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巨大芽孢杆菌去包被孢子的萌发

Germination of the decoated spores of Bacillus megaterium.

作者信息

Nakatani Y, Imagawa M, Takubo Y, Nishikawa J, Nishihara T, Kondo M

出版信息

Microbiol Immunol. 1985;29(12):1139-49. doi: 10.1111/j.1348-0421.1985.tb00904.x.

Abstract

Decoated spores of Bacillus megaterium ATCC 12872 were prepared by extracting the inner coat components with an alkaline solution containing sodium dodecyl sulfate and dithiothreitol (SDS-DTT) from outer coat-deficient mutant spores, which were produced from one of the mutants isolated and named MAE-05 by us. The decoated mutant spores germinated as well as the intact spores of the mutant and the parent, indicating that the outer and inner spore cats cannot be essential structures for the initiation of germination. When the SDS-DTT-treated MAE-05 spores were converted to H-spores by incubation in citrate-phosphate buffer (pH 3.5) at 30 C for 3 hr, they lost their germinability by glucose and KNO3. Ca-spores, prepared by treating H-spores with 10 mM calcium acetate at 37 C for 60 min, regained the germinability. Experiments on the interaction of 45Ca with the cortex and the inner membrane isolated from H-spores suggested that the calcium present in the inner membrane might be related to germinability.

摘要

巨大芽孢杆菌ATCC 12872的脱壳孢子是通过用含有十二烷基硫酸钠和二硫苏糖醇(SDS-DTT)的碱性溶液从外膜缺陷型突变体孢子中提取内膜成分制备的,这些突变体孢子是我们分离并命名为MAE-05的其中一个突变体产生的。脱壳突变体孢子的萌发情况与突变体和亲本的完整孢子一样,这表明孢子的外膜和内膜对于萌发起始并非必需结构。当经SDS-DTT处理的MAE-05孢子在30℃的柠檬酸盐-磷酸盐缓冲液(pH 3.5)中孵育3小时转化为H型孢子时,它们失去了对葡萄糖和硝酸钾的可萌发能力。通过在37℃用10 mM醋酸钙处理H型孢子60分钟制备的Ca型孢子恢复了可萌发能力。关于45Ca与从H型孢子分离的皮层和内膜相互作用的实验表明,内膜中存在的钙可能与可萌发能力有关。

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