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鼠伤寒沙门氏菌、胡萝卜软腐欧文氏菌、铜绿假单胞菌和恶臭假单胞菌lexA基因的核苷酸序列分析与比较。

Nucleotide sequence analysis and comparison of the lexA genes from Salmonella typhimurium, Erwinia carotovora, Pseudomonas aeruginosa and Pseudomonas putida.

作者信息

Garriga X, Calero S, Barbé J

机构信息

Department of Genetics and Microbiology, Autonomous University of Barcelona, Bellaterra, Spain.

出版信息

Mol Gen Genet. 1992 Dec;236(1):125-34. doi: 10.1007/BF00279651.

Abstract

The complete nucleotide sequences of the lexA genes from Salmonella typhimurium, Erwinia carotovora, Pseudomonas aeruginosa and Pseudomonas putida were determined; the DNA sequences of the lexA genes from these bacteria were 86%, 76%, 61% and 59% similar, respectively, to the Escherichia coli K12 gene. The predicted amino acid sequences of the S. typhimurium, E. carotovora and P. putida LexA proteins are 202 residues long whereas that of P. aeruginosa is 204. Two putative LexA repressor binding sites were localized upstream of each of the heterologous genes, the distance between them being 5 bp in S. typhimurium and E. carotovora, as in the lexA gene of E. coli, and 3 bp in P. putida and P. aeruginosa. The first lexA site present in the lexA operator of all five bacteria is very well conserved. However, the second lexA box is considerably more variable. The Ala-84--Gly-85 bond, at which the LexA repressor of E. coli is cleaved during the induction of the SOS response, is also found in the LexA proteins of S. typhimurium and E. carotovora. Likewise, the amino acids Ser-119 and Lys-156 are present in all of these three LexA repressors. These residues also exist in the LexA proteins of P. putida and P. aeruginosa, but they are displaced by 4 and 6 residues, respectively. Furthermore, the structure and sequence of the DNA-binding domain of the LexA repressor of E. coli are highly conserved in the S. typhimurium, E. carotovora, P. aeruginosa and P. putida LexA proteins.

摘要

测定了鼠伤寒沙门氏菌、胡萝卜软腐欧文氏菌、铜绿假单胞菌和恶臭假单胞菌lexA基因的完整核苷酸序列;这些细菌lexA基因的DNA序列与大肠杆菌K12基因的相似性分别为86%、76%、61%和59%。鼠伤寒沙门氏菌、胡萝卜软腐欧文氏菌和恶臭假单胞菌LexA蛋白的预测氨基酸序列长度为202个残基,而铜绿假单胞菌的为204个。在每个异源基因的上游定位了两个假定的LexA阻遏物结合位点,它们之间的距离在鼠伤寒沙门氏菌和胡萝卜软腐欧文氏菌中为5 bp,与大肠杆菌lexA基因中的情况相同,在恶臭假单胞菌和铜绿假单胞菌中为3 bp。所有五种细菌的lexA操纵子中存在的第一个lexA位点非常保守。然而,第二个lexA框的变异性要大得多。在SOS反应诱导过程中大肠杆菌LexA阻遏物被切割的Ala-84--Gly-85键,也存在于鼠伤寒沙门氏菌和胡萝卜软腐欧文氏菌的LexA蛋白中。同样,所有这三种LexA阻遏物中都存在氨基酸Ser-119和Lys-156。这些残基也存在于恶臭假单胞菌和铜绿假单胞菌的LexA蛋白中,但它们分别被4个和6个残基取代。此外,大肠杆菌LexA阻遏物的DNA结合结构域的结构和序列在鼠伤寒沙门氏菌、胡萝卜软腐欧文氏菌、铜绿假单胞菌和恶臭假单胞菌的LexA蛋白中高度保守。

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