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Production, purification and characterization of l-asparaginase from streptomyces gulbargensis

L-asparaginase is an anti-neoplastic agent used in the lymphoblastic leukaemia chemotherapy. In the present study a novel strain, Streptomyces gulbargensis was explored for the production of extra-cellular L-asparaginase using groundnut cake extract. The optimum pH, temperature, inoculum size and ag...

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Autores principales: Amena, S., Vishalakshi, N., Prabhakar, M., Dayanand, A., Lingappa, K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Microbiologia 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3768618/
https://www.ncbi.nlm.nih.gov/pubmed/24031478
http://dx.doi.org/10.1590/S1517-838220100001000025
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author Amena, S.
Vishalakshi, N.
Prabhakar, M.
Dayanand, A.
Lingappa, K.
author_facet Amena, S.
Vishalakshi, N.
Prabhakar, M.
Dayanand, A.
Lingappa, K.
author_sort Amena, S.
collection PubMed
description L-asparaginase is an anti-neoplastic agent used in the lymphoblastic leukaemia chemotherapy. In the present study a novel strain, Streptomyces gulbargensis was explored for the production of extra-cellular L-asparaginase using groundnut cake extract. The optimum pH, temperature, inoculum size and agitation speed for enzyme production were pH 8.5, 40°C, 1x10(8)spores/ml and 200 rev/min respectively. Maltose (0.5%) and L-asparagine (0.5%) proved to be the best carbon and nitrogen sources respectively. The enzyme was purified 82.12 fold and the apparent molecular weight of the enzyme was found to be 85 kDa. The optima pH and temperature for the enzyme were 9.0 and 40°C respectively. The enzyme was more stable at the alkaline pH than at the acidic one and it retained 55% of the activity at 80°C for 60 min.
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spelling pubmed-37686182013-09-12 Production, purification and characterization of l-asparaginase from streptomyces gulbargensis Amena, S. Vishalakshi, N. Prabhakar, M. Dayanand, A. Lingappa, K. Braz J Microbiol Industrial Microbiology L-asparaginase is an anti-neoplastic agent used in the lymphoblastic leukaemia chemotherapy. In the present study a novel strain, Streptomyces gulbargensis was explored for the production of extra-cellular L-asparaginase using groundnut cake extract. The optimum pH, temperature, inoculum size and agitation speed for enzyme production were pH 8.5, 40°C, 1x10(8)spores/ml and 200 rev/min respectively. Maltose (0.5%) and L-asparagine (0.5%) proved to be the best carbon and nitrogen sources respectively. The enzyme was purified 82.12 fold and the apparent molecular weight of the enzyme was found to be 85 kDa. The optima pH and temperature for the enzyme were 9.0 and 40°C respectively. The enzyme was more stable at the alkaline pH than at the acidic one and it retained 55% of the activity at 80°C for 60 min. Sociedade Brasileira de Microbiologia 2010 2010-03-01 /pmc/articles/PMC3768618/ /pubmed/24031478 http://dx.doi.org/10.1590/S1517-838220100001000025 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
Amena, S.
Vishalakshi, N.
Prabhakar, M.
Dayanand, A.
Lingappa, K.
Production, purification and characterization of l-asparaginase from streptomyces gulbargensis
title Production, purification and characterization of l-asparaginase from streptomyces gulbargensis
title_full Production, purification and characterization of l-asparaginase from streptomyces gulbargensis
title_fullStr Production, purification and characterization of l-asparaginase from streptomyces gulbargensis
title_full_unstemmed Production, purification and characterization of l-asparaginase from streptomyces gulbargensis
title_short Production, purification and characterization of l-asparaginase from streptomyces gulbargensis
title_sort production, purification and characterization of l-asparaginase from streptomyces gulbargensis
topic Industrial Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3768618/
https://www.ncbi.nlm.nih.gov/pubmed/24031478
http://dx.doi.org/10.1590/S1517-838220100001000025
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