Engineering of the pyruvate dehydrogenase bypass in Saccharomyces cerevisiae for high-level production of isoprenoids

被引:275
作者
Shiba, Yoichiro
Paradise, Eric M.
Kirby, James
Ro, Dae-Kyun
Keasing, Jay D.
机构
[1] Univ Calif Berkeley, Dept Chem Engn, Berkeley Ctr Synthet Biol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Calif Inst Quantitat Biomed Res, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Lab, Phys Biosci Div, Berkeley, CA 94720 USA
关键词
acetaldehyde dehydrogenase; acetyl-CoA synthetase; amorphadiene; isoprenoids;
D O I
10.1016/j.ymben.2006.10.005
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
Amorphadiene, a sesquiterpene precursor to the anti-malarial drug artemisinin, is synthesized by the cyclization of farnesyl pyrophosphate (FPP). Saccharomyces cerevisiae produces FPP through the mevalonate pathway using acetyl-CoA as a starting compound. In order to enhance the supply of acetyl-CoA to the mevalonate pathway and achieve high-level production of amorphadiene, we engineered the pyruvate dehydrogenase bypass in S. cerevisiae. Overproduction of acetaldehyde dehydrogenase and introduction of a Salmonella enterica acetyl-CoA synthetase variant increased the carbon flux into the mevalonate pathway resulting in increased amorphadiene production. This work will be generally applicable to the production of a broad range of isoprenoids in yeast. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:160 / 168
页数:9
相关论文
共 39 条
[1]   Synthesis of atypical cyclic and acyclic hydroxy carotenoids in Escherichia coli transformants [J].
Albrecht, M ;
Takaichi, S ;
Misawa, N ;
Schnurr, G ;
Böger, P ;
Sandmann, G .
JOURNAL OF BIOTECHNOLOGY, 1997, 58 (03) :177-185
[2]   Identifying gene targets for the metabolic engineering of lycopene biosynthesis in Escherichia coli [J].
Alper, H ;
Jin, YS ;
Moxley, JF ;
Stephanopoulos, G .
METABOLIC ENGINEERING, 2005, 7 (03) :155-164
[3]  
[Anonymous], 1989, Molecular Cloning
[4]   STEREOSELECTIVE TOTAL SYNTHESIS OF (+)-ARTEMISININ, THE ANTIMALARIAL CONSTITUENT OF ARTEMISIA-ANNUA L [J].
AVERY, MA ;
CHONG, WKM ;
JENNINGSWHITE, C .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (03) :974-979
[5]   Total synthesis of baccatin III and taxol [J].
Danishefsky, SJ ;
Masters, JJ ;
Young, WB ;
Link, JT ;
Snyder, LB ;
Magee, TV ;
Jung, DK ;
Isaacs, RCA ;
Bornmann, WG ;
Alaimo, CA ;
Coburn, CA ;
DiGrandi, MJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (12) :2843-2859
[6]  
Daum G, 1998, YEAST, V14, P1471, DOI 10.1002/(SICI)1097-0061(199812)14:16<1471::AID-YEA353>3.0.CO
[7]  
2-Y
[8]   Overproduction of acetyl-coenzyme A synthetase isoenzymes in respiring Saccharomyces cerevisiae cells does not reduce acetate production after exposure to glucose excess [J].
de Jong-Gubbels, P ;
van den Berg, MA ;
Luttick, MAH ;
Steensma, HY ;
van Dijken, JP ;
Pronk, JT .
FEMS MICROBIOLOGY LETTERS, 1998, 165 (01) :15-20
[9]   Genetic engineering of Taxol biosynthetic genes in Saccharomyces cerevisiae [J].
DeJong, JM ;
Liu, YL ;
Bollon, AP ;
Long, RM ;
Jennewein, S ;
Williams, D ;
Croteau, RB .
BIOTECHNOLOGY AND BIOENGINEERING, 2006, 93 (02) :212-224
[10]   The Saccharomyces cerevisiae acetyl-coenzyme A synthetase encoded by the ACS1 gene, but not the ACS2-encoded enzyme, is subject to glucose catabolite inactivation [J].
deJongGubbels, P ;
vandenBerg, MA ;
Steensma, HY ;
vanDijken, JP ;
Pronk, JT .
FEMS MICROBIOLOGY LETTERS, 1997, 153 (01) :75-81