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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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