Wendisch V F, de Graaf A A, Sahm H, Eikmanns B J
Institute of Biotechnology 1, Research Center Jülich, Germany.
J Bacteriol. 2000 Jun;182(11):3088-96. doi: 10.1128/JB.182.11.3088-3096.2000.
Growth of Corynebacterium glutamicum on mixtures of the carbon sources glucose and acetate is shown to be distinct from growth on either substrate alone. The organism showed nondiauxic growth on media containing acetate-glucose mixtures and simultaneously metabolized these substrates. Compared to those for growth on acetate or glucose alone, the consumption rates of the individual substrates were reduced during acetate-glucose cometabolism, resulting in similar total carbon consumption rates for the three conditions. By (13)C-labeling experiments with subsequent nuclear magnetic resonance analyses in combination with metabolite balancing, the in vivo activities for pathways or single enzymes in the central metabolism of C. glutamicum were quantified for growth on acetate, on glucose, and on both carbon sources. The activity of the citric acid cycle was high on acetate, intermediate on acetate plus glucose, and low on glucose, corresponding to in vivo activities of citrate synthase of 413, 219, and 111 nmol. (mg of protein)(-1). min(-1), respectively. The citric acid cycle was replenished by carboxylation of phosphoenolpyruvate (PEP) and/or pyruvate (30 nmol. mg of protein. min(-1)) during growth on glucose. Although levels of PEP carboxylase and pyruvate carboxylase during growth on acetate were similar to those for growth on glucose, anaplerosis occurred solely by the glyoxylate cycle (99 nmol. mg of protein. min(-1)). Surprisingly, the anaplerotic function was fulfilled completely by the glyoxylate cycle (50 nmol. mg of protein. min(-1)) on glucose plus acetate also. Consistent with the predictions deduced from the metabolic flux analyses, a glyoxylate cycle-deficient mutant of C. glutamicum, constructed by targeted deletion of the isocitrate lyase and malate synthase genes, exhibited impaired growth on acetate-glucose mixtures.
谷氨酸棒杆菌在葡萄糖和乙酸盐碳源混合物上的生长表现出与单独在任一底物上生长不同。该生物体在含有乙酸盐 - 葡萄糖混合物的培养基上呈现非双相生长,并同时代谢这些底物。与单独在乙酸盐或葡萄糖上生长相比,在乙酸盐 - 葡萄糖共代谢期间,各个底物的消耗速率降低,导致三种条件下的总碳消耗速率相似。通过随后结合代谢物平衡的核磁共振分析的¹³C标记实验,对谷氨酸棒杆菌在乙酸盐、葡萄糖以及两种碳源上生长时中央代谢途径或单个酶的体内活性进行了定量。柠檬酸循环的活性在乙酸盐上较高,在乙酸盐加葡萄糖上中等,在葡萄糖上较低,相应的柠檬酸合酶体内活性分别为413、219和111 nmol·(mg蛋白质)⁻¹·min⁻¹。在葡萄糖上生长期间,磷酸烯醇式丙酮酸(PEP)和/或丙酮酸的羧化作用补充了柠檬酸循环(30 nmol·(mg蛋白质)⁻¹·min⁻¹)。尽管在乙酸盐上生长期间PEP羧化酶和丙酮酸羧化酶的水平与在葡萄糖上生长时相似,但回补作用仅通过乙醛酸循环发生(99 nmol·(mg蛋白质)⁻¹·min⁻¹)。令人惊讶的是,在葡萄糖加乙酸盐上,乙醛酸循环也完全实现了回补功能(50 nmol·(mg蛋白质)⁻¹·min⁻¹)。与从代谢通量分析得出的预测一致,通过靶向缺失异柠檬酸裂合酶和苹果酸合酶基因构建的谷氨酸棒杆菌乙醛酸循环缺陷型突变体,在乙酸盐 - 葡萄糖混合物上生长受损。