首页> 外文期刊>Biotechnology for Biofuels >Transcriptional analysis of Clostridium beijerinckii NCIMB 8052 to elucidate role of furfural stress during acetone butanol ethanol fermentation
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Transcriptional analysis of Clostridium beijerinckii NCIMB 8052 to elucidate role of furfural stress during acetone butanol ethanol fermentation

机译:拜氏梭菌NCIMB 8052的转录分析,阐明糠醛胁迫在丙酮丁醇乙醇发酵中的作用

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Background Furfural is the prevalent microbial inhibitor generated during pretreatment and hydrolysis of lignocellulose biomass to monomeric sugars, but the response of acetone butanol ethanol (ABE) producing Clostridium beijerinckii NCIMB 8052 to this compound at the molecular level is unknown. To discern the effect of furfural on C. beijerinckii and to gain insight into molecular mechanisms of action and detoxification, physiological changes of furfural-stressed cultures during acetone butanol ethanol (ABE) fermentation were studied, and differentially expressed genes were profiled by genome-wide transcriptional analysis. Results A total of 5,003 C. beijerinckii NCIMB 8052 genes capturing about 99.7% of the genome were examined. About 111 genes were differentially expressed (up- or down-regulated) by C. beijerinckii when it was challenged with furfural at acidogenic growth phase compared with 721 genes that were differentially expressed (up- or down-regulated) when C. beijerinckii was challenged with furfural at solventogenic growth phase. The differentially expressed genes include genes related to redox and cofactors, membrane transporters, carbohydrate, amino sugar and nucleotide sugar metabolisms, heat shock proteins, DNA repair, and two-component signal transduction system. While C. beijerinckii exposed to furfural stress during the acidogenic growth phase produced 13% more ABE than the unstressed control, ABE production by C. beijerinckii ceased following exposure to furfural stress during the solventogenic growth phase. Conclusion Genome-wide transcriptional response of C. beijerinckii to furfural stress was investigated for the first time using microarray analysis. Stresses emanating from ABE accumulation in the fermentation medium; redox balance perturbations; and repression of genes that code for the phosphotransferase system, cell motility and flagellar proteins (and combinations thereof) may have caused the premature termination of C. beijerinckii 8052 growth and ABE production following furfural challenge at the solventogenic phase.This study provides insights into basis for metabolic engineering of C. beijerinckii NCIMB 8052 for enhanced tolerance of lignocellulose-derived microbial inhibitory compounds, thereby improving bioconversion of lignocellulose biomass hydrolysates to biofuels and chemicals. Indeed, two enzymes encoded by Cbei_3974 and Cbei_3904 belonging to aldo/keto reductase (AKR) and short-chain dehydrogenase/reductase (SDR) families have been identified to be involved in furfural detoxification and tolerance.
机译:背景糠醛是木质纤维素生物质的预处理和水解过程中产生的普遍的微生物抑制剂,但是在分子水平上丙酮丁醇乙醇(ABE)产生拜氏梭菌NCIMB 8052对该化合物的反应尚不清楚。为了辨别糠醛对拜氏梭菌的影响并深入了解作用和解毒的分子机制,研究了丙酮丁醇乙醇(ABE)发酵过程中糠醛胁迫培养物的生理变化,并通过全基因组对差异表达的基因进行了分析。转录分析。结果检查了总共5003个捕获约99.7%基因组的拜氏梭菌NCIMB 8052基因。当在产酸生长期受到糠醛挑战时,约111种基因被拜氏梭菌差异表达(上调或下调),而当挑战挑战拜氏梭菌时,约有721个基因差异表达(上调或下调)。在产溶剂的生长期具有糠醛。差异表达的基因包括与氧化还原和辅助因子,膜转运蛋白,碳水化合物,氨基糖和核苷酸糖代谢,热休克蛋白,DNA修复和两组分信号转导系统有关的基因。尽管在产酸生长阶段暴露于糠醛胁迫下的拜氏梭菌比未受胁迫的对照产生的ABE多13%,但在溶剂生成生长阶段暴露于糠醛胁迫后,拜氏梭菌停止生产ABE。结论使用芯片分析首次研究了拜氏梭菌对糠醛胁迫的全基因组转录应答。源自发酵培养基中ABE积累的压力;氧化还原平衡扰动;和磷酸化编码磷酸转移酶系统,细胞运动性和鞭毛蛋白(及其组合)的基因可能导致溶剂化阶段糠醛攻击后拜氏梭菌8052生长和ABE产生的提前终止。本研究提供了见解NCIMB 8052可以用于C. beijerinckii的代谢工程,以提高对木质纤维素衍生的微生物抑制化合物的耐受性,从而改善木质纤维素生物质水解产物向生物燃料和化学品的生物转化。实际上,已经鉴定出由Cbei_3974和Cbei_3904编码的两种酶,分别属于醛基/酮基还原酶(AKR)和短链脱氢酶/还原酶(SDR)家族,参与糠醛解毒和耐受。

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