生命科学仪器
生命科學儀器
생명과학의기
LIFE SCIENCES INSTRUMENT
2011年
3期
48-50
,共3页
张波%李军立%李玉锋%何洋%刘震东%谢紫莹
張波%李軍立%李玉鋒%何洋%劉震東%謝紫瑩
장파%리군립%리옥봉%하양%류진동%사자형
暗紫贝母%鳞茎%外植体%愈伤组织%不定芽%诱导率
暗紫貝母%鱗莖%外植體%愈傷組織%不定芽%誘導率
암자패모%린경%외식체%유상조직%불정아%유도솔
F.unibracteata%bulblet%explant%callus%adventitious bud%induction rate
目的:对暗紫贝母愈伤组织和不定芽诱导进行研究。方法:以暗紫贝母新鲜鳞茎为外植体,在附加NAA和6-BA不同浓度配比的MS培养基上进行离体培养。结果:鲜鳞茎能诱导形成愈伤组织和不定芽。其中,NAA1.2mg/L+6-BA1.8mg/L的MS培养基中外植体愈伤组织诱导率最高,达53.3%;NAA1.2mg/L+6-BA1.6mg/L的MS培养基中外植体不定芽诱导率最高,达73.3%。结论:建立了暗紫贝母愈伤组织和不定芽诱导的培养方法。
目的:對暗紫貝母愈傷組織和不定芽誘導進行研究。方法:以暗紫貝母新鮮鱗莖為外植體,在附加NAA和6-BA不同濃度配比的MS培養基上進行離體培養。結果:鮮鱗莖能誘導形成愈傷組織和不定芽。其中,NAA1.2mg/L+6-BA1.8mg/L的MS培養基中外植體愈傷組織誘導率最高,達53.3%;NAA1.2mg/L+6-BA1.6mg/L的MS培養基中外植體不定芽誘導率最高,達73.3%。結論:建立瞭暗紫貝母愈傷組織和不定芽誘導的培養方法。
목적:대암자패모유상조직화불정아유도진행연구。방법:이암자패모신선린경위외식체,재부가NAA화6-BA불동농도배비적MS배양기상진행리체배양。결과:선린경능유도형성유상조직화불정아。기중,NAA1.2mg/L+6-BA1.8mg/L적MS배양기중외식체유상조직유도솔최고,체53.3%;NAA1.2mg/L+6-BA1.6mg/L적MS배양기중외식체불정아유도솔최고,체73.3%。결론:건립료암자패모유상조직화불정아유도적배양방법。
Objictive: Study on the induction of callus and adventitious buds from F.unibracteata. Methods: Explants from the fresh bulb-scale sections of F.unibracteata were in-vitro cultured using Murashige and Skoog (MS) medium supplemented with different ratios concentration of NAA and 6-BA. Results: The fresh bulb-scale sections could be induced to the callus and adventitious buds. The callus induction rate of the explants in MS medium with NAA(1.2 mg/L) and 6-BA(1.8 mg/L) was the highest, reaching 53.3%. The adventitious buds induction rate of the explants in MS medium with NAA(1.2 mg/L) and 6-BA(1.6 mg/L) was the highest, reaching 73.3%. Conclusion: Th is study established the culture methods of callus and adventitious buds from F.unibracteata.