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Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles
Linear α,ω-dinitriles are important precursors for the polymer industry. Most prominently, adiponitrile is produced on an annual scale of ca. 1 million tons. However, a drawback of today’s dominating process is the need for large amounts of highly toxic hydrogen cyanide. In this contribution, an alt...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269433/ https://www.ncbi.nlm.nih.gov/pubmed/30504854 http://dx.doi.org/10.1038/s41467-018-07434-0 |
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author | Betke, Tobias Maier, Manuel Gruber-Wölfler, Heidrun Gröger, Harald |
author_facet | Betke, Tobias Maier, Manuel Gruber-Wölfler, Heidrun Gröger, Harald |
author_sort | Betke, Tobias |
collection | PubMed |
description | Linear α,ω-dinitriles are important precursors for the polymer industry. Most prominently, adiponitrile is produced on an annual scale of ca. 1 million tons. However, a drawback of today’s dominating process is the need for large amounts of highly toxic hydrogen cyanide. In this contribution, an alternative approach towards such linear dinitriles is presented based on dehydration of readily available α,ω-dialdoximes at ambient conditions by means of aldoxime dehydratases. In contrast to existing production routes this biocatalytic route enables a highly regio- and chemoselective approach towards dinitriles without the use of hydrogen cyanide or harsh reaction conditions. In addition, a selective synthesis of adiponitrile with substrate loadings of up to 100 g/L and high yields of up to 80% was achieved. Furthermore, a lab scale process on liter scale leading to > 99% conversion at 50 g/L underlines the potential and robustness of this method for technical applicability. |
format | Online Article Text |
id | pubmed-6269433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62694332018-12-03 Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles Betke, Tobias Maier, Manuel Gruber-Wölfler, Heidrun Gröger, Harald Nat Commun Article Linear α,ω-dinitriles are important precursors for the polymer industry. Most prominently, adiponitrile is produced on an annual scale of ca. 1 million tons. However, a drawback of today’s dominating process is the need for large amounts of highly toxic hydrogen cyanide. In this contribution, an alternative approach towards such linear dinitriles is presented based on dehydration of readily available α,ω-dialdoximes at ambient conditions by means of aldoxime dehydratases. In contrast to existing production routes this biocatalytic route enables a highly regio- and chemoselective approach towards dinitriles without the use of hydrogen cyanide or harsh reaction conditions. In addition, a selective synthesis of adiponitrile with substrate loadings of up to 100 g/L and high yields of up to 80% was achieved. Furthermore, a lab scale process on liter scale leading to > 99% conversion at 50 g/L underlines the potential and robustness of this method for technical applicability. Nature Publishing Group UK 2018-11-30 /pmc/articles/PMC6269433/ /pubmed/30504854 http://dx.doi.org/10.1038/s41467-018-07434-0 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Betke, Tobias Maier, Manuel Gruber-Wölfler, Heidrun Gröger, Harald Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles |
title | Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles |
title_full | Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles |
title_fullStr | Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles |
title_full_unstemmed | Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles |
title_short | Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles |
title_sort | biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269433/ https://www.ncbi.nlm.nih.gov/pubmed/30504854 http://dx.doi.org/10.1038/s41467-018-07434-0 |
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