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In vitro clonal propagation of Pisum sativum L.
Authors:Miroslav Griga  Eva Tejklová  František J. Novák  Marie Kubaláková
Affiliation:(1) OSEVA-Plant Breeding and Seed Corporation, Plant Breeding Station for Legumes, CS-751 17 Horní Mo"scaron"t"ecaron"nice, Czechoslovakia;(2) OSEVA-Plant Breeding and Seed Corporation, Research and Breeding Institute of Technical Crops and Legumes, CS-787 01 "Scaron"umperk-Temenice, Czechoslovakia;(3) Institute of Experimental Botany, Czechoslovak Academy of Sciences, Sokolovská 6, CS-772 00 Olomouc, Czechoslovakia
Abstract:A system of in vitro clonal propagation has been developed in Pisum sativum L. (cv. Bohatýr). A modified MS-medium supplemented with 20 mgrM 6-benzylaminopurine (BAP) and 0.1 mgrM agr-naphthaleneacetic acid (NAA) was used to induce multiple shoot formation from shoot apices, axillary buds of the first normal leaf, axillary buds of the first and second primary scales and axillary buds of cotyledons of 4 to 6 day old pea seedlings. Meristem explants maintained a high proliferation ability in each subculture in the course of 20 months of the culture. Regenerated shoots were rooted in the same basal medium containing 5 mgrM NAA. Rooted plants were cultured in hydroponic pots filled with half-strength MS-medium to attain anthesis and seed maturity. The phenotypic uniformity of the regenerants was evaluated. Cytological investigation confirmed the diploid stage (2n=14) of regenerants and their progeny. Histological studies revealed that proliferating shoots originated from axillary and adventitious buds. In vitro propagation is discussed as related to pea breeding.
Keywords:Pisum sativum L.  pea  shoot tip culture  axillary bud culture  regeneration  organogenesis  in vitro clonal propagation
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