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 in | Biotechnology progress Vol. 20; no. 4; pp. 1259 - 1262 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
USA
American Chemical Society
01.07.2004
American Institute of Chemical Engineers |
Subjects | |
Online Access | Get full text |
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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. |
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Bibliography: | ArticleID:BTPR49957 ark:/67375/WNG-5HPNL0RZ-H istex:3C0A8C94F890EB9A16C120B8022D4A7C7DEAE4D0 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 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 8756-7938 1520-6033 |
DOI: | 10.1021/bp049957m |