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Zymophore identification enables the discovery of novel phenylalanine ammonia lyase enzymes
The suite of biological catalysts found in Nature has the potential to contribute immensely to scientific advancements, ranging from industrial biotechnology to innovations in bioenergy and medical intervention. The endeavour to obtain a catalyst of choice is, however, wrought with challenges. Herei...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651878/ https://www.ncbi.nlm.nih.gov/pubmed/29057979 http://dx.doi.org/10.1038/s41598-017-13990-0 |
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author | Weise, Nicholas J. Ahmed, Syed T. Parmeggiani, Fabio Galman, James L. Dunstan, Mark S. Charnock, Simon J. Leys, David Turner, Nicholas J. |
author_facet | Weise, Nicholas J. Ahmed, Syed T. Parmeggiani, Fabio Galman, James L. Dunstan, Mark S. Charnock, Simon J. Leys, David Turner, Nicholas J. |
author_sort | Weise, Nicholas J. |
collection | PubMed |
description | The suite of biological catalysts found in Nature has the potential to contribute immensely to scientific advancements, ranging from industrial biotechnology to innovations in bioenergy and medical intervention. The endeavour to obtain a catalyst of choice is, however, wrought with challenges. Herein we report the design of a structure-based annotation system for the identification of functionally similar enzymes from diverse sequence backgrounds. Focusing on an enzymatic activity with demonstrated synthetic and therapeutic relevance, five new phenylalanine ammonia lyase (PAL) enzymes were discovered and characterised with respect to their potential applications. The variation and novelty of various desirable traits seen in these previously uncharacterised enzymes demonstrates the importance of effective sequence annotation in unlocking the potential diversity that Nature provides in the search for tailored biological tools. This new method has commercial relevance as a strategy for assaying the ‘evolvability’ of certain enzyme features, thus streamlining and informing protein engineering efforts. |
format | Online Article Text |
id | pubmed-5651878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56518782017-10-26 Zymophore identification enables the discovery of novel phenylalanine ammonia lyase enzymes Weise, Nicholas J. Ahmed, Syed T. Parmeggiani, Fabio Galman, James L. Dunstan, Mark S. Charnock, Simon J. Leys, David Turner, Nicholas J. Sci Rep Article The suite of biological catalysts found in Nature has the potential to contribute immensely to scientific advancements, ranging from industrial biotechnology to innovations in bioenergy and medical intervention. The endeavour to obtain a catalyst of choice is, however, wrought with challenges. Herein we report the design of a structure-based annotation system for the identification of functionally similar enzymes from diverse sequence backgrounds. Focusing on an enzymatic activity with demonstrated synthetic and therapeutic relevance, five new phenylalanine ammonia lyase (PAL) enzymes were discovered and characterised with respect to their potential applications. The variation and novelty of various desirable traits seen in these previously uncharacterised enzymes demonstrates the importance of effective sequence annotation in unlocking the potential diversity that Nature provides in the search for tailored biological tools. This new method has commercial relevance as a strategy for assaying the ‘evolvability’ of certain enzyme features, thus streamlining and informing protein engineering efforts. Nature Publishing Group UK 2017-10-20 /pmc/articles/PMC5651878/ /pubmed/29057979 http://dx.doi.org/10.1038/s41598-017-13990-0 Text en © The Author(s) 2017 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 Weise, Nicholas J. Ahmed, Syed T. Parmeggiani, Fabio Galman, James L. Dunstan, Mark S. Charnock, Simon J. Leys, David Turner, Nicholas J. Zymophore identification enables the discovery of novel phenylalanine ammonia lyase enzymes |
title | Zymophore identification enables the discovery of novel phenylalanine ammonia lyase enzymes |
title_full | Zymophore identification enables the discovery of novel phenylalanine ammonia lyase enzymes |
title_fullStr | Zymophore identification enables the discovery of novel phenylalanine ammonia lyase enzymes |
title_full_unstemmed | Zymophore identification enables the discovery of novel phenylalanine ammonia lyase enzymes |
title_short | Zymophore identification enables the discovery of novel phenylalanine ammonia lyase enzymes |
title_sort | zymophore identification enables the discovery of novel phenylalanine ammonia lyase enzymes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651878/ https://www.ncbi.nlm.nih.gov/pubmed/29057979 http://dx.doi.org/10.1038/s41598-017-13990-0 |
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