In vivo assay to identify bacteria with β-glucosidase activity

[Background]: β-Glucosidase assay is performed with purified or semipurified enzymes extracted from cell lysis. However, in screening studies, to find bacteria with β-glucosidase activity among many tested bacteria, a fast method without cell lysis is desirable. In that objective, we report an in vivo β-glucosidase assay as a fast method to find a β-glucosidase producer strain. [Results]: The method consists in growing the strains for testing in a medium supplemented with the artificial substrate p-nitrophenyl-β-glucopyranoside (pNPG). The presence of β-glucosidases converts the substrate to p-nitrophenol (pNP), a molecule that can be easily measured in the supernatant spectrophotometrically at 405 nm. The assay was evaluated using two Bifidobacterium strains: Bifidobacterium longum B7254 strain that lacks β-glucosidase activity and Bifidobacterium pseudocatenulatum B7003 strain that shows β-glucosidase activity. The addition of sodium carbonate during pNP measurement increases the sensitivity of pNP detection and avoids the masking of absorbance by the culture medium. Furthermore, we show that pNP is a stable enzymatic product, not metabolized by bacteria, but with an inhibitory effect on cell growth. The β-glucosidase activity was measured as units of enzyme per gram per minute per dry cell weight. This method also allowed the identification of Lactobacillus strains with higher β-glucosidase activity among several lactobacillus species. [Conclusion]: This in vivo β-glucosidase assay can be used as an enzymatic test on living cells without cell disruption. The method is simple, quantitative, and recommended, especially in studies screening for bacteria not only with β-glucosidase activity but also with high β-glucosidase activity.

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Bibliographic Details
Main Authors: Strahsburger, Erwin, López de Lacey, Ana M., Marotti, Ilaria, Di Gioia, Diana, Biavati, Bruno, Dinelli, Giovanni
Other Authors: Università di Bologna
Format: artículo biblioteca
Published: Elsevier 2017
Subjects:β-Glucosidase assay, Screening, β-Glucosidase producer strain, Antimicrobial, p-Nitrophenyl-β-glucopyranoside, Bifidobacterium, Cell lysis, Enzymatic test, Lactobacillus, p-Nitrophenol,
Online Access:http://hdl.handle.net/10261/171408
http://dx.doi.org/10.13039/501100005969
http://dx.doi.org/10.13039/501100003339
http://dx.doi.org/10.13039/501100000780
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spelling dig-ictan-es-10261-1714082020-12-10T15:45:45Z In vivo assay to identify bacteria with β-glucosidase activity Strahsburger, Erwin López de Lacey, Ana M. Marotti, Ilaria Di Gioia, Diana Biavati, Bruno Dinelli, Giovanni Università di Bologna European Commission Consejo Superior de Investigaciones Científicas (España) β-Glucosidase assay Screening β-Glucosidase producer strain Antimicrobial p-Nitrophenyl-β-glucopyranoside Bifidobacterium Cell lysis Enzymatic test Lactobacillus p-Nitrophenol [Background]: β-Glucosidase assay is performed with purified or semipurified enzymes extracted from cell lysis. However, in screening studies, to find bacteria with β-glucosidase activity among many tested bacteria, a fast method without cell lysis is desirable. In that objective, we report an in vivo β-glucosidase assay as a fast method to find a β-glucosidase producer strain. [Results]: The method consists in growing the strains for testing in a medium supplemented with the artificial substrate p-nitrophenyl-β-glucopyranoside (pNPG). The presence of β-glucosidases converts the substrate to p-nitrophenol (pNP), a molecule that can be easily measured in the supernatant spectrophotometrically at 405 nm. The assay was evaluated using two Bifidobacterium strains: Bifidobacterium longum B7254 strain that lacks β-glucosidase activity and Bifidobacterium pseudocatenulatum B7003 strain that shows β-glucosidase activity. The addition of sodium carbonate during pNP measurement increases the sensitivity of pNP detection and avoids the masking of absorbance by the culture medium. Furthermore, we show that pNP is a stable enzymatic product, not metabolized by bacteria, but with an inhibitory effect on cell growth. The β-glucosidase activity was measured as units of enzyme per gram per minute per dry cell weight. This method also allowed the identification of Lactobacillus strains with higher β-glucosidase activity among several lactobacillus species. [Conclusion]: This in vivo β-glucosidase assay can be used as an enzymatic test on living cells without cell disruption. The method is simple, quantitative, and recommended, especially in studies screening for bacteria not only with β-glucosidase activity but also with high β-glucosidase activity. The study was funded by the University of Bologna, RFO Program number J61J10000790001. Erwin Strahsburger received a scholarship within the Erasmus Mundus Program. Ana M. Lopez de Lacey received a fellowship within the JAE-CSIC predoctoral Programme. The study was also financially funded by the Universidad Arturo Prat, internal projects number VRIIP0218-15 and VRIIP01-14. Peer Reviewed 2018-10-23T10:12:32Z 2018-10-23T10:12:32Z 2017 2018-10-23T10:12:32Z artículo http://purl.org/coar/resource_type/c_6501 doi: 10.1016/j.ejbt.2017.08.010 e-issn: 0717-3458 Electronic Journal of Biotechnology 30: 83-87 (2017) http://hdl.handle.net/10261/171408 10.1016/j.ejbt.2017.08.010 http://dx.doi.org/10.13039/501100005969 http://dx.doi.org/10.13039/501100003339 http://dx.doi.org/10.13039/501100000780 Publisher's version https://doi.org/10.1016/j.ejbt.2017.08.010 Sí open Elsevier
institution ICTAN ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-ictan-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del ICTAN España
topic β-Glucosidase assay
Screening
β-Glucosidase producer strain
Antimicrobial
p-Nitrophenyl-β-glucopyranoside
Bifidobacterium
Cell lysis
Enzymatic test
Lactobacillus
p-Nitrophenol
β-Glucosidase assay
Screening
β-Glucosidase producer strain
Antimicrobial
p-Nitrophenyl-β-glucopyranoside
Bifidobacterium
Cell lysis
Enzymatic test
Lactobacillus
p-Nitrophenol
spellingShingle β-Glucosidase assay
Screening
β-Glucosidase producer strain
Antimicrobial
p-Nitrophenyl-β-glucopyranoside
Bifidobacterium
Cell lysis
Enzymatic test
Lactobacillus
p-Nitrophenol
β-Glucosidase assay
Screening
β-Glucosidase producer strain
Antimicrobial
p-Nitrophenyl-β-glucopyranoside
Bifidobacterium
Cell lysis
Enzymatic test
Lactobacillus
p-Nitrophenol
Strahsburger, Erwin
López de Lacey, Ana M.
Marotti, Ilaria
Di Gioia, Diana
Biavati, Bruno
Dinelli, Giovanni
In vivo assay to identify bacteria with β-glucosidase activity
description [Background]: β-Glucosidase assay is performed with purified or semipurified enzymes extracted from cell lysis. However, in screening studies, to find bacteria with β-glucosidase activity among many tested bacteria, a fast method without cell lysis is desirable. In that objective, we report an in vivo β-glucosidase assay as a fast method to find a β-glucosidase producer strain. [Results]: The method consists in growing the strains for testing in a medium supplemented with the artificial substrate p-nitrophenyl-β-glucopyranoside (pNPG). The presence of β-glucosidases converts the substrate to p-nitrophenol (pNP), a molecule that can be easily measured in the supernatant spectrophotometrically at 405 nm. The assay was evaluated using two Bifidobacterium strains: Bifidobacterium longum B7254 strain that lacks β-glucosidase activity and Bifidobacterium pseudocatenulatum B7003 strain that shows β-glucosidase activity. The addition of sodium carbonate during pNP measurement increases the sensitivity of pNP detection and avoids the masking of absorbance by the culture medium. Furthermore, we show that pNP is a stable enzymatic product, not metabolized by bacteria, but with an inhibitory effect on cell growth. The β-glucosidase activity was measured as units of enzyme per gram per minute per dry cell weight. This method also allowed the identification of Lactobacillus strains with higher β-glucosidase activity among several lactobacillus species. [Conclusion]: This in vivo β-glucosidase assay can be used as an enzymatic test on living cells without cell disruption. The method is simple, quantitative, and recommended, especially in studies screening for bacteria not only with β-glucosidase activity but also with high β-glucosidase activity.
author2 Università di Bologna
author_facet Università di Bologna
Strahsburger, Erwin
López de Lacey, Ana M.
Marotti, Ilaria
Di Gioia, Diana
Biavati, Bruno
Dinelli, Giovanni
format artículo
topic_facet β-Glucosidase assay
Screening
β-Glucosidase producer strain
Antimicrobial
p-Nitrophenyl-β-glucopyranoside
Bifidobacterium
Cell lysis
Enzymatic test
Lactobacillus
p-Nitrophenol
author Strahsburger, Erwin
López de Lacey, Ana M.
Marotti, Ilaria
Di Gioia, Diana
Biavati, Bruno
Dinelli, Giovanni
author_sort Strahsburger, Erwin
title In vivo assay to identify bacteria with β-glucosidase activity
title_short In vivo assay to identify bacteria with β-glucosidase activity
title_full In vivo assay to identify bacteria with β-glucosidase activity
title_fullStr In vivo assay to identify bacteria with β-glucosidase activity
title_full_unstemmed In vivo assay to identify bacteria with β-glucosidase activity
title_sort in vivo assay to identify bacteria with β-glucosidase activity
publisher Elsevier
publishDate 2017
url http://hdl.handle.net/10261/171408
http://dx.doi.org/10.13039/501100005969
http://dx.doi.org/10.13039/501100003339
http://dx.doi.org/10.13039/501100000780
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AT digioiadiana invivoassaytoidentifybacteriawithbglucosidaseactivity
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