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Characterization of Thermostable Cellulase from Bacillus licheniformis PANG L Isolated from the Himalayan Soil

This study aimed to isolate, purify, and characterize a potential thermophilic cellulase-producing bacterium from the Himalayan soil. Eleven thermophilic bacteria were isolated, and the strain PANG L was found to be the most potent cellulolytic producer. Morphological, physiological, biochemical, an...

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Autores principales: Shyaula, Manita, Regmi, Sunil, Khadka, Deegendra, Poudel, Ram Chandra, Dhakal, Agni, Koirala, Devesh, Sijapati, Jaishree, Singh, Anjana, Maharjan, Jyoti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484656/
https://www.ncbi.nlm.nih.gov/pubmed/37692921
http://dx.doi.org/10.1155/2023/3615757
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author Shyaula, Manita
Regmi, Sunil
Khadka, Deegendra
Poudel, Ram Chandra
Dhakal, Agni
Koirala, Devesh
Sijapati, Jaishree
Singh, Anjana
Maharjan, Jyoti
author_facet Shyaula, Manita
Regmi, Sunil
Khadka, Deegendra
Poudel, Ram Chandra
Dhakal, Agni
Koirala, Devesh
Sijapati, Jaishree
Singh, Anjana
Maharjan, Jyoti
author_sort Shyaula, Manita
collection PubMed
description This study aimed to isolate, purify, and characterize a potential thermophilic cellulase-producing bacterium from the Himalayan soil. Eleven thermophilic bacteria were isolated, and the strain PANG L was found to be the most potent cellulolytic producer. Morphological, physiological, biochemical, and molecular characterization identified PANG L as Bacillus licheniformis. This is the first study on the isolation of thermostable cellulase-producing Bacillus licheniformis from the Himalayan soil. This bacterium was processed for the production of cellulase enzyme. The optimum conditions for cellulase production were achieved at 45°C after 48 h of incubation at pH 6.5 in media-containing carboxymethyl cellulose (CMC) and yeast extract as carbon and nitrogen sources, respectively, in a thermo-shaker at 100 rpm. The enzyme was partially purified by 80% ammonium sulphate precipitation followed by dialysis, resulting in a 1.52-fold purification. The optimal activity of partially purified cellulase was observed at a temperature of 60°C and pH 5. The cellulase enzyme was stable within the pH ranges of 3–5 and retained 67% of activity even at 55°C. Cellulase activity was found to be enhanced in the presence of metal ions such as Cd(2+), Pb(2+), and Ba(2+). The enzyme showed the highest activity when CMC was used as a substrate, followed by cellobiose. The K(m) and V(max) values of the enzyme were 1.8 mg/ml and 10.92 μg/ml/min, respectively. The cellulase enzyme obtained from Bacillus licheniformis PANG L had suitable catalytic properties for use in industrial applications.
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spelling pubmed-104846562023-09-08 Characterization of Thermostable Cellulase from Bacillus licheniformis PANG L Isolated from the Himalayan Soil Shyaula, Manita Regmi, Sunil Khadka, Deegendra Poudel, Ram Chandra Dhakal, Agni Koirala, Devesh Sijapati, Jaishree Singh, Anjana Maharjan, Jyoti Int J Microbiol Research Article This study aimed to isolate, purify, and characterize a potential thermophilic cellulase-producing bacterium from the Himalayan soil. Eleven thermophilic bacteria were isolated, and the strain PANG L was found to be the most potent cellulolytic producer. Morphological, physiological, biochemical, and molecular characterization identified PANG L as Bacillus licheniformis. This is the first study on the isolation of thermostable cellulase-producing Bacillus licheniformis from the Himalayan soil. This bacterium was processed for the production of cellulase enzyme. The optimum conditions for cellulase production were achieved at 45°C after 48 h of incubation at pH 6.5 in media-containing carboxymethyl cellulose (CMC) and yeast extract as carbon and nitrogen sources, respectively, in a thermo-shaker at 100 rpm. The enzyme was partially purified by 80% ammonium sulphate precipitation followed by dialysis, resulting in a 1.52-fold purification. The optimal activity of partially purified cellulase was observed at a temperature of 60°C and pH 5. The cellulase enzyme was stable within the pH ranges of 3–5 and retained 67% of activity even at 55°C. Cellulase activity was found to be enhanced in the presence of metal ions such as Cd(2+), Pb(2+), and Ba(2+). The enzyme showed the highest activity when CMC was used as a substrate, followed by cellobiose. The K(m) and V(max) values of the enzyme were 1.8 mg/ml and 10.92 μg/ml/min, respectively. The cellulase enzyme obtained from Bacillus licheniformis PANG L had suitable catalytic properties for use in industrial applications. Hindawi 2023-08-31 /pmc/articles/PMC10484656/ /pubmed/37692921 http://dx.doi.org/10.1155/2023/3615757 Text en Copyright © 2023 Manita Shyaula et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Shyaula, Manita
Regmi, Sunil
Khadka, Deegendra
Poudel, Ram Chandra
Dhakal, Agni
Koirala, Devesh
Sijapati, Jaishree
Singh, Anjana
Maharjan, Jyoti
Characterization of Thermostable Cellulase from Bacillus licheniformis PANG L Isolated from the Himalayan Soil
title Characterization of Thermostable Cellulase from Bacillus licheniformis PANG L Isolated from the Himalayan Soil
title_full Characterization of Thermostable Cellulase from Bacillus licheniformis PANG L Isolated from the Himalayan Soil
title_fullStr Characterization of Thermostable Cellulase from Bacillus licheniformis PANG L Isolated from the Himalayan Soil
title_full_unstemmed Characterization of Thermostable Cellulase from Bacillus licheniformis PANG L Isolated from the Himalayan Soil
title_short Characterization of Thermostable Cellulase from Bacillus licheniformis PANG L Isolated from the Himalayan Soil
title_sort characterization of thermostable cellulase from bacillus licheniformis pang l isolated from the himalayan soil
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484656/
https://www.ncbi.nlm.nih.gov/pubmed/37692921
http://dx.doi.org/10.1155/2023/3615757
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