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谷氨酸棒杆菌中L-赖氨酸生产的代谢通量工程——葡萄糖-6-磷酸脱氢酶的过表达与修饰

Metabolic flux engineering of L-lysine production in Corynebacterium glutamicum--over expression and modification of G6P dehydrogenase.

作者信息

Becker Judith, Klopprogge Corinna, Herold Andrea, Zelder Oskar, Bolten Christoph J, Wittmann Christoph

机构信息

Biochemical Engineering, Saarland University, Im Stadtwald, 66123 Saarbrücken, Germany.

出版信息

J Biotechnol. 2007 Oct 31;132(2):99-109. doi: 10.1016/j.jbiotec.2007.05.026. Epub 2007 Jun 6.

Abstract

In the present work, metabolic flux engineering of Corynebacterium glutamicum was carried out to increase lysine production. The strategy focused on engineering of the pentose phosphate pathway (PPP) flux by different genetic modifications. Over expression of the zwf gene, encoding G6P dehydrogenase, in the feedback-deregulated lysine-producing strain C. glutamicum ATCC 13032 lysC(fbr) resulted in increased lysine production on different carbon sources including the two major industrial sugars, glucose and sucrose. The additional introduction of the A243T mutation into the zwf gene and the over expression of fructose 1,6-bisphosphatase resulted in a further successive improvement of lysine production. Hereby the point mutation resulted in higher affinity of G6P dehydrogenase towards NADP and reduced sensitivity against inhibition by ATP, PEP and FBP. Overall, the lysine yield increased up to 70% through the combination of the different genetic modifications. Through strain engineering formation of trehalose was reduced by up to 70% due to reduced availability of its precursor G6P. Metabolic flux analysis revealed a 15% increase of PPP flux in response to over expression of the zwf gene. Overall a strong apparent NADPH excess resulted. Redox balancing indicated that this excess is completely oxidized by malic enzyme.

摘要

在本研究中,对谷氨酸棒杆菌进行了代谢通量工程改造以提高赖氨酸产量。该策略聚焦于通过不同的基因修饰来改造磷酸戊糖途径(PPP)通量。在反馈解除调控的产赖氨酸菌株谷氨酸棒杆菌ATCC 13032 lysC(fbr)中过表达编码葡萄糖-6-磷酸脱氢酶的zwf基因,导致在包括两种主要工业糖葡萄糖和蔗糖在内的不同碳源上赖氨酸产量增加。在zwf基因中额外引入A243T突变并过表达果糖-1,6-二磷酸酶,导致赖氨酸产量进一步连续提高。由此,点突变导致葡萄糖-6-磷酸脱氢酶对NADP的亲和力更高,并降低了对ATP、PEP和FBP抑制的敏感性。总体而言,通过不同基因修饰的组合,赖氨酸产量提高了70%。通过菌株工程,由于海藻糖前体葡萄糖-6-磷酸的可用性降低,海藻糖的形成减少了70%。代谢通量分析表明,响应zwf基因的过表达,PPP通量增加了15%。总体上产生了强烈的明显NADPH过量。氧化还原平衡表明,这种过量被苹果酸酶完全氧化。

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