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铜绿假单胞菌中异柠檬酸裂解酶的功能与转录调控

Function and transcriptional regulation of the isocitrate lyase in Pseudomonas aeruginosa.

作者信息

Kretzschmar Utta, Khodaverdi Viola, Jeoung Jae-Hun, Görisch Helmut

机构信息

Fachgebiet Technische Biochemie, Institut für Biotechnologie, Technische Universität Berlin, Seestr. 13, 13353 Berlin, Germany.

出版信息

Arch Microbiol. 2008 Aug;190(2):151-8. doi: 10.1007/s00203-008-0381-7. Epub 2008 Jun 24.

Abstract

Pseudomonas aeruginosa ATCC 17933 is capable of growing aerobically on ethanol as sole source of carbon and energy. This requires the glyoxylate cycle for replenishing C4-compounds to the TCA cycle. The enzyme isocitrate lyase (ICL) catalyzes the first step of this glyoxylate shunt. Its activity was induced more than 10-fold in response to the carbon sources ethanol or acetate instead of glucose or succinate. We could prove that in P. aeruginosa ICL is essential for aerobic as well as anaerobic utilization of C2-sources. Transcriptional regulation of icl gene (aceA) expression was monitored on different carbon sources by using an aceA-lacZ gene fusion. A strong correlation between promoter and ICL activity indicated regulation at the transcriptional level. But ICL was not simply induced by the mere presence of ethanol in the growth medium as was demonstrated by cultivation on mixed substrates. P. aeruginosa showed diauxic growth on media containing ethanol-succinate or ethanol-glucose mixtures and did not transcribe the aceA gene to metabolize ethanol until succinate or glucose, respectively, were exhausted. Inactivation of the chromosomal aceA gene in P. aeruginosa led to an inability to grow on ethanol and acetate. Promoter activity studies showed that all genes necessary to oxidize ethanol were downregulated in the ICL-negative mutant. But on mixed substrates like ethanol-succinate or ethanol-glucose the mutant exhibited growth and utilized ethanol as well, probably as energy source only.

摘要

铜绿假单胞菌ATCC 17933能够在以乙醇作为唯一碳源和能源的条件下进行有氧生长。这需要乙醛酸循环来为三羧酸循环补充C4化合物。异柠檬酸裂解酶(ICL)催化乙醛酸支路的第一步反应。与葡萄糖或琥珀酸相比,其活性在乙醇或乙酸盐作为碳源时被诱导提高了10倍以上。我们能够证明,在铜绿假单胞菌中,ICL对于C2源的有氧和无氧利用都是必不可少的。通过使用aceA - lacZ基因融合体,监测了不同碳源上icl基因(aceA)表达的转录调控。启动子与ICL活性之间的强相关性表明存在转录水平的调控。但正如在混合底物上培养所证明的那样,ICL并非仅仅由生长培养基中乙醇的存在而简单诱导。铜绿假单胞菌在含有乙醇 - 琥珀酸或乙醇 - 葡萄糖混合物的培养基上呈现双相生长,并且在琥珀酸或葡萄糖分别耗尽之前不会转录aceA基因来代谢乙醇。铜绿假单胞菌染色体上aceA基因的失活导致其无法在乙醇和乙酸盐上生长。启动子活性研究表明,在ICL阴性突变体中,氧化乙醇所需的所有基因均被下调。但在乙醇 - 琥珀酸或乙醇 - 葡萄糖等混合底物上,该突变体仍能生长并利用乙醇,可能仅将其作为能源。

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