Evolution of polyhydroxyalkanoate (PHA) production system by "enzyme evolution": Successful case studies of directed evolution

被引:118
|
作者
Taguchi, S [1 ]
Doi, Y
机构
[1] Hokkaido Univ, Grad Sch Engn, Div Mol Chem, Sapporo, Hokkaido 0608628, Japan
[2] Riken Inst Phys & Chem Res, Polymer Chem Lab, Wako, Saitama 3510198, Japan
[3] Tokyo Inst Technol, Dept Innovat & Engn Mat, Midori Ku, Yokohama, Kanagawa 2268502, Japan
关键词
biodegradable polyesters; copolymerization; enzyme evolution; polyhydroxyalkanoate; synthase;
D O I
10.1002/mabi.200300111
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Biotechnological studies towards the biosynthesis of polyhydroxyalkanoates (PHAs) biopolyesters have extensively progressed through the development of various metabolic engineering strategies. Historically, efficient PHA production has been achieved using the fermentation technology of naturally occurring PHA-producing bacteria based on external substrate manipulation (1st generation), and subsequent reinforcement with recombinant gene technology (2nd generation). More recently, "enzyme evolution" is becoming the 3rd generation approach for PHA production. A break-through in the chemical synthesis of macromolecules with desirable properties was achieved by the development of prominent chemical catalysts via "catalyst evolution", as represented by a series of Ziegler-Natta catalysts. Thus, one can easily accept the concept that the molecular evolution of the biocatalysts (enzymes) relevant to PHA synthesis will provide us with a chance to create novel PHA materials with high performance. The first trial of an in vitro enzyme evolution in PHA biosynthesis was reported by our group in 2001. The following literature data, as well as our own experimental results devoted to this new approach, have been accumulated over a short time. This review article focuses specifically on the concept and current case studies of the application of "enzyme evolution" to PHA biosynthesis.
引用
收藏
页码:145 / 156
页数:12
相关论文
共 50 条
  • [1] Directed enzyme evolution
    Farinas, ET
    Bulter, T
    Arnold, FH
    [J]. CURRENT OPINION IN BIOTECHNOLOGY, 2001, 12 (06) : 545 - 551
  • [2] DIRECTED EVOLUTION OF AN RNA ENZYME
    BEAUDRY, AA
    JOYCE, GF
    [J]. SCIENCE, 1992, 257 (5070) : 635 - 641
  • [3] Directed evolution of enzyme catalysis
    Kuchner, O
    Arnold, FH
    [J]. BIOFUTUR, 1999, (185) : B1 - B11
  • [4] Directed evolution of enzyme stability
    Eijsink, VGH
    Gåseidnes, S
    Borchert, TV
    van den Burg, B
    [J]. BIOMOLECULAR ENGINEERING, 2005, 22 (1-3): : 21 - 30
  • [5] Directed evolution of a psychrophilic enzyme
    Wintrobe, PL
    Arnold, FH
    [J]. FASEB JOURNAL, 1999, 13 (07): : A1535 - A1535
  • [6] Directed evolution of enzyme catalysts
    Kuchner, O
    Arnold, FH
    [J]. TRENDS IN BIOTECHNOLOGY, 1997, 15 (12) : 523 - 530
  • [7] Milestones in directed enzyme evolution
    Tao, HY
    Cornish, VW
    [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 2002, 6 (06) : 858 - 864
  • [8] Molecular system identification for enzyme directed evolution and design
    Guan, Xiangying
    Chakrabarti, Raj
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2017, 147 (12):
  • [9] Directed evolution of thermotolerant malic enzyme for improved malate production
    Morimoto, Yumi
    Honda, Kohsuke
    Ye, Xiaoting
    Okano, Kenji
    Ohtake, Hisao
    [J]. JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 2014, 117 (02) : 147 - 152
  • [10] Optimising enzyme function by directed evolution
    Dalby, PA
    [J]. CURRENT OPINION IN STRUCTURAL BIOLOGY, 2003, 13 (04) : 500 - 505