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本文引用的文献

1
The Pseudomonas putida Crc global regulator controls the expression of genes from several chromosomal catabolic pathways for aromatic compounds.恶臭假单胞菌Crc全局调控因子控制来自几个染色体芳香族化合物分解代谢途径的基因表达。
J Bacteriol. 2004 Mar;186(5):1337-44. doi: 10.1128/JB.186.5.1337-1344.2004.
2
The HWE histidine kinases, a new family of bacterial two-component sensor kinases with potentially diverse roles in environmental signaling.HWE组氨酸激酶,一类新型细菌双组分传感激酶,在环境信号传导中可能具有多种作用。
J Bacteriol. 2004 Jan;186(2):445-53. doi: 10.1128/JB.186.2.445-453.2004.
3
Integrated regulation in response to aromatic compounds: from signal sensing to attractive behaviour.对芳香化合物响应的综合调控:从信号感知到吸引行为。
Environ Microbiol. 2003 Dec;5(12):1226-41. doi: 10.1111/j.1462-2920.2003.00472.x.
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The growth of micro-organisms in relation to their energy supply.微生物生长与其能量供应的关系。
J Gen Microbiol. 1960 Dec;23:457-69. doi: 10.1099/00221287-23-3-457.
5
Expression of the Pseudomonas putida OCT plasmid alkane degradation pathway is modulated by two different global control signals: evidence from continuous cultures.恶臭假单胞菌OCT质粒烷烃降解途径的表达受两种不同的全局控制信号调节:来自连续培养的证据。
J Bacteriol. 2003 Aug;185(16):4772-8. doi: 10.1128/JB.185.16.4772-4778.2003.
6
Genomic analysis of the aromatic catabolic pathways from Pseudomonas putida KT2440.恶臭假单胞菌KT2440芳香族化合物分解代谢途径的基因组分析。
Environ Microbiol. 2002 Dec;4(12):824-41. doi: 10.1046/j.1462-2920.2002.00370.x.
7
Inactivation of cytochrome o ubiquinol oxidase relieves catabolic repression of the Pseudomonas putida GPo1 alkane degradation pathway.细胞色素 o 泛醇氧化酶的失活可解除恶臭假单胞菌 GPo1 烷烃降解途径的分解代谢阻遏。
J Bacteriol. 2002 Jul;184(14):3785-93. doi: 10.1128/JB.184.14.3785-3793.2002.
8
Integration of global regulation of two aromatic-responsive sigma(54)-dependent systems: a common phenotype by different mechanisms.两个芳香族响应σ⁵⁴依赖系统的全局调控整合:不同机制导致的共同表型。
J Bacteriol. 2002 Feb;184(3):760-70. doi: 10.1128/JB.184.3.760-770.2002.
9
The Pfam protein families database.Pfam蛋白质家族数据库。
Nucleic Acids Res. 2002 Jan 1;30(1):276-80. doi: 10.1093/nar/30.1.276.
10
In vivo UV laser footprinting of the Pseudomonas putidasigma 54Pu promoter reveals that integration host factor couples transcriptional activity to growth phase.恶臭假单胞菌54Pu启动子的体内紫外激光足迹法表明,整合宿主因子将转录活性与生长阶段联系起来。
J Biol Chem. 2002 Jan 18;277(3):2169-75. doi: 10.1074/jbc.M108162200. Epub 2001 Nov 1.

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.

DOI:10.1128/JB.187.11.3678-3686.2005
PMID:15901690
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1112034/
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。