Co-metabolic formation of substituted phenylacetic acids by styrene-degrading bacteria
[Display omitted] •Styrene degradation via phenylacetic acid was shown for the strains described.•Co-metabolic transformation of substituted styrenes was shown.•Formation of several phenylacetic acids, e.g. ibuprofen, was reported.•α-Methylated substrates were transformed enantioselectively with an...
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| Published in: | Biotechnology reports (Amsterdam, Netherlands) Vol. 6; no. C; pp. 20 - 26 |
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| Main Authors: | , , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
Netherlands
Elsevier B.V
01.06.2015
Elsevier |
| Subjects: | |
| ISSN: | 2215-017X, 2215-017X |
| Online Access: | Get full text |
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| Summary: | [Display omitted]
•Styrene degradation via phenylacetic acid was shown for the strains described.•Co-metabolic transformation of substituted styrenes was shown.•Formation of several phenylacetic acids, e.g. ibuprofen, was reported.•α-Methylated substrates were transformed enantioselectively with an ee of up to 40%.•Pseud. fluorescens ST was identified as promising biocatalyst for phenylacetic acids.
Some soil bacteria are able to metabolize styrene via initial side-chain oxygenation. This catabolic route is of potential biotechnological relevance due to the occurrence of phenylacetic acid as a central metabolite.
The styrene-degrading strains Rhodococcus opacus 1CP, Pseudomonas fluorescens ST, and the novel isolates Sphingopyxis sp. Kp5.2 and Gordonia sp. CWB2 were investigated with respect to their applicability to co-metabolically produce substituted phenylacetic acids. Isolates were found to differ significantly in substrate tolerance and biotransformation yields. Especially, P. fluorescens ST was identified as a promising candidate for the production of several phenylacetic acids. The biotransformation of 4-chlorostyrene with cells of strain ST was shown to be stable over a period of more than 200 days and yielded about 38mmolproductgcelldryweight−1 after nearly 350 days. Moreover, 4-chloro-α-methylstyrene was predominantly converted to the (S)-enantiomer of the acid with 40% enantiomeric excess. |
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| Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
| ISSN: | 2215-017X 2215-017X |
| DOI: | 10.1016/j.btre.2015.01.003 |