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异柠檬酸裂合酶的失活导致恶臭假单胞菌中链长度聚(3-羟基链烷酸酯)产量增加。

Inactivation of isocitrate lyase leads to increased production of medium-chain-length poly(3-hydroxyalkanoates) in Pseudomonas putida.

作者信息

Klinke S, Dauner M, Scott G, Kessler B, Witholt B

机构信息

Institute of Biotechnology, Swiss Federal Institute of Technology Zurich, CH-8093 Zurich, Switzerland.

出版信息

Appl Environ Microbiol. 2000 Mar;66(3):909-13. doi: 10.1128/AEM.66.3.909-913.2000.

Abstract

Medium-chain-length (mcl) poly(3-hydroxyalkanoates) (PHAs) are storage polymers that are produced from various substrates and accumulate in Pseudomonas strains belonging to rRNA homology group I. In experiments aimed at increasing PHA production in Pseudomonas strains, we generated an mcl PHA-overproducing mutant of Pseudomonas putida KT2442 by transposon mutagenesis, in which the aceA gene was knocked out. This mutation inactivated the glyoxylate shunt and reduced the in vitro activity of isocitrate dehydrogenase, a rate-limiting enzyme of the citric acid cycle. The genotype of the mutant was confirmed by DNA sequencing, and the phenotype was confirmed by biochemical experiments. The aceA mutant was not able to grow on acetate as a sole carbon source due to disruption of the glyoxylate bypass and exhibited two- to fivefold lower isocitrate dehydrogenase activity than the wild type. During growth on gluconate, the difference between the mean PHA accumulation in the mutant and the mean PHA accumulation in the wild-type strain was 52%, which resulted in a significant increase in the amount of mcl PHA at the end of the exponential phase in the mutant P. putida KT217. On the basis of a stoichiometric flux analysis we predicted that knockout of the glyoxylate pathway in addition to reduced flux through isocitrate dehydrogenase should lead to increased flux into the fatty acid synthesis pathway. Therefore, enhanced carbon flow towards the fatty acid synthesis pathway increased the amount of mcl PHA that could be accumulated by the mutant.

摘要

中链长度(mcl)的聚(3-羟基脂肪酸酯)(PHA)是由多种底物产生的储存聚合物,并积累在属于rRNA同源组I的假单胞菌菌株中。在旨在提高假单胞菌菌株中PHA产量的实验中,我们通过转座子诱变产生了恶臭假单胞菌KT2442的mcl PHA高产突变体,其中aceA基因被敲除。这种突变使乙醛酸循环失活,并降低了柠檬酸循环的限速酶异柠檬酸脱氢酶的体外活性。通过DNA测序确认了突变体的基因型,并通过生化实验确认了其表型。由于乙醛酸旁路的破坏,aceA突变体不能以乙酸盐作为唯一碳源生长,并且其异柠檬酸脱氢酶活性比野生型低两到五倍。在以葡萄糖酸盐为碳源生长期间,突变体中PHA的平均积累量与野生型菌株中PHA的平均积累量之间的差异为52%,这导致在突变体恶臭假单胞菌KT217的指数期末mcl PHA的量显著增加。基于化学计量通量分析,我们预测除了通过异柠檬酸脱氢酶的通量降低之外,乙醛酸途径的敲除应该导致进入脂肪酸合成途径的通量增加。因此,增强的碳流向脂肪酸合成途径增加了突变体能够积累的mcl PHA的量。

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