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
.jpg)
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/141899
Ver los metadatos del registro completo
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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 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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publishedVersion |
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http://sedici.unlp.edu.ar/handle/10915/141899 |
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eng |
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eng |
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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 |
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openAccess |
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