Kreft J, Burger K J, Goebel W
Mol Gen Genet. 1983;190(3):384-9. doi: 10.1007/BF00331063.
Bifunctional recombinant plasmids were constructed, comprised of the E. coli vectors pBR322, pBR325 and pACYC184 and different plasmids from Gram-positive bacteria, e.g. pBSU161-1 of B. subtilis and pUB110 and pC221 of S. aureus. The beta-lactamase (bla) gene and the chloramphenicol acetyltransferase (cat) gene from the E. coli plasmids were not transcribed and therefore not expressed in B. subtilis. However, tetracycline resistance from the E. coli plasmids was expressed in B. subtilis. Transcription of the tetracycline resistance gene(s) started in B. subtilis at or near the original E. coli promoter, the sequence of which is almost identical with the sequence recognized by sigma 55 of B. subtilis RNA polymerase.
构建了双功能重组质粒,其由大肠杆菌载体pBR322、pBR325和pACYC184以及来自革兰氏阳性菌的不同质粒组成,例如枯草芽孢杆菌的pBSU161-1以及金黄色葡萄球菌的pUB110和pC221。大肠杆菌质粒中的β-内酰胺酶(bla)基因和氯霉素乙酰转移酶(cat)基因在枯草芽孢杆菌中不转录,因此不表达。然而,大肠杆菌质粒的四环素抗性在枯草芽孢杆菌中表达。四环素抗性基因的转录在枯草芽孢杆菌中于原始大肠杆菌启动子处或其附近开始,该启动子的序列与枯草芽孢杆菌RNA聚合酶的σ55识别的序列几乎相同。