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Functional expression and utilization of bacterial cytochrome C__-

Research Project

Project/Area Number 03556010
Research Category

Grant-in-Aid for Developmental Scientific Research (B)

Allocation TypeSingle-year Grants
Research Field 応用微生物学・発酵学
Research InstitutionThe University of Tokyo

Principal Investigator

KODAMA Tohru  The university of Tokyo, Department of Agriculture, Professor, 農学部, 教授 (30011901)

Co-Investigator(Kenkyū-buntansha) SHIBANO Yuzi  Suntory, Institute for fundamental research, Head manager, 基礎研究所微生物科学研究室, 室長
MIYAWAKI Osato  The university of Tokyo Department of Agriculture, Associate professor, 農学部, 助教授 (80012053)
天知 輝夫  サントリー(株), 基礎研究所, 所長
Project Period (FY) 1991 – 1992
Project Status Completed (Fiscal Year 1992)
Budget Amount *help
¥15,800,000 (Direct Cost: ¥15,800,000)
Fiscal Year 1992: ¥3,900,000 (Direct Cost: ¥3,900,000)
Fiscal Year 1991: ¥11,900,000 (Direct Cost: ¥11,900,000)
Keywordscytochrome C__- / electro chemistry / シトロクロムC / 電気化学反応
Research Abstract

Cytochrome c__-_<552> gene was cloned from the total DNA of the cells of Hydrogen obacter thermophilus. The gene was shown to contain a signal sequence. As a next step, the gene without the signal sequence was prepared. When Escherichia coli was transformed with the plasmid containing this gene and was cultivated under nitrate respiration, it produced cytochrome c__-_<552> within cytoplasm fraction.
Cytochrome c__-_<551> gene was also cloned from the total DNA of the cells of Pseudomonas aeruginosa. When Pseudomonas aeruginosa was transformed with the plasmid containig this gene, it produced cytochrome c__-_<551> within periplasm fraction. The production rate was as high as 0.7 % of the total protein of the cell-free extract. An attempt was made to produce cytochrome c__-_<551> by using the other microorganisms (Escherichia coli or Pseudomonas putida), however, successful production could not be obtained.
Reactivity of the two proteins (cytochrome c__-_<552> and cytochrome c__-_<551>) toward electrode was also investigated. Both cytochromes were shown to react with Pt-electrode in a solution state. Cytochrome c__-_<552> protein could react with Au-electrode in the presence of promotor, however, in its absence reactivity was not observed.

Report

(3 results)
  • 1992 Annual Research Report   Final Research Report Summary
  • 1991 Annual Research Report
  • Research Products

    (3 results)

All Other

All Publications (3 results)

  • [Publications] Hiroyuki ARAI: "Nitrite activates the transcription of the Pseudomonas aeruginosa nitrite reductase and cytochrome C_<551> under anaerobic conditions" FEBS Letters. 288. 227-228 (1991)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] Hiroyuki Arai: "Nitrite actives the transcription of the Pseudomonas aeruginosa nitrite reductase and cytochrome c__-_<551> under anaerobic conditions" FEBS Letters. 288. 227-228 (1991)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] Arai,H.et al.: "Anaerobically Induced Expression of the Nitrite Reductase Cytochrome c-551 Operon from Pseudomonas aeruginosa" FEBS Letters. 280. 351-353 (1991)

    • Related Report
      1991 Annual Research Report

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Published: 1991-04-01   Modified: 2016-04-21  

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