Global gene expression analysis of glucose overflow metabolism in Escherichia coli and reduction of aerobic acetate formation

被引:90
|
作者
Veit, Andrea
Polen, Tino
Wendisch, Volker F.
机构
[1] Univ Munster, Inst Mol Microbiol & Biotechnol, D-48149 Munster, Germany
[2] Res Ctr Juelich, Inst Biotechnol 1, D-52428 Julich, Germany
关键词
Escherichia coli MG1655; aerobic acetate formation; overflow metabolism; TCA cycle; DNA microarray; chemostat cultivation; global gene expression analysis; acetate switch;
D O I
10.1007/s00253-006-0680-3
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
During aerobic growth on glucose, Escherichia coli produces acetate in the so-called overflow metabolism. DNA microarray analysis was used to determine the global gene expression patterns of chemostat cultivations of E. coli MG1655 that were characterized by different acetate formation rates during aerobic growth on glucose. A correlation analysis identified that expression of ten genes (sdhCDAB, sucB, sucC, acnB, lpdA, fumC and mdh) encoding the TCA cycle enzymes succinate dehydrogenase, alpha-ketoglutarate dehydrogenase, succinyl-CoA synthetase, aconitase, fumarase and malate dehydrogenase, respectively, and of the acs-yjcH-actP operon for acetate utilization correlated negatively with acetate formation. Relieving transcriptional control of the sdhCDAB-b0725-sucABCD operon by chromosomal promoter exchange mutagenesis yielded a strain with increased specific activities of the TCA cycle enzymes succinate dehydrogenase, alpha-ketoglutarate dehydrogenase and succinyl-CoA synthetase, which are encoded by this operon. The resulting strain produced less acetate and directed more carbon towards carbon dioxide formation than the parent strain MG1655 while maintaining high growth and glucose consumption rates.
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页码:406 / 421
页数:16
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