Warner Jessica B, Lolkema Juke S
Molecular Microbiology, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Kerklaan 30, 9751 NN Haren, The Netherlands1.
Microbiology (Reading). 2002 Nov;148(Pt 11):3405-3412. doi: 10.1099/00221287-148-11-3405.
Bacillus subtilis 168 was assayed for its growth on tricarboxylic acid (TCA) cycle intermediates and related compounds as the sole carbon sources. Growth of the organism was supported by citrate, D-isocitrate, succinate, fumarate and L-malate, whereas no growth was observed in the presence of cis-aconitate,2-oxoglutarate, D-malate, oxaloacetate and tricarballylate. Growth of the organism on the tricarboxylates citrate and D-isocitrate required the presence of functional CitM, an Mg(2+)-citrate transporter, whereas its growth on succinate, fumarate and L-malate appeared to be CitM-independent. Interestingly, the naturally occurring enantiomer D-isocitrate was favoured over L-isocitrate by the organism. Like citrate, D-isocitrate was shown to be an inducer of citM expression in B. subtilis. The addition of 1 mM Mg(2+) to the growth medium improved growth of the organism on both citrate and D-isocitrate, suggesting that D-isocitrate was taken up by CitM in complex with divalent metal ions. Subsequently, the ability of CitM to transport D-isocitrate was demonstrated by competition experiments and by heterologous exchange in right-side-out membrane vesicles prepared from E. coli cells expressing citM. None of the other TCA cycle intermediates and related compounds tested were recognized by CitM. Uptake experiments using radioactive (63)Ni(2+) provided direct evidence that D-isocitrate is transported in complex with divalent metal ions.
对枯草芽孢杆菌168进行了检测,以研究其在三羧酸(TCA)循环中间体及相关化合物作为唯一碳源时的生长情况。该生物体可在柠檬酸盐、D -异柠檬酸盐、琥珀酸盐、富马酸盐和L -苹果酸盐上生长,而在顺乌头酸盐、2 -氧代戊二酸、D -苹果酸盐、草酰乙酸盐和三羧甲基丙烷酸盐存在的情况下未观察到生长。该生物体在三羧酸盐柠檬酸盐和D -异柠檬酸盐上的生长需要功能性的CitM(一种Mg(2 +) -柠檬酸盐转运蛋白)的存在,而其在琥珀酸盐、富马酸盐和L -苹果酸盐上的生长似乎不依赖于CitM。有趣的是,该生物体更倾向于天然存在的对映体D -异柠檬酸盐而非L -异柠檬酸盐。与柠檬酸盐一样,D -异柠檬酸盐被证明是枯草芽孢杆菌中citM表达的诱导剂。向生长培养基中添加1 mM Mg(2 +)可改善该生物体在柠檬酸盐和D -异柠檬酸盐上的生长,这表明D -异柠檬酸盐是与二价金属离子形成复合物后被CitM摄取的。随后,通过竞争实验以及在表达citM的大肠杆菌细胞制备的外翻膜囊泡中的异源交换,证明了CitM转运D -异柠檬酸盐的能力。所测试的其他TCA循环中间体及相关化合物均未被CitM识别。使用放射性(63)Ni(2 +)进行的摄取实验提供了直接证据,表明D -异柠檬酸盐是与二价金属离子形成复合物进行转运的。