Simultaneous Multienzymatic Screening with Fluorogenic Probes

Detalhes bibliográficos
Autor(a) principal: Lima,Maria L. S. O.
Data de Publicação: 2018
Outros Autores: Chaves,Michel R. B., Nascimento,Renato M. C. do, Gonçalves,Caroline C. S., Marsaioli,Anita J.
Tipo de documento: Relatório
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532018000501149
Resumo: The simultaneous screening of multiple enzyme activities in a single assay has numerous advantages over the traditional format, since it decreases sampling errors, allows savings in reagents and consumables and reduces the time and labor required to conduct the assays. In the present study, a direct and sensitive assay for the simultaneous detection of epoxide hydrolase and esterase (or lipase) activities was developed. Signal overlap is avoided by synthesizing fluorogenic probes with enzyme-specific alkyl linkers, connected to different fluorophores (resorfurin and umbelliferone), which exhibit emission spectra at different wavelengths. The simultaneous assays were conducted in microplate format with the fluorogenic probes monitored in the same well that uses microorganisms as enzyme source. Our results show that the fluorescent signal from each of the probes used here can be discriminated, allowing multiple enzyme activity detection and quantitation.
id SBQ-2_ad6fc4241c1679d7a49841cf547128e0
oai_identifier_str oai:scielo:S0103-50532018000501149
network_acronym_str SBQ-2
network_name_str Journal of the Brazilian Chemical Society (Online)
repository_id_str
spelling Simultaneous Multienzymatic Screening with Fluorogenic Probesmultienzymatic screeningsimultaneous detectionfluorogenic probeshydrolasescascade reactionThe simultaneous screening of multiple enzyme activities in a single assay has numerous advantages over the traditional format, since it decreases sampling errors, allows savings in reagents and consumables and reduces the time and labor required to conduct the assays. In the present study, a direct and sensitive assay for the simultaneous detection of epoxide hydrolase and esterase (or lipase) activities was developed. Signal overlap is avoided by synthesizing fluorogenic probes with enzyme-specific alkyl linkers, connected to different fluorophores (resorfurin and umbelliferone), which exhibit emission spectra at different wavelengths. The simultaneous assays were conducted in microplate format with the fluorogenic probes monitored in the same well that uses microorganisms as enzyme source. Our results show that the fluorescent signal from each of the probes used here can be discriminated, allowing multiple enzyme activity detection and quantitation.Sociedade Brasileira de Química2018-05-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532018000501149Journal of the Brazilian Chemical Society v.29 n.5 2018reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20170188info:eu-repo/semantics/openAccessLima,Maria L. S. O.Chaves,Michel R. B.Nascimento,Renato M. C. doGonçalves,Caroline C. S.Marsaioli,Anita J.eng2018-07-04T00:00:00Zoai:scielo:S0103-50532018000501149Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2018-07-04T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Simultaneous Multienzymatic Screening with Fluorogenic Probes
title Simultaneous Multienzymatic Screening with Fluorogenic Probes
spellingShingle Simultaneous Multienzymatic Screening with Fluorogenic Probes
Lima,Maria L. S. O.
multienzymatic screening
simultaneous detection
fluorogenic probes
hydrolases
cascade reaction
title_short Simultaneous Multienzymatic Screening with Fluorogenic Probes
title_full Simultaneous Multienzymatic Screening with Fluorogenic Probes
title_fullStr Simultaneous Multienzymatic Screening with Fluorogenic Probes
title_full_unstemmed Simultaneous Multienzymatic Screening with Fluorogenic Probes
title_sort Simultaneous Multienzymatic Screening with Fluorogenic Probes
author Lima,Maria L. S. O.
author_facet Lima,Maria L. S. O.
Chaves,Michel R. B.
Nascimento,Renato M. C. do
Gonçalves,Caroline C. S.
Marsaioli,Anita J.
author_role author
author2 Chaves,Michel R. B.
Nascimento,Renato M. C. do
Gonçalves,Caroline C. S.
Marsaioli,Anita J.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Lima,Maria L. S. O.
Chaves,Michel R. B.
Nascimento,Renato M. C. do
Gonçalves,Caroline C. S.
Marsaioli,Anita J.
dc.subject.por.fl_str_mv multienzymatic screening
simultaneous detection
fluorogenic probes
hydrolases
cascade reaction
topic multienzymatic screening
simultaneous detection
fluorogenic probes
hydrolases
cascade reaction
description The simultaneous screening of multiple enzyme activities in a single assay has numerous advantages over the traditional format, since it decreases sampling errors, allows savings in reagents and consumables and reduces the time and labor required to conduct the assays. In the present study, a direct and sensitive assay for the simultaneous detection of epoxide hydrolase and esterase (or lipase) activities was developed. Signal overlap is avoided by synthesizing fluorogenic probes with enzyme-specific alkyl linkers, connected to different fluorophores (resorfurin and umbelliferone), which exhibit emission spectra at different wavelengths. The simultaneous assays were conducted in microplate format with the fluorogenic probes monitored in the same well that uses microorganisms as enzyme source. Our results show that the fluorescent signal from each of the probes used here can be discriminated, allowing multiple enzyme activity detection and quantitation.
publishDate 2018
dc.date.none.fl_str_mv 2018-05-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/report
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format report
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532018000501149
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532018000501149
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.21577/0103-5053.20170188
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.29 n.5 2018
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
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
_version_ 1750318180791746560