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大肠杆菌中细胞形状基因dacA-rodA-pbpA簇的组织与亚克隆

Organization and subcloning of the dacA-rodA-pbpA cluster of cell shape genes in Escherichia coli.

作者信息

Stoker N G, Broome-Smith J K, Edelman A, Spratt B G

出版信息

J Bacteriol. 1983 Aug;155(2):847-53. doi: 10.1128/jb.155.2.847-853.1983.

Abstract

The transducing bacteriophage lambda pBS10 carries a small cluster of Escherichia coli penicillin-binding protein/cell shape genes, including pbpA, rodA, and dacA. Deletion mapping and subcloning showed that these genes, and the gene for a cytoplasmic membrane protein of molecular weight 54,000, are located within a 5.6-kilobase region and are probably contiguous. The dacA gene, which codes for penicillin-binding protein 5, was cloned on a 1.5-kilobase fragment into a low-copy-number plasmid vector, but insertion into high-copy-number plasmids produced deleterious effects on bacterial growth, and the plasmids could not be stably maintained. The direction of transcription of dacA was determined. The rodA gene was cloned on a 1.6-kilobase fragment into both low- and high-copy-number plasmids, and the identification of its gene product is described in the accompanying paper (Stoker et al., J. Bacteriol. 155:854-859). The pbpA gene, which codes for penicillin-binding protein 2, was cloned on a 3.7-kilobase fragment in low-copy-number plasmids, but insertion of the fragment into high-copy-number plasmids resulted in deleterious effects on bacterial growth, and the plasmids could not be stably maintained.

摘要

转导噬菌体λ pBS10携带一小簇大肠杆菌青霉素结合蛋白/细胞形状基因,包括pbpA、rodA和dacA。缺失图谱分析和亚克隆表明,这些基因以及一个分子量为54,000的细胞质膜蛋白基因位于一个5.6千碱基区域内,且可能是连续的。编码青霉素结合蛋白5的dacA基因被克隆到一个1.5千碱基的片段上,导入低拷贝数质粒载体,但导入高拷贝数质粒对细菌生长产生有害影响,且这些质粒不能稳定维持。确定了dacA的转录方向。rodA基因被克隆到一个1.6千碱基的片段上,导入低拷贝数和高拷贝数质粒,其基因产物的鉴定见随附论文(斯托克等人,《细菌学杂志》155:854 - 859)。编码青霉素结合蛋白2的pbpA基因被克隆到低拷贝数质粒的一个3.7千碱基片段上,但将该片段导入高拷贝数质粒对细菌生长产生有害影响,且这些质粒不能稳定维持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3777/217758/6d56deac615c/jbacter00243-0414-a.jpg

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