Iron nutrition of plants and interactions with vascular wilt disease and light
Date
1989
Authors
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Journal ISSN
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Publisher
Montana State University - Bozeman, College of Agriculture
Abstract
The relationship between iron nutritional status and Verticillium Wilt disease in tomato possessing
single gene resistance to Race 1 of Verticillium dahliae was investigated using hydroponic culture
media. Iron limiting conditions increased the sensitivity of resistant tomatoes to the pathogen as
expressed by wilting and chlorosis. Distance of fungal vascular invasion was approximately the same
in both iron replete and iron limited treatments. Comparison of near-isolines revealed that the
magnitude of disease expressed in Fe deficient Pixie II (resistant) was considerably less than that
expressed by the susceptible Pixie variety. Infection of tomato did not enhance iron stress severity as
quantified by root peroxidase activity and chlorophyll content of young leaves.
The release of iron from horse spleen ferritin through photochemical reduction of Fe(III) to Fe(II) was
studied in vitro. Spectrophotometric measurement of the Fe(ferrozine)3^2+ complex (specific for
Fe(II)) was used to quantify rates of Fe mobilization: Cool white fluorescent plus incandescent light
effectively promoted the rate of Fe release. Compounds known to be present in plants may provide
further regulation of photorelease. Reductive removal from ferritin was inhibited by phosphate, and
hydroxide, whereas citrate, oxalate, tartrate, and caffeate enhanced the release. Of the organic acids
studied, caffeate was the only compound which induced detectable Fe release in the absence of
irradiation. Rate constants ranged from 2.7 x 10^-3 sec^-1 (pH = 4.6) to 2.1 x 10^-3 sec^-1 (pH = 7.1)
at 26.5°C. Synthesis of the photosynthetic apparatus is dependent on both light and iron. Thus, the
findings provide one possible mechanism coupling chloroplast iron demand with iron release from
ferritin.
Treatments known to alter either phenolic metabolism or overall enzyme activity were utilized to
examine the Fe reductive mechanisms involved in iron stress response at the roots. Although specific
compounds caused elevation of internal o-dihydroxyphenol content, the overall root reduction capacity
of Fe stressed plants was significantly suppressed. However, plant roots retained significant capacity to
reduce Fe after tissues were subjected to severe protein denaturizing treatments. Thus, indications for
both secreted reductant and enzymatic reduction mechanisms were observed.