Biosynthesis of Plant Isoprenoids: Perspectives for Microbial Engineering

被引:332
作者
Kirby, James [1 ]
Keasling, Jay D. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Calif Berkeley, Calif Inst Quantitat Biomed Res, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Chem Engn, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Lab, Phys Biosci Div, Berkeley, CA 94720 USA
[5] Joint Bioenergy Inst, Emeryville, CA 94608 USA
基金
美国国家科学基金会; 比尔及梅琳达.盖茨基金会;
关键词
terpenes; P450; yeast; Escherichia coli; gene discovery; ESCHERICHIA-COLI STRAINS; CELL-SUSPENSION CULTURES; HIGH-LEVEL PRODUCTION; 1-DEOXY-D-XYLULOSE-5-PHOSPHATE SYNTHASE; FUNCTIONAL EXPRESSION; MOLECULAR-CLONING; CYTOCHROMES P450; SACCHAROMYCES-CEREVISIAE; CINNAMATE; 4-HYDROXYLASE; CAROTENOID ACCUMULATION;
D O I
10.1146/annurev.arplant.043008.091955
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Isoprenoids are a large and highly diverse group of natural products with many functions in plant primary and secondary metabolism. Isoprenoids are synthesized from common prenyl diphosphate precursors through the action of terpene synthases and terpene-modifying enzymes such as cytochrome P450 monooxygenases. Many isoprenoids have important applications in areas such as human health and nutrition, and much effort has been directed toward their production in microbial hosts. However, many hurdles must be overcome in the elucidation and functional microbial expression of the genes responsible for biosynthesis of ail isoprenoid of interest. Here, we review investigations into isoprenoid function and gene discovery in plants as well as the latest advances in isoprenoid pathway engineering in both plant and microbial hosts.
引用
收藏
页码:335 / 355
页数:21
相关论文
共 105 条
[1]   Biosynthesis of terpenes:: Studies on 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate reductase [J].
Adam, P ;
Hecht, S ;
Eisenreich, WG ;
Kaiser, J ;
Gräwert, T ;
Arigoni, D ;
Bacher, A ;
Rohdich, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (19) :12108-12113
[2]   Terpenoid metabolism in wild-type and transgenic Arabidopsis plants [J].
Aharoni, A ;
Giri, AP ;
Deuerlein, S ;
Griepink, F ;
de Kogel, WJ ;
Verstappen, FWA ;
Verhoeven, HA ;
Jongsma, MA ;
Schwab, W ;
Bouwmeester, HJ .
PLANT CELL, 2003, 15 (12) :2866-2884
[3]   Terpenoids: Opportunities for biosynthesis of natural product drugs using engineered microorganisms [J].
Ajikumar, Parayil Kumaran ;
Tyo, Keith ;
Carlsen, Simon ;
Mucha, Oliver ;
Phon, Too Heng ;
Stephanopoulos, Gregory .
MOLECULAR PHARMACEUTICS, 2008, 5 (02) :167-190
[4]   Construction of lycopene-overproducing E-coli strains by combining systematic and combinatorial gene knockout targets [J].
Alper, H ;
Miyaoku, K ;
Stephanopoulos, G .
NATURE BIOTECHNOLOGY, 2005, 23 (05) :612-616
[5]   Global transcription machinery engineering: A new approach for improving cellular phenotype [J].
Alper, Hal ;
Stephanopoulos, Gregory .
METABOLIC ENGINEERING, 2007, 9 (03) :258-267
[6]   Characterization of lycopene-overproducing E-coli strains in high cell density fermentations [J].
Alper, Hal ;
Miyaoku, Kohei ;
Stephanopoulos, Gregory .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2006, 72 (05) :968-974
[7]   A P450BM-3 mutant hydroxylates alkanes, cycloalkanes, arenes and heteroarenes [J].
Appel, D ;
Lutz-Wahl, S ;
Fischer, P ;
Schwaneberg, U ;
Schmid, RD .
JOURNAL OF BIOTECHNOLOGY, 2001, 88 (02) :167-171
[8]   Euphorbium: Modern research on its active principle, resiniferatoxin, revives an ancient medicine [J].
Appendino, G ;
Szallasi, A .
LIFE SCIENCES, 1997, 60 (10) :681-696
[9]   Cloning of three A-type cytochromes p450, CYP71E1, CYP98, and CYP99 from Sorghum bicolor (L.) Moench by a PCR approach and identification by expression in Escherichia coli of CYP71E1 as a multifunctional cytochrome p450 in the biosynthesis of the cyanogenic glucoside dhurrin [J].
Bak, S ;
Kahn, RA ;
Nielsen, HL ;
Moller, BL ;
Halkier, BA .
PLANT MOLECULAR BIOLOGY, 1998, 36 (03) :393-405
[10]   Increasing expression of P450 and P450-reductase proteins from monocots in heterologous systems [J].
Batard, Y ;
Hehn, A ;
Nedelkina, S ;
Schalk, M ;
Pallett, K ;
Schaller, H ;
Werck-Reichhart, D .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2000, 379 (01) :161-169