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枯草芽孢杆菌中特定区域的转录:谷氨酸脱氢酶启动子的鉴定

Compartment-specific transcription in Bacillus subtilis: identification of the promoter for gdh.

作者信息

Rather P N, Moran C P

机构信息

Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia 30322.

出版信息

J Bacteriol. 1988 Nov;170(11):5086-92. doi: 10.1128/jb.170.11.5086-5092.1988.

Abstract

Glucose dehydrogenase beings to accumulate in the forespore between 2 and 3 h after the onset of endospore formation in Bacillus subtilis. The promoter for the structural gene for glucose dehydrogenase (gdh) was shown to be located 800 base pairs upstream from the coding sequence by examining the effects of integrating plasmids into the gdh region of the chromosome. The location of the gdh promoter was confirmed by primer extension analysis and by the identification of two single-base substitutions in the gdh promoter that prevented its function. The results of cell fractionation experiments with a strain that contained a transcriptional fusion of the gdh promoter and lacZ indicated that the forespore-specific accumulation of glucose dehydrogenase during sporulation is probably due to forespore-specific transcription of gdh.

摘要

在枯草芽孢杆菌中,芽孢形成开始后2至3小时内,葡萄糖脱氢酶开始在前芽孢中积累。通过研究将质粒整合到染色体gdh区域的效果,发现葡萄糖脱氢酶(gdh)结构基因的启动子位于编码序列上游800个碱基对处。通过引物延伸分析以及鉴定gdh启动子中两个阻止其功能的单碱基取代,证实了gdh启动子的位置。用含有gdh启动子与lacZ转录融合的菌株进行细胞分级分离实验的结果表明,孢子形成过程中葡萄糖脱氢酶在前芽孢中的特异性积累可能是由于gdh在前芽孢中的特异性转录。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b58/211575/f70842624b9b/jbacter00189-0097-a.jpg

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