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Production and partial characterization of extracellular amylase enzyme from Bacillus amyloliquefaciens P-001
Amylases are one of the most important enzymes in present-day biotechnology. The present study was concerned with the production and partial characterization of extracellular amylase from Bacillus amyloliquefaciens P-001. The effect of various fermentation conditions on amylase production through sh...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing AG
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3631119/ https://www.ncbi.nlm.nih.gov/pubmed/23626928 http://dx.doi.org/10.1186/2193-1801-2-154 |
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author | Deb, Promita Talukdar, Saimon Ahmad Mohsina, Kaniz Sarker, Palash Kumar Sayem, SM Abu |
author_facet | Deb, Promita Talukdar, Saimon Ahmad Mohsina, Kaniz Sarker, Palash Kumar Sayem, SM Abu |
author_sort | Deb, Promita |
collection | PubMed |
description | Amylases are one of the most important enzymes in present-day biotechnology. The present study was concerned with the production and partial characterization of extracellular amylase from Bacillus amyloliquefaciens P-001. The effect of various fermentation conditions on amylase production through shake-flask culture was investigated. Enzyme production was induced by a variety of starchy substrate but corn flour was found to be a suitable natural source for maximum production. Tryptone and ammonium nitrate (0.2%) as nitrogen sources gave higher yield compared to other nitrogen sources. Maximum enzyme production was obtained after 48 hrs of incubation in a fermentation medium with initial pH 9.0 at 42°C under continuous agitation at 150 rpm. The size of inoculum was also optimized which was found to be 1% (v/v). Enzyme production was 2.43 times higher after optimizing the production conditions as compared to the basal media. Studies on crude amylase revealed that optimum pH, temperature and reaction time of enzyme activity was 6.5, 60°C and 40 minutes respectively. About 73% of the activity retained after heating the crude enzyme solution at 50°C for 30 min. The enzyme was activated by Ca(2+) (relative activity 146.25%). It was strongly inhibited by Mn(2+), Zn(2+) and Cu(2+), but less affected by Mg(2+) and Fe(2+). |
format | Online Article Text |
id | pubmed-3631119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer International Publishing AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-36311192013-04-25 Production and partial characterization of extracellular amylase enzyme from Bacillus amyloliquefaciens P-001 Deb, Promita Talukdar, Saimon Ahmad Mohsina, Kaniz Sarker, Palash Kumar Sayem, SM Abu Springerplus Research Amylases are one of the most important enzymes in present-day biotechnology. The present study was concerned with the production and partial characterization of extracellular amylase from Bacillus amyloliquefaciens P-001. The effect of various fermentation conditions on amylase production through shake-flask culture was investigated. Enzyme production was induced by a variety of starchy substrate but corn flour was found to be a suitable natural source for maximum production. Tryptone and ammonium nitrate (0.2%) as nitrogen sources gave higher yield compared to other nitrogen sources. Maximum enzyme production was obtained after 48 hrs of incubation in a fermentation medium with initial pH 9.0 at 42°C under continuous agitation at 150 rpm. The size of inoculum was also optimized which was found to be 1% (v/v). Enzyme production was 2.43 times higher after optimizing the production conditions as compared to the basal media. Studies on crude amylase revealed that optimum pH, temperature and reaction time of enzyme activity was 6.5, 60°C and 40 minutes respectively. About 73% of the activity retained after heating the crude enzyme solution at 50°C for 30 min. The enzyme was activated by Ca(2+) (relative activity 146.25%). It was strongly inhibited by Mn(2+), Zn(2+) and Cu(2+), but less affected by Mg(2+) and Fe(2+). Springer International Publishing AG 2013-04-10 /pmc/articles/PMC3631119/ /pubmed/23626928 http://dx.doi.org/10.1186/2193-1801-2-154 Text en © Deb et al.; licensee Springer. 2013 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Deb, Promita Talukdar, Saimon Ahmad Mohsina, Kaniz Sarker, Palash Kumar Sayem, SM Abu Production and partial characterization of extracellular amylase enzyme from Bacillus amyloliquefaciens P-001 |
title | Production and partial characterization of extracellular amylase enzyme from Bacillus amyloliquefaciens P-001 |
title_full | Production and partial characterization of extracellular amylase enzyme from Bacillus amyloliquefaciens P-001 |
title_fullStr | Production and partial characterization of extracellular amylase enzyme from Bacillus amyloliquefaciens P-001 |
title_full_unstemmed | Production and partial characterization of extracellular amylase enzyme from Bacillus amyloliquefaciens P-001 |
title_short | Production and partial characterization of extracellular amylase enzyme from Bacillus amyloliquefaciens P-001 |
title_sort | production and partial characterization of extracellular amylase enzyme from bacillus amyloliquefaciens p-001 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3631119/ https://www.ncbi.nlm.nih.gov/pubmed/23626928 http://dx.doi.org/10.1186/2193-1801-2-154 |
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