Co-production of ferulic acid and p-coumaric acid from distiller grain by a putative feruloyl esterase discovered in metagenome assembled genomes

The brewing industry generates a large amount of distillation waste, causing environmental pollution and resource wastage. In this study, a putative gene encoding feruloyl esterase detected in 33 bins using metagenomic sequencing, was expressed to exogenously to generate a recombinase with a molecul...

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Veröffentlicht in:Journal of cleaner production Jg. 439; S. 140814
Hauptverfasser: Zhang, Jiaqi, Tang, Hongzhi, Yu, Xun, Xue, Dongsheng, Li, Mei, Xing, Xingyue, Chen, Hao, Chen, Jia, Wang, Chongju, Gong, Chunjie
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Sprache:Englisch
Veröffentlicht: Elsevier Ltd 01.02.2024
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ISSN:0959-6526, 1879-1786
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Abstract The brewing industry generates a large amount of distillation waste, causing environmental pollution and resource wastage. In this study, a putative gene encoding feruloyl esterase detected in 33 bins using metagenomic sequencing, was expressed to exogenously to generate a recombinase with a molecular weight of 40.8 KDa. The feruloyl esterase has been optimized through codon optimization and signal peptide truncation to exhibit optimal activity at pH 6.0 and 50 °C, specifically when using 4-nitrophenyl trans-ferulate as its substrate. By employing this enzyme, p-coumaric acid and ferulic acid were simultaneously produced using brewing waste of distilled spent grain with husk. The yield of the two phenolic acids amounted to 91.2 μg and 89.25 μg from 1 g of distilled spent grain with husk, respectively. Although the yield obtained was lower than that from wheat bran and corn cob, the strategy serves as a model for the high-value utilization of brewing waste and has hold application potential. The integration of enzyme catalysis and metagenomic sequencing revealed a significant importance for clean production from agricultural processing industrial waste. The strategy for ferulic acid and p-coumaric acid production from distilled spent grain with husk by catalysis of a feruloyl esterase from Metagenomic sequencing of forest soils. Natural biomass containing hemicellulose could be degraded by the feruloyl esterase to produce high-value chemicals. It provided a gentle and environmentally friendly method for the biomass utilization. [Display omitted] •An encoding gene for feruloyl esterase was obtained through metagenomic sequencing.•The enzyme catalyzed the co-production of p-coumaric acid and ferulic acid.•A method for recovering chemicals from distilled spent grain with husk is provided.•The yield of p-coumaric acid and ferulic acid amounted to 91.2 μg/g and 89.25 μg/g.
AbstractList The brewing industry generates a large amount of distillation waste, causing environmental pollution and resource wastage. In this study, a putative gene encoding feruloyl esterase detected in 33 bins using metagenomic sequencing, was expressed to exogenously to generate a recombinase with a molecular weight of 40.8 KDa. The feruloyl esterase has been optimized through codon optimization and signal peptide truncation to exhibit optimal activity at pH 6.0 and 50 °C, specifically when using 4-nitrophenyl trans-ferulate as its substrate. By employing this enzyme, p-coumaric acid and ferulic acid were simultaneously produced using brewing waste of distilled spent grain with husk. The yield of the two phenolic acids amounted to 91.2 μg and 89.25 μg from 1 g of distilled spent grain with husk, respectively. Although the yield obtained was lower than that from wheat bran and corn cob, the strategy serves as a model for the high-value utilization of brewing waste and has hold application potential. The integration of enzyme catalysis and metagenomic sequencing revealed a significant importance for clean production from agricultural processing industrial waste.
The brewing industry generates a large amount of distillation waste, causing environmental pollution and resource wastage. In this study, a putative gene encoding feruloyl esterase detected in 33 bins using metagenomic sequencing, was expressed to exogenously to generate a recombinase with a molecular weight of 40.8 KDa. The feruloyl esterase has been optimized through codon optimization and signal peptide truncation to exhibit optimal activity at pH 6.0 and 50 °C, specifically when using 4-nitrophenyl trans-ferulate as its substrate. By employing this enzyme, p-coumaric acid and ferulic acid were simultaneously produced using brewing waste of distilled spent grain with husk. The yield of the two phenolic acids amounted to 91.2 μg and 89.25 μg from 1 g of distilled spent grain with husk, respectively. Although the yield obtained was lower than that from wheat bran and corn cob, the strategy serves as a model for the high-value utilization of brewing waste and has hold application potential. The integration of enzyme catalysis and metagenomic sequencing revealed a significant importance for clean production from agricultural processing industrial waste. The strategy for ferulic acid and p-coumaric acid production from distilled spent grain with husk by catalysis of a feruloyl esterase from Metagenomic sequencing of forest soils. Natural biomass containing hemicellulose could be degraded by the feruloyl esterase to produce high-value chemicals. It provided a gentle and environmentally friendly method for the biomass utilization. [Display omitted] •An encoding gene for feruloyl esterase was obtained through metagenomic sequencing.•The enzyme catalyzed the co-production of p-coumaric acid and ferulic acid.•A method for recovering chemicals from distilled spent grain with husk is provided.•The yield of p-coumaric acid and ferulic acid amounted to 91.2 μg/g and 89.25 μg/g.
ArticleNumber 140814
Author Tang, Hongzhi
Xing, Xingyue
Xue, Dongsheng
Li, Mei
Gong, Chunjie
Zhang, Jiaqi
Chen, Jia
Yu, Xun
Chen, Hao
Wang, Chongju
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  organization: Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Key Laboratory of Fermentation Engineering (Ministry of Education), National “111” Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan, 430068, PR China
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  givenname: Hongzhi
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  organization: State Key Laboratory of Microbial Metabolism, and School of Life Sciences & Biotechnology, Shanghai Jiao Tong University, Shanghai, 200240, PR China
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  givenname: Xun
  orcidid: 0000-0001-7248-8082
  surname: Yu
  fullname: Yu, Xun
  organization: Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Key Laboratory of Fermentation Engineering (Ministry of Education), National “111” Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan, 430068, PR China
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  givenname: Dongsheng
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  givenname: Mei
  orcidid: 0009-0007-8969-0499
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  organization: Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Key Laboratory of Fermentation Engineering (Ministry of Education), National “111” Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan, 430068, PR China
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  givenname: Xingyue
  surname: Xing
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  organization: Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Key Laboratory of Fermentation Engineering (Ministry of Education), National “111” Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan, 430068, PR China
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  givenname: Hao
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  givenname: Jia
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  organization: Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Key Laboratory of Fermentation Engineering (Ministry of Education), National “111” Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan, 430068, PR China
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  givenname: Chongju
  surname: Wang
  fullname: Wang, Chongju
  organization: Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Key Laboratory of Fermentation Engineering (Ministry of Education), National “111” Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan, 430068, PR China
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  givenname: Chunjie
  orcidid: 0000-0003-2198-6342
  surname: Gong
  fullname: Gong, Chunjie
  email: gongcj606@163.com
  organization: Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Key Laboratory of Fermentation Engineering (Ministry of Education), National “111” Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan, 430068, PR China
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Keywords Agricultural processing industrial waste
Feruloyl esterase
Distilled spent grain with husk
Phenolic acid
Metagenome
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Snippet The brewing industry generates a large amount of distillation waste, causing environmental pollution and resource wastage. In this study, a putative gene...
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SubjectTerms Agricultural processing industrial waste
catalytic activity
corn cobs
distillation
Distilled spent grain with husk
ferulic acid
Feruloyl esterase
genes
hulls
industrial wastes
industry
Metagenome
metagenomics
molecular weight
p-coumaric acid
Phenolic acid
pollution
recombinases
signal peptide
spent grains
wheat bran
Title Co-production of ferulic acid and p-coumaric acid from distiller grain by a putative feruloyl esterase discovered in metagenome assembled genomes
URI https://dx.doi.org/10.1016/j.jclepro.2024.140814
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