Redox Cofactor Metabolic Engineering with Escherichia coli

被引:0
|
作者
Wang Baiyun [1 ,2 ,3 ]
Wang Xiaoyue [1 ,2 ,3 ]
Wang Zhiwen [1 ,2 ,3 ]
Chen Tao [1 ,2 ,3 ]
Zhao Xueming [1 ,2 ,3 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Key Lab Syst Bioengn, Minist Educ, Tianjin 300072, Peoples R China
[3] Tianjin Univ, Sch Chem Engn & Technol, SynBio Res Platform, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
redox cofactor; E; coli; metabolic engineering; biotransformation; PENTOSE-PHOSPHATE PATHWAY; SUCCINIC ACID PRODUCTION; WHOLE-CELL BIOCATALYSIS; MEVALONATE PATHWAY; NADH/NAD(+) RATIO; OVEREXPRESSION; DEHYDROGENASE; YIELD; BIOSYNTHESIS; AVAILABILITY;
D O I
10.7536/PC140322
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Redox cofactor plays an important role in maintaining cellular redox balance and driving catabolic or anabolic reactions. As the driving force of biochemical reactions and redox carriers, redox cofactor has received much attention for enhancing biotransformation process in recent years. The Gram-negative bacterium Escherichia coli (E. coli) has been studied extensively on a fundamental and applied level and has become a predominant host microorganism for industrial applications. Metabolic engineering of E. coli for the enhanced biochemical production such as bioethanol, organic acids, biopolymer, complex natural compounds and so on, has been significantly promoted by the redox cofactor engineering. This review introduced various strategies to improve productivity and product titers by engineered E. coli through metabolic engineering pathways and key enzymes involved redox cofactor. Advanced metabolic engineering strategies in redox cofactor include metabolic engineering of pathway involved in NAD(P)H biosynthesis, mutual transformation of redox cofactor, expression of heterogeneous redox cofactor dependent enzymes, manipulation of pyridine biosynthesis and NAD transportation. These strategies have been successfully implemented in recombinant E. coli to increase cellular availability of desired redox cofactor or change cofactor specificity of key enzymes. While current cofactor strategies just focus on natural metabolic pathways and enzymes, novel strategy needs to be developed for manipulating redox cofactor completely according to the will of the human.
引用
收藏
页码:1609 / 1618
页数:10
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  • [1] Identifying gene targets for the metabolic engineering of lycopene biosynthesis in Escherichia coli
    Alper, H
    Jin, YS
    Moxley, JF
    Stephanopoulos, G
    [J]. METABOLIC ENGINEERING, 2005, 7 (03) : 155 - 164
  • [2] Engineering the isobutanol biosynthetic pathway in Escherichia coli by comparison of three aldehyde reductase/alcohol dehydrogenase genes
    Atsumi, Shota
    Wu, Tung-Yun
    Eckl, Eva-Maria
    Hawkins, Sarah D.
    Buelter, Thomas
    Liao, James C.
    [J]. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2010, 85 (03) : 651 - 657
  • [3] Metabolic engineering of Escherichia coli to minimize byproduct formate and improving succinate productivity through increasing NADH availability by heterologous expression of NAD+-dependent formate dehydrogenase
    Balzer, Grant J.
    Thakker, Chandresh
    Bennett, George N.
    San, Ka-Yiu
    [J]. METABOLIC ENGINEERING, 2013, 20 : 1 - 8
  • [4] Engineered ketol-acid reductoisomerase and alcohol dehydrogenase enable anaerobic 2-methylpropan-1-ol production at theoretical yield in Escherichia coli
    Bastian, Sabine
    Liu, Xiang
    Meyerowitz, Joseph T.
    Snow, Christopher D.
    Chen, Mike M. Y.
    Arnold, Frances H.
    [J]. METABOLIC ENGINEERING, 2011, 13 (03) : 345 - 352
  • [5] The effect of NAPRTase overexpression on the total levels of NAD, the NADH/NAD+ ratio, and the distribution of metabolites in Escherichia coli
    Berríos- Rivera, SJ
    San, KY
    Bennett, GN
    [J]. METABOLIC ENGINEERING, 2002, 4 (03) : 238 - 247
  • [6] Bruschi F, 2011, CURR OPIN BIOTECH S1, V22, pS7
  • [7] Canonaco F, 2001, FEMS MICROBIOL LETT, V204, P247, DOI 10.1111/j.1574-6968.2001.tb10892.x
  • [8] Overexpression and biochemical characterization of soluble pyridine nucleotide transhydrogenase from Escherichia coli
    Cao, Zhengyu
    Song, Ping
    Xu, Qin
    Su, Ruirui
    Zhu, Guoping
    [J]. FEMS MICROBIOLOGY LETTERS, 2011, 320 (01) : 9 - 14
  • [9] Improving NADPH availability for natural product biosynthesis in Escherichia coli by metabolic engineering
    Chemler, Joseph A.
    Fowler, Zachary L.
    McHugh, Kyle P.
    Koffas, Mattheos A. G.
    [J]. METABOLIC ENGINEERING, 2010, 12 (02) : 96 - 104
  • [10] Metabolic engineering of Escherichia coli: A sustainable industrial platform for bio-based chemical production
    Chen, Xianzhong
    Zhou, Li
    Tian, Kangming
    Kumar, Ashwani
    Singh, Suren
    Prior, Bernard A.
    Wang, Zhengxiang
    [J]. BIOTECHNOLOGY ADVANCES, 2013, 31 (08) : 1200 - 1223