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首页> 外文期刊>FEMS Microbiology Letters >Cloning and characterization of the gene encoding penicillin-binding protein A of Streptomyces griseus
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Cloning and characterization of the gene encoding penicillin-binding protein A of Streptomyces griseus

机译:灰链霉菌青霉素结合蛋白A编码基因的克隆与鉴定

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摘要

An internal segment of the penicillin-binding protein gene, pbpA, of Streptomyces griseus was amplified from genomic DNA using the polymerase chain reaction and used as a hybridization probe to isolate the complete gene from a cosmid library. pbpA encodes a 485 amino acid sequence that conserves three motifs of PBPs, SXXK, SXN, and KTG. The pbpA gene was located downstream of a gene homologous to the Bacillus subtilis spoVE gene. The pbpA gene was disrupted by replacing an ApaI fragment of the pbpA gene in S. griseus chromosome with an apramycin resistance gene cassette or directly inserting this apramycin resistance gene cassette at the NcoI site of pbpA penicillin- binding domain. No obvious defects in growth, sporulation, or spore sonication resistance were observed in the constructed pbpA mutants, suggesting that PBPA is not essential for growth and sporulation under normal laboratory conditions in S. griseus. (C) 2000 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved. [References: 26]
机译:使用聚合酶链反应从基因组DNA扩增灰链霉菌青霉素结合蛋白基因pbpA的内部片段,并将其用作杂交探针,从粘粒文库中分离出完整的基因。 pbpA编码一个485个氨基酸序列,该序列保留了PBP,SXXK,SXN和KTG的三个基序。 pbpA基因位于与枯草芽孢杆菌spoVE基因同源的基因的下游。通过用阿霉素抗性基因盒代替灰霉链球菌染色体中的pbpA基因的ApaI片段,或将该阿普霉素抗性基因盒直接插入pbpA青霉素结合域的NcoI位点,来破坏pbpA基因。在构建的pbpA突变体中未观察到明显的生长,孢子形成或孢子超声抗性缺陷,这表明在正常实验室条件下,PBPA对于灰霉菌在正常实验室条件下的生长和孢子形成不是必不可少的。 (C)2000年欧洲微生物学会联合会。由Elsevier Science B.V.保留所有权利。 [参考:26]

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