Thermal resistance of proteolytic enzymes produced by psychrotrophic bacteria isolated from buffalo milk
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/188751 |
Resumo: | Background and Objective: Psychrotrophic bacteria produce extracellular proteases, resulting in deterioration and reduced shelf life of dairy products. In this study, 21 species of psychotropic bacteria isolated from buffalo milk were selected and the thermal resistance of the proteases produced by these bacteria was evaluated. Materials and Methods: The isolates were tested to evaluate proteolytic activity of buffalo milk agar. The cell-free supernatants from the growing of isolates were obtained for the quantification of enzymatic activity under different pH values (5.5, 7.0 and 8.0). Thermal resistance and the clotting ability of proteolytic enzymes in buffalo and bovine milk substrates were also evaluated. One-way ANOVA test with a critical probability of p<0.05 followed by the Tukey’s test was used to evaluate the results. Results: All strains were able to produce proteolysis in buffalo milk agar; additionally, all cell-free supernatants showed enzymatic activity, with values of >1 U mLG1 under at least one of the pH tested. Five isolates produced cell-free supernatants resistant to pasteurization (63.5EC/30 min), following which they were able to coagulate buffalo and bovine milk. The crude enzyme of P. fluorescens PL5.4 showed the greatest enzymatic activity within a wide pH range (4-10) and at an optimum temperature of 40EC. The cell-free supernatant of this isolate resisted to tests with detergents and organic solvents. However, it was not possible to identify the type of protease. Conclusion: The results of this study showed the negative impact of the presence of psychrotrophic bacteria producing proteolytic enzymes in buffalo milk. This is because the enzymes studied caused changes in milk samples, revealing a negative impact on the production of derived products. This is significant, since the buffalo milk produced in Brazil is directed to the production of dairy products. |
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Bogo, MarcieleCruz, Karine LauerRevello, Alvaro GonzalezCorrea, Ana Paula FolmerBrandelli, AdrianoFrazzon, Ana Paula GuedesMotta, Amanda de Souza da2019-02-14T02:32:32Z20170022-0302http://hdl.handle.net/10183/188751001086105Background and Objective: Psychrotrophic bacteria produce extracellular proteases, resulting in deterioration and reduced shelf life of dairy products. In this study, 21 species of psychotropic bacteria isolated from buffalo milk were selected and the thermal resistance of the proteases produced by these bacteria was evaluated. Materials and Methods: The isolates were tested to evaluate proteolytic activity of buffalo milk agar. The cell-free supernatants from the growing of isolates were obtained for the quantification of enzymatic activity under different pH values (5.5, 7.0 and 8.0). Thermal resistance and the clotting ability of proteolytic enzymes in buffalo and bovine milk substrates were also evaluated. One-way ANOVA test with a critical probability of p<0.05 followed by the Tukey’s test was used to evaluate the results. Results: All strains were able to produce proteolysis in buffalo milk agar; additionally, all cell-free supernatants showed enzymatic activity, with values of >1 U mLG1 under at least one of the pH tested. Five isolates produced cell-free supernatants resistant to pasteurization (63.5EC/30 min), following which they were able to coagulate buffalo and bovine milk. The crude enzyme of P. fluorescens PL5.4 showed the greatest enzymatic activity within a wide pH range (4-10) and at an optimum temperature of 40EC. The cell-free supernatant of this isolate resisted to tests with detergents and organic solvents. However, it was not possible to identify the type of protease. Conclusion: The results of this study showed the negative impact of the presence of psychrotrophic bacteria producing proteolytic enzymes in buffalo milk. This is because the enzymes studied caused changes in milk samples, revealing a negative impact on the production of derived products. This is significant, since the buffalo milk produced in Brazil is directed to the production of dairy products.application/pdfengInternational journal of dairy science. Champaign, IL. Vol. 12, no. 5 (2017), p. 339-347Resistência bacterianaPeptídeo hidrolasesProteóliseBactériasPseudomonasLeite de búfalaPsychrotrophicProteolysisThermal resistanceCoagulationEnzymesPseudomonasThermal resistance of proteolytic enzymes produced by psychrotrophic bacteria isolated from buffalo milkEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001086105.pdf.txt001086105.pdf.txtExtracted Texttext/plain1634http://www.lume.ufrgs.br/bitstream/10183/188751/2/001086105.pdf.txtb8b0a28fa5e425581ae545d82dd463feMD52ORIGINAL001086105.pdfTexto completo (inglês)application/pdf685424http://www.lume.ufrgs.br/bitstream/10183/188751/1/001086105.pdf4687adfdd3c0b12b7ede277d06b9c11bMD5110183/1887512021-05-26 04:28:26.654253oai:www.lume.ufrgs.br:10183/188751Repositório InstitucionalPUBhttps://lume.ufrgs.br/oai/requestlume@ufrgs.bropendoar:2021-05-26T07:28:26Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Thermal resistance of proteolytic enzymes produced by psychrotrophic bacteria isolated from buffalo milk |
title |
Thermal resistance of proteolytic enzymes produced by psychrotrophic bacteria isolated from buffalo milk |
spellingShingle |
Thermal resistance of proteolytic enzymes produced by psychrotrophic bacteria isolated from buffalo milk Bogo, Marciele Resistência bacteriana Peptídeo hidrolases Proteólise Bactérias Pseudomonas Leite de búfala Psychrotrophic Proteolysis Thermal resistance Coagulation Enzymes Pseudomonas |
title_short |
Thermal resistance of proteolytic enzymes produced by psychrotrophic bacteria isolated from buffalo milk |
title_full |
Thermal resistance of proteolytic enzymes produced by psychrotrophic bacteria isolated from buffalo milk |
title_fullStr |
Thermal resistance of proteolytic enzymes produced by psychrotrophic bacteria isolated from buffalo milk |
title_full_unstemmed |
Thermal resistance of proteolytic enzymes produced by psychrotrophic bacteria isolated from buffalo milk |
title_sort |
Thermal resistance of proteolytic enzymes produced by psychrotrophic bacteria isolated from buffalo milk |
author |
Bogo, Marciele |
author_facet |
Bogo, Marciele Cruz, Karine Lauer Revello, Alvaro Gonzalez Correa, Ana Paula Folmer Brandelli, Adriano Frazzon, Ana Paula Guedes Motta, Amanda de Souza da |
author_role |
author |
author2 |
Cruz, Karine Lauer Revello, Alvaro Gonzalez Correa, Ana Paula Folmer Brandelli, Adriano Frazzon, Ana Paula Guedes Motta, Amanda de Souza da |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Bogo, Marciele Cruz, Karine Lauer Revello, Alvaro Gonzalez Correa, Ana Paula Folmer Brandelli, Adriano Frazzon, Ana Paula Guedes Motta, Amanda de Souza da |
dc.subject.por.fl_str_mv |
Resistência bacteriana Peptídeo hidrolases Proteólise Bactérias Pseudomonas Leite de búfala |
topic |
Resistência bacteriana Peptídeo hidrolases Proteólise Bactérias Pseudomonas Leite de búfala Psychrotrophic Proteolysis Thermal resistance Coagulation Enzymes Pseudomonas |
dc.subject.eng.fl_str_mv |
Psychrotrophic Proteolysis Thermal resistance Coagulation Enzymes Pseudomonas |
description |
Background and Objective: Psychrotrophic bacteria produce extracellular proteases, resulting in deterioration and reduced shelf life of dairy products. In this study, 21 species of psychotropic bacteria isolated from buffalo milk were selected and the thermal resistance of the proteases produced by these bacteria was evaluated. Materials and Methods: The isolates were tested to evaluate proteolytic activity of buffalo milk agar. The cell-free supernatants from the growing of isolates were obtained for the quantification of enzymatic activity under different pH values (5.5, 7.0 and 8.0). Thermal resistance and the clotting ability of proteolytic enzymes in buffalo and bovine milk substrates were also evaluated. One-way ANOVA test with a critical probability of p<0.05 followed by the Tukey’s test was used to evaluate the results. Results: All strains were able to produce proteolysis in buffalo milk agar; additionally, all cell-free supernatants showed enzymatic activity, with values of >1 U mLG1 under at least one of the pH tested. Five isolates produced cell-free supernatants resistant to pasteurization (63.5EC/30 min), following which they were able to coagulate buffalo and bovine milk. The crude enzyme of P. fluorescens PL5.4 showed the greatest enzymatic activity within a wide pH range (4-10) and at an optimum temperature of 40EC. The cell-free supernatant of this isolate resisted to tests with detergents and organic solvents. However, it was not possible to identify the type of protease. Conclusion: The results of this study showed the negative impact of the presence of psychrotrophic bacteria producing proteolytic enzymes in buffalo milk. This is because the enzymes studied caused changes in milk samples, revealing a negative impact on the production of derived products. This is significant, since the buffalo milk produced in Brazil is directed to the production of dairy products. |
publishDate |
2017 |
dc.date.issued.fl_str_mv |
2017 |
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2019-02-14T02:32:32Z |
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Estrangeiro info:eu-repo/semantics/article |
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dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10183/188751 |
dc.identifier.issn.pt_BR.fl_str_mv |
0022-0302 |
dc.identifier.nrb.pt_BR.fl_str_mv |
001086105 |
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0022-0302 001086105 |
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http://hdl.handle.net/10183/188751 |
dc.language.iso.fl_str_mv |
eng |
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eng |
dc.relation.ispartof.pt_BR.fl_str_mv |
International journal of dairy science. Champaign, IL. Vol. 12, no. 5 (2017), p. 339-347 |
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