Comparison of the metabolic response to over-production of p-coumaric acid in two yeast strains

被引:55
作者
Rodriguez, Angelica [1 ,3 ]
Chen, Yun [2 ]
Khoomrung, Sakda [2 ,4 ]
Ozdemir, Emre [1 ]
Borodina, Irina [1 ]
Nielsen, Jens [1 ,2 ]
机构
[1] Tech Univ Denmark, Novo Nordisk Fdn, Ctr Biosustainabil, Kemitorvet 220, DK-2800 Lyngby, Denmark
[2] Chalmers Univ Technol, Dept Biol & Biol Engn, SE-41296 Gothenburg, Sweden
[3] Delft Univ Technol, Dept Biotechnol, Ind Microbiol Sect, Maasweg 9, NL-2629 HZ Delft, Netherlands
[4] Mahidol Univ, Siriraj Hosp, Fac Med, Ctr Appl Thai Tradit Med,Siriraj Metabol & Phen C, Bangkok 10700, Thailand
关键词
Saccharomyces cerevisiae; p-Coumaric acid; Transcriptome; Metabolome data; Transporters; SACCHAROMYCES-CEREVISIAE; OXIDATIVE STRESS; GENE; ETHANOL; INTEGRATION; SET; EXPRESSION; TOLERANCE; MEMBRANE; PATHWAY;
D O I
10.1016/j.ymben.2017.10.013
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 development of robust and efficient cell factories requires understanding of the metabolic changes triggered by the production of the targeted compound. Here we aimed to study how production of p-coumaric acid, a precursor of multiple secondary aromatic metabolites, influences the cellular metabolism of Saccharomyces cerevisiae. We evaluated the growth and p-coumaric acid production in batch and chemostat cultivations and analyzed the transcriptome and intracellular metabolome during steady state in low-and high-producers of p-coumaric acid in two strain backgrounds, S288c or CEN.PK. We found that the same genetic modifications resulted in higher production of p-coumaric acid in the CEN.PK background than in the S288c background. Moreover, the CEN.PK strain was less affected by the genetic engineering as was evident from fewer changes in the transcription profile and intracellular metabolites concentrations. Surprisingly, for both strains we found the largest transcriptional changes in genes involved in transport of amino acids and sugars, which were downregulated. Additionally, in S288c amino acid and protein biosynthesis processes were also affected. We systematically overexpressed or deleted genes with significant transcriptional changes in CEN.PK low and high-producing strains. The knockout of some of the downregulated transporters triggered a 20-50% improvement in the synthesis of p-CA in the CEN.PK high-producing strain. This study demonstrates the importance of transporters in the engineering of cell factories for production of small molecules.
引用
收藏
页码:265 / 272
页数:8
相关论文
共 46 条
[1]  
[Anonymous], 2010, ANN PLANT REV
[2]   Production of plant secondary metabolites: a historical perspective [J].
Bourgaud, F ;
Gravot, A ;
Milesi, S ;
Gontier, E .
PLANT SCIENCE, 2001, 161 (05) :839-851
[3]  
Brachmann CB, 1998, YEAST, V14, P115
[4]   Quantitative Evaluation of Intracellular Metabolite Extraction Techniques for Yeast Metabolomics [J].
Canelas, Andre B. ;
ten Pierick, Angela ;
Ras, Cor ;
Seifar, Reza M. ;
van Dam, Jan C. ;
van Gulik, Walter M. ;
Heijnen, Joseph J. .
ANALYTICAL CHEMISTRY, 2009, 81 (17) :7379-7389
[5]   Expanding the chemical palate of cells by combining systems biology and metabolic engineering [J].
Curran, Kathleen A. ;
Alper, Hal S. .
METABOLIC ENGINEERING, 2012, 14 (04) :289-297
[6]   Yeast genetic strain and plasmid collections [J].
Entian, Karl-Dieter ;
Koetter, Peter .
YEAST GENE ANALYSIS, SECOND EDITION, 2007, 36 :629-666
[7]  
Germann S. M., 2016, BIOTECHNOL J
[8]  
Gietz RD, 2002, METHOD ENZYMOL, V350, P87
[9]   Yeast osmoregulation [J].
Hohmann, Stefan ;
Krantz, Marcus ;
Nordlander, Bodil .
OSMOSENSING AND OSMOSIGNALING, 2007, 428 :29-+
[10]  
Jamieson DJ, 1998, YEAST, V14, P1511, DOI 10.1002/(SICI)1097-0061(199812)14:16<1511::AID-YEA356>3.0.CO