Pugsley A P, Cole S T
J Gen Microbiol. 1986 Aug;132(8):2297-307. doi: 10.1099/00221287-132-8-2297.
A series of plasmids encoding hybrid proteins comprising various lengths of the NH2-terminal region of colicin N coupled to almost complete beta-galactosidase or alkaline phosphatase polypeptides was constructed by transposon mutagenesis of ColN plasmid derivatives. Synthesis of the hybrid proteins, like that of colicin N itself, was regulated by the SOS response. Large quantities of the hybrid proteins accumulated in the cytoplasm (beta-galactosidase) or particulate fractions (alkaline phosphatase). When the gene fusions were expressed in cells that were producing colicin E2 and expressing the ColE2 lysis gene, only very low levels of the hybrid proteins were found in the medium. The results suggest that the amino-terminal part of colicin N does not contain sufficient biochemical information to promote the release of the hybrid proteins into the medium.
通过对大肠杆菌素N(ColN)质粒衍生物进行转座子诱变,构建了一系列编码杂合蛋白的质粒,这些杂合蛋白包含大肠杆菌素N不同长度的NH2末端区域,并与几乎完整的β-半乳糖苷酶或碱性磷酸酶多肽相连。杂合蛋白的合成,与大肠杆菌素N自身的合成一样,受SOS反应调控。大量杂合蛋白积聚在细胞质(β-半乳糖苷酶)或颗粒部分(碱性磷酸酶)中。当基因融合体在产生大肠杆菌素E2并表达ColE2裂解基因的细胞中表达时,在培养基中仅发现极低水平的杂合蛋白。结果表明,大肠杆菌素N的氨基末端部分不包含足够的生化信息来促进杂合蛋白释放到培养基中。