Jacob J, Evers S, Bischoff K, Carlier C, Courvalin P
Unité des Agents Antibactériens, CNRS, Institut Pasteur, Paris, France.
FEMS Microbiol Lett. 1994 Jul 1;120(1-2):13-7. doi: 10.1111/j.1574-6968.1994.tb07000.x.
The sat4 streptothricin resistance gene from Campylobacter coli BE/G4 was cloned into pUC18, and its nucleotide sequence was determined. Streptothricin acetyltransferase activity was detected in Escherichia coli cells containing recombinant plasmid pAT132 which carries the sat4 gene as an insert. The deduced amino acid sequence displayed 21-27% amino acid identity with streptothricin acetyltransferases from E. coli and streptothricin producers Streptomyces lavendulae and Streptomyces noursei. The sat4 gene was detected by hybridization in clinical and environmental isolates of Campylobacter spp.
将来自空肠弯曲菌BE/G4的sat4链丝菌素抗性基因克隆到pUC18中,并测定其核苷酸序列。在含有重组质粒pAT132的大肠杆菌细胞中检测到链丝菌素乙酰转移酶活性,该重组质粒携带插入的sat4基因。推导的氨基酸序列与来自大肠杆菌以及链丝菌素产生菌薰衣草链霉菌和诺尔斯链霉菌的链丝菌素乙酰转移酶显示出21%-27%的氨基酸同一性。通过杂交在弯曲菌属的临床和环境分离株中检测到sat4基因。