Plant Physiology 86:1089-1094 (1988)
© 1988 American Society of Plant Biologists
Metabolism and Enzymology
The Regulation of Gelation of Phloem Exudate from Cucurbita Fruit by Dilution, Glutathione, and Glutathione Reductase
M. Carol Alosi1,
Diane L. Melroy2 and
Roderic B. Park
Department of Botany, University of California, Berkeley, California 94720
The average glutathione equivalent concentration in phloem exudate collected from squash fruit (Cucurbita moschata [Duchesne] Poir. var Butternut) and pumpkin fruit (Cucurbita pepo [L.] var Jack-o-lattern) was 1.02 and 0.60 millimolar, respectively. Glutathione reductase (EC 1.6.4.2) activity in phloem exudate from squash and pumpkin fruit averaged 0.48 and 1.74 micromole NADPH oxidized per minute per milliliter, respectively. Protein concentrations in fruit phloem exudates averaged 67 milligrams per milliliter for squash and 57 milligrams per milliliter for pumpkin. The phloem-specific P-proteins account for most of the protein content of exudate. Pure exudate from fruit does not gel for hours or days, but when diluted with neutral or alkaline aqueous solutions, exudate gels rapidly. Exudate solutions undergo biphasic pH changes with dilution. We suggest that P-protein undergoes conformational change upon dilution, exposing titratable groups and sulfhydryl residues. Oxidation of the latter forms the intermolecular disulfide bridges of the gel. The gelation of diluted exudate is regulated by factors (oxygen, pH, glutathione, NADPH) which affect the maintenance of reduced sulfhydryl residues and the activity of glutathione reductase. While these factors may also act in vivo to regulate redox conditions in phloem, their relationship to hypothetical sol/gel transitions or motile and nonmotile phases in the transport conduit is unknown.
1 Supported by National Science Foundation Postdoctoral Fellowship Grant BSR-84-08023.
2 Present address: United States Department of Agriculture, Agricultural Research Service, Beltsville, MD 20705.
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