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光叶楮组织培养繁殖技术研究

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开展光叶楮(Broussouetia papyrifera)外植体消毒、侧芽诱导、继代增殖和生根诱导试验.以75%乙醇+0.15%升汞消毒外植体,干净外植体获得率达40%;采用MS+ 6-BA 2.0 mg/L+ NAA 0.5 mg/L培养基,侧芽诱导分化率达80%;采用MS+ 6-BA 1.0 mg/L+ NAA 0.5 mg/L继代培养,增殖倍数达3.96倍;采用1/2MS+ IBA1.0 mg/L或GGR6 0.5~1.0 mg/L进行生根培养,瓶苗生根率达100%,形成了可以产业化的光叶楮组织培养技术流程.
Study on Tissue Culture Breeding Technology of Broussonetia papyrifera
The tissue culture technology of Broussonetia papyrifera was studied by explants disinfection,lateral bud induction,subculture multiplication and root induction.Explants were sterilized using 75% ethanol and 0.15% mercuric chloride,the survival rate was 40%.The lateral buds planted in MS medium containg 6-BA 2.0 mg/L and NAA 0.5 mg/L showed the highest bud differentiation rate (80%).The optimum medium for subculture was MS + 6-BA 1.0 mg/L + NAA 0.5 mg/L,the proliferation times was 3.96.The rooting rate of 100% could be obtained by using 1/2MS + IBA1.0 mg/L or GGR6 0.5 ~ 1.0 mg/L.The results of this study fomed a high potential of large scale commercial production of B.papyrifera.

Broussonetia papyriferatissue culture

朱永钊、曾雷、张弘

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陈禾洞省级自然保护区管理处,广东从化510950

广东省林业科学研究院 广东广州510520

光叶楮 组织培养

广东省林业科技创新专项

2012KJCX015-01

2014

林业与环境科学
广东省林学会,广东省林业科学研究院

林业与环境科学

影响因子:0.62
ISSN:1006-4427
年,卷(期):2014.30(4)
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