Freese E, Fortnagel P
J Bacteriol. 1967 Dec;94(6):1957-69. doi: 10.1128/jb.94.6.1957-1969.1967.
Mutants deficient in sporulation were isolated and characterized with respect to antibiotic and protease activity, transformability, growth, and sporulation. All but two mutants could grow on minimal medium containing glucose. The inability of most mutants to incorporate uracil into trichloroacetic acid-precipitable material (ribonucleic acid) during the developmental period, and their response to a number of carbon sources, were used to characterize their biochemical blocks. Reproducible measurements of these responses were possible when the pH of the culture, which changed during growth and greatly influenced the rate of uracil uptake, was adjusted to 6.5. By their response to ribose and glutamate, the sporulation mutants could then be divided into four groups. All mutants of the first three groups produced antibiotic activity against Staphylococcus aureus, whereas all mutants, except one, of the fourth group produced none or very little of this activity. Mutants which did not respond to glutamate belonged to the first three groups; they also grew slowly or not at all on glutamate as sole carbon source. One of these mutants lacked succinic dehydrogenase activity. The results indicate that most of our sporulation mutants are unable to produce or utilize a natural carbon precursor, which is normally used as a slowly available carbon and energy source via the Krebs cycle when other carbon sources are used up. It enters the Krebs cycle as a precursor of alpha-ketoglutarate, probably via acetylcoenzyme A. All mutants of group four are blocked in this pathway before alpha-ketoglutarate.
分离出了孢子形成缺陷型突变体,并对其抗生素和蛋白酶活性、转化能力、生长及孢子形成进行了表征。除两个突变体外,其他所有突变体都能在含有葡萄糖的基本培养基上生长。利用大多数突变体在发育期间无法将尿嘧啶掺入三氯乙酸可沉淀物质(核糖核酸)以及它们对多种碳源的反应,来表征其生化阻断情况。当将生长过程中会发生变化且极大影响尿嘧啶摄取速率的培养基pH值调至6.5时,就能够对这些反应进行可重复测量。根据孢子形成突变体对核糖和谷氨酸的反应,可将其分为四组。前三组的所有突变体都对金黄色葡萄球菌产生抗生素活性,而第四组除一个突变体外的所有突变体均不产生或仅产生极少的这种活性。对谷氨酸无反应的突变体属于前三组;它们在以谷氨酸作为唯一碳源时生长缓慢或根本不生长。其中一个突变体缺乏琥珀酸脱氢酶活性。结果表明,我们的大多数孢子形成突变体无法产生或利用一种天然碳前体,当其他碳源耗尽时,这种碳前体通常会通过三羧酸循环作为一种缓慢可用的碳和能源。它可能通过乙酰辅酶A作为α-酮戊二酸的前体进入三羧酸循环。第四组的所有突变体在α-酮戊二酸之前的这条途径中被阻断。