Tissue Culture and Rapid Propagation of Jacaranda mimosifolia
Wang Mi-li
Abstract
Wang Mi-li
Abstract
The hypocotyls of Jacaranda mimosaefolia used as explants,the tissue culture and rapid propagation system were studied.The results showed that the seed germination rate of J.mimosaefolia reached up to 55.6% after warm water immersion for 60 minutes at 40℃-45℃.The optimum mediums for induction of adventitious buds and callus were MS+6-BA 2.0 mg L-1+NAA 0.1 mg L-1+2,4-D 0.1 mg L-1,and MS+6-BA 0.5 mg L-1+NAA 1.0 mg L-1+2,4-D 1.0 mg L-1,respectively.The optimum mediums for proliferation of adventitious buds and callus were modified MS+6-BA 0.5 mg L-1+NAA 0.5 mg L-1+IBA 0.5 mg L-1,and MS+6-BA 1.0 mg L-1+NAA 0.5 mg L-1+ZT 3.0 mg L-1,respectively.The optimum medium for callus differentiation was MS+6-BA 1.0 mg L-1+NAA 0.5 mg L-1+2,4-D 0.5 mg L-1.The optimum rooting medium was 1/2MS supplemented with 20 g L-1 sugar and NAA 0.5 mg L-1 and 2.0 g L-1 active carbon(AC) with rooting up to 78.3%.
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The hypocotyls of Jacaranda mimosaefolia used as explants,the tissue culture and rapid propagation system were studied.The results showed that the seed germination rate of J.mimosaefolia reached up to 55.6% after warm water immersion for 60 minutes at 40℃-45℃.The optimum mediums for induction of adventitious buds and callus were MS+6-BA 2.0 mg L-1+NAA 0.1 mg L-1+2,4-D 0.1 mg L-1,and MS+6-BA 0.5 mg L-1+NAA 1.0 mg L-1+2,4-D 1.0 mg L-1,respectively.The optimum mediums for proliferation of adventitious buds and callus were modified MS+6-BA 0.5 mg L-1+NAA 0.5 mg L-1+IBA 0.5 mg L-1,and MS+6-BA 1.0 mg L-1+NAA 0.5 mg L-1+ZT 3.0 mg L-1,respectively.The optimum medium for callus differentiation was MS+6-BA 1.0 mg L-1+NAA 0.5 mg L-1+2,4-D 0.5 mg L-1.The optimum rooting medium was 1/2MS supplemented with 20 g L-1 sugar and NAA 0.5 mg L-1 and 2.0 g L-1 active carbon(AC) with rooting up to 78.3%.
Key concepts: Callus, Explant culture, Hypocotyl, Botany, Tissue culture, Germination, Sucrose, Chemistry