- Open Access
Xylose utilization stimulates mitochondrial production of isobutanol and 2-methyl-1-butanol in Saccharomyces cerevisiae
Biotechnology for Biofuels volume 12, Article number: 223 (2019)
Branched-chain higher alcohols (BCHAs), including isobutanol and 2-methyl-1-butanol, are promising advanced biofuels, superior to ethanol due to their higher energy density and better compatibility with existing gasoline infrastructure. Compartmentalizing the isobutanol biosynthetic pathway in yeast mitochondria is an effective way to produce BCHAs from glucose. However, to improve the sustainability of biofuel production, there is great interest in developing strains and processes to utilize lignocellulosic biomass, including its hemicellulose component, which is mostly composed of the pentose xylose.
In this work, we rewired the xylose isomerase assimilation and mitochondrial isobutanol production pathways in the budding yeast Saccharomyces cerevisiae. We then increased the flux through these pathways by making gene deletions of BAT1, ALD6, and PHO13, to develop a strain (YZy197) that produces as much as 4 g/L of BCHAs (3.10 ± 0.18 g isobutanol/L and 0.91 ± 0.02 g 2-methyl-1-butanol/L) from xylose. This represents approximately a 28-fold improvement on the highest isobutanol titers obtained from xylose previously reported in yeast and the first report of 2-methyl-1-butanol produced from xylose. The yield of total BCHAs is 57.2 ± 5.2 mg/g xylose, corresponding to ~ 14% of the maximum theoretical yield. Respirometry experiments show that xylose increases mitochondrial activity by as much as 7.3-fold compared to glucose.
The enhanced levels of mitochondrial BCHA production achieved, even without disrupting ethanol byproduct formation, arise mostly from xylose activation of mitochondrial activity and are correlated with slow rates of sugar consumption.
Branched-chain higher alcohols (BCHAs), including isobutanol, isopentanol and 2-methyl-1-butanol (2-MbOH), are promising alternatives to the first-generation biofuel ethanol. These alcohols have better fuel properties than ethanol, such as higher energy density, ease of refining, and better compatibility with existing gasoline engines and infrastructures . Several organisms have been engineered to produce isobutanol and other branched-chain alcohols by combining the biosynthetic and degradation pathways of branched-chain amino acids [2,3,4,5,6,7,8,9,10]. Isobutanol biosynthesis begins from pyruvate with acetolactate synthase (ALS), encoded in Saccharomyces cerevisiae by ILV2, followed by ketol-acid reductoisomerase (KARI), encoded by ILV5, and then dehydroxyacid dehydratase (DHAD), encoded by ILV3 . This upstream pathway results in the production of the valine precursor α-ketoisovalerate (α-KIV), which can be converted to isobutanol through the Ehrlich degradation pathway. This involves the decarboxylation of α-KIV by various α-ketoacid decarboxylases (α-KDCs), including those encoded by PDC1 and ARO10, followed by reduction of the resulting isobutyraldehyde by various endogenous alcohol dehydrogenases (ADHs) (Fig. 1a). The 2-methyl-1-butanol biosynthetic pathway has considerable overlap with the upstream pathway of isobutanol biosynthesis and identical downstream Ehrlich degradation pathway. However, in this case the isoleucine precursor α-keto-β-methylvalerate (α-KMV) is synthesized by Ilv2p from one pyruvate and one α-ketobutyrate produced by threonine deaminase (ILV1) (Fig. 1b). In yeast, the gene products of the upstream pathway, ILV2, ILV3, and ILV5 (collectively referred to as the ILV genes), are naturally located in mitochondria, where α-KIV is thus produced (ILV1 and α-KMV are also mitochondrial). Yet the downstream pathway, composed of KDCs and ADHs, is naturally located in the cytosol. Alternative strategies have been used to overcome this physical fragmentation of the natural pathways, including colocalizing all enzymes in the cytosol , or in mitochondria .
To improve the environmental sustainability of biofuels, it is desirable to produce them from lignocellulosic biomass instead of starch or simple sugars [13,14,15]. Lignocellulosic biomass is primarily composed of three biopolymers: cellulose (~ 40–50%), hemicellulose (~ 25–35%) and lignin (~ 15–20%). The first two can be hydrolyzed into fermentable sugars: glucose from cellulose and mostly pentoses from hemicellulose [16, 17]. To enhance the economic viability of lignocellulosic biofuels, it is necessary to convert as much of the feedstock into valuable products, including the hemicellulose. As the primary component of hemicellulose, d-xylose (xylose) is the second most abundant sugar in lignocellulosic hydrolysates after glucose . While yeast does not naturally assimilate xylose, several yeast strains have been developed to grow and produce ethanol from xylose [19,20,21,22,23,24,25].
Two different approaches have been taken to engineer xylose assimilation in yeast, both of which rely on converting xylose into xylulose-5-phosphate to feed glycolysis through the pentose phosphate pathway (PPP) (Fig. 1). In one strategy, called the isomerase pathway, xylose is isomerized to d-xylulose using a xylose isomerase (XI) [19, 21]. Alternatively, in the oxidoreductase pathway, xylose is converted to d-xylulose by sequential redox reactions carried out by xylose reductase (XR) and xylitol dehydrogenase (XDH), passing through xylitol as an intermediate [20, 22,23,24,25] (Fig. 1). In either strategy, the d-xylulose produced is phosphorylated to xylulose-5-phosphate by xylulokinase (XK), which feeds into the PPP.
Here, we describe a new strain engineered to produce isobutanol from xylose, which uses the mitochondrial isobutanol biosynthetic pathway  in a strain engineered with the isomerase xylose utilization pathway . Previous efforts, using the isomerase xylose utilization and the cytosolic isobutanol biosynthetic pathways [27, 28], resulted in strains that produced up to approximately 110 mg/L of isobutanol . Our strain produces as much as 3.10 ± 0.18 g/L of isobutanol as well as 0.91 ± 0.02 g/L of 2-MbOH, representing a 28-fold improvement from previously reported isobutanol titers, the highest xylose-derived isobutanol yields and productivities, as well the first report of 2-MbOH production from xylose. This study shows that xylose stimulates the activity of yeast mitochondria, thereby benefitting the mitochondrial isobutanol biosynthetic pathway for BCHA production from this pentose.
Construction of a yeast strain to produce isobutanol from xylose
To develop S. cerevisiae strains that produce isobutanol from xylose, we introduced the mitochondrial isobutanol biosynthetic pathway  into the xylose-utilizing strain H145E10-XYLA3-1 (called Y58 in this study, Table 1) . Y58 was evolved from a yeast strain engineered with the Piromyces xylose isomerase XYLA, and the xylulose kinase XYL3 from Pichia stipitis, which together convert d-xylose to d-xylulose-5-P [19, 26]. The d-xylulose-5-P feeds into the glycolytic pathway through the non-oxidative pentose phosphate pathway (PPP), allowing the cell to metabolize xylose for cell growth and ethanol production  (Fig. 1). Using linearized plasmid pYZ34 (Table 2), we integrated the mitochondrial isobutanol pathway into genomic δ-sites (YARCdelta5) of Y58. This pathway consists of three genes for branched-chain amino acid biosynthesis (ILV2, ILV5, and ILV3, collectively referred to as the ILV genes), as well as genes encoding the Ehrlich degradation enzymes (CoxIVMLS-ARO10 and CoxIVMLS-LlAdhARE1) targeted to mitochondria using the COXIV mitochondrial localization signal (CoxIVMLS). This so-called mitochondrial isobutanol pathway boosts the production of branched-chain alcohols, relative to overexpressing the same enzymes in their native compartments . After screening 20 colonies for isobutanol production in 48 h of high cell-density fermentation in 15% xylose we found that the best producer, YZy165 (Table 1), makes 162 mg/L of isobutanol, which is about sevenfold higher than the parental strain Y58 (24 ± 5 mg/L) (Additional file 1: Figure S1).
Improvement of isobutanol production by targeted gene deletions
Previous studies have shown that deletion of PHO13 enhances xylose fermentation in S. cerevisiae [22, 29, 30]. PHO13 encodes a promiscuous alkaline phosphatase that dephosphorylates metabolites and proteins. Although the precise role of this enzyme in boosting xylose utilization is not completely understood, it has been shown to have phosphatase activity on xylulose-5-phosphate  (Fig. 1). In addition, PHO13 deletion causes transcriptional changes that affect the oxidative pentose phosphate pathway (PPP), other pathways that regenerate NADPH, and TAL1. The later encodes transaldolase, a bottleneck enzyme of the PPP whose activity, combined with that of Pho13p, leads to the accumulation of sedoheptulose as a byproduct . When we deleted PHO13 in YZy165 (YZy178, Table 1), we observed a modest increase in isobutanol yield (2.3 ± 0.5 mg/g xylose from 1.7 ± 0.3 mg/g xylose, Fig. 2a) and approximately 36% reduction in ethanol titers (27.9 ± 0.3 g/L from 37.8 ± 1.9 g/L, Fig. 2b) from 15% xylose in 72 h high cell-density fermentations. However, deletion of PHO13 also results in a proportional reduction in xylose consumption (Fig. 2c), which leads to practically unchanged isobutanol titers (Fig. 2a and Additional file 1: Figure S2). The parental strain Y58 is already engineered to overexpress enzymes in the PPP (Table 1), which could explain the small effects on cell growth and isobutanol production of deleting PHO13.
The aldehyde dehydrogenase encoded by ALD6 has been shown to divert the isobutyraldehyde precursor to isobutyrate at the expense of isobutanol production [31, 32] (Fig. 1). In addition, Ald6p is involved in converting the ethanol produced from fermentation to acetic acid, which reduces cell growth and product yields [33,34,35]. Disruption of ALD6 in YZy165 (YZy183, Table 1) indeed leads to a 1.7-fold improvement in isobutanol production from xylose (Fig. 2a). Because Ald6p is a cytosolic enzyme, this result suggests that a fraction of isobutyraldehyde reduction may actually occur in the cytosol. This is consistent with the high activity of the mitochondrial α-KIV carrier, which transports α-KIV produced in mitochondria to the cytosol, where it can be decarboxylated by endogenous cytosolic ketoacid decarboxylases to isobutyraldehyde . However, the largest effect of deleting ALD6 is a substantial boost in cell growth measured by optical density (OD600, Additional file 1: Figure S2f), ethanol titers (Fig. 2b), and xylose consumption (Fig. 2c), suggesting that much of the improvement to isobutanol production may come from decreasing acetic acid production and boosting biomass formation. Moreover, deletion of both ALD6 and PHO13 (YZy182, Table 1) did not result in further increase in isobutanol production (Fig. 2a).
We also explored the effect of deleting the mitochondrial branched-chain amino acid transaminase encoded by BAT1, which converts the α-KIV precursor to valine exclusively in mitochondria (Fig. 1a). We found that deleting BAT1 in YZy165 results in a strain (YZy173, Table 1) that produces 358 ± 13 mg/L isobutanol (from 15% xylose in 72 h high cell-density fermentations), which is a substantial improvement relative to deletions of PHO13 (YZy178) or ALD6 (YZy183) alone, and 2.5-times higher than the isobutanol produced by the parental YZy165 strain (Fig. 2a).
When we combined multiple deletions in the same strain (Table 1), we sometimes saw modest improvements in isobutanol production relative to the strain containing BAT1 deleted (YZy173). Deleting both BAT1 and PHO13 (YZy177) produces the same titers as deleting PHO13 alone (YZy178), which is less than half of what the BAT1 deletion alone (YZy173) produces; yet the yield in the double knockout strain (YZy177) is 76% higher than that in the ΔPHO13 strain (YZy178, Fig. 2a). The improvement in yield observed in YZy177 relative to YZy178 is a consequence of a substantial reduction in xylose consumption in YZy177 (Fig. 2c, Additional file 1: Figure S2), a trend perceived in the deletion of PHO13 alone (when comparing YZy178 and the parental strain YZy165), which is exacerbated when combined with a BAT1 deletion and ultimately explains the lower titers obtained with YZy177. When we deleted both BAT1 and ALD6 (YZy184), we saw an increase in isobutanol titers relative to the strain carrying only a BAT1 deletion (YZy173) but also a lower yield (Fig. 2a, Additional file 1: Figure S2a, b), seemingly due to the accelerated xylose consumption observed in all strains with an ALD6 deletion (Additional file 1: Figure S2e). However, the yields and titers of this double knockout are much higher than those of the strain with only ALD6 deleted (YZy183). Finally, the strain carrying all three deletions (YZy181) achieves the same isobutanol titers (409 ± 25 mg/L) as the strain with only BAT1 and ALD6 (YZy184) and the highest overall yields after 72 h of fermentation (5.2 ± 0.4 mg/g), which are 2.8- and 3.0-fold higher than the parental strain (YZy165) (Fig. 2a, Additional file 1: Figure S2a, b). This suggests that the negative impact of PHO13 deletion on xylose consumption is repealed by the additional deletion of ALD6, (consistent with the improvement in xylose consumption in YZy182 relative to YZy178), while preserving the yield enhancement brought also by the PHO13 deletion. Nevertheless, the biggest strain improvement comes from deleting BAT1, which is a hallmark of mitochondrial isobutanol production .
Improvement of isobutanol production with additional copies of the mitochondrial biosynthetic pathway
Considering the possibility that stronger overexpression of the isobutanol biosynthetic pathway could further improve production, we set out to introduce additional copies of the mitochondrial isobutanol pathway using 2μ plasmids. Because YZy181 is derived from Y58, a uracil prototrophic strain [19, 26], we first introduced a missense mutation in the URA3 gene of YZy181 to make YZy171 (Table 1, see “Methods”) with a ura3 mutant allele compatible with the URA3 auxotrophic marker in our 2μ plasmids. Next, we transformed YZy171 with one of the three possible 2µ plasmids : pJA182 (containing the ILV genes, CoxIVMLS-ARO10, and CoxIVMLS-LlAdhARE1), pJA180 (containing the same genes, except CoxIVMLS-LlKivd, instead of CoxIVMLS-ARO10), or pRS426 (an empty plasmid control, Table 2). We also used these plasmids to transform YZy176, a strain derived from deleting PHO13, ALD6, and BAT1 from Y58 and introducing a missense mutant ura3 allele (as a control strain lacking the isobutanol biosynthetic pathway in δ-integration sites).
For each test strain transformation, we screened 22 colonies (3 for each empty plasmid control) for isobutanol production in 48 h high cell-density fermentations in 15% xylose. We found that most colonies of YZy171 transformed with 2μ plasmids containing biosynthetic pathways produce significantly higher isobutanol titers compared to colonies with empty plasmids (Additional file 1: Figure S3). This enhancement is more pronounced in some colonies harboring pJA180, with the best strain (isolated as YZy197, Table 1) producing over 1 g/L. Interestingly, the pJA180 plasmid contains a different α-KDC (CoxIVMLS-LlKivd) from the one introduced into δ-sites of YZy171 (CoxIVMLS-ARO10); thus, YZy197 overexpresses both α-KDCs. We also found increased isobutanol production in colonies of YZy176 (lacking α-KDC in its δ-sites) transformed with pJA180 or pJA182. However, strains transformed with either plasmid produce approximately equal levels of isobutanol, and about the same as strains of YZy171 transformed with pJA182 (containing the same α-KDC, CoxIVMLS-ARO10, introduced in its δ-sites). Therefore, our results suggest that having the two different α-KDCs overexpressed simultaneously in the same strain, YZy197, is beneficial for isobutanol production.
Production of isobutanol and 2-methyl-1-butanol from different sugars in buffered media
We have previously shown that the mitochondrial isobutanol pathway can also lead to the conversion of glucose to other branched-chain higher alcohols (BCHAs) besides isobutanol, including 2-MbOH , which is another advanced biofuel (our strains are unable to produce isopentanol because of the leu2–3 auxotrophic marker in their parent strain, Y58, Table 1). Therefore, we explored the ability of YZy197 to produce both isobutanol and 2-MbOH from xylose, as well as from glucose or galactose in CaCO3-buffered media (see “Methods”). Using buffered medium maintains the pH of fermentations slightly above pH 6, which substantially improves BCHA production (Additional file 1: Figure S4). We found that YZy197 can produce both isobutanol and 2-MbOH from all three sugars in buffered media (Fig. 3).
Our results show that YZy197 is more proficient at making BCHAs from xylose than from glucose or galactose. Fermentations in 10% xylose produce 2.05 ± 0.21 g/L of isobutanol and 0.91 ± 0.02 g/L of 2-MbOH (Fig. 3a), whereas in 10% glucose they produce 1.07 ± 0.01 g/L of isobutanol and 0.68 ± 0.05 g/L of 2-MbOH (Fig. 3b); and in 10% galactose they produce 1.32 ± 0.12 g/L of isobutanol and 0.93 ± 0.16 g/L of 2-MbOH (Fig. 3c). In addition, the rate of conversion of glucose is higher than that of xylose: 100% of the glucose load is consumed in approximately 48 h, while approximately 45% of xylose remains after the same period of time, and more than 120 h are needed to consume all the xylose. However, the titers of isobutanol and 2-MbOH obtained from 10% xylose in the first 48 h of fermentation are higher than those from glucose, or galactose in the same amount of time (Fig. 3a–c). This is consistent with the higher yields we obtain from xylose compared to other sugars (Fig. 3 and Additional file 1: Table S1).
BCHA production in batch fermentations in different media
We carried out fermentations with YZy197 in SC-Ura medium containing different initial concentrations of xylose (4%, 8%, and 15%), glucose (15%) or galactose (15%) (Additional file 1: Figure S5 and Fig. 3). As expected, we found that higher concentrations of any sugar result in substantially higher isobutanol titers (Fig. 3 and Additional file 1: Figure S5), achieving the highest titer of 2.72 ± 0.10 g/L in 15% xylose (Fig. 3d). However, the titers of 2-MbOH are largely unchanged with increasing sugar concentrations (Additional file 1: Table S1), achieving similar values at 10% (0.91 ± 0.02 g/L) or 15% (0.86 ± 0.02 g/L) xylose. In addition, initial xylose consumption rates drop with increasing xylose concentrations and remain consistently low in fermentations starting at 15% xylose (Additional file 1: Figure S6a), which prevents full conversion even after 192 h (Fig. 3d). In contrast, increasing initial glucose concentrations raises its consumption rate (Additional file 1: Figure S7a).
We also analyzed the isobutanol yields and productivities at different xylose concentrations. We found that higher xylose concentrations result in higher isobutanol yields (Fig. 4a), which correlate with decreased rates of xylose consumption (Additional file 1: Figure S6a, b), achieving a maximum overall yield of 23.0 ± 4.8 mg/g xylose in 15% xylose. Daily isobutanol yields start lower in fermentations starting with 8% or 10% xylose, but increase with time (Fig. 4b), (fermentations starting with 4% xylose ended before 24 h, so we could only measure one daily yield). On the other hand, fermentations starting with 15% xylose start with higher daily yields and remain relatively unchanged throughout most of the fermentation. Furthermore, initial isobutanol productivities are similar in all initial xylose concentrations in which they can be reliably measured (8%, 10%, and 15% xylose) but decline faster in fermentations at lower xylose concentrations (Fig. 4c); (again, we could not reliably measure productivities or consumption rates in fermentations starting with 4% xylose, because the substrate is fully consumed in less than 24 h). These results are thus consistent with our observation that reduced rates of xylose consumption at higher xylose concentrations result in increased isobutanol yields (Fig. 4a and Additional file 1: Figure S6).
We also tested YZy197 fermentations using Verduyn’s medium, a vitamin-enriched minimal medium that uses only ammonium salts as nitrogen source . This medium has been effectively used for yeast xylose assimilation [38, 39] and isobutanol production from xylose . Time course experiments (as described above), in 10 mL of CaCO3-buffered medium with 10% xylose (see “Methods”), revealed that YZy197 still produces significant amounts of isobutanol and 2-MbOH (Additional file 1: Figure S5c), although at slightly lower titers and productivities compared to those obtained in SC-Ura, 10% xylose (Fig. 3a). Therefore, YZy197 is effective at producing BCHAs from xylose in both synthetic-rich (SC-Ura) and minimal (Verduyn’s) media.
Fed-batch fermentation for isobutanol production from xylose
To maximize isobutanol production from xylose, we carried out fed-batch fermentations at high sugar concentrations. Our results from batch fermentations revealed that higher xylose concentrations lead to higher isobutanol yields (Fig. 4a), productivities (Fig. 4c), and titers (Fig. 3d). Therefore, we set out to conduct fed-batch fermentations in which every 24 h we manually fed enough xylose to keep concentrations at approximately 10% or 15%, based on the calculated or measured xylose consumption rates (see “Methods”). The amount of xylose added in the first feeding at 24 h was calculated based on the xylose consumption rates obtained from batch fermentations (Additional file 1: Figure S6). The rest of the daily xylose feedings were calculated based on the measured rates of xylose consumption during the previous 24 h in the actual running fermentations. With this approach, we kept xylose concentrations at approximately 10% (103 ± 8 g/L, Additional file 1: Figure S8a) and 15% (154 ± 11 g/L, Additional file 1: Figure S8b) in fed-batch fermentations for 192 h.
Our results show that fed-batch fermentations in which xylose concentrations are kept high lead to improved isobutanol production (Fig. 5 and Additional file 1: Figure S8). YZy197 produces 2.96 ± 0.06 g/L of isobutanol in fermentations kept at approximately 10% xylose (Fig. 5a and Additional file 1: Figure S8c), and 3.10 ± 0.18 g/L of isobutanol (Fig. 5b and Additional file 1: Figure S8d) in those kept at 15% xylose, corresponding to as much as a 44% increase relative to batch fermentations (where xylose concentrations continuously drop). Even though the isobutanol titer is only improved by 5% in the higher xylose concentration, xylose consumption is lower at 15% xylose, which improves the yield. The maximum daily yield of 38.8 ± 2.4 mg/g xylose, achieved in the second day of fed-batch fermentations in 15% xylose, corresponds to 9.4% of the maximum theoretical yield (411 mg/g) and a 50% increase from the maximum daily yield achieved in batch fermentations starting with same amount of xylose (Table 3, Additional file 1: Table S1 and Figure S8). The compounded isobutanol yield of the fed-batch fermentation in 15% xylose during the first 96 h is thus higher than in any other fermentation (Additional file 1: Figure S8g), peaking after 48 h, when it reaches 35.8 ± 1.1 mg/g xylose, which is 74% higher than in the batch fermentation starting with the same xylose concentration (Fig. 5c).
Isobutanol productivities also benefit from keeping xylose concentrations high in fed-batch fermentations (Additional file 1: Figure S8f, h, and Table S1), achieving the highest values again on the second day. The maximum daily productivities are similar for both 10% and 15% xylose fed-batch fermentations (34.6 ± 3.1 mg/L/h and 35.7 ± 2.4 mg/L/h, respectively, Additional file 1: Figure S8f), but the maximum compounded productivity is slightly higher in fed-batch fermentations in 10% xylose (32.6 ± 1.7 mg/L/h, Fig. 5d and Additional file 1: Table S1). The fact that the maximum values are achieved on the second day of fermentation is likely due to the adaptation period at the beginning of fermentation that takes place during the first day. Our results from fed-batch experiments are consistent with our findings in batch experiments that higher xylose concentrations boost isobutanol yields and productivities (Fig. 4a).
Activation of mitochondrial activity by xylose
To test whether mitochondria are more active in xylose than in glucose or galactose, we carried out respirometry experiments to measure the oxygen consumption rate (OCR) of YZy197 in different concentrations of these sugars, ranging from 2 to 15%. We found that mitochondrial activity is indeed significantly higher in xylose than in glucose or galactose and that it is further stimulated with increasing sugar concentration (Fig. 6). At low sugar concentrations, the OCR is considerably lower, but even at 2% sugar, the OCR in xylose is twofold higher than in glucose. As sugar concentrations increase, so do the OCRs, but the rise in OCR is much more pronounced with increasing concentrations of xylose than of glucose or galactose. In fact, the OCR is 9.7-fold higher in 15% than in 2% xylose, while only 3- and 3.5-fold higher with the same increases in glucose or galactose, respectively (Fig. 6). Thus, the OCR in high (15%) sugar concentrations is 7.3 times higher in xylose than in glucose, and 3.3 times higher than in galactose. These results show that mitochondrial activity is significantly higher in xylose than in glucose or galactose, most notably at concentrations ranging from 8 to 15%, which could explain why mitochondrial isobutanol production is enhanced in xylose, especially at high concentrations.
We have engineered a xylose-utilizing yeast strain to produce BCHAs, including isobutanol and 2-MbOH, from this sugar. Yeast strains able to assimilate xylose have been previously engineered with the cytosolic isobutanol pathway [27, 28] to produce up to 110 mg/L of isobutanol from xylose . In contrast, our strain engineered with the mitochondrial isobutanol pathway can produce as much as 3.10 ± 0.18 g/L of isobutanol and 0.91 ± 0.02 g/L of 2-MbOH. This is about a 28-fold improvement in isobutanol titers from the highest previous report, as well as the first account of a C5 BCHA (2-MbOH), produced from xylose (Table 3). Although our strain and those previously reported [27, 28] all utilize xylose via the xylose isomerase pathway, there are significant differences in their genetic backgrounds, as well as in the xylose isomerases and xylulokinases they use, which may account for some of the difference in isobutanol production between these strains. However, we speculate that mitochondrial compartmentalization of the isobutanol pathway is a key factor in the performance of our strain, especially in light of the stimulatory effect of xylose on mitochondrial activity. In a parallel study, we show that the mitochondrial isobutanol biosynthetic pathway introduced into another strain of equally divergent background, engineered to utilize xylose via the oxidoreductase pathway (instead of the isomerase pathway), can produce similarly high levels of isobutanol from xylose of up to 2.6 ± 0.1 g/L . Thus, targeting the isobutanol biosynthetic pathway to mitochondria seems to be beneficial when producing BCHAs from xylose.
Mitochondrial production of BCHAs is higher in xylose than in other sugars. The parent strain Y58 was developed to efficiently grow and produce ethanol from xylose [19, 26], but it retains the ability to do the same in other sugars, including glucose and galactose. This gave us the opportunity to compare the performance of mitochondrial BCHA biosynthesis in these different sugars. Our results show that isobutanol and 2-MbOH titers and yields are, respectively, as much as 57% and 126% higher when produced from xylose (15%) than when produced from an equal amount of glucose; and as much as 33% and 30%, respectively, higher than when produced from the same amount of galactose (Additional file 1: Table S1). This suggests that mitochondrial metabolism is more active in xylose than in glucose, consistent with our observation that cells produce more ethanol from glucose than from xylose, which significantly impacts BCHA yields and titers .
There are different mechanisms by which xylose may enhance mitochondrial isobutanol production. We initially hypothesized that the reason could be related to the rate of sugar consumption, which is significantly lower in xylose compared to glucose (Fig. 3) and is inversely proportional to xylose initial concentrations (Fig. 3 and Additional file 1: Figure S6a, b) as well as isobutanol yields (Fig. 4). This hypothesis is consistent with observations we made in a separate study . However, this trend does not occur in glucose or galactose (Additional file 1: Figure S6c, d), suggesting that an additional mechanism is involved during xylose assimilation. A more likely mechanism for the enhanced production of isobutanol in xylose is the higher mitochondrial activity observed in this sugar. Previous studies have shown that xylose is not recognized by S. cerevisiae as a fermentable carbon source the way glucose or galactose are [42,43,44,45,46]. Transcriptional data have also shown that xylose induces respiratory proteins . Our own respirometry experiments confirmed that xylose enhances mitochondrial activity in YZy197 by more than sevenfold relative to glucose (Fig. 6). This stimulatory effect on mitochondrial activity is more pronounced at higher xylose concentrations, consistent with the enhanced isobutanol yields we observe in fed-batch fermentations in which we maintain high xylose concentrations (Fig. 5 and Additional file 1: Figure S8). Moreover, the reduced xylose consumption rate at higher xylose concentrations comes at the expense of reduced xylose fermentation, enabled by the higher amount of energy obtained from respiration, and consistent with the lower ethanol yields we observe. Therefore, it is likely that, by evading the Crabtree effect , xylose stimulates overall mitochondrial activity, including isobutanol production in this organelle. We anticipate that this effect of xylose on yeast metabolism will boost other metabolic pathways targeted to mitochondria .
The results obtained from the different gene deletion strains we tested reinforce the importance of mitochondrial activity in our strains. Deletion of BAT1 produces by far the largest boost in production (Fig. 2). Not only does Bat1p withdraw α-KIV from isobutanol biosynthesis, but the valine produced by this competing reaction also interferes with the upstream BCHA biosynthetic pathway by inhibiting Ilv2p via Ilv6p . Both of these inhibitory mechanisms of Bat1p occur exclusively in mitochondria; thus, the large increase in isobutanol production observed with its deletion alone strongly implicates mitochondrial activity in the biosynthesis of this alcohol in our strains. Once BAT1 is deleted, the contributions from deleting PHO13 and ALD6 are marginal (only 14% higher than the BAT1 deletion), again demonstrating the dominant role of mitochondrial activity in isobutanol production relative to the cytosolic Ehrlich pathway or even xylose assimilation efficiency.
We found that overexpressing two different α-KDCs (ARO10 and LlKivd) in the same strain (YZy197) leads to about 30% higher isobutanol production than overexpressing either α-KDC alone at equal levels (Additional file 1: Figure S3). We hypothesize that heterodimer formation may lead to higher protein stability or enzymatic activity [48,49,50]. Another possibility is that having two genes encoding different α-KDCs increases the mRNA levels and thus enzyme concentration for this enzymatic step in the pathway [51,52,53,54]. These are intriguing possibilities, which we are currently exploring.
Our best strains developed in this study (YZy197), and a concurrent study (SR8-Iso) , achieve the highest reported levels of BCHA production from xylose. Nevertheless, their titers, yields, and productivities are insufficient for industrial application. The main reason is that most of the xylose assimilated by these strains is diverted to ethanol production. Thus, future work to remove or control ethanol biosynthesis will be key in developing industrially relevant strains to produce BCHAs from xylose. Deletion of the three pyruvate decarboxylase genes (PDC1, PDC5, and PDC6), which divert metabolic flux away from BCHAs and toward ethanol, results in strains that are notably difficult to work with because they lose the ability to grow on high glucose concentrations [55,56,57]. This complication may be avoided when cells grow on xylose instead of glucose, given that yeast does not recognize xylose as a fermentable carbon source . If this is not the case, however, the timing and levels of PDC1 expression may be controlled, for example optogenetically , in a xylose-utilizing strain, which would significantly improve BCHA production from xylose.
In this study, we engineered a yeast strain that assimilates xylose via the xylose isomerase pathway with the mitochondrial isobutanol biosynthetic pathway. After deleting PHO13, ALD6, and BAT1 to enhance xylose assimilation and isobutanol production, and introducing additional copies of the mitochondrial isobutanol pathway, we obtained a strain that produces as much as 3.10 ± 0.18 g/L of isobutanol and 0.91 ± 0.02 g/L of 2-MbOH from xylose (Table 3). This represents the highest isobutanol titer and yield ever reported from xylose (28- and 9.5-fold higher than previous reports , respectively.), as well as the first report of 2-MbOH production from this sugar. We provide evidence that mitochondrial activity is significantly higher in xylose than in glucose, probably because the Crabtree effect is averted due to the inability of yeast to recognize xylose as a fermentative carbon source, which likely stimulates mitochondrial isobutanol biosynthesis. Slow xylose consumption rates may also benefit mitochondrial isobutanol production. The effect of xylose on mitochondrial activity makes using the mitochondrial isobutanol biosynthetic pathway to produce BCHAs from xylose advantageous. Furthermore, the benefits that xylose brings to BCHA production in mitochondria will likely translate to other metabolic pathways targeted to this organelle.
Chemicals, reagents and general molecular biology methods
All chemicals and solvents were purchased from Sigma (St. Louis, Missouri, USA). Plasmid construction was performed through standard restriction enzyme cloning and isothermal assembly . Target gene-disruption cassettes were amplified with polymerase chain reaction (PCR). Phusion High-Fidelity DNA Polymerase, Taq DNA polymerase, T4 DNA ligase, T5 Exonuclease, Taq DNA ligase, Calf Intestinal Alkaline Phosphatase (CIP), deoxynucleotide (dNTP) solution mix, and restriction enzymes were purchased from New England BioLabs (NEB, Ipswich, MA, USA) or Thermo Fisher Scientifics (Waltham, MA, USA). QIAprep Spin Miniprep, QIAquick PCR Purification, and QIAquick Gel Extraction Kits (Qiagen, Valencia, CA, USA) were used for plasmids isolation and DNA fragments purification according to the manufacturer’s protocols. The oligonucleotides used (Additional file 1: Table S2) were obtained from Integrated DNA Technologies (IDT, Coraville, Iowa, USA). The strain of Escherichia coli DH5α was used for routine construction and amplification of plasmids. All the constructed plasmids were verified by DNA sequencing (GENEWIZ, South Plainfield, NJ, USA).
The plasmids used in this study are listed in Table 2. Three new PCR template plasmids containing gene disruption cassettes flanked by mutant loxP sites (lox71 and lox66) were constructed for gene deletion and drug-resistant marker recycling: pYZ17 (KanMX), pYZ55 (HphMX), pYZ84 (NatMX). Cre-mediated recombination between same oriented lox71 and lox66 of inserts derived from these plasmids results in deletion of the drug resistance marker and a defective double mutant loxP site (lox72) which has a very low affinity for Cre recombinase . Plasmid pYZ17 was first constructed by replacing the two loxP sites in pUG6  with mutant lox71 and lox66 sites using the isothermal assembly method . Two overlapping DNA fragments were amplified from pUG6 using primer pairs Yfz_Oli67 & Yfz_Oli68, and Yfz_Oli69 & Yfz_Oli70, respectively (Additional file 1: Table S2). Plasmids pYZ55 and pYZ84 were constructed using restriction cloning by replacing the fragment between BglII and SacI in pYZ17 with fragments cut with BglII and SacI from pAG26 and pAG36 , respectively. The antibiotic resistant markers were amplified from these plasmids (pYZ17, pYZ55 and pYZ84) using a pair of primers containing the annealing sequences: primer 1 (5′-TACGCTGCAGGTCGACAACC-3′) and primer 2 (5′-CTAGTGGATCTGATATCACC-3′) with 5′ extensions containing 70 base pairs of homology to the sequences upstream and downstream of the ORF of the gene targeted for deletion.
We used a previously developed plasmid, pYZ23 , to target multiple copies of gene cassettes into genomic δ-sites YARCdelta5, the 337 bp long-terminal-repeat of S. cerevisiae Ty1 retrotransposons (YARCTy1-1, SGD ID: S000006792). The selection marker in pYZ23 is the shBleMX6 gene, which encodes a protein conferring resistance to zeocin and allows a selection of varying number of integration events based on varying zeocin concentrations. The level of zeocin resistance reflects the number of copies of the integration: resistance to higher concentration of zeocin correlates with a higher number of gene cassette copies integrated into δ-sites. The δ-integration plasmid pYZ34 (δ-integration of ILV2, ILV5, ILV3, CoxIVMLS-ARO10, and CoxIVMLS-LlAdhARE1) was constructed by subcloning the gene cassette from previously described plasmid pJA182  using restriction site pairs XmaI/AscI (to extract gene cassettes) and MreI/AscI (to open pYZ23). Integration plasmid was linearized with PmeI prior to yeast transformation.
Yeast strains, yeast transformation and growth media
All S. cerevisiae strains in this study (Table 1) were constructed from a xylose-utilizing strain Y58 (originally called H145E10-XYLA3-1), kindly provided by Dr. Gregory Stephanopoulos . H145E10-XYLA3-1 (MATa, leu2-3, 112, URA3, trp1-1∆::(PTDH3-RKI1-TCYC1, PTDH3-RPE1-TCYC1, TRP1), his2∆::(PTDH3-TKL1-TCYC1, HIS2), ade1∆::(PTDH3-PsTAL1-TCYC1, ADE1), ChVI::(PTDH3-PsXYL3-TCYC1, 32 copies of PTDH3-PsXYLA-TCYC1), arg4∆::(GRE3E193K, ARG4)) is evolved from H131-A3CS, a strain previously engineered and evolved to assimilate xylose by overexpressing codon-optimized xylose isomerase (XYLA) from Piromyces sp., xylulokinase (PsXYL3) from Pichia stipitis, and the non-oxidative pentose phosphate pathway (PPP) [19, 26].
Deletions of BAT1, ALD6, and PHO13 were obtained using PCR-based homologous recombination. DNA fragments containing lox71–lox66-flanked antibiotic resistance cassettes were amplified with PCR from pYZ55 (containing the hygromycin resistance gene hphMX4), pYZ17 (containing the G418 resistance gene KanMX), or pYZ84 (containing the nourseothricin resistance gene NAT1), using primers with 50–70 base pairs of homology to upstream and downstream of the ORF of the gene targeted for deletion. Transformation of gel-purified PCR fragments was done using the lithium acetate method . Transformed cells were first plated onto nonselective plates with 10 g/L yeast extract, 20 g/L peptone, 0.15 g/L tryptophan and 20 g/L xylose (YPX) and grown overnight at 30 °C. Lawns were then replica-plated onto YPX plates with 300 µg/mL hygromycin (Invitrogen, Carlsbad, CA, USA), 200 µg/mL nourseothricin (WERNER BioAgents, Jena, Germany), or 200 µg/mL Geneticin (G-418 sulfate) (Gibco, Life Technologies, Grand Island, NY, USA), and grown for another 3 days at 30 °C until colonies appeared. All strains with gene deletions were genotyped with positive and negative controls to confirm the removal of the ORF of interest.
Integrations into genomic δ-sites were performed by transforming strains with PmeI-linearized pYZ34 and using the lithium acetate method . Transformed cells were first incubated in YPX liquid medium for 6 h and then plated onto nonselective YPX agar plates for overnight growth. On the next day, the cells were replica-plated onto YPX agar plates with different concentrations (800, 1500 or 2000 µg/mL) of zeocin (Invitrogen, Carlsbad, CA, USA), and incubated at 30 °C until colonies appeared.
To restore the ura3 auxotrophic marker in YZy181 and Y58 (to make YZy171 and YZy176), an 825-bp double-stranded DNA fragment of the ORF of URA3 (orotidine-5′-phosphate decarboxylase) with three stop codons (taatgatag) inserted between Lys134 and Gln135 was synthesized from GENEWIZ (GENEWIZ, South Plainfield, NJ, USA) and transformed into the URA3 allele. We then selected on 5-fluoroorotic acid (5-FOA, Zymo Research, Orange, CA, USA) for Ura− strains.
Unless otherwise specified, yeast cells were grown on either YPX medium (10 g/L yeast extract, 20 g/L peptone, 0.15 g/L tryptophan and 20 g/L xylose) or synthetic complete (SC) drop-out medium (20 g/L glucose, 1.5 g/L yeast nitrogen base without amino acids or ammonium sulfate, 5 g/L ammonium sulfate, 36 mg/L inositol, and 2 g/L amino acid drop-out mixture).
High cell density fermentations were carried out in sterile 24-well microtiter plates (Cat. 229524, CELLTREAT Scientific Products, Pepperell, MA, USA) or in 50-mL conical tubes in an orbital shaker (Eppendorf, New Brunswick, USA) at 30 °C and at 200 rpm agitation. For plate fermentations, single colonies were first grown overnight in 1 mL of synthetic complete (SC) or synthetic complete minus uracil (SC-ura) medium supplemented with 2% xylose. The next day, 10 µL of the overnight culture was used to inoculate 1 mL of SC (or SC-ura) + 2% xylose medium in a fresh 24-well plate, and grown for 20 h. The following day, the plates were centrifuged at 1000 rpm for 5 min, the supernatant was discarded, and cells were re-suspended in 1 mL of SC (or SC-ura) supplemented with 15% xylose. The plates, in triplicates, were covered with sterile adhesive SealPlate® sealing films (Cat. # STR-SEAL-PLT; Excel Scientific, Victorville, CA, USA) and incubated for 48 h, 72 h or 96 h, respectively, at 30 °C and with shaking at 200 rpm. The sealing film was used in all 24-well plate fermentations to keep semi-aerobic conditions in all wells and to prevent evaporation, “edge effects”, and cross-contamination between wells. At the end of the fermentations, the optical density at 600 nm (OD600) of the culture in each well was measured. Plates were then centrifuged for 5 min at 1000 rpm. The supernatant (approximately 1 mL) from each well was processed and analyzed using HPLC as described below.
Longer time course experiments (192 h) of high cell density fermentations were carried out semi-aerobically in sterile 50-mL conical tubes. Overnight cultures were prepared by inoculating 5 mL of liquid SC-ura medium supplemented with 2% xylose with a single colony from agar plates. The following day, 10 mL of liquid SC-ura medium supplemented with 2% xylose was inoculated with 100 µL of overnight cultures and grown for 20 h at 30 °C in 50 mL conical tubes. The next day, cell cultures were centrifuged for 5 min at 3000 rpm and re-suspended in 10 mL of SC-ura or Verduyn’s medium  minus uracil, supplemented with different amounts of xylose (4%, 8%, 10%, or 15%), glucose (10% or 15%) or galactose (10% or 15%). Dry autoclaved calcium carbonate (CaCO3) was added to 1% concentration to the resuspended culture to maintain a pH range of approximately 6.2–6.6 during the fermentation. We used CaCO3 as a pH buffering agent to prevent acidification during fermentation [63, 64]. Samples of 0.3 mL were taken at different time intervals during fermentation (0, 24, 48, 72, 96, 120, 144, 168, and 192 h), and processed for HPLC analysis as described below.
Fermentations were carried out in sterile 50-mL conical tubes, semi-anaerobically and with CaCO3 as described above. Starting 24 h after resuspending cells in fresh SC-ura media with 15% xylose, and every 24 h thereafter, xylose was added manually using concentrated xylose feed (50% xylose in SC-ura medium). The amount of xylose added the first 24 h was calculated based on the xylose consumption rate obtained from batch fermentation studies (Additional file 1: Figure S6). The amount of xylose added for the rest of the feedings was calculated based on the rate of xylose consumption during the previous 24 h for each individual fermentation, aiming to keep a xylose concentration of approximately 10% or 15% throughout the fermentation. Samples of 0.3 mL were taken at 0, 24, 48, 72, 96, 120, 144, 168, and 192 h for both OD600 measurements and HPLC analysis.
The concentrations of xylose, ethanol, isobutanol, and 2-methyl-1-butanol were determined with high-performance liquid chromatography (HPLC) using an Agilent 1260 Infinity instrument (Agilent Technologies, Santa Clara, CA, USA). Samples were centrifuged at 13,300 rpm for 40 min at 4 °C to remove residual cells and other solid debris, and analyzed using an Aminex HPX-87H ion-exchange column (Bio-Rad, Hercules, CA, USA). The column was eluted with a mobile phase of 5 mM sulfuric acid at 55 °C and with a flow rate of 0.6 mL/min for 50 min. The chemical concentrations were monitored with a refractive index detector (RID) and quantified by comparing the peak areas to those of standard solutions.
Oxygen consumption rate measurements
Oxygen consumption rates (OCRs) of YZy197 in media supplemented with different carbon sources were measured using a Seahorse XF96 Analyzer (Agilent Seahorse Bioscience, MA, USA) according to the manufacturer’s instructions. Yeast cells were grown to mid-log phase in SC-ura medium supplemented with different amounts (2%, 4%, 8%, 10%, or 15%) of xylose, glucose, or galactose. Cells were then washed and resuspended to OD600 of 1.0 in the fresh medium which was used for growth. 180 µL of resuspended cells was seeded in poly-l-lysine-coated XF96 plate via centrifugation (500g for 3 min) and then incubated for 30 min at 30 °C prior to measurement. The Seahorse XF96 sensor cartridge was sequentially hydrated at 30 °C with sterile water (overnight) and XF Calibrant (60 min) following the manufacturer’s instructions. The Seahorse XF96 Analyzer was set to maintain the temperature at 30 °C. Both the mixing time and measuring time were set to 3 min in each cycle.
Availability of data and materials
The authors declare that all data supporting the findings of this study are available within the paper (and its Additional files).
branched-chain higher alcohols
pentose phosphate pathway
Choi YJ, Lee J, Jang YS, Lee SY. Metabolic engineering of microorganisms for the production of higher alcohols. MBio. 2014;5(5):e01524-01514.
Avalos JL, Fink GR, Stephanopoulos G. Compartmentalization of metabolic pathways in yeast mitochondria improves the production of branched-chain alcohols. Nat Biotechnol. 2013;31(4):335–41.
Atsumi S, Hanai T, Liao JC. Non-fermentative pathways for synthesis of branched-chain higher alcohols as biofuels. Nature. 2008;451(7174):86-U13.
Lin PP, Mi L, Moriok AH, Yoshino MM, Konishi S, Xu SC, Papanek BA, Riley LA, Guss AM, Liao JC. Consolidated bioprocessing of cellulose to isobutanol using Clostridium thermocellum. Metab Eng. 2015;31:44–52.
Smith KM, Cho KM, Liao JC. Engineering Corynebacterium glutamicum for isobutanol production. Appl Microbiol Biotechnol. 2010;87(3):1045–55.
Blombach B, Riester T, Wieschalka S, Ziert C, Youn JW, Wendisch VF, Eikmanns BJ. Corynebacterium glutamicum tailored for efficient isobutanol production. Appl Environ Microb. 2011;77(10):3300–10.
Black WB, Zhang LY, Kamoku C, Liao JC, Li H. Rearrangement of coenzyme A-acylated carbon chain enables synthesis of isobutanol via a novel pathway in Ralstonia eutropha. ACS Synth Biol. 2018;7(3):794–800.
Lu J, Brigham CJ, Gai CS, Sinskey AJ. Studies on the production of branched-chain alcohols in engineered Ralstonia eutropha. Appl Microbiol Biotechnol. 2012;96(1):283–97.
Varman AM, Xiao Y, Pakrasi HB, Tang YJJ. Metabolic engineering of Synechocystis sp. strain PCC 6803 for isobutanol production. Appl Environ Microbiol. 2013;79(3):908–14.
Miao R, Liu X, Englund E, Lindberg P, Lindblad P. Isobutanol production in Synechocystis PCC 6803 using heterologous and endogenous alcohol dehydrogenases. Metab Eng Commun. 2017;5:45–53.
Hazelwood LA, Daran JM, van Maris AJA, Pronk JT, Dickinson JR. The ehrlich pathway for fusel alcohol production: a century of research on Saccharomyces cerevisiae metabolism. Appl Environ Microbiol. 2008;74(8):2259–66.
Brat D, Weber C, Lorenzen W, Bode HB, Boles E. Cytosolic re-localization and optimization of valine synthesis and catabolism enables increased isobutanol production with the yeast Saccharomyces cerevisiae. Biotechnol Biofuels. 2012;5:65.
Valdivia M, Galan JL, Laffarga J, Ramos JL. Biofuels 2020: biorefineries based on lignocellulosic materials. Microb Biotechnol. 2016;9(5):585–94.
Limayem A, Ricke SC. Lignocellulosic biomass for bioethanol production: current perspectives, potential issues and future prospects. Prog Energy Combust Sci. 2012;38(4):449–67.
Chundawat SPS, Beckham GT, Himmel ME, Dale BE. Deconstruction of lignocellulosic biomass to fuels and chemicals. Annu Rev Chem Biomol Eng. 2011;2:121–45.
Buzala KP, Kalinowska H, Przybysz P, Malachowska E. Conversion of various types of lignocellulosic biomass to fermentable sugars using kraft pulping and enzymatic hydrolysis. Wood Sci Technol. 2017;51(4):873–85.
Lane S, Dong J, Jin YS. Value-added biotransformation of cellulosic sugars by engineered Saccharomyces cerevisiae. Bioresour Technol. 2018;260:380–94.
Mosier N, Wyman C, Dale B, Elander R, Lee YY, Holtzapple M, Ladisch M. Features of promising technologies for pretreatment of lignocellulosic biomass. Bioresour Technol. 2005;96(6):673–86.
Zhou H. Metabolic engineering of yeast for xylose uptake and fermentation. Ph. D. Massachusetts Institute of Technology; 2011.
Li X, Park A, Estrela R, Kim SR, Jin YS, Cate JH. Comparison of xylose fermentation by two high-performance engineered strains of Saccharomyces cerevisiae. Biotechnol Rep. 2016;9:53–6.
Lee SM, Jellison T, Alper HS. Systematic and evolutionary engineering of a xylose isomerase-based pathway in Saccharomyces cerevisiae for efficient conversion yields. Biotechnol Biofuels. 2014;7(1):122.
Kim SR, Skerker JM, Kang W, Lesmana A, Wei N, Arkin AP, Jin YS. Rational and evolutionary engineering approaches uncover a small set of genetic changes efficient for rapid xylose fermentation in Saccharomyces cerevisiae. PLoS ONE. 2013;8(2):e57048.
Cadete RM, de las Heras AM, Sandstrom AG, Ferreira C, Girio F, Gorwa-Grauslund MF, Rosa CA, Fonseca C. Exploring xylose metabolism in Spathaspora species: XYL1.2 from Spathaspora passalidarum as the key for efficient anaerobic xylose fermentation in metabolic engineered Saccharomyces cerevisiae. Biotechnol Biofuels. 2016;9:167.
Runquist D, Hahn-Hagerdal B, Bettiga M. Increased ethanol productivity in xylose-utilizing Saccharomyces cerevisiae via a randomly mutagenized xylose reductase. Appl Environ Microbiol. 2010;76(23):7796–802.
Ho NW, Chen Z, Brainard AP. Genetically engineered Saccharomyces yeast capable of effective cofermentation of glucose and xylose. Appl Environ Microbiol. 1998;64(5):1852–9.
Zhou H, Cheng JS, Wang BL, Fink GR, Stephanopoulos G. Xylose isomerase overexpression along with engineering of the pentose phosphate pathway and evolutionary engineering enable rapid xylose utilization and ethanol production by Saccharomyces cerevisiae. Metab Eng. 2012;14(6):611–22.
Generoso WC, Brinek M, Dietz H, Oreb M, Boles E. Secretion of 2,3-dihydroxyisovalerate as a limiting factor for isobutanol production in Saccharomyces cerevisiae. FEMS Yeast Res. 2017. https://doi.org/10.1093/femsyr/fox029.
Brat D, Boles E. Isobutanol production from d-xylose by recombinant Saccharomyces cerevisiae. FEMS Yeast Res. 2013;13(2):241–4.
Kwak S, Jin YS. Production of fuels and chemicals from xylose by engineered Saccharomyces cerevisiae: a review and perspective. Microb Cell Fact. 2017;16(1):82.
Ni H, Laplaza JM, Jeffries TW. Transposon mutagenesis to improve the growth of recombinant Saccharomyces cerevisiae on d-xylose. Appl Environ Microbiol. 2007;73(7):2061–6.
Park SH, Kim S, Hahn JS. Metabolic engineering of Saccharomyces cerevisiae for the production of isobutanol and 3-methyl-1-butanol. Appl Microbiol Biotechnol. 2014;98(21):9139–47.
Lee KM, Kim SK, Lee YG, Park KH, Seo JH. Elimination of biosynthetic pathways for l-valine and l-isoleucine in mitochondria enhances isobutanol production in engineered Saccharomyces cerevisiae. Bioresour Technol. 2018;268:271–7.
Boubekeur S, Camougrand N, Bunoust O, Rigoulet M, Guerin B. Participation of acetaldehyde dehydrogenases in ethanol and pyruvate metabolism of the yeast Saccharomyces cerevisiae. Eur J Biochem. 2001;268(19):5057–65.
Pampulha ME, Loureiro-Dias MC. Energetics of the effect of acetic acid on growth of Saccharomyces cerevisiae. FEMS Microbiol Lett. 2000;184(1):69–72.
Saint-Prix F, Bonquist L, Dequin S. Functional analysis of the ALD gene family of Saccharomyces cerevisiae during anaerobic growth on glucose: the NADP+-dependent Ald6p and Ald5p isoforms play a major role in acetate formation. Microbiology. 2004;150(Pt 7):2209–20.
Hammer SK, Avalos JL. Uncovering the role of branched-chain amino acid transaminases in Saccharomyces cerevisiae isobutanol biosynthesis. Metab Eng. 2017;44:302–12.
Verduyn C, Postma E, Scheffers WA, Van Dijken JP. Effect of benzoic acid on metabolic fluxes in yeasts: a continuous-culture study on the regulation of respiration and alcoholic fermentation. Yeast. 1992;8(7):501–17.
Verhoeven MD, de Valk SC, Daran JG, van Maris AJA, Pronk JT. Fermentation of glucose–xylose–arabinose mixtures by a synthetic consortium of single-sugar-fermenting Saccharomyces cerevisiae strains. FEMS Yeast Res. 2018;18(8):foy075. https://doi.org/10.1093/femsyr/foy075
Kong II, Turner TL, Kim H, Kim SR, Jin YS. Phenotypic evaluation and characterization of 21 industrial Saccharomyces cerevisiae yeast strains. FEMS Yeast Res. 2018;18(1):foy001. https://doi.org/10.1093/femsyr/foy001
Lane S, Zhang Y, Yun EJ, Ziolkowski L, Zhang G, Jin Y-S, Avalosd JL. Xylose assimilation enhances production of isobutanol in engineered yeast. Biotechnol Bioeng. 2019 (In revision).
Zhao EM, Zhang Y, Mehl J, Park H, Lalwani MA, Toettcher JE, Avalos JL. Optogenetic regulation of engineered cellular metabolism for microbial chemical production. Nature. 2018;555(7698):683–7.
Jin YS, Laplaza JM, Jeffries TW. Saccharomyces cerevisiae engineered for xylose metabolism exhibits a respiratory response. Appl Environ Microbiol. 2004;70(11):6816–25.
Osiro KO, Brink DP, Borgstrom C, Wasserstrom L, Carlquist M, Gorwa-Grauslund MF. Assessing the effect of d-xylose on the sugar signaling pathways of Saccharomyces cerevisiae in strains engineered for xylose transport and assimilation. FEMS Yeast Res. 2018;18(1):fox096.
Brink DP, Borgstrom C, Tueros FG, Gorwa-Grauslund MF. Real-time monitoring of the sugar sensing in Saccharomyces cerevisiae indicates endogenous mechanisms for xylose signaling. Microb Cell Fact. 2016;15(1):183.
Osiro KO, Borgström C, Brink DP, Fjölnisdóttir BL, Gorwa-Grauslund MF. Exploring the xylose paradox in Saccharomyces cerevisiae through in vivo sugar signal omics of targeted deletants. Microb Cell Fact. 2019;18(1):88.
Belinchon MM, Gancedo JM. Xylose and some non-sugar carbon sources cause catabolite repression in Saccharomyces cerevisiae. Arch Microbiol. 2003;180(4):293–7.
Hammer SK, Avalos JL. Harnessing yeast organelles for metabolic engineering. Nat Chem Biol. 2017;13(8):823–32.
Berthold CL, Gocke D, Wood MD, Leeper FJ, Pohl M, Schneider G. Structure of the branched-chain keto acid decarboxylase (KdcA) from Lactococcus lactis provides insights into the structural basis for the chemoselective and enantioselective carboligation reaction. Acta Crystallogr D. 2007;63(12):1217–24.
Kneen MM, Stan R, Yep A, Tyler RP, Saehuan C, McLeish MJ. Characterization of a thiamin diphosphate-dependent phenylpyruvate decarboxylase from Saccharomyces cerevisiae. FEBS J. 2011;278(11):1842–53.
Gocke D, Nguyen CL, Pohl M, Stillger T, Walter L, Müller M. Branched-chain keto acid decarboxylase from Lactococcus lactis (KdcA), a valuable thiamine diphosphate-dependent enzyme for asymmetric C–C bond formation. Adv Synth Catal. 2007;349(8–9):1425–35.
Nouaille S, Mondeil S, Finoux AL, Moulis C, Girbal L, Cocaign-Bousquet M. The stability of an mRNA is influenced by its concentration: a potential physical mechanism to regulate gene expression. Nucleic Acids Res. 2017;45(20):11711–24.
Lin J, Amir A. Homeostasis of protein and mRNA concentrations in growing cells. Nat Commun. 2018;9:4496.
Liu YS, Beyer A, Aebersold R. On the dependency of cellular protein levels on mRNA abundance. Cell. 2016;165(3):535–50.
Takahashi Y, Nishikawa M, Takiguchi N, Suehara T, Takakura Y. Saturation of transgene protein synthesis from mRNA in cells producing a large number of transgene mRNA. Biotechnol Bioeng. 2011;108(10):2380–9.
Flikweert MT, Van Der Zanden L, Janssen WM, Steensma HY, Van Dijken JP, Pronk JT. Pyruvate decarboxylase: an indispensable enzyme for growth of Saccharomyces cerevisiae on glucose. Yeast. 1996;12(3):247–57.
van Maris AJA, Luttik MAH, Winkler AA, van Dijken JP, Pronk JT. Overproduction of threonine aldolase circumvents the biosynthetic role of pyruvate decarboxylase in glucose-limited chemostat cultures of Saccharomyces cerevisiae. Appl Environ Microb. 2003;69(4):2094–9.
Milne N, Wahl SA, van Maris AJA, Pronk JT, Daran JM. Excessive by-product formation: a key contributor to low isobutanol yields of engineered Saccharomyces cerevisiae strains. Metab Eng Commun. 2016;3:39–51.
Gibson DG, Young L, Chuang RY, Venter JC, Hutchison CA, Smith HO. Enzymatic assembly of DNA molecules up to several hundred kilobases. Nat Methods. 2009;6(5):343-U341.
Albert H, Dale EC, Lee E, Ow DW. Site-specific integration of DNA into wild-type and mutant lox sites placed in the plant genome. Plant J. 1995;7(4):649–59.
Guldener U, Heck S, Fielder T, Beinhauer J, Hegemann JH. A new efficient gene disruption cassette for repeated use in budding yeast. Nucleic Acids Res. 1996;24(13):2519–24.
Goldstein AL, McCusker JH. Three new dominant drug resistance cassettes for gene disruption in Saccharomyces cerevisiae. Yeast. 1999;15(14):1541–53.
Gietz RD, Woods RA. Transformation of yeast by lithium acetate/single-stranded carrier DNA/polyethylene glycol method. Methods Enzymol. 2002;350:87–96.
Salek SS, van Turnhout AG, Kleerebezem R, van Loosdrecht MCM. pH control in biological systems using calcium carbonate. Biotechnol Bioeng. 2015;112(5):905–13.
Ma WL, Liu YF, Shin HD, Li JH, Chen J, Du GC, Liu L. Metabolic engineering of carbon overflow metabolism of Bacillus subtilis for improved N-acetyl-glucosamine production. Bioresour Technol. 2018;250:642–9.
Christianson TW, Sikorski RS, Dante M, Shero JH, Hieter P. Multifunctional yeast high-copy-number shuttle vectors. Gene. 1992;110(1):119–22.
We thank Dr. Gregory Stephanopoulos for providing strain Y58. We thank Dr. Coleen Murphy and Dr. Joshua D. Rabinowitz for allowing us to use their Seahorse XF96 Analyzer.
This work was supported by the U.S. Department of Energy, Office of Science, Office of Biological and Environmental Research Award Numbers DE-SC0019363 (to J.L.A.) and DE-SC0018420 (to YS.J.); as well as the NSF CAREER Award CBET-1751840, The Pew Charitable Trusts, The Alfred P. Sloan Foundation, and The Yang Family Foundation for Engineering from Princeton University SEAS (to J.L.A.).
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Zhang, Y., Lane, S., Chen, JM. et al. Xylose utilization stimulates mitochondrial production of isobutanol and 2-methyl-1-butanol in Saccharomyces cerevisiae. Biotechnol Biofuels 12, 223 (2019). https://doi.org/10.1186/s13068-019-1560-2
- Branched-chain higher alcohols
- Saccharomyces cerevisiae
- Mitochondrial engineering