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珙桐体细胞胚胎发生技术研究OA北大核心CSTPCD

Somatic Embryogenesis in Davidia involucrata

中文摘要英文摘要

研究探讨基本培养基类型对珙桐愈伤组织诱导的影响、植物生长调节剂对胚性愈伤组织诱导及体胚发育的影响,初步建立以未成熟合子胚为外植体,通过体细胞胚胎发生途径再生珙桐植株的培养方案.结果表明,在含有3%蔗糖、0.3%凝胶、800 mg/L水解酪蛋白、400 mg/L L-谷氨酰胺的MS、1/2MS和 WPM基本培养基上均可诱导出愈伤组织,以MS+2.0 mg/L 2,4-D+0.5 mg/L 6-BA诱导率最高,可达94.0%;胚性愈伤组织在MS+0.5 mg/L NAA+1.0 mg/L 6-BA的培养基上诱导效果较好;在MS+0.5 mg/L NAA+1.0 mg/L 6-BA培养基上,体胚诱导率可达22.9%;成熟体胚在1/2MS+0.5 mg/L 6-BA+0.25 mg/L IBA的萌发培养基上能正常萌发,其后在添加1 g/L活性炭的萌发培养基上转化成完整小植株.组织细胞学观察表明,珙桐体胚起源于胚性愈伤组织,经历了球形期、心形期、鱼雷期和子叶期发育阶段,这与 自然条件下的合子胚形成过程相似.

The effects of basic medium types on the callus induction of Davidia involucrata and plant growth regulators on embryogenic callus induction and somatic embryo development were studied.A cul-ture scheme for the regeneration of D.involucrata plants by somatic embryogenesis with immature zygotic embryos as explants was preliminarily established.The results showed that callus could be induced on MS,1/2MS and WPM basic media containing 3%sucrose,0.3%gel,800 mg/L hydrolyzed casein,400 mg/L L-glutamine,and MS+2.0 mg/L 2,4-D+0.5 mg/L 6-BA had the highest induction rate of 94.0%.The em-bryogenic callus was induced on MS+0.5 mg/L NAA+1.0 mg/L 6-BA medium.On MS+0.5 mg/L NAA+1.0 mg/L 6-BA medium,the induction rate of somatic embryos reached 22.9%.Mature somatic embryos could germinate normally on the germination medium of 1/2MS+0.5 mg/L 6-BA+0.25 mg/L IBA,and then transformed into complete plantlets on the germination medium supplemented with 1 g/L activated carbon.Histocytological observation showed that the somatic embryos originated from embryo-genic callus and underwent the development stages of globular-,heart-,torpedo-and cotyledonary-stage,which was similar to the formation process of zygotic embryos under natural conditions.

令狐高曼;季晓莲;段榕怡;刘睿;戴钊;董嘉明;徐金颢;康永祥

西北农林科技大学林学院,陕西杨陵 712100杨凌职业技术学院,陕西杨陵 712100

林学

珙桐胚性愈伤组织体细胞胚植株再生组织细胞学

Davidia involucrataembryogenic callussomatic embryosplantlet regenerationhistocytology

《西北林学院学报》 2024 (002)

70-78 / 9

秦岭珍稀植物红豆杉、珙桐高效繁育技术研究与示范(SXLK2021-01-03).

10.3969/j.issn.1001-7461.2024.02.09

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