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缺失大肠杆菌中的 yghZ 可促进以木糖为碳源在糠醛存在下的生长。

Deletion of yghZ in Escherichia coli promotes growth in presence of furfural with xylose as carbon source.

机构信息

Institute of Biotechnology, Amity University, Manesar, Haryana 122413, India.

Microbial Engineering Group, International Center for Genetic Engineering and Biotechnology, New Delhi 110067, India.

出版信息

FEMS Microbiol Lett. 2024 Jan 9;371. doi: 10.1093/femsle/fnae028.

DOI:10.1093/femsle/fnae028
PMID:38664064
Abstract

Thermo-acidic pretreatment of lignocellulosic biomass is required to make it amenable to microbial metabolism and results in generation of furfural due to breakdown of pentose sugars. Furfural is toxic to microbial metabolism and results in reduced microbial productivity and increased production costs. This study asks if deletion of yghZ gene which encodes a NADPH-dependent aldehyde reductase enzyme results in improved furfural tolerance in Escherichia coli host. The ∆yghZ strain-SSK201-was tested for tolerance to furfural in presence of 5% xylose as a carbon source in AM1 minimal medium. At 96 h and in presence of 1.0 g/L furfural, the culture harboring strain SSK201 displayed 4.5-fold higher biomass, 2-fold lower furfural concentration and 15.75-fold higher specific growth rate (µ) as compared to the parent strain SSK42. The furfural tolerance advantage of SSK201 was retained when the carbon source was switched to glucose in AM1 medium and was lost in rich LB medium. The findings have potential to be scaled up to a hydrolysate culture medium, which contains furan inhibitors and lack nutritionally rich components, under bioreactor cultivation and observe growth advantage of the ∆yghZ host. It harbors potential to generate robust industrial strains which can convert lignocellulosic carbon into metabolites of interest in a cost-efficient manner.

摘要

木质纤维素生物质的热酸预处理使其易于微生物代谢,并由于戊糖的分解而产生糠醛。糠醛对微生物代谢有毒,导致微生物生产力降低和生产成本增加。本研究探讨了缺失编码 NADPH 依赖型醛还原酶的 yghZ 基因是否会导致大肠杆菌宿主对糠醛的耐受性提高。在 AM1 最小培养基中以 5%木糖作为碳源时,测试了缺失 yghZ 基因的 ∆yghZ 菌株-SSK201 对糠醛的耐受性。在 96 小时和 1.0 g/L 糠醛存在的情况下,与亲本菌株 SSK42 相比,携带菌株 SSK201 的培养物显示出 4.5 倍更高的生物量、2 倍更低的糠醛浓度和 15.75 倍更高的比生长速率(µ)。当碳源在 AM1 培养基中切换为葡萄糖时,SSK201 的糠醛耐受性优势得以保留,而在富含 LB 培养基中则丧失。这些发现有可能在生物反应器培养中扩展到水解培养基,该培养基含有呋喃抑制剂且缺乏营养丰富的成分,并观察到 ∆yghZ 宿主的生长优势。它具有产生能够以具有成本效益的方式将木质纤维素碳转化为有价值代谢物的稳健工业菌株的潜力。

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