| Project/Area Number |
06453171
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| Research Category |
Grant-in-Aid for General Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Research Field |
Bioproduction chemistry/Bioorganic chemistry
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| Research Institution | The University of Tokyo |
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Principal Investigator |
YAMAZAKI Sunao Univ.of Tokyo, Fac.Agriculture, 農学部, 教授 (00011982)
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| Co-Investigator(Kenkyū-buntansha) |
YOSHIMURA Etsuro Univ.of Tokyo, Fac.Agric., 農学部, 助教授 (10130303)
OKUBO Akira Univ.of Tokyo, Fac.Agric., 農学部, 助教授 (20111479)
SATOH Toshio Univ.of Hiroshima, Fac.Sci., 理学部, 教授 (90087130)
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| Project Period (FY) |
1994 – 1995
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| Project Status |
Completed (Fiscal Year 1995)
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| Budget Amount *help |
¥8,200,000 (Direct Cost: ¥8,200,000)
Fiscal Year 1995: ¥2,800,000 (Direct Cost: ¥2,800,000)
Fiscal Year 1994: ¥5,400,000 (Direct Cost: ¥5,400,000)
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| Keywords | denitrifier / molybdenum / metalloenzyme / DMSO respiration / respiration enzyme / DMSO reductase / electron transfer / Rhodobacter sphaeroides / Rhodobacter Sphaeroides |
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| Research Abstract |
Dimethyl sulfoxide (DMSO) respiration is known to support the cell growth of many bacteria under unaerobic conditions. The terminal enzyme of the DMSO respiration, DMSO reeducates, was studied. The gene enconding DMSO reductase, which contains a molybdenum cofactor, of the photosynthetic bacterium Rhodobacter sphaeroides f.sp.denitirficans was isolated using an oligonucleotide probe, which was synthsized based on an internal amino acid sequence of the purified enzyme. The DMSO reductase gene coded 822 amino acids (2466 base pairs, Mw 89,206) as a precursor form having a signal peptide of 42 amino acids. The deduced amino acid sequence had high homology with those of some enzymes containing a molybdenum cofactor : trimethyl amine N-oxide reductase (48%), biotin sulfoxide reductase (44%), and DMSO reductase (29%) of Escherichia coli.
DMSO reductase has a broad substrate specificity. It assimilates not only DMSO but also TMAO,methionine sulfoxide, biotin sulfoxide and other synthetic alkyl aryl sulfoxides. It has extremely high stereospecificity in reduction of S-form and R-form was obtained in a optically-pure form. Stereo-selective conversion by this enzyme was of great use for organic synthesis.
Global emission of dimethyl sulfide (DMS) from aquatic environmentis recentlyrevealed to be related with biological activity of reduction of sulfur compounds. Presence of DMSO and its reducing enzymes and emission of DMS in hydrosphere should be clarified further to understand the biological contribution to environment.
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