Galactosidases are enzymes (glycoside hydrolases) that catalyze the hydrolysis of galactosides into monosaccharides.

Galactosides can be classified as either alpha or beta. If the galactoside is classified as an alpha-galactoside, the enzyme is called alpha-galactosidase, and is responsible for catalyzing the hydrolysis of substrates that contain α-galactosidic residues, such as glycosphingolipids or glycoproteins.[1] On the other hand, if it is a beta-galactoside, it is called beta-galactosidase, and is responsible for breaking down the disaccharide lactose into its monosaccharide components, glucose and galactose[2] Both varieties of galactosidase are categorized under the EC number 3.2.1.

Two recombinant forms of alpha-galactosidase are called agalsidase alfa (INN) and agalsidase beta (INN). Lack of alpha-galactosidase activity in leukocytes has been linked to Fabry Disease.[3]

Galactosidases have a variety of uses, including the production of prebiotics, the biosynthesis of transgalactosylated products, and the removal of lactose.

B-galactosidase forms the basis of lac z operon in bacteria which can be used to control gene expression.

Uses

B-galactosidase can be used to track the efficiency of bacterial transformation with a recombinant plasmid in a process called Blue/White Color Screening. B-galactosidase is made up of 4 identical polypeptide chains, i.e. it has 4 identical subunits. When B-galactosidase is separated into 2 fragments, it has the unique property of regaining enzymatic activity upon the rejoining of the inactive fragments.[4] In the process called alpha-complementation, one of the fragments (omega) is encoded by a part of a gene of the lac operon that is found in the chromosome of the bacteria, while the other fragment (alpha) is encoded by the other part of the gene that is found in the plasmid. It is only when both parts of the gene are being expressed that both the omega and alpha fragments are produced. When both fragments are present they would come together to restore the activity of B-galactosidase. However, by placing the target gene within the locus responsible for encoding the alpha fragment, one can track the presence of the desired gene in the plasmid. When the target gene is present, the alpha-fragment gene would be inactive and the alpha fragment won't be produced. In that case B-galactosidase will not be active. When the target gene is not found in the vector, the alpha fragment gene would be active, producing the alpha fragment and allowing for B-galactosidase to gain its activity. To trace the activity of B-galactosidase a colorless analog of lactose is used, X-gal. The hydrolysis of X-gal by B-galactosidase produces galactose, a blue colored compound. Therefore, when the bacteria is transformed with the recombinant plasmid B-galactosidase is inactive and the colonies appear white, but when bacteria are transformed with the original plasmid, lacking the target gene, B-galactosidase is active and the colonies appear blue.[5]

References

  1. ↑ King, Robert C.; Mulligan, Pamela K.; Stansfield, William D. A Dictionary of Genetics (8 ed.).
  2. ↑ King, Robert C.; Mulligan, Pamela K.; Stansfield, William D. A Dictionary of Genetics (8th ed.). Oxford University Press. ISBN 9780199376865.
  3. ↑ Kint, J. A. (1970-02-27). "Fabry's Disease: Alpha-Galactosidase Deficiency". Science. 167 (3922): 1268–1269. Bibcode:1970Sci...167.1268K. doi:10.1126/science.167.3922.1268. ISSN 0036-8075. PMID 5411915.
  4. ↑ Broome, Ann-Marie; Bhavsar, Nihir; Ramamurthy, Gopal; Newton, Gail; Basilion, James (Spring 2017). "Expanding the utility of β-galactosidase complementation: piece by piece". Molecular Pharmaceutics. 7 (1): 60–74. doi:10.1021/mp900188e. PMC 2835542. PMID 19899815.
  5. ↑ Clark, David; Pazdernik, Nanette (2013). Molecular Biology. Oxford, UK: Elsevier. p. 201. ISBN 9780123785947.
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