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首页> 外文期刊>Journal of bacteriology >Regulation of Clostridium acetobutylicum metabolism as revealed by mixed-substrate steady-state continuous cultures: role of NADH/NAD ratio and ATP pool.
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Regulation of Clostridium acetobutylicum metabolism as revealed by mixed-substrate steady-state continuous cultures: role of NADH/NAD ratio and ATP pool.

机译:混合底物稳态连续培养揭示了丙酮丁醇梭菌代谢的调节:NADH / NAD比和ATP池的作用。

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摘要

Glycerol-glucose-fed (molar ratio of 2) chemostat cultures of Clostridium acetobutylicum were glucose limited but glycerol sufficient and had a high intracellular NADH/NAD ratio (I. Vasconcelos, L. Girbal, and P. Soucaille, J. Bacteriol. 176:1443-1450, 1994). We report here that the glyceraldehyde-3-phosphate dehydrogenase, one of the key enzymes of the glycolytic pathway, is inhibited by high NADH/NAD ratios. Partial substitution of glucose by pyruvate while maintaining glycerol concentration at a constant level allowed a higher consumption of glycerol in steady-state continuous cultures. However, glycerol-sufficient cultures had a constant flux through the glyceraldehyde-3-phosphate dehydrogenase and a constant NADH/NAD ratio. A high substitution of glucose by pyruvate [P/(G+P) value of 0.67 g/g] provided a carbon-limited culture with butanol and butyrate as the major end products. In this alcohologenic culture, the induction of the NADH-dependent butyraldehyde and the ferredoxin-NAD(P) reductases and the higher expression of alcohol dehydrogenases were related to a high NADH/NAD ratio and a low intracellular ATP concentration. In three different steady-state cultures, the in vitro phosphotransbutyrylase and butyrate-kinase activities decreased with the intracellular ATP concentration, suggesting a transcriptional regulation of these two genes, which are arranged in an operon (K. A. Walter, R. V. Nair, R. V. Carry, G. N. Bennett, and E. T. Papoutsakis, Gene 134:107-111, 1993).
机译:丙酮丁醇梭菌的甘油-葡萄糖喂养的(恒摩尔比为2)化学恒温培养物受葡萄糖限制,但甘油充足,且细胞内NADH / NAD比率高(I.Vasconcelos,L.Girbal和P.Soucaille,J.Bacteriol.176 :1443-1450,1994)。我们在这里报告说,甘油醛-3-磷酸脱氢酶,糖酵解途径的关键酶之一,被高NADH / NAD比抑制。通过丙酮酸部分替代葡萄糖,同时将甘油浓度保持在恒定水平,可以在稳态连续培养中消耗更多的甘油。然而,甘油充足的培养物具有通过3-磷酸甘油醛脱氢酶的恒定通量和恒定的NADH / NAD比。丙酮酸对葡萄糖的高取代[P /(G + P)值为0.67 g / g]提供了以丁醇和丁酸酯为主要终产物的限碳培养物。在这种产醇培养物中,NADH依赖性丁醛和铁氧还蛋白-NAD(P)还原酶的诱导以及醇脱氢酶的较高表达与高NADH / NAD比和低细胞内ATP浓度有关。在三种不同的稳态培养物中,体外磷酸转丁酰酶和丁酸激酶活性随细胞内ATP浓度的降低而降低,表明这两个基因的转录调控排列在操纵子中(KA Walter,RV Nair,RV Carry,GN Bennett和ET Papoutsakis,Gene 134:107-111,1993)。

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