In: Transgenic Research, 2001, vol. 10, no. 6, p. 533-543
|
In: Transgenic Research, 2006, vol. 15, no. 1, p. 69-82
|
In: The Plant Journal, 2009, vol. 58, no. 2, p. 287 - 298
Plant immune responses to pathogens are often associated with enhanced production of reactive oxygen species (ROS), known as the oxidative burst, and with rapid hypersensitive host cell death (the hypersensitive response, HR) at sites of attempted infection. It is generally accepted that the oxidative burst acts as a promotive signal for HR, and that HR is highly correlated with efficient disease...
|
In: Molecular Plant-Microbe Interactions, 2008, vol. 21, no. 11, p. 1482-1497
Volatile, low–molecular weight terpenoids have been implicated in plant defenses, but their direct role in resistance against microbial pathogens is not clearly defined. We have examined a possible role of terpenoid metabolism in the induced defense of Arabidopsis thaliana plants against leaf infection with the bacterial pathogen Pseudomonas syringae. Inoculation of plants with...
|
In: Journal of Phytopathology, 2005, vol. 153, p. 27-36
The reduction of atmospheric sulphur dioxide pollution is causing increasing problems of sulphur deficiency in sulphur-demanding crop plants in northern Europe. Elemental sulphur and many sulphur containing compounds such as cysteine-rich antifungal proteins, glucosinolates (GSL) and phytoalexins play important roles in plant disease resistance. The aim of this work was to analyse the effect of...
|