Towner K J, Carter G I
Department of Microbiology, University Hospital, Nottingham, U.K.
FEMS Microbiol Lett. 1990 Jun 15;58(1):19-22. doi: 10.1016/0378-1097(90)90095-8.
A 1.3 kb HindIII fragment encoding the type VII trimethoprim-resistant dihydrofolate reductase gene was cloned into pBR322. Unidirectional deletion of this cloned fragment with exonuclease III identified the start of the dihydrofolate reductase gene. An internal 300bp EcoRV fragment was identified which could be used as a specific non-radioactive DNA probe to distinguish bacteria carrying the type VII gene from those carrying genes encoding other known dihydrofolate reductase types.
将编码VII型耐甲氧苄啶二氢叶酸还原酶基因的1.3 kb HindIII片段克隆到pBR322中。用核酸外切酶III对该克隆片段进行单向缺失,确定了二氢叶酸还原酶基因的起始位置。鉴定出一个300bp的内部EcoRV片段,它可作为一种特异性非放射性DNA探针,用于区分携带VII型基因的细菌与携带编码其他已知二氢叶酸还原酶类型基因的细菌。