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Selective Enzymatic Transformation to Aldehydes in vivo by Fungal Carboxylate Reductase from Neurospora crassa
Author(s) -
Schwendenwein Daniel,
Fiume Giuseppe,
Weber Hansjörg,
Rudroff Florian,
Winkler Margit
Publication year - 2016
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.201600914
Subject(s) - neurospora crassa , chemistry , biotransformation , enzyme , carboxylate , yield (engineering) , biochemistry , escherichia coli , stereochemistry , transformation (genetics) , substrate (aquarium) , crassa , combinatorial chemistry , mutant , materials science , metallurgy , gene , oceanography , geology
The enzymatic reduction of carboxylic acids is in its infancy with only a handful of biocatalysts available to this end. We have increased the spectrum of carboxylate‐reducing enzymes (CARs) with the sequence of a fungal CAR from Neurospora crassa OR74A ( Nc CAR). Nc CAR was efficiently expressed in E. coli using an autoinduction protocol at low temperature. It was purified and characterized in vitro , revealing a broad substrate acceptance, a pH optimum at pH 5.5–6.0, a T m of 45 °C and inhibition by the co‐product pyrophosphate which can be alleviated by the addition of pyrophosphatase. The synthetic utility of Nc CAR was demonstrated in a whole‐cell biotransformation using the Escherichia coli K‐12 MG1655 RARE strain in order to suppress overreduction to undesired alcohol. The fragrance compound piperonal was prepared from piperonylic acid (30 mM) on gram scale in 92 % isolated yield in >98% purity. This corresponds to a productivity of 1.5 g/L/h.