CHLOROPLAST STRUCTURE AND FUNCTION IN CULTURED TOBACCO TISSUE

Abstract

A comparative study was made of the ability of cultured pith tissue, leaves of buds induced from callus, and mature leaf tissue of Nicotiana tabacum L. ‘Maryland Mammoth’ to fix carbon, as determined by light‐induced C 14 O 2 incorporation. Photosynthetic ability was then correlated with the fine structure of chloroplasts from these tissues. The light to dark incorporation ratio for C 14 O 2 was at least 3 times as great in the leaf tissue as in growing cultured tissue. The chlorophyll content of the leaf tissue was 10 times as great. The carbon fixation pattern of all the tissues, as determined by radioautographs of chromatogramed extracts, was qualitatively the same. The rate of sucrose synthesis differed greatly, since 20% of the total radioactivity of the extracts from mature leaf tissue appeared in sucrose, while only 1.0% was found in sucrose from callus extracts. The incorporation of C 14 O 2 into sugars was inhibited in all the tissue by DCMU (3,4‐dichlorophenyl,1, 1‐dimethylurea). Cultured tissue past the log phase of growth was intermediate between the younger cultured tissue and the leaf tissue in its chlorophyll content and ability to incorporate C 14 O 2 in the light. Proplastids from dark‐grown callus possessed stroma lamellae, but prolamellar bodies were not observed. The chloroplasts from growing callus were partially differentiated in comparison with chloroplasts from mature leaf tissue, since each granum had only 4‐7 lamellae. Chloroplasts from callus past the log phase of growth were indistinguishable from those in mature leaves. This study establishes that the differentiation of chloroplasts in cultured tissue is a function of the growth rate of the tissue. The growth rate and degree of differentiation of the tissue can be regulated, so a well‐defined system is available for the experimental study of chloroplast differentiation.