From data mining of chitinophaga sp. Genome to enzyme discovery of a hyperthermophilic metallocarboxypeptidase
Autor(a) principal: | |
---|---|
Data de Publicação: | 2021 |
Outros Autores: | , , , |
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. |
id |
UNSP_0c91c4dd629a7fd9781240973abf810f |
---|---|
oai_identifier_str |
oai:repositorio.unesp.br:11449/205871 |
network_acronym_str |
UNSP |
network_name_str |
Repositório Institucional da UNESP |
repository_id_str |
2946 |
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) |
repository.mail.fl_str_mv |
|
_version_ |
1808128872135262208 |