In silico analysis of bioethanol overproduction by genetically modified microorganisms in coculture fermentation.

Biotechnology Research International Pub Date : 2015-01-01 Epub Date: 2015-02-16 DOI:10.1155/2015/238082
Lisha K Parambil, Debasis Sarkar
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引用次数: 11

Abstract

Lignocellulosic biomass is an attractive sustainable carbon source for fermentative production of bioethanol. In this context, use of microbial consortia consisting of substrate-selective microbes is advantageous as it eliminates the negative impacts of glucose catabolite repression. In this study, a detailed in silico analysis of bioethanol production from glucose-xylose mixtures of various compositions by coculture fermentation of xylose-selective Escherichia coli strain ZSC113 and glucose-selective wild-type Saccharomyces cerevisiae is presented. Dynamic flux balance models based on available genome-scale metabolic networks of the microorganisms have been used to analyze bioethanol production and the maximization of ethanol productivity is addressed by computing optimal aerobic-anaerobic switching times. A set of genetic engineering strategies for ethanol overproduction by E. coli strain ZSC113 have been evaluated for their efficiency in the context of batch coculture process. Finally, simulations are carried out to determine the pairs of genetically modified E. coli strain ZSC113 and S. cerevisiae that significantly enhance ethanol productivity in batch coculture fermentation.

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共培养发酵中转基因微生物生物乙醇生产过剩的计算机分析。
木质纤维素生物质是发酵生产生物乙醇的一种有吸引力的可持续碳源。在这种情况下,使用由底物选择性微生物组成的微生物联合体是有利的,因为它消除了葡萄糖分解代谢抑制的负面影响。在这项研究中,详细分析了由不同组成的葡萄糖-木糖混合物通过木糖选择性大肠杆菌菌株ZSC113和葡萄糖选择性野生型酿酒酵母共培养发酵生产生物乙醇。基于微生物基因组尺度代谢网络的动态通量平衡模型已被用于分析生物乙醇的生产,并通过计算最佳的好氧-厌氧切换时间来实现乙醇产量的最大化。在批量共培养过程中,对大肠杆菌菌株ZSC113乙醇过量生产的一系列基因工程策略进行了评估。最后,进行了模拟实验,确定了在分批共培养发酵中显著提高乙醇产量的转基因大肠杆菌菌株ZSC113和酿酒酵母菌株对。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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