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Laccase engineering by rational and evolutionary design
Laccases are considered as green catalysts of great biotechnological potential. This has attracted a great interest in designing laccases a la carte with enhanced stabilities or activities tailored to specific conditions for different fields of application. Over 20 years, numerous efforts have been...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Basel
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323517/ https://www.ncbi.nlm.nih.gov/pubmed/25586560 http://dx.doi.org/10.1007/s00018-014-1824-8 |
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author | Pardo, Isabel Camarero, Susana |
author_facet | Pardo, Isabel Camarero, Susana |
author_sort | Pardo, Isabel |
collection | PubMed |
description | Laccases are considered as green catalysts of great biotechnological potential. This has attracted a great interest in designing laccases a la carte with enhanced stabilities or activities tailored to specific conditions for different fields of application. Over 20 years, numerous efforts have been taken to engineer these multicopper oxidases and to understand their reaction mechanisms by site-directed mutagenesis, and more recently, using computational calculations and directed evolution tools. In this work, we review the most relevant contributions made in the field of laccase engineering, from the comprehensive study of their structure–function relationships to the tailoring of outstanding biocatalysts. |
format | Online Article Text |
id | pubmed-4323517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Basel |
record_format | MEDLINE/PubMed |
spelling | pubmed-43235172015-02-18 Laccase engineering by rational and evolutionary design Pardo, Isabel Camarero, Susana Cell Mol Life Sci Multi-Author Review Laccases are considered as green catalysts of great biotechnological potential. This has attracted a great interest in designing laccases a la carte with enhanced stabilities or activities tailored to specific conditions for different fields of application. Over 20 years, numerous efforts have been taken to engineer these multicopper oxidases and to understand their reaction mechanisms by site-directed mutagenesis, and more recently, using computational calculations and directed evolution tools. In this work, we review the most relevant contributions made in the field of laccase engineering, from the comprehensive study of their structure–function relationships to the tailoring of outstanding biocatalysts. Springer Basel 2015-01-14 2015 /pmc/articles/PMC4323517/ /pubmed/25586560 http://dx.doi.org/10.1007/s00018-014-1824-8 Text en © The Author(s) 2015 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Multi-Author Review Pardo, Isabel Camarero, Susana Laccase engineering by rational and evolutionary design |
title | Laccase engineering by rational and evolutionary design |
title_full | Laccase engineering by rational and evolutionary design |
title_fullStr | Laccase engineering by rational and evolutionary design |
title_full_unstemmed | Laccase engineering by rational and evolutionary design |
title_short | Laccase engineering by rational and evolutionary design |
title_sort | laccase engineering by rational and evolutionary design |
topic | Multi-Author Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323517/ https://www.ncbi.nlm.nih.gov/pubmed/25586560 http://dx.doi.org/10.1007/s00018-014-1824-8 |
work_keys_str_mv | AT pardoisabel laccaseengineeringbyrationalandevolutionarydesign AT camarerosusana laccaseengineeringbyrationalandevolutionarydesign |