Downregulation of fungal cytochrome c peroxidase expression by antifungal quinonemethide triterpenoidsopen access
- Authors
- Seo, W.-D.; Lee, D.-Y.; Park, K.H.; Kim, J.-H.
- Issue Date
- 2016
- Publisher
- Korean Society for Applied Biological Chemistry
- Keywords
- Anti-fungal; Antioxidant; Cytochrome c peroxidase; Quinonemethide triterpenoid
- Citation
- Journal of Applied Biological Chemistry, v.59, no.4, pp 281 - 284
- Pages
- 4
- Indexed
- SCOPUS
KCI
- Journal Title
- Journal of Applied Biological Chemistry
- Volume
- 59
- Number
- 4
- Start Page
- 281
- End Page
- 284
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/16764
- DOI
- 10.3839/jabc.2016.048
- ISSN
- 1976-0442
2234-7941
- Abstract
- To handle the development of antifungal drug resistance, the development of new structural modules and new modes of action for antifungals have been highlighted recently. Here, the antifungal activity of quinonemethidal triterpenoids such as celastrol, dihydrocelastrol, iguestein, pristimerin, and tingenone isolated from Tripterygium regelii were identified (MIC 0.269-19.02 ?M). C. glabrata was the most susceptible to quinonemethide among the tested fungi. Furthermore, quinonemethide suppressed cyctochrome c peroxidase expression dramatically, decreasing fungal viability caused by the accumulation of hydrogen peroxide. Thus, cyctochrome c peroxidase downregulation of quinonemethide may be a key mode of action for antifungals. ? The Korean Society for Applied Biological Chemistry 2016.
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Collections - 농업생명과학대학 > 환경생명화학과 > Journal Articles

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