Puchkov E O, Yurkova T V, Golubev W I
Institute of Biochemistry and Physiology of Microorganisms, Russian Academy of Sciences, Pushchino, Russian Federation.
Biochim Biophys Acta. 1998 Jun 5;1381(1):61-7. doi: 10.1016/s0304-4165(98)00012-9.
Killer toxin (microcin) produced by Cryptococcus humicola 9-6 induced interaction of the fluorogenic dyes, ethidium bromide, propidium iodide, and hemimagnesium 8-anilino-1-naphtalenesulfonate, with the sensitive strain of Cryptococcus terreus VKM Y-2253. The toxin also made the cells susceptible to cetyltrimethylammonium bromide and leaky for K+. When excited at 360 nm, cell-bound ethidium (propidium) fluorescence was enhanced by 8-anilino-1-naphtalensulfonate, and cell-bound 8-anilino-1-naphtalensulfonate fluorescence was quenched by ethidium (propidium), indicating energy transfer from 8-anilino-1-naphtalensulfonate to ethidium (propidium). These results suggest that at least a portion of the probe molecules had the same binding site, possibly the cytoplasmic membrane. The parameters of kinetics of microcin action were evaluated fluorometrically. They were found to be identical for all probes and depended on microcin concentration. The fluorescence increment of ethidium and 8-anilino-1-naphtalensulfonate upon binding to microcin-treated cells correlated with the fraction of stainable cells and viability.
土生隐球酵母9-6产生的杀伤毒素(微菌素)诱导了荧光染料溴化乙锭、碘化丙啶和半镁8-苯胺基-1-萘磺酸盐与土生隐球酵母敏感菌株VKM Y-2253之间的相互作用。该毒素还使细胞对十六烷基三甲基溴化铵敏感,并导致钾离子泄漏。当在360nm激发时,细胞结合的溴化乙锭(碘化丙啶)荧光被8-苯胺基-1-萘磺酸盐增强,而细胞结合的8-苯胺基-1-萘磺酸盐荧光被溴化乙锭(碘化丙啶)淬灭,这表明能量从8-苯胺基-1-萘磺酸盐转移到溴化乙锭(碘化丙啶)。这些结果表明,至少一部分探针分子具有相同的结合位点,可能是细胞质膜。用荧光法评估了微菌素作用的动力学参数。发现所有探针的参数相同,且取决于微菌素浓度。溴化乙锭和8-苯胺基-1-萘磺酸盐与经微菌素处理的细胞结合后的荧光增量与可染色细胞的比例和活力相关。