详细信息

麻花秦艽休眠芽的玻璃化超低温保存及植株再生    

Cryopreservation and Plantlet Regeneration of Dormant Buds of Gentiana straminea by Vitrification

文献类型:期刊文献

中文题名:麻花秦艽休眠芽的玻璃化超低温保存及植株再生

英文题名:Cryopreservation and Plantlet Regeneration of Dormant Buds of Gentiana straminea by Vitrification

作者:晋玲[1];刘进[1];张延红[1];朱田田[1];陈红刚[1]

第一作者:晋玲

机构:[1]甘肃中医学院药学系,甘肃兰州730000

第一机构:甘肃中医药大学药学院(西北中藏药协同创新中心办公室)

年份:2012

卷号:35

期号:9

起止页码:1374

中文期刊名:中药材

外文期刊名:Journal of Chinese Medicinal Materials

收录:MEDLINE(收录号:23451488);CSTPCD;;Scopus(收录号:2-s2.0-84883867428);北大核心:【北大核心2011】;CSCD:【CSCD2011_2012】;PubMed;

基金:甘肃省中医药管理局项目(GZK-2010-Z2);国家中医药管理局项目(04-C52L23)

语种:中文

中文关键词:麻花秦艽;休眠芽;超低温保存;玻璃化法

外文关键词:Gentiana straminea Maxim. ; Dormant buds; Cryopreservation; Vitrification method

摘要:目的:采用玻璃化超低温技术保存濒危药用植物麻花秦艽的休眠芽。方法:以休眠芽作试材,研究休眠芽大小、不同的预处理方法、装载时间和玻璃化保护液等因素对休眠芽超低温保存效果的影响。结果:10~11 mm大小的休眠芽在含有0.3 mol/L、0.5 mol/L、0.7 mol/L蔗糖的MS培养基中暗培养各1 d,在装载液(2 mol/L甘油+0.4 mol/L蔗糖)中20℃处理20 min,于玻璃化保护液PVS2(30%甘油+15%乙二醇+15%二甲基亚砜+0.4mol/L蔗糖)中0℃处理40 min,换新鲜PVS2保护液并迅速投入液氮,液氮中保存24 h后,在40℃水浴中解冻2~3 min,用含1.2 mol/L蔗糖的1/2MS无机盐液体培养基洗涤2次,每次10 min,无菌滤纸吸干后接种到恢复培养基中,在22℃条件下暗培养1周后转入正常条件培养,再生率高达83.3%。结论:建立了高效的麻花秦艽休眠芽玻璃化超低温保存技术体系。
Objective: To investigate the detailed techniques for cryopreservation of Gentiana straminea dormant buds by vitrifica- tion. Methods : Dormant buds as an experimental material, the influence of the different size of dormant buds, preeuhure and PVS etc. on eryopreservation of C, entiana straminea were studied. Results: The optimal procedures were as follows: 10 - 11 mm long dormant buds which were cultured on MS medium supplemented with different sucrose concentration (0. 3,0. 5 or 0. 7 tool/L) for 1 day respective- ly. The buds were immersed in loading solution for 20 rain at 20 ~C, and then treated in PVS2 solution for 40 rain at 0 ~C and finally plunged into liquid nitrogen quickly. After 24 hours, the buds were rapidly thawed in a water bath at 40 ~C for 2 ~ 3 min and washed twice with MS medium supplemented with 1/2 MS liquid medium containing 1.2 mol/L sucrose. Finally the buds Were transferred to re- generation medium( MS + 0. 5 mg/L 6-BA + 0. lmg/L NAA + 3% sucrose + 0. 7% agar), the survival rate was up to 83.3%. Conclusion: A high-efficiency cryopreservation protocol of Gentiana straminea is set up.

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