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α‐Galactosidase from Saccharomyces carlsbergensis
Author(s) -
LAZO Pedro S.,
OCHOA Amparo G.,
GASCÓN Santiago
Publication year - 1977
Publication title -
european journal of biochemistry
Language(s) - English
Resource type - Journals
eISSN - 1432-1033
pISSN - 0014-2956
DOI - 10.1111/j.1432-1033.1977.tb11677.x
Subject(s) - invertase , saccharomyces , sephadex , chromatography , yeast , enzyme , biochemistry , polyacrylamide gel electrophoresis , chemistry , membrane , saccharomyces cerevisiae
1. The α‐galactosidase of Saccharomyces carlsbergensis is an inducible enzyme which is localized mainly outside the cell membrane and which is secreted into the culture medium in increasing amounts during the growth cycle. 2. The soluble form of α‐galactosidase localized inside the cell appears to have the same characteristics as the external one, contrasting with the different forms found in the case of invertase. Although some activity is membrane‐bound, this activity, when solubilized with detergent, has the same characteristics as the external form of the enzyme. 3. A procedure has been developed by which the enzyme has been purified using batch adsorption with DEAE‐Sephadex and column chromatography in DEAE‐Sephadex, DEAE‐cellulose and Sephadex G‐200, using the supernatant of a culture of Saccharomyces carlsbergensis grown in yeast nitrogen base complemented with galactose. 4. The purified enzyme, which is homogeneous by chromatographic criteria and polyacrylamide gel electrophoresis, appears to be glycoprotein. 5. Invertase copurifies with the α‐galactosidase but because of its lower stability, together with the fact that the synthesis of both enzymes can be controlled separately, it was possible to obtain preparations in which the contaminant activity was approximately 1%.

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