Veiga da Cunha M, Foster M A
Department of Biochemistry, University of Oxford, United Kingdom.
J Bacteriol. 1992 Feb;174(3):1013-9. doi: 10.1128/jb.174.3.1013-1019.1992.
The simultaneous fermentation of glycerol and sugar by lactobacillus brevis B22 and Lactobacillus buchneri B190 increases both the growth rate and total growth. The reduction of glycerol to 1,3-propanediol by the lactobacilli was found to influence the metabolism of the sugar cofermented by channelling some of the intermediate metabolites (e.g., pyruvate) towards NADH-producing (rather than NADH-consuming) reactions. Ultimately, the absolute requirement for NADH to prevent the accumulation of 3-hydroxypropionaldehyde leads to a novel lactate-glycerol cofermentation. As a result, additional ATP can be made not only by (i) converting pyruvate to acetate via acetyl phosphate rather than to the ethanol usually found and (ii) oxidizing part of the intermediate pyruvate to acetate instead of the usual reduction to lactate but also by (iii) reoxidation of accumulated lactate to acetate via pyruvate. The conversion of lactate to pyruvate is probably catalyzed by NAD-independent lactate dehydrogenases that are found only in the cultures oxidizing lactate and producing 1,3-propanediol, suggesting a correlation between the expression of these enzymes and a raised intracellular NAD/NADH ratio. The enzymes metabolizing glycerol (glycerol dehydratase and 1,3-propanediol dehydrogenase) were expressed in concert without necessary induction by added glycerol, although their expression may also be influenced by the intracellular NAD/NADH ratio set by the different carbohydrates fermented.
短乳杆菌B22和布氏乳杆菌B190对甘油和糖的同步发酵可提高生长速率和总生长量。研究发现,乳杆菌将甘油还原为1,3 - 丙二醇会影响共发酵糖的代谢,它通过将一些中间代谢物(如丙酮酸)导向产生NADH(而非消耗NADH)的反应来实现。最终,由于绝对需要NADH来防止3 - 羟基丙醛的积累,从而导致了一种新型的乳酸 - 甘油共发酵。结果,不仅可以通过以下方式产生额外的ATP:(i)经由乙酰磷酸将丙酮酸转化为乙酸盐,而不是转化为通常生成的乙醇;(ii)将部分中间丙酮酸氧化为乙酸盐,而不是通常还原为乳酸盐;还可以通过(iii)经由丙酮酸将积累的乳酸盐再氧化为乙酸盐。乳酸盐向丙酮酸的转化可能由仅在氧化乳酸盐并产生1,3 - 丙二醇的培养物中发现的不依赖NAD的乳酸脱氢酶催化,这表明这些酶的表达与细胞内升高的NAD/NADH比值之间存在相关性。代谢甘油的酶(甘油脱水酶和1,3 - 丙二醇脱氢酶)协同表达,无需添加甘油的诱导,尽管它们的表达也可能受到由不同发酵碳水化合物设定的细胞内NAD/NADH比值的影响。