García J A, Pastrana R, Prieto I, Salas M
Gene. 1983 Jan-Feb;21(1-2):65-76. doi: 10.1016/0378-1119(83)90148-8.
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.
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。