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Immune-enhancing alkali-soluble glucans produced by wild-type and mutant Saccharomyces cerevisiae

Authors
Ha, CHLim, KHJang, SHYun, CWPaw, HDKim, SWKang, CWChang, HI
Issue Date
Apr-2006
Publisher
KOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY
Keywords
alkali-soluble glucan; mannoprotein; yeast cell wall; random mutation
Citation
JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, v.16, no.4, pp.576 - 583
Indexed
SCIE
SCOPUS
KCI
Journal Title
JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY
Volume
16
Number
4
Start Page
576
End Page
583
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/123144
ISSN
1017-7825
Abstract
The alkali-soluble glucan of the yeast cell wall contains and (1,6)-D-linkages and is known to systemically enhance the immune system. In the previous study [6], in order to isolate cell wall mutants, a wild-type strain was mutagenized by exposure to ultraviolet light, and the mutants were then selected via treatment with laminarinase (endo-beta-(1,3)-D-glucanase). The mass of alkali- and water-soluble glucans produced by the mutant was measured to be 33.8 mg/g of the dry mass of the yeast cell. Our results showed that the mutants generated the amount of alkali-soluble glucan 10-fold higher than that generated by the wildtype. Structural analysis showed that the alkali-soluble glucan from the mutants was associated with a higher degree of beta(1,6)-D-linkage than was observed in conjunction with the wild-type. Yeast cell wall P-glucan was shown to interact with macrophages via receptors, thereby inducing the release of tumor necrosis factor alpha (TNF-alpha) and nitric oxide. Alkali-soluble beta-glucans, both from water-soluble and water-insoluble glucan, exhibited a higher degree of macrophage activity with regard to both the secretion Of tumor necrosis factor alpha (TNF-alpha) and nitric oxide and direct phagocytosis, than did the positive control(1 mu g of lipopolysaccharide).
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