Literature DB >> 15063716

Coronalon: a powerful tool in plant stress physiology.

Göde Schüler1, Axel Mithöfer, Ian T Baldwin, Susanne Berger, Jürgen Ebel, Jonathan G Santos, Gabriele Herrmann, Dirk Hölscher, Robert Kramell, Toni M Kutchan, Helmut Maucher, Bernd Schneider, Irene Stenzel, Claus Wasternack, Wilhelm Boland.   

Abstract

Coronalon, a synthetic 6-ethyl indanoyl isoleucine conjugate, has been designed as a highly active mimic of octadecanoid phytohormones that are involved in insect and disease resistance. The spectrum of biological activities that is affected by coronalon was investigated in nine different plant systems specifically responding to jasmonates and/or 12-oxo-phytodienoic acid. In all bioassays analyzed, coronalon demonstrated a general strong activity at low micromolar concentrations. The results obtained showed the induction of (i) defense-related secondary metabolite accumulation in both cell cultures and plant tissues, (ii) specific abiotic and biotic stress-related gene expression, and (iii) root growth retardation. The general activity of coronalon in the induction of plant stress responses together with its simple and efficient synthesis suggests that this compound might serve as a valuable tool in the examination of various aspects in plant stress physiology. Moreover, coronalon might become employed in agriculture to elicit plant resistance against various aggressors.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15063716     DOI: 10.1016/S0014-5793(04)00239-X

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  29 in total

1.  B1-phytoprostanes trigger plant defense and detoxification responses.

Authors:  Christiane Loeffler; Susanne Berger; Alexandre Guy; Thierry Durand; Gerhard Bringmann; Michael Dreyer; Uta von Rad; Jörg Durner; Martin J Mueller
Journal:  Plant Physiol       Date:  2004-12-23       Impact factor: 8.340

2.  Up-regulation of lipoxygenase, phospholipase, and oxylipin-production in the induced chemical defense of the red alga Gracilaria chilensis against epiphytes.

Authors:  Florian Weinberger; Ulrich Lion; Ludovic Delage; Bernard Kloareg; Philippe Potin; Jessica Beltrán; Verónica Flores; Sylvain Faugeron; Juan Correa; Georg Pohnert
Journal:  J Chem Ecol       Date:  2011-06-15       Impact factor: 2.626

3.  Pseudomonas syringae manipulates systemic plant defenses against pathogens and herbivores.

Authors:  Jianping Cui; Adam K Bahrami; Elizabeth G Pringle; Gustavo Hernandez-Guzman; Carol L Bender; Naomi E Pierce; Frederick M Ausubel
Journal:  Proc Natl Acad Sci U S A       Date:  2005-01-18       Impact factor: 11.205

4.  Enhancement of lignan biosynthesis in suspension cultures of Linum nodiflorum by coronalon, indanoyl-isoleucine and methyl jasmonate.

Authors:  Anna Berim; Otmar Spring; Jürgen Conrad; Matthias Maitrejean; Wilhelm Boland; Maike Petersen
Journal:  Planta       Date:  2005-09-01       Impact factor: 4.116

5.  12-hydroxyjasmonic acid glucoside is a COI1-JAZ-independent activator of leaf-closing movement in Samanea saman.

Authors:  Yoko Nakamura; Axel Mithöfer; Erich Kombrink; Wilhelm Boland; Shin Hamamoto; Nobuyuki Uozumi; Kentaro Tohma; Minoru Ueda
Journal:  Plant Physiol       Date:  2011-01-12       Impact factor: 8.340

Review 6.  Chemical and genetic exploration of jasmonate biosynthesis and signaling paths.

Authors:  Erich Kombrink
Journal:  Planta       Date:  2012-07-28       Impact factor: 4.116

7.  Variation of herbivore-induced volatile terpenes among Arabidopsis ecotypes depends on allelic differences and subcellular targeting of two terpene synthases, TPS02 and TPS03.

Authors:  Mengsu Huang; Christian Abel; Reza Sohrabi; Jana Petri; Ina Haupt; John Cosimano; Jonathan Gershenzon; Dorothea Tholl
Journal:  Plant Physiol       Date:  2010-05-12       Impact factor: 8.340

8.  The role of jasmonates in floral nectar secretion.

Authors:  Venkatesan Radhika; Christian Kost; Wilhelm Boland; Martin Heil
Journal:  PLoS One       Date:  2010-02-19       Impact factor: 3.240

9.  A type III polyketide synthase from Wachendorfia thyrsiflora and its role in diarylheptanoid and phenylphenalenone biosynthesis.

Authors:  S Brand; D Hölscher; A Schierhorn; A Svatos; J Schröder; B Schneider
Journal:  Planta       Date:  2006-02-16       Impact factor: 4.116

10.  Synthesis of 6-substituted 1-oxoindanoyl isoleucine conjugates and modeling studies with the COI1-JAZ co-receptor complex of lima bean.

Authors:  Yoko Nakamura; Christian Paetz; Wolfgang Brandt; Anja David; Martha Rendón-Anaya; Alfredo Herrera-Estrella; Axel Mithöfer; Wilhelm Boland
Journal:  J Chem Ecol       Date:  2014-07-10       Impact factor: 2.626

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.