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Properties of a new fungal ß-Galactosidase with potential application in the dairy industry
Cruz, Rubens; Cruz, Vinícius D'Arcádia; Belote, Juliana Gisele; Khenayfes, Marcelo de Oliveira; Dorta, Claudia; Oliveira, Luiza Helena dos Santos.
  • Cruz, Rubens; Universidade Estadual de São Paulo de Assis. Faculdade de Ciências e Letras. Departamento de Ciências Biológicas.
  • Cruz, Vinícius D'Arcádia; Universidade Estadual de São Paulo de Assis. Faculdade de Ciências e Letras. Departamento de Ciências Biológicas.
  • Belote, Juliana Gisele; Universidade Estadual de São Paulo de Assis. Faculdade de Ciências e Letras. Departamento de Ciências Biológicas.
  • Khenayfes, Marcelo de Oliveira; Universidade Estadual de São Paulo de Assis. Faculdade de Ciências e Letras. Departamento de Ciências Biológicas.
  • Dorta, Claudia; Universidade Estadual de São Paulo de Assis. Faculdade de Ciências e Letras. Departamento de Ciências Biológicas.
  • Oliveira, Luiza Helena dos Santos; Universidade Estadual de São Paulo de Assis. Faculdade de Ciências e Letras. Departamento de Ciências Biológicas.
Rev. microbiol ; 30(3): 265-71, jul.-set. 1999. tab, graf
Article in Portuguese, English | LILACS | ID: lil-253783
RESUMO
ß-Galactosidase or ß-D-galactohydrolase (EC.3.2.1.23) is an important enzyme industrially used for the hydrolysis of lactose from milk and milk whey for several applications. Lately, the importance of this enzyme was enhanced by its galactosyltransferase activity, which is responsible for the synthesis of transgalctosylated oligosaccharides (TOS) that act as functional foods, with several beneficial effects on consumers. Penicillium simplicissimum, a strain isolated from soil, when grown in semi-solid medium showed good productivity of ß-galactosidase with galactosyltransferase activity. The optimum pH for hydrolysis was in 4.0-4.6 range and the optimum pH for galactosyltransferase activity was in the 6.0-7.0 range. The optimum temperature for hydrolysis and transferase activity was 55-60§C and 50§C, respectively, and the enzyme showed high thermostability for the hydrolytic activity. The enzyme showed a potential for several industrial applications such as removal of 67 (per cent) of the lactose from milk and 84 (per cent) of the lactose from milk whey when incubated at their original pH (4.5 and 6.34, respectively) under optimum temperature conditions. When incubated with a 40 (per cent) lactose solution in 150 mM McIlvaine buffer, pH 4.5, at 55§C the enzyme converted 86.5 (per cent) of the lactose to its component monosaccharides. When incubated with a 60 (per cent) lactose solution in the same buffer but at pH 6.5 and 50§C, the enzyme can synthetize up to 30.5 (per cent) TOS, with 39.5 (per cent) lactose and 30 (per cent) monosaccharides remaining in the preparation.
Subject(s)
Full text: Available Index: LILACS (Americas) Main subject: Beta-Galactosidase / Fungicides, Industrial Language: English / Portuguese Journal: Rev. microbiol Journal subject: Microbiology Year: 1999 Type: Article

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Full text: Available Index: LILACS (Americas) Main subject: Beta-Galactosidase / Fungicides, Industrial Language: English / Portuguese Journal: Rev. microbiol Journal subject: Microbiology Year: 1999 Type: Article