Bausch C, Peekhaus N, Utz C, Blais T, Murray E, Lowary T, Conway T
Department of Microbiology, The Ohio State University, Columbus, Ohio 43210, USA.
J Bacteriol. 1998 Jul;180(14):3704-10. doi: 10.1128/JB.180.14.3704-3710.1998.
The presence of two systems in Escherichia coli for gluconate transport and phosphorylation is puzzling. The main system, GntI, is well characterized, while the subsidiary system, GntII, is poorly understood. Genomic sequence analysis of the region known to contain genes of the GntII system led to a hypothesis which was tested biochemically and confirmed: the GntII system encodes a pathway for catabolism of L-idonic acid in which D-gluconate is an intermediate. The genes have been named accordingly: the idnK gene, encoding a thermosensitive gluconate kinase, is monocistronic and transcribed divergently from the idnD-idnO-idnT-idnR operon, which encodes L-idonate 5-dehydrogenase, 5-keto-D-gluconate 5-reductase, an L-idonate transporter, and an L-idonate regulatory protein, respectively. The metabolic sequence is as follows: IdnT allows uptake of L-idonate; IdnD catalyzes a reversible oxidation of L-idonate to form 5-ketogluconate; IdnO catalyzes a reversible reduction of 5-ketogluconate to form D-gluconate; IdnK catalyzes an ATP-dependent phosphorylation of D-gluconate to form 6-phosphogluconate, which is metabolized further via the Entner-Doudoroff pathway; and IdnR appears to act as a positive regulator of the IdnR regulon, with L-idonate or 5-ketogluconate serving as the true inducer of the pathway. The L-idonate 5-dehydrogenase and 5-keto-D-gluconate 5-reductase reactions were characterized both chemically and biochemically by using crude cell extracts, and it was firmly established that these two enzymes allow for the redox-coupled interconversion of L-idonate and D-gluconate via the intermediate 5-ketogluconate. E. coli K-12 strains are able to utilize L-idonate as the sole carbon and energy source, and as predicted, the ability of idnD, idnK, idnR, and edd mutants to grow on L-idonate is altered.
大肠杆菌中存在两种用于葡萄糖酸盐转运和磷酸化的系统,这令人感到困惑。主要系统GntI已得到充分表征,而辅助系统GntII却了解甚少。对已知包含GntII系统基因的区域进行基因组序列分析,得出了一个假设,该假设经过生化测试并得到证实:GntII系统编码一条L-艾杜糖酸分解代谢途径,其中D-葡萄糖酸盐是一种中间产物。这些基因也因此被命名:编码热敏葡萄糖酸盐激酶的idnK基因是单顺反子,其转录方向与idnD-idnO-idnT-idnR操纵子相反,该操纵子分别编码L-艾杜糖酸5-脱氢酶、5-酮-D-葡萄糖酸盐5-还原酶、一种L-艾杜糖酸转运蛋白和一种L-艾杜糖酸调节蛋白。代谢顺序如下:IdnT允许L-艾杜糖酸的摄取;IdnD催化L-艾杜糖酸可逆氧化形成5-酮葡萄糖酸盐;IdnO催化5-酮葡萄糖酸盐可逆还原形成D-葡萄糖酸盐;IdnK催化D-葡萄糖酸盐的ATP依赖性磷酸化形成6-磷酸葡萄糖酸盐,其通过Entner-Doudoroff途径进一步代谢;IdnR似乎作为IdnR调节子的正调控因子,L-艾杜糖酸或5-酮葡萄糖酸盐作为该途径的真正诱导剂。通过使用粗细胞提取物对L-艾杜糖酸5-脱氢酶和5-酮-D-葡萄糖酸盐5-还原酶反应进行了化学和生化表征,并且确切证实这两种酶通过中间产物5-酮葡萄糖酸盐实现L-艾杜糖酸和D-葡萄糖酸盐的氧化还原偶联相互转化。大肠杆菌K-12菌株能够利用L-艾杜糖酸作为唯一的碳源和能源,正如预测的那样,idnD、idnK、idnR和edd突变体在L-艾杜糖酸上生长的能力发生了改变。