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枯草芽孢杆菌pbpF基因的克隆、核苷酸序列及调控,该基因编码一种假定的A类高分子量青霉素结合蛋白。

Cloning, nucleotide sequence, and regulation of the Bacillus subtilis pbpF gene, which codes for a putative class A high-molecular-weight penicillin-binding protein.

作者信息

Popham D L, Setlow P

机构信息

Department of Biochemistry, University of Connecticut Health Center, Farmington 06032.

出版信息

J Bacteriol. 1993 Aug;175(15):4870-6. doi: 10.1128/jb.175.15.4870-4876.1993.

Abstract

The partial nucleotide sequence of a gene encoding a Bacillus subtilis homolog to the Escherichia coli ponA gene, encoding penicillin-binding protein 1A, was previously reported. The remaining part of this gene, termed pbpF, was isolated, and its nucleotide sequence was completed. Deletion of this gene did not alter the profile of B. subtilis penicillin-binding proteins observed after gel electrophoresis and resulted in no observable phenotype. A transcriptional pbpF-lacZ fusion was weakly expressed during vegetative growth. Expression diminished during the first hours of sporulation but was slightly induced in the forespore compartment during late sporulation. This sporulation expression was dependent on spoIIIG, which encodes the forespore-specific transcription factor sigma G. A single transcription start site which was apparently directly dependent on E sigma A was detected in vegetative cells.

摘要

先前已报道了一个编码枯草芽孢杆菌中与大肠杆菌ponA基因同源基因的部分核苷酸序列,该大肠杆菌ponA基因编码青霉素结合蛋白1A。该基因的其余部分,称为pbpF,已被分离出来,其核苷酸序列也已完成。该基因的缺失并未改变凝胶电泳后观察到的枯草芽孢杆菌青霉素结合蛋白的图谱,也未产生可观察到的表型。一个转录的pbpF-lacZ融合体在营养生长期间弱表达。在芽孢形成的最初几个小时表达减弱,但在芽孢形成后期在前芽孢区室中略有诱导。这种芽孢形成期的表达依赖于spoIIIG,它编码前芽孢特异性转录因子σG。在营养细胞中检测到一个显然直接依赖于EσA的单一转录起始位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/513e/204940/d8cbf27aac73/jbacter00057-0308-a.jpg

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