Jackson M P, Newland J W, Holmes R K, O'Brien A D
Department of Microbiology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814-4799.
Microb Pathog. 1987 Feb;2(2):147-53. doi: 10.1016/0882-4010(87)90106-9.
A nucleotide sequence analysis was performed on the Shiga-like toxin I genes previously cloned from the Escherichia coli bacteriophage 933J. Two structural genes designated slt-I A and slt-I B were found to be oriented on a single transcriptional unit with slt-I A preceding slt-I B. A 12 base pair gap separated the in-phase open reading frames of slt-I A and slt-I B. Putative ribosome binding sites were identified 5' to both the slt-I A and slt-I B genes. Translation of the SLT-I nucleotide sequence revealed that both the A and B subunits were synthesized with signal peptides. The molecular weight calculated for the mature A subunit was 32,211 while the molecular weight of the mature B subunit was 7690.
对先前从大肠杆菌噬菌体933J中克隆的志贺样毒素I基因进行了核苷酸序列分析。发现两个结构基因,分别命名为slt-I A和slt-I B,位于一个单一的转录单元上,slt-I A位于slt-I B之前。一个12个碱基对的缺口将slt-I A和slt-I B的同相位开放阅读框隔开。在slt-I A和slt-I B基因的5'端均鉴定出推定的核糖体结合位点。对SLT-I核苷酸序列的翻译显示,A和B亚基均由信号肽合成。成熟A亚基的计算分子量为32,211,而成熟B亚基的分子量为7690。