Abstract
Isolated sugar maple callus was grown on defined medium containing 0.2 kinetin and 2.0 ppm indoleacetic acid. Selected components of the basal medium were varied but did not result in increased tissue growth. The presence of 1, 5, or 25 ppm gibberellic acid in the culture medium did not increase the secretion of starch digesting materials by the tissue. The diameter of the starch digestion zone was not influenced by changing the acidity of the medium in the range of pH which supported tissue growth. The ability of isolated callus tissues from various species to digest extracellular starch was examined. It was found that equal amounts of various tissues do not possess an equal capacity for the in vitro secretion of extracellular materials, most probably enzymes, into the culture medium. It was found that isolated sugar maple tissue metabolized sucrose, galactose, and cellobiose while mannose and rhamnose were not used.Isolated sugar maple tissue which had been subcultured on the same medium for a long period was found to undergo nutritional changes which enabled the tissue to adapt to the medium. The starch-digestion enzyme activity of the tissue was found to increase when sugar maple tissue was placed on soluble starch medium.
Published Version
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