共 73 条
Terminal Alkenes from Acrylic Acid Derivatives via Non-Oxidative Enzymatic Decarboxylation by Ferulic Acid Decarboxylases
被引:29
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
来源:
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;
奥地利科学基金会;
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.
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页码:3736 / 3745
页数:10
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