Nano F E, Shepherd W D, Watkins M M, Kuhl S A, Kaplan S
Gene. 1985;34(2-3):219-26. doi: 10.1016/0378-1119(85)90130-1.
A broad-host-range plasmid was constructed that allows the in vitro formation of beta-galactosidase fusions. DNA from the photosynthetic bacterium Rhodopseudomonas sphaeroides was cloned into this plasmid and a number of R. sphaeroides isolates were recovered that had varying levels of beta-galactosidase activity. beta-galactosidase antigenic activity from the fusion strains could be localized immunologically in polypeptides with an Mr of 120 000 or greater. Expression of beta-galactosidase activity under control of fusion derivatives was either very low or nonexistent in Escherichia coli relative to R. sphaeroides, indicating that R. sphaeroides promoters or translational start signals function poorly in E. coli.
构建了一种广宿主范围的质粒,该质粒允许体外形成β-半乳糖苷酶融合体。将光合细菌球形红假单胞菌的DNA克隆到该质粒中,并获得了一些具有不同水平β-半乳糖苷酶活性的球形红假单胞菌分离株。融合菌株的β-半乳糖苷酶抗原活性可通过免疫定位到分子量为120000或更大的多肽中。相对于球形红假单胞菌,融合衍生物控制下的β-半乳糖苷酶活性在大肠杆菌中的表达非常低或不存在,这表明球形红假单胞菌启动子或翻译起始信号在大肠杆菌中功能不佳。