Enhanced fermentative performance under stresses of multiple lignocellulose-derived inhibitors by overexpression of a typical 2-Cys peroxiredoxin from Kluyveromyces marxianus
© The Author(s) 2017
Received: 13 August 2016
Accepted: 21 March 2017
Published: 28 March 2017
Bioethanol from lignocellulosic materials is of great significance to the production of renewable fuels due to its wide sources. However, multiple inhibitors generated from pretreatments represent great challenges for its industrial-scale fermentation. Despite the complex toxicity mechanisms, lignocellulose-derived inhibitors have been reported to be related to the levels of intracellular reactive oxygen species (ROS), which makes oxidoreductase a potential target for the enhancement of the tolerance of yeasts to these inhibitors.
A typical 2-Cys peroxiredoxin from Kluyveromyces marxianus Y179 (KmTPX1) was identified, and its overexpression was achieved in Saccharomyces cerevisiae 280. Strain TPX1 with overexpressed KmTPX1 gene showed an enhanced tolerance to oxidative stresses. Serial dilution assay indicated that KmTPX1 gene contributed to a better cellular growth behavior, when the cells were exposed to multiple lignocellulose-derived inhibitors, such as formic acid, acetic acid, furfural, ethanol, and salt. In particular, KmTPX1 expression also possessed enhanced tolerance to a mixture of formic acid, acetic acid, and furfural (FAF) with a shorter lag period. The maximum glucose consumption rate and ethanol generation rate in KmTPX1-expressing strain were significantly improved, compared with the control. The mechanism of improved tolerance to FAF depends on the lower level of intracellular ROS for cell survival under stress.
A new functional gene KmTPX1 from K. marxianus is firstly associated with the enhanced tolerance to multiple lignocellulose-derived inhibitors in S. cerevisiae. We provided a possible detoxification mechanism of the KmTPX1 for further theoretical research; meanwhile, we provided a powerful potential for application of the KmTPX1 overexpressing strain in ethanol production from lignocellulosic materials.
KeywordsLignocellulose Inhibitors Tolerance Peroxiredoxin Ethanol fermentation Kluyveromyces marxianus
Fuel ethanol has been the earliest and most mature biofuel product so far and widely considered as one of the most promising biomass energies. Bioethanol from lignocellulosic materials represents the most promising renewable fuel due to its wide range of sources. However, the complex structure of lignocellulose requires a pretreatment step to produce monosaccharides for Saccharomyces cerevisiae. Current efficient pretreatment of lignocellulose by steam explosion, acids, or alkali may generate inhibitors to restrain the growth of yeasts in the fermentation, which represents a great challenge for the scale-up of ethanol production from lignocellulosic materials .
Lignocellulose-derived inhibitors in hydrolysates include weak acids (formic acid and acetic acid), furan derivatives (furfural and 5-hydroxymethyl furfural), and phenolic compounds (phenol and O-methoxyphenol) . Toxic mechanisms of inhibitors in lignocellulosic hydrolysates are supposed to be extremely complicated. The inhibitors may be removed by detoxification of lignocellulosic hydrolysates , which should not be regarded as the preferred choice considering loss of sugars and increased costs. Therefore, exploring the toxicity of distinctive inhibitors to cells and its mechanism, and developing excellent strains with enhanced tolerance are becoming a more critical component of ethanol production from lignocellulosic materials. However, mechanisms of toxicities of these inhibitors in yeasts are very complex and greatly variable depending on strains .
Inhibitors like acetic acid, furfural, and phenol have been reported to be related to the redox state inside cells, inducing reactive oxygen species (ROS) generation [4–6]. Acetic acid generally affects cell metabolism and stabilities of proteins by a drop in intracellular pH and potential, leading to a net negative effect on yeasts’ cell growth and proliferation . Acetic acid diffusing across plasma membrane damages cells by accumulating ROS , and therefore the expression of some oxidoreductases like mitochondrial cytochrome C oxidase chaperone gene (encoded by COX20) may improve tolerance to weak acids, especially acetic acid in S. cerevisiae . Moreover, an enhancement of intracellular proline concentration by the addition of proline or overexpression of a proline synthesis-related gene (PRO1) led to an obvious increase in tolerance to both acetic acid and furfural ; unlike acetic acid, the toxicity of furfural results from the inhibition of glycolytic and fermentative enzymes essential to central metabolic pathways, which reduces cell growth rates eventually . Interestingly, furfural also induces the accumulation of ROS inside cells by lowering activities of intracellular oxidoreductases . Consequently, some oxidoreductases, such as alcohol dehydrogenase ADH1  and ADH6 , 3-methylglyoxal reductase GRE2 , aldehyde reductase ARI1 , and xylose reductase XYL1 , help yeast cells convert furfural into the less toxic alcohols and then increase tolerance to furfural; phenolic compounds alter the permeability of biological membranes and caused irreversible damages to the cells. Phenolic compounds are supposed to be even more toxic than furfural by generating ROS like peroxides and superoxides inside the cells . It has been indicated that oxidoreductases could be quite effective in enhancing the tolerance of yeast cells to phenolic compounds in lignocellulosic hydrolysates . But beyond that, ionic liquids and hydrogen peroxide have become a new kind of inhibitors as the pretreatment technologies evolve. Hence, oxidoreductases have shown a perfect application in the enhancement of tolerance to multiple inhibitors from pretreatment of lignocellulose.
High-throughput sequencing is a powerful tool to gain insight into new genes and their new functions [16–19]. Our previous study on the transcriptional analysis of the non-conventional yeast Kluyveromyces marxianus, which possesses the advantages of high-temperature resistance, rapid growth rate, and diversity of substrates, identified lots of differentially expressed genes (DEGs) . A greatly up-regulated gene under aerobic conditions (ORP controlled at −130 mV) from K. marxianus Y179 has attracted our attention. According to the sequence alignment, this gene (KmTPX1) belongs to a large and highly conserved peroxiredoxin family. KmTPX1 is homologous to one of the five peroxiredoxins (Prxs) in S. cerevisiae (TSA1/TPX1) , which is the most abundant Prxs in cells . Tsa1p in S. cerevisiae has been reported to participate in oxidation–reduction reactions to remove excess ROS like peroxides , and the antioxidant role of Tsa1p in regulating the concentrations of intracellular peroxides protects cells from DNA damage and cell death [24, 25]. However, so far, no reports have combined Tsa1p in S. cerevisiae with tolerance to lignocellulose-derived inhibitors, and the homologous protein in K. marxianus (encoded by KmTPX1) has never been studied.
Therefore, in this study, KmTPX1 gene was cloned and then overexpressed in S. cerevisiae to analyze its potential functions in yeast cells. Afterwards, tolerance of the recombinant S. cerevisiae to multiple inhibitors or stressors in lignocellulosic hydrolysates was evaluated. The enhanced tolerance to formic acid, acetic acid, furfural, and salt makes great difference to ethanol production from lignocellulosic materials and provides more theoretical references for its industrial scale-up in the future.
Results and discussion
Identification of a hypothetical typical 2-Cys peroxiredoxin from K. marxianus
Furthermore, the construction of evolutionary tree by several typical 2-Cys Prxs from S. cerevisiae, Kluyveromyces lactis, Scheffersomyces stipites, and Candida tropicalis indicates that the evolutionary distance between KmTPX1 and Prxs from K. lactis is the shortest, followed by Tsa1p from S. cerevisiae. The other four Prxs from S. cerevisiae have the lowest homologies with KmTPX1, which makes us even more certain that KmTPX1 should be identified as a hypothetical typical 2-Cys Prx (Fig. 1b).
Simultaneously, a simple function annotation was conducted using amino acid sequence from K. marxianus,Y179. Firstly, we determined the accurate positions of two cysteine residues in KmTPX1, which were found at the sites of 47 and 171, respectively. Besides, an active domain, PXXXTXXCp, has been reported to exist in all Prxs , and this domain lies in amino acids between the 40th and 47th sites in KmTPX1. Meanwhile, the 146th Arg, another active site, is supposed to be close to the above active domain in 3D structure while it is far away from Cp in 2D sequence [26, 27]. Finally, Tairum et al.  constructed the three-dimensional structure model of Tsa1 protein, which showed that the 50th Glu and the 46th Arg are two essential sites for disulfide formation. These two functional sites in KmTPX1 were also found to be highly conserved from the alignment results (Fig. 1c).
Enhanced tolerance of TPX1 strain to oxidative stresses
To validate the possible functions of KmTPX1, we constructed the overexpression vector containing the gene KmTPX1, and the overexpression was achieved in S. cerevisiae 280 after verification by restriction enzyme digestion. Meanwhile, real-time quantitative PCR was performed to test the levels of expression. Expression of KmTPX1 gene in strain TPX1 can be detected, compared with the control strain 423 containing only empty vector (an additional file shows this in more detail [see Additional file 1]).
On the other hand, we carried out liquid fermentation experiments at different concentrations of H2O2 to further confirm our findings (Fig. 2b). There were no obvious differences in growth between two strains under low concentration (0.2 mM). An elevated concentration of 3 mM could inhibit the growth of the control strain 423 significantly, while strain TPX1 had been less affected, which was in line with the results reported by Kim et al. . Consequently, an enhanced tolerance of S. cerevisiae 280 with a normally functioning KmTPX1 gene provided a good foundation for further analysis and validation of other possible functions.
Responses to multiple lignocellulose-derived inhibitors in KmTPX1-overexpressing yeast
Lignocellulose-derived inhibitors, such as acetic acid, furfural, and phenol, induce the generation of intracellular ROS that is closely related to the redox state in cells. Hence, we further explored the potential applications of gene KmTPX1 in an enhanced tolerance of yeasts to the mixed inhibitors in the lignocellulosic hydrolysates. As a result, weak acids (formic acid and acetic acid), phenolic compounds (phenol and O-methoxyphenol), and furan derivative (furfural and 5-HMF), as the representative inhibitors in hydrolysates, were selected to test their effects on S. cerevisiae overexpressing KmTPX1.
Considering the possibilities of applications in industrial-scale ethanol production from lignocellulosic materials, the enhanced tolerance to a single inhibitor makes little sense. So we further evaluated the abilities of KmTPX1 to tolerate a mixture of lignocellulose-derived inhibitors. An improved tolerance of strain TPX1 to mixed FAF inhibitors was observed. Interestingly, a much more obvious difference in cell growth was detected when the two strains were exposed to mixed FAFH inhibitors, which might be attributed to the comprehensive stress compared with the FAF inhibitors. A similar publication reported that the addition of proline or overexpression of a proline synthesis-related gene (encoded by PRO1) might also achieve enhanced tolerance to a mixture of furfural, acetic acid, and phenol . In this case, a generally elevated tolerance of yeasts to the mixed lignocellulose-derived inhibitors due to some key genes makes a major breakthrough in the biofuel industry.
Besides, our tests on phenol and O-methoxyphenol indicated that KmTPX1 did not work for these two inhibitors despite marginally increased tolerance to O-methoxyphenol. Except for lignocellulose-derived inhibitors, phenol and O-methoxyphenol are also two typical environmental pollutants, which might make a great difference if we achieved both enhanced tolerance and degradation. The elevated effect of KmTPX1 on these two inhibitors was not obvious, which can be attributed to two main reasons: on the one hand, test conditions were not quite suitable; on the other hand, some doubts remain on whether these two inhibitors will generate ROS.
In particular, we also evaluated the tolerance of strain TPX1 to salt, ethanol, and high temperature from a global perspective of ethanol production. An enhanced tolerance of strain TPX1 to high concentration of salt was just as expected, which showed similar results with some related Prxs [29, 30]. This finding is of great significance to reducing the costs for scale-up of ethanol production. Surprisingly, KmTPX1 played a positive role in growth at high concentrations of ethanol. No previous results showed that ethanol had possible relations with intracellular redox states, so oxidoreductases might also be applied in increasing tolerance to ethanol. Therefore, this special result makes great sense in the field of ethanol fermentation. Finally, no significant effect of KmTPX1 in cell growth at high temperature was observed in spite of the relations between high temperature and intracellular ROS . In contrast, another Prx family protein, thioredoxin from Endocarpon pusillum, showed a positive role in increasing yeast tolerance to high temperature .
The principal advantage of KmTPX1 gene tends to increase the tolerance to mixed lignocellulose-derived inhibitors. Although some other oxidoreductases have been proved to promote cell growth when exposed to a single inhibitor, a comprehensively enhanced tolerance to multiple stressors may provide more references and potential applications for ethanol production from lignocellulosic materials.
Effect of initial pH on acetic acid tolerance in transgenic yeast cells
KmTPX1 gene has shown a distinct effect on increasing tolerance of S. cerevisiae to multiple lignocellulose-derived inhibitors. In our experiments, a lack of adequate nutrition in SC medium led to an obvious reduction in tolerance to acetic acid. Concentrations of acetic acid in lignocellulosic hydrolysates have been reported to achieve up to 5 g/L , so the relatively low concentration of acetic acid in FAF affects its possibility of application in industrial-scale production. Ionization of some inhibitors under certain pH values may change the degree of toxicity of the compounds. Therefore, the initial pH of the medium was adjusted to improve cell growth as much as possible under the current conditions .
Batch fermentation by KmTPX1-overexpressing yeast with FAF
Fermentative performance under FAF inhibitors in 3-L bioreactors
Lag phase, h
1.30 ± 0.06
0.80 ± 0.05
1.49 ± 0.12
0.61 ± 0.01
Initial glucose, g/L
51.84 ± 2.60
51.45 ± 1.89
50.86 ± 1.01
50.56 ± 2.27
Residual glucose, g/L
23.22 ± 1.24
34.78 ± 1.91
21.41 ± 0.83
11.03 ± 0.51
20.38 ± 1.02
8.50 ± 1.33
Glucose consumption rate, g/L/h
0.86 ± 0.04
0.47 ± 0.08
1.06 ± 0.02
0.33 ± 0.02
0.36 ± 0.01
0.18 ± 0.01
0.42 ± 0.02
0.18 ± 0.03
As shown in Fig. 5 and Additional file 2: Figure S2, the overexpression of KmTPX1 gene in cells helped accelerate the process of ethanol fermentation under inhibitors and greatly reduce the lag phase in both flasks and bioreactors, which showed a similar trend. Considering the experiments in the 3-L bioreactors as an example (Fig. 5; Table 1), fermentative performance was greatly enhanced whether controlling the pH or not. Without adjusting the initial pH after the addition of inhibitors (Fig. 5a, b), the lag phase was slashed by almost 24 h compared with that in the control strain. Glucose consumption rate and ethanol productivity of TPX1 were achieved up to 0.86 and 0.36 g/L/h, respectively, both of which were double those of the control strain. Particularly, a lower residual glucose concentration for strain TPX1 was observed because of an accelerated fermentative process (Table 1). This may make great differences to industrial-scale ethanol production.
In addition, controlling pH at 4.5 greatly improved both the fermentative performance and the tolerance to acetic acid in TPX1 strain. As mentioned above, the poor nutrition in SC media led to the decrease of acetic acid concentration in FAF inhibitors. Fortunately, adjusting the initial pH in serial dilution assay helped solve this problem. Therefore, fermentations were conducted in bioreactors to control the pH at around 4.5 in media throughout the process. As shown in Fig. 5c, d and Table 1, TPX1 strain could tolerate the FAF inhibitors containing an elevated concentration of acetic acid without an obvious lag phase. The glucose consumption and ethanol production achieved a reasonable result within 48 h; in contrast, the control strain hardly grew under the same conditions, which was mainly manifested in the extremely low consumption rate of glucose (less than 10 g/L within 48 h).
Consequently, KmTPX1 gene overexpressed in S. cerevisiae increased the tolerance to lignocellulose-derived inhibitors, thus shortening the lag period and accelerating the fermentation process. Besides, a shorter lag period is supposed to be the general characterization for strains with an enhanced tolerance [9, 29]. We would see a better fermentative performance in strain TPX1, as was described previously by Kim et al. , if higher concentrations of initial glucose and final ethanol were adopted.
Increasing stress tolerance related to intracellular ROS levels
Despite the complicated mechanisms that lignocellulose-derived inhibitors are toxic to cells, they may induce cells to generate intracellular ROS, either FAF or phenol [4–6]. Intracellular ROS damages cells by altering the growth and metabolism characteristics. Therefore, oxidoreductases help remove the excess ROS, maintaining it at a normal level, to achieve an elevated tolerance and reduce damages to cells. Intracellular ROS in cells with an increased tolerance has been reported to decrease under inhibitors, no matter what strategies were adopted [9, 29, 34].
Fortunately, the measurement of intracellular ROS provided strong supports for our inference. Without FAF inhibitors, the level of intracellular ROS in TPX1 was slightly lower than that in 423, which was proved to have no differences. Rather, with inhibitors of FAF, the level of intracellular ROS in control strain increased dramatically, achieving up to 3 times more than that in strain TPX1, and a lower amount of ROS was an important guarantee of growth, metabolism, and multiplication of yeasts (Fig. 6b). Above all, our results and some previous reports all confirmed that oxidoreductases maintained a normal level of oxidoreductases, which eventually manifested as an apparently enhanced tolerance of S. cerevisiae to multiple lignocellulose-derived inhibitors [9, 29, 34].
Ethanol production from lignocellulosic materials has been considered as one of the most promising substitutions for fossil fuels. In this study, through a comprehensive transcriptional analysis, we identified a typical 2-Cys peroxiredoxin from K. marxianus Y179 (KmTPX1). Meanwhile, the overexpression of KmTPX1 gene has been proved to regulate the levels of intracellular ROS, which correspondingly increased the tolerance of S. cerevisiae to both oxidative stress and multiple lignocellulose-derived inhibitors. Particularly, a reasonable fermentation profile of the overexpressing strain TPX1 was achieved in the presence of FAF inhibitors. These findings lay a good foundation for further research on industrial-scale ethanol production from lignocellulosic materials.
Strains, media, and growth conditions
Strains, plasmids, and primers used in this study
K. marxianus, wild-type
S. cerevisiae, MAT a, his3-1, leu2-0, met 15-0, ura3
E. coli, for genetic manipulation
S. cerevisiae overexpressing KmTPX1 gene, transformed from 280
S. cerevisiae with pRS423 plasmid, transformed from 280
Source and reference
Yeast episomal vector with HIS3 marker
KmTPX1 in pRS423
Plasmid construction and transformation
To construct an overexpression vector with the KmTPX1 gene, plasmid pRS423  was used for DNA manipulation and cloning. DNA manipulation was performed by standard procedures . KmTPX1 gene fragment was amplified from genome of K. marxianus Y179 with primers TPX1-F and TPX1-R. The obtained fragment with a coding region and a native promoter of KmTPX1 gene was inserted into pRS423 to generate pRS423–TPX1 after digestion with SacI and SacII (Table 2; Additional file 1: Figure S1a). The constructs were verified by both digestion of restriction enzyme and sequencing (Additional file 1: Figure S1b).
Transformation of E. coli cells was performed using the CaCl2 method . For screening the transformants, ampicillin (100 μg/mL) was added into LB selective plates. Yeast transformation was conducted using the LiAc/PEG method described by Gietz et al. , and the transformants were screened by SC medium without histidine (SC-His). Transformants with the recombinant plasmid of pRS423–TPX1 were marked as TPX1, and strains with the plasmid pRS423 were set as control (423) in this study. All transformants were verified by PCR.
Stress tolerance assay
To test the functions of KmTPX1 gene, serial dilution assay was performed using strain TPX1, and strain 423 was used as the control. Yeast cells were cultivated in SC-His medium with 1 mM H2O2 for 16–18 h at 30 °C and 150 rpm and then collected by centrifugation at 3000×g for 5 min. The collected cells (final cell density 10 g/L of DCW) were serially diluted with distilled water, after which 10 μL of the diluted cells was loaded onto SC-His agar plates containing a single or mixed lignocellulose-derived inhibitors. The inhibitors applied in this section included 3 mM H2O2, 0.3 g/L formic acid, 1.5 g/L acetic acid, 1.0 g/L furfural, 0.23 g/L phenol, 0.3 g/L O-methoxyphenol, 0.5 g/L 5-HMF, 5% (v/v) ethanol, 3 M NaCl, FAF mixture (0.3 g/L formic acid, 1.5 g/L acetic acid and 0.6 g/L furfural), and FAFH mixture (0.2 g/L formic acid, 0.8 g/L acetic acid, 0.3 g/L furfural, and 0.3 g/L 5-HMF). All plates were incubated for 2–3 days at 30 °C and then photographed. For high-temperature test, plates were incubated at 42 °C.
Fermentation experiments with H2O2 were also conducted to further verify the potential function of KmTPX1. Overnight cultures of two strains were inoculated into 100 mL SC-His medium supplemented with 0.2 mM or 3 mM H2O2, adjusting the initial cell density to around 0.05 g/L of DCW. The fermentation was performed at 30 °C and 150 rpm, and the samples were taken every 12 h to test cell growth.
The potential of an enhanced acetic acid tolerance was tested by serial dilution assay as was described above with the concentration of acetic acid increasing from 1.5 to 5 g/L. Effects of pH on acetic acid tolerance were evaluated by adjusting the initial pH to 4.5 with 3 N NaOH. The concentrations of acetic acid in SD-His plates were 1.5, 4, 5, and 10 g/L, respectively (Fig. 4).
Laboratory-scale batch fermentation
To evaluate the fermentative performance of strain TPX1, batch fermentation was conducted in bioreactors for 60 h. Pre-cultures of yeast cells were carried out in 100 mL of SC-His medium in 250-mL flasks for 16–18 h, and then 5% of cells were inoculated in a 3-L fermenter with 1 L of SC-His medium containing 50 g/L of glucose and FAF mixture (0.3 g/L formic acid, 1.2 g/L acetic acid, and 0.5 g/L furfural) at 30 °C and 150 rpm. The initial cell density was adjusted to 0.08–0.09 g/L of DCW, and the aeration rate was kept at 0.05 vvm.
To test the effect of initial pH on the fermentation and tolerance of TPX1 strain, batch fermentation was performed at an elevated concentration of acetic acid in FAF inhibitors (0.3 g/L formic acid, 5 g/L acetic acid, and 0.5 g/L furfural). Before inoculation, the initial pH of the medium with inhibitors was adjusted to around 4.5, and other environmental parameters were kept the same as above.
Samples were taken every 12 h to test cell growth, sugar and ethanol.
Expression pattern analysis of differentially expressed genes related to oxidative stress from transcriptome of K. marxianus Y179  was clustered using Cluster software  and Java TreeView software . The hierarchical clustering of the chosen experimental conditions and genes was carried out using Euclidean Distance as the formula of the distance matrix. Evolutionary tree of some typical 2-Cys Prxs from Y179 and its allied species using MEGA 4 software , and amino acid sequences applied are listed as follows: KmTSA1/KmTPX1, Tsa1 protein from K. marxianus Y179 in this study; KlTSA1, Tsa1 protein from K. lactis (Accession No. XP_451603.1); ScTSA1, Tsa1 protein from S. cerevisiae (Accession No. NP_013684.1); ScTSA2, Tsa2 protein from S. cerevisiae (Accession No. NP_010741.1); SsTSA1, Tsa1 protein from S. stipitis (Accession No. XP_001382622.1); CtTSA1, Tsa1 protein from C. tropicalis (Accession No. XP_002547929.1); ScPRX1, Pxr1 protein from S. cerevisiae (Accession No. NP_009489.1); ScAHP1, Ahp1 protein from S. cerevisiae (Accession No. NP_013210.1); and ScDOT5, Dot5 protein from S. cerevisiae (Accession No. NP_012255.3). Alignment was conducted using the National Center for Biotechnology Information (NCBI) Basic Local Alignment Search Tool (BLAST) software (http://clustalw.ddbj.nig.ac.jp/).
ROS level analysis
Levels of ROS inside cells were tested by a common method using 2′,7′-dichlorofluorescein diacetate (DCFH-DA, Sigma-35845, dissolved in absolute ethanol) as an indicator. Cells after pre-culture were cultivated for 16–18 h in SD-His medium with FAF (0.3 g/L formic acid, 1.2 g/L acetic acid, and 0.5 g/L furfural) at 30 °C and 150 rpm. Cell pellets were washed twice with distilled water and then re-suspended in 0.5 mL of 10 mM PBS (pH 7.0) containing 10 μM DCFH-DA. After incubation at 37 °C for 60 min, fluorescence was measured by a Multiskan spectrum microplate spectrophotometer (PerkinElmer, USA).
The cell concentration was measured in dry cell weight (DCW) following the previous protocol . Concentrations of glucose, ethanol, and glycerol were analyzed by Aminex HPX-87H column (300 × 7.8 mm; Bio-Rad, Hercules) in HPLC system, which used 0.01 mol/L H2SO4 as the mobile phase and was eluted at 50 °C with a flow rate of 0.5 mL/min. All analyses in this study were done in duplicate except indicated, and the mean values are shown in the Results and discussion section.
reactive oxygen species
differentially expressed genes
oxidoreduction potential (mV)
a mixture of formic acid, acetic acid and furfural inhibitors
a mixture of formic acid, acetic acid, furfural, and 5-HMF inhibitors
synthetic complete medium
SC medium without histidine
dry cell weight (g/L)
JQG designed the research, performed most of the experiments, collected data, and prepared the manuscript. WJY conceived the concept and design of the experiment. HLF, SBH, and YML carried out microbiological sampling study and conducted part of the analyses. SJZ and FWB participated in the design of the experiment. The manuscript was written with the contributions of all the authors. All authors read and approved the final manuscript.
All authors declare that they have no competing interests.
Availability of data and materials
All data generated or analyzed during this study are included in the published article.
This study was supported by projects of International Cooperation and Exchanges NSFC (51561145014), the China Postdoctoral Science Foundation (2015M571316), and the National Key Laboratory project of Microbial Metabolism (MMLKF16-04).
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