Ghei O K, Kay W W
J Bacteriol. 1973 Apr;114(1):65-79. doi: 10.1128/jb.114.1.65-79.1973.
The transport of the tricarboxylic acid cycle C(4)-dicarboxylic acids was studied in both the wild-type strain and tricarboxylic acid cycle mutants of Bacillus subtilis. Active transport of malate, fumarate, and succinate was found to be inducible by these dicarboxylic acids or by precursors to them, whereas glucose or closely related metabolites catabolite-repressed their uptake. l-Malate was found to be the best dicarboxylic acid transport inducer in succinic dehydrogenase, fumarase, and malic dehydrogenase mutants. Succinate and fumarate are accumulated over 100-fold in succinic dehydrogenase and fumarase mutants, respectively, whereas mutants lacking malate dehydrogenase were unable to accumulate significant quantities of the C(4)-dicarboxylic acids. The stereospecificity of this transport system was studied from a comparison of the rates of competitive inhibition of both succinate uptake and efflux in a succinate dehydrogenase mutant by utilizing thirty dicarboxylic acid analogues. The system was specific for the C(4)-dicarboxylic acids of the tricarboxylic acid cycle, neither citrate nor alpha-ketoglutarate were effective competitive inhibitors. Of a wide variety of metabolic inhibitors tested, inhibiors of oxidative phosphorylation and of the formation of proton gradients were the most potent inhibitors of transport. From the kinetics of dicarboxylic acid transport (K(m) approximately 10(-4) M for succinate or fumarate in succinic acid dehydrogenase and fumarase mutants) and from the competitive inhibition studies, it was concluded that an inducible dicarboxylic acid transport system mediates the entry of malate, fumarate, or succinate into B. subtilis. Mutants devoid of alpha-ketoglutarate dehydrogenase were shown to accumulate both alpha-ketoglutarate and glutamate, and these metabolites subsequently inhibited the transport of all the C(4)-dicarboxylic acids, suggesting a regulatory role.
在枯草芽孢杆菌的野生型菌株和三羧酸循环突变体中研究了三羧酸循环C(4)-二羧酸的转运。发现苹果酸、富马酸和琥珀酸的主动转运可被这些二羧酸或其前体诱导,而葡萄糖或密切相关的代谢物会对它们的摄取产生分解代谢物阻遏作用。在琥珀酸脱氢酶、延胡索酸酶和苹果酸脱氢酶突变体中,l-苹果酸被发现是最佳的二羧酸转运诱导剂。琥珀酸脱氢酶和延胡索酸酶突变体分别积累了超过100倍的琥珀酸和富马酸,而缺乏苹果酸脱氢酶的突变体无法积累大量的C(4)-二羧酸。通过利用30种二羧酸类似物比较琥珀酸脱氢酶突变体中琥珀酸摄取和流出的竞争性抑制速率,研究了该转运系统的立体特异性。该系统对三羧酸循环的C(4)-二羧酸具有特异性,柠檬酸和α-酮戊二酸都不是有效的竞争性抑制剂。在测试的多种代谢抑制剂中,氧化磷酸化抑制剂和质子梯度形成抑制剂是最有效的转运抑制剂。从二羧酸转运动力学(琥珀酸脱氢酶和延胡索酸酶突变体中琥珀酸或富马酸的K(m)约为10(-4) M)以及竞争性抑制研究得出结论,一种可诱导的二羧酸转运系统介导苹果酸、富马酸或琥珀酸进入枯草芽孢杆菌。缺乏α-酮戊二酸脱氢酶的突变体被证明会积累α-酮戊二酸和谷氨酸盐,并且这些代谢物随后会抑制所有C(4)-二羧酸的转运,表明其具有调节作用。