New enzymes for chemical synthesis exploring natural product biosynthesis

被引:0
作者
Tao, Junhua
Burkart, Michael D.
机构
[1] BioVerdant Inc, San Diego, CA 92121 USA
[2] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
关键词
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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
As a result of recent advances in large-scale DNA sequencing and enzyme directed evolution technologies, biocatalysis is becoming a transformational technology uniquely suited for chemical synthesis and green chemistry development. Nature has; evolved enzymes to create molecules that range from simple gases to complex natural products, yet many of these tools remain unutilized by synthetic chemists. in order to further expand the synthetic applications of biotransformation, it is essential that biocatalysts display attributes complementary or superior to chemical catalysis, such as high synthetic efficiency, exquisite stereocontrol and use of economic starting materials. In this review, several new classes of enzymatic transformations deriving from natural product biosynthesis are selected to discuss their potential for chemical synthesis.
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页码:3 / 7
页数:5
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共 55 条
[1]   2,4-Dioxyenases catalyzing N-heterocyclic-ring cleavage and formation of carbon monoxide - Purification and some properties of 1H-3-hydroxy-4-oxoquinaldine 2,4-dioxygenase from Arthrobacter sp Ru61a and comparison with 1H-3-hydroxy-4-oxoquinoline 2,4-dioxygenase from Pseudomonas putida 33/1 [J].
Bauer, I ;
Max, N ;
Fetzner, S ;
Lingens, F .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 240 (03) :576-583
[2]   Mechanism and control in biological amine methylation [J].
Blackburn, GM ;
Gamblin, SJ ;
Wilson, JR .
HELVETICA CHIMICA ACTA, 2003, 86 (12) :4000-4006
[3]   Enzymatic tools for engineering natural product glycosylation [J].
Blanchard, Sophie ;
Thorson, Jon S. .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2006, 10 (03) :263-271
[4]   Crystal structure of the non-haem iron halogenase SyrB2 in syringomycin biosynthesis [J].
Blasiak, LC ;
Vaillancourt, FH ;
Walsh, CT ;
Drennan, CL .
NATURE, 2006, 440 (7082) :368-371
[5]   Epothilone C macrolactonization and hydrolysis are catalyzed by the isolated thioesterase domain of epothilone polyketide synthase [J].
Boddy, CN ;
Schneider, TL ;
Hotta, K ;
Walsh, CT ;
Khosla, C .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (12) :3428-3429
[6]   Characterization of the glycosyltransferase activity of DesVII:: Analysis of and implications for the biosynthesis of macrolide antibiotics [J].
Borisova, SA ;
Zhao, LS ;
Melancon, CE ;
Kao, CL ;
Liu, HW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (21) :6534-6535
[7]  
Borman S, 2006, CHEM ENG NEWS, V84, P13, DOI 10.1021/cen-v084n044.p013
[8]   Aromatic dioxygenases: molecular biocatalysis and applications [J].
Boyd, DR ;
Sharma, ND ;
Allen, CCR .
CURRENT OPINION IN BIOTECHNOLOGY, 2001, 12 (06) :564-573
[9]   Halogenating enzymes in the biosynthesis of antibiotics [J].
Burd, VN ;
van Pee, KH .
BIOCHEMISTRY-MOSCOW, 2003, 68 (10) :1132-1135
[10]   The mechanism of ACV synthetase [J].
Byford, MF ;
Baldwin, JE ;
Shiau, CY ;
Schofield, CJ .
CHEMICAL REVIEWS, 1997, 97 (07) :2631-2649