吉林林业科技
吉林林業科技
길림임업과기
JILIN FORESTRY SCICNCE AND TECHNOLOGY
2014年
6期
8-10,13
,共4页
李金英%赵春莉%谭莎%段加红
李金英%趙春莉%譚莎%段加紅
리금영%조춘리%담사%단가홍
蓝靛果忍冬%继代增殖%生根培养
藍靛果忍鼕%繼代增殖%生根培養
람전과인동%계대증식%생근배양
Lonicera edulis Turcz%Subculture multiplication%Rooting culture
以野生蓝靛果忍冬组培苗为材料进行继代增殖和生根培养研究，结果表明：继代增殖最适培养基为MS＋BA2．0 mg? L-1＋IBA0．2 mg? L-1＋GA30．3 mg? L-1，增殖系数为5．5；适宜的生根培养基为1/2MS＋IBA1．0 mg? L-1，生根率达到100％。
以野生藍靛果忍鼕組培苗為材料進行繼代增殖和生根培養研究，結果錶明：繼代增殖最適培養基為MS＋BA2．0 mg? L-1＋IBA0．2 mg? L-1＋GA30．3 mg? L-1，增殖繫數為5．5；適宜的生根培養基為1/2MS＋IBA1．0 mg? L-1，生根率達到100％。
이야생람전과인동조배묘위재료진행계대증식화생근배양연구，결과표명：계대증식최괄배양기위MS＋BA2．0 mg? L-1＋IBA0．2 mg? L-1＋GA30．3 mg? L-1，증식계수위5．5；괄의적생근배양기위1/2MS＋IBA1．0 mg? L-1，생근솔체도100％。
The subculture multiplication and rooting culture study was carried on wild Lonicera edulis Turcz tissue culture seedling.The result showed that the proper culture medium for subculture multiplication was MS +BA2.0 mg? L-1 +IBA0.2 mg? L-1 +GA30.3 mg? L-1 .The multiplication factor was 5.5.Moreover, the proper rooting culture was 1/2MS+IBA1.0 mg? L-1 .The rooting ratio was 100%.
