热带亚热带植物学报
熱帶亞熱帶植物學報
열대아열대식물학보
JOURNAL OF TROPICAL AND SUBTROPICAL BOTANY
2014年
4期
406-412
,共7页
宋运贤%张强%杜雪玲%彭贺%唐润%张园园%陈耀锋
宋運賢%張彊%杜雪玲%彭賀%唐潤%張園園%陳耀鋒
송운현%장강%두설령%팽하%당윤%장완완%진요봉
马兜铃%茎段%TDZ%不定芽诱导%AgNO3
馬兜鈴%莖段%TDZ%不定芽誘導%AgNO3
마두령%경단%TDZ%불정아유도%AgNO3
Aristolochia debillis%Stem%TDZ%Adventitious bud induction%AgNO3
为建立马兜铃(Aristolochia debilis Sieb. et Zucc)不含腋芽茎段的不定芽诱导体系,采用正交设计方法研究植物生长调节剂、预培养方式和AgNO3对不定芽诱导的影响。结果表明:植物生长调节物质对不定芽诱导的影响以TDZ>6-BA>IAA,其中TDZ的影响极显著(P<0.01),6-BA的影响显著(P<0.05)。不定芽诱导的最适培养基为MS+0.5 mg L-1 TDZ+0.1 mg L-1 IAA+0.5 mg L-16-BA+2 mg L-1 AgNO3+3%蔗糖+0.6%琼脂(pH 5.8);预培养方式为在MS+0.1 mg L-12,4-D+3%蔗糖+0.6%琼脂培养基上暗培养2 d。马兜铃不含腋芽茎段的不定芽诱导率最高可达37.5%。
為建立馬兜鈴(Aristolochia debilis Sieb. et Zucc)不含腋芽莖段的不定芽誘導體繫,採用正交設計方法研究植物生長調節劑、預培養方式和AgNO3對不定芽誘導的影響。結果錶明:植物生長調節物質對不定芽誘導的影響以TDZ>6-BA>IAA,其中TDZ的影響極顯著(P<0.01),6-BA的影響顯著(P<0.05)。不定芽誘導的最適培養基為MS+0.5 mg L-1 TDZ+0.1 mg L-1 IAA+0.5 mg L-16-BA+2 mg L-1 AgNO3+3%蔗糖+0.6%瓊脂(pH 5.8);預培養方式為在MS+0.1 mg L-12,4-D+3%蔗糖+0.6%瓊脂培養基上暗培養2 d。馬兜鈴不含腋芽莖段的不定芽誘導率最高可達37.5%。
위건립마두령(Aristolochia debilis Sieb. et Zucc)불함액아경단적불정아유도체계,채용정교설계방법연구식물생장조절제、예배양방식화AgNO3대불정아유도적영향。결과표명:식물생장조절물질대불정아유도적영향이TDZ>6-BA>IAA,기중TDZ적영향겁현저(P<0.01),6-BA적영향현저(P<0.05)。불정아유도적최괄배양기위MS+0.5 mg L-1 TDZ+0.1 mg L-1 IAA+0.5 mg L-16-BA+2 mg L-1 AgNO3+3%자당+0.6%경지(pH 5.8);예배양방식위재MS+0.1 mg L-12,4-D+3%자당+0.6%경지배양기상암배양2 d。마두령불함액아경단적불정아유도솔최고가체37.5%。
In order to establish adventitious bud induction system from stem segments without axillary bud of Aristolochia debilis Sieb. et Zucc, the effects of plant growth regulators, pre-culture pattern and AgNO3 on the induction rate were studied by using orthogonal design method. The results showed that the effects of plant growth regulators on adventitious bud reduction from stems were in the order of TDZ>6-BA>IAA, in which TDZ and 6-BA had signiifcant inlfuence at 0.01 and 0.05 levels, respectively. The optimum medium for adventitious bud induction was MS+0.5 mg L-1 TDZ+0.1 mg L-1 IAA+0.5 mg L-1 6-BA+2.0 mg L-1 AgNO3+3%sucrose+0.6%agar (pH 5.8). After the explants were pre-cultured on MS+0.1 mg L-1 2,4-D+3%sucrose+0.6%agar (pH 5.8) in dark for 2 days, and then transferred on adventitious bud induction medium, the rate of adventitious bud induction could reach to 37.5%.