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Discovery of Novel Bacterial Chalcone Isomerases by a Sequence‐Structure‐Function‐Evolution Strategy for Enzymatic Synthesis of (S)‐Flavanones
Chalcone isomerase (CHI) is a key enzyme in the biosynthesis of flavonoids in plants. The first bacterial CHI (CHI(era)) was identified from Eubacterium ramulus, but its distribution, evolutionary source, substrate scope, and stereoselectivity are still unclear. Here, we describe the identification...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361940/ https://www.ncbi.nlm.nih.gov/pubmed/34129275 http://dx.doi.org/10.1002/anie.202107182 |
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author | Meinert, Hannes Yi, Dong Zirpel, Bastian Schuiten, Eva Geißler, Torsten Gross, Egon Brückner, Stephan I. Hartmann, Beate Röttger, Carsten Ley, Jakob P. Bornscheuer, Uwe T. |
author_facet | Meinert, Hannes Yi, Dong Zirpel, Bastian Schuiten, Eva Geißler, Torsten Gross, Egon Brückner, Stephan I. Hartmann, Beate Röttger, Carsten Ley, Jakob P. Bornscheuer, Uwe T. |
author_sort | Meinert, Hannes |
collection | PubMed |
description | Chalcone isomerase (CHI) is a key enzyme in the biosynthesis of flavonoids in plants. The first bacterial CHI (CHI(era)) was identified from Eubacterium ramulus, but its distribution, evolutionary source, substrate scope, and stereoselectivity are still unclear. Here, we describe the identification of 66 novel bacterial CHIs from Genbank using a novel Sequence‐Structure‐Function‐Evolution (SSFE) strategy. These novel bacterial CHIs show diversity in substrate specificity towards various hydroxylated and methoxylated chalcones. The mutagenesis of CHI(era) according to the substrate binding models of these novel bacterial CHIs resulted in several variants with greatly improved activity towards these chalcones. Furthermore, the preparative scale conversion catalyzed by bacterial CHIs has been performed for five chalcones and revealed (S)‐selectivity with up to 96 % ee, which provides an alternative biocatalytic route for the synthesis of (S)‐flavanones in high yields. |
format | Online Article Text |
id | pubmed-8361940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83619402021-08-17 Discovery of Novel Bacterial Chalcone Isomerases by a Sequence‐Structure‐Function‐Evolution Strategy for Enzymatic Synthesis of (S)‐Flavanones Meinert, Hannes Yi, Dong Zirpel, Bastian Schuiten, Eva Geißler, Torsten Gross, Egon Brückner, Stephan I. Hartmann, Beate Röttger, Carsten Ley, Jakob P. Bornscheuer, Uwe T. Angew Chem Int Ed Engl Communications Chalcone isomerase (CHI) is a key enzyme in the biosynthesis of flavonoids in plants. The first bacterial CHI (CHI(era)) was identified from Eubacterium ramulus, but its distribution, evolutionary source, substrate scope, and stereoselectivity are still unclear. Here, we describe the identification of 66 novel bacterial CHIs from Genbank using a novel Sequence‐Structure‐Function‐Evolution (SSFE) strategy. These novel bacterial CHIs show diversity in substrate specificity towards various hydroxylated and methoxylated chalcones. The mutagenesis of CHI(era) according to the substrate binding models of these novel bacterial CHIs resulted in several variants with greatly improved activity towards these chalcones. Furthermore, the preparative scale conversion catalyzed by bacterial CHIs has been performed for five chalcones and revealed (S)‐selectivity with up to 96 % ee, which provides an alternative biocatalytic route for the synthesis of (S)‐flavanones in high yields. John Wiley and Sons Inc. 2021-06-30 2021-07-26 /pmc/articles/PMC8361940/ /pubmed/34129275 http://dx.doi.org/10.1002/anie.202107182 Text en © 2021 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Meinert, Hannes Yi, Dong Zirpel, Bastian Schuiten, Eva Geißler, Torsten Gross, Egon Brückner, Stephan I. Hartmann, Beate Röttger, Carsten Ley, Jakob P. Bornscheuer, Uwe T. Discovery of Novel Bacterial Chalcone Isomerases by a Sequence‐Structure‐Function‐Evolution Strategy for Enzymatic Synthesis of (S)‐Flavanones |
title | Discovery of Novel Bacterial Chalcone Isomerases by a Sequence‐Structure‐Function‐Evolution Strategy for Enzymatic Synthesis of (S)‐Flavanones |
title_full | Discovery of Novel Bacterial Chalcone Isomerases by a Sequence‐Structure‐Function‐Evolution Strategy for Enzymatic Synthesis of (S)‐Flavanones |
title_fullStr | Discovery of Novel Bacterial Chalcone Isomerases by a Sequence‐Structure‐Function‐Evolution Strategy for Enzymatic Synthesis of (S)‐Flavanones |
title_full_unstemmed | Discovery of Novel Bacterial Chalcone Isomerases by a Sequence‐Structure‐Function‐Evolution Strategy for Enzymatic Synthesis of (S)‐Flavanones |
title_short | Discovery of Novel Bacterial Chalcone Isomerases by a Sequence‐Structure‐Function‐Evolution Strategy for Enzymatic Synthesis of (S)‐Flavanones |
title_sort | discovery of novel bacterial chalcone isomerases by a sequence‐structure‐function‐evolution strategy for enzymatic synthesis of (s)‐flavanones |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361940/ https://www.ncbi.nlm.nih.gov/pubmed/34129275 http://dx.doi.org/10.1002/anie.202107182 |
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