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Comparative Biochemistry of the Oxidative Burst Produced by Rose and French Bean Cells Reveals Two Distinct Mechanisms1

G. Paul Bolwell, Dewi R. Davies, Chris Gerrish, Chung-Kyoon Auh2, and Terence M. Murphy*

Division of Biochemistry, School of Biological Sciences, Royal Holloway, and Bedford New College, University of London, Egham, Surrey TW20 0EX, United Kingdom (G.P.B., D.R.D., C.G.); and Section of Plant Biology, Division of Biological Sciences, University of California, Davis, California 95616 (C.-K.A., T.M.M.)

Cultured cells of rose (Rosa damascena) treated with an elicitor derived from Phytophthora spp. and suspension-cultured cells of French bean (Phaseolus vulgaris) treated with an elicitor derived from the cell walls of Colletotrichum lindemuthianum both produced H2O2. It has been hypothesized that in rose cells H2O2 is produced by a plasma membrane NAD(P)H oxidase (superoxide synthase), whereas in bean cells H2O2 is derived directly from cell wall peroxidases following extracellular alkalinization and the appearance of a reductant. In the rose/Phytophthora spp. system treated with N,N-diethyldithiocarbamate, superoxide was detected by a N,N'-dimethyl-9,9'-biacridium dinitrate-dependent chemiluminescence; in contrast, in the bean/C. lindemuthianum system, no superoxide was detected, with or without N,N-diethyldithiocarbamate. When rose cells were washed free of medium (containing cell wall peroxidase) and then treated with Phytophthora spp. elicitor, they accumulated a higher maximum concentration of H2O2 than when treated without the washing procedure. In contrast, a washing treatment reduced the H2O2 accumulated by French bean cells treated with C. lindemuthianum elicitor. Rose cells produced reductant capable of stimulating horseradish (Armoracia lapathifolia) peroxidase to form H2O2 but did not have a peroxidase capable of forming H2O2 in the presence of reductant. Rose and French bean cells thus appear to be responding by different mechanisms to generate the oxidative burst.


1   This work was supported in part by the U.S. Department of Agriculture National Research Initiative-Cooperative State Research Service (grant no. 94-37100-0788) to T.M.M.
2   Present address: Department of Plant Pathology, North Carolina State University, Raleigh, NC 27695.
*   Corresponding author; e-mail tmmurphy{at}ucdavis.edu; fax 1-916-752-5410.

Plant Physiol. (1998) 116: 1379-1385
Copyright Clearance Center:   0032-0889/98/116/1379/07
© 1998 American Society of Plant Physiologists




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