2002•Journal of Nanjing Forestry UnversityRequires access

Tissue Culture and Plant Regeneration of Cerasus campanulata

Guang Wang

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Abstract

Stabilized shoot cultures were achieved when the explant sources were the juvenile branches of Cerasus campanulata in spring.The inducing rate of fasciculated shoots was 87.5% when the inducing medium of 1/4MS with BA 1.0 mg/L and IBA 0.01 mg/L were used.The adventitious shoots were propagated most rapidly when subcultured on the medium of MS with BA 1.0 mg/L,IBA 0.1 mg/L and GA 3 0.3 mg/L,or MS with KT1.0 mg/L,NAA 0.1 mg/L and GA 3 0.3 mg/L.The elongation of adventitious shoots was greatly affected by gibberellin.The adventitious shoots were cut and rooted in the rooting medium of 1/2MS with NAA 1.0 mg/L IBA 1.0 mg/L and BA 0.75 mg/L.The tooting rate was more than 90%.The surviving rate was 95% when the intact shoots were moved to the greenhouse.

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Stabilized shoot cultures were achieved when the explant sources were the juvenile branches of Cerasus campanulata in spring.The inducing rate of fasciculated shoots was 87.5% when the inducing medium of 1/4MS with BA 1.0 mg/L and IBA 0.01 mg/L were used.The adventitious shoots were propagated most rapidly when subcultured on the medium of MS with BA 1.0 mg/L,IBA 0.1 mg/L and GA 3 0.3 mg/L,or MS with KT1.0 mg/L,NAA 0.1 mg/L and GA 3 0.3 mg/L.The elongation of adventitious shoots was greatly affected by gibberellin.The adventitious shoots were cut and rooted in the rooting medium of 1/2MS with NAA 1.0 mg/L IBA 1.0 mg/L and BA 0.75 mg/L.The tooting rate was more than 90%.The surviving rate was 95% when the intact shoots were moved to the greenhouse.

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Available abstract

Stabilized shoot cultures were achieved when the explant sources were the juvenile branches of Cerasus campanulata in spring.The inducing rate of fasciculated shoots was 87.5% when the inducing medium of 1/4MS with BA 1.0 mg/L and IBA 0.01 mg/L were used.The adventitious shoots were propagated most rapidly when subcultured on the medium of MS with BA 1.0 mg/L,IBA 0.1 mg/L and GA 3 0.3 mg/L,or MS with KT1.0 mg/L,NAA 0.1 mg/L and GA 3 0.3 mg/L.The elongation of adventitious shoots was greatly affected by gibberellin.The adventitious shoots were cut and rooted in the rooting medium of 1/2MS with NAA 1.0 mg/L IBA 1.0 mg/L and BA 0.75 mg/L.The tooting rate was more than 90%.The surviving rate was 95% when the intact shoots were moved to the greenhouse.

Key concepts: Shoot, Explant culture, Elongation, Botany, Murashige and Skoog medium, Tissue culture, Horticulture, Biology

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