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2015 Fiscal Year Final Research Report

Synthetic mechanism and physiological role of nitric oxidce in yeasts

Research Project

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Project/Area Number 25252065
Research Category

Grant-in-Aid for Scientific Research (A)

Allocation TypeSingle-year Grants
Section一般
Research Field Applied molecular and cellular biology
Research InstitutionNara Institute of Science and Technology

Principal Investigator

Takagi Hiroshi  奈良先端科学技術大学院大学, バイオサイエンス研究科, 教授 (50275088)

Co-Investigator(Kenkyū-buntansha) KAWAMOTO Susumu  千葉大学, 真菌医学研究センター, 教授 (80125921)
CHIBANA Hiroji  千葉大学, 真菌医学研究センター, 准教授 (30333488)
Research Collaborator WATANABE Daisuke  
NASUNO Ryo  
Project Period (FY) 2013-10-21 – 2016-03-31
Keywords酵母 / 一酸化窒素 / 酸化ストレス / シグナル伝達 / 病原真菌
Outline of Final Research Achievements

The flavoprotein Tah18 is involved in NO synthase (NOS)-like activity and Tah18-dependent NO synthesis confers high-temperature stress tolerance on the budding yeast Saccharomyces cerevisiae. We showed that NOS-like activity requiring Tah18 induced cell death upon treatment with H2O2. Our findings indicate that the Tah18-Dre2 complex regulates cell death as a molecular switch via Tah18-dependent NOS-like activity in response to oxidative stresses. We also studied the antioxidative mechanism by NO. NO increased the transcription of the CTR1 gene encoding copper transporter, the intracellular copper content, the activity of superoxide dismutase Sod1, and the cell viability in a manner dependent on Mac1. Thus, Tah18-dependent NO synthesis exhibits dual effects, cell protection and death, in yeast. Our results also suggest that NO is involved in the growth, infection and pathogenicity of the pathogenic yeasts and fungi, Candida glabrata, Cryptococcus neoformans and Aspergillus fumigatus.

Free Research Field

応用微生物学

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Published: 2017-05-10  

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