Bekker O B, Elizarov S M, Alekseeva M T, Liubimova I K, Danilenko V N
Mikrobiologiia. 2008 Sep-Oct;77(5):630-8.
The level of resistance to antibiotics of various chemical structure in actinobacteria of the genus Streptomyces is shown to be regulated by Ca2+ ions. The inhibitors of Ca2+/calmodulin and Ca2+/phospholipid-dependent serine/threonine protein kinases (STPK) are found to reduce antibiotic resistance of actinobacteria. The effect of Ca2+ -dependent phosphorylation on the activity of the enzymatic aminoglycoside phosphotransferase system protecting actinobacteria from aminoglycoside antibiotics was studied. It is shown that inhibitors of Ca2+/calmodulin and Ca2+/phospholipid-dependent STPK reduced the Ca2+ -induced kanamycin resistance in Streptomyces lividans cells transformed by a hybrid plasmid which contained the aminoglycoside phosphotransferase VIII (APHVIII) gene. In S. coelicolor A3(2) cells, the protein kinase PK25 responsible for APHVIII phosphorylation in vitro was identified. It is suggested that STPK play a major role in the regulation of antibiotic resistance in actinobacteria.
研究表明,链霉菌属放线菌对各种化学结构抗生素的耐药水平受Ca2+离子调控。发现Ca2+/钙调蛋白和Ca2+/磷脂依赖性丝氨酸/苏氨酸蛋白激酶(STPK)的抑制剂可降低放线菌的抗生素耐药性。研究了Ca2+依赖性磷酸化对保护放线菌免受氨基糖苷类抗生素影响的酶促氨基糖苷磷酸转移酶系统活性的作用。结果表明,Ca2+/钙调蛋白和Ca2+/磷脂依赖性STPK的抑制剂降低了由含有氨基糖苷磷酸转移酶VIII(APHVIII)基因的杂交质粒转化的淡紫链霉菌细胞中Ca2+诱导的卡那霉素耐药性。在天蓝色链霉菌A3(2)细胞中,鉴定出了负责体外APHVIII磷酸化的蛋白激酶PK25。提示STPK在放线菌抗生素耐药性调控中起主要作用。