2014•GuihaiaRequires access

Tissue culture and rapid propagation of Lysionotus aeschynanthoides

Fu Chuan

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Abstract

Tissue culture and rapid propagation technique of Lysionotus aeschynanthoides were studied. The results showed that the axillary buds of Lysionotus aeschynanthoides could directly germinate in MS+6-BA 1.0 mg·L-1+IBA 0.1 mg·L-1and the germination rate was 75%. The primary culture medium for bud induction from stem segments was MS+6-BA 1.0 mg·L-1+IBA 0.1 mg·L-1. The subculture medium for bud multiplication and seedlings growing was 1/2MS+NAA 0.2 mg·L-1,and proliferation coefficient was 6.0/60 d. Callus could be inducted through the pedicels explants in subculture but could not develop further. The optimal rooting medium was 1/2 MS+BA 0.2 mg·L-1+NAA 0.8 mg·L-1+AC 0.1%+5% banana juice,and rooting rate was 100%. The rooting plantlets were transplanted in greenhouse that simulated the natural growing environment of L. aeschynanthoids,the survival rate was more than 95%.

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Tissue culture and rapid propagation technique of Lysionotus aeschynanthoides were studied. The results showed that the axillary buds of Lysionotus aeschynanthoides could directly germinate in MS+6-BA 1.0 mg·L-1+IBA 0.1 mg·L-1and the germination rate was 75%. The primary culture medium for bud induction from stem segments was MS+6-BA 1.0 mg·L-1+IBA 0.1 mg·L-1. The subculture medium for bud multiplication and seedlings growing was 1/2MS+NAA 0.2 mg·L-1,and proliferation coefficient was 6.0/60 d. Callus could be inducted through the pedicels explants in subculture but could not develop further. The optimal rooting medium was 1/2 MS+BA 0.2 mg·L-1+NAA 0.8 mg·L-1+AC 0.1%+5% banana juice,and rooting rate was 100%. The rooting plantlets were transplanted in greenhouse that simulated the natural growing environment of L. aeschynanthoids,the survival rate was more than 95%.

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Available abstract

Tissue culture and rapid propagation technique of Lysionotus aeschynanthoides were studied. The results showed that the axillary buds of Lysionotus aeschynanthoides could directly germinate in MS+6-BA 1.0 mg·L-1+IBA 0.1 mg·L-1and the germination rate was 75%. The primary culture medium for bud induction from stem segments was MS+6-BA 1.0 mg·L-1+IBA 0.1 mg·L-1. The subculture medium for bud multiplication and seedlings growing was 1/2MS+NAA 0.2 mg·L-1,and proliferation coefficient was 6.0/60 d. Callus could be inducted through the pedicels explants in subculture but could not develop further. The optimal rooting medium was 1/2 MS+BA 0.2 mg·L-1+NAA 0.8 mg·L-1+AC 0.1%+5% banana juice,and rooting rate was 100%. The rooting plantlets were transplanted in greenhouse that simulated the natural growing environment of L. aeschynanthoids,the survival rate was more than 95%.

Key concepts: Subculture (biology), Tissue culture, Explant culture, Germination, Axillary bud, Pedicel, Callus, Botany

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