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作 者:毕海林[1,2] 木永青 郭淼 和加卫[1] 王朝文[1] 和志娇[1] 杨燕林[1] 杨正松[1,2] BI Hai-lin;MU Yong-qing;GUO Miao;HE Jia-wei;WANG Chao-wen;HE Zhi-jiao;YANG Yan-lin;YANG Zheng-song(Alpine Economic Plant Research Institute,Yunnan Academy of Agricultural Sciences,Lijiang 674199,China;LijiangLanma Biotechnology Development Limited Company in Yunnan Province,Lijiang 674100,China)
机构地区:[1]云南省农业科学院高山经济植物研究所,云南丽江674199 [2]丽江蓝玛生物科技开发有限责任公司,云南丽江674100
出 处:《江西农业学报》2023年第3期51-55,共5页Acta Agriculturae Jiangxi
基 金:云南省技术创新人才项目(2019HB092);云南省基础研究计划项目“滇西北重要野生植物种质资源发掘利用”(202101BC 070003);高山农业科技创新及成果展示转化专项(530000210000000017045)。
摘 要:以吉塞拉6号带腋芽茎段为外植体,对大樱桃矮化砧木吉塞拉6号进行了组织培养和快速繁殖技术研究。结果表明,较佳的启动培养基:MS+0.5 mg/L 6-BA+0.2 mg/L NAA,较佳的增殖培养基:MS+1.0 mg/L 6-BA+0.2 mg/L NAA;较佳的生根培养基:1/2 MS+0.5 mg/L IBA+2.0 g/L AC。生根培养第13天进行试管苗炼苗,第20天进行移栽,移栽后的成活率较高,分别为最佳的生根诱导和移栽时间;粉碎苔藓是吉塞拉6号较好的瓶外生根基质。The stem segment with axillary buds of Gisela 6 was used as explants,and the tissue culture and rapid propagation techniques of Sweet Cherry Dwarf Rootstock Gisela 6 were studied.The results showed that the better initiating medium was MS+0.5 mg/L 6-BA+0.2 mg/L NAA,and the better proliferative medium was MS+1.0 mg/L 6-BA+0.2 mg/L NAA.The better rooting medium was 1/2 MS+0.5 mg/L IBA+2.0 g/L AC.On the 13th day for rooting culture and on the 20th day for transplanting,the high survival rate was achieved after transplanting,which was the optimal time for root induction and transplanting time.Smash moss was better rooting substrate for Gisela 6 outside the bottle.
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