Dalal F R, Gots R E, Gots J S
J Bacteriol. 1966 Feb;91(2):507-13. doi: 10.1128/jb.91.2.507-513.1966.
Dalal, Fram R. (University of Pennsylvania, Philadelphia), Ronald E. Gots, and Joseph S. Gots. Mechanism of adenine inhibition in adenine-sensitive mutants of Salmonella typhimurium. J. Bacteriol. 91: 507-513. 1966.-The inhibition of growth of Salmonella typhimurium by adenine was studied with three adenine-sensitive mutants. These mutants were acutely sensitive to inhibition by adenine, were prototrophic in their growth requirements, and represented mutational events in three different genetic loci. In all cases, inhibition by adenine was relieved noncompetitively by thiamine (or its pyrimidine moiety), pantothenate (or its pantoyl moiety), and methionine alone or, more efficiently, in the presence of lysine. Kinetics of reversal indicated that adenine inhibited the synthesis of the reversing agents, probably at the level of a common factor required for their syntheses, such as the folic acid coenzymes. Support for this inference has been found by the facts that one of the mutants was identified as a partial auxotroph for p-aminobenzoic acid, and sulfadiazine could sensitize the wild type to acute inhibition by adenine.
达拉尔,弗拉姆·R.(宾夕法尼亚大学,费城),罗纳德·E.戈茨,约瑟夫·S.戈茨。鼠伤寒沙门氏菌腺嘌呤敏感突变体中腺嘌呤抑制的机制。《细菌学杂志》91: 507 - 513。1966年。——利用三个腺嘌呤敏感突变体研究了腺嘌呤对鼠伤寒沙门氏菌生长的抑制作用。这些突变体对腺嘌呤抑制极为敏感,在生长需求上是原养型的,代表了三个不同基因位点的突变事件。在所有情况下,单独的硫胺素(或其嘧啶部分)、泛酸盐(或其泛酰部分)和蛋氨酸,或者在赖氨酸存在时更有效地解除了腺嘌呤的抑制作用。逆转动力学表明,腺嘌呤抑制了逆转剂的合成,可能是在它们合成所需的共同因子水平上,如叶酸辅酶。有以下事实支持这一推断:其中一个突变体被鉴定为对对氨基苯甲酸部分营养缺陷型,并且磺胺嘧啶可使野生型对腺嘌呤的急性抑制敏感。