Immobilization of lactase from Kluyveromyces lactis greatly reduces the inhibition promoted by glucose. Full hydrolysis of lactose in milk

The kinetic constants (Km, Vmax, and inhibition constants for the different products) of soluble and different immobilized preparations of β‐galactosidase from Kluyveromyces lactis were determined. For the soluble enzyme, the Km was 3.6 mM, while the competitive inhibition constant by galactose was...

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Published inBiotechnology progress Vol. 20; no. 4; pp. 1259 - 1262
Main Authors Mateo, C, Monti, R, Pessela, B.C.C, Fuentes, M, Torres, R, Guisan, J.M, Fernandez-Lafuente, R
Format Journal Article
LanguageEnglish
Published USA American Chemical Society 01.07.2004
American Institute of Chemical Engineers
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Summary:The kinetic constants (Km, Vmax, and inhibition constants for the different products) of soluble and different immobilized preparations of β‐galactosidase from Kluyveromyces lactis were determined. For the soluble enzyme, the Km was 3.6 mM, while the competitive inhibition constant by galactose was 45 mM and the noncompetitive one by glucose was 758 mM. The immobilized preparations conserved similar values of Km and competitive inhibition, but in some instances much higher values for the noncompetitive inhibition constants were obtained. Thus, when glyoxyl or glutaraldehyde supports were used to immobilize the enzyme, the noncompetitive inhibition was greatly reduced (Ki ≈ 15 000 and >40 000 mM, respectively), whereas when using sugar chains to immobilize the enzyme the behavior had an effect very similar to the soluble enzyme. These results presented a great practical relevance. While using the soluble enzyme or the enzyme immobilized via the sugar chain as biocatalysts in the hydrolysis of lactose in milk only around 90% of the substrate was hydrolyzed, by using of these the enzyme immobilized via the glyoxyl or the glutaraldehyde groups, more than 99% of the lactose in milk was hydrolyzed.
Bibliography:ArticleID:BTPR49957
ark:/67375/WNG-5HPNL0RZ-H
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Escuela de Química, Facultad de Ciencias, Edificio Camilo Torres, Ciudad Universitaria, Universidad Industrial de Santander, Bucaramanga, Colombia
Faculdade de Ciências Farmacêuticas (UNESP) Rodovia Araraquara‐Jaú Km. 1, CEP 14801–902 Araraquara, S. P., Brasil
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ISSN:8756-7938
1520-6033
DOI:10.1021/bp049957m