Enhancement of Farnesyl Diphosphate Pool as Direct Precursor of Sesquiterpenes Through Metabolic Engineering of the Mevalonate Pathway in Saccharomyces cerevisiae

被引:128
作者
Asadollahi, Mohammad A. [1 ,2 ]
Maury, Jerome [1 ]
Schalk, Michel [3 ]
Clark, Anthony [4 ]
Nielsen, Jens [1 ]
机构
[1] Tech Univ Denmark, Ctr Microbial Biotechnol, Dept Syst Biol, DK-2800 Lyngby, Denmark
[2] Univ Isfahan, Biotechnol Grp, Fac Adv Sci & Technol, Esfahan, Iran
[3] Firmenich Co, Corp R&D Div, Geneva, Switzerland
[4] Firmenich Inc, Corp R&D Div, Princeton, NJ USA
关键词
metabolic engineering; Saccharomyces cerevisiae; sesquiterpene; mevalonate pathway; farnesyl diphosphate; squalene; HYDROXYMETHYLGLUTARYL-COA REDUCTASE; ACTIVATED PROTEIN-KINASE; HIGH-LEVEL PRODUCTION; TRANSCRIPTIONAL REGULATION; BIOSYNTHETIC-PATHWAY; SQUALENE SYNTHETASE; CATALYTIC DOMAIN; ARTEMISIA-ANNUA; YEAST SNF1; SYNTHASE;
D O I
10.1002/bit.22668
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
The mevalonate pathway in the yeast Saccharomyces cerevisiae was deregulated in order to enhance the intracellular pool of farnesyl diphosphate (FPP), the direct precursor for the biosynthesis of sesquiterpenes. Overexpression of the catalytic domain of HMG1, both from the genome and plasmid, resulted in higher production of cubebol, a plant originating sesquiterpene, and increased squalene accumulation. Down-regulation of ERG9 by replacing its native promoter with the regulatable MET3 promoter, enhanced cubebol titers but simultaneous overexpression of tHMG1 and repression of ERG9 did not further improve cubebol production. Furtheremore, the concentrations of squalene and ergosterol were measured in the engineered strains. Unexpectedly, significant accumulation of squalene and restoring the ergosterol biosynthesis were observed in the ERG9 repressed strains transformed with the plasmids harboring cubebol synthase gene. This could be explained by a toxicity effect of cubebol, possibly resulting in higher transcription levels for the genes under control of MET3 promoter, which could lead to accumulation of squalene and ergosterol. Biotechnol. Bioeng. 2010;106: 86-96. (C) 2010 Wiley Periodicals, Inc.
引用
收藏
页码:86 / 96
页数:11
相关论文
共 44 条
[1]   Production of plant Sesquiterpenes in Saccharomyces cerevisiae:: Effect of ERG9 repression on sesquiterpene biosynthesis [J].
Asadollahi, Mohammad A. ;
Maury, Jerome ;
Moller, Kasper ;
Nielsen, Kristian Fog ;
Schalk, Michel ;
Clark, Anthony ;
Nielsen, Jens .
BIOTECHNOLOGY AND BIOENGINEERING, 2008, 99 (03) :666-677
[2]   Enhancing sesquiterpene production in Saccharomyces cerevisiae through in silico driven metabolic engineering [J].
Asadollahi, Mohammad A. ;
Maury, Jerome ;
Patil, Kiran Raosaheb ;
Schalk, Michel ;
Clark, Anthony ;
Nielsen, Jens .
METABOLIC ENGINEERING, 2009, 11 (06) :328-334
[3]  
BASSON ME, 1987, GENETICS, V117, P645
[4]  
Connolly J.D., 1991, DICT TERPENOIDS
[5]   Effects of overproduction of the catalytic domain of 3-hydroxy-3-methylglutaryl coenzyme A reductase on squalene synthesis in Saccharomyces cerevisiae [J].
Donald, KAG ;
Hampton, RY ;
Fritz, IB .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (09) :3341-3344
[6]   Carbon catabolite repression of invertase during batch cultivations of Saccharomyces cerevisiae:: the role of glucose, fructose, and mannose [J].
Dynesen, J ;
Smits, HP ;
Olsson, L ;
Nielsen, J .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1998, 50 (05) :579-582
[7]   Metabolic engineering of taxadiene biosynthesis in yeast as a first step towards Taxol (Paclitaxel) production [J].
Engels, Benedikt ;
Dahm, Pia ;
Jennewein, Stefan .
METABOLIC ENGINEERING, 2008, 10 (3-4) :201-206
[8]   Cloning-free PCR-based allele replacement methods [J].
Erdeniz, N ;
Mortensen, UH ;
Rothstein, R .
GENOME RESEARCH, 1997, 7 (12) :1174-1183
[9]   A highly conserved signal controls degradation of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase in eukaryotes [J].
Gardner, RG ;
Hampton, RY .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (44) :31671-31678
[10]  
HAMPTON R, 1996, TRENDS BIOCHEM SCI, V21, P142