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. 1964 Jan;4(1 Pt 2):155–165. doi: 10.1016/s0006-3495(64)86935-6

Metabolism of Acid Mucopolysaccharides

Albert Dorfman
PMCID: PMC1367622  PMID: 14104075

Abstract

The biosynthesis of the acid mucopolysaccharides, hyaluronic acid and chondroitin sulfuric acid, occurs by way of uridine nucleotides which contain the monosaccharide units of the respective polysaccharides. The mechanism of alternation of groups is as yet unknown. Certain of the acid mucopolysaccharides are covalently bound to protein by way of serine. In the case of the protein-polysaccharide complex of cartilage, there is evidence to suggest that the polysaccharide may be linked to the serine by way of galactose. Chondroitin sulfuric acid B may be isolated almost free of amino acids from the tissues and urine of patients with the Hurler syndrome without the use of proteolytic enzymes, acid, or alkali. This contrasts markedly with the tight binding of this compound to protein in normal tissue. It is suggested that the metabolic defect in this disease may reside in a defect of the peptide or linkage of the peptide to polysaccharide resulting in failure of the acid mucopolysaccharide to be fixed normally in connective tissue. Such a defect may result in interference with normal regulation of polysaccharide synthesis with a resultant increased synthesis. It is proposed that such a mechanism may obtain in other heritable connective tissue diseases as well as other storage diseases.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. CIFONELLI J. A., DORFMAN A. The biosynthesis of hyaluronic acid by group A streptococcus. V. The uridine nucleotides of group A streptococcus. J Biol Chem. 1957 Oct;228(2):547–557. [PubMed] [Google Scholar]
  2. D'ABRAMO F., LIPMANN F. The formation of adenosine-3'-phosphate-5'-phosphosulfate in extracts of chick embryo cartilage and its conversion into chondroitin sulfate. Biochim Biophys Acta. 1957 Jul;25(1):211–213. doi: 10.1016/0006-3002(57)90452-3. [DOI] [PubMed] [Google Scholar]
  3. DAVIDSON E. A., MEYER K. Chondroitin, a new mucopolysaccharide. J Biol Chem. 1954 Dec;211(2):605–611. [PubMed] [Google Scholar]
  4. DORFMAN A., ROSEMAN S., MOSES F. E., LUDOWIEG J., MAYEDA M. The biosynthesis of hyaluronic acid by group A Streptococcus. II. Origin of the N-acetylglucosamine moiety. J Biol Chem. 1955 Feb;212(2):583–591. [PubMed] [Google Scholar]
  5. FREIMER E. H., KRAUSE R. M., McCARTY M. Studies of L forms and protoplasts of group A streptococci. I. Isolation, growth, and bacteriologic characteristics. J Exp Med. 1959 Dec 1;110:853–874. doi: 10.1084/jem.110.6.853. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. GROSS J. I., MATHEWS M. B., DORFMAN A. Sodium chondroitin sulfate-protein complexes of cartilage. II. Metabolism. J Biol Chem. 1960 Oct;235:2889–2892. [PubMed] [Google Scholar]
  7. KOBATA A. Isolation and identification of two novel uridine nucleotide oligosaccharide conjugates from human milk. Biochem Biophys Res Commun. 1962 May 11;7:346–350. doi: 10.1016/0006-291x(62)90312-1. [DOI] [PubMed] [Google Scholar]
  8. KRAUSE R. M. Studies on the bacteriophages of hemolytic streptococci. II. Antigens released from the streptococcal cell wall by a phage-associated lysin. J Exp Med. 1958 Dec 1;108(6):803–821. doi: 10.1084/jem.108.6.803. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. LYON M. F. Gene action in the X-chromosome of the mouse (Mus musculus L.). Nature. 1961 Apr 22;190:372–373. doi: 10.1038/190372a0. [DOI] [PubMed] [Google Scholar]
  10. MARKOVITZ A., CIFONELLI J. A., DORFMAN A. The biosynthesis of hyaluronic acid by group A Streptococcus. VI. Biosynthesis from uridine nucleotides in cell-free extracts. J Biol Chem. 1959 Sep;234:2343–2350. [PubMed] [Google Scholar]
  11. MATHEWS M. B., INOUYE M. The determination of chondroitin sulfate C-type polysaccharides in mixtures with other acid mucopolysaccharides. Biochim Biophys Acta. 1961 Nov 11;53:509–513. doi: 10.1016/0006-3002(61)90209-8. [DOI] [PubMed] [Google Scholar]
  12. MEYER K., GRUMBACH M. M., LINKER A., HOFFMAN P. Excretion of sulfated mucopolysaccharides in gargoylism (Hurler's syndrome). Proc Soc Exp Biol Med. 1958 Feb;97(2):275–279. doi: 10.3181/00379727-97-23714. [DOI] [PubMed] [Google Scholar]
  13. MOSCONA A., MOSCONA H. The dissociation and aggregation of cells from organ rudiments of the early chick embryo. J Anat. 1952 Jul;86(3):287–301. [PMC free article] [PubMed] [Google Scholar]
  14. ROSEMAN S., LUDOWIEG J., MOSES F. E., DORFMAN A. The biosynthesis of hyaluronic acid by group A Streptococcus. II. Origin of the glucuronic acid. J Biol Chem. 1954 Feb;206(2):665–669. [PubMed] [Google Scholar]
  15. ROSEMAN S., MOSES F. E., LUDOWIEG J., DORFMAN A. The biosynthesis of hyaluronic acid by group A Streptococcus. I. Utilization of 1-C14-glucose. J Biol Chem. 1953 Jul;203(1):213–225. [PubMed] [Google Scholar]
  16. THORP F. K., DORFMAN A. The occurrence of intracellular chondroitin sulfate. J Cell Biol. 1963 Jul;18:13–17. doi: 10.1083/jcb.18.1.13. [DOI] [PMC free article] [PubMed] [Google Scholar]

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