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在自然丰度下通过2H NMR定量测定肠膜明串珠菌发酵过程中葡萄糖向乙醇的前R和前S亚甲基位置的氢转移的非等效性。

Non-equivalence of hydrogen transfer from glucose to the pro-R and pro-S methylene positions of ethanol during fermentation by Leuconostoc mesenteroides quantified by 2H NMR at natural abundance.

作者信息

Robins Richard J, Pétavy François, Nemmaoui Youssef, Ayadi Farouk, Silvestre Virginie, Zhang Ben-Li

机构信息

Interdisciplinary Chemistry: Synthesis, Analysis, Modelling (CEISAM), UMR CNRS 6230, University of Nantes, 2 rue de la Houssinière, Nantes, France.

出版信息

J Biol Chem. 2008 Apr 11;283(15):9704-12. doi: 10.1074/jbc.M710272200. Epub 2008 Feb 7.

Abstract

The anaerobic fermentation of glucose by Leuconostoc mesenteroides via the reductive pentose phosphate pathway leads to the accumulation of lactic acid and ethanol. The isotope redistribution coefficients (a(ij)) that characterize the specific derivation of each hydrogen atom in ethanol in relation to the non-exchangeable hydrogen atoms in glucose and the medium water have been determined using quantitative (2)H NMR. First, it is confirmed that the hydrogens of the methylene group are related only to the 1 and 3 positions of glucose via the NAD(P)H pool and not to the 4 position, in contrast to ethanol produced by Saccharomyces cerevisiae. Second, it is found that the conversion factors (C(f)) for the transfer of hydrogen to the pro-S and pro-R positions of the methylene group are not equivalent: the C(f)-1-R:C(f)-1-S ratio is 2.1, whereas the C(f)-3-R:C(f)-3-S ratio is 0.8. It is shown that this non-equivalence is not determined by the stereochemistry of the terminal NADH- and NADPH-dependent alcohol dehydrogenases, but is dependent on the cofactor selectivities of the reductive and oxidative steps of the reduced nucleotide cycle.

摘要

嗜柠檬酸明串珠菌通过还原性磷酸戊糖途径对葡萄糖进行厌氧发酵会导致乳酸和乙醇的积累。利用定量氘核磁共振已确定了同位素再分配系数(a(ij)),该系数表征了乙醇中每个氢原子相对于葡萄糖和培养基水中不可交换氢原子的特定来源。首先,已证实亚甲基的氢仅通过NAD(P)H池与葡萄糖的1位和3位相关,而与4位无关,这与酿酒酵母产生的乙醇不同。其次,发现氢转移至亚甲基的前手性S和前手性R位置的转换因子(C(f))并不相等:C(f)-1-R:C(f)-1-S的比值为2.1,而C(f)-3-R:C(f)-3-S的比值为0.8。结果表明,这种不等性不是由末端依赖NADH和NADPH的醇脱氢酶的立体化学决定的,而是取决于还原核苷酸循环的还原步骤和氧化步骤的辅因子选择性。

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