Biocatalytic hydroxylation of n-butane with in situ cofactor regeneration at low temperature and under normal pressure
The hydroxylation of n-alkanes, which proceeds in the presence of a P450-monooxygenase advantageously at temperatures significantly below room temperature, is described. In addition, an enzymatic hydroxylation of the “liquid gas” n-butane with in situ cofactor regeneration, which does not require hi...
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doaj-1fad91934f3b4507bf388879cd46819e2021-02-02T00:50:50ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972012-02-018118619110.3762/bjoc.8.201860-5397-8-20Biocatalytic hydroxylation of n-butane with in situ cofactor regeneration at low temperature and under normal pressureSvenja Staudt0Christina A. Müller1Jan Marienhagen2Christian Böing3Stefan Buchholz4Ulrich Schwaneberg5Harald Gröger6Department of Chemistry and Pharmacy, University of Erlangen-Nürnberg, Henkestr. 42, 91054 Erlangen, GermanyDepartment of Biotechnology, RWTH Aachen University, Worringerweg 1, 52074 Aachen, GermanyDepartment of Biotechnology, RWTH Aachen University, Worringerweg 1, 52074 Aachen, GermanyEvonik Oxeno GmbH, Paul-Baumann-Straße 1, 45772 Marl, GermanyEvonik Degussa GmbH, Industrial Chemicals, Paul-Baumann-Straße 1, 45772 Marl, GermanyDepartment of Biotechnology, RWTH Aachen University, Worringerweg 1, 52074 Aachen, GermanyDepartment of Chemistry and Pharmacy, University of Erlangen-Nürnberg, Henkestr. 42, 91054 Erlangen, GermanyThe hydroxylation of n-alkanes, which proceeds in the presence of a P450-monooxygenase advantageously at temperatures significantly below room temperature, is described. In addition, an enzymatic hydroxylation of the “liquid gas” n-butane with in situ cofactor regeneration, which does not require high-pressure conditions, was developed. The resulting 2-butanol was obtained as the only regioisomer, at a product concentration of 0.16 g/L.https://doi.org/10.3762/bjoc.8.20biotransformationscofactor regenerationgreen chemistryhydroxylationP450-monooxygenase |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Svenja Staudt Christina A. Müller Jan Marienhagen Christian Böing Stefan Buchholz Ulrich Schwaneberg Harald Gröger |
spellingShingle |
Svenja Staudt Christina A. Müller Jan Marienhagen Christian Böing Stefan Buchholz Ulrich Schwaneberg Harald Gröger Biocatalytic hydroxylation of n-butane with in situ cofactor regeneration at low temperature and under normal pressure Beilstein Journal of Organic Chemistry biotransformations cofactor regeneration green chemistry hydroxylation P450-monooxygenase |
author_facet |
Svenja Staudt Christina A. Müller Jan Marienhagen Christian Böing Stefan Buchholz Ulrich Schwaneberg Harald Gröger |
author_sort |
Svenja Staudt |
title |
Biocatalytic hydroxylation of n-butane with in situ cofactor regeneration at low temperature and under normal pressure |
title_short |
Biocatalytic hydroxylation of n-butane with in situ cofactor regeneration at low temperature and under normal pressure |
title_full |
Biocatalytic hydroxylation of n-butane with in situ cofactor regeneration at low temperature and under normal pressure |
title_fullStr |
Biocatalytic hydroxylation of n-butane with in situ cofactor regeneration at low temperature and under normal pressure |
title_full_unstemmed |
Biocatalytic hydroxylation of n-butane with in situ cofactor regeneration at low temperature and under normal pressure |
title_sort |
biocatalytic hydroxylation of n-butane with in situ cofactor regeneration at low temperature and under normal pressure |
publisher |
Beilstein-Institut |
series |
Beilstein Journal of Organic Chemistry |
issn |
1860-5397 |
publishDate |
2012-02-01 |
description |
The hydroxylation of n-alkanes, which proceeds in the presence of a P450-monooxygenase advantageously at temperatures significantly below room temperature, is described. In addition, an enzymatic hydroxylation of the “liquid gas” n-butane with in situ cofactor regeneration, which does not require high-pressure conditions, was developed. The resulting 2-butanol was obtained as the only regioisomer, at a product concentration of 0.16 g/L. |
topic |
biotransformations cofactor regeneration green chemistry hydroxylation P450-monooxygenase |
url |
https://doi.org/10.3762/bjoc.8.20 |
work_keys_str_mv |
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1724312801128742912 |