首页> 美国卫生研究院文献>Journal of Bacteriology >Defective and plaque-forming lambda transducing bacteriophage carrying penicillin-binding protein-cell shape genes: genetic and physical mapping and identification of gene products from the lip-dacA-rodA-pbpA-leuS region of the Escherichia coli chromosome.
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Defective and plaque-forming lambda transducing bacteriophage carrying penicillin-binding protein-cell shape genes: genetic and physical mapping and identification of gene products from the lip-dacA-rodA-pbpA-leuS region of the Escherichia coli chromosome.

机译:带有青霉素结合蛋白-细胞形状基因的有缺陷的噬菌斑形成λ转导噬菌体:大肠杆菌染色体lip-dacA-rodA-pbpA-leuS区基因产物的遗传和物理定位及鉴定。

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摘要

A series of defective lambda transducing phage carrying genes from the lip-leuS region of the Escherichia coli chromosome (min 14 on the current linkage map) has been isolated. The phage defined the gene order as lac---lip-dacA-rodA-pbpA-leuS---gal. These included the structural genes for penicillin-binding protein 2 (pbpA) and penicillin-binding protein 5 (dacA) as well as a previously unidentified cell shape gene that we have called rodA. rodA mutants were spherical and very similar to pbpA mutants but were distinguishable from them in that they had no defects in the activity of penicillin-binding protein 2. The separation into two groups of spherical mutants with mutations that mapped close to lip was confirmed by complementation analysis. The genes dacA, rodA, and pbpA lie within a 12-kilobase region, and represent a cluster of genes involved in cell shape determination and peptidoglycan synthesis. A restriction map of the lip-leuS region was established, and restriction fragments were cloned from defective transducing phage into appropriate lambda vectors to generate plaque-forming phage that carried genes from this region. Analysis of the proteins synthesized from lambda transducing phage in ultraviolet light-irradiated cells of E. coli resulted in the identification of the leuS, pbpA, dacA, and lip gene products, but the product of the rodA gene was not identified. The nine proteins that were synthesized from the lip-leuS region accounted for 57% of its coding capacity. Phage derivatives were constructed that allowed about 50-fold amplification of the levels of penicillin-binding proteins 2 and 5 in the cytoplasmic membrane.
机译:从大肠杆菌染色体的唇-leuS区(当前连锁图上的第14分钟)分离出了一系列带有缺陷的lambda转导噬菌体携带基因。噬菌体将基因顺序定义为lac --- lip-dacA-rodA-pbpA-leuS --- gal。这些包括青霉素结合蛋白2(pbpA)和青霉素结合蛋白5(dacA)的结构基因,以及我们以前称为roA的先前未鉴定的细胞形状基因。 rodA突变体是球形的,与pbpA突变体非常相似,但与它们的区别在于它们在青霉素结合蛋白2的活性方面没有缺陷。通过互补,证实了将两组突变体分离到靠近嘴唇的球形突变体的分离。分析。基因dacA,rodA和pbpA位于12碱基对的区域内,代表与细胞形状确定和肽聚糖合成有关的基因簇。建立了lip-leuS区域的限制性图谱,并将限制性片段从有缺陷的转导噬菌体克隆到合适的λ载体中,以产生噬菌斑形成噬菌体,其携带来自该区域的基因。分析从λ噬菌体转导的噬菌体在紫外线照射的大肠杆菌细胞中合成的蛋白质,可鉴定出leuS,pbpA,dacA和lip基因产物,但未鉴定出rodA基因的产物。从唇-leuS区合成的九种蛋白质占其编码能力的57%。构建了噬菌体衍生物,其可使细胞质膜中青霉素结合蛋白2和5的水平扩增约50倍。

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