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由于odhA缺失导致的代谢通量改变致使谷氨酸棒杆菌中L-谷氨酸过量产生。

Altered metabolic flux due to deletion of odhA causes L-glutamate overproduction in Corynebacterium glutamicum.

作者信息

Asakura Yoko, Kimura Eiichiro, Usuda Yoshihiro, Kawahara Yoshio, Matsui Kazuhiko, Osumi Tsuyoshi, Nakamatsu Tsuyoshi

机构信息

Ajinomoto Co., Inc., Kawasaki, Kanagawa 210-8681, Japan.

出版信息

Appl Environ Microbiol. 2007 Feb;73(4):1308-19. doi: 10.1128/AEM.01867-06. Epub 2006 Dec 8.

Abstract

L-glutamate overproduction in Corynebacterium glutamicum, a biotin auxotroph, is induced by biotin limitation or by treatment with certain fatty acid ester surfactants or with penicillin. We have analyzed the relationship between the inductions, 2-oxoglutarate dehydrogenase complex (ODHC) activity, and L-glutamate production. Here we show that a strain deleted for odhA and completely lacking ODHC activity produces L-glutamate as efficiently as the induced wild type (27.8 mmol/g [dry weight] of cells for the ohdA deletion strain compared with only 1.0 mmol/g [dry weight] of cells for the uninduced wild type). This level of production is achieved without any induction or alteration in the fatty acid composition of the cells, showing that L-glutamate overproduction can be caused by the change in metabolic flux alone. Interestingly, the L-glutamate productivity of the odhA-deleted strain is increased about 10% by each of the L-glutamate-producing inductions, showing that the change in metabolic flux resulting from the odhA deletion and the inductions have additive effects on L-glutamate overproduction. Tween 40 was indicated to induce drastic metabolic change leading to L-glutamate overproduction in the odhA-deleted strain. Furthermore, optimizing the metabolic flux from 2-oxoglutarate to L-glutamate by tuning glutamate dehydrogenase activity increased the l-glutamate production of the odhA-deleted strain.

摘要

谷氨酸棒杆菌是一种生物素营养缺陷型细菌,其L-谷氨酸过量生产可由生物素限制、用某些脂肪酸酯表面活性剂或青霉素处理诱导产生。我们分析了这些诱导因素、2-氧代戊二酸脱氢酶复合体(ODHC)活性与L-谷氨酸生产之间的关系。在此我们表明,odhA基因缺失且完全缺乏ODHC活性的菌株产生L-谷氨酸的效率与诱导后的野生型一样高(odhA基因缺失菌株每克[干重]细胞可产生27.8 mmol的L-谷氨酸,而未诱导的野生型每克[干重]细胞仅产生1.0 mmol)。这种生产水平的实现无需对细胞脂肪酸组成进行任何诱导或改变,这表明L-谷氨酸过量生产可能仅由代谢通量的变化引起。有趣的是,odhA基因缺失菌株的L-谷氨酸生产力在每次L-谷氨酸生产诱导下提高约10%,这表明odhA基因缺失和诱导所导致的代谢通量变化对L-谷氨酸过量生产具有累加效应。已表明吐温40可诱导odhA基因缺失菌株发生剧烈的代谢变化,从而导致L-谷氨酸过量生产。此外,通过调节谷氨酸脱氢酶活性来优化从2-氧代戊二酸到L-谷氨酸的代谢通量,可提高odhA基因缺失菌株的L-谷氨酸产量。

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