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大肠杆菌K-12中编码好氧甘油-3-磷酸脱氢酶的glpD基因启动子和操纵子的结构

Structures of the promoter and operator of the glpD gene encoding aerobic sn-glycerol-3-phosphate dehydrogenase of Escherichia coli K-12.

作者信息

Ye S Z, Larson T J

机构信息

Department of Biochemistry and Nutrition, Virginia Polytechnic Institute and State University, Blacksburg 24061.

出版信息

J Bacteriol. 1988 Sep;170(9):4209-15. doi: 10.1128/jb.170.9.4209-4215.1988.

Abstract

The nucleotide sequence of a 690-base-pair DNA segment containing the control region for the glpD gene encoding aerobic sn-glycerol-3-phosphate dehydrogenase was determined. An ATG translation initiation codon with an adjacent ribosome-binding site was found which preceded an open reading frame continuing 61 codons to the end of the DNA that was sequenced. The start site for transcription, identified by using primer extension analysis, was located 42 base pairs upstream from the proposed Met start codon. The transcription start site was preceded by a region containing typical -10 and -35 sequences found in bacterial promoters. A binding site for the cyclic AMP-cyclic AMP receptor protein complex (identified by comparison with the consensus-binding sequence and verified by using DNase I footprinting) was located just upstream from the -35 sequence, centered at position -63. The interaction site for the glp repressor was identified by using DNase I footprinting. It consisted of a 49-base-pair region which started at the -10 sequence and continued to position +38. This region contained two directly repeated sequences, each possessing hyphenated dyad symmetry, which suggests that the operator is tandemly repeated. The presence of two adjacent operators may explain why expression of the glpD gene is the most sensitive to repressor when compared with expression of the other operons that are members of the glp regulon.

摘要

测定了一段690个碱基对的DNA片段的核苷酸序列,该片段包含编码好氧甘油-3-磷酸脱氢酶的glpD基因的控制区。发现了一个带有相邻核糖体结合位点的ATG翻译起始密码子,其位于一个开放阅读框之前,该开放阅读框一直延续到测序DNA的末端,共61个密码子。通过引物延伸分析确定的转录起始位点位于推测的甲硫氨酸起始密码子上游42个碱基对处。转录起始位点之前是一个含有细菌启动子中典型的-10和-35序列的区域。环腺苷酸-环腺苷酸受体蛋白复合物的结合位点(通过与共有结合序列比较确定,并通过DNase I足迹法验证)位于-35序列上游,中心位于-63位。通过DNase I足迹法确定了glp阻遏物的相互作用位点。它由一个49个碱基对的区域组成,从-10序列开始,一直延续到+38位。该区域包含两个直接重复序列,每个序列都具有带连字符的二元对称,这表明操纵基因是串联重复的。两个相邻操纵基因的存在可能解释了为什么与glp操纵子中的其他操纵子相比,glpD基因的表达对阻遏物最为敏感。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bd2/211429/34482a80b7ab/jbacter00187-0432-a.jpg

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