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对一株对铜敏感的恶臭假单胞菌菌株中copABCD操纵子的表征

Characterization of copABCD operon from a copper-sensitive Pseudomonas putida strain.

作者信息

Adaikkalam Vellaichamy, Swarup Sanjay

机构信息

Department of Biological Sciences, National University of Singapore, Singapore.

出版信息

Can J Microbiol. 2005 Mar;51(3):209-16. doi: 10.1139/w04-135.

Abstract

We describe an operon, copABCD, that encodes copper-binding and sequestering proteins for copper homeostasis in the copper-sensitive strain Pseudomonas putida PNL-MK25. This is the second operon characterized as being involved in copper homeostasis, in addition to a P1-type ATPase encoded by cueAR, which was previously shown to be active in the same strain. In this study, 3 copper-responsive mutants were obtained through mini-Tn5::gfp mutagenesis and were found to exhibit reduced tolerance to copper. Sequencing analysis of the transposon-tagged region in the 3 mutants revealed insertions in 2 genes of an operon homologous to the copABCD of P. syringae and pcoABCD of Escherichia coli. Gene expression studies demonstrated that the P. putida copABCD is inducible starting from 3 micromol/L copper levels. Copper-sensitivity studies revealed that the tolerance of the mutant strains was reduced only marginally (only 0.16-fold) in comparison to a 6-fold reduced tolerance of the cueAR mutant. Thus, the cop operon in this strain has a minimal role when compared with its role both in other copper-resistant strains, such as P. syringae pv. syringae, and in the cueAR operon of the same strain. We propose that the reduced function of the copABCD operon is likely to be due to the presence of fewer metal-binding domains in the encoded proteins.

摘要

我们描述了一个操纵子copABCD,它编码铜结合和螯合蛋白,用于在对铜敏感的恶臭假单胞菌PNL-MK25中维持铜稳态。这是第二个被鉴定参与铜稳态的操纵子,除了之前显示在同一菌株中具有活性的由cueAR编码的P1型ATP酶。在本研究中,通过mini-Tn5::gfp诱变获得了3个铜响应突变体,发现它们对铜的耐受性降低。对这3个突变体中转座子标签区域的测序分析显示,在一个与丁香假单胞菌的copABCD和大肠杆菌的pcoABCD同源的操纵子的2个基因中存在插入。基因表达研究表明,恶臭假单胞菌的copABCD从3微摩尔/升的铜水平开始可诱导表达。铜敏感性研究表明,与cueAR突变体6倍的耐受性降低相比,突变菌株的耐受性仅略有降低(仅0.16倍)。因此,与它在其他抗铜菌株(如丁香假单胞菌丁香致病变种)以及同一菌株的cueAR操纵子中的作用相比,该菌株中的cop操纵子作用最小。我们认为,copABCD操纵子功能降低可能是由于其编码蛋白中金属结合结构域较少。

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