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

被引:209
作者
Petersson, Annell
Almeida, Joao R. M.
Modig, Tobias
Karhumaa, Kaisa
Hahn-Hagerdal, Barbel
Gorwa-Grauslund, Marie F.
Liden, Gunnar
机构
[1] Lund Univ, Dept Chem Engn, S-22100 Lund, Sweden
[2] Lund Univ, Dept Appl Microbiol, S-22100 Lund, Sweden
关键词
5-hydroxymethyl furfural; ADH6; genome-wide analysis; lignocellulose hydrolysates; Saccharomyces cerevisiae;
D O I
10.1002/yea.1370
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:455 / 464
页数:10
相关论文
共 33 条
[1]  
BANERJEE N, 1976, P ANN CONV SUG TECHN, V41, pG75
[2]   The fermentation performance of nine strains of Saccharomyces cerevisiae in batch and fed-batch cultures in dilute-acid wood hydrolysate [J].
Brandberg, T ;
Franzén, CJ ;
Gustafsson, L .
JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 2004, 98 (02) :122-125
[3]   PROLONGED INCUBATION IN CALCIUM-CHLORIDE IMPROVES THE COMPETENCE OF ESCHERICHIA-COLI-CELLS [J].
DAGERT, M ;
EHRLICH, SD .
GENE, 1979, 6 (01) :23-28
[4]   Effects of lignocellulose degradation products on ethanol fermentations of glucose and xylose by Saccharomyces cerevisiae, Zymomonas mobilis, Pichia stipitis, and Candida shehatae [J].
Delgenes, JP ;
Moletta, R ;
Navarro, JM .
ENZYME AND MICROBIAL TECHNOLOGY, 1996, 19 (03) :220-225
[5]   The catabolism of amino acids to long chain and complex alcohols in Saccharomyces cerevisiae [J].
Dickinson, JR ;
Eshantha, L ;
Salgado, J ;
Hewlins, MJE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (10) :8028-8034
[6]   A review of the production of ethanol from softwood [J].
Galbe, M ;
Zacchi, G .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2002, 59 (06) :618-628
[7]   STUDIES ON THE TRANSFORMATION OF INTACT YEAST-CELLS BY THE LIAC/S-DNA/PEG PROCEDURE [J].
GIETZ, RD ;
SCHIESTL, RH ;
WILLEMS, AR ;
WOODS, RA .
YEAST, 1995, 11 (04) :355-360
[8]   Simultaneous genomic overexpression of seven glycolytic enzymes in the yeast Saccharomyces cerevisiae [J].
Hauf, J ;
Zimmermann, FK ;
Müller, S .
ENZYME AND MICROBIAL TECHNOLOGY, 2000, 26 (9-10) :688-698
[9]   Investigation of limiting metabolic steps in the utilization of xylose by recombinant Saccharomyces cerevisiae using metabolic engineering [J].
Karhumaa, K ;
Hahn-Hägerdal, B ;
Gorwa-Grauslund, MF .
YEAST, 2005, 22 (05) :359-368
[10]   Screening of two complementary collections of Saccharomyces cerevisiae to identify enzymes involved in stereo-selective reductions of specific carbonyl compounds:: an alternative to protein purification [J].
Katz, M ;
Hahn-Hägerdal, B ;
Gorwa-Grauslund, MF .
ENZYME AND MICROBIAL TECHNOLOGY, 2003, 33 (2-3) :163-172