CAJ | 학술논문

[目的]该研究以紫茉莉（Mirabilis jalapaL.）为供试植物,建立愈伤组织诱导及继代培养体系,为后期的细胞悬浮培养奠定基础。[方法]以MS为基础培养基,加入不同浓度的6-BA、2,4-D、NAA、KT,设计L16（44）正交试验。[结果]得出最佳愈伤组织诱导组合为：6-BA 0 mg/L＋2,4-D 1 mg/L＋NAA 1 mg/L＋KT 1.5 mg/L,以附加2,4-D 1 mg/L＋KT 0.5 mg/L的继代培养基上生长的愈伤组织适合细胞悬浮培养。[结论]筛选出适合紫茉莉愈伤组织培养的激素条件,可为紫茉莉组培相关研究奠定基础。
[목적]해연구이자말리（Mirabilis jalapaL.）위공시식물,건립유상조직유도급계대배양체계,위후기적세포현부배양전정기출。[방법]이MS위기출배양기,가입불동농도적6-BA、2,4-D、NAA、KT,설계L16（44）정교시험。[결과]득출최가유상조직유도조합위：6-BA 0 mg/L＋2,4-D 1 mg/L＋NAA 1 mg/L＋KT 1.5 mg/L,이부가2,4-D 1 mg/L＋KT 0.5 mg/L적계대배양기상생장적유상조직괄합세포현부배양。[결론]사선출괄합자말리유상조직배양적격소조건,가위자말리조배상관연구전정기출。
[Objective] Mimbilis jalapa L. was used as the test plant to establish the system of callus induction and subculture for cell suspension culture.[Method] The experiment was designed L16,（44） orthogonal test by adding different type and coneentration of plant gruwth regulating substances,6-BA. 2.4-D.NAA,KT based on MS culture medium. [Resultl The results showed that the appropriate medium tot callus induetion is： 6-BA 0 mg/L ＋2,4-D 1 mg/L ＋ NAA 1 mg/L ＋ KT 1.5 mg/L.Based on the conclusion.the callus growing on the subculture medium with 2,4-D 1 lng/L ＋ KT 0.5 mg/L was better for （;ell suspension culture. [Conclusion] The suitable hormone level fur Mi,-at,ilis jalapa L callus induction was screened out.These could provide basis for related researches.