Literature DB >> 12240387

Assembling the biosynthetic puzzle of crucifer metabolites: indole-3-acetaldoxime is incorporated efficiently into phytoalexins but glucobrassicin is not.

M S Pedras1, S Montaut, Y Xu, A Q Khan, A Loukaci.   

Abstract

First biosynthetic studies utilizing tetradeuterated precursors indicate that the indole glucosinolate glucobrassicin is not a precursor of the phytoalexin brassinin, and that indole-3-acetaldoxime is an efficient precursor.

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Year:  2001        PMID： 12240387     DOI： 10.1039/b103442c

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  3 in total

1.  CYP83A1 and CYP83B1, two nonredundant cytochrome P450 enzymes metabolizing oximes in the biosynthesis of glucosinolates in Arabidopsis.

Authors:  Peter Naur; Bent Larsen Petersen; Michael Dalgaard Mikkelsen; Søren Bak; Hasse Rasmussen; Carl Erik Olsen; Barbara Ann Halkier
Journal:  Plant Physiol       Date:  2003-09       Impact factor: 8.340

2.  Camalexin is synthesized from indole-3-acetaldoxime, a key branching point between primary and secondary metabolism in Arabidopsis.

Authors:  Erich Glawischnig; Bjarne Gram Hansen; Carl Erik Olsen; Barbara Ann Halkier
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-17       Impact factor: 11.205

3.  Cell wall composition and penetration resistance against the fungal pathogen Colletotrichum higginsianum are affected by impaired starch turnover in Arabidopsis mutants.

Authors:  Timo Engelsdorf; Cornelia Will; Jörg Hofmann; Christine Schmitt; Brian B Merritt; Leonie Rieger; Marc S Frenger; André Marschall; Rochus B Franke; Sivakumar Pattathil; Lars M Voll
Journal:  J Exp Bot       Date:  2017-01-01       Impact factor: 6.992
  3 in total

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