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来自蜡样芽孢杆菌的氨甲酰妥布霉素 A 抗性基因。

Zwittermicin A resistance gene from Bacillus cereus.

作者信息

Milner J L, Stohl E A, Handelsman J

机构信息

Department of Plant Pathology, University of Wisconsin-Madison 53706, USA.

出版信息

J Bacteriol. 1996 Jul;178(14):4266-72. doi: 10.1128/jb.178.14.4266-4272.1996.

Abstract

Zwittermicin A is a novel aminopolyol antibiotic produced by Bacillus cereus that is active against diverse bacteria and lower eukaryotes (L.A. Silo-Suh, B.J. Lethbridge, S.J. Raffel, H. He, J. Clardy, and J. Handelsman, Appl. Environ. Microbiol. 60:2023-2030, 1994). To identify a determinant for resistance to zwittermicin A, we constructed a genomic library from B. cereus UW85, which produces zwittermicin A, and screened transformants of Escherichia coli DH5alpha, which is sensitive to zwittermicin A, for resistance to zwittermicin A. Subcloning and mutagenesis defined a genetic locus, designated zmaR, on a 1.2-kb fragment of DNA that conferred zwittermicin A resistance on E. coli. A DNA fragment containing zmaR hybridized to a corresponding fragment of genomic DNA from B. cereus UW85. Corresponding fragments were not detected in mutants of B. cereus UW85 that were sensitive to zwittermicin A, and the plasmids carrying zmaR restored resistance to the zwittermicin A-sensitive mutants, indicating that zmaR was deleted in the zwittermicin A-sensitive mutants and that zmaR is functional in B. cereus. Sequencing of the 1.2-kb fragment of DNA defined an open reading frame, designated ZmaR. Neither the nucleotide sequence nor the predicted protein sequence had significant similarity to sequences in existing databases. Cell extracts from an E. coli strain carrying zmaR contained a 43.5-kDa protein whose molecular mass and N-terminal sequence matched those of the protein predicted by the zmaR sequence. The results demonstrate that we have isolated a gene, zmaR, that encodes a zwIttermicin A resistance determinant that is functional in both B. cereus and E. coli.

摘要

茨维特霉素A是一种由蜡样芽孢杆菌产生的新型氨基多元醇抗生素,对多种细菌和低等真核生物具有活性(L.A. 西洛 - 苏、B.J. 莱思布里奇、S.J. 拉费尔、H. 贺、J. 克拉迪和J. 汉德尔斯曼,《应用与环境微生物学》60:2023 - 2030,1994)。为了鉴定对茨维特霉素A的抗性决定因素,我们构建了一个来自能产生茨维特霉素A的蜡样芽孢杆菌UW85的基因组文库,并筛选对茨维特霉素A敏感的大肠杆菌DH5α的转化子以获得对茨维特霉素A的抗性。亚克隆和诱变确定了一个位于1.2 kb DNA片段上的基因座,命名为zmaR,它赋予大肠杆菌对茨维特霉素A的抗性。一个含有zmaR的DNA片段与来自蜡样芽孢杆菌UW85的基因组DNA的相应片段杂交。在对茨维特霉素A敏感的蜡样芽孢杆菌UW85突变体中未检测到相应片段,并且携带zmaR的质粒恢复了对茨维特霉素A敏感突变体的抗性,表明zmaR在对茨维特霉素A敏感的突变体中被删除,并且zmaR在蜡样芽孢杆菌中具有功能。对1.2 kb DNA片段的测序确定了一个开放阅读框,命名为ZmaR。核苷酸序列和预测的蛋白质序列与现有数据库中的序列均无显著相似性。携带zmaR的大肠杆菌菌株的细胞提取物含有一种43.5 kDa的蛋白质,其分子量和N端序列与zmaR序列预测的蛋白质的分子量和N端序列相匹配。结果表明我们分离到了一个基因zmaR,它编码一种在蜡样芽孢杆菌和大肠杆菌中均具有功能的茨维特霉素A抗性决定因素。

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