Suppr超能文献

编码大肠杆菌K12的2-氧代戊二酸脱氢酶的sucA基因的核苷酸序列。

Nucleotide sequence of the sucA gene encoding the 2-oxoglutarate dehydrogenase of Escherichia coli K12.

作者信息

Darlison M G, Spencer M E, Guest J R

出版信息

Eur J Biochem. 1984 Jun 1;141(2):351-9. doi: 10.1111/j.1432-1033.1984.tb08199.x.

Abstract

The nucleotide sequence of a 3180-base-pair segment of DNA, containing the sucA gene encoding the 2-oxoglutarate dehydrogenase component (E1o) of the 2-oxoglutarate dehydrogenase complex of Escherichia coli, has been determined by the dideoxy chain-termination method. The sucA structural gene contains 2796 base pairs (932 codons, excluding the initiation codon AUG) and encodes a polypeptide having a glutamine residue at the amino terminus, a glutamate residue at the carboxy-terminus and a calculated Mr = 104905. The predicted amino acid composition is in good agreement with published information obtained by hydrolysis of the purified enzyme. There is a striking lack of sequence homology between the 2-oxoglutarate dehydrogenase (E1o) and the corresponding pyruvate dehydrogenase (E1p), which suggests that the two components are not closely related in evolutionary terms. The location and polarity of the sucA gene, relative to the restriction map of the corresponding segment of DNA, are consistent with it being the proximal gene of the suc operon, as defined in previous genetic and post-infection labelling studies, but it could also form part of a more complex regulatory unit. The sucA gene is preceded by a segment of DNA that contains many substantial regions of hyphenated dyad symmetry including an IS-like sequence of the type that is thought to function as an intercistronic regulatory element. This segment also contains three putative RNA polymerase binding sites and a good ribosome binding site.

摘要

通过双脱氧链终止法测定了一段3180个碱基对的DNA片段的核苷酸序列,该片段包含编码大肠杆菌2-氧代戊二酸脱氢酶复合体中2-氧代戊二酸脱氢酶组分(E1o)的sucA基因。sucA结构基因包含2796个碱基对(932个密码子,不包括起始密码子AUG),编码一种多肽,该多肽在氨基末端有一个谷氨酰胺残基,在羧基末端有一个谷氨酸残基,计算得出的分子量为104905。预测的氨基酸组成与通过纯化酶水解获得的已发表信息高度一致。2-氧代戊二酸脱氢酶(E1o)与相应的丙酮酸脱氢酶(E1p)之间明显缺乏序列同源性,这表明这两个组分在进化上没有密切关系。sucA基因相对于相应DNA片段的限制酶切图谱的位置和极性,与它是suc操纵子的近端基因一致,如先前的遗传和感染后标记研究中所定义的,但它也可能是一个更复杂调控单元的一部分。sucA基因之前有一段DNA,其中包含许多具有大量间断二元对称的区域,包括一个被认为起顺反子间调控元件作用的IS样序列。该片段还包含三个假定的RNA聚合酶结合位点和一个良好的核糖体结合位点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验