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A biocatalytic method for the chemoselective aerobic oxidation of aldehydes to carboxylic acids

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논문

A biocatalytic method for the chemoselective aerobic oxidation of aldehydes to carboxylic acids

학술지

Green chemistry : an international journal and green chemistry resource : GC

저자명

Knaus, Tanja; Tseliou, Vasilis; HumphreysCurrent address: Gilead Alberta ULC, 1021 Hayter Road NW, Edmonton, AB T6S 1A1, Canada., Luke D.; Scrutton, Nigel S.; Mutti, Francesco G.

초록

<P>Herein, we present a study on the oxidation of aldehydes to carboxylic acids using three recombinant aldehyde dehydrogenases (ALDHs). The ALDHs were used in purified form with a nicotinamide oxidase (NOx), which recycles the catalytic NAD<SUP>+</SUP> at the expense of dioxygen (air at atmospheric pressure). The reaction was studied also with lyophilised whole cell as well as resting cell biocatalysts for more convenient practical application. The optimised biocatalytic oxidation runs in phosphate buffer at pH 8.5 and at 40 &deg;C. From a set of sixty-one aliphatic, aryl-aliphatic, benzylic, hetero-aromatic and bicyclic aldehydes, fifty were converted with elevated yield (up to >99%). The exceptions were a few <I>ortho</I>-substituted benzaldehydes, bicyclic heteroaromatic aldehydes and 2-phenylpropanal. In all cases, the expected carboxylic acid was shown to be the only product (>99% chemoselectivity). Other oxidisable functionalities within the same molecule (<I>e.g.</I> hydroxyl, alkene, and heteroaromatic nitrogen or sulphur atoms) remained untouched. The reaction was scaled for the oxidation of 5-(hydroxymethyl)furfural (2 g), a bio-based starting material, to afford 5-(hydroxymethyl)furoic acid in 61% isolated yield. The new biocatalytic method avoids the use of toxic or unsafe oxidants, strong acids or bases, or undesired solvents. It shows applicability across a wide range of substrates, and retains perfect chemoselectivity. Alternative oxidisable groups were not converted, and other classical side-reactions (<I>e.g.</I> halogenation of unsaturated functionalities, Dakin-type oxidation) did not occur. In comparison to other established enzymatic methods such as the use of oxidases (where the concomitant oxidation of alcohols and aldehydes is common), ALDHs offer greatly improved selectivity.</P><P>Graphic Abstract</P><P>Aldehyde dehydrogenases enable the chemospecific oxidation of structurally diverse aldehydes to carboxylic acids in aqueous environment and using only air.<BR/><IMG SRC='http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=c8gc01381k'/><BR/></P>

발행연도

2018

발행기관

The Royal Society of Chemistry

ISSN

1463-9262

ISSN

1463-9270

20

17

페이지

pp.3931-3943

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논문; 2018-01-01

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