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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.
Afiliación
  • Shyaula M; Central Department of Microbiology, Tribhuvan University, Kirtipur, Kathmandu, Nepal.
  • Regmi S; Nepal Academy of Science and Technology, Khumaltar, Lalitpur, Nepal.
  • Khadka D; Nepal Academy of Science and Technology, Khumaltar, Lalitpur, Nepal.
  • Poudel RC; Nepal Academy of Science and Technology, Khumaltar, Lalitpur, Nepal.
  • Dhakal A; Nepal Academy of Science and Technology, Khumaltar, Lalitpur, Nepal.
  • Koirala D; Nepal Academy of Science and Technology, Khumaltar, Lalitpur, Nepal.
  • Sijapati J; Nepal Academy of Science and Technology, Khumaltar, Lalitpur, Nepal.
  • Singh A; Nepal Academy of Science and Technology, Khumaltar, Lalitpur, Nepal.
  • Maharjan J; Central Department of Microbiology, Tribhuvan University, Kirtipur, Kathmandu, Nepal.
Int J Microbiol ; 2023: 3615757, 2023.
Article en En | MEDLINE | ID: mdl-37692921
ABSTRACT
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 Cd2+, Pb2+, and Ba2+. The enzyme showed the highest activity when CMC was used as a substrate, followed by cellobiose. The Km and Vmax 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.

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Int J Microbiol Año: 2023 Tipo del documento: Article País de afiliación: Nepal

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Int J Microbiol Año: 2023 Tipo del documento: Article País de afiliación: Nepal