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Biosynthesis of pectin, a plant cell wall polysaccharide

Research Project

Project/Area Number 12640627
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field 植物生理
Research InstitutionSaitama University

Principal Investigator

TSUMURAYA Yoichi  Saitama University, Faculty of Science, Professor, 理学部, 教授 (10142233)

Project Period (FY) 2000 – 2002
Project Status Completed (Fiscal Year 2002)
Budget Amount *help
¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 2002: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 2001: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 2000: ¥1,100,000 (Direct Cost: ¥1,100,000)
Keywordscell wall / pectin / galactoronic acid / galacturonosyltransferase
Research Abstract

Pectins are plant cell wall polysaccharides consisting mainly of contiguous unbranched (1→4)-linked α-galacturonic acid (GalA) residues, and participate in various physiological functions including regulation of cell strength, wall porocity, and intercellular adhesion and communication. A membrane preparation of 7-d-old seedlings from azuki bean (Vigna angularis) contained galacturonosyltransferase (GTase) capable of transferring [^<14>C] GalA from UDP-[^<14>C]GalA into polygalacturonic acid (polyGalA) as an exogenous acceptor. The enzyme was maximally active at pH 6.8-7.5 and 25-35℃ in the presence of 5 mM Mn^<2÷> and 0.5% (w/v) TritonX-100. Acid-soluble low-M_r (average M_r 10,000) polyGalA was a more efficient acceptor substrate than acid-insoluble polymer (M_r 70,000). The apparent Michaelis constants for UDP-GalA and low-M_r polyGalA were 0.11 mM and 0.02 mg/ml, respectively. Various pectins with different degrees of methyl-esterification (DE) were poor acceptors, and the enzyme activity tended to decrease with decreasing DE of the pectins. The transfer products from incubation of the enzyme with UDP-[^<14>C]GalA and the low-M_r polyGalA yielded [^<14>C]GalA_2 as the major product upon digestion with an endopolygalacturonase, confirming the incorporation of GalA into polyGalA through contiguous α-1,4-linkages.

Report

(4 results)
  • 2002 Annual Research Report   Final Research Report Summary
  • 2001 Annual Research Report
  • 2000 Annual Research Report
  • Research Products

    (5 results)

All Other

All Publications (5 results)

  • [Publications] Y.Takeuchi: "In vitro biosynthesis of homogalacturona by a membrane-bound galacturonosyl transferase from epicotyls of azuki bean"Bioscience, Biotechnology, and Biochemistry. 65. 1519-1527 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Y.Takeuchi: "In vitro biosynthesis of homogalacturonan by a membrane-bound galacturonosyltransferase from epilotyls of azuki bean"Bioscience, Biotechnology and Biochemistry. 65, No.7. 1519-1527 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] T.Takeuchi: "In vitro biosynthesis of homogalacturonan by a membrane-bound galacturonosyltransterase from epilotyls of azuki bean"Bioscience, Biotechnology, and Biochemistry. 65(7). 1519-1527 (2001)

    • Related Report
      2002 Annual Research Report
  • [Publications] Y.Takeuchi: "<Invitro>___-biosynthesis of homogalacturonan by a membrane-bound galacturonosyltransterase from epicotyls of azuki bean"Bioscience,Biotechnology,and Biochemistry. 65(7). 1519-1527 (2001)

    • Related Report
      2001 Annual Research Report
  • [Publications] Y.Takeuchi: "In vitro biosynthesis of homogalacturonan by a membrane-bound galacturonosyltrans-ferase from epicotyls of azuki bean"Bioscience, Biotechnology, and Biochemistry. (印刷中).

    • Related Report
      2000 Annual Research Report

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Published: 2000-04-01   Modified: 2016-04-21  

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