Literature DB >> 10680168

Phytoalexins from crucifers: synthesis, biosynthesis, and biotransformation.

M S Pedras1, F I Okanga, I L Zaharia, A Q Khan.   

Abstract

Phytoalexins play a significant role in the defense response of plants. These secondary metabolites, which are synthesized de novo in response to diverse forms of stress, including fungal infection, are part of the plants' chemical and biochemical defense mechanisms. Phytoalexins from crucifers are structurally and biogenetically related, but display significantly different biological activities. Here, we review work reporting the chemical structures, synthesis, biosynthesis and metabolism of cruciferous phytoalexins, as well as their biological activity towards different microorganisms.

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Year:  2000        PMID: 10680168     DOI: 10.1016/s0031-9422(99)00494-x

Source DB:  PubMed          Journal:  Phytochemistry        ISSN: 0031-9422            Impact factor:   4.072


  19 in total

1.  The Biosynthetic Pathways for Shikimate and Aromatic Amino Acids in Arabidopsis thaliana.

Authors:  Vered Tzin; Gad Galili
Journal:  Arabidopsis Book       Date:  2010-05-17

Review 2.  Tropospheric ozone as a fungal elicitor.

Authors:  Paolo Zuccarini
Journal:  J Biosci       Date:  2009-03       Impact factor: 1.826

3.  The multifunctional enzyme CYP71B15 (PHYTOALEXIN DEFICIENT3) converts cysteine-indole-3-acetonitrile to camalexin in the indole-3-acetonitrile metabolic network of Arabidopsis thaliana.

Authors:  Christoph Böttcher; Lore Westphal; Constanze Schmotz; Elke Prade; Dierk Scheel; Erich Glawischnig
Journal:  Plant Cell       Date:  2009-06-30       Impact factor: 11.277

4.  Palladium-Catalyzed Chemoselective Activation of sp3 vs sp2 C-H Bonds: Oxidative Coupling To Form Quaternary Centers.

Authors:  Gang Hong; Pradip D Nahide; Uday Kumar Neelam; Peter Amadeo; Arjun Vijeta; John M Curto; Charles E Hendrick; Kelsey F VanGelder; Marisa C Kozlowski
Journal:  ACS Catal       Date:  2019-03-08       Impact factor: 13.084

Review 5.  New insight into the biosynthesis and regulation of indole compounds in Arabidopsis thaliana.

Authors:  Bjarne Gram Hansen; Barbara Ann Halkier
Journal:  Planta       Date:  2005-06-02       Impact factor: 4.116

6.  Structure-activity study of brassinin derivatives as indoleamine 2,3-dioxygenase inhibitors.

Authors:  Paul Gaspari; Tinku Banerjee; William P Malachowski; Alexander J Muller; George C Prendergast; James DuHadaway; Shauna Bennett; Ashley M Donovan
Journal:  J Med Chem       Date:  2006-01-26       Impact factor: 7.446

7.  Phytotoxin production and phytoalexin elicitation by the phytopathogenic fungus Sclerotinia sclerotiorum.

Authors:  M Soledade C Pedras; Pearson W K Ahiahonu
Journal:  J Chem Ecol       Date:  2004-11       Impact factor: 2.626

8.  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

Review 9.  Molecular diversity of spirooxindoles. Synthesis and biological activity.

Authors:  Tetyana L Pavlovska; Ruslan Gr Redkin; Victoria V Lipson; Dmytro V Atamanuk
Journal:  Mol Divers       Date:  2015-09-29       Impact factor: 2.943

10.  In planta sequential hydroxylation and glycosylation of a fungal phytotoxin: Avoiding cell death and overcoming the fungal invader.

Authors:  M S Pedras; I L Zaharia; Y Gai; Y Zhou; D E Ward
Journal:  Proc Natl Acad Sci U S A       Date:  2001-01-09       Impact factor: 11.205

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