An Enzymatic–Colorimetric Assay for the Quantification of <i>Bifidobacterium</i>

Autores
Bibiloni, Rodrigo; Pérez, Pablo Fernando; De Antoni, Graciela Liliana
Año de publicación
2000
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
An enzymatic-colorimetric assay for the quantification of Bifidobacterium was developed. The method, based upon the standard detection of fructose-6-phosphate phosphoketolase activity, was optimized with respect to bacterial cell pretreatment, time of incubation, and substrate concentration. The relationship between bacterial biomass and phosphoketolase activity was linear in a wide spectrum of bacterial densities. Higher sensitivity over the standard method was achieved by using 0.25% Triton X-100 in the reaction mixture to pretreat the bacterial cells. Because autoaggregation is a frequent feature among Bifidobacterium strains, this simple and reproducible method offers good advantage over viable plate count and turbidimetric techniques. The methodology can also be applied to the assessment of adherent Bifidobacterium strains to human epithelial cells.
Centro de Investigación y Desarrollo en Criotecnología de Alimentos
Materia
Ciencias Exactas
Química
Bifidobacterium
enzymatic-colorimetric assay
Bacteria
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-nd/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/141899

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network_name_str SEDICI (UNLP)
spelling An Enzymatic–Colorimetric Assay for the Quantification of <i>Bifidobacterium</i>Bibiloni, RodrigoPérez, Pablo FernandoDe Antoni, Graciela LilianaCiencias ExactasQuímicaBifidobacteriumenzymatic-colorimetric assayBacteriaAn enzymatic-colorimetric assay for the quantification of <i>Bifidobacterium</i> was developed. The method, based upon the standard detection of fructose-6-phosphate phosphoketolase activity, was optimized with respect to bacterial cell pretreatment, time of incubation, and substrate concentration. The relationship between bacterial biomass and phosphoketolase activity was linear in a wide spectrum of bacterial densities. Higher sensitivity over the standard method was achieved by using 0.25% Triton X-100 in the reaction mixture to pretreat the bacterial cells. Because autoaggregation is a frequent feature among <i>Bifidobacterium</i> strains, this simple and reproducible method offers good advantage over viable plate count and turbidimetric techniques. The methodology can also be applied to the assessment of adherent <i>Bifidobacterium</i> strains to human epithelial cells.Centro de Investigación y Desarrollo en Criotecnología de Alimentos2000-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf322-326http://sedici.unlp.edu.ar/handle/10915/141899enginfo:eu-repo/semantics/altIdentifier/issn/0362-028Xinfo:eu-repo/semantics/altIdentifier/issn/1944-9097info:eu-repo/semantics/altIdentifier/doi/10.4315/0362-028x-63.3.322info:eu-repo/semantics/altIdentifier/pmid/10716559info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-nd/4.0/Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-10-15T11:24:29Zoai:sedici.unlp.edu.ar:10915/141899Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-15 11:24:30.001SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv An Enzymatic–Colorimetric Assay for the Quantification of <i>Bifidobacterium</i>
title An Enzymatic–Colorimetric Assay for the Quantification of <i>Bifidobacterium</i>
spellingShingle An Enzymatic–Colorimetric Assay for the Quantification of <i>Bifidobacterium</i>
Bibiloni, Rodrigo
Ciencias Exactas
Química
Bifidobacterium
enzymatic-colorimetric assay
Bacteria
title_short An Enzymatic–Colorimetric Assay for the Quantification of <i>Bifidobacterium</i>
title_full An Enzymatic–Colorimetric Assay for the Quantification of <i>Bifidobacterium</i>
title_fullStr An Enzymatic–Colorimetric Assay for the Quantification of <i>Bifidobacterium</i>
title_full_unstemmed An Enzymatic–Colorimetric Assay for the Quantification of <i>Bifidobacterium</i>
title_sort An Enzymatic–Colorimetric Assay for the Quantification of <i>Bifidobacterium</i>
dc.creator.none.fl_str_mv Bibiloni, Rodrigo
Pérez, Pablo Fernando
De Antoni, Graciela Liliana
author Bibiloni, Rodrigo
author_facet Bibiloni, Rodrigo
Pérez, Pablo Fernando
De Antoni, Graciela Liliana
author_role author
author2 Pérez, Pablo Fernando
De Antoni, Graciela Liliana
author2_role author
author
dc.subject.none.fl_str_mv Ciencias Exactas
Química
Bifidobacterium
enzymatic-colorimetric assay
Bacteria
topic Ciencias Exactas
Química
Bifidobacterium
enzymatic-colorimetric assay
Bacteria
dc.description.none.fl_txt_mv An enzymatic-colorimetric assay for the quantification of <i>Bifidobacterium</i> was developed. The method, based upon the standard detection of fructose-6-phosphate phosphoketolase activity, was optimized with respect to bacterial cell pretreatment, time of incubation, and substrate concentration. The relationship between bacterial biomass and phosphoketolase activity was linear in a wide spectrum of bacterial densities. Higher sensitivity over the standard method was achieved by using 0.25% Triton X-100 in the reaction mixture to pretreat the bacterial cells. Because autoaggregation is a frequent feature among <i>Bifidobacterium</i> strains, this simple and reproducible method offers good advantage over viable plate count and turbidimetric techniques. The methodology can also be applied to the assessment of adherent <i>Bifidobacterium</i> strains to human epithelial cells.
Centro de Investigación y Desarrollo en Criotecnología de Alimentos
description An enzymatic-colorimetric assay for the quantification of <i>Bifidobacterium</i> was developed. The method, based upon the standard detection of fructose-6-phosphate phosphoketolase activity, was optimized with respect to bacterial cell pretreatment, time of incubation, and substrate concentration. The relationship between bacterial biomass and phosphoketolase activity was linear in a wide spectrum of bacterial densities. Higher sensitivity over the standard method was achieved by using 0.25% Triton X-100 in the reaction mixture to pretreat the bacterial cells. Because autoaggregation is a frequent feature among <i>Bifidobacterium</i> strains, this simple and reproducible method offers good advantage over viable plate count and turbidimetric techniques. The methodology can also be applied to the assessment of adherent <i>Bifidobacterium</i> strains to human epithelial cells.
publishDate 2000
dc.date.none.fl_str_mv 2000-03
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/141899
url http://sedici.unlp.edu.ar/handle/10915/141899
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/0362-028X
info:eu-repo/semantics/altIdentifier/issn/1944-9097
info:eu-repo/semantics/altIdentifier/doi/10.4315/0362-028x-63.3.322
info:eu-repo/semantics/altIdentifier/pmid/10716559
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-nd/4.0/
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-nd/4.0/
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
dc.format.none.fl_str_mv application/pdf
322-326
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
instacron:UNLP
reponame_str SEDICI (UNLP)
collection SEDICI (UNLP)
instname_str Universidad Nacional de La Plata
instacron_str UNLP
institution UNLP
repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
repository.mail.fl_str_mv alira@sedici.unlp.edu.ar
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