Superoxide‐producing NAD(P)H oxidases in plasma membrane vesicles from elicitor responsive bean plants |
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Authors: | Peter Van Gestelen Han Asard Nele Horemans Roland J. Caubergs |
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Affiliation: | P. Van (corresponding author, e‐mail;), H. Asard, N. Horemans and R. J. Caubergs, Gestelen Dept of Biology, Univ. of Antwerp (RUCA), Groenenborgerlaan 171, B‐2020 Antwerp, Belgium. |
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Abstract: | Higher plants produce active oxygen species (AOS) that regulate their defence responses against pathogenic elicitation. Etiolated bean seedlings ( Phaseolus vulgaris L. cv. Limburgse vroege) were used to measure the in vivo‐induced AOS production and to search for plasma membrane bound NAD(P)H‐dependent oxidases producing AOS. Immersed bean plants showed a substantial production of H2O2, as determined by the peroxidase (EC 1.11.1.7)‐dependent oxidation of 3,5‐dichloro‐2‐hydroxybenzenesulfonic acid (DHBS). Addition of the elicitor polygalacturonase (PGase, EC 3.2.1.15) from Aspergillus japonicus or the phosphatase inhibitor, cantharidin, resulted in a transient increase of AOS synthesis. Plasma membrane vesicles, purified from etiolated bean seedlings, showed an NAD(P)H‐dependent superoxide (O2−) production that was highly stimulated with naphthoquinones. Protein solubilisation and anion exchange chromatography resolved a basal and three naphthoquinone‐stimulated NAD(P)H‐dependent O2− oxidase fractions. The natural phenol, apigenin, was also a strong inducer of the naphthoquinone‐dependent enzymes, when it was used in the presence of peroxidase. Although, the relation of these different in vitro‐determined plasma membrane NAD(P)H‐dependent O2− oxidases to the in vivo elicitation of H 2O2 has not been elucidated so far. |
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