XIAO Wang,TU Hong-yan,DENG Chong-hui.Establishment of Embryogenic Cell Suspension and Protoplast Culture of Hedychium coccineum[J].Northern Horticulture,2015,39(05):104-108.[doi:10.11937/bfyy.201505032]
红姜花胚性细胞悬浮体系的建立和原生质体培养
- Title:
- Establishment of Embryogenic Cell Suspension and Protoplast Culture of Hedychium coccineum
- 文献标志码:
- A
- 摘要:
- 以红姜花(Hedychium coccineum)未成熟花丝和花药为试材,研究了红姜花胚性愈伤组织的诱导、细胞悬浮体系的建立以及原生质体的培养。结果表明:在MS+4 mg/L 2,4-D+4 mg/L NAA+1 mg/L 6-BA+30 g/L 蔗糖+7 g/L 琼脂上经过120 d培养诱导出了愈伤组织,愈伤组织在增殖培养基上经过继代筛选获得浅黄色、松散易碎的胚性愈伤组织。胚性愈伤组织通过3个月的悬浮培养,得到均质稳定的胚性细胞悬浮系。以胚性悬浮细胞 (ECS) 为起始材料分离原生质体,酶解试验表明,在原生质体分离过程中,用于原生质体分离的酶液需要保持一定的渗透压以保护原生质体不被破坏。当甘露醇的浓度为0.14 mol/L 时,原生质体产量最高,达到2.25×105个/mL PCV ECS (packed cell volume,PCV)。在看护培养系统中,原生质体经过7 d 的培养,细胞第一次分裂,经过14 d培养,细胞分裂频率达到12.3%,28 d时,细胞团形成频率达到4.2%。所形成的细胞团具有典型的胚性细胞特征。
- Abstract:
- Embryogenci cell suspensions were established for the ornamental ginger Hedychium coccineum using filaments and anthers.Embryagenic indction,cell suspension culture system establishment and protolast culture of Hedychium coccineum were studied.The results showed that,after culture for 120 days,calli were induced on induced medium (Murashige and Skoog (MS) basal medium supplemented with 4 mg/L 2,4-D+4 mg/L NAA+1 mg/L 6-BA+30 g/L sucrose+7 g/L agar).The calli were then transferred on proliferated medium (MS basal medium+1 mg/L 2,4-D+0.25 mg/L NAA+0.25 mg/L 6-BA)and light yellow and friable embryogenic callus were obtained.These embryogenic callus were suspended in liquid medium,and after 3 months culture,a homogeneous and stable embryogenic cell suspension (ECS),composed of small cell aggregates,was established.Viable protoplasts were isolated from ECS in a enzyme mixture of 3.0% (w/v) cellulose R-10,2% (w/v) macerozyme R-10 and 0.25% (w/v) pectinase Y-23 for 7 hours,enzyme solution with 0.14 mol/L manntitol resulted in the highest yield of 2.25×105 protoplasts per mL PCV ECS.Feeder layer culture systems were used for protoplast culture.Frequency of cell division at 14 days and colony formation at 28 days were 12.3% and 4.2% respectively.However,all protoplast-derived cell colonies could not develop further.
参考文献/References:
[1] 高江云,盛春玲,杨淑霞.红姜花(姜科)同步大量开花的适应意义[J].生物多样性,2012,20(3):376-385. [2] 涂红艳,肖望,邓崇会.红姜花体细胞胚胎发生及植株再生的研究[J].园艺学报,2014,41(10):2139-2146. [3] Murashige T,Skoog F.A revised medium for rapid growth and bioassays with tobacco tissue cultures[J].Physiology Plantarum,1962,5:473-497. [4] Gamborg O L,Miller R A,Ojima K.Nutrient requirements of suspension cultures of soybean root cells[J].Experimental Cell Research,1968,50:151-158. [5] 李浚明.植物组织培养教程[M].2版.北京:中国农业大学出版社,2002:59-102. [6] Xiao W,Huang X L,Huang X,et al.Plant regeneration from protoplasts of Musa acuminata cv.Mas (AA) via somatic embryogenesis[J].Plant Cell Tissue Organ Culture,2007,90:191-200. [7] Patnaik G,Wilson D,Cooking E C.Importance of enzyme purification for increased plating efficiency and plant regeneration from single protoplasts of Petunia parodii.Z[J].Pflanzenphysiol,1981,102:199-205. [8] Tegeder M,Gebhardt D,Schieder O,et al.Thidiazuron induced plant regeneration from protoplast of Vicia faba cv.Mythos[J].Plant Cell Reports,1995,15:164-169. [9] Kreuger M,Van Holst J G.Arabinogalactan proteins are essential in somatic embryogenesis of Daucus carota L [J].Planta,1993,189:243-248. [10]Egertsdotter U,Von Arnold S.Importance of arabinogalactan proteins for the development of somatic embryos of Norway spruce (Picea abies) [J].Physiology Plantarum,1995,93:334-345. [11]Letarte J,Simion E,Miner M,et al.Arabinogalactans and arabinogalactan-protein induce embryogenesis in wheat (Triticum aestivum L.) microspore culture[J].Plant Cell Reports,2006,24:691-698.
备注/Memo
第一作者简介:肖望(1970-),女,博士,教授,现主要从事姜科植物生物技术研究和植物生理学教学工作。E-mail:exiao7379@sina.com. 基金项目:广东省自然科学基金博士启动资助项目(10451030301004286);广东省高等院校学科与专业建设专项资金资助项目(2013KJCX0137);广州市科技计划资助项目(2014J4100151)。