Enzymatic Promiscuity for Organic Synthesis and Cascade Process

Author(s): Qi Wu, Bo-Kai Liu, Xian-Fu Lin

Journal Name: Current Organic Chemistry

Volume 14 , Issue 17 , 2010

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Enzymatic promiscuity, namely the possibility that one active site of an enzyme can catalyze several different chemical transformations, has been an important research field and valuable synthesis tool for protein engineering and synthetic chemistry. This review will focus on promiscuous enzyme-mediated reactions that are useful in organic synthesis. Examples include promiscuous hydrolysis reactions, Michael addition, Markovnikov addition, aldol condensation, Henry reaction, Mannich reaction, Epoxidation reaction, Baeyer-Villiger oxidation, radical polymerization and tandem reactions catalyzed by natural enzymes or engineered enzymes with existing or induced catalytic promiscuity. Among these examples, many enzymes from different family have been verified to be able to catalyze the same type of reaction through distinct mechanism. Many complex compounds or important intermediates can be synthesized using promiscuous enzymes or through novel synthesis pathways. These examples support the enormous potential of enzymatic promiscuity in synthetic chemistry.

Keywords: Enzymatic promiscuity, Organic synthesis, Application, Michael addition, Oxidation, promiscuity, synthesis, catalytic promiscuity, substrate promiscuity, condition promiscuity, Hydrolysis, hydrolases, AP, acrylamide, solvents, chemoselectivity, (DA), (AA), DMSO, Triazole, CAL-B mutant, C-C Bond, CAL-B, lipase-MY, 1ipasePL, enantioselectivity, D-aminoacylase, (MJML), DMF, Aldol reaction, (DDG), heterocyclic aldehydes, MPS, kcat/Km, AMDase, (PLP), HbHNL, (MML), Haloperoxidases, H2O2, PFE, Pseudomonas sp, (UHP), (TMPME), Baeyer-Villiger Oxidation, Metalloenzymes, CA[Mn], (BARS1), Grob fragmentation, Mhpc, (CDNB), Lipase

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Article Details

Year: 2010
Page: [1966 - 1988]
Pages: 23
DOI: 10.2174/138527210792927591
Price: $58

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