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Production of alkaline protease from Cellulosimicrobium cellulans

Cellulosimicrobium cellulans is one of the microorganisms that produces a wide variety of yeast cell wall-degrading enzymes, β-1,3-glucanase, protease and chitinase. Dried cells of Saccharomyces cerevisiae were used as carbon and nitrogen source for cell growth and protease production. The medium co...

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Detalles Bibliográficos
Autores principales: Ferracini-Santos, Luciana, Sato, Hélia H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Microbiologia 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3768500/
https://www.ncbi.nlm.nih.gov/pubmed/24031317
http://dx.doi.org/10.1590/S1517-83822009000100008
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author Ferracini-Santos, Luciana
Sato, Hélia H
author_facet Ferracini-Santos, Luciana
Sato, Hélia H
author_sort Ferracini-Santos, Luciana
collection PubMed
description Cellulosimicrobium cellulans is one of the microorganisms that produces a wide variety of yeast cell wall-degrading enzymes, β-1,3-glucanase, protease and chitinase. Dried cells of Saccharomyces cerevisiae were used as carbon and nitrogen source for cell growth and protease production. The medium components KH(2)PO(4), KOH and dried yeast cells showed a significant effect (p<0.05) on the factorial fractional design. A second design was prepared using two factors: pH and percentage of dried yeast cells. The results showed that the culture medium for the maximum production of protease was 0.2 g/l of MgSO(4).7H(2)O, 2.0 g/l of (NH(4))(2)SO(4) and 8% of dried yeast cells in 0.15M phosphate buffer at pH 8.0. The maximum alkaline protease production was 7.0 ± 0.27 U/ml over the center point. Crude protease showed best activity at 50ºC and pH 7.0-8.0, and was stable at 50ºC.
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spelling pubmed-37685002013-09-12 Production of alkaline protease from Cellulosimicrobium cellulans Ferracini-Santos, Luciana Sato, Hélia H Braz J Microbiol Industrial Microbiology Cellulosimicrobium cellulans is one of the microorganisms that produces a wide variety of yeast cell wall-degrading enzymes, β-1,3-glucanase, protease and chitinase. Dried cells of Saccharomyces cerevisiae were used as carbon and nitrogen source for cell growth and protease production. The medium components KH(2)PO(4), KOH and dried yeast cells showed a significant effect (p<0.05) on the factorial fractional design. A second design was prepared using two factors: pH and percentage of dried yeast cells. The results showed that the culture medium for the maximum production of protease was 0.2 g/l of MgSO(4).7H(2)O, 2.0 g/l of (NH(4))(2)SO(4) and 8% of dried yeast cells in 0.15M phosphate buffer at pH 8.0. The maximum alkaline protease production was 7.0 ± 0.27 U/ml over the center point. Crude protease showed best activity at 50ºC and pH 7.0-8.0, and was stable at 50ºC. Sociedade Brasileira de Microbiologia 2009 2009-03-01 /pmc/articles/PMC3768500/ /pubmed/24031317 http://dx.doi.org/10.1590/S1517-83822009000100008 Text en © Sociedade Brasileira de Microbiologia http://creativecommons.org/licenses/by-nc/3.0/ All the content of the journal, except where otherwise noted, is licensed under a Creative Commons License
spellingShingle Industrial Microbiology
Ferracini-Santos, Luciana
Sato, Hélia H
Production of alkaline protease from Cellulosimicrobium cellulans
title Production of alkaline protease from Cellulosimicrobium cellulans
title_full Production of alkaline protease from Cellulosimicrobium cellulans
title_fullStr Production of alkaline protease from Cellulosimicrobium cellulans
title_full_unstemmed Production of alkaline protease from Cellulosimicrobium cellulans
title_short Production of alkaline protease from Cellulosimicrobium cellulans
title_sort production of alkaline protease from cellulosimicrobium cellulans
topic Industrial Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3768500/
https://www.ncbi.nlm.nih.gov/pubmed/24031317
http://dx.doi.org/10.1590/S1517-83822009000100008
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