Distribution of pyruvate dehydrogenase complex activities between chloroplasts and mitochondria from leaves of different species

Protoplasts from barley (Hordeum vulgare) pea (Pisum sativum), wheat (Triticum aestivum) and spinach (Spinacia oleracea) leaves were fractionated into chloroplast- and mitochondrion-enriched fractions, Pyruvate dehydrogenase complex capacities in mitochondria (mtPDC) and chloroplasts (cpPDC) were me...

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Veröffentlicht in:Plant physiology (Bethesda) 1994-12, Vol.106 (4), p.1633-1638
Hauptverfasser: Lernmark, U. (University of Umea, Umea, Sweden), Gardestrom, P
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Sprache:eng
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Zusammenfassung:Protoplasts from barley (Hordeum vulgare) pea (Pisum sativum), wheat (Triticum aestivum) and spinach (Spinacia oleracea) leaves were fractionated into chloroplast- and mitochondrion-enriched fractions, Pyruvate dehydrogenase complex capacities in mitochondria (mtPDC) and chloroplasts (cpPDC) were measured in appropriate fractions under conditions optimal for each isozyme. The total cellular capacity of PDC was similar in barley and pea but about 50% lower in wheat and spinach. In pea a distribution of 87% mtPDC and 13% cpPDC was found on a cellular basis. In barley, wheat and spinach the subcellular distribution was the opposite, with about 15% mtPDC and 85% cpPDC. cpPDC activity was constant at about 0.1 nmol cell-1 h-1 in cells from different regions along the developing barley leaf and showed no correlation with developmental patterns of photosynthetic parameters such as increasing Chl and NADP-glyceraldehyde-3-phosphate dehydrogenase activity. Similarly the capacity of the mitochondrial isoform did not change during barley leaf development and had a developmental pattern similar to that of citrate synthase and fumarase. Differences in subcellular distribution of PDCs in barley and pea are proposed to be due to differences in regulation not to changes in isozyme proportions during leaf development or to species-specific differences in phosphorylation state of mtPDC after organelle separation
ISSN:0032-0889
1532-2548
1532-2548
DOI:10.1104/pp.106.4.1633