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Advances in 4-Hydroxyphenylacetate-3-hydroxylase Monooxygenase
Catechols have important applications in the pharmaceutical, food, cosmetic, and functional material industries. 4-hydroxyphenylacetate-3-hydroxylase (4HPA3H), a two-component enzyme system comprising HpaB (monooxygenase) and HpaC (FAD oxidoreductase), demonstrates significant potential for catechol...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10537072/ https://www.ncbi.nlm.nih.gov/pubmed/37764475 http://dx.doi.org/10.3390/molecules28186699 |
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author | Yang, Kai Zhang, Qianchao Zhao, Weirui Hu, Sheng Lv, Changjiang Huang, Jun Mei, Jiaqi Mei, Lehe |
author_facet | Yang, Kai Zhang, Qianchao Zhao, Weirui Hu, Sheng Lv, Changjiang Huang, Jun Mei, Jiaqi Mei, Lehe |
author_sort | Yang, Kai |
collection | PubMed |
description | Catechols have important applications in the pharmaceutical, food, cosmetic, and functional material industries. 4-hydroxyphenylacetate-3-hydroxylase (4HPA3H), a two-component enzyme system comprising HpaB (monooxygenase) and HpaC (FAD oxidoreductase), demonstrates significant potential for catechol production because it can be easily expressed, is highly active, and exhibits ortho-hydroxylation activity toward a broad spectrum of phenol substrates. HpaB determines the ortho-hydroxylation efficiency and substrate spectrum of the enzyme; therefore, studying its structure–activity relationship, improving its properties, and developing a robust HpaB-conducting system are of significance and value; indeed, considerable efforts have been made in these areas in recent decades. Here, we review the classification, molecular structure, catalytic mechanism, primary efforts in protein engineering, and industrial applications of HpaB in catechol synthesis. Current trends in the further investigation of HpaB are also discussed. |
format | Online Article Text |
id | pubmed-10537072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105370722023-09-29 Advances in 4-Hydroxyphenylacetate-3-hydroxylase Monooxygenase Yang, Kai Zhang, Qianchao Zhao, Weirui Hu, Sheng Lv, Changjiang Huang, Jun Mei, Jiaqi Mei, Lehe Molecules Review Catechols have important applications in the pharmaceutical, food, cosmetic, and functional material industries. 4-hydroxyphenylacetate-3-hydroxylase (4HPA3H), a two-component enzyme system comprising HpaB (monooxygenase) and HpaC (FAD oxidoreductase), demonstrates significant potential for catechol production because it can be easily expressed, is highly active, and exhibits ortho-hydroxylation activity toward a broad spectrum of phenol substrates. HpaB determines the ortho-hydroxylation efficiency and substrate spectrum of the enzyme; therefore, studying its structure–activity relationship, improving its properties, and developing a robust HpaB-conducting system are of significance and value; indeed, considerable efforts have been made in these areas in recent decades. Here, we review the classification, molecular structure, catalytic mechanism, primary efforts in protein engineering, and industrial applications of HpaB in catechol synthesis. Current trends in the further investigation of HpaB are also discussed. MDPI 2023-09-19 /pmc/articles/PMC10537072/ /pubmed/37764475 http://dx.doi.org/10.3390/molecules28186699 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Yang, Kai Zhang, Qianchao Zhao, Weirui Hu, Sheng Lv, Changjiang Huang, Jun Mei, Jiaqi Mei, Lehe Advances in 4-Hydroxyphenylacetate-3-hydroxylase Monooxygenase |
title | Advances in 4-Hydroxyphenylacetate-3-hydroxylase Monooxygenase |
title_full | Advances in 4-Hydroxyphenylacetate-3-hydroxylase Monooxygenase |
title_fullStr | Advances in 4-Hydroxyphenylacetate-3-hydroxylase Monooxygenase |
title_full_unstemmed | Advances in 4-Hydroxyphenylacetate-3-hydroxylase Monooxygenase |
title_short | Advances in 4-Hydroxyphenylacetate-3-hydroxylase Monooxygenase |
title_sort | advances in 4-hydroxyphenylacetate-3-hydroxylase monooxygenase |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10537072/ https://www.ncbi.nlm.nih.gov/pubmed/37764475 http://dx.doi.org/10.3390/molecules28186699 |
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