Vizváryová M, Stuchlík S, Grones J, Macor M, Turna J
Department of Molecular Biology, Comenius University, Bratislava, Slovakia.
Folia Microbiol (Praha). 1999;44(6):625-8. doi: 10.1007/BF02825651.
Escherichia coli strain which contains a marker of tetracycline resistance gene (TcR) placed by P1 transduction beside the chromosomal deletion of ampC gene (delta ampC) coding for beta-lactamase was constructed. Such introduction of TcR marker permits a fast and simple selection for the transfer of delta ampC by P1 transduction into industrial E. coli strains. This approach was used for constructing an E. coli strain suitable for penicillin acylase production.
构建了一种大肠杆菌菌株,该菌株通过P1转导在编码β-内酰胺酶的ampC基因(delta ampC)的染色体缺失旁边放置了四环素抗性基因(TcR)标记。TcR标记的这种引入允许通过P1转导将delta ampC快速简单地选择转移到工业大肠杆菌菌株中。该方法用于构建适合青霉素酰化酶生产的大肠杆菌菌株。