Est16, a New Esterase Isolated from a Metagenomic Library of a Microbial Consortium Specializing in Diesel Oil Degradation

Detalhes bibliográficos
Autor(a) principal: Pereira, Mariana Rangel [UNESP]
Data de Publicação: 2015
Outros Autores: Mercaldi, Gustavo Fernando, Maester, Thais Carvalho [UNESP], Balan, Andrea, Macedo Lemos, Eliana Gertrudes de [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1371/journal.pone.0133723
http://hdl.handle.net/11449/160684
Resumo: Lipolytic enzymes have attracted attention from a global market because they show enormous biotechnological potential for applications such as detergent production, leather processing, cosmetics production, and use in perfumes and biodiesel. Due to the intense demand for biocatalysts, a metagenomic approach provides methods of identifying new enzymes. In this study, an esterase designated as Est16 was selected from 4224 clones of a fosmid metagenomic library, revealing an 87% amino acid identity with an esterase/lipase (accession number ADM63076.1) from an uncultured bacterium. Phylogenetic studies showed that the enzyme belongs to family V of bacterial lipolytic enzymes and has sequence and structural similarities with an aryl-esterase from Pseudomonas fluorescens and a patented Anti-Kazlauskas lipase (patent number US20050153404). The protein was expressed and purified as a highly soluble, thermally stable enzyme that showed a preference for basic pH. Est16 exhibited activity toward a wide range of substrates and the highest catalytic efficiency against p-nitrophenyl butyrate and p-nitrophenyl valerate. Est16 also showed tolerance to the presence of organic solvents, detergents and metals. Based on molecular modeling, we showed that the large alpha-beta domain is conserved in the patented enzymes but not the substrate pocket. Here, it was demonstrated that a metagenomic approach is suitable for discovering the lipolytic enzyme diversity and that Est16 has the biotechnological potential for use in industrial processes.
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spelling Est16, a New Esterase Isolated from a Metagenomic Library of a Microbial Consortium Specializing in Diesel Oil DegradationLipolytic enzymes have attracted attention from a global market because they show enormous biotechnological potential for applications such as detergent production, leather processing, cosmetics production, and use in perfumes and biodiesel. Due to the intense demand for biocatalysts, a metagenomic approach provides methods of identifying new enzymes. In this study, an esterase designated as Est16 was selected from 4224 clones of a fosmid metagenomic library, revealing an 87% amino acid identity with an esterase/lipase (accession number ADM63076.1) from an uncultured bacterium. Phylogenetic studies showed that the enzyme belongs to family V of bacterial lipolytic enzymes and has sequence and structural similarities with an aryl-esterase from Pseudomonas fluorescens and a patented Anti-Kazlauskas lipase (patent number US20050153404). The protein was expressed and purified as a highly soluble, thermally stable enzyme that showed a preference for basic pH. Est16 exhibited activity toward a wide range of substrates and the highest catalytic efficiency against p-nitrophenyl butyrate and p-nitrophenyl valerate. Est16 also showed tolerance to the presence of organic solvents, detergents and metals. Based on molecular modeling, we showed that the large alpha-beta domain is conserved in the patented enzymes but not the substrate pocket. Here, it was demonstrated that a metagenomic approach is suitable for discovering the lipolytic enzyme diversity and that Est16 has the biotechnological potential for use in industrial processes.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Brazilian Ctr Res Energy & Mat CNPEM, Natl Lab Biosci LNBio, Campinas, SP, BrazilUniv Sao Paulo, Sao Paulo, SP, BrazilSao Paulo State Univ, Dept Technol, Jaboticabal, SP, BrazilUniv Estadual Campinas, Inst Biol, Campinas, SP, BrazilUniv Sao Paulo, Inst Biomed Sci 2, Dept Microbiol, Sao Paulo, SP, BrazilSao Paulo State Univ, Dept Technol, Jaboticabal, SP, BrazilFAPESP: 2011/09136-7Public Library ScienceBrazilian Ctr Res Energy & Mat CNPEMUniversidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Universidade Estadual de Campinas (UNICAMP)Pereira, Mariana Rangel [UNESP]Mercaldi, Gustavo FernandoMaester, Thais Carvalho [UNESP]Balan, AndreaMacedo Lemos, Eliana Gertrudes de [UNESP]2018-11-26T16:16:18Z2018-11-26T16:16:18Z2015-07-27info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article16application/pdfhttp://dx.doi.org/10.1371/journal.pone.0133723Plos One. San Francisco: Public Library Science, v. 10, n. 7, 16 p., 2015.1932-6203http://hdl.handle.net/11449/16068410.1371/journal.pone.0133723WOS:000358594300026WOS000358594300026.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPlos One1,164info:eu-repo/semantics/openAccess2024-06-07T15:32:23Zoai:repositorio.unesp.br:11449/160684Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T21:31:05.812676Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Est16, a New Esterase Isolated from a Metagenomic Library of a Microbial Consortium Specializing in Diesel Oil Degradation
title Est16, a New Esterase Isolated from a Metagenomic Library of a Microbial Consortium Specializing in Diesel Oil Degradation
spellingShingle Est16, a New Esterase Isolated from a Metagenomic Library of a Microbial Consortium Specializing in Diesel Oil Degradation
Pereira, Mariana Rangel [UNESP]
title_short Est16, a New Esterase Isolated from a Metagenomic Library of a Microbial Consortium Specializing in Diesel Oil Degradation
title_full Est16, a New Esterase Isolated from a Metagenomic Library of a Microbial Consortium Specializing in Diesel Oil Degradation
title_fullStr Est16, a New Esterase Isolated from a Metagenomic Library of a Microbial Consortium Specializing in Diesel Oil Degradation
title_full_unstemmed Est16, a New Esterase Isolated from a Metagenomic Library of a Microbial Consortium Specializing in Diesel Oil Degradation
title_sort Est16, a New Esterase Isolated from a Metagenomic Library of a Microbial Consortium Specializing in Diesel Oil Degradation
author Pereira, Mariana Rangel [UNESP]
author_facet Pereira, Mariana Rangel [UNESP]
Mercaldi, Gustavo Fernando
Maester, Thais Carvalho [UNESP]
Balan, Andrea
Macedo Lemos, Eliana Gertrudes de [UNESP]
author_role author
author2 Mercaldi, Gustavo Fernando
Maester, Thais Carvalho [UNESP]
Balan, Andrea
Macedo Lemos, Eliana Gertrudes de [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Brazilian Ctr Res Energy & Mat CNPEM
Universidade de São Paulo (USP)
Universidade Estadual Paulista (Unesp)
Universidade Estadual de Campinas (UNICAMP)
dc.contributor.author.fl_str_mv Pereira, Mariana Rangel [UNESP]
Mercaldi, Gustavo Fernando
Maester, Thais Carvalho [UNESP]
Balan, Andrea
Macedo Lemos, Eliana Gertrudes de [UNESP]
description Lipolytic enzymes have attracted attention from a global market because they show enormous biotechnological potential for applications such as detergent production, leather processing, cosmetics production, and use in perfumes and biodiesel. Due to the intense demand for biocatalysts, a metagenomic approach provides methods of identifying new enzymes. In this study, an esterase designated as Est16 was selected from 4224 clones of a fosmid metagenomic library, revealing an 87% amino acid identity with an esterase/lipase (accession number ADM63076.1) from an uncultured bacterium. Phylogenetic studies showed that the enzyme belongs to family V of bacterial lipolytic enzymes and has sequence and structural similarities with an aryl-esterase from Pseudomonas fluorescens and a patented Anti-Kazlauskas lipase (patent number US20050153404). The protein was expressed and purified as a highly soluble, thermally stable enzyme that showed a preference for basic pH. Est16 exhibited activity toward a wide range of substrates and the highest catalytic efficiency against p-nitrophenyl butyrate and p-nitrophenyl valerate. Est16 also showed tolerance to the presence of organic solvents, detergents and metals. Based on molecular modeling, we showed that the large alpha-beta domain is conserved in the patented enzymes but not the substrate pocket. Here, it was demonstrated that a metagenomic approach is suitable for discovering the lipolytic enzyme diversity and that Est16 has the biotechnological potential for use in industrial processes.
publishDate 2015
dc.date.none.fl_str_mv 2015-07-27
2018-11-26T16:16:18Z
2018-11-26T16:16:18Z
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1371/journal.pone.0133723
Plos One. San Francisco: Public Library Science, v. 10, n. 7, 16 p., 2015.
1932-6203
http://hdl.handle.net/11449/160684
10.1371/journal.pone.0133723
WOS:000358594300026
WOS000358594300026.pdf
url http://dx.doi.org/10.1371/journal.pone.0133723
http://hdl.handle.net/11449/160684
identifier_str_mv Plos One. San Francisco: Public Library Science, v. 10, n. 7, 16 p., 2015.
1932-6203
10.1371/journal.pone.0133723
WOS:000358594300026
WOS000358594300026.pdf
dc.language.iso.fl_str_mv eng
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dc.publisher.none.fl_str_mv Public Library Science
publisher.none.fl_str_mv Public Library Science
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instname_str Universidade Estadual Paulista (UNESP)
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