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Discovery and characterizaton of a novel lipase with transesterification activity from hot spring metagenomic library

A new gene encoding a lipase (designated as Lip-1) was identified from a metagenomic bacterial artificial chromosome(BAC) library prepared from a concentrated water sample collected from a hot spring field in Niujie, Eryuan of Yunnan province in China. The open reading frame of this gene encoded 622...

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Detalles Bibliográficos
Autores principales: Yan, Wei, Li, Furong, Wang, Li, Zhu, Yaxin, Dong, Zhiyang, Bai, Linhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397106/
https://www.ncbi.nlm.nih.gov/pubmed/28459005
http://dx.doi.org/10.1016/j.btre.2016.12.007
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author Yan, Wei
Li, Furong
Wang, Li
Zhu, Yaxin
Dong, Zhiyang
Bai, Linhan
author_facet Yan, Wei
Li, Furong
Wang, Li
Zhu, Yaxin
Dong, Zhiyang
Bai, Linhan
author_sort Yan, Wei
collection PubMed
description A new gene encoding a lipase (designated as Lip-1) was identified from a metagenomic bacterial artificial chromosome(BAC) library prepared from a concentrated water sample collected from a hot spring field in Niujie, Eryuan of Yunnan province in China. The open reading frame of this gene encoded 622 amino acid residues. It was cloned, fused with the oleosin gene and over expressed in Escherichia coli to prepare immobilized lipase artificial oil body AOB-sole-lip-1. The monomeric Sole-lip-1 fusion protein presented a molecular mass of 102.4 kDa. Enzyme assays using olive oil and methanol as the substrates in petroleum ether confirmed its transesterification activity. Hexadecanoic acid methyl ester, 8,11-Octadecadienoic acid methyl ester, 8-Octadecenoic acid methyl ester, and Octadecanoic acid methyl ester were detected. It showed favorable transesterification activity with optimal temperature 45 °C. Besides, the maximal biodiesel yield was obtained when the petroleum ether system as the organic solvent and the substrate methanol in 350 mmol/L (at a molar ratio of methanol of 10.5:1) and the water content was 1%. In light of these advantages, this lipase presents a promising resource for biodiesel production.
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spelling pubmed-53971062017-04-28 Discovery and characterizaton of a novel lipase with transesterification activity from hot spring metagenomic library Yan, Wei Li, Furong Wang, Li Zhu, Yaxin Dong, Zhiyang Bai, Linhan Biotechnol Rep (Amst) Article A new gene encoding a lipase (designated as Lip-1) was identified from a metagenomic bacterial artificial chromosome(BAC) library prepared from a concentrated water sample collected from a hot spring field in Niujie, Eryuan of Yunnan province in China. The open reading frame of this gene encoded 622 amino acid residues. It was cloned, fused with the oleosin gene and over expressed in Escherichia coli to prepare immobilized lipase artificial oil body AOB-sole-lip-1. The monomeric Sole-lip-1 fusion protein presented a molecular mass of 102.4 kDa. Enzyme assays using olive oil and methanol as the substrates in petroleum ether confirmed its transesterification activity. Hexadecanoic acid methyl ester, 8,11-Octadecadienoic acid methyl ester, 8-Octadecenoic acid methyl ester, and Octadecanoic acid methyl ester were detected. It showed favorable transesterification activity with optimal temperature 45 °C. Besides, the maximal biodiesel yield was obtained when the petroleum ether system as the organic solvent and the substrate methanol in 350 mmol/L (at a molar ratio of methanol of 10.5:1) and the water content was 1%. In light of these advantages, this lipase presents a promising resource for biodiesel production. Elsevier 2016-12-23 /pmc/articles/PMC5397106/ /pubmed/28459005 http://dx.doi.org/10.1016/j.btre.2016.12.007 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Yan, Wei
Li, Furong
Wang, Li
Zhu, Yaxin
Dong, Zhiyang
Bai, Linhan
Discovery and characterizaton of a novel lipase with transesterification activity from hot spring metagenomic library
title Discovery and characterizaton of a novel lipase with transesterification activity from hot spring metagenomic library
title_full Discovery and characterizaton of a novel lipase with transesterification activity from hot spring metagenomic library
title_fullStr Discovery and characterizaton of a novel lipase with transesterification activity from hot spring metagenomic library
title_full_unstemmed Discovery and characterizaton of a novel lipase with transesterification activity from hot spring metagenomic library
title_short Discovery and characterizaton of a novel lipase with transesterification activity from hot spring metagenomic library
title_sort discovery and characterizaton of a novel lipase with transesterification activity from hot spring metagenomic library
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397106/
https://www.ncbi.nlm.nih.gov/pubmed/28459005
http://dx.doi.org/10.1016/j.btre.2016.12.007
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