Immune-enhancing alkali-soluble glucans produced by wild-type and mutant Saccharomyces cerevisiae
- Authors
- Ha, CH; Lim, KH; Jang, SH; Yun, CW; Paw, HD; Kim, SW; Kang, CW; Chang, HI
- Issue Date
- 4월-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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Collections - College of Life Sciences and Biotechnology > Division of Life Sciences > 1. Journal Articles
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