Abstract

SYNOPSIS The technique of “in-organelle” DNA digestion was assessed with regard to its applicability to the production of eucalypt chloroplast DNA (cpDNA) restriction fragments. Because of the waxy cuticle, high incidence of thickened tissue and presence of phenolic compounds in eucalypt leaves, it was necessary to devise an effective protocol for the isolation of high yields of purified chloroplasts. Eucalyptus grandis S/N M6 was selected as the model for this purpose. “In organelle” digestion of the resultant E. grandis chloroplasts (450–600 μg chlorophyll) with Bgl II, followed by electrophoretic separation of fragments, produced a well resolved profile clearly distinguishable from that of an outgroup, Spinacea oleracea. However, the described chloroplast isolation procedure was found to be non-optimal when applied to E. grandis TAG 5, E. grandis TAG 14, E. nitens and E. macarthurii (yields ranged from 0,0 to 5,3 μ g chlorophyll/g fresh mass). On account of the requirement that the chloroplast extracti...

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