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园艺学报 ›› 2005, Vol. 32 ›› Issue (6): 1080-1083.

• 研究报告 • 上一篇    下一篇

不同基因型梨叶片离体培养和植株再生

刘翠琼;汤浩茹;罗 娅
  

  1. (四川农业大学林学园艺学院, 雅安625014)
  • 收稿日期:2005-01-14 修回日期:2005-05-24 出版日期:2005-12-25 发布日期:2005-12-25

Leaf Culture and Plantlet Regeneration of Pears with Different Genotypes

Liu Cuiqiong;Tang Haoru;Luo Ya   

  1. (College of Forestry and Horticulture, Sichuan Agricultural University, Ya'an 625014, China)
  • Received:2005-01-14 Revised:2005-05-24 Online:2005-12-25 Published:2005-12-25

摘要: 以‘巴梨’、‘身不知’和‘早酥’梨试管苗叶片为外植体, 对不定芽进行了诱导、增殖和生
根。重点探讨了基本培养基、植物生长调节剂配比、AgNO3 不同浓度和NH4+-N与NO3--N比例对不定芽再生的影响。结果表明, MS + TDZ 0.5 mg/L + IBA 0.1 mg/L为‘巴梨’叶片不定芽发生的最佳培养基。在QL + TDZ 1.0 mg/L +NAA 0.1 mg/L培养基上, 暗培养3周后转光下培养, ‘身不知’和‘早酥’分别获得89.6%、81.2%的不定芽再生率和3.45、3.73的平均再生芽数; 对‘巴梨’和‘早酥’不定芽再生有效促进的AgNO3 浓度范围为0.1~0.5 mg/L, 0.1~4.0 mg/L的AgNO3、1∶2~7的NH4+-N∶NO 3--N和21.50mmol/L的K+对‘身不知’叶片再生均有促进作用, 缺乏NH4+-N不利于不定芽的再生; 转移到MS+BA1.0 mg/L + IBA 0.1 mg/L培养基上能快速增殖; 在MS、1 /4MS + IBA 1.0~2.5 mg/L +蔗糖5~15 g/L +活性炭0.5~1.0 g/L上获得了不同程度的生根苗。

关键词: 梨, 叶片, 再生, 组织培养

Abstract: Taking leaves from the vitro cuttings of Pyrus communis L. ‘Bartlett’, P. pyrifolia Nak.‘Shenbuzhi’and P. bretschneideri Rhed. ‘Zaosu’as explants, the adventitious bud were induced, propagated, and rooted. The effects of basic media, plant growth regulators and their concentration, AgNO3 with
different concentration and the ratios of the nitrate: ammonium on adventitious bud regeneration were studied.The results showed that the best bud regeneration medium from leaves of‘Bartlett’wasMS + TDZ 0.5 mg/L+ IBA 0.1 mg/L. The bud regeneration rate of ‘Shenbuzhi’ and ‘Zaosu’ respectively from leaves was reached 89.6% and 81.2% , with an average regeneration buds of 3.45 and 3.73 on QL + TDZ 1.0 mg/L +NAA 0.1 mg/L after three weeks dark pretreatment. The bud regeneration frequency of‘Shenbuzhi’from
leaves was enhanced on medium containing AgNO3 0.1 - 4.0 mg/L, 1∶2 - 7 of the nitrate: ammonium with K+ 21.50 mmol/L, while inhibited without nitrate; The subculture medium for in vitro proliferation of three cultivars was MS +BA 1.0 mg/L + IBA 0.1 mg/L; The rooting rate in varying degrees was obtained in the media of MS, 1 /4MS supplemented with IBA at 1.0 - 2.5 mg/L and sucrose at 5 - 15 g/L and AC ( actived charcoal) at 0.5 - 1.0 g/L.

Key words: Pear, Leaf, Regeneration, Tissue culture

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