Iron nutrition-mediated chloroplast development
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Updated: Aug 8, 2026

A Colorimetric Method for Measuring Iron Content in Plants
Published on: September 7, 2018
1Department of Plant and Soil Biology, University of California, Berkeley, California 94720.
Abstract:
Membrane development in chloroplasts was explored by resupplying iron to iron-deficient sugar beet (Beta vulgaris L. cv F58-554H1) and monitoring changes in lamellar components during regreening. The synthesis of chlorophyll a, chlorophyll b, and Q, the first stable electron acceptor of photosystem II, exhibited a lag phase during the first 24 to 48 hours of resupply. In contrast, the per area amounts of P(700) and cytochrome f increased linearly over the first 48 hours. During the early regreening period, the Q to P(700) ratio was 2.6 and decreased to 0.7 after 96 hours of regreening. The rate of photosynthesis (net CO(2) uptake) per chlorophyll increased during the first 48 hours of resupply, then by 96 hours decreased to values typical of control plants. The results suggest that there was preferential synthesis of the measured photosystem I components during the first 24 to 48 hours, while from 48 to 96 hours there was rapid synthesis of all components. The iron nutrition-mediated chloroplast development system provides a useful experimental approach for studying biomembrane synthesis and structural-functional relations of the photosynthetic apparatus.
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