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Breeding of yeast which ferments directly cellulose

Research Project

Project/Area Number 11460049
Research Category

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

Allocation TypeSingle-year Grants
Section一般
Research Field 応用微生物学・応用生物化学
Research InstitutionOsaka Prefecture University

Principal Investigator

ARAI Motoo  Graduate School of Agricultur and Biological Sciences, Osaka Prefecture University Professor, 農学生命科学研究科, 教授 (80081537)

Co-Investigator(Kenkyū-buntansha) KAWAGUCHI Takashi  The sama as above, Associate Professor, 農学生命科学研究科, 助教授 (70195056)
Project Period (FY) 1999 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥9,200,000 (Direct Cost: ¥9,200,000)
Fiscal Year 2000: ¥2,700,000 (Direct Cost: ¥2,700,000)
Fiscal Year 1999: ¥6,500,000 (Direct Cost: ¥6,500,000)
Keywordscellulose / cellulase / gene / cloning / expression / セルロース / セルラーゼ / キシラナーゼ / マンノシダーゼ / 遺伝子 / 糸状菌 / バイオマス
Research Abstract

For utilization of biomass cellulosic substances are important because they are dominant organic substances on the earth. Cellulases consist of complex system and they hydrolyze cellulosic substances synergistically. We isolated Aspergillus aculeatus which shows synergism with Trichoderma cellulase. When the cellulase from Aspergillus aculeatus was mixed with Trichoderma cellulase, enzyme showed potent synergisty and hydrolyzed completely cellulosic substances. The research elucidated essential cellulase components. The enzyme genes were cloned and then these genes were introduced into yeast cells. Finally, we can expected the yeast which produced ethanol directly from cellulose.
The genes of 1 β-glucosidase, 2 Avicelases, 2 CM-cellulases, β-mannosidase, 1 xylanase were cloned. These genes were expressed in yeast cells. β-mannosidase gene was introduced into Aspergillus. The enzyme production improved in fungal cells.

Report

(3 results)
  • 2000 Annual Research Report   Final Research Report Summary
  • 1999 Annual Research Report
  • Research Products

    (8 results)

All Other

All Publications (8 results)

  • [Publications] G.Takada et al: "Cloning and Sequencing of β-Mannosidase Gene from Asp. aculeatus No.F.50"Biosci.Biotechnol.Biochem.. 63. 206-209 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] A.Ohnishi et al: "Analysis of a catalytic Acidic Pair in the Active Center of Cellulase from Asp.aculeatus"Biosci.Biotechnol.Biochem.. 63. 2157-2162 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] G.Takada et al.: "Cloning and Sequencing of β-Mannosidase Gene from Asp.aculeatus No.F-50"Biosci.Biotechnol.Biochem.. 63. 206-209 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] A.Ohnishi et al.: "Analysis of a Catalytic Acidic Pair in the Active Center of Cellulase from Asp.aculeatus"Biosci.Biotechnol.Biochem.. 63. 2157-2162

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] G.Takada et al: "Cloning and sequencing β-Mannosidase Gene from Asp.aculeatas No.F50"Biosci.Biotechnol.Biochem.. 63. 206-209 (1999)

    • Related Report
      2000 Annual Research Report
  • [Publications] A.Ohnishi et al: "Analysis of a Catalytic Acidic Pair in the Active Center of Cellulase from Asp.aculeatas"Biosci.Biotechnol.Biochem.. 63. 2157-2162 (1999)

    • Related Report
      2000 Annual Research Report
  • [Publications] A. Ohnishi, et al.: "Analysis of a catalytic acidic pair in the active center of cellulase from Aspergillus aculeatus"Bioscience, Biotechnology, and Biochemistry. 63(12). 2157-2162 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] T. Ooi, et. al.: "Analysis of 5'-upstream non-coding region of FI-carboxy methyl cellulase from Aspergillus aculeatus"Biotechnol. Lett.. 21. 735-739 (1999)

    • Related Report
      1999 Annual Research Report

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Published: 1999-04-01   Modified: 2016-04-21  

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