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枯草芽孢杆菌CGMCC 0833中不同添加剂存在下聚γ-谷氨酸生物合成的改善及代谢通量的重新分布

Improvement of poly(gamma-glutamic acid) biosynthesis and redistribution of metabolic flux with the presence of different additives in Bacillus subtilis CGMCC 0833.

作者信息

Wu Qun, Xu Hong, Shi Ningning, Yao Jun, Li Sha, Ouyang Pingkai

机构信息

College of Life Science and Pharmacy, Nanjing University of Technology, Nanjing, China.

出版信息

Appl Microbiol Biotechnol. 2008 Jun;79(4):527-35. doi: 10.1007/s00253-008-1462-x. Epub 2008 Apr 29.

DOI:10.1007/s00253-008-1462-x
PMID:18443783
Abstract

Tween-80, dimethyl sulfoxide (DMSO), and glycerol could be used as novel materials to regulate the central carbon metabolic pathway and improve gamma-PGA biosynthesis by Bacillus subtilis CGMCC 0833. With glycerol in the medium, the activity of 2-oxoglutarate dehydrogenase complex at the key node of 2-oxoglutarate was depressed, more carbon flux distribution was directed to synthesize glutamate, the substrate of gamma-PGA, which led to overproducing of gamma-PGA, reached 31.7 g/l, compared to the original value of 26.7 g/l. When Tween-80 or DMSO was in the medium, the activity of isocitrate dehydrogenase was stimulated, the branch flux from 2-oxoglutarate to glutamate was also enhanced due to the increasing of total flux from iso-citrate to 2-oxoglutarate, then a large amount of glutamate was produced, and formation of gamma-PGA was also improved, which was a different process compared with that of glycerol. Moreover, with the addition of Tween-80 or DMSO, cell membrane permeability was increased, which facilitated the uptake of extracellular substrates and the secretion of gamma-PGA by this strain; therefore, gamma-PGA production was further stimulated, and 34.4 and 32.7 g/l gamma-PGA were obtained, respectively. This work firstly employed additives to improve the biosynthesis of gamma-PGA and would be helpful in understanding the biosynthesis mechanism of gamma-PGA by Bacillus species deeply.

摘要

吐温80、二甲基亚砜(DMSO)和甘油可作为新型材料,用于调节中心碳代谢途径并提高枯草芽孢杆菌CGMCC 0833的γ-聚谷氨酸生物合成。培养基中添加甘油时,2-酮戊二酸关键节点处的2-酮戊二酸脱氢酶复合体活性受到抑制,更多的碳通量分布导向合成γ-聚谷氨酸的底物谷氨酸,从而导致γ-聚谷氨酸过量生产,达到31.7 g/L,相比原来的26.7 g/L有所提高。当培养基中存在吐温80或DMSO时,异柠檬酸脱氢酶的活性受到刺激,由于从异柠檬酸到2-酮戊二酸的总通量增加,从2-酮戊二酸到谷氨酸的分支通量也增强,进而产生大量谷氨酸,γ-聚谷氨酸的形成也得到改善,这与甘油的情况是不同的过程。此外,添加吐温80或DMSO后,细胞膜通透性增加,这促进了该菌株对细胞外底物的摄取以及γ-聚谷氨酸的分泌;因此,γ-聚谷氨酸的产量进一步提高,分别获得了34.4 g/L和32.7 g/L的γ-聚谷氨酸。这项工作首次采用添加剂来改善γ-聚谷氨酸的生物合成,将有助于深入理解芽孢杆菌属合成γ-聚谷氨酸的生物合成机制。

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