Antifungal activity and expression patterns of extracellular chitinase and β-1, 3-glucanase in Wickerhamomyces anomalus EG2 treated with chitin and glucan. (September 2017)
- Record Type:
- Journal Article
- Title:
- Antifungal activity and expression patterns of extracellular chitinase and β-1, 3-glucanase in Wickerhamomyces anomalus EG2 treated with chitin and glucan. (September 2017)
- Main Title:
- Antifungal activity and expression patterns of extracellular chitinase and β-1, 3-glucanase in Wickerhamomyces anomalus EG2 treated with chitin and glucan
- Authors:
- Hong, Sin-Hyoung
Song, Yong-Su
Seo, Dong-Jun
Kim, Kil-Yong
Jung, Woo-Jin - Abstract:
- Abstract: In this study, the expression patterns of extracellular chitinase and β-1, 3-glucanase from cultured Wickerhamomyces anomalus EG2 treated with chitin, glucan, and chemical chitinase inhibitors (kinetin, caffeine, and acetazolamide) were investigated using SDS-PAGE. Relationship between enzyme expression and antifungal activity from yeast plays a very important role for biocontrol of phytopathoges. To determine antifungal activity against phytopathogens, W. anomalus EG2 was shown to strongly inhibit hyphal growth of Fusarium oxysporum KACC 40032 and Rhizoctonia solani KACC 40111. Slight chitinase activity was observed 12 h after incubation in both PDB and YPD medium without colloidal chitin. The molecular weight of chitinase was approximately 124 kDa β-1, 3-Glucanase isoenzyme (GN1 and GN2) was observed distinctly on SDS-PAGE gels when laminarin was used as a substrate. β-1, 3-Glucanase isoenzyme was not observed when using glucan-containing high polymer complex (GHPC) as a substrate. Production of chitinase from W. anomalus EG2 was inhibited slightly by acetazolamide. Abnormal and cluster-shaped cells of W. anomalus EG2 were observed in both PDB and YPD medium treated with colloidal chitin. These results indicated that W. anomalus EG2 could be applied commercially as a biological control agent of phytopathogens and as a bioinhibitor of yeast cell growth. Highlights: W. anomalus EG2 was shown to strongly inhibit hyphal growth of F. oxysporum and R. solani .Abstract: In this study, the expression patterns of extracellular chitinase and β-1, 3-glucanase from cultured Wickerhamomyces anomalus EG2 treated with chitin, glucan, and chemical chitinase inhibitors (kinetin, caffeine, and acetazolamide) were investigated using SDS-PAGE. Relationship between enzyme expression and antifungal activity from yeast plays a very important role for biocontrol of phytopathoges. To determine antifungal activity against phytopathogens, W. anomalus EG2 was shown to strongly inhibit hyphal growth of Fusarium oxysporum KACC 40032 and Rhizoctonia solani KACC 40111. Slight chitinase activity was observed 12 h after incubation in both PDB and YPD medium without colloidal chitin. The molecular weight of chitinase was approximately 124 kDa β-1, 3-Glucanase isoenzyme (GN1 and GN2) was observed distinctly on SDS-PAGE gels when laminarin was used as a substrate. β-1, 3-Glucanase isoenzyme was not observed when using glucan-containing high polymer complex (GHPC) as a substrate. Production of chitinase from W. anomalus EG2 was inhibited slightly by acetazolamide. Abnormal and cluster-shaped cells of W. anomalus EG2 were observed in both PDB and YPD medium treated with colloidal chitin. These results indicated that W. anomalus EG2 could be applied commercially as a biological control agent of phytopathogens and as a bioinhibitor of yeast cell growth. Highlights: W. anomalus EG2 was shown to strongly inhibit hyphal growth of F. oxysporum and R. solani . Production of chitinase from W. anomalus EG2 was inhibited slightly by acetazolamide. The molecular weight of chitinase was approximately 124 kDa. Abnormal and cluster-shaped cells of W. anomalus EG2 were observed in both PDB and YPD medium treated with colloidal chitin. … (more)
- Is Part Of:
- Microbial pathogenesis. Volume 110(2017)
- Journal:
- Microbial pathogenesis
- Issue:
- Volume 110(2017)
- Issue Display:
- Volume 110, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 110
- Issue:
- 2017
- Issue Sort Value:
- 2017-0110-2017-0000
- Page Start:
- 159
- Page End:
- 164
- Publication Date:
- 2017-09
- Subjects:
- Wickerhamomyces anomalus EG2 -- Chitinase -- β-1, 3-Glucanase -- Chitinase inhibitors -- Antifungal activity
Pathogenic microorganisms -- Periodicals
Pathology, Molecular -- Periodicals
Communicable Diseases -- microbiology -- Periodicals
Communicable Diseases -- parasitology -- Periodicals
Micro-organismes pathogènes -- Périodiques
Pathologie moléculaire -- Périodiques
Electronic journals
616.9041 - Journal URLs:
- http://www.sciencedirect.com/science/journal/08824010 ↗
http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=0882-4010;screen=info;ECOIP ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.micpath.2017.06.038 ↗
- Languages:
- English
- ISSNs:
- 0882-4010
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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