Long-duration,high-frequency plant regeneration from cereal tissue cultures |
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Authors: | Murray W. Nabors James W. Heyser Thomas A. Dykes Kirby J. DeMott |
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Affiliation: | (1) Department of Botany and Plant Pathology, Colorado State University, 80523 Fort Collins, CO, USA;(2) Present address: LS-6, MS-890, Los Alamos National Laboratory, 87545 Los Alamos, NM, USA |
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Abstract: | By visual examination of calli derived from germinating seeds of wheat, oats, rice, proso millet, and pearl millet it has been possible to visually select embryogenic (E) callus which, on transfer to a regeneration medium, forms plants an average of 33 times more frequently than non-embryogenic (NE) callus of equal mass. Embryogenic callus consists of small isodiametric cells averaging 31 m in diameter; NE callus consists of long tubular cells averaging 52 m in width and 355 m in length. Production of E callus is in many cases promoted by media containing 2,4-di- or 2,4,5-trichlorophenoxyacetic acid (2,4-D or 2,4,5-T) plus indole-3-acetic acid or tryptophan+kinetin. Production on NE callus is promoted by media containing 2,4-D or 2,4,5-T alone. As a result of initial experiments to optimize both media for E callus production and media for plant regeneration, callus derived in six passages from an average of 26 seeds could produce about 1,000 regenerated plants.Abbreviations 2,4-D 2,4-dichlorophenoxyacetic acid - 2,4,5-T 2,4,5-trichlorophenoxyacetic acid - IAA indole-3-acetic acid - Kin kinetin - Trp L-tryptophan - E embryogenic - NE non-embryogenic |
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Keywords: | Cereals (regeneration from calli) Embryogenesis, somatic Regeneration from calli Tissue culture (regeneration) |
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