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Directed evolution of the aryl-alcohol oxidase: Beyond the lab bench

Aryl-alcohol oxidase (AAO) is a fungal GMC flavoprotein secreted by white-rot fungi that supplies H(2)O(2) to the ligninolytic consortium. This enzyme can oxidize a wide array of aromatic alcohols in a highly enantioselective manner, an important trait in organic synthesis. The best strategy to adap...

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Detalles Bibliográficos
Autores principales: Viña-Gonzalez, Javier, Alcalde, Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7358221/
https://www.ncbi.nlm.nih.gov/pubmed/32695272
http://dx.doi.org/10.1016/j.csbj.2020.06.037
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author Viña-Gonzalez, Javier
Alcalde, Miguel
author_facet Viña-Gonzalez, Javier
Alcalde, Miguel
author_sort Viña-Gonzalez, Javier
collection PubMed
description Aryl-alcohol oxidase (AAO) is a fungal GMC flavoprotein secreted by white-rot fungi that supplies H(2)O(2) to the ligninolytic consortium. This enzyme can oxidize a wide array of aromatic alcohols in a highly enantioselective manner, an important trait in organic synthesis. The best strategy to adapt AAO to industrial needs is to engineer its properties by directed evolution, aided by computational analysis. The aim of this review is to describe the strategies and challenges we faced when undertaking laboratory evolution of AAO. After a comprehensive introduction into the structure of AAO, its function and potential applications, the different directed evolution enterprises designed to express the enzyme in an active and soluble form in yeast are described, as well as those to unlock new activities involving the oxidation of secondary aromatic alcohols and the synthesis of furandicarboxylic acids.
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spelling pubmed-73582212020-07-20 Directed evolution of the aryl-alcohol oxidase: Beyond the lab bench Viña-Gonzalez, Javier Alcalde, Miguel Comput Struct Biotechnol J Review Article Aryl-alcohol oxidase (AAO) is a fungal GMC flavoprotein secreted by white-rot fungi that supplies H(2)O(2) to the ligninolytic consortium. This enzyme can oxidize a wide array of aromatic alcohols in a highly enantioselective manner, an important trait in organic synthesis. The best strategy to adapt AAO to industrial needs is to engineer its properties by directed evolution, aided by computational analysis. The aim of this review is to describe the strategies and challenges we faced when undertaking laboratory evolution of AAO. After a comprehensive introduction into the structure of AAO, its function and potential applications, the different directed evolution enterprises designed to express the enzyme in an active and soluble form in yeast are described, as well as those to unlock new activities involving the oxidation of secondary aromatic alcohols and the synthesis of furandicarboxylic acids. Research Network of Computational and Structural Biotechnology 2020-06-29 /pmc/articles/PMC7358221/ /pubmed/32695272 http://dx.doi.org/10.1016/j.csbj.2020.06.037 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review Article
Viña-Gonzalez, Javier
Alcalde, Miguel
Directed evolution of the aryl-alcohol oxidase: Beyond the lab bench
title Directed evolution of the aryl-alcohol oxidase: Beyond the lab bench
title_full Directed evolution of the aryl-alcohol oxidase: Beyond the lab bench
title_fullStr Directed evolution of the aryl-alcohol oxidase: Beyond the lab bench
title_full_unstemmed Directed evolution of the aryl-alcohol oxidase: Beyond the lab bench
title_short Directed evolution of the aryl-alcohol oxidase: Beyond the lab bench
title_sort directed evolution of the aryl-alcohol oxidase: beyond the lab bench
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7358221/
https://www.ncbi.nlm.nih.gov/pubmed/32695272
http://dx.doi.org/10.1016/j.csbj.2020.06.037
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