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一种异源还原酶会影响重组酿酒酵母的氧化还原平衡。

A heterologous reductase affects the redox balance of recombinant Saccharomyces cerevisiae.

作者信息

Meinander Nina, Zacchi Guido, Hahn-Hägerdal Bärbel

机构信息

Applied Microbiology.

Chemical Engineering l, Lund Institute of Technology/University of Lund, PO Box 124, S-22100 Lund, Sweden.

出版信息

Microbiology (Reading). 1996 Jan;142 ( Pt 1):165-172. doi: 10.1099/13500872-142-1-165.

Abstract

Recombinant Saccharomyces cerevisiae harbouring the xylose reductase (XR) gene XYL1 from Pichia stipitis was grown in anoxic chemostat culture at two different dilution rates. At each dilution rate a transient experiment, encompassing a shift in the sugar content of the medium from glucose to glucose plus xylose was performed. The steady states at the beginning and the end of the transients were compared in terms of specific product fluxes from glucose metabolism. At both dilution rates, the specific glycerol flux decreased and the specific acetate and CO2 fluxes increased. The specific ethanol flux was not affected. At the lower dilution rate, the production of biomass decreased during the transient, but at the higher dilution rate it increased. The changes in product pattern can be explained as being due to the redox perturbation caused by the consumption of reduced cofactors in the XR-catalysed reaction. Regeneration of NAD partly through xylose reduction instead of glycerol production decreased the formation of glycerol. Additionally, xylose reduction activated those pathways which produce reduced cofactors, such as acetate formation and the pentose phosphate pathway, indicated by increased acetate and CO2 production. The dual cofactor specificity of XR, with a preference for NADPH over NADH, was evident from the effects of xylose reduction on product fluxes. Comparison of the xylose reduction rates at low and high glucose flux indicated that the supply of reduced cofactors partly controlled the reaction rate. At the higher dilution rate, control by some other factor such as xylose transport or XR activity increased. Calculation of carbon balances at the steady states showed that all substrate carbon was recovered in biomass or products. Based on the specific product fluxes, calculations of quantitative cofactor balances at the steady states was attempted. However, sensitivity calculations showed that analysis errors in the range of 5% caused substantial errors in the cofactor balance, without affecting the carbon balance.

摘要

携带来自树干毕赤酵母木糖还原酶(XR)基因XYL1的重组酿酒酵母在两种不同稀释率下于缺氧恒化器培养中生长。在每个稀释率下,进行了一个瞬态实验,该实验包括培养基中糖含量从葡萄糖转变为葡萄糖加木糖的过程。根据葡萄糖代谢的特定产物通量,比较了瞬态开始和结束时的稳态。在两种稀释率下,特定甘油通量均降低,特定乙酸盐和二氧化碳通量增加。特定乙醇通量未受影响。在较低稀释率下,瞬态期间生物量产量下降,但在较高稀释率下则增加。产物模式的变化可解释为是由于XR催化反应中还原型辅因子消耗引起的氧化还原扰动。部分通过木糖还原而非甘油生产来再生NAD降低了甘油的形成。此外,木糖还原激活了那些产生还原型辅因子的途径,如乙酸盐形成和戊糖磷酸途径,这通过乙酸盐和二氧化碳产量增加得以表明。XR对NADPH的偏好高于NADH的双重辅因子特异性,从木糖还原对产物通量的影响中明显可见。低葡萄糖通量和高葡萄糖通量下木糖还原率的比较表明,还原型辅因子的供应部分控制了反应速率。在较高稀释率下,由其他一些因素如木糖转运或XR活性的控制作用增强。稳态下碳平衡的计算表明,所有底物碳均在生物量或产物中得到回收。基于特定产物通量,尝试了稳态下定量辅因子平衡的计算。然而,敏感性计算表明,5%范围内的分析误差在辅因子平衡中会导致相当大的误差,而不影响碳平衡。

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