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由酿酒酵母ADH6基因编码的一种5-羟甲基糠醛还原酶赋予了对HMF的耐受性。

A 5-hydroxymethyl furfural reducing enzyme encoded by the Saccharomyces cerevisiae ADH6 gene conveys HMF tolerance.

作者信息

Petersson Anneli, Almeida João R M, Modig Tobias, Karhumaa Kaisa, Hahn-Hägerdal Bärbel, Gorwa-Grauslund Marie F, Lidén Gunnar

机构信息

Department of Chemical Engineering, Lund University, PO Box 124, S-221 00 Lund, Sweden.

出版信息

Yeast. 2006 Apr 30;23(6):455-64. doi: 10.1002/yea.1370.

Abstract

The fermentation of lignocellulose hydrolysates by Saccharomyces cerevisiae for fuel ethanol production is inhibited by 5-hydroxymethyl furfural (HMF), a furan derivative which is formed during the hydrolysis of lignocellulosic materials. The inhibition can be avoided if the yeast strain used in the fermentation has the ability to reduce HMF to 5-hydroxymethylfurfuryl alcohol. To enable the identification of enzyme(s) responsible for HMF conversion in S. cerevisiae, microarray analyses of two strains with different abilities to convert HMF were performed. Based on the expression data, a subset of 15 reductase genes was chosen to be further examined using an overexpression strain collection. Three candidate genes were cloned from two different strains, TMB3000 and the laboratory strain CEN.PK 113-5D, and overexpressed using a strong promoter in the strain CEN.PK 113-5D. Strains overexpressing ADH6 had increased HMF conversion activity in cell-free crude extracts with both NADPH and NADH as co-factors. In vitro activities were recorded of 8 mU/mg with NADH as co-factor and as high as 1200 mU/mg for the NADPH-coupled reduction. Yeast strains overexpressing ADH6 also had a substantially higher in vivo conversion rate of HMF in both aerobic and anaerobic cultures, showing that the overexpression indeed conveyed the desired increased reduction capacity.

摘要

酿酒酵母发酵木质纤维素水解产物生产燃料乙醇的过程会受到5-羟甲基糠醛(HMF)的抑制,HMF是一种呋喃衍生物,在木质纤维素材料水解过程中形成。如果发酵中使用的酵母菌株有能力将HMF还原为5-羟甲基糠醇,就可以避免这种抑制。为了鉴定酿酒酵母中负责HMF转化的酶,对两种具有不同HMF转化能力的菌株进行了微阵列分析。基于表达数据,选择了15个还原酶基因的子集,使用过表达菌株文库进行进一步检测。从两种不同菌株TMB3000和实验室菌株CEN.PK 113-5D中克隆了三个候选基因,并在菌株CEN.PK 113-5D中使用强启动子进行过表达。过表达ADH6的菌株在以NADPH和NADH作为辅因子的无细胞粗提物中,HMF转化活性有所提高。以NADH作为辅因子时,体外活性记录为8 mU/mg,而对于NADPH偶联的还原反应,活性高达1200 mU/mg。过表达ADH6的酵母菌株在需氧和厌氧培养中HMF的体内转化率也显著更高,表明过表达确实赋予了所需的增强还原能力。

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