From data mining of chitinophaga sp. Genome to enzyme discovery of a hyperthermophilic metallocarboxypeptidase

Detalhes bibliográficos
Autor(a) principal: Fernandes, Gabriela Cabral [UNESP]
Data de Publicação: 2021
Outros Autores: Sierra, Elwi Guillermo Machado [UNESP], Brear, Paul, Pereira, Mariana Rangel, Lemos, Eliana G. M. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.3390/microorganisms9020393
http://hdl.handle.net/11449/205871
Resumo: For several centuries, microorganisms and enzymes have been used for many different applications. Although many enzymes with industrial applications have already been reported, different screening technologies, methods and approaches are constantly being developed in order to allow the identification of enzymes with even more interesting applications. In our work, we have performed data mining on the Chitinophaga sp. genome, a gram-negative bacterium isolated from a bacterial consortium of sugarcane bagasse isolated from an ethanol plant. The analysis of 8 Mb allowed the identification of the chtcp gene, previously annotated as putative Cht4039. The corresponding codified enzyme, denominated as ChtCP, showed the HEXXH conserved motif of family M32 from thermostable carboxypeptidases. After expression in E. coli, the recombinant enzyme was characterized biochemically. ChtCP showed the highest activity versus benziloxicarbonil Ala-Trp at pH 7.5, suggesting a preference for hydrophobic substrates. Surprisingly, the highest activity of ChtCP observed was between 55 °C and 75 °C, and 62% activity was still displayed at 100 °C. We observed that Ca2+, Ba2+, Mn2+ and Mg2+ ions had a positive effect on the activity of ChtCP, and an increase of 30 °C in the melting temperature was observed in the presence of Co2+. These features together with the structure of ChtCP at 1.2 Å highlight the relevance of ChtCP for further biotechnological applications.
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spelling From data mining of chitinophaga sp. Genome to enzyme discovery of a hyperthermophilic metallocarboxypeptidaseChitinophaga spM32 family of peptidasesMetallocarboxypeptidaseFor several centuries, microorganisms and enzymes have been used for many different applications. Although many enzymes with industrial applications have already been reported, different screening technologies, methods and approaches are constantly being developed in order to allow the identification of enzymes with even more interesting applications. In our work, we have performed data mining on the Chitinophaga sp. genome, a gram-negative bacterium isolated from a bacterial consortium of sugarcane bagasse isolated from an ethanol plant. The analysis of 8 Mb allowed the identification of the chtcp gene, previously annotated as putative Cht4039. The corresponding codified enzyme, denominated as ChtCP, showed the HEXXH conserved motif of family M32 from thermostable carboxypeptidases. After expression in E. coli, the recombinant enzyme was characterized biochemically. ChtCP showed the highest activity versus benziloxicarbonil Ala-Trp at pH 7.5, suggesting a preference for hydrophobic substrates. Surprisingly, the highest activity of ChtCP observed was between 55 °C and 75 °C, and 62% activity was still displayed at 100 °C. We observed that Ca2+, Ba2+, Mn2+ and Mg2+ ions had a positive effect on the activity of ChtCP, and an increase of 30 °C in the melting temperature was observed in the presence of Co2+. These features together with the structure of ChtCP at 1.2 Å highlight the relevance of ChtCP for further biotechnological applications.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Department of Technology São Paulo State University (UNESP)São Paulo State University (UNESP) School of Agricultural and Veterinarian SciencesLaboratorio de Investigación en Microbiología Facultad de Ciencias Básicas y Biomédicas Universidad Simón BolívarDepartment of Biochemistry University of CambridgeCAPES Foundation Ministry of Education of Brazil, DFDepartment of Technology São Paulo State University (UNESP)São Paulo State University (UNESP) School of Agricultural and Veterinarian SciencesCAPES: 001FAPESP: 2016/23892-2CNPq: 401886/2016-1Universidade Estadual Paulista (Unesp)Universidad Simón BolívarUniversity of CambridgeMinistry of Education of BrazilFernandes, Gabriela Cabral [UNESP]Sierra, Elwi Guillermo Machado [UNESP]Brear, PaulPereira, Mariana RangelLemos, Eliana G. M. [UNESP]2021-06-25T10:22:38Z2021-06-25T10:22:38Z2021-02-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1-18http://dx.doi.org/10.3390/microorganisms9020393Microorganisms, v. 9, n. 2, p. 1-18, 2021.2076-2607http://hdl.handle.net/11449/20587110.3390/microorganisms90203932-s2.0-85100799983Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMicroorganismsinfo:eu-repo/semantics/openAccess2021-10-22T19:32:21Zoai:repositorio.unesp.br:11449/205871Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T17:53:21.392128Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv From data mining of chitinophaga sp. Genome to enzyme discovery of a hyperthermophilic metallocarboxypeptidase
title From data mining of chitinophaga sp. Genome to enzyme discovery of a hyperthermophilic metallocarboxypeptidase
spellingShingle From data mining of chitinophaga sp. Genome to enzyme discovery of a hyperthermophilic metallocarboxypeptidase
Fernandes, Gabriela Cabral [UNESP]
Chitinophaga sp
M32 family of peptidases
Metallocarboxypeptidase
title_short From data mining of chitinophaga sp. Genome to enzyme discovery of a hyperthermophilic metallocarboxypeptidase
title_full From data mining of chitinophaga sp. Genome to enzyme discovery of a hyperthermophilic metallocarboxypeptidase
title_fullStr From data mining of chitinophaga sp. Genome to enzyme discovery of a hyperthermophilic metallocarboxypeptidase
title_full_unstemmed From data mining of chitinophaga sp. Genome to enzyme discovery of a hyperthermophilic metallocarboxypeptidase
title_sort From data mining of chitinophaga sp. Genome to enzyme discovery of a hyperthermophilic metallocarboxypeptidase
author Fernandes, Gabriela Cabral [UNESP]
author_facet Fernandes, Gabriela Cabral [UNESP]
Sierra, Elwi Guillermo Machado [UNESP]
Brear, Paul
Pereira, Mariana Rangel
Lemos, Eliana G. M. [UNESP]
author_role author
author2 Sierra, Elwi Guillermo Machado [UNESP]
Brear, Paul
Pereira, Mariana Rangel
Lemos, Eliana G. M. [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidad Simón Bolívar
University of Cambridge
Ministry of Education of Brazil
dc.contributor.author.fl_str_mv Fernandes, Gabriela Cabral [UNESP]
Sierra, Elwi Guillermo Machado [UNESP]
Brear, Paul
Pereira, Mariana Rangel
Lemos, Eliana G. M. [UNESP]
dc.subject.por.fl_str_mv Chitinophaga sp
M32 family of peptidases
Metallocarboxypeptidase
topic Chitinophaga sp
M32 family of peptidases
Metallocarboxypeptidase
description For several centuries, microorganisms and enzymes have been used for many different applications. Although many enzymes with industrial applications have already been reported, different screening technologies, methods and approaches are constantly being developed in order to allow the identification of enzymes with even more interesting applications. In our work, we have performed data mining on the Chitinophaga sp. genome, a gram-negative bacterium isolated from a bacterial consortium of sugarcane bagasse isolated from an ethanol plant. The analysis of 8 Mb allowed the identification of the chtcp gene, previously annotated as putative Cht4039. The corresponding codified enzyme, denominated as ChtCP, showed the HEXXH conserved motif of family M32 from thermostable carboxypeptidases. After expression in E. coli, the recombinant enzyme was characterized biochemically. ChtCP showed the highest activity versus benziloxicarbonil Ala-Trp at pH 7.5, suggesting a preference for hydrophobic substrates. Surprisingly, the highest activity of ChtCP observed was between 55 °C and 75 °C, and 62% activity was still displayed at 100 °C. We observed that Ca2+, Ba2+, Mn2+ and Mg2+ ions had a positive effect on the activity of ChtCP, and an increase of 30 °C in the melting temperature was observed in the presence of Co2+. These features together with the structure of ChtCP at 1.2 Å highlight the relevance of ChtCP for further biotechnological applications.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-25T10:22:38Z
2021-06-25T10:22:38Z
2021-02-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.3390/microorganisms9020393
Microorganisms, v. 9, n. 2, p. 1-18, 2021.
2076-2607
http://hdl.handle.net/11449/205871
10.3390/microorganisms9020393
2-s2.0-85100799983
url http://dx.doi.org/10.3390/microorganisms9020393
http://hdl.handle.net/11449/205871
identifier_str_mv Microorganisms, v. 9, n. 2, p. 1-18, 2021.
2076-2607
10.3390/microorganisms9020393
2-s2.0-85100799983
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Microorganisms
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1-18
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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