Biosynthesis of acetylacetone inspired by its biodegradation
Abstract 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-b...
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doaj-8c4dceaf10ea4f7e830e04423024f4352020-11-25T02:15:09ZengBMCBiotechnology for Biofuels1754-68342020-05-0113111010.1186/s13068-020-01725-9Biosynthesis of acetylacetone inspired by its biodegradationYifei Zhou0Yamei Ding1Wenjie Gao2Jichao Wang3Xiutao Liu4Mo Xian5Xinjun Feng6Guang Zhao7CAS Key Laboratory of Biobased Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of SciencesInstitute of Oceanology, Chinese Academy of SciencesCAS Key Laboratory of Biobased Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of SciencesCAS Key Laboratory of Biobased Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of SciencesCAS Key Laboratory of Biobased Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of SciencesCAS Key Laboratory of Biobased Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of SciencesCAS Key Laboratory of Biobased Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of SciencesCAS Key Laboratory of Biobased Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of SciencesAbstract 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.http://link.springer.com/article/10.1186/s13068-020-01725-9Acetylacetone biosynthesisAcetylacetone-cleaving enzymeRational designSite-directed mutagenesisβ-Dicarbonyl compounds |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yifei Zhou Yamei Ding Wenjie Gao Jichao Wang Xiutao Liu Mo Xian Xinjun Feng Guang Zhao |
spellingShingle |
Yifei Zhou Yamei Ding Wenjie Gao Jichao Wang Xiutao Liu Mo Xian Xinjun Feng Guang Zhao Biosynthesis of acetylacetone inspired by its biodegradation Biotechnology for Biofuels Acetylacetone biosynthesis Acetylacetone-cleaving enzyme Rational design Site-directed mutagenesis β-Dicarbonyl compounds |
author_facet |
Yifei Zhou Yamei Ding Wenjie Gao Jichao Wang Xiutao Liu Mo Xian Xinjun Feng Guang Zhao |
author_sort |
Yifei Zhou |
title |
Biosynthesis of acetylacetone inspired by its biodegradation |
title_short |
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_sort |
biosynthesis of acetylacetone inspired by its biodegradation |
publisher |
BMC |
series |
Biotechnology for Biofuels |
issn |
1754-6834 |
publishDate |
2020-05-01 |
description |
Abstract 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. |
topic |
Acetylacetone biosynthesis Acetylacetone-cleaving enzyme Rational design Site-directed mutagenesis β-Dicarbonyl compounds |
url |
http://link.springer.com/article/10.1186/s13068-020-01725-9 |
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