Co-purification of galactosyltransferases from chick-embryo liver
- 15 April 1985
- journal article
- research article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 227 (2) , 573-582
- https://doi.org/10.1042/bj2270573
Abstract
Two galactosyltransferases with nearly identical Mr values were purified 5000-7000-fold from microsomal membranes of chick-embryo livers by using several affinity columns. One enzyme transfers galactose from UDP-galactose to form a β-(1→4)-linkage to GlcNAc (N-acetylglucosamine) or AsAgAGP [asialo-agalacto-(alpha 1-acid glycoprotein)]. The other enzyme forms a β-(1→3)-linkage to AsOSM [asialo-(ovine submaxillary mucin)]. Both enzymes were solubilized (85%) from a microsomal pellet by using 1% Triton X-100 in 0.1 M-NaCl. The supernatant activities were subjected to DEAE-Sepharose chromatography and four affinity columns: UDP-hexanolamine-Sepharose, alpha-lactalbumin-Sepharose, GlcNAc-Sepharose and either AsAgAGP-Sepharose or AsOSM-Sepharose. The AsAgAGP enzyme [(1→4)-transferase] and the AsOSM enzyme [(1→3)-transferase] behave identically on the DEAE-Sepharose and UDP-hexanolamine-Sepharose columns, and similarly on the alpha-lactalbumin-Sepharose column. Final separation of the two enzymes, however, could only be achieved on affinity columns of their immobilized respective acceptors. Both purified enzymes migrate as a single band on sodium dodecyl sulphate/polyacrylamide-gel electrophoresis after silver staining, and both have an apparent Mr of 68 000. The enzymes were radioiodinated and again subjected to sodium dodecyl sulphate/polyacrylamide-gel electrophoresis. Radioautographic analyses showed only one, intensely radioactive, band. Activity stains performed for both transferases after cellulose acetate electrophoresis indicate that, with this system too, both activities have identical mobilities, and co-migrate, as well, with the major, silver-stained, protein band. Kinetic studies with the purified enzymes show that the Km value for GlcNAc, for the (1→4)-transferase, is 4mM; for the (1→3)-transferase the Km value for AsOSM is 5mM, in terms of GalNAc (N-acetylgalactosamine) equivalents. Both enzymes have a Km value of 25 microM for UDP-galactose.This publication has 27 references indexed in Scilit:
- Transport and topology of galactosyltransferase in endomembranes of HeLa cells.The Journal of cell biology, 1983
- Two α‐3‐d‐Galactosyltransferases in Rabbit Stomach Mucosa with Different Acceptor Substrate SpecificitiesEuropean Journal of Biochemistry, 1983
- A comparison of the isoelectric points of mouse liver UDP-glucuronosyltransferase enzymes conjugating the twelve benzo[a]pyrene phenolsBiochemical and Biophysical Research Communications, 1982
- Role of galactosyl-transferases in rat gastric epithelial glycoprotein synthesisBiochimica et Biophysica Acta (BBA) - Enzymology, 1980
- Purification by affinity chromatography and some properties of microsomal galactosyltransferase from pig thyroidBiochimica et Biophysica Acta (BBA) - Enzymology, 1979
- Ia antigenic specificities are oligosaccharide in nature: hapten-inhibition studies.The Journal of Experimental Medicine, 1977
- A Molecular Model for Cell InteractionsThe Quarterly Review of Biology, 1973
- EVIDENCE FOR CELL-SURFACE GLYCOSYLTRANSFERASESThe Journal of cell biology, 1971
- The synthesis of complex carbohydrates by multiglycosyltransferase systems and their potential function in intercellular adhesionChemistry and Physics of Lipids, 1970
- Preparation of Iodine-131 Labelled Human Growth Hormone of High Specific ActivityNature, 1962