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大肠杆菌K-12的argF调控区的核苷酸序列。

Nucleotide sequence of the argF regulatory region of Escherichia coli K-12.

作者信息

Moore S K, Garvin R T, James E

出版信息

Gene. 1981 Dec;16(1-3):119-32. doi: 10.1016/0378-1119(81)90068-8.

Abstract

The deoxyribonucleotide sequence has been determined for the regulatory region of the arginine F gene (argF) of Escherichia coli K-12. The location of the argF coding region was deduced by comparison of the DNA sequence to the sequence predicted from the primary structure of the N-terminus of the argF gene product, the subunit of the "F" isoenzyme of ornithine transcarbamylase. Transcription of the argF gene was found to initiate at a position approx. 40 bp preceding the N-terminal codon for OTCase. Comparison of the region surrounding the origin of transcription with a computer-generated "model promoter sequence" revealed structural similarities between the two sequences, in particular, the promoter-associated stretches known as the "Pribnow box" and "minus 35 contact site". Another feature noted for the argF promoter region was its extreme abundance of A : T nucleotide pairs. In the region preceding the start site for argF translation, a sequence was observed to be complementary to the 3' end of the 16S RNA component of the E. coli ribosome. Both the length and the nucleotide sequence of the argF leader region indicate that the argF gene does not contain an attenuator proposed to exist in other operons concerned with amino acid biosynthesis.

摘要

已确定大肠杆菌K - 12精氨酸F基因(argF)调控区的脱氧核糖核苷酸序列。通过将DNA序列与根据argF基因产物(鸟氨酸转氨甲酰酶“F”同工酶的亚基)N端一级结构预测的序列进行比较,推断出argF编码区的位置。发现argF基因的转录起始于距鸟氨酸转氨甲酰酶N端密码子约40 bp的位置。将转录起始位点周围区域与计算机生成的“模型启动子序列”进行比较,发现这两个序列在结构上有相似之处,特别是与启动子相关的延伸区域,即所谓的“Pribnow框”和“-35接触位点”。argF启动子区域的另一个特点是其A:T核苷酸对极其丰富。在argF翻译起始位点之前的区域,观察到一个序列与大肠杆菌核糖体16S RNA组分的3'端互补。argF前导区的长度和核苷酸序列均表明,argF基因不包含其他与氨基酸生物合成相关的操纵子中所提出的衰减子。

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