Protoplast culture and plant regeneration in Lycium barbarum L.
Identifieur interne : 003E70 ( Main/Exploration ); précédent : 003E69; suivant : 003E71Protoplast culture and plant regeneration in Lycium barbarum L.
Auteurs : I. Ratushnyak [Russie] ; M. Piven [Russie] ; A. Rudas [Russie]Source :
- Plant Cell, Tissue and Organ Culture [ 0167-6857 ] ; 1989-01-01.
Abstract
Abstract: Protoplasts were isolated from leaves of the woody plant Lycium barbarum L. and cultured in liquid nutrient medium TM-2 at a density of 104–105 cells ml-1. After ten days of culture, regenerated colonies were transferred to the agar-solidified medium TM-3, and 5–7 days later to regeneration media PRM or TM-4. Formation of shoots was observed after 30–40 days. Completely formed and rooted plants were transferred to the soil. Cytological and morphological analysis of the regenerated plants revealed relative genetic stability of this species in the process ‘protoplast — plant’. The results obtained allow us to conclude that L. barbarum can be used in the experiments on somatic hybridization or direct gene transfer.
Url:
DOI: 10.1007/BF00046866
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Abstract: Protoplasts were isolated from leaves of the woody plant Lycium barbarum L. and cultured in liquid nutrient medium TM-2 at a density of 104–105 cells ml-1. After ten days of culture, regenerated colonies were transferred to the agar-solidified medium TM-3, and 5–7 days later to regeneration media PRM or TM-4. Formation of shoots was observed after 30–40 days. Completely formed and rooted plants were transferred to the soil. Cytological and morphological analysis of the regenerated plants revealed relative genetic stability of this species in the process ‘protoplast — plant’. The results obtained allow us to conclude that L. barbarum can be used in the experiments on somatic hybridization or direct gene transfer.</div>
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