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Screening, purification and characterization of cellulase from cellulase producing bacteria in molasses
OBJECTIVES: This study was conducted to isolate, screening and purification of cellulase from bacteria present in sugar industry waste (molasses) and characterization by morphological and biochemical analysis. RESULTS: Based on experiments, three bacterial strains produced clear transparent zone int...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032522/ https://www.ncbi.nlm.nih.gov/pubmed/29973263 http://dx.doi.org/10.1186/s13104-018-3558-4 |
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author | Islam, Farjana Roy, Narayan |
author_facet | Islam, Farjana Roy, Narayan |
author_sort | Islam, Farjana |
collection | PubMed |
description | OBJECTIVES: This study was conducted to isolate, screening and purification of cellulase from bacteria present in sugar industry waste (molasses) and characterization by morphological and biochemical analysis. RESULTS: Based on experiments, three bacterial strains produced clear transparent zone into carboxymethyl cellulose (CMC) agar plate were identified as cellulase producing bacteria. Different culture parameters such as pH, temperature, incubation period, substrate concentration and carbon sources were optimized for enzyme production. According to the morphological and biochemical tests, the isolated strains were identified as Paenibacillus sp., Bacillus sp. and Aeromonas sp. The first strain Paenibacillus sp. showed high potentiality for maximum cellulase production (0.9 µmol ml(−1) min(−1)) at pH 7.0 after 24 h of incubation at 40 °C in a medium containing 1.0% CMC. Then Paenibacillus sp. was selected for enzyme purification by ammonium sulfate precipitation, DEAE-cellulose and CM-cellulose column chromatography, respectively. In last step of purification, specific activity, recovery and purification fold were 2655 U/mg, 35.7% and 9.7, respectively. The molecular weight of the purified cellulase was found to be 67 kDa by SDS-PAGE, had an optimal pH and temperature at 7.0 and 40 °C. According to substrate specificity, the purified cellulase had high specificity on CMC substrate which indicated it to be an endo-β-1,4-glucanase. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-018-3558-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6032522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60325222018-07-11 Screening, purification and characterization of cellulase from cellulase producing bacteria in molasses Islam, Farjana Roy, Narayan BMC Res Notes Research Note OBJECTIVES: This study was conducted to isolate, screening and purification of cellulase from bacteria present in sugar industry waste (molasses) and characterization by morphological and biochemical analysis. RESULTS: Based on experiments, three bacterial strains produced clear transparent zone into carboxymethyl cellulose (CMC) agar plate were identified as cellulase producing bacteria. Different culture parameters such as pH, temperature, incubation period, substrate concentration and carbon sources were optimized for enzyme production. According to the morphological and biochemical tests, the isolated strains were identified as Paenibacillus sp., Bacillus sp. and Aeromonas sp. The first strain Paenibacillus sp. showed high potentiality for maximum cellulase production (0.9 µmol ml(−1) min(−1)) at pH 7.0 after 24 h of incubation at 40 °C in a medium containing 1.0% CMC. Then Paenibacillus sp. was selected for enzyme purification by ammonium sulfate precipitation, DEAE-cellulose and CM-cellulose column chromatography, respectively. In last step of purification, specific activity, recovery and purification fold were 2655 U/mg, 35.7% and 9.7, respectively. The molecular weight of the purified cellulase was found to be 67 kDa by SDS-PAGE, had an optimal pH and temperature at 7.0 and 40 °C. According to substrate specificity, the purified cellulase had high specificity on CMC substrate which indicated it to be an endo-β-1,4-glucanase. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-018-3558-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-04 /pmc/articles/PMC6032522/ /pubmed/29973263 http://dx.doi.org/10.1186/s13104-018-3558-4 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Note Islam, Farjana Roy, Narayan Screening, purification and characterization of cellulase from cellulase producing bacteria in molasses |
title | Screening, purification and characterization of cellulase from cellulase producing bacteria in molasses |
title_full | Screening, purification and characterization of cellulase from cellulase producing bacteria in molasses |
title_fullStr | Screening, purification and characterization of cellulase from cellulase producing bacteria in molasses |
title_full_unstemmed | Screening, purification and characterization of cellulase from cellulase producing bacteria in molasses |
title_short | Screening, purification and characterization of cellulase from cellulase producing bacteria in molasses |
title_sort | screening, purification and characterization of cellulase from cellulase producing bacteria in molasses |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032522/ https://www.ncbi.nlm.nih.gov/pubmed/29973263 http://dx.doi.org/10.1186/s13104-018-3558-4 |
work_keys_str_mv | AT islamfarjana screeningpurificationandcharacterizationofcellulasefromcellulaseproducingbacteriainmolasses AT roynarayan screeningpurificationandcharacterizationofcellulasefromcellulaseproducingbacteriainmolasses |