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Purification and characterization of beta-glucosidase from Melanocarpus sp. MTCC 3922
Kaur, Jatinder; Chadha, Bhupinder S; Kumar, Badhan A; Kaur, Ghatora S; Saini, Harvinder S.
Afiliação
  • Kaur, Jatinder; Guru Nanak Dev University. Department of Microbiology. Amritsar. IN
  • Chadha, Bhupinder S; Guru Nanak Dev University. Department of Microbiology. Amritsar. IN
  • Kumar, Badhan A; Guru Nanak Dev University. Department of Microbiology. Amritsar. IN
  • Kaur, Ghatora S; Guru Nanak Dev University. Department of Microbiology. Amritsar. IN
  • Saini, Harvinder S; Guru Nanak Dev University. Department of Microbiology. Amritsar. IN
Electron. j. biotechnol ; 10(2): 260-270, Apr. 15, 2007. ilus, graf, tab
Artigo em Inglês | LILACS | ID: lil-499175
Biblioteca responsável: CL1.1
ABSTRACT
This study reports the purification and characterization of beta-glucosidase from a newly isolated thermophilic fungus, Melanocarpus sp. Microbial Type Culture Collection (MTCC) 3922. The molecular weight of beta-glucosidase was determined to be ~ 92 and 102 kDa with SDS PAGE and gel filtration, respectively, and pI of ~ 4.1. It was optimally active at 60 C and pH 6.0, though was stable at 50 C and pH 5.0 - 6.0. The presence of DTT, mercaptoethanol and metal ions such as Na+, K+, Ca2+, Mg2+and Zn2+ positively influenced the activity of beta-glucosidase but the activity was inhibited in the presence of CuSO4. beta-Glucosidase recognized pNP- beta-glucopyranoside (pNPG) as the preferred substrate, and showed very low affinity for pNP- beta-D-cellobioside. Km and Vmax for the hydrolysis of pNPG by beta-glucosidase was calculated as 3.3 mM and 43.68 ‘molmin-1mg protein-1, respectively and k cat was quantified as 4 x 10³ min-1. beta-Glucosidase activity was enhanced appreciably in the presence of alcohols (methanol and ethanol) moreover, purified beta-glucosidase showed putative transglycosylation activity that was positively catalyzed in presence of methanol as an acceptor molecule
Assuntos

Texto completo: Disponível Coleções: Bases de dados internacionais Base de dados: LILACS Assunto principal: Ascomicetos / Beta-Glucosidase Limite: Animais Idioma: Inglês Revista: Electron. j. biotechnol Assunto da revista: Biotecnologia Ano de publicação: 2007 Tipo de documento: Artigo País de afiliação: Índia Instituição/País de afiliação: Guru Nanak Dev University/IN
Texto completo: Disponível Coleções: Bases de dados internacionais Base de dados: LILACS Assunto principal: Ascomicetos / Beta-Glucosidase Limite: Animais Idioma: Inglês Revista: Electron. j. biotechnol Assunto da revista: Biotecnologia Ano de publicação: 2007 Tipo de documento: Artigo País de afiliação: Índia Instituição/País de afiliação: Guru Nanak Dev University/IN
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