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枯草芽孢杆菌葡萄糖酸盐操纵子(gnt)的组织与转录

Organization and transcription of the gluconate operon, gnt, of Bacillus subtilis.

作者信息

Fujita Y, Fujita T, Miwa Y, Nihashi J, Aratani Y

出版信息

J Biol Chem. 1986 Oct 15;261(29):13744-53.

PMID:3020045
Abstract

The gluconate (gnt) operon of Bacillus subtilis has been cloned and sequenced. Analysis of the sequence (5482 base pairs) revealed four open reading frames, each of which was preceded by a Shine-Dalgarno sequence. These four frames were designated from the 5'-end as gntR, gntK, gntP, and gntZ. The gntR and gntK genes overlapped by 5 bases. The gntK and gntP gene products (consisting of 513 and 448 amino acids) were identified as gluconate kinase and permease, respectively, by means of insertional inactivation and deletion analysis of these genes subcloned in plasmid pC194. The functions of the gntR and gntZ gene products (243 and 468 amino acids) are presently unknown. S1 nuclease mapping and subcloning in a promoter probe vector (pPL603B) provided evidence that the gnt operon was transcribed as a polycistronic mRNA. Besides the gnt promoter about 40 base pairs upstream of the gntR gene, we detected two overlapping internal promoters between the gntP and gntZ genes. The gnt transcripts terminate about 45 base pairs downstream of the gntZ gene.

摘要

枯草芽孢杆菌的葡萄糖酸盐(gnt)操纵子已被克隆并测序。对该序列(5482个碱基对)的分析揭示了四个开放阅读框,每个阅读框之前都有一个Shine-Dalgarno序列。这四个阅读框从5'端开始分别命名为gntR、gntK、gntP和gntZ。gntR和gntK基因重叠5个碱基。通过对克隆在质粒pC194中的这些基因进行插入失活和缺失分析,gntK和gntP基因产物(分别由513和448个氨基酸组成)被鉴定为葡萄糖酸盐激酶和通透酶。gntR和gntZ基因产物(分别为243和468个氨基酸)的功能目前尚不清楚。S1核酸酶图谱分析以及在启动子探针载体(pPL603B)中的亚克隆提供了证据,表明gnt操纵子转录为多顺反子mRNA。除了gntR基因上游约40个碱基对处的gnt启动子外,我们在gntP和gntZ基因之间检测到两个重叠的内部启动子。gnt转录本在gntZ基因下游约45个碱基对处终止。

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