The existence of cytokinins both as a free form and as a constituent of t‐RNA was investigated in young fruits of Moringa pterigosperma Gaertn. Purified methanol extract was separated into butanol insoluble and butanol soluble fractions. The cytokinin(s) in the butanol insoluble fraction was tentatively identified as zeatin nucleotide. The butanol soluble fraction contained cytokinins and was chromatographed on Sephadex LH‐20 with 35% ethanol. The two active fractions from LH‐20 column coincided with zeatin and zeatin riboside. Cytokinin per g tissue was high in early stages of fruit growth and then remained more or less constant. Alkaline phosphatase hydrolysis of t‐RNA hydrolysate of fruit tissue showed considerable cytokinin activity.
Changes in cytokinin activity in the flag, first, second, and third leaves and in the developing grain of rice (Oryza sativa L.) were studied using the soybean callus bioassay in relation to the movement of photosynthate during different developmental stages. Cytokininlike activity in leaves was highest at the 85th day after transplantation. The flag leaf maintained higher cytokinin activity than other upper leaves. In grains high cytokininlike activity during the 1st week after anthesis is correlated with the grain setting and cell division period. The concentration gradient of cytokininlike substances in the upper parts of the plant was highest in the panicle after anthesis. The data suggest that the developing rice grains attract most of their photoassimilate from their nearest neighbours, the metabolically active flag, first, and second leaves.
The presence of rhamnose bound indole‐3‐acetic acid (IAA) was reported from acetone extract of anthers and carpels of the flowers of Peltophorum ferrugineum. Hydrolysis of the sugar ester gave IAA and rhamnose. Identification of IAA was based on physical measurements supported by bioassay. Bound and free IAA were not detected in petals, seeds and seed coats.
Endogenous cytokinin activity was determined in the flowers of Cosmos sulphureus Cav. from bud emergence to full bloom using the soybean callus bioassay. Cytokinin activity was low early in flower development but increased prior to full bloom. In Sephadex LH-20 column chromatography of flower extracts, the cytokinins present co-eluted with zeatin, zeatin riboside and glucoside cytokinin. While the former two predominated prior to full bloom, cytokinin glucoside activity appeared to be at a maximum at full bloom. The possible relevance of these findings is discussed in relation to flower development.
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