Terminal Alkenes from Acrylic Acid Derivatives via Non-Oxidative Enzymatic Decarboxylation by Ferulic Acid Decarboxylases

被引:28
作者
Aleku, Godwin A. [1 ]
Prause, Christoph [3 ]
Bradshaw-Allen, Ruth T. [1 ]
Plasch, Katharina [3 ]
Glueck, Silvia M. [2 ,3 ]
Bailey, Samuel S. [1 ]
Payne, Karl A. P. [1 ]
Parker, David A. [4 ]
Faber, Kurt [3 ]
Leys, David [1 ]
机构
[1] Univ Manchester, Manchester Inst Biotechnol, Sch Chem, 131 Princess St, Manchester M1 7DN, Lancs, England
[2] ACIB, A-8010 Graz, Austria
[3] Karl Franzens Univ Graz, Dept Chem, Heinrichstr 28, A-8010 Graz, Austria
[4] Shell Int Explorat & Prod Inc, Westhollow Technol Ctr, Innovat Biodomain, Houston, TX USA
基金
奥地利科学基金会; 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
Biocatalysis; Ferulic acid decarboxylase; Prenylated flavin; Decarboxylation; Terminal alkenes; REVERSIBLE PYRROLE-2-CARBOXYLATE DECARBOXYLASE; 1,3-DIPOLAR CYCLOADDITION REACTIONS; BACTERIAL UBIQUINONE BIOSYNTHESIS; EXPRESSING STREPTOMYCES-LIVIDANS; CARBON-DIOXIDE FIXATION; HYDROXYSTYRENE DERIVATIVES; STRUCTURAL-CHARACTERIZATION; STYRENE PRODUCTION; REDUCTIVE AMINASE; ESCHERICHIA-COLI;
D O I
10.1002/cctc.201800643
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Fungal ferulic acid decarboxylases (FDCs) belong to the UbiD-family of enzymes and catalyse the reversible (de)carboxylation of cinnamic acid derivatives through the use of a prenylated flavin cofactor. The latter is synthesised by the flavin prenyltransferase UbiX. Herein, we demonstrate the applicability of FDC/UbiX expressing cells for both isolated enzyme and whole-cell biocatalysis. FDCs exhibit high activity with total turnover numbers (TTN) of up to 55000 and turnover frequency (TOF) of up to 370min(-1). Co-solvent compatibility studies revealed FDC's tolerance to some organic solvents up 20% v/v. Using the in-vitro (de)carboxylase activity of holo-FDC as well as whole-cell biocatalysts, we performed a substrate profiling study of three FDCs, providing insights into structural determinants of activity. FDCs display broad substrate tolerance towards a wide range of acrylic acid derivatives bearing (hetero)cyclic or olefinic substituents at C3 affording conversions of up to >99%. The synthetic utility of FDCs was demonstrated by a preparative-scale decarboxylation.
引用
收藏
页码:3736 / 3745
页数:10
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