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对编码核苷转运蛋白的大肠杆菌nupG基因调控区的分析。

Analysis of the regulatory region of the Escherichia coli nupG gene, encoding a nucleoside-transport protein.

作者信息

Munch-Petersen A, Jensen N

机构信息

Institute of Biological Chemistry B, University of Copenhagen, Denmark.

出版信息

Eur J Biochem. 1990 Jul 5;190(3):547-51. doi: 10.1111/j.1432-1033.1990.tb15608.x.

Abstract

The S1-mapping procedure, when applied to an 800-bp fragment upstream of the nupG structural gene of Escherichia coli revealed one transcription-initiation site. The corresponding promoter is negatively regulated by the cytR and the deoR repressors. The expression of the gene is activated by the complex between cAMP and its receptor protein. In strains lacking cAMP the promoter expression is reduced and it is no longer regulated by the cytR repressor, whereas the deoR regulation is retained.

摘要

将S1映射程序应用于大肠杆菌nupG结构基因上游800 bp的片段时,发现了一个转录起始位点。相应的启动子受到cytR和deoR阻遏物的负调控。该基因的表达由cAMP与其受体蛋白之间的复合物激活。在缺乏cAMP的菌株中,启动子表达降低,且不再受cytR阻遏物调控,而deoR调控得以保留。

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