Institut de Biochimie Cellulaire et Neurochimie du CNRS, 1 rue Camille St-Saëns, F-33077, Bordeaux Cedex, France.
Curr Genet. 1984 Sep;8(7):507-16. doi: 10.1007/BF00410437.
One mutant resistant to carbonylcyanide m-chlorophenylhydrazone (CCCP), an uncoupler of oxidative phosphorylation, was isolated in Saccharomyces cerevisiae.Genetic analysis showed that a single nuclear gene is responsible for increased resistance; this gene was dominant.The mutant showed cross-resistance or collateral sensitivity to several chemically-unrelated inhibitors (cycloheximide, dinitrophenol, tributhyltin chloride, chloramphenicol).The resistance of the mutant is related to a decreased uptake of CCCP which is not expressed in glucose-starved cells. It was shown that glucose induced a CCCP efflux which was more efficient in the mutant than in the wild-type cells. This effect was correlated to a greater acidification of the internal pH by glucose addition in the mutant cells.It was proposed that resistance was not due to a change of permeability of the plasmic membrane itself but to the change of internal pH which determines the extent of accumulation of weak acids or bases.
在酿酒酵母中分离到一株对羰基氰化物 m-氯代苯腙(CCCP),一种氧化磷酸化解偶联剂有抗性的突变株。遗传分析表明,一个单一的核基因负责增加抗性;该基因是显性的。该突变株对几种化学上无关的抑制剂(放线菌酮、二硝基酚、三丁基锡氯化物、氯霉素)表现出交叉抗性或伴生性敏感。突变株的抗性与 CCCP 的摄取减少有关,而在饥饿葡萄糖的细胞中不表达。结果表明,葡萄糖诱导 CCCP 外流,在突变株中比在野生型细胞中更有效。这种效应与葡萄糖添加使内部 pH 更酸化相关,在突变细胞中。有人提出,抗性不是由于质膜本身通透性的改变,而是由于内部 pH 的改变,这决定了弱酸碱的积累程度。