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A. Macleod, A. Millar (1962)
EFFECTS OF GIBBERELLIC ACID ON BARLEY ENDOSPERMJournal of The Institute of Brewing, 68
J. Varner, 7212 Bellona (1964)
Gibberellic Acid Controlled Synthesis of α-Amylase in Barley EndospermPlant Physiology, 39
H. Brown, F. Escombe
On the depletion of the endosperm of Hordenm vulgare during germinationProceedings of the Royal Society of London, 63
J. Varner (1965)
Gibberellic Acid Controlled Synthesis of alpha-Amylase in Barley Endosperm.Plant physiology, 39 3
L. Shuster, R. Gifford (1962)
Changes in 3'-nucleotidase during the germination of wheatembryos.Archives of biochemistry and biophysics, 96
(1890)
Die Kleberschicht des Gras - Endosperms als Diastase aussclheidendes Driisen - gewebe
K. Kirby (1965)
ISOLATION AND CHARACTERIZATION OF RIBOSOMAL RIBONUCLEIC ACID.The Biochemical journal, 96
C. Wilson (1963)
Chromatographic separation of ribonucleases in corn.Biochimica et biophysica acta, 68
L. Paleg (1960)
Physiological Effects of Gibberellic Acid: I. On Carbohydrate Metabolism and Amylase Activity of Barley Endosperm.Plant physiology, 35 3
(1965)
RAM CHANDRA, AND ,M
D. Briggs (1963)
BIOCHEMISTRY OF BARLEY GERMINATION ACTION OF GIBBERELLIC ACID ON BARLEY ENDOSPERMJournal of The Institute of Brewing, 69
1 CHANDRA. 1964. Hornional control of enzyme synthesis in barlev enclospermii
(1960)
Studies on the a-anivlase activatilng substance. IV. On the amylase activating actioIn of gibberellin. Hakko Kyokaishi
Abstract Gibberellic acid enhances the synthesis of α-amylase in isolated aleurone layers of barley-seeds (Hordeum vulgare var. Himalaya). In the presence of 20 mm calcium chloride the amount of enzyme obtained from isolated aleurone layers is quantitatively comparable to that of the half-seeds used in earlier studies. After a lag period of 6 to 8 hours enzyme is produced at a linear rate. Gibberellic acid does not merely trigger α-amylase synthesis, but it is continuously required during the period of enzyme formation. Enzyme synthesis is inhibited by inhibitors of protein and RNA synthesis. Small amounts of actinomycin D differentially inhibit enzyme release and enzyme synthesis suggesting 2 distinct processes. Gibberellic acid similarly enhances the formation of ribonuclease which increases linearly over a 48 hour period. During the first 24 hours the enzyme is retained by the aleurone cells and this is followed by a rapid release of ribonuclease during the next 24 hour period. The capacity to release the enzyme is generated between 20 and 28 hours after the addition of the hormone. Ribonuclease formation is inhibited by inhibitors of protein and RNA synthesis. These inhibitors also prevent the formation of the release mechanism if added at the appropriate moment. This content is only available as a PDF. © 1967 American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)
Plant Physiology – Oxford University Press
Published: Mar 1, 1967
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