Tietze E, Brevet J, Tschäpe H, Voigt W
Institut für Experimentelle Epidemiologie, DDR, Wernigerode.
J Basic Microbiol. 1988;28(1-2):129-36. doi: 10.1002/jobm.3620280116.
Streptothricin resistance determinants have been cloned from the transposons Tn1825 and Tn1826 to the vector plasmid pUC8. The recombinant plasmids were characterized with respect to their physical structure. The resistance properties of their hosts were characterized with respect to the minimal inhibitory concentration of streptothricin and the activity of the streptothricin acetyltransferase. The proteins encoded by the cloned resistance determinants were analysed in a maxicell system. The results of our investigations suggest that the resistance to streptothricin is mediated by the activity of a streptothricin acetyltransferase with both, Tn1825 and Tn1826. However, the resistance determinant of Tn1825 is more complex than Tn1826 and additional functions involved in realizing the resistance phenotype must be recognized.
链丝菌素抗性决定簇已从转座子Tn1825和Tn1826克隆到载体质粒pUC8中。对重组质粒的物理结构进行了表征。根据链丝菌素的最小抑菌浓度和链丝菌素乙酰转移酶的活性,对其宿主的抗性特性进行了表征。在最大细胞系统中分析了克隆的抗性决定簇编码的蛋白质。我们的研究结果表明,Tn1825和Tn1826对链丝菌素的抗性均由链丝菌素乙酰转移酶的活性介导。然而,Tn1825的抗性决定簇比Tn1826更复杂,必须认识到实现抗性表型所涉及的其他功能。