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带有R1质粒的大肠杆菌对链霉素的高水平抗性及遗传决定因素分析

High-level resistance to streptomycin in Escherichia coli with R1 plasmid and the analysis of genetic determinants.

作者信息

Braná H, Hubácek J

出版信息

Folia Microbiol (Praha). 1979;24(2):136-42. doi: 10.1007/BF02927297.

Abstract

Some properties of streptomycin-resistant mutants of Escherichia coli were analyzed. In a R+ culture, the phenotype under study may be significantly selected at a frequency of 10(-5) on media with higher streptomycin level. The lrs mutation is present in the cells prior to the action of streptomycin and remains in the cells even after curing of the R1 plasmid. The mapping of the lrs gene by conjugation with a concomitant transfer of chromosome and the R1 plasmid in different Hfr strains of E. coli failed to establish the localization of this gene in the tested chromosome regions. The presence of a cryptic plasmid was detected in cells with the lrs mutation after curing of the R1 plasmid. This plasmid codes neither fertility functions nor chloramphenicol-acetyltransferase, streptomycin-adenyltransferase, or ampicillin-beta-lactamase.

摘要

对大肠杆菌链霉素抗性突变体的一些特性进行了分析。在R⁺培养物中,在链霉素水平较高的培养基上,所研究的表型可能以10⁻⁵的频率被显著选择。lrs突变在链霉素作用之前就存在于细胞中,即使在R1质粒消除后仍保留在细胞中。通过与不同大肠杆菌Hfr菌株的染色体和R1质粒同时转移进行接合来绘制lrs基因图谱,但未能在测试的染色体区域确定该基因的定位。在R1质粒消除后,在具有lrs突变的细胞中检测到一种隐蔽质粒。该质粒既不编码育性功能,也不编码氯霉素乙酰转移酶、链霉素腺苷转移酶或氨苄青霉素β-内酰胺酶。

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