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松毛翠的离体快繁体系建立及种质试管保存 被引量:13

Rapid Propagation System and Germplasm Preservation in vitro of Phyllodoce caerulea
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摘要 The tender buds of Phyllodoce caerulea were used as explants for this experiment.The most suitable culture media were screened for shoots regeneration directly from bases of the tender buds,rooting and germplasm preservation in vitro with a uniform design.The results showed that DR+TDZ4.00 mg·L-1was the most suitable for shoots regeneration,and the rate of regeneration was more than 98.5%.MS(modified)+IBA0.05 mg·L-1+NAA0.01 mg·L-1+KT0.10 mg·L-1was the most suitable for rooting,and the rate of rooting was more than 97.8%.N-68+B92.30 mg·L-1+ phloridzin 1.50 mg·L-1was the most suitable for preservation in vitro for 42 months.Stems each with one node were cut from the regenerated shoots and cultured for propagation,and a 35-fold proliferation rate was achieved within 40 days.The method of "deferring growth with dwarfing" was utilized for germplasm preservation in vitro at normal temperature.In vitro culture and germplasm preservation in vitro system of Phyllodoce caerulea had been successfully established. The tender buds of Phyllodoce caerulea were used as explants for this experiment. The most suitable culture media were screened for shoots regeneration directly from bases of the tender buds, rooting and germplasm preservation in vitro with a uniform design. The results showed that DR + TDZ4.00 mg· L- 1 was the most suitable for shoots regeneration, and the rate of regeneration was more than 98.5 %. MS(modified) + IBA0.05 mg·L- 1 + NAA0.01 mg· L- 1 + KT0.10 mg·L- 1 was the most suitable for rooting, and the rate of rooting was more than 97.8%. N-68 + B92.30 mg·L-1 + phloridzin 1.50 mg·L-lwas the most suitable for preservatiofi in vitro for 42 months. Stems each with one node were cut from the regenerated shoots and cultured for propagation, and a 35-fold proliferation rate was achieved within 40 days. The method of "deferring growth with dwarfing" was utilized for germplasm preservation in vitro at normal temperature. In vitro culture and germplasm preservation in vitro system of Phyllodoce caerulea had been successfully established.
出处 《林业科学》 EI CAS CSCD 北大核心 2009年第7期140-144,共5页 Scientia Silvae Sinicae
基金 吉林省科技厅自然科学基金资助项目(200705C05) 通化师范学院自然科学基金资助项目(XS070079)
关键词 松毛翠 种质试管保存 均匀设计 根皮苷 Phyllodoce caerulea germplasm preservation in vitro uniform design phloridzin
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