathway gene expression.

Interestingly, the sorbitol dehydrogenases SOR1 and SOR2, suggested to have the biochemical ability to oxidize xylitol, are highly expressed compared to the reference in the positive strain both in the presence and absence of xylose, and are strongly repressed vs. the pooled reference in the negative strains in both conditions across the time course. Because there is only one nucleotide difference between the coding sequences of SOR1 and SOR2, the probes on the array for these genes are only different by 1 base out of 60 and thus there is likely to be cross-hybridization of the mRNA's from the two SOR genes. It is also possible that there is hybridization of XDH1 mRNA to these probes, as there are only a few differences between XDH1 and the SOR1/2 probes on the microarray (6 for SOR1 and 7 for SOR2). Although we cannot determine which of the mRNA's (SOR1, SOR2 or XDH1) are hybridizing to the probes, it is nevertheless obvious that there is a distinct difference between the positive and negative spores in the expression levels of at least one of these putative dehydrogenase genes. No striking difference in the expression level of the xylulokinase, XKS1, was observed between any conditions or between any spores. The lack of change in the expression of XKS1 is somewhat unsurprising, as it has been previously reported that low levels of XKS1 are sufficient to allow xylose metabolism, while over-expression can enhance xylose fermentation in an engineered strain [29], [62]. Taken together, these data strongly suggest that the presence of XDH1 in the positive spores permits continued expression of some members of the endogenous xylose pathway when grown in xylose.

To further understand the transcriptome-wide response of these strains, we identified genes that changed significantly across the time course, compared these genes with other microarray datasets to identify any clear physiological responses, and looked for categories of functional enrichment within groups of up or down-regulated genes. Using Significance Analysis of Microarrays [SAM] [63] with a false discovery rate of 1%, we identified a list of 1266 genes whose expression levels were significantly changed over time. Specifically, we carried out a SAM analysis using the two-class (paired timecourse) option to identify genes whose expression changed over time within the positive spores, comparing the xylose to the no carbon condition. Next, we identified genes whose expression changed over time when comparing the positive to the negative spores in the presence of xylose, again using SAM with a two-class (paired timecourse) option. From the union of these two gene lists, we removed genes whose expression levels changed significantly over time within the negative strain, comparing the xylose to the no carbon condition (another two-class, paired timecourse analysis). Using this strategy, we generated an inclusive list of genes whose expression values change over time due to differences between the positive and negative strain, or due to differences between the presence and absence of xylose specifically in the positive strain. To identify the physiological responses that are associated with these gene expression differences, we retrieved data for these 1266 genes using HIDRA [64] from three other yeast microarray experiments [65]–[67] and organized the genes by K-means clustering with K

10 [68] (Figure 8, Datasets S1, S2). For consistency with the other datasets, each of the four time-course experiments performed in this work were zero-transformed. To the right of the experiments from this paper are, respectively, a measure of how each gene's expression level correlates with increased growth rate [65], a gene expression time course over the diauxic shift [66], gene expression across a set of carbon sources (ethanol, sucrose, fructose, glucose, galactose, and raffinose) [67], and a series of time courses in various conditions including starvation, steady state growth, and other stresses [67]. We observed 5 groups (labeled on the right of the heat map) that appear to be strongly driven by similarity of the positive strain in 2% xylose to either growth rate or a stress response. For example, the genes in groups 1 and 4 (Figure 8) are more highly expressed over the time course in the positive strain in xylose when compared to the positive strain in no carbon source or the negative strain in either condition, and these genes also show a positive correlation with growth rate. As expected, when GO::TermFinder [69] is used on these groups to look for functional enrichment of biological processes, we observed processes known to be up-regulated in conjunction with a higher growth rate. Specifically, group 1 was significantly enriched for vesicle-mediated transport (GO:0016192, p

2.11e-8) and cellular localization (GO:0051641, p

3.13e-8) among others (Dataset S3) and group 4 is enriched for translation (GO:0006412, p

2.26e-41) and ribosome biogenesis (GO:0042254, p

5.87e-23) along with related processes (Dataset S4). Group 5 shows the same pattern, but largely with the opposite response, meaning that these are genes whose expression is negatively correlated with growth, and we observed that they are expressed at a lower relative level in the positive strain in xylose when compared to the no carbon condition or the negative strain in either condition; but we observed no functional enrichment in this group. Interestingly, within group 5 there is a small group of genes (labeled ‡) whose expression is induced over time relative to the reference in the positive strain in xylose, and repressed over time in the other conditions. This group includes SNO4, THI4, and HSP32, which are genes all at least putatively involved in thiamin biosynthesis. Thiamin biosynthesis is known to be important for sugar metabolism, and is a pathway in which higher expression of certain components has likely been selected for in a variety of industrial yeasts [7]. There is also a small group of genes within group 1 (labeled †) that behaves differently than the rest of the group, as it is strongly repressed relative to the reference in the positive strain in xylose. Within this group of seven genes, four of them could be involved in intracellular redox balancing as they all use NADP(H) as a cofactor (TRR1, OYE2, GDH1, ADH6). In general, these three groups suggest that XDH1 in the positive strain permits a “growth-like” transcriptional response in the presence of xylose, whereas in the absence of xylose or the absence of XDH1 the strains are exhibiting an expression pattern consistent with lack of growth and starvation (e.g. groups 4 and 5). We also observed two other groups that did not fit this pattern, but instead the positive strain in xylose exhibited a response more akin to various stresses. For example, in group 2 we observed lower relative expression in the positive strain in xylose compared to the other three conditions despite the fact that these genes are all strongly correlated with growth rate, and included functional enrichment for RNA metabolism (GO:0016070, p

1.56e-6) and ribosome biogenesis (GO:0042254, p

1.33e-5) (Dataset S5). Instead, they appear to be more similar to the expression patterns in strains experiencing nitrogen depletion, stationary phase, diamide, DTT, or hydrogen peroxide treatment, and 37°C heat shock. We observed a similar response in group 3, in which the expression level is opposite what we might expect if growth rate was the main cause of the expression differences but similar if the strains were exhibiting an environmental stress response. Interestingly, this group was enriched for pentose metabolic process (GO:0019321, p

5.7e-3) and response to oxidative stress (GO:0006979, p

7.88e-3) (Dataset S6). These data suggest that despite the fact that this set of genes is normally repressed in response to a higher growth rate, some of these genes may be responding to the presence of xylose.

Figure 8

Gene expression timecourse.

There were also three groups of genes that did not have an obvious visual relationship with either growth rate or stress response. Group (a) appears to be more highly expressed in the positive strain in xylose compared to no carbon or the negative strain in either condition. While this group contains no functional enrichment using GO::TermFinder, it does contain a number of genes related to carbon metabolism, including PFK1, PFK2, PGI1, GCR1, and GND1. The final two groups (b and c) both appear to be expressed at a lower level in the positive strain in xylose compared to the other three conditions. Both groups have functional enrichment for various processes related to transcription and its regulation (Datasets S7, S8). In general genes in these three groups (a–c) show larger magnitude expression changes (induction or repression relative to the reference) in the non-growth conditions than in the positive strain in the presence of xylose. These clusters could support the conclusion that in the absence of xylose or the absence of XDH1, strains are exhibiting a response (perhaps starvation) that is simply not induced in the presence of xylose in the positive strain. In summary, these microarray data suggest that the positive strain in the presence of xylose is capable of “growth” when compared to the negative strain or lack of xylose, but it is still exhibiting a less pronounced stress-like response. These data are not inconsistent with the positive strain recognizing and using xylose as a carbon source.

Discussion

In this work we have shown that naturally occurring strains of Saccharomyces cerevisiae are capable of utilizing xylose without engineering or directed evolution, and have determined the genetic basis for this phenotype. While it has been known for many years that the xylose isomer xylulose is fermentable by S. cerevisiae, it has generally been thought that this species is incapable of metabolizing xylose. However, recent work has shown natural genetic variation for xylose utilization does exist, and that natural selection and breeding can improve xylose utilization in natural strains of S. cerevisiae [9]. By screening through many industrial and clinical isolates, we discovered variation within this species that permits utilization of this sugar, fermentation of which is an important prerequisite for the efficient generation of ethanol from lignocellulosic biomass sources. We have also shown that this ability to utilize xylose by Saccharomyces is conferred by the presence of a single gene, a novel putative xylitol dehydrogenase that we have named XDH1. This gene is both necessary and sufficient to permit xylose utilization in the normally non-xylose-utilizing S288c laboratory strain, and is absent from the reference genome sequence of S288c.

We also characterized the transcriptional response of one of our xylose-utilizing strains of S. cerevisiae to xylose in the presence and absence of XDH1. While these data do not allow us to draw conclusions as to whether or not this gene permits actual fermentation (rather than simply utilization) of xylose, we can make a number of observations. First, it is clear that the endogenous xylose pathway is capable of responding at the transcriptional level to the presence of xylose when this novel XDH is present. Secondly, we can infer that this sugar and its downstream metabolites are likely being funneled into central carbon metabolism via the pentose phosphate pathway as is consistent with what has previously been observed. This suggests that industrial or laboratory strains of S. cerevisiae may be more poised to ferment this pentose than previously thought, implying that we can better harness the standing genetic potential that already exists in nature and use it in combination with directed evolution and metabolic engineering to make an industrially applicable xylose fermentation strain.

The idea that Saccharomyces might be more “ready” to ferment xylose than previously thought is further supported by our genetic dissection of the xylose metabolic pathway endogenous to S. cerevisiae. We corroborated previous data that shows the xylulokinase encoded by XKS1 is functional and supports metabolism of xylose. We also demonstrated that GRE3 and YPR1, encoding two aldo-keto reductases, are each sufficient to allow xylose utilization in our strain background. The observation that a novel xylitol dehydrogenase is responsible for the xylose utilization phenotype, and the observation that the genes in the reference strain encoding enzymes putatively thought to oxidize xylitol (SOR1, SOR2, XYL2) are in fact detrimental to the phenotype, further support that the idea of a redox imbalance in S. cerevisiae favoring xylitol production over further metabolism is true [70], [71]. Finally, our results also suggest that some property of the XDH1 is able to reduce the cofactor imbalance and may be capable of pushing xylitol through the xylose metabolic pathway.

We also discovered Saccharomyces sensu stricto interspecific hybrids in our screen that appear to robustly utilize xylose by a mechanism independent of XDH1. Some of these strains are even more effective at utilizing xylose than the S. cerevisiae wine strains we have characterized here, and we are currently attempting to identify the locus (or loci) responsible for these other xylose phenotypes. Based upon the results in Table 2 that show S. bayanus xylose-positive strains that do not possess XDH1, it is likely that there is at least one other trait that is as yet unidentified. There may also be additional components of the xylose utilization pathway for which hypomorphic alleles exist in natural strains, as XDH1 is present in xylose-negative segregants of some xylose-positive strains we identified. We also suggest that the only other previously described [9], [72] xylose phenotype native to S. cerevisiae is likely to be XDH1-dependent, given that wine strains were included in the initial breeding. Because we and others have assayed strains that only contain a small sample of the variation that likely exists in the Saccharomyces gene pool, it is likely that there is additional variation present in nature that may be able to contribute to a xylose-positive phenotype.

Finally, we have developed a novel application of high-throughput sequencing for quickly mapping an unknown trait by BSA. Because we were able to identify a clear segregation pattern for our phenotype of interest, in this case a single locus, we were able to easily pool segregants and use sequencing to narrow down the genomic location using the high frequency of polymorphisms that segregated with our locus. Applying sequencing technology in addition to tiling arrays was critical as our phenotype resided in a region of the genome that is not present in the reference genome. Given that the number of genes responsible is small, we suggest that this application of high-throughput sequencing could be used broadly for associating other unknown genotypes to well-characterized phenotypes. It will be particularly applicable to other species that have small genomes and for which the genome sequence or tiling arrays are not readily available, or for such species that may contain variation not captured in their respective reference genomes.

While effective conversion of xylose to ethanol in an industrial setting by Saccharomyces yeasts has not yet reached its full potential, much progress has been made recently. We suggest that uncovering and studying the genes responsible for xylose utilization in wild strains of Saccharomyces may contribute directly to further improvements in lignocellulosic biomass fermentation. Additionally, the functions of these genes might continue to shed light on problematic areas in the metabolism of xylose, helping to inform directed evolution and metabolic engineering approaches.

Materials and Methods

Strains

Strains used in this study are shown in Table S1 and Table S6. In order to cross diploid HO/HO wine strains to a haploid S288c strain, wine strains were transformed with either pGS35 (CEN/ARS, KanMX) or pGS36 (CEN/ARS, Hph) and the resulting transformants carrying the plasmid were sporulated (Hph is the gene that permits hygromycin B resistance). Spores were mixed with a haploid ho S288c strain carrying either pGS35 if the wine strain carried pGS36 or vice versa, and plated onto YPD plates supplemented with G418 (200µg/mL) and hygromycin B (150µg/mL).

Media, Growth Conditions, and Growth Quantification

To screen for xylose utilization, single colonies were pre-grown to saturation at 25°C in YP with 2% glucose and then diluted 1 [ratio]

50 into YP with 2% xylose (Sigma) or no carbon source. 100µL cultures were grown for 5 days at 25°C in a sealed 96-well plate and absorbance was read at 595nm every 15 minutes in a TECAN Genios plate reader with orbital shaking. Xylose positives were identified by visual inspection of increasing OD in xylose compared to no carbon source, and were confirmed by retesting in both YP and Minimal [73] media.

Because growth on xylose is not exponential, we did not calculate a doubling time. Instead, to quantify xylose utilization we calculated a slope (change in OD over time) across the linear range of OD increase, from 20 to 80 hours in a typical TECAN growth experiment following the initial trehalose growth. Growth curves were done in at least triplicate (see Table S6 for all deletion strains), and a t-test was used to determine significant differences in rate of OD increase between deletion strains and “wild type” xylose positives.

Gene Expression Arrays

To analyze gene expression, cultures were pre-grown to saturation in YP with 2% glucose and diluted 1 [ratio]

50 into a 1.1L culture of minimal medium [73] with 2% xylose or no carbon source. 100mL samples were collected starting immediately after inoculation (t

0) and at subsequent 8 hour intervals for 72 hours by filtering with 0.45µm analytical test filter funnels (Nalgene) and were snap frozen in liquid nitrogen. RNA was extracted using a modified version of the hot phenol protocol, as described [74], [75]. A pooled reference sample was created by combining 350ng of each of the 120 RNA samples (10 time points for 6 strains in 2 conditions). 325ng of each total RNA sample and reference were labeled with Cy dyes (Amersham) using the Agilent Low RNA Input Linear Amplification Kit, and hybridized to Agilent Yeast Gene Expression Arrays (v2, 8x15K) for 17 hours at 65°C at 10rpm in a hybridization oven (Shel Lab). Arrays were scanned at 5µm resolution on an Agilent Scanner, and Agilent Feature Extraction v9.5.3.1 was used for extraction of data from the scanned images, and data normalization and calculation of log₂ ratios. Gene expression data have been deposited in the GEO database with accession number GSE19121.

Bulk Segregant Analysis

Xylose-positive segregants of Simi White (Lallemand), Lalvin AC, and SIHA Activ-Hefe 4 were crossed once to S288c (GSY147), and the resulting diploids were then sporulated. F2 segregants were scored for xylose utilization in the TECAN plate reader as described above. 1.5mL of overnight YPD culture of each segregant grown was spun down, resuspended, and frozen in 300µL of sorbitol solution (0.9M sorbitol, 0.1M Tris pH 8, 0.1M EDTA). Samples were pooled by phenotype at this stage and genomic DNA was extracted as described [76]. The pools contained 39 positives and 39 negatives for Simi White, 19 positives and 16 negatives for Lalvin AC, and 16 positives and 16 negatives for SIHA.

Genomic DNA was labeled as described [77], and microarray-assisted BSA was done using Affymetrix GeneChip S. cerevisiae Tiling 1.0R Array basically as described [52], [78]. Briefly, a ratio of the log₂ intensities for the perfect match probes was plotted across every chromosome for each nucleotide. The plots for each chromosome were scanned visually for local peaks in intensity. Tiling array data have been deposited in the GEO database with accession number GSE19121.

The same pools of genomic DNA were used for BSA by sequencing. 5µg of genomic DNA were prepared for sequencing using the Illumina Genomic DNA Sample Kit. Flow cells were prepared using the Illumina Standard Cluster Generation Kit v2, and samples were sequenced on the Illumina Genome Analyzer II. GAII data were analyzed with the Illumina 1.3.2 pipeline, and reads (with qualities) were aligned to the S288c genome with MAQ v0.7.1 [56] using default parameters. Reads from the positive pools that did not align to the reference genome were combined, and reads that contained any uncalled bases (“N”>

1) were removed from further analysis. De novo assembly was performed on this filtered set of un-mapped reads using Velvet v0.7.55 [57] with default parameters and hash length

13. All raw high throughput sequence data have been deposited in the SRA database with accession number SRP001391.

Cloning

The novel XDH was cloned into the NotI site of pRS316 [59] from GSY2469 (Simi White derivative) and GSY1362 (Lalvin AC derivative) by PCR using primers that contained NotI restriction sites. Primers are listed in Table S5. FY2 (S288c) was then transformed with the resulting plasmids (pGS104 and pGS105) via a slightly modified lithium acetate method [79]. Plasmids are listed in Table S6. Growth was assayed as described above in the TECAN plate reader.

Plasmid loss experiments were done as follows. The original transformant that was used to generate a TECAN growth curve was also streaked for single colonies on a YPD plate. These were grown and replica plated onto YPD and SC-URA plates, and colonies were picked from the YPD plate that either retained the plasmid (grew on the SC-URA replica plate) or lost the plasmid during mitosis (did not grow on the SC-URA replica plate) and were tested again in the TECAN.

Deletion Construction

Homologous recombination was used to create a disruption of the novel XDH. Primers are listed in Table S5. Briefly, KanMX6 was amplified from pFA6-KanMX6 [80], and approximately 400 bases up and downstream of the XDH homolog were amplified separately using primers that overlapped with the 5′ and 3′ primers used to amplify KanMX6. The three fragments were joined using Phusion DNA polymerase (Finnzymes) and the resulting deletion cassette was integrated into GSY2469 and GSY2468 (Simi White derivatives) by lithium acetate transformation. Correct integration of the deletion was confirmed by PCR and by showing opposing segregation of G418 resistance and the xylose trait in a cross to another xylose-positive haploid derivative.

To genetically dissect the endogenous xylose pathway, deletions of the xylose pathway genes were crossed into a haploid Simi White derivative that was previously backcrossed twice to S288c (GSY2469). Diploid strains heterozygous for deletions of GCY1, GRE3, YPR1, YJR096W, XYL2, and XKS1 were purchased from Invitrogen. Deletions of SOR1 and SOR2 were not available from the deletion collection as they are in large genomic regions of essentially 100% identity. Deletions were constructed as described [81], except with approximately 80 bases of homology to the regions immediately up and downstream of the SOR1/2 open reading frames rather than 40. Transformants were crossed to pgu1Δ and lrg1Δ to differentiate between sor1Δ and sor2Δ. Segregation of deletions was tracked by colony PCR when creating strains with more than two deletions, as the deletions are all marked with G418^R. Primers are listed in Table S5, and strains are listed in Table S6.

Supporting Information

Dataset S1

Data from Figure 8 organized by K-means (k

10) clustering (.cdt file).

(1.16 MB TXT)

Click here for additional data file.^{(1.1M, txt)}

Dataset S2

K-means groups for Figure 8 (.kgg file).

(0.01 MB TXT)

Click here for additional data file.^{(12K, txt)}

Dataset S3

GO Term Enrichment for “Group 1” from Figure 8.

(0.02 MB XLS)

Click here for additional data file.^{(21K, xls)}

Dataset S4

GO Term Enrichment for “Group 4” from Figure 8.

(0.03 MB XLS)

Click here for additional data file.^{(32K, xls)}

Dataset S5

GO Term Enrichment for “Group 2” from Figure 8.

(0.01 MB XLS)

Click here for additional data file.^{(8.6K, xls)}

Dataset S6

GO Term Enrichment for “Group 3” from Figure 8.

(0.01 MB XLS)

Click here for additional data file.^{(1.2K, xls)}

Dataset S7

GO Term Enrichment for “Group (b)” from Figure 8.

(0.01 MB XLS)

Click here for additional data file.^{(3.9K, xls)}

Dataset S8

GO Term Enrichment for “Group (c)” from Figure 8.

(0.07 MB XLS)

Click here for additional data file.^{(68K, xls)}

Figure S1

MUSCLE alignment of top 25 BLAST hits to XDH1 and neighbor-joining tree based on the multiple sequence alignment.

(2.51 MB TIF)

Click here for additional data file.^{(2.3M, tif)}

Table S1

Strains screened for xylose utilization.

(0.09 MB XLS)

Click here for additional data file.^{(93K, xls)}

Table S2

Linkage (Tetrad) Analysis of xylose trait to various chromosome XV genes.

(0.01 MB XLS)

Click here for additional data file.^{(15K, xls)}

Table S3

Illumina Sequencing Results (using MAQ to map reads to S288c genome).

(0.02 MB XLS)

Click here for additional data file.^{(18K, xls)}

Table S4

Linkage analysis of Velvet nodes amplified by PCR to xylose positive trait (S288c yor365cΔ×Simi White derivative).

(0.02 MB XLS)

Click here for additional data file.^{(17K, xls)}

Table S5

Primers used in this study.

(0.04 MB XLS)

Click here for additional data file.^{(35K, xls)}

Table S6

Strains and plasmids used in this study.

(0.04 MB XLS)

Click here for additional data file.^{(36K, xls)}

Acknowledgments

We wish to thank Maitreya Dunham and Douglas Ruderfer for analyzing the tiling microarray BSA data. We thank Ziming Weng and Phil Lacroute for help with generating the high-throughput sequence reads, as well as Devin Scannell for help with de novo assembly. We also thank Barbara Dunn, Dan Kvitek, Yuya Kobayashi, and R. Frank Rosenzweig for critical reading of this manuscript.

Footnotes

The authors have declared that no competing interests exist.

We wish to thank the Stanford Global Climate and Energy Project (GCEP) (grant # 33450), as well the NIH-NIGMS Genetics & Developmental Biology Training Program (grant # NIHGM007790) for funding. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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