Identification and in silico characterization of two novel genes encoding peptidases S8 found by functional screening in a metagenomic library of Yucatán underground water

Metagenomics is a culture-independent technology that allows access to novel and potentially useful genetic resources from a wide range of unknown microorganisms. In this study, a fosmid metagenomic library of tropical underground water was constructed, and clones were functionally screened for extracellular proteolytic activity. One of the positive clones, containing a 41,614-bp insert, had two genes with 60% and 68% identity respectively with a peptidase S8 of Chitinimonas koreensis. When these genes were individually sub-cloned, in both cases their sub-clones showed proteolytic phenotype, confirming that they both encode functional proteases. These genes -named PrAY5 and PrAY6- are next to each other. They are similar in size (1845bp and 1824bp respectively) and share 66.5% identity. An extensive in silico characterization showed that their ORFs encode complex zymogens having a signal peptide at their 5'end, followed by a pro-peptide, a catalytic region, and a PPC domain at their 3' end. Their translated sequences were classified as peptidases S8A by sequence comparisons against the non-redundant database and corroborated by Pfam and MEROPS. Phylogenetic analysis of the catalytic region showed that they encode novel proteases that clustered with the sub-family S8_13, which according to the CDD database at NCBI, is an uncharacterized subfamily. They clustered in a clade different from the other three proteases S8 found so far by functional metagenomics, and also different from proteases S8 found in sequenced environmental samples, thereby expanding the range of potentially useful proteases that have been identified by metagenomics. I-TASSER modeling corroborated that they may be subtilases, thus possibly they participate in the hydrolysis of proteins with broad specificity for peptide bonds, and have a preference for a large uncharged residue in P1.

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Main Authors: Apolinar Hernández, Max M., Peña Ramírez, Yuri Jorge Jesús Doctor autor/a 12328, Pérez Rueda, Ernesto autor/a, Canto Canché, Blondy B. autor/a, De los Santos Briones, César autor/a 12483, O'Connor Sánchez, Aileen autor/a 14441
Format: Texto biblioteca
Language:eng
Subjects:Enzimas proteolíticas, Proteinasas de serina, Metagenómica, Recursos de germoplasma, Aguas subterráneas, Filogenética, Artfrosur,
Online Access:http://www.sciencedirect.com/science/article/pii/S0378111916306254
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id KOHA-OAI-ECOSUR:8943
record_format koha
institution ECOSUR
collection Koha
country México
countrycode MX
component Bibliográfico
access En linea
En linea
databasecode cat-ecosur
tag biblioteca
region America del Norte
libraryname Sistema de Información Bibliotecario de ECOSUR (SIBE)
language eng
topic Enzimas proteolíticas
Proteinasas de serina
Metagenómica
Recursos de germoplasma
Aguas subterráneas
Filogenética
Artfrosur
Enzimas proteolíticas
Proteinasas de serina
Metagenómica
Recursos de germoplasma
Aguas subterráneas
Filogenética
Artfrosur
spellingShingle Enzimas proteolíticas
Proteinasas de serina
Metagenómica
Recursos de germoplasma
Aguas subterráneas
Filogenética
Artfrosur
Enzimas proteolíticas
Proteinasas de serina
Metagenómica
Recursos de germoplasma
Aguas subterráneas
Filogenética
Artfrosur
Apolinar Hernández, Max M.
Peña Ramírez, Yuri Jorge Jesús Doctor autor/a 12328
Pérez Rueda, Ernesto autor/a
Canto Canché, Blondy B. autor/a
De los Santos Briones, César autor/a 12483
O'Connor Sánchez, Aileen autor/a 14441
Identification and in silico characterization of two novel genes encoding peptidases S8 found by functional screening in a metagenomic library of Yucatán underground water
description Metagenomics is a culture-independent technology that allows access to novel and potentially useful genetic resources from a wide range of unknown microorganisms. In this study, a fosmid metagenomic library of tropical underground water was constructed, and clones were functionally screened for extracellular proteolytic activity. One of the positive clones, containing a 41,614-bp insert, had two genes with 60% and 68% identity respectively with a peptidase S8 of Chitinimonas koreensis. When these genes were individually sub-cloned, in both cases their sub-clones showed proteolytic phenotype, confirming that they both encode functional proteases. These genes -named PrAY5 and PrAY6- are next to each other. They are similar in size (1845bp and 1824bp respectively) and share 66.5% identity. An extensive in silico characterization showed that their ORFs encode complex zymogens having a signal peptide at their 5'end, followed by a pro-peptide, a catalytic region, and a PPC domain at their 3' end. Their translated sequences were classified as peptidases S8A by sequence comparisons against the non-redundant database and corroborated by Pfam and MEROPS. Phylogenetic analysis of the catalytic region showed that they encode novel proteases that clustered with the sub-family S8_13, which according to the CDD database at NCBI, is an uncharacterized subfamily. They clustered in a clade different from the other three proteases S8 found so far by functional metagenomics, and also different from proteases S8 found in sequenced environmental samples, thereby expanding the range of potentially useful proteases that have been identified by metagenomics. I-TASSER modeling corroborated that they may be subtilases, thus possibly they participate in the hydrolysis of proteins with broad specificity for peptide bonds, and have a preference for a large uncharged residue in P1.
format Texto
topic_facet Enzimas proteolíticas
Proteinasas de serina
Metagenómica
Recursos de germoplasma
Aguas subterráneas
Filogenética
Artfrosur
author Apolinar Hernández, Max M.
Peña Ramírez, Yuri Jorge Jesús Doctor autor/a 12328
Pérez Rueda, Ernesto autor/a
Canto Canché, Blondy B. autor/a
De los Santos Briones, César autor/a 12483
O'Connor Sánchez, Aileen autor/a 14441
author_facet Apolinar Hernández, Max M.
Peña Ramírez, Yuri Jorge Jesús Doctor autor/a 12328
Pérez Rueda, Ernesto autor/a
Canto Canché, Blondy B. autor/a
De los Santos Briones, César autor/a 12483
O'Connor Sánchez, Aileen autor/a 14441
author_sort Apolinar Hernández, Max M.
title Identification and in silico characterization of two novel genes encoding peptidases S8 found by functional screening in a metagenomic library of Yucatán underground water
title_short Identification and in silico characterization of two novel genes encoding peptidases S8 found by functional screening in a metagenomic library of Yucatán underground water
title_full Identification and in silico characterization of two novel genes encoding peptidases S8 found by functional screening in a metagenomic library of Yucatán underground water
title_fullStr Identification and in silico characterization of two novel genes encoding peptidases S8 found by functional screening in a metagenomic library of Yucatán underground water
title_full_unstemmed Identification and in silico characterization of two novel genes encoding peptidases S8 found by functional screening in a metagenomic library of Yucatán underground water
title_sort identification and in silico characterization of two novel genes encoding peptidases s8 found by functional screening in a metagenomic library of yucatán underground water
url http://www.sciencedirect.com/science/article/pii/S0378111916306254
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spelling KOHA-OAI-ECOSUR:89432024-03-11T15:22:58ZIdentification and in silico characterization of two novel genes encoding peptidases S8 found by functional screening in a metagenomic library of Yucatán underground water Apolinar Hernández, Max M. Peña Ramírez, Yuri Jorge Jesús Doctor autor/a 12328 Pérez Rueda, Ernesto autor/a Canto Canché, Blondy B. autor/a De los Santos Briones, César autor/a 12483 O'Connor Sánchez, Aileen autor/a 14441 textengMetagenomics is a culture-independent technology that allows access to novel and potentially useful genetic resources from a wide range of unknown microorganisms. In this study, a fosmid metagenomic library of tropical underground water was constructed, and clones were functionally screened for extracellular proteolytic activity. One of the positive clones, containing a 41,614-bp insert, had two genes with 60% and 68% identity respectively with a peptidase S8 of Chitinimonas koreensis. When these genes were individually sub-cloned, in both cases their sub-clones showed proteolytic phenotype, confirming that they both encode functional proteases. These genes -named PrAY5 and PrAY6- are next to each other. They are similar in size (1845bp and 1824bp respectively) and share 66.5% identity. An extensive in silico characterization showed that their ORFs encode complex zymogens having a signal peptide at their 5'end, followed by a pro-peptide, a catalytic region, and a PPC domain at their 3' end. Their translated sequences were classified as peptidases S8A by sequence comparisons against the non-redundant database and corroborated by Pfam and MEROPS. Phylogenetic analysis of the catalytic region showed that they encode novel proteases that clustered with the sub-family S8_13, which according to the CDD database at NCBI, is an uncharacterized subfamily. They clustered in a clade different from the other three proteases S8 found so far by functional metagenomics, and also different from proteases S8 found in sequenced environmental samples, thereby expanding the range of potentially useful proteases that have been identified by metagenomics. I-TASSER modeling corroborated that they may be subtilases, thus possibly they participate in the hydrolysis of proteins with broad specificity for peptide bonds, and have a preference for a large uncharged residue in P1.Metagenomics is a culture-independent technology that allows access to novel and potentially useful genetic resources from a wide range of unknown microorganisms. In this study, a fosmid metagenomic library of tropical underground water was constructed, and clones were functionally screened for extracellular proteolytic activity. One of the positive clones, containing a 41,614-bp insert, had two genes with 60% and 68% identity respectively with a peptidase S8 of Chitinimonas koreensis. When these genes were individually sub-cloned, in both cases their sub-clones showed proteolytic phenotype, confirming that they both encode functional proteases. These genes -named PrAY5 and PrAY6- are next to each other. They are similar in size (1845bp and 1824bp respectively) and share 66.5% identity. An extensive in silico characterization showed that their ORFs encode complex zymogens having a signal peptide at their 5'end, followed by a pro-peptide, a catalytic region, and a PPC domain at their 3' end. Their translated sequences were classified as peptidases S8A by sequence comparisons against the non-redundant database and corroborated by Pfam and MEROPS. Phylogenetic analysis of the catalytic region showed that they encode novel proteases that clustered with the sub-family S8_13, which according to the CDD database at NCBI, is an uncharacterized subfamily. They clustered in a clade different from the other three proteases S8 found so far by functional metagenomics, and also different from proteases S8 found in sequenced environmental samples, thereby expanding the range of potentially useful proteases that have been identified by metagenomics. I-TASSER modeling corroborated that they may be subtilases, thus possibly they participate in the hydrolysis of proteins with broad specificity for peptide bonds, and have a preference for a large uncharged residue in P1.Adobe Acrobat profesional 6.0 o superiorEnzimas proteolíticasProteinasas de serinaMetagenómicaRecursos de germoplasmaAguas subterráneasFilogenéticaArtfrosurDisponible en líneaGenehttp://www.sciencedirect.com/science/article/pii/S0378111916306254Disponible para usuarios de ECOSUR con su clave de acceso