Gene Deletion Leads to Improved Valinomycin Production by Streptomyces sp. CBMAI 2042

Detalhes bibliográficos
Autor(a) principal: Paulo,Bruno S.
Data de Publicação: 2019
Outros Autores: Sigrist,Renata, Angolini,Célio F. F., Eberlin,Marcos N., Oliveira,Luciana G. de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532019000300673
Resumo: The genus Streptomyces represents one of the largest producers of molecules with antibiotic activity. The whole genome sequencing of the endophytic microorganism Streptomyces sp. CBMAI 2042 revealed 35 gene clusters encoding for secondary metabolism including 3 non-ribosomal peptide synthetases (NRPS) and 7 NRPS-hybrids. Combining genome mining and cultivation profile analysis, the depsipeptide ionophore valinomycin was identified as one of the main metabolites produced by this strain. To better understand the metabolic machinery codified in CBMAI 2042 genome an adenylation domain from a hybrid NRPS cluster was deleted through a double crossing knockout experiment. Though the deletion was not plentiful to elucidate the encoded NRP metabolite related to the adenilation domain, an astounding increase of 10.5-fold in valinomycin production was observed in the mutant. These results suggest a metabolic flux redistribution of common substrates as an outcome of a gene target deletion.
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spelling Gene Deletion Leads to Improved Valinomycin Production by Streptomyces sp. CBMAI 2042genome mininggene target deletionvalinomycinThe genus Streptomyces represents one of the largest producers of molecules with antibiotic activity. The whole genome sequencing of the endophytic microorganism Streptomyces sp. CBMAI 2042 revealed 35 gene clusters encoding for secondary metabolism including 3 non-ribosomal peptide synthetases (NRPS) and 7 NRPS-hybrids. Combining genome mining and cultivation profile analysis, the depsipeptide ionophore valinomycin was identified as one of the main metabolites produced by this strain. To better understand the metabolic machinery codified in CBMAI 2042 genome an adenylation domain from a hybrid NRPS cluster was deleted through a double crossing knockout experiment. Though the deletion was not plentiful to elucidate the encoded NRP metabolite related to the adenilation domain, an astounding increase of 10.5-fold in valinomycin production was observed in the mutant. These results suggest a metabolic flux redistribution of common substrates as an outcome of a gene target deletion.Sociedade Brasileira de Química2019-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532019000300673Journal of the Brazilian Chemical Society v.30 n.3 2019reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20180207info:eu-repo/semantics/openAccessPaulo,Bruno S.Sigrist,RenataAngolini,Célio F. F.Eberlin,Marcos N.Oliveira,Luciana G. deeng2019-02-14T00:00:00Zoai:scielo:S0103-50532019000300673Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2019-02-14T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Gene Deletion Leads to Improved Valinomycin Production by Streptomyces sp. CBMAI 2042
title Gene Deletion Leads to Improved Valinomycin Production by Streptomyces sp. CBMAI 2042
spellingShingle Gene Deletion Leads to Improved Valinomycin Production by Streptomyces sp. CBMAI 2042
Paulo,Bruno S.
genome mining
gene target deletion
valinomycin
title_short Gene Deletion Leads to Improved Valinomycin Production by Streptomyces sp. CBMAI 2042
title_full Gene Deletion Leads to Improved Valinomycin Production by Streptomyces sp. CBMAI 2042
title_fullStr Gene Deletion Leads to Improved Valinomycin Production by Streptomyces sp. CBMAI 2042
title_full_unstemmed Gene Deletion Leads to Improved Valinomycin Production by Streptomyces sp. CBMAI 2042
title_sort Gene Deletion Leads to Improved Valinomycin Production by Streptomyces sp. CBMAI 2042
author Paulo,Bruno S.
author_facet Paulo,Bruno S.
Sigrist,Renata
Angolini,Célio F. F.
Eberlin,Marcos N.
Oliveira,Luciana G. de
author_role author
author2 Sigrist,Renata
Angolini,Célio F. F.
Eberlin,Marcos N.
Oliveira,Luciana G. de
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Paulo,Bruno S.
Sigrist,Renata
Angolini,Célio F. F.
Eberlin,Marcos N.
Oliveira,Luciana G. de
dc.subject.por.fl_str_mv genome mining
gene target deletion
valinomycin
topic genome mining
gene target deletion
valinomycin
description The genus Streptomyces represents one of the largest producers of molecules with antibiotic activity. The whole genome sequencing of the endophytic microorganism Streptomyces sp. CBMAI 2042 revealed 35 gene clusters encoding for secondary metabolism including 3 non-ribosomal peptide synthetases (NRPS) and 7 NRPS-hybrids. Combining genome mining and cultivation profile analysis, the depsipeptide ionophore valinomycin was identified as one of the main metabolites produced by this strain. To better understand the metabolic machinery codified in CBMAI 2042 genome an adenylation domain from a hybrid NRPS cluster was deleted through a double crossing knockout experiment. Though the deletion was not plentiful to elucidate the encoded NRP metabolite related to the adenilation domain, an astounding increase of 10.5-fold in valinomycin production was observed in the mutant. These results suggest a metabolic flux redistribution of common substrates as an outcome of a gene target deletion.
publishDate 2019
dc.date.none.fl_str_mv 2019-03-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532019000300673
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532019000300673
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.21577/0103-5053.20180207
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.30 n.3 2019
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
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reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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