Biocatalysts from alkaloid producing plants

被引:27
作者
Kries, Hajo [1 ]
O'Connor, Sarah E. [1 ]
机构
[1] John Innes Ctr Plant Sci Res, Dept Biol Chem, Norwich Res Pk, Norwich NR4 7UH, Norfolk, England
基金
英国生物技术与生命科学研究理事会; 欧洲研究理事会;
关键词
PICTET-SPENGLER REACTION; CATHARANTHUS-ROSEUS; OPIUM POPPY; IRIDOID BIOSYNTHESIS; NOSCAPINE BIOSYNTHESIS; SYNTHETIC BIOLOGY; ENZYME; STEP; SYNTHASE; TETRAHYDROISOQUINOLINES;
D O I
10.1016/j.cbpa.2015.12.006
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
Metabolic pathways leading to benzylisoquinoline and monoterpene indole alkaloids in plants are revealing remarkable new reactions. Understanding of the enzymes involved in alkaloid biosynthesis provides access to a variety of applications in biocatalysis and bioengineering. In chemo-enzymatic settings, plant biocatalysts can transform medically important scaffolds. Additionally, synthetic biologists are taking alkaloid pathways as templates to assemble pathways in microorganisms that are tailored to the needs of medicinal chemistry. In light of these many recent discoveries, it is expected that plants will continue to be a source of novel biocatalysts for the foreseeable future.
引用
收藏
页码:22 / 30
页数:9
相关论文
共 54 条
  • [1] The chemical logic of plant natural product biosynthesis
    Anarat-Cappillino, Guelbenk
    Sattely, Elizabeth S.
    [J]. CURRENT OPINION IN PLANT BIOLOGY, 2014, 19 : 51 - 58
  • [2] A Pair of Tabersonine 16-Hydroxylases Initiates the Synthesis of Vindoline in an Organ-Dependent Manner in Catharanthus roseus
    Besseau, Sebastien
    Kellner, Franziska
    Lanoue, Arnaud
    Thamm, Antje M. K.
    Salim, Vonny
    Schneider, Bernd
    Geu-Flores, Fernando
    Hoefer, Rene
    Guirimand, Gregory
    Guihur, Anthony
    Oudin, Audrey
    Glevarec, Gaelle
    Foureau, Emilien
    Papon, Nicolas
    Clastre, Marc
    Giglioli-Guivarc'h, Nathalie
    St-Pierre, Benoit
    Werck-Reichhart, Daniele
    Burlat, Vincent
    De Luca, Vincenzo
    O'Connor, Sarah E.
    Courdavault, Vincent
    [J]. PLANT PHYSIOLOGY, 2013, 163 (04) : 1792 - 1803
  • [3] Engineering the third wave of biocatalysis
    Bornscheuer, U. T.
    Huisman, G. W.
    Kazlauskas, R. J.
    Lutz, S.
    Moore, J. C.
    Robins, K.
    [J]. NATURE, 2012, 485 (7397) : 185 - 194
  • [4] BIOMIMETIC SYNTHESIS OF CATHENAMINE AND 19-EPICATHENAMINE, KEY INTERMEDIATES TO HETEROYOHIMBINE ALKALOIDS
    BROWN, RT
    LEONARD, J
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1979, (20) : 877 - 879
  • [5] De novo production of the plant-derived alkaloid strictosidine in yeast
    Brown, Stephanie
    Clastre, Marc
    Courdavault, Vincent
    O'Connor, Sarah E.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (11) : 3205 - 3210
  • [6] Short-chain dehydrogenase/reductase catalyzing the final step of noscapine biosynthesis is localized to laticifers in opium poppy
    Chen, Xue
    Facchini, Peter J.
    [J]. PLANT JOURNAL, 2014, 77 (02) : 173 - 184
  • [7] Dang TTT, 2015, NAT CHEM BIOL, V11, P104, DOI [10.1038/nchembio.1717, 10.1038/NCHEMBIO.1717]
  • [8] An enzyme-coupled biosensor enables (S)-reticuline production in yeast from glucose
    DeLoache, William C.
    Russ, Zachary N.
    Narcross, Lauren
    Gonzales, Andrew M.
    Martin, Vincent J. J.
    Dueber, John E.
    [J]. NATURE CHEMICAL BIOLOGY, 2015, 11 (07) : 465 - +
  • [9] Eisenreich W., 2013, The handbook of plant metabolomics, P25
  • [10] Farrow SC, 2015, NAT CHEM BIOL, V11, P728, DOI [10.1038/NCHEMBIO.1879, 10.1038/nchembio.1879]