Khan M A, Isaacson R E
Department of Veterinary Pathobiology, University of Illinois, Urbana, Illinois 61801, USA.
J Bacteriol. 1998 Sep;180(17):4746-9. doi: 10.1128/JB.180.17.4746-4749.1998.
An Escherichia coli DNA fragment was identified that contained part of the beta-glucoside (bgl) operon. This fragment was identified because it contained a promoter that was responsible for the expression of a reporter gene, the chloramphenicol acetyltransferase gene, in a mouse liver during bacterial infection but not when a bacterial clone was grown in vitro. This fragment contained a promoter and a rho-independent transcription terminator which were flanked by the 3' end of bglG and the 5' end of bglF. Reverse transcription-PCR confirmed that cat-specific mRNA was produced in infected mouse liver but not in vitro. mRNA encoding the positive regulator of the bgl operon, bglG, also was detected in mouse liver infected with an E. coli strain. These results demonstrated that expression of the bgl operon occurs in infected mouse liver and suggests a unique role for this operon in vivo.
鉴定出一个大肠杆菌DNA片段,其包含部分β-葡萄糖苷(bgl)操纵子。鉴定出该片段是因为它含有一个启动子,该启动子在细菌感染期间负责在小鼠肝脏中表达报告基因氯霉素乙酰转移酶基因,但在体外培养细菌克隆时则不然。该片段包含一个启动子和一个不依赖ρ因子的转录终止子,其两侧分别是bglG的3'端和bglF的5'端。逆转录-聚合酶链反应证实,感染的小鼠肝脏中产生了cat特异性mRNA,而体外则没有。在感染大肠杆菌菌株的小鼠肝脏中也检测到了编码bgl操纵子正调控因子bglG的mRNA。这些结果表明,bgl操纵子在感染的小鼠肝脏中表达,并提示该操纵子在体内具有独特作用。