Recent Advances in Understanding the Origin of the Apoplastic Oxidative Burst in Plant Cells

• Published in: Free radical research Vol. 31; no. sup1; pp. 137 - 145
• Main Authors: Bolwell, G. Paul, Blee, Kristopher A., Butt, Vernon S., Davies, Dewi R., Cardner, Sara L., Gerrish, Chris, Minibayeva, Farida, Rowntree, Ellen G., Wojtaszek, Przemyslaw
• Format: Journal Article
• Language: English
• Published: England Taylor & Francis 01.01.1999
• Subjects: ADF, Actin depolymerising factor; Alkalinisation; Calcium - metabolism; CDPK, calcium-dependent protein kinase; Cell Wall - metabolism; DDC, N,N diethyl-dithiocarbamate; DPI, diphenylene iodonium; ECM, extracellular matrix; Elicitor; French bean; Hydrogen-Ion Concentration; LRR, leucine-rich receptor; Models, Biological; Multienzyme Complexes - metabolism; NADH, NADPH Oxidoreductases - metabolism; Oxidative burst; PAL, phenylalanine ammonia-lyase; Peroxidase; Peroxidases - metabolism; Plants; Plants - metabolism; PP1, protein phosphatase 1; Respiratory Burst; ROS, reactive oxygen species; Signal Transduction; Space life sciences; Substrate Specificity
• ISSN: 1071-5762; 1029-2470
• DOI: 10.1080/10715769900301431

The origin of the oxidative burst during plant-pathogen interactions remains controversial. A number of possibilities have been identified, which involve the protoplast, plasmalemma or apoplast. The apoplastic production of H2O2 requires three components, an extracellular peroxidase, ion fluxes leading to extracellular alkalinisation and release of a substrate. Fatty acids are the major compounds that appear in the apoplast following elicitation, which can activate H2O2 production by peroxidases in vitro. However, the reaction with peroxidases appears to be novel and is uncharacterised at present. The apoplastic mechanism also cannot be readily distinguished from the operation of a plasma membrane NADPH oxidase system by the use of the inhibitors diphenylene iodonium and N,N diethyl-dithiocarbamate since it is also inhibited by these. These inhibitors have often in the past been used to define the involvement of the latter in the oxidative burst. In common with the NADPH oxidase system, the peroxidase responsible has been cloned but unlike the NADPH oxidase it has been shown to function in vitro to generate H2O2. In vivo studies of the oxidative burst have shown that the alkalinisation is essential and the underlying ion fluxes may be regulated by cAMP. Calcium fluxes are also essential. Although the oxidative activity of peroxidase requires calcium the fluxes have obvious other function. These may include activation of release of substrate and through the activation of a CDPK, regulation of enzymes involved in phytoalexin and cell wall phenolic production such as PAL.