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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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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. |
format | Online Article Text |
id | pubmed-5397106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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