首页|山竹高效再生体系的建立

山竹高效再生体系的建立

扫码查看
本研究以山竹不定胚诱导的无菌苗叶片为外植体,通过优化山竹叶片诱导再生的培养条件,建立了山竹再生培养技术体系方法。结果显示,叶片转入WPM+1.0 mg?L-1GA3+1.0 mg?L-16-BA+0.5 mg?L-1TDZ培养基中,诱导结节性愈伤组织的比例为62.4%。转入添加0.7 mg?L -1 TDZ+0.5 mg?L -16-BA的WPM胚性愈伤组织诱导培养基中,诱导出36%的球状胚性愈伤组织。8周后球状胚性愈伤组织转入不定芽诱导培养,在含有WPM+2.0 mg?L-16-BA+0.5 mg?L-1 NAA的培养基中,增殖系数达12.54。当不定芽长到20 mm左右时,转接到生根培养基中进行生根诱导,诱导生根的最适培养基为1/2MS+0.5 mg?L-16-BA+0.5 mg?L-1 NAA+0.1 mg?L-1 IBA,生根率为85.2%。
Establishment of highly efifcient regeneration system of mangosteen (Garcinia mangostana)
This study established the system ofin vitro culture and multiplication of mangosteen (Garcinia mangostana) using explants from germinated seedlings. The results showed that after 6 weeks of culture inocu-lation, high percentage (62.4%) of nodular callus formations were established from aseptically leaf explants on WPM medium with 1.0 mg·L-1 GA3+1.0 mg·L-16-BA +0.5 mg·L-1 TDZ, and 36% globular callus formations were induced on WPM medium with 0.7 mg·L-1 TDZ+0.5 mg·L-1 6-BA. After 8 weeks of culture, the multipli-cation coefifcient of globular embryogenic callus reached 12.54 on WPM medium supplemented with 2.0 mg·L-1 6-BA and 0.5 mg?L-1 NAA. Subsequently, adventitious buds with 20 mm length were transferred to rooting me-dium for rooting culture. And the best medium for rooting was 1/2MS+0.5 mg?L-1 6-BA+0.5 mg?L-1 NAA+0.1 mg?L-1 IBA+1.0% AC, and the rooting rate was 85.2%.

Garcinia mangostananodular callusembryonic callusadventitious embryo

李敬阳、李艳霞、林妃、许奕、黄东梅、唐粉玲、李羽佳、金志强

展开 >

华中农业大学植物科学技术学院,武汉430070

中国热带农业科学院海口实验站,海口570102

山竹 结节愈伤组织 胚性愈伤组织 不定胚

资助海南省科技厅重点研发计划中国热带农业科学院海口实验站科研专项经费

ZDYF2016054HKZKY140101

2016

植物生理学报
中国植物生理学会,中国科学院上海生命科学研究院植物生理生态研究所

植物生理学报

CSTPCDCSCD北大核心
影响因子:1.532
ISSN:2095-1108
年,卷(期):2016.52(9)
  • 1