Tochikubo K
J Bacteriol. 1971 Nov;108(2):652-61. doi: 10.1128/jb.108.2.652-661.1971.
The chemical and enzymatic properties of the cytochrome system in the particulate preparations obtained from dormant spores, germinated spores, young vegetative cells, and vegetative cells of Bacillus subtilis PCI219 were investigated. Difference spectra of particulate fractions from dormant spores of this strain suggested the presence of cytochromes a, a(3), b, c(+c(1)), and o. All of the cytochrome components were present in dormant spores and in germinated spores and vegetative cells at all stages which were investigated. Concentrations of cytochromes a, a(3), b, and c(+c(1)) increased during germination, outgrowth, and vegetative growth, but that of cytochrome o was highest in dormant spores. As the cytochrome components were reducible by reduced nicotinamide adenine dinucleotide (NADH), they were believed to be metabolically active. Difference spectra of whole-cell suspensions of dormant spores and vegetative cells were coincident with those of the particulate fractions. NADH oxidase and cytochrome c oxidase were present in dormant spores, germinated spores, and vegetative cells at all stages after germination, but succinate cytochrome c reductase was not present in dormant spores. Cytochrome c oxidase and succinate cytochrome c reductase activities increased with growth, but NADH oxidase activity was highest in germinated spores and lowest in vegetative cells. There was no striking difference between the effects of respiratory inhibitors on NADH oxidase in dormant spores and those on NADH oxidase in vegetative cells.
对枯草芽孢杆菌PCI219的休眠孢子、萌发孢子、幼嫩营养细胞和营养细胞中获得的颗粒制剂中的细胞色素系统的化学和酶学性质进行了研究。该菌株休眠孢子颗粒级分的差异光谱表明存在细胞色素a、a3、b、c(+c1)和o。在所有研究阶段,所有细胞色素成分均存在于休眠孢子、萌发孢子和营养细胞中。细胞色素a、a3、b和c(+c1)的浓度在萌发、生长和营养生长过程中增加,但细胞色素o的浓度在休眠孢子中最高。由于细胞色素成分可被还原型烟酰胺腺嘌呤二核苷酸(NADH)还原,因此认为它们具有代谢活性。休眠孢子和营养细胞的全细胞悬浮液的差异光谱与颗粒级分的光谱一致。NADH氧化酶和细胞色素c氧化酶在休眠孢子、萌发孢子以及萌发后各阶段的营养细胞中均存在,但琥珀酸细胞色素c还原酶在休眠孢子中不存在。细胞色素c氧化酶和琥珀酸细胞色素c还原酶活性随生长而增加,但NADH氧化酶活性在萌发孢子中最高,在营养细胞中最低。呼吸抑制剂对休眠孢子中NADH氧化酶的作用与对营养细胞中NADH氧化酶的作用之间没有显著差异。