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枯草芽孢杆菌噬菌体 phi 29 DNA 末端连接蛋白编码基因在大肠杆菌中的克隆与表达。

Cloning and expression in Escherichia coli of the gene coding for the protein linked to the ends of Bacillus subtilis phage phi 29 DNA.

作者信息

García J A, Pastrana R, Prieto I, Salas M

出版信息

Gene. 1983 Jan-Feb;21(1-2):65-76. doi: 10.1016/0378-1119(83)90148-8.

Abstract

A phi 29 DNA fragment containing gene 3, coding for the 5'-terminal protein, and several other early genes has been cloned in a pBR322 derivative plasmid (pKC30) under the control of the pL promoter of bacteriophage lambda. Four polypeptides of Mr 27000, 18500, 17500 and 12500 were labelled with [35S]methionine after heat induction, accounting for about 15% of the de novo synthesized protein. The Mr 27000 and 12500 proteins were characterized as p3, the 5'-terminal protein, and p4, involved in the control of late transcription, respectively. Protein p3 synthesized in Escherichia coli was active in the in vitro formation of the initiation complex p3-dAMP when supplemented with extracts from Bacillus subtilis infected with a sus3 mutant.

摘要

一个含有基因3(编码5'-末端蛋白)和其他几个早期基因的φ29 DNA片段已在噬菌体λ的pL启动子控制下克隆到pBR322衍生质粒(pKC30)中。热诱导后,用[35S]甲硫氨酸标记了分子量为27000、18500、17500和12500的四种多肽,约占从头合成蛋白的15%。分子量为27000和12500的蛋白分别被鉴定为p3(5'-末端蛋白)和p4(参与晚期转录的控制)。在大肠杆菌中合成的蛋白p3,当补充来自感染sus3突变体的枯草芽孢杆菌的提取物时,在体外形成起始复合物p3-dAMP时具有活性。

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