Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1980 Oct;144(1):92–96. doi: 10.1128/jb.144.1.92-96.1980

Immunochemical studies of the mannans of Saccharomyces cerevisiae X2180-1A-5 and Saccharomyces cerevisiae 4484-24D-1 mutant strains, with special reference to their phosphate content.

Y Okubo, N Shibata, T Matsumoto, M Suzuki, C Schuerch, S Suzuki
PMCID: PMC294596  PMID: 6158512

Abstract

The mannans from Saccharomyces cerevisiae mutant strains X2180-1A-5 and 4484-24D-1, both of which were shown to contain small amounts of phosphate (less than 0.2%), were fractionated on a column of diethylaminoethyl-Sephadex into five subfractions designated as fractions I to V. These subfractions contain different amounts of phosphate, ranging from 0.03 to 0.09 (strain X2180-1A-5) and from 0.01 to 0.17% (strain 4484-24D-1). Fractions I to IV from strain X2180-1A-5 showed nearly identical precipitin activities against the homologous anti-whole cell serum, whereas fraction V, containing the largest amount of phosphate and protein among this mannan subfraction series, showed unexpectedly weaker precipitin activity than those of the other fractions. A synthetic mannan consisting or consecutive alpha-1 leads to 6-linked D-mannopyranosyl residues was found to be cross-reactive with all the mannan subfractions of strain X2180-1A-5 against anti-X2180-1A-5 serum. On the other hand, antibody-precipitating activities of the mannan subfractions of the latter strain were proportional to their phosphate content, although the increments of precipitated antibody nitrogen among the subfractions were quite small. However, fraction V of this mannan subfraction series, containing the largest amounts of phosphate and protein, showed lower precipitin activity than did the other four fractions. These findings indicate that mannans containing no phosphate or relatively small amounts of phosphate, such as those investigated in the present study, are less heterogeneous in the densities of the branching moieties than are highly phosphorylated mannans. These findings suggest that the transfer step of mannosyl-1-phosphate into the precursor(s) of the wild-type strain mannans during the biosynthetic process corresponds to the key reaction responsible for the anionic heterogeneity due to the density heterogeneity of the antigenic determinants.

Full text

PDF
96

Images in this article

Selected References

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

  1. AMES B. N., DUBIN D. T. The role of polyamines in the neutralization of bacteriophage deoxyribonucleic acid. J Biol Chem. 1960 Mar;235:769–775. [PubMed] [Google Scholar]
  2. Antalis C., Fogel S., Ballou C. E. Genetic control of yeast mannan structure. Mapping the first gene concerned with mannan biosynthesis. J Biol Chem. 1973 Jul 10;248(13):4655–4659. [PubMed] [Google Scholar]
  3. Ballou C. E., Kern K. A., Raschke W. C. Genetic control of yeast mannan structure. Complementation studies and properties of mannan mutants. J Biol Chem. 1973 Jul 10;248(13):4667–4671. [PubMed] [Google Scholar]
  4. Friis J., Ottolenghi P. The genetically determined binding of alcian blue by a minor fraction of yeast cell walls. C R Trav Lab Carlsberg. 1970;37(15):327–341. [PubMed] [Google Scholar]
  5. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  6. Nakajima T., Ballou C. E. Characterization of the carbohydrate fragments obtained from Saccharomyces cerevisiae mannan by alkaline degradation. J Biol Chem. 1974 Dec 10;249(23):7679–7684. [PubMed] [Google Scholar]
  7. Nakajima T., Ballou C. E. Structure of the linkage region between the polysaccharide and protein parts of Saccharomyces cerevisiae mannan. J Biol Chem. 1974 Dec 10;249(23):7685–7694. [PubMed] [Google Scholar]
  8. Okubo Y., Honma Y., Suzuki S. Relationship between phosphate content and serological activities of the mannans of Candida albicans strains NIH A-207, NIH B-792, and J-1012. J Bacteriol. 1979 Jan;137(1):677–680. doi: 10.1128/jb.137.1.677-680.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Okubo Y., Ichikawa T., Suzuki S. Relationship between phosphate content and immunochemical properties of subfractions of bakers' yeast mannan. J Bacteriol. 1978 Oct;136(1):63–68. doi: 10.1128/jb.136.1.63-68.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Raschke W. C., Kern K. A., Antalis C., Ballou C. E. Genetic control of yeast mannan structure. Isolation and characterization of mannan mutants. J Biol Chem. 1973 Jul 10;248(13):4660–4666. [PubMed] [Google Scholar]
  11. Rosenfeld L., Ballou C. E. Genetic control of yeast mannan structure. Biochemical basis for the transformation of saccharomyces cerevisiae somatic antigen. J Biol Chem. 1974 Apr 10;249(7):2319–2321. [PubMed] [Google Scholar]
  12. Sentandreu R., Northcote D. H. The structure of a glycopeptide isolated from the yeast cell wall. Biochem J. 1968 Sep;109(3):419–432. doi: 10.1042/bj1090419. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Sunayama H. Studies on the antigenic activities of yeasts. IV. Analysis of the antigenic determinant groups of the mannan of Candida albicans serotype A. Jpn J Microbiol. 1970 Jan;14(1):27–39. doi: 10.1111/j.1348-0421.1970.tb00488.x. [DOI] [PubMed] [Google Scholar]
  14. Thieme T. R., Ballou C. E. Nature of the phosphodiester linkage of the phosphomannan from the yeast Kloeckera brevis. Biochemistry. 1971 Oct 26;10(22):4121–4129. doi: 10.1021/bi00798a017. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES