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恶臭假单胞菌全局调控蛋白Crc的水平和活性会根据生长条件而变化。

Levels and activity of the Pseudomonas putida global regulatory protein Crc vary according to growth conditions.

作者信息

Ruiz-Manzano Ana, Yuste Luis, Rojo Fernando

机构信息

Departamento de Biotecnología, Centro Nacional de Biotecnología, CSIC, Campus de la Universidad Autónoma de Madrid, Cantoblanco, 28049 Madrid, Spain.

出版信息

J Bacteriol. 2005 Jun;187(11):3678-86. doi: 10.1128/JB.187.11.3678-3686.2005.

Abstract

The global regulatory protein Crc is involved in the repression of several catabolic pathways for sugars, hydrocarbons, and nitrogenated and aromatic compounds in Pseudomonas putida and Pseudomonas aeruginosa when other preferred carbon sources are present in the culture medium (catabolite repression), therefore modulating carbon metabolism. We have analyzed whether the levels or the activity of Crc is regulated. Crc activity was followed by its ability to inhibit the induction by alkanes of the P. putida OCT plasmid alkane degradation pathway when cells grow in a complete medium, where the effect of Crc is very strong. The abundance of crc transcripts and the amounts of Crc protein were higher under repressing conditions than under nonrepressing conditions. The presence of crc on a high-copy-number plasmid considerably increased Crc levels, but this impaired its ability to inhibit the alkane degradation pathway. Crc shows similarity to a family of nucleases that have highly conserved residues at their catalytic sites. Mutation of the corresponding residues in Crc (Asp220 and His246) led to proteins that can inhibit induction of the alkane degradation pathway when present at normal or elevated levels in the cell. Repression by these mutant proteins occurred only under repressing conditions. These results suggest that both the amounts and the activity of Crc are modulated and support previous proposals that Crc may form part of a signal transduction pathway. Furthermore, the activity of the mutant proteins suggests that Crc is not a nuclease.

摘要

全局调控蛋白Crc参与恶臭假单胞菌和铜绿假单胞菌中糖、碳氢化合物以及含氮和芳香族化合物的几种分解代谢途径的抑制,当培养基中存在其他更优碳源时(分解代谢物阻遏),从而调节碳代谢。我们分析了Crc的水平或活性是否受到调控。当细胞在完全培养基中生长时,通过其抑制恶臭假单胞菌OCT质粒烷烃降解途径被烷烃诱导的能力来跟踪Crc活性,在完全培养基中Crc的作用非常强。在阻遏条件下,crc转录本的丰度和Crc蛋白的量高于非阻遏条件。crc存在于高拷贝数质粒上会显著增加Crc水平,但这会损害其抑制烷烃降解途径的能力。Crc与一类在催化位点具有高度保守残基的核酸酶家族相似。Crc中相应残基(Asp220和His246)的突变导致蛋白质在细胞中以正常或升高水平存在时能够抑制烷烃降解途径的诱导。这些突变蛋白的阻遏作用仅在阻遏条件下发生。这些结果表明Crc的量和活性都受到调节,并支持先前的观点,即Crc可能是信号转导途径的一部分。此外,突变蛋白的活性表明Crc不是核酸酶。

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