Metabolic engineering of Saccharomyces cerevisiae for production of fatty acid ethyl esters, an advanced biofuel, by eliminating non-essential fatty acid utilization pathways

被引:81
作者
Valle-Rodriguez, Juan Octavio [1 ]
Shi, Shuobo [1 ,2 ]
Siewers, Verena [1 ]
Nielsen, Jens [1 ]
机构
[1] Chalmers Univ Technol, Dept Chem & Biol Engn, SE-41296 Gothenburg, Sweden
[2] ASTAR, Inst Chem & Engn Sci, Metab Engn Res Lab, Singapore 138669, Singapore
基金
欧洲研究理事会; 瑞典研究理事会;
关键词
Advanced biofuel; Biodiesel; Metabolic engineering; Saccharomyces cerevisiae; Triacylglycerols; Steryl esters; ESCHERICHIA-COLI; WAX ESTER; FUNCTIONAL EXPRESSION; LIPID-ACCUMULATION; GENE DISRUPTION; YEAST; BIODIESEL; BIOSYNTHESIS; SYNTHETASE; CHEMICALS;
D O I
10.1016/j.apenergy.2013.10.003
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Microbial production of fatty acid derived chemicals and fuels is currently of great interest due to the limited resources and increasing prices of petroleum and petroleum-based products. The development of Saccharomyces cerevisiae as a fatty acid ethyl ester (FAEE) cell factory would represent an opportunity for biodiesel production due to its successful history in the biotechnology area. However, fatty acid (FA) biosynthesis is highly regulated and usually not high enough for developing an efficient production process. In S. cerevisiae, FAs are degraded by beta-oxidation and a large fraction is utilized to synthesize steryl esters (SEs) and triacylglycerols (TAGs), which are not essential for the cell. Here, by eliminating nonessential FA utilization pathways, we developed a metabolic engineering strategy resulting in a S. cerevisiae strain that can overproduce FAs and in turn use these for producing FAEEs (biodiesel). Compared to the wild-type, there is an about 3-fold increase in free FA content in a strain devoid of both TAG and SE formation, a 4-fold increase in free FA content in a strain that is incapable of beta-oxidation, and a 5-fold increase of free FAs in a strain lacking all of these non-essential FA utilization pathways. It is also demonstrated that there are similar positive effects on FAEE production in these deletion strains. The highest production of FAEEs is 17.2 mg/l in the strain in which all these pathways were blocked. The results of this study serve as a basis for further strategies to improve the production of FA derivatives in S. cerevisiae. (C) 2013 The Authors. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:226 / 232
页数:7
相关论文
共 40 条
[1]   A METHOD FOR GENE DISRUPTION THAT ALLOWS REPEATED USE OF URA3 SELECTION IN THE CONSTRUCTION OF MULTIPLY DISRUPTED YEAST STRAINS [J].
ALANI, E ;
CAO, L ;
KLECKNER, N .
GENETICS, 1987, 116 (04) :541-545
[2]  
[Anonymous], 2012, Molecular Cloning: A Laboratory Manual
[3]   Control of Lipid Accumulation in the Yeast Yarrowia lipolytica [J].
Beopoulos, Athanasios ;
Mrozova, Zuzana ;
Thevenieau, France ;
Le Dall, Marie-Therese ;
Hapala, Ivan ;
Papanikolaou, Seraphim ;
Chardot, Thierry ;
Nicaud, Jean-Marc .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2008, 74 (24) :7779-7789
[4]   A POSITIVE SELECTION FOR MUTANTS LACKING OROTIDINE-5'-PHOSPHATE DECARBOXYLASE ACTIVITY IN YEAST - 5-FLUORO-OROTIC ACID RESISTANCE [J].
BOEKE, JD ;
LACROUTE, F ;
FINK, GR .
MOLECULAR & GENERAL GENETICS, 1984, 197 (02) :345-346
[5]   Oleate Inhibits Steryl Ester Synthesis and Causes Liposensitivity in Yeast [J].
Connerth, Melanie ;
Czabany, Tibor ;
Wagner, Andrea ;
Zellnig, Guenther ;
Leitner, Erich ;
Steyrer, Ernst ;
Daum, Guenther .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (35) :26832-26841
[6]   Systems biology of yeast: enabling technology for development of cell factories for production of advanced biofuels [J].
de Jong, Bouke ;
Siewers, Verena ;
Nielsen, Jens .
CURRENT OPINION IN BIOTECHNOLOGY, 2012, 23 (04) :624-630
[7]   STRUCTURE AND TRANSCRIPTIONAL CONTROL OF THE SACCHAROMYCES-CEREVISIAE POX1 GENE ENCODING ACYL-COENZYME-A OXIDASE [J].
DMOCHOWSKA, A ;
DIGNARD, D ;
MALESZKA, R ;
THOMAS, DY .
GENE, 1990, 88 (02) :247-252
[8]   Cloning-free PCR-based allele replacement methods [J].
Erdeniz, N ;
Mortensen, UH ;
Rothstein, R .
GENOME RESEARCH, 1997, 7 (12) :1174-1183
[9]   High-efficiency yeast transformation using the LiAc/SS carrier DNA/PEG method [J].
Gietz R.D. ;
Schiestl R.H. .
Nature Protocols, 2007, 2 (1) :31-34
[10]   A new efficient gene disruption cassette for repeated use in budding yeast [J].
Guldener, U ;
Heck, S ;
Fiedler, T ;
Beinhauer, J ;
Hegemann, JH .
NUCLEIC ACIDS RESEARCH, 1996, 24 (13) :2519-2524