Prospects of microbial cell factories developed through systems metabolic engineering

被引:53
|
作者
Gustavsson, Martin [1 ,2 ]
Lee, Sang Yup [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Metab & Biomol Engn Natl Res Lab, Dept Chem & Biomol Engn,Inst BioCentury,Plus Prog, BioProc Engn Res Ctr,Ctr Syst & Synthet Biotechno, 291 Daehak Ro, Daejeon 34141, South Korea
[2] KTH Royal Inst Technol, Sch Biotechnol, Div Ind Biotechnol, AlbaNova Univ Ctr, S-10691 Stockholm, Sweden
来源
MICROBIAL BIOTECHNOLOGY | 2016年 / 9卷 / 05期
基金
瑞典研究理事会; 新加坡国家研究基金会;
关键词
L-THREONINE PRODUCTION; ESCHERICHIA-COLI; GENE-EXPRESSION; FERMENTATION; ETHANOL; STRAINS; TRANSPORTER; STRATEGIES; TOLERANCE; PATHWAYS;
D O I
10.1111/1751-7915.12385
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
While academic-level studies on metabolic engineering of microorganisms for production of chemicals and fuels are ever growing, a significantly lower number of such production processes have reached commercial-scale. In this work, we review the challenges associated with moving from laboratory-scale demonstration of microbial chemical or fuel production to actual commercialization, focusing on key requirements on the production organism that need to be considered during the metabolic engineering process. Metabolic engineering strategies should take into account technoeconomic factors such as the choice of feedstock, the product yield, productivity and titre, and the cost effectiveness of midstream and downstream processes. Also, it is important to develop an industrial strain through metabolic engineering for pathway construction and flux optimization together with increasing tolerance to products and inhibitors present in the feedstock, and ensuring genetic stability and strain robustness under actual fermentation conditions.
引用
收藏
页码:610 / 617
页数:8
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