[Objective] The aim was to optimize the culture conditions for asexual reproduction system of Populus euramericana 108.[Method] Orthogonal designs were adopted optimize the culture conditions of the regeneration syste...[Objective] The aim was to optimize the culture conditions for asexual reproduction system of Populus euramericana 108.[Method] Orthogonal designs were adopted optimize the culture conditions of the regeneration system for direct differentiation from leaves and induced callus from stems of P.euramericana 108 aseptic seeding.[Result] Leaves of P.euramericana 108 directly regenerated and differentiated under illumination,while stem segments preferred to regenerate and differentiate through callus induction under illumination.The differentiation medium of adventitious buds from leaves was MS medium （agar 7.0 g/L,pH 6.0,sucrose 20 g/L） added with 0.6 mg/L 6-BA and 0.2 mg/L NAA; callus induction medium of stem segments was WPM solid medium added with 0.75 mg/L KT and 1.5 mg/L 2,4-D.Rooting induction medium for adventitious buds was WPM solid culture （sucrose 30 g/L） added with 2.0 mg/L IBA.[Conclusion] The culture conditions for regeneration system of differentiation from leaves and induced callus of stems were optimized,which provides basis for the construction of tissue culture and genetic transformation system.展开更多
文摘[Objective] The aim was to optimize the culture conditions for asexual reproduction system of Populus euramericana 108.[Method] Orthogonal designs were adopted optimize the culture conditions of the regeneration system for direct differentiation from leaves and induced callus from stems of P.euramericana 108 aseptic seeding.[Result] Leaves of P.euramericana 108 directly regenerated and differentiated under illumination,while stem segments preferred to regenerate and differentiate through callus induction under illumination.The differentiation medium of adventitious buds from leaves was MS medium （agar 7.0 g/L,pH 6.0,sucrose 20 g/L） added with 0.6 mg/L 6-BA and 0.2 mg/L NAA; callus induction medium of stem segments was WPM solid medium added with 0.75 mg/L KT and 1.5 mg/L 2,4-D.Rooting induction medium for adventitious buds was WPM solid culture （sucrose 30 g/L） added with 2.0 mg/L IBA.[Conclusion] The culture conditions for regeneration system of differentiation from leaves and induced callus of stems were optimized,which provides basis for the construction of tissue culture and genetic transformation system.
