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Biosynthesis of acetylacetone inspired by its biodegradation

BACKGROUND: Acetylacetone is a commercially bulk chemical with diverse applications. However, the traditional manufacturing methods suffer from many drawbacks such as multiple steps, harsh conditions, low yield, and environmental problems, which hamper further applications of petrochemical-based ace...

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Autores principales: Zhou, Yifei, Ding, Yamei, Gao, Wenjie, Wang, Jichao, Liu, Xiutao, Xian, Mo, Feng, Xinjun, Zhao, Guang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226712/
https://www.ncbi.nlm.nih.gov/pubmed/32454892
http://dx.doi.org/10.1186/s13068-020-01725-9
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author Zhou, Yifei
Ding, Yamei
Gao, Wenjie
Wang, Jichao
Liu, Xiutao
Xian, Mo
Feng, Xinjun
Zhao, Guang
author_facet Zhou, Yifei
Ding, Yamei
Gao, Wenjie
Wang, Jichao
Liu, Xiutao
Xian, Mo
Feng, Xinjun
Zhao, Guang
author_sort Zhou, Yifei
collection PubMed
description BACKGROUND: Acetylacetone is a commercially bulk chemical with diverse applications. However, the traditional manufacturing methods suffer from many drawbacks such as multiple steps, harsh conditions, low yield, and environmental problems, which hamper further applications of petrochemical-based acetylacetone. Compared to conventional chemical methods, biosynthetic methods possess advantages such as being eco-friendly, and having mild conditions, high selectivity and low potential costs. It is urgent to develop biosynthetic route for acetylacetone to avoid the present problems. RESULTS: The biosynthetic pathway of acetylacetone was constructed by reversing its biodegradation route, and the acetylacetone was successfully produced by engineered Escherichia coli (E. coli) by overexpression of acetylacetone-cleaving enzyme (Dke1) from Acinetobacter johnsonii. Several promising amino acid residues were selected for enzyme improvement based on sequence alignment and structure analysis, and the acetylacetone production was improved by site-directed mutagenesis of Dke1. The double-mutant (K15Q/A60D) strain presented the highest acetylacetone-producing capacity which is 3.6-fold higher than that of the wild-type protein. Finally, the strain accumulated 556.3 ± 15.2 mg/L acetylacetone in fed-batch fermentation under anaerobic conditions. CONCLUSIONS: This study presents the first intuitive biosynthetic pathway for acetylacetone inspired by its biodegradation, and shows the potential for large-scale production.
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spelling pubmed-72267122020-05-18 Biosynthesis of acetylacetone inspired by its biodegradation Zhou, Yifei Ding, Yamei Gao, Wenjie Wang, Jichao Liu, Xiutao Xian, Mo Feng, Xinjun Zhao, Guang Biotechnol Biofuels Research BACKGROUND: Acetylacetone is a commercially bulk chemical with diverse applications. However, the traditional manufacturing methods suffer from many drawbacks such as multiple steps, harsh conditions, low yield, and environmental problems, which hamper further applications of petrochemical-based acetylacetone. Compared to conventional chemical methods, biosynthetic methods possess advantages such as being eco-friendly, and having mild conditions, high selectivity and low potential costs. It is urgent to develop biosynthetic route for acetylacetone to avoid the present problems. RESULTS: The biosynthetic pathway of acetylacetone was constructed by reversing its biodegradation route, and the acetylacetone was successfully produced by engineered Escherichia coli (E. coli) by overexpression of acetylacetone-cleaving enzyme (Dke1) from Acinetobacter johnsonii. Several promising amino acid residues were selected for enzyme improvement based on sequence alignment and structure analysis, and the acetylacetone production was improved by site-directed mutagenesis of Dke1. The double-mutant (K15Q/A60D) strain presented the highest acetylacetone-producing capacity which is 3.6-fold higher than that of the wild-type protein. Finally, the strain accumulated 556.3 ± 15.2 mg/L acetylacetone in fed-batch fermentation under anaerobic conditions. CONCLUSIONS: This study presents the first intuitive biosynthetic pathway for acetylacetone inspired by its biodegradation, and shows the potential for large-scale production. BioMed Central 2020-05-15 /pmc/articles/PMC7226712/ /pubmed/32454892 http://dx.doi.org/10.1186/s13068-020-01725-9 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhou, Yifei
Ding, Yamei
Gao, Wenjie
Wang, Jichao
Liu, Xiutao
Xian, Mo
Feng, Xinjun
Zhao, Guang
Biosynthesis of acetylacetone inspired by its biodegradation
title Biosynthesis of acetylacetone inspired by its biodegradation
title_full Biosynthesis of acetylacetone inspired by its biodegradation
title_fullStr Biosynthesis of acetylacetone inspired by its biodegradation
title_full_unstemmed Biosynthesis of acetylacetone inspired by its biodegradation
title_short Biosynthesis of acetylacetone inspired by its biodegradation
title_sort biosynthesis of acetylacetone inspired by its biodegradation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226712/
https://www.ncbi.nlm.nih.gov/pubmed/32454892
http://dx.doi.org/10.1186/s13068-020-01725-9
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