Metabolic engineering of a phosphoketolase pathway for pentose catabolism in Saccharomyces cerevisiae

被引:100
作者
Sonderegger, M [1 ]
Schümperli, M [1 ]
Sauer, U [1 ]
机构
[1] ETH, Inst Biotechnol, CH-8093 Zurich, Switzerland
关键词
D O I
10.1128/AEM.70.5.2892-2897.2004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Low ethanol yields on xylose hamper economically viable ethanol production from hemicellulose-rich plant material with Saccharomyces cerevisiae. A major obstacle is the limited capacity of yeast for anaerobic reoxidation of NADH. Net reoxidation of NADH could potentially be achieved by channeling carbon fluxes through a recombinant phosphoketolase pathway. By heterologous expression of phosphotransacetylase and acetaldehyde dehydrogenase in combination with the native phosphoketolase, we installed a functional phosphoketolase pathway in the xylose-fermenting Saccharomyces cerevisiae strain TMB3001c. Consequently the ethanol yield was increased by 25% because less of the by-product xylitol was formed. The flux through the recombinant phosphoketolase pathway was about 30% of the optimum flux that would be required to completely eliminate xylitol and glycerol accumulation. Further overexpression of phosphoketolase, however, increased acetate accumulation and reduced the fermentation rate. By combining the phosphoketolase pathway with the ald6 mutation, which reduced acetate formation, a strain with an ethanol yield 20% higher and a xylose fermentation rate 40% higher than those of its parent was engineered.
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页码:2892 / 2897
页数:6
相关论文
共 41 条
[1]   Expression of bifunctional enzymes with xylose reductase and xylitol dehydrogenase activity in Saccharomyces cerevisiae alters product formation during xylose fermentation [J].
Anderlund, M ;
Radström, P ;
Hahn-Hägerdal, B .
METABOLIC ENGINEERING, 2001, 3 (03) :226-235
[2]  
ARISTIDOU A, 1999, Patent No. 9946363
[3]   A modified Saccharomyces cerevisiae strain that consumes L-arabinose and produces ethanol [J].
Becker, J ;
Boles, E .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (07) :4144-4150
[4]   NADH-LINKED ALDOSE REDUCTASE - THE KEY TO ANAEROBIC ALCOHOLIC FERMENTATION OF XYLOSE BY YEASTS [J].
BRUINENBERG, PM ;
DEBOT, PHM ;
VANDIJKEN, JP ;
SCHEFFERS, WA .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1984, 19 (04) :256-260
[5]   Functional characterization and localization of acetyl-CoA hydrolase, Ach1p, in Saccharomyces cerevisiae [J].
Buu, LM ;
Chen, YC ;
Lee, FJS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (19) :17203-17209
[6]   Decreasing acetic acid accumulation by a glycerol overproducing strain of Saccharomyces cerevisiae by deleting the ALD6 aldehyde dehydrogenase gene [J].
Eglinton, JM ;
Heinrich, AJ ;
Pollnitz, AP ;
Langridge, P ;
Henschke, PA ;
Lopes, MD .
YEAST, 2002, 19 (04) :295-301
[7]   Anaerobic xylose fermentation by recombinant Saccharomyces cerevisiae carrying XYL1, XYL2, and XKS1 in mineral medium chemostat cultures [J].
Eliasson, A ;
Christensson, C ;
Wahlbom, CF ;
Hahn-Hägerdal, B .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (08) :3381-3386
[8]   INDUCTION OF XYLULOSE-5-PHOSPHATE PHOSPHOKETOLASE IN A VARIETY OF YEASTS GROWN ON D-XYLOSE - THE KEY TO EFFICIENT XYLOSE METABOLISM [J].
EVANS, CT ;
RATLEDGE, C .
ARCHIVES OF MICROBIOLOGY, 1984, 139 (01) :48-52
[9]  
Gietz RD, 2002, METHOD ENZYMOL, V350, P87
[10]  
Gottschalk G., 1986, Bacterial Metabolism