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Partial characterization of proteases from Spretomyces clavuligerus using an inexpensive medium
Moreira, Keila Aparecida; Cavalcanti, Maria Taciana Holanda; Duarte, Helena Simões; Tambourgi, Elias Basile; Melo, Eduardo Henrique Magalhäes de; Silva, Valdinete Lins; Porto, Ana Lúcia Figueiredo; Lima Filho, José Luiz de.
  • Moreira, Keila Aparecida; Universidade Federal de Pernambuco. Departamento de Bioquímica e Laboratório de Imunopatologia Keizo Asami. Recife. BR
  • Cavalcanti, Maria Taciana Holanda; Universidade Federal de Pernambuco. Departamento de Bioquímica e Laboratório de Imunopatologia Keizo Asami. Recife. BR
  • Duarte, Helena Simões; Universidade Federal Rural de Pernambuco. Departamento de Morfologia e Fisiologia Animal. Recife. BR
  • Tambourgi, Elias Basile; Universidade Estadual de Campinas. Faculdade de Engenharia Química. Departamento de Separaçäo Quimica. Campinas. BR
  • Melo, Eduardo Henrique Magalhäes de; Universidade Federal de Pernambuco. Departamento de Bioquímica. Recife. BR
  • Silva, Valdinete Lins; Universidade Federal de Pernambuco. Departamento de Engenharia Química. Recife. BR
  • Porto, Ana Lúcia Figueiredo; Universidade Federal de Pernambuco. Laboratório de Imunopatologia Keizo Asami. Recife. BR
  • Lima Filho, José Luiz de; Universidade Federal de Pernambuco. Departamento de Bioquímica e Laboratório de Imunopatologia Keizo Asami. Recife. BR
Braz. j. microbiol ; 32(3): 215-220, July-Sept., 2001.
Article in English | LILACS | ID: lil-316972
RESUMO
The partial characterization of extracellular proteases from Streptomyces clavuligerus NRRL 3585 and 644 mutant was investigated. The enzyme production was carried out in batch fermentation using soy bean filtrate as nitrogen source. Maximum activity was obtained after 96h of fermentation with an initial pH of 7.0. The enzyme was partially purified by ammonium sulphate precipitation. Enzymes from the two strains retained 37 per cent of their initial activities at pH 8.0 after 2 h incubation at 25§C. Enzyme half-life at pH 8.0 and 60§C was 40.30 and 53.32 min, respectively for both strains (partially purified extract). The optimum pH was obtained at pH 7.0-8.0 and 8.4 for enzymes produced for 3585 and 644 strains (crude extract), respectively, and 8.4 and 8.0 for enzymes from the partially purified extract 3585 and 644 strains, respectively. The optimum temperature for the crude extract was 21§C for both strains. However, for the partially preparation the optimum temperature was 50§C and 40ºC for S. clavuligerus NRRL 3585 and 644 strains respectively.
Subject(s)
Full text: Available Index: LILACS (Americas) Main subject: Protease Inhibitors / Streptomyces / In Vitro Techniques / Enzyme Activation / Clinical Enzyme Tests / Enzymes Language: English Journal: Braz. j. microbiol Journal subject: Microbiology Year: 2001 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Estadual de Campinas/BR / Universidade Federal Rural de Pernambuco/BR / Universidade Federal de Pernambuco/BR

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Full text: Available Index: LILACS (Americas) Main subject: Protease Inhibitors / Streptomyces / In Vitro Techniques / Enzyme Activation / Clinical Enzyme Tests / Enzymes Language: English Journal: Braz. j. microbiol Journal subject: Microbiology Year: 2001 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Estadual de Campinas/BR / Universidade Federal Rural de Pernambuco/BR / Universidade Federal de Pernambuco/BR