Griffiths Phillippa L, Park Robert W A, Connerton Ian F
1 Department of Biochemistry, Imperial College of Science, Technology and Medicine, Exhibition Road, London SW7 2AZ, UK.
2 Department of Microbiology, University of Reading, PO Box 228, Reading RG6 2AJ, UK.
Microbiology (Reading). 1995 Jun;141 ( Pt 6):1359-1367. doi: 10.1099/13500872-141-6-1359.
A gene encoding a protein of apparent molecular mass 56 kDa that shares 31% identity with the amino acid sequence of trigger factor from Escherichia coli (a protein thought to be involved in cell division), was cloned from Campylobacter jejuni NCTC 11168. The clone was selected from a lambda ZAP II genomic DNA library following an immuno-screen using antiserum raised against glycine-extractable proteins from C. jejuni. The gene has two potential initiation codons, giving rise to two possible nested protein products. Complex differential growth-phase-dependent transcripts give rise to these products.
从空肠弯曲菌NCTC 11168中克隆出一个编码表观分子量为56 kDa蛋白质的基因,该蛋白质与大肠杆菌触发因子的氨基酸序列有31%的同源性(触发因子是一种被认为参与细胞分裂的蛋白质)。该克隆是从λZAP II基因组DNA文库中筛选出来的,筛选时使用了针对空肠弯曲菌甘氨酸可提取蛋白产生的抗血清进行免疫筛选。该基因有两个潜在的起始密码子,可产生两种可能的嵌套蛋白质产物。复杂的依赖生长阶段的差异转录本产生了这些产物。