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谷氨酸棒杆菌L-赖氨酸生物合成的琥珀酰化分支中最后两个未知基因dapC和dapF的鉴定与表征。

Identification and characterization of the last two unknown genes, dapC and dapF, in the succinylase branch of the L-lysine biosynthesis of Corynebacterium glutamicum.

作者信息

Hartmann Michael, Tauch Andreas, Eggeling Lothar, Bathe Brigitte, Möckel Bettina, Pühler Alfred, Kalinowski Jörn

机构信息

Lehrstuhl für Genetik, Universität Bielefeld, Universitätsstrasse 25, D-33615 Bielefeld, Germany.

出版信息

J Biotechnol. 2003 Sep 4;104(1-3):199-211. doi: 10.1016/s0168-1656(03)00156-1.

Abstract

The inspection of the complete genome sequence of Corynebacterium glutamicum ATCC 13032 led to the identification of dapC and dapF, the last two unknown genes of the succinylase branch of the L-lysine biosynthesis. The deduced DapF protein of C. glutamicum is characterized by a two-domain structure and a conserved diaminopimelate (DAP) epimerase signature. Overexpression of dapF resulted in an 8-fold increase of the specific epimerase activity. A defined deletion in the dapF gene led to a reduced growth of C. glutamicum in a medium with excess carbon but limited ammonium availability. The predicted DapC protein of C. glutamicum shared 29% identical amino acids with DapC from Bordetella pertussis, the only enzymatically characterized N-succinyl-aminoketopimelate aminotransferase. Overexpression of the dapC gene in C. glutamicum resulted in a 9-fold increase of the specific aminotransferase activity. A C. glutamicum mutant with deleted dapC showed normal growth characteristics with excess carbon and limited ammonium. Even a mutation of the two genes dapC and ddh, interrupting both branches of the split pathway, could be established in C. glutamicum. Overexpression of the dapF or the dapC gene in an industrial C. glutamicum strain resulted in an increased L-lysine production, indicating that both genes might be relevant targets for the development of improved production strains.

摘要

对谷氨酸棒杆菌ATCC 13032全基因组序列的检测,鉴定出了dapC和dapF,它们是L-赖氨酸生物合成琥珀酰化分支中最后两个未知基因。谷氨酸棒杆菌推导的DapF蛋白具有双结构域结构和保守的二氨基庚二酸(DAP)差向异构酶特征。dapF的过表达导致比差向异构酶活性提高了8倍。dapF基因的特定缺失导致谷氨酸棒杆菌在碳过量但铵供应有限的培养基中生长减缓。谷氨酸棒杆菌预测的DapC蛋白与百日咳博德特氏菌的DapC有29%的相同氨基酸,后者是唯一经酶学鉴定的N-琥珀酰氨基酮戊二酸氨基转移酶。谷氨酸棒杆菌中dapC基因的过表达导致比氨基转移酶活性提高了9倍。缺失dapC的谷氨酸棒杆菌突变体在碳过量和铵有限的情况下表现出正常的生长特性。甚至在谷氨酸棒杆菌中可以构建同时缺失dapC和ddh这两个基因的突变体,从而中断分支途径的两个分支。在一株工业谷氨酸棒杆菌菌株中过表达dapF或dapC基因,导致L-赖氨酸产量增加,这表明这两个基因可能都是改良生产菌株开发的相关靶点。

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