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pecS:一个控制菊欧文氏菌中果胶酶、纤维素酶和蓝色色素产生的基因座。

pecS: a locus controlling pectinase, cellulase and blue pigment production in Erwinia chrysanthemi.

作者信息

Reverchon S, Nasser W, Robert-Baudouy J

机构信息

Laboratoire de Génétique Moléculaire des Microorganismes, CNRS-URA 1486, INSA Bâtiment 406, Villeurbanne, France.

出版信息

Mol Microbiol. 1994 Mar;11(6):1127-39. doi: 10.1111/j.1365-2958.1994.tb00389.x.

Abstract

Erwinia chrysanthemi mutants (designated as pecS) displaying derepressed pectate lyase and cellulase synthesis were isolated. In addition, the pecS mutation is responsible for production of an extracellular insoluble blue pigment whose synthesis is cryptic in the wild-type 3937 strain. Transduction analysis indicates that the phenotype is due to a single mutation located near the xyl marker on the strain 3937 chromosome. This mutation was complemented by an R-prime plasmid carrying the xyl and argG genes of E. chrysanthemi, suggesting that the pecS product acts in trans to modulate pectinase, cellulase and blue pigment production. Insertion mutagenesis of the cloned region and recombination of the corresponding mutations in the bacterial chromosome by marker exchange revealed the existence of two divergently transcribed genes, pecS and pecM, that are both involved in the pectate lyase and cellulase regulation. The nucleotide sequences of pecS and pecM were determined. The pecS gene encodes a 166 amino acid polypeptide that shows similarity to the MprA regulatory protein of Escherichia coli whereas the pecM gene encodes a 297 amino acid polypeptide that was shown to be an integral membrane protein. The possible functions of the PecS and PecM proteins derived from the mutant phenotype and sequence analysis are discussed in terms of signal transduction and transcription regulation.

摘要

分离出了表现出果胶酸裂解酶和纤维素酶合成去阻遏的菊欧文氏菌突变体(命名为pecS)。此外,pecS突变导致产生一种细胞外不溶性蓝色色素,其合成在野生型3937菌株中是隐蔽的。转导分析表明,该表型是由于3937菌株染色体上靠近木糖标记处的一个单一突变所致。该突变被携带菊欧文氏菌木糖和argG基因的R-prime质粒互补,这表明pecS产物以反式作用调节果胶酶、纤维素酶和蓝色色素的产生。对克隆区域进行插入诱变,并通过标记交换在细菌染色体中重组相应突变,揭示了两个反向转录的基因pecS和pecM的存在,它们都参与果胶酸裂解酶和纤维素酶的调控。测定了pecS和pecM的核苷酸序列。pecS基因编码一种166个氨基酸的多肽,与大肠杆菌的MprA调节蛋白相似,而pecM基因编码一种297个氨基酸的多肽,已证明它是一种整合膜蛋白。根据信号转导和转录调控讨论了从突变体表型和序列分析得出的PecS和PecM蛋白的可能功能。

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