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Structure type: oligomer
Trivial name: avenacin B-1
Compound class: glycoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_983931,SB_192

• Article ID: 12767
  Trojanowska MR, Osbourn AE, Daniels MJ, Threlfall DR "Biosynthesis of avenacins and phytosterols in roots of Avena sativa cv. Image" - Phytochemistry 54(2) (2000) 153-164
  

  In keeping with the proposal that avenacin biosynthesis is restricted to the tips of primary roots of oat seedlings, the incorporation of radioactivity from R-[2-]mevalonic acid (MVA) into avenacins and β-amyrin by serial sections of primary roots was found to be more-or-less restricted to root tip sections. Squalene synthase (SQS) (EC 2.5.1.21) and 2,3-oxidosqualene:β-amyrin cyclase (OSβAC) (EC 5.4.99) were also most active in these sections. The incorporation of radiolabel from R-[2-]MVA into cycloartenol and 24-methylene cycloartanol by, and the 2,3-oxidosqualene:cycloartenol cyclase (OSCC) (EC 5.4.99) activity in, the various serial sections were consistent with phytosterol biosynthesis occurring in all the sections of the root with some tailing-off in the rate of synthesis in the more distal sections.

  Avena sativa; Poaceae; biosynthesis; saponins; avenacins; phytosterols

  NCBI PubMed ID: 10872206
  Publication DOI: 10.1016/s0031-9422(00)00062-5
  Journal NLM ID: 0151434
  Publisher: Elsevier
  Correspondence: miranda.trojanowska@bbsrc.ac.uk
  Institutions: Department of Biological Sciences, University of Hull, Hull, UK, The Sainsbury Laboratory, Norwich Research Park, Colney, UK
  Methods: TLC, radiolabeling, radioactivity measurement, HPLC, extraction, CC
  
   
  
  Avena sativa cv. Image
  CSDB ID 68238 (all data & tools)

Show legend Show as text

Structure type: oligomer
Trivial name: avenacin B-2
Compound class: glycoside
Contained glycoepitopes: IEDB_139965,IEDB_142488,IEDB_146664,IEDB_983931,SB_192

• Article ID: 12767
  Trojanowska MR, Osbourn AE, Daniels MJ, Threlfall DR "Biosynthesis of avenacins and phytosterols in roots of Avena sativa cv. Image" - Phytochemistry 54(2) (2000) 153-164
  

  In keeping with the proposal that avenacin biosynthesis is restricted to the tips of primary roots of oat seedlings, the incorporation of radioactivity from R-[2-]mevalonic acid (MVA) into avenacins and β-amyrin by serial sections of primary roots was found to be more-or-less restricted to root tip sections. Squalene synthase (SQS) (EC 2.5.1.21) and 2,3-oxidosqualene:β-amyrin cyclase (OSβAC) (EC 5.4.99) were also most active in these sections. The incorporation of radiolabel from R-[2-]MVA into cycloartenol and 24-methylene cycloartanol by, and the 2,3-oxidosqualene:cycloartenol cyclase (OSCC) (EC 5.4.99) activity in, the various serial sections were consistent with phytosterol biosynthesis occurring in all the sections of the root with some tailing-off in the rate of synthesis in the more distal sections.

  Avena sativa; Poaceae; biosynthesis; saponins; avenacins; phytosterols

  NCBI PubMed ID: 10872206
  Publication DOI: 10.1016/s0031-9422(00)00062-5
  Journal NLM ID: 0151434
  Publisher: Elsevier
  Correspondence: miranda.trojanowska@bbsrc.ac.uk
  Institutions: Department of Biological Sciences, University of Hull, Hull, UK, The Sainsbury Laboratory, Norwich Research Park, Colney, UK
  Methods: TLC, radiolabeling, radioactivity measurement, HPLC, extraction, CC
  
   
  
  Avena sativa cv. Image
  CSDB ID 68239 (all data & tools)