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Study of ecosystem assessment for oxidative damaged base by oxidative radical reaction

Research Project

Project/Area Number 16K12607
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Environmental impact assessment
Research InstitutionIbaraki University

Principal Investigator

KURUSU Yasurou  茨城大学, 農学部, 教授 (60272118)

Project Period (FY) 2016-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2018: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2017: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywords酸化損傷塩基 / 酸化ラジカル反応 / 自然突然変異 / 酸化ラジカル / DNA修復
Outline of Final Research Achievements

One of the most lesions in DNA caused by reactive oxygen species (ROS) is the oxidized base 7,8-dihydro-8-oxoguanine (8-oxoG). The product of three of the Escherichia coli mut genes, mutM, mutY, and mutT, are devoted exclusively to preventing mutations due to 8-oxoG and are important components of the defense against this type of oxidative damage. However, other bacteria for DNA repair systems to prevent 8-oxoG such as MutT are unclear. Here, we used some strains, such as an Bacillus subtilis, Lactobacillus reuteri, Pseudoalteromonas sp from deep sea, Synechocystis sp. PCC6803, and E. coli as a control. We measured the amount of 8-oxoG in chromosomal DNA. Also, cells highly accumulated 8-oxoG in DNA at low temperature than at appropriate temperature in all of bacteria. These results indicated that accumulation of 8-oxoG by ROS is highly active in exponential growth and at low temperature and prevention of DNA mutation by 8-oxoG are due to MutY and MutM rather than MutT.

Academic Significance and Societal Importance of the Research Achievements

これまで、生物進化の原動力は、ウィルス、トランスポゾン、プラスミド等による遺伝子の水平伝搬、すなわち外的要因を中心に研究されてきた。本研究は、細胞内酸化ラジカル反応により生成する酸化損傷塩基8OHdGを細胞内変異原、すなわち内的要因として位置付け、8-OHdGを生物進化の新たな指標として、そのポテンシャルを評価する点に意義がある。

Report

(5 results)
  • 2018 Annual Research Report   Final Research Report ( PDF )
  • 2017 Research-status Report
  • 2016 Research-status Report
  • Products Report
  • Research Products

    (10 results)

All 2022 2020 2019 2018 2017 2016

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Open Access: 1 results) Presentation (9 results) (of which Int'l Joint Research: 2 results)

  • [Journal Article] Complete genome sequence of a psychrophilic bacterium, Pseudoal teromonas sp. strain APM04, isolated from the seafloor of the South Mariana Trough, Pacific Ocean2022

    • Author(s)
      Mahoko Taguchi, Yong Guo, Tomoyasu Nishizawa, Shigeru Chohnan, Yasurou Kurusu
    • Journal Title

      Microbiology Resource Announcements

      Volume: 11 Issue: 8

    • DOI

      10.1128/mra.00374-22

    • Related Report
      Products Report
    • Peer Reviewed / Open Access
  • [Presentation] 深海微生物のゲノム進化に関する解析2020

    • Author(s)
      田口 真秀子、久留主 泰朗
    • Organizer
      第93回日本生化学会大会
    • Related Report
      Products Report
  • [Presentation] 地球環境の変遷に伴う細胞内変異原の生物進化への影響2019

    • Author(s)
      和田浩樹 久留主泰朗
    • Organizer
      ブルーアースサイエンステク2019
    • Related Report
      2018 Annual Research Report
  • [Presentation] Characterization and Diversity of Mutts That Degrade Oxidative Damaged Nucleotide, 8-oxo-dGTP, in Various Bacteria2019

    • Author(s)
      Yasurou Kurusu, Hiroki Wada
    • Organizer
      asm microbe 2019
    • Related Report
      2018 Annual Research Report
    • Int'l Joint Research
  • [Presentation] Genomic analysis of psychrotrophic bacterium Pseudoalteromonas sp. PS1M32019

    • Author(s)
      Yoshihito Nikaidou, Akihiko Maruyama, Yasurou Kurusu
    • Organizer
      12th International Marine Biotechnology Conference
    • Related Report
      2018 Annual Research Report
    • Int'l Joint Research
  • [Presentation] 細菌ゲノムDNA中における酸化損傷塩基8-oxo-dGの生成と抑制について2018

    • Author(s)
      二階堂惟人、久留主泰朗
    • Organizer
      第16回微生物研究会
    • Related Report
      2017 Research-status Report
  • [Presentation] 細菌における酸化損傷塩基分解遺伝子mutTの機能解析2018

    • Author(s)
      和田浩樹、久留主泰朗
    • Organizer
      第16回微生物研究会
    • Related Report
      2017 Research-status Report
  • [Presentation] 大腸菌dksA変異株におけるプラスミド複製と安定分配の解析2017

    • Author(s)
      中内瑛巴 大山加奈絵 久留主泰朗
    • Organizer
      第11回日本ゲノム微生物学会
    • Place of Presentation
      慶応大学湘南藤沢キャンパス
    • Year and Date
      2017-03-02
    • Related Report
      2016 Research-status Report
  • [Presentation] 大腸菌の低温培養時における酸化損傷塩基のゲノム内蓄積について2016

    • Author(s)
      宮城隆太 久留主泰朗
    • Organizer
      第15回微生物研究会
    • Place of Presentation
      日本大学湘南キャンパス
    • Related Report
      2016 Research-status Report
  • [Presentation] 大腸菌dksA変異株内におけるプラスミドのコピー数について2016

    • Author(s)
      中内瑛巴 大山加奈絵 久留主泰朗
    • Organizer
      第15回微生物研究会
    • Place of Presentation
      日本大学湘南キャンパス
    • Related Report
      2016 Research-status Report

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Published: 2016-04-21   Modified: 2023-03-30  

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