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在几个缺乏依赖rpoS的代谢途径基因的大肠杆菌突变体中,乙酸代谢和生物量生产发生了改变。

Altered acetate metabolism and biomass production in several Escherichia coli mutants lacking rpoS-dependent metabolic pathway genes.

作者信息

Rahman Mahbuba, Shimizu Kazuyuki

机构信息

Department of Bioscience and Bioinformatics, Faculty of Computer Science and System Engineering, Kyushu Institute of Technology, Iizuka, Fukuoka 820-8502, Japan.

出版信息

Mol Biosyst. 2008 Feb;4(2):160-9. doi: 10.1039/b712023k. Epub 2007 Sep 26.

Abstract

The stress responsive sigma factor RpoS regulates the expression of tktB and talAgenes of the non-oxidative pentose phosphate (PP) pathway, and fumCand acnA genes of the TCA cycle at the stationary phase of growth. In the present study, batch cultivations were performed using tktB, talA, fumC or acnA-knockout mutants of Escherichia coli to observe the metabolic changes at different phases of growth compared to the wild type strain. Although the specific growth rates of the mutants were similar to the wild type, acetate yield was nearly half in all mutants except the acnA mutant. Altered acetate yield in the mutants was also accompanied by variations in the biomass yield. While the biomass yield in both the tktB and talA mutants was increased by 13.8%, biomass was 5.5% and 13.8% lower in the fumC and acnA mutants, respectively. Upregulation of global regulators such as rpoS and soxRS, the acs, aceA, aceB genes, and several TCA cycle genes such as fumC, acnA and sucA, is consistent with higher acetate consumption and biomass yield in the tktB and talA mutants. On the other hand, the fumC and acnA mutants, with their impaired TCA cycles, were unable to utilize acetate for biomass production in spite of the higher expression of rpoS and soxRS.

摘要

应激反应性σ因子RpoS在生长稳定期调节非氧化戊糖磷酸途径(PP途径)的tktB和talA基因以及三羧酸循环(TCA循环)的fumC和acnA基因的表达。在本研究中,使用大肠杆菌的tktB、talA、fumC或acnA基因敲除突变体进行分批培养,以观察与野生型菌株相比在不同生长阶段的代谢变化。尽管突变体的比生长速率与野生型相似,但除acnA突变体外,所有突变体的乙酸产量几乎减半。突变体中乙酸产量的改变还伴随着生物量产量的变化。tktB和talA突变体的生物量产量均增加了13.8%,而fumC和acnA突变体的生物量分别降低了5.5%和13.8%。全局调节因子如rpoS和soxRS、acs、aceA、aceB基因以及几个TCA循环基因如fumC、acnA和sucA的上调,与tktB和talA突变体中更高的乙酸消耗和生物量产量一致。另一方面,fumC和acnA突变体的TCA循环受损,尽管rpoS和soxRS表达较高,但仍无法利用乙酸进行生物量生产。

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