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Novel and innovative mechanism of ATP biosynthesis based on the plasmolysis as a proton-driven force in alkalophilic bacteria

Research Project

Project/Area Number 16K14893
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Applied microbiology
Research InstitutionSetsunan University

Principal Investigator

Murata Kousaku  摂南大学, 理工学部, 教授 (90142299)

Co-Investigator(Kenkyū-buntansha) 橋本 渉  京都大学, 農学研究科, 教授 (30273519)
丸山 如江  摂南大学, 理工学部, 助教 (90397563)
Project Period (FY) 2016-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2017: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2016: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Keywords好アルカリ性細菌 / 原形質分離 / ATP合成機構 / プロトン勾配 / 細菌内膜動的構造 / プロトン駆動力 / F0F1ATPase / pHジャンプ / Aeromonas属細菌 / 内膜皺構造 / 細胞膜機能 / 廃グリセロール / アエロモナス属細菌 / 窒素固定細菌 / 有機酸生産
Outline of Final Research Achievements

It has been postulated that alkalophilic bacteria synthesize ATP by the action of membrane-bound F0F1-ATPase, thereby utilizing proton (H+) chemical gradient formed across the cytoplasmic membrane as an energy source. However, in alkaline growth conditions, it seems difficult to accumulate H+ outside the membrane, since H+ is readily converted to H2O through the reaction with OH- present in external milieu at extremely high concentration. We found that the cells of Aeromonas sp. strain L, a Gram negative rod, repeat plasmolysis in accordance with cell growth (i.e. cell division) and postulated the possibility that the physicochemical structures induced during a contraction and expansion of cytoplasmic membrane will prepare place for H+ accumulation and form chemical gradient of H+ across the cell membrane. This physicochemical mechanism for the ATP synthesis will be expected to exclude the unclear hitherto explanation as to the ATP synthesis in alkalophilic bacteria.

Report

(3 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Research-status Report

URL: 

Published: 2016-04-21   Modified: 2019-03-29  

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