Análise e expressão de genes de PKS II e de carboidrases provenientes de bibliotecas metagenômicas

Detalhes bibliográficos
Autor(a) principal: Gomes, Elisângela Soares [UNESP]
Data de Publicação: 2015
Tipo de documento: Tese
Idioma: por
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://hdl.handle.net/11449/126393
Resumo: The Clone metagenomic B5pl37 (insert of 23kb length) was obtained by a PCR prospect for gene set Polyketide Synthases type II (PKSII) in a library cosmidial eucalyptus grove soil sample (SE). The PKSII are responsible for producing many bioactive molecules, among which the antibiotics were noticeable. Part of the sequence of the insert (27-43% coverage) showed similarity of 77-78% with bacteria Streptomycetaceae family (BLASTN tool, Genbank). In PKS II gene annotation was possible to identify genes related to the degradation of lignocellulosic important compounds for the production of second generation biofuel (2G): A β-glucosidase, a cellulose and a Multicopper oxidase (MCO). Considering the industrial importance of these genes, this study aimed to characterize in silico and in vitro /in vivo thereof. The in silico analyzes helped identify the architecture of the active site (protein structure obtained by homology) and enzyme families (based on phenetic groups with sequences of known enzyme activity). The in vitro / vivo experiments were performed in pET28a expression vector in Escherichia coli for cellulase (E. coli strains BL21; Artics and C41) and β-glucosidase (E. coli BL21), while the gene MCO in vitro synthesis for a subsequent study it was submitted. We had done the kinetic characterization of β- glucosidase (best performance in the expression and purification), which obtained the catalytic parameters: Vmax 0.79 uM / min; km from 0.46 mM. The respective temperature and the pH optimum for the enzyme was 37 ° C and pH7-7,5; and the enzyme was able to maintain an activity above 80% at a pH of 6.5-8.0 and temperature range 35-40 ° C. With respect to PKSII, the preparatory processes have been started to insert the expression in the same host specialized for expression of Streptomyces coelicolor antibiotic M1152 (courtesy of Juan P. Gomez-Escribano, John Innes Centre, Norwich, UK). Cosmidial exchange vector was carried out ...
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spelling Análise e expressão de genes de PKS II e de carboidrases provenientes de bibliotecas metagenômicasCelulaseMetagenômicaExpressão gênicaGenesEnzimasMetagenomicsThe Clone metagenomic B5pl37 (insert of 23kb length) was obtained by a PCR prospect for gene set Polyketide Synthases type II (PKSII) in a library cosmidial eucalyptus grove soil sample (SE). The PKSII are responsible for producing many bioactive molecules, among which the antibiotics were noticeable. Part of the sequence of the insert (27-43% coverage) showed similarity of 77-78% with bacteria Streptomycetaceae family (BLASTN tool, Genbank). In PKS II gene annotation was possible to identify genes related to the degradation of lignocellulosic important compounds for the production of second generation biofuel (2G): A β-glucosidase, a cellulose and a Multicopper oxidase (MCO). Considering the industrial importance of these genes, this study aimed to characterize in silico and in vitro /in vivo thereof. The in silico analyzes helped identify the architecture of the active site (protein structure obtained by homology) and enzyme families (based on phenetic groups with sequences of known enzyme activity). The in vitro / vivo experiments were performed in pET28a expression vector in Escherichia coli for cellulase (E. coli strains BL21; Artics and C41) and β-glucosidase (E. coli BL21), while the gene MCO in vitro synthesis for a subsequent study it was submitted. We had done the kinetic characterization of β- glucosidase (best performance in the expression and purification), which obtained the catalytic parameters: Vmax 0.79 uM / min; km from 0.46 mM. The respective temperature and the pH optimum for the enzyme was 37 ° C and pH7-7,5; and the enzyme was able to maintain an activity above 80% at a pH of 6.5-8.0 and temperature range 35-40 ° C. With respect to PKSII, the preparatory processes have been started to insert the expression in the same host specialized for expression of Streptomyces coelicolor antibiotic M1152 (courtesy of Juan P. Gomez-Escribano, John Innes Centre, Norwich, UK). Cosmidial exchange vector was carried out ...O clone metagenômico B5pl37 (inserto de 23 Kb) foi obtido por meio de uma prospecção por PCR para o conjunto gênico de Policetídeos Sintases tipo II (PKSII) em uma biblioteca cosmidial de amostra de solo de bosque de eucaliptos (S.E.). As PKSII são responsáveis pela produção de inúmeras moléculas bioativas, dentre os quais se destacam os antibióticos policetídicos. Parte da sequência do inserto (cobertura de 27-43%) apresentou similaridade de 77-78% com bactérias da família Streptomycetaceae (ferramenta BlastN, Genbank). Além da PKS II, a anotação gênica permitiu identificar genes relacionados à degradação de compostos lignocelulósicos importantes para a produção de combustíveis de segunda geração (2G): uma β- glicosidase, uma celulase e uma Multicopper oxidase (MCO). Considerando a importância industrial destes genes, este trabalho teve como objetivo a caracterização in silico e in vitro/vivo dos mesmos. As análises in silico auxiliaram a identificar a arquitetura do sítio ativo (modelo de estrutura proteica obtida por homologia) e famílias enzimáticas (com base em agrupamentos fenéticos com sequências de enzimas de atividade conhecida). Quanto às análises in vitro/vivo, foram realizados experimentos de expressão em vetor pET28a em Escherichia coli para as enzimas celulase (linhagens de E.coli BL21; C41 e Artics) e β-glicosidase (E.coli BL21), enquanto o gene MCO foi submetido à síntese in vitro para um estudo posterior. Foi feita a caracterização cinética da β-glicosidase (melhor rendimento na expressão e purificação), que obteve os parâmetros catalíticos: Vmax de 0,79 μM/min; km de 0,46 mM.. Os respectivos valores de temperatura e pH ótimos para a enzima foram 37°C e pH7-7,5; e a enzima foi capaz de manter uma atividade acima de 80% para uma faixa de pH 6,5-8,0 e temperatura 35- 40°C. Com relação à PKSII, foram iniciados os processos preparatórios para a...Universidade Estadual Paulista (Unesp)Lemos, Eliana Gertrudes de Macedo [UNESP]Universidade Estadual Paulista (Unesp)Gomes, Elisângela Soares [UNESP]2015-08-20T17:09:40Z2015-08-20T17:09:40Z2015-02-12info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisxi, 107 p. : il.application/pdfGOMES, Elisângela Soares. Análise e expressão de genes de PKS II e de carboidrases provenientes de bibliotecas metagenômicas. 2015. xi, 107 p. Tese (doutorado) - Universidade Estadual Paulista Júlio de Mesquita Filho, Faculdade de Ciências Agrárias e Veterinárias de Jaboticabal, 2015.http://hdl.handle.net/11449/126393000837967000837967.pdf33004102070P63254990612451836Alephreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPporinfo:eu-repo/semantics/openAccess2024-06-05T18:49:00Zoai:repositorio.unesp.br:11449/126393Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T13:49:26.927054Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Análise e expressão de genes de PKS II e de carboidrases provenientes de bibliotecas metagenômicas
title Análise e expressão de genes de PKS II e de carboidrases provenientes de bibliotecas metagenômicas
spellingShingle Análise e expressão de genes de PKS II e de carboidrases provenientes de bibliotecas metagenômicas
Gomes, Elisângela Soares [UNESP]
Celulase
Metagenômica
Expressão gênica
Genes
Enzimas
Metagenomics
title_short Análise e expressão de genes de PKS II e de carboidrases provenientes de bibliotecas metagenômicas
title_full Análise e expressão de genes de PKS II e de carboidrases provenientes de bibliotecas metagenômicas
title_fullStr Análise e expressão de genes de PKS II e de carboidrases provenientes de bibliotecas metagenômicas
title_full_unstemmed Análise e expressão de genes de PKS II e de carboidrases provenientes de bibliotecas metagenômicas
title_sort Análise e expressão de genes de PKS II e de carboidrases provenientes de bibliotecas metagenômicas
author Gomes, Elisângela Soares [UNESP]
author_facet Gomes, Elisângela Soares [UNESP]
author_role author
dc.contributor.none.fl_str_mv Lemos, Eliana Gertrudes de Macedo [UNESP]
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Gomes, Elisângela Soares [UNESP]
dc.subject.por.fl_str_mv Celulase
Metagenômica
Expressão gênica
Genes
Enzimas
Metagenomics
topic Celulase
Metagenômica
Expressão gênica
Genes
Enzimas
Metagenomics
description The Clone metagenomic B5pl37 (insert of 23kb length) was obtained by a PCR prospect for gene set Polyketide Synthases type II (PKSII) in a library cosmidial eucalyptus grove soil sample (SE). The PKSII are responsible for producing many bioactive molecules, among which the antibiotics were noticeable. Part of the sequence of the insert (27-43% coverage) showed similarity of 77-78% with bacteria Streptomycetaceae family (BLASTN tool, Genbank). In PKS II gene annotation was possible to identify genes related to the degradation of lignocellulosic important compounds for the production of second generation biofuel (2G): A β-glucosidase, a cellulose and a Multicopper oxidase (MCO). Considering the industrial importance of these genes, this study aimed to characterize in silico and in vitro /in vivo thereof. The in silico analyzes helped identify the architecture of the active site (protein structure obtained by homology) and enzyme families (based on phenetic groups with sequences of known enzyme activity). The in vitro / vivo experiments were performed in pET28a expression vector in Escherichia coli for cellulase (E. coli strains BL21; Artics and C41) and β-glucosidase (E. coli BL21), while the gene MCO in vitro synthesis for a subsequent study it was submitted. We had done the kinetic characterization of β- glucosidase (best performance in the expression and purification), which obtained the catalytic parameters: Vmax 0.79 uM / min; km from 0.46 mM. The respective temperature and the pH optimum for the enzyme was 37 ° C and pH7-7,5; and the enzyme was able to maintain an activity above 80% at a pH of 6.5-8.0 and temperature range 35-40 ° C. With respect to PKSII, the preparatory processes have been started to insert the expression in the same host specialized for expression of Streptomyces coelicolor antibiotic M1152 (courtesy of Juan P. Gomez-Escribano, John Innes Centre, Norwich, UK). Cosmidial exchange vector was carried out ...
publishDate 2015
dc.date.none.fl_str_mv 2015-08-20T17:09:40Z
2015-08-20T17:09:40Z
2015-02-12
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv GOMES, Elisângela Soares. Análise e expressão de genes de PKS II e de carboidrases provenientes de bibliotecas metagenômicas. 2015. xi, 107 p. Tese (doutorado) - Universidade Estadual Paulista Júlio de Mesquita Filho, Faculdade de Ciências Agrárias e Veterinárias de Jaboticabal, 2015.
http://hdl.handle.net/11449/126393
000837967
000837967.pdf
33004102070P6
3254990612451836
identifier_str_mv GOMES, Elisângela Soares. Análise e expressão de genes de PKS II e de carboidrases provenientes de bibliotecas metagenômicas. 2015. xi, 107 p. Tese (doutorado) - Universidade Estadual Paulista Júlio de Mesquita Filho, Faculdade de Ciências Agrárias e Veterinárias de Jaboticabal, 2015.
000837967
000837967.pdf
33004102070P6
3254990612451836
url http://hdl.handle.net/11449/126393
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv xi, 107 p. : il.
application/pdf
dc.publisher.none.fl_str_mv Universidade Estadual Paulista (Unesp)
publisher.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.source.none.fl_str_mv Aleph
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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