Riede I
J Bacteriol. 1987 Jul;169(7):2956-61. doi: 10.1128/jb.169.7.2956-2961.1987.
The lysis gene t of the T-even-like bacteriophage K3 has been cloned and sequenced. The gene codes for a protein with a predicted molecular weight of 25,200. Expression of the complete lysis protein was impossible, but peptides complementing T4 amber mutants in t are described. No known lysis protein of other phages is homologous to protein T. Also, the Escherichia coli phospholipase A is different from protein T. CelB, the lysis protein of the colicin E2 operon, shows a similarity to protein T. Sequences of colicins A, E1, and E2 are related to gene 38 sequences, the gene preceding t and coding for the phage adhesin. A common origin for colicin genes and phage genes is discussed, and a protein region in colicins that is responsible for receptor recognition is predicted.
类T偶数噬菌体K3的裂解基因t已被克隆和测序。该基因编码一种预测分子量为25200的蛋白质。完整裂解蛋白的表达是不可能的,但描述了能互补T4在t位点的琥珀突变体的肽段。其他噬菌体的已知裂解蛋白与蛋白T没有同源性。此外,大肠杆菌磷脂酶A与蛋白T不同。大肠杆菌素E2操纵子的裂解蛋白CelB与蛋白T有相似性。大肠杆菌素A、E1和E2的序列与基因38序列相关,基因38位于t之前,编码噬菌体粘附素。讨论了大肠杆菌素基因和噬菌体基因的共同起源,并预测了大肠杆菌素中负责受体识别的蛋白质区域。