Quantitative Trait Loci (QTL)-Guided Metabolic Engineering of a Complex Trait

被引:15
|
作者
Maurer, Matthew J. [1 ]
Sutardja, Lawrence [2 ]
Pinel, Dominic [1 ]
Bauer, Stefan [1 ,5 ]
Muehlbauer, Amanda L. [1 ]
Ames, Tyler D. [1 ,6 ]
Skerker, Jeffrey M. [1 ,2 ,3 ]
Arkin, Adam P. [1 ,2 ,4 ]
机构
[1] Univ Calif Berkeley, Energy Biosci Inst, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[3] Lawrence Berkeley Natl Lab, Biol Syst & Engn Div, Berkeley, CA 94720 USA
[4] Lawrence Berkeley Natl Lab, Environm Genom & Syst Biol Div, Berkeley, CA 94720 USA
[5] Zymergen, Emeryville, CA USA
[6] Phosplatin Therapeut, New York, NY USA
来源
ACS SYNTHETIC BIOLOGY | 2017年 / 6卷 / 03期
关键词
biofuel; CRISPR-Cas9; genetic engineering; hydrolysate; strain development; quantitative trait loci; SACCHAROMYCES-CEREVISIAE STRAINS; RECIPROCAL SIGN EPISTASIS; SPENT SULFITE LIQUOR; GENETIC INTERACTIONS; FITNESS LANDSCAPES; ETHANOL-PRODUCTION; GENOME SEQUENCE; YEAST STRAINS; TOLERANCE; FERMENTATION;
D O I
10.1021/acssynbio.6b00264
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Engineering complex phenotypes for industrial and synthetic biology applications is difficult and often confounds rational design. Bioethanol production from lignocellulosic feedstocks is a complex trait that requires multiple host systems to utilize, detoxify, and metabolize a mixture of sugars and inhibitors present in plant hydrolysates. Here, we demonstrate an integrated approach to discovering and optimizing host factors that impact fitness of Saccharomyces cerevisiae during fermentation of a Miscanthus x giganteus plant hydrolysate. We first used high-resolution Quantitative Trait Loci (QTL) mapping and systematic bulk Reciprocal Hemizygosity Analysis (bRHA) to discover 17 loci that differentiate hydrolysate tolerance between an industrially related (JAY291) and a laboratory (S288C) strain. We then used this data to identify a subset of favorable allelic loci that were most amenable for strain engineering. Guided by this "genetic blueprint", and using a dual-guide Cas9-based method to efficiently perform multikilobase locus replacements, we engineered an S288C-derived strain with superior hydrolysate tolerance than JAY291. Our methods should be generalizable to engineering any complex trait in S. cerevisiae, as well as other organisms.
引用
收藏
页码:566 / 581
页数:16
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