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从罗伊氏乳杆菌中鉴定并克隆一种质粒编码的红霉素抗性决定子。

Identification and cloning of a plasmid-encoded erythromycin resistance determinant from Lactobacillus reuteri.

作者信息

Axelsson L T, Ahrné S E, Andersson M C, Ståhl S R

机构信息

Department of Microbiology, Swedish University of Agricultural Sciences, Uppsala.

出版信息

Plasmid. 1988 Sep;20(2):171-4. doi: 10.1016/0147-619x(88)90023-6.

Abstract

Plasmid analysis, plasmid curing, cloning, and hybridization experiments were used to study four Lactobacillus reuteri strains showing high resistance to erythromycin. Plasmid curing with acriflavine resulted in a loss of erythromycin resistance in a frequency of 1-10%. For three of the strains this was accompanied by a loss of a 6.9-MDa plasmid, which was shown to be identical for the different strains and designated pLUL631. The erythromycin (erm) gene was located on a 5.5-MDa plasmid in the fourth strain. A restriction map of pLUL631 was constructed and the location of the erm gene on the plasmid was identified by cloning in Escherichia coli. By using a Streptococcus lactis-E. coli shuttle vector, the erm gene was also transformed to S. lactis and expressed. The erm gene from L. reuteri was shown to be related to the erm gene from pIP501 (Streptococcus agalactiae) by DNA-DNA hybridization.

摘要

通过质粒分析、质粒消除、克隆和杂交实验,对四株对红霉素具有高抗性的罗伊氏乳杆菌菌株进行了研究。用吖啶黄素进行质粒消除,导致红霉素抗性以1%-10%的频率丧失。对于其中三株菌株,这伴随着一个6.9-MDa质粒的丢失,该质粒在不同菌株中显示相同,并命名为pLUL631。第四株菌株的红霉素(erm)基因位于一个5.5-MDa质粒上。构建了pLUL631的限制性图谱,并通过在大肠杆菌中克隆确定了erm基因在质粒上的位置。通过使用乳酸链球菌-大肠杆菌穿梭载体,erm基因也被转化到乳酸链球菌中并表达。通过DNA-DNA杂交表明,罗伊氏乳杆菌的erm基因与pIP501(无乳链球菌)的erm基因相关。

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