Please wait a minute...

中国生物工程杂志

CHINA BIOTECHNOLOGY
中国生物工程杂志  2012, Vol. 32 Issue (11): 49-54    
研究报告     
三叶半夏(Pinelliaternata (Thunb.) Breit)的间歇浸没培养
贾明良1,2, 张本厚2, 高伟平2, 陈集双1,2, 欧阳平凯1
1. 南京工业大学生物资源工程研究所 南京 210009;
2. 南京工业大学大丰海洋产业研究院 大丰 224145
Micropropagation of Pinellia Ternata (Thunb.) Breit in a Bioreactor Using Temporary Immersion System
JIA Ming-liang1,2, ZHANG Ben-hou2, GAO Wei-ping2, CHEN Ji-shuang1,2, OUYANG Ping-kai1
1. Institute of Bioresourse Engineering, Nanjing University of Technology, Nanjing 210009, China;
2. Dafeng Marine Industrial Institute, Nanjing University of Technology, Dafeng 224145, China
 全文: PDF(810 KB)   HTML
摘要: 目的:利用间歇浸没培养反应器对药用植物三叶半夏(Pinellia ternata (Thunb.) Breit)进行组培快繁研究。方法:以增殖倍数、鲜重、平均鲜重、折干率和组培苗状态为指标,一方面对三叶半夏叶片、叶柄及丛生芽体进行培养,考察适合间歇浸没培养的外植体类型;另一方面以叶柄为外植体对三叶半夏进行间歇浸没培养、固体培养和液体摇瓶培养,考察三种培养方式对其生长的影响。结果:不同的外植体在反应器内培养时,从增殖情况来看,丛生芽作为外植体得到的增殖倍数高达39.15,叶柄为27.65,叶片为18.05。鲜重方面与增殖倍数具有相同的规律。从平均鲜重和折干率来看,无显著差异。由组培苗形态来看,以叶柄诱导的组培苗最为健壮,而以丛生芽诱导的组培苗则较为细弱。不同培养方式下的增殖倍数分别为:间歇浸没培养方式最高为24.73,其次固体培养为14.75,液体摇瓶培养为12.26,差异显著。平均鲜重和折干率均为间歇浸没培养最优。由组培苗形态来看固体培养优于间歇浸没培养,反应器得到的组培苗较为细弱。在保卫细胞长宽和叶绿体个数上两者没有显著性差异。而液体摇瓶培养玻璃化导致叶绿体个数减少,不适合培养三叶半夏的。结论:较适合间歇浸没培养的外植体类型为叶柄和丛生芽,以叶柄为优。间歇浸没培养方式相对于传统的固体和液体培养在各项生理指标上表现较好,具有大规模培养三叶半夏的潜力。
关键词: 三叶半夏生物反应器间歇浸没培养植物组织培养    
Abstract: Objactive: To improve a new system for micropropagation of Pinellia ternata (Thunb.) Breit. in a temporary immersion bioreactor. Methods: Average number of tubers per plantlet (NTPs), Fresh weight (FW), Average fresh weight per plantlet (FWPs), Dry weight/Fresh weight (DW/FW) and the status of plantlet were studied refering standards. Firstly, leaves, petioles and cluster buds were cultured to establish the best explants type in the temporary immersion system. Secondly, petioles were cultured in the temporary immersion system, solid and liquid culture methods to compare the training effect. Results: Different types of explants were cultured in this temporary immersion system. Highest NTPs of 39.15 was achieved by culturing cluster bud. The petiole was 27.65 and the leaf was 18.05. Fresh weight has the same rule with NTPs. FWPs and DW/FW both have no significant differences. The plantlets induced by petioles were the most robust and which were more in thin induced by cluster buds. NTPs induced by petioles were achieved by different culture methods were as follows: temporary immersion system was 24.73, solid culture method was 14.75 and liquid culture method was 12.26. FWPs and DW/FW of temporary immersion system were optimal. The solid method and temporary immersion system were the suitable culturing methods for. The status of plantlets cultured by solid method was better than temporary immersion system. And the plantlets of temporary immersion system were thinner. Length of stoma guard cell (LSGC), Width of stoma guard cell (WSGC) and Average number of chloroplast per stoma guard cell (NCPs) have no significant difference between the two methods. The vitrification of plantlets cultured by liquid method has less number of chloroplasts, so the liquid method was not suitable for cultivation of Pinellia ternata (Thunb.) Breit. Conclusion: Petioles and cluster buds are suitable for the temporary immersion culture, and the petiole is better. Compared with conventional solid and liquid culture, temporary immersion culture system behaved as the best in various physiological indexes and that this system has the potential of large-scale micropropagation for this medicinal plant.
Key words: Pinellia ternata (Thunb.)    Breit    Bioreactor    Temporary immersion system    Plant tissue culture
收稿日期: 2012-09-19 出版日期: 2012-11-25
ZTFLH:  Q819  
基金资助: 江苏省高层次创新创业人才引进计划资助项目(51207204)
通讯作者: 陈集双,电子信箱:biochenjs@njut.edu.cn     E-mail: biochenjs@njut.edu.cn
服务  
把本文推荐给朋友
加入引用管理器
E-mail Alert
RSS
作者相关文章  
贾明良
张本厚
高伟平
陈集双
欧阳平凯

引用本文:

贾明良, 张本厚, 高伟平, 陈集双, 欧阳平凯. 三叶半夏(Pinelliaternata (Thunb.) Breit)的间歇浸没培养[J]. 中国生物工程杂志, 2012, 32(11): 49-54.

JIA Ming-liang, ZHANG Ben-hou, GAO Wei-ping, CHEN Ji-shuang, OUYANG Ping-kai. Micropropagation of Pinellia Ternata (Thunb.) Breit in a Bioreactor Using Temporary Immersion System. China Biotechnology, 2012, 32(11): 49-54.

链接本文:

https://manu60.magtech.com.cn/biotech/CN/        https://manu60.magtech.com.cn/biotech/CN/Y2012/V32/I11/49

[1] 国家药典委员会. 中华人民共和国药典2010年版. 北京: 中国医药科技出版社, 2010. 110-112. Pharmacopoeia Commission of People's Republic of China. Pharmacopoeia of People's Republic of China 2010. Beijing: China medical science and technology press, 2010. 110-112.
[2] 吴伯骥,肖亮,覃章铮. 从三叶半夏(Pinellia ternata (Thunb.)Breit.) 叶肉原生质体再生植株. 中国科学(B辑), 1986,3(3):267-271. Wu B J,Xiao L,Qin Z Z. Mesophyll protoplast culture and plant regeneration of Pinellia ternata (Thunb.)Breit. Since China(B), 1986,3(3):267-271.
[3] 罗成科,彭正松,蔡鹏. 三叶半夏叶片一步成苗离体培养技术. 广西植物, 2007(2):260-264. Luo C K,Peng ZH S,Cai P. In-vitro regeneration of PinellIa ternata from leaf explants.Guihaia, 2007(2):260-264.
[4] 赵望锋,王力华.间歇浸没式生物反应器在大规模组织培养中的应用研究.安徽农业科学, 2007,35(2):317-320,323. Zhao W F,Wang L H,Study on temporary immersion in bioreactor in tissue culture.Journal of Anhui Agrisci, 2007,35(2):317-320,323.
[5] Etienne H, Berthouly M. Temporary immersion systems in plant micropropagation. Plant Cell, Tissue and Organ Culture, 2002,69(3):215-231.
[6] 杨柳,秦钢,杨丽涛,等.利用间歇浸没式生物反应器进行果蔗组培快繁.热带作物学报,2010,31(4):614-620. Yang L,Qin G,Yang L T,et al. Optimization of saccharum sinensis roxb rapid multiplication in temporary immersion bioreactors system. Chinese Journal of Tropical Crops, 2010,31(4):614-620.
[7] Yan H B, Yang L T, Li Y R.Axillary shoot proliferation and tuberization of Dioscorea fordii Prain et Burk. Plant Cell, Tissue and Organ Culture, 2011,104(2):193-198.
[8] Yan H B, Yang L T, Li Y R. Improved growth and quality of Siraitia grosvenorii plantlets using a temporary immersion system. Plant Cell, Tissue and Organ Culture, 2010,103(1):131-135.
[9] 贾明良,陈集双,覃佐东.间歇浸没植物组织器官的培养反应器:中国, ZL 200920116327.X.2010-03-10. Jia M L,Chen J S,Qin Z D. One kind of temporary immersion bioreactor in plant micropropagation: China, ZL 200920116327.X.2010-03-10.
[10] 陈集双,郭巧萍.半夏多倍体植株的制备方法:中国, ZL101524050A.2012-05-16. Chen J S,Guo Q P. Preparation of ployploid plants pinellia: China, ZL101524050A.2012-05-16.
[11] 张苏锋,谢素霞.半夏组织培养快速繁殖的研究. 信阳师范学院学报(自然科学版),1998,11(1):86-88. Zhang S F,Xie S X. Study on tissue culture and rap id propagat i on of pinellia ternata. Journal of Xinyang Teachers College (Natural Science Edition),1998,11(1):86-88.
[12] 何奕昆,刘刚,路铁刚,等. 半夏茎尖培养及块茎的品质改良.植物学报,1994,36(1):39-44. He Y k, Liu G, Lu T G, et al. Stem apex culture and quality improvement of tubercles ofpinellia ternata. Acta Bot anica Sinica,1994,36(1):39-44.
[1] 靳露,周航,曹云,王振守,曹荣月. 高通量灌流培养模型在生物工艺开发中的应用研究[J]. 中国生物工程杂志, 2020, 40(8): 63-73.
[2] 梁振鑫,刘芳,张玮,刘庆友,李力. 抗p185 erb B2人鼠嵌合抗体ChAb26转基因小鼠乳腺生物反应器的制备与验证 *[J]. 中国生物工程杂志, 2019, 39(8): 40-51.
[3] 郭玉蕾,唐亮,孙瑞强,李尤,陈依军. 高通量微型生物反应器的研究进展[J]. 中国生物工程杂志, 2018, 38(8): 69-75.
[4] 李亚芳,赵颖慧,刘赛宝,王伟,曾为俊,王金泉,陈洪岩,孟庆文. 鸡OV启动子表达HA对禽流感病毒攻击提供完全保护 *[J]. 中国生物工程杂志, 2018, 38(7): 67-74.
[5] 孙静静,周伟伟,周雷鸣,赵巧辉,李桂林. 杂交瘤细胞体外大规模培养研究进展[J]. 中国生物工程杂志, 2018, 38(10): 82-89.
[6] 苏晓蕊, 李伟国, 王延辉, 高晓静, 闪伊红, 谭菲菲, 李向东, 田克恭. 重组杆状病毒细小VP2蛋白40L生物反应器放大工艺研究[J]. 中国生物工程杂志, 2017, 37(10): 60-64.
[7] 林优红, 程霞英, 严依雯, 梁宗锁, 杨宗岐. 衣藻叶绿体表达重组蛋白及表达优化策略[J]. 中国生物工程杂志, 2017, 37(10): 118-125.
[8] 刘婷婷, 梁梓强, 梁士可, 郭技星, 王方海. 利用生物工程技术生产蜘蛛丝的研究进展[J]. 中国生物工程杂志, 2016, 36(5): 132-137.
[9] 赵绘存. 基于专利信息可视化的生物反应器发展态势分析[J]. 中国生物工程杂志, 2016, 36(1): 115-121.
[10] 张丹凤, 余自青, 吴锁伟, 饶力群, 万向元. 植物生物反应器在分子医药农业中的应用[J]. 中国生物工程杂志, 2016, 36(1): 86-94.
[11] 申斓, 周爱东, 吴小芹. 植物细胞培养生物反应器的种类特点及展望[J]. 中国生物工程杂志, 2015, 35(8): 109-115.
[12] 梁振鑫, 尹富强, 刘庆友, 李力. 转基因动物乳腺生物反应器相关技术及研究进展[J]. 中国生物工程杂志, 2015, 35(2): 92-98.
[13] 张斯敏, 高越, 方彧聃, 张金脉, 张敬之. 乳腺生物反应器特异高效表达载体的构建[J]. 中国生物工程杂志, 2014, 34(7): 49-55.
[14] 林美玲, 唐寅, 张明, 易小萍, 黄明志. 重组HSV-Ⅱ病毒疫苗的微载体悬浮培养生产工艺研究[J]. 中国生物工程杂志, 2014, 34(3): 68-78.
[15] 雷学青, 卢哲, 高保燕, 张文源, 李爱芬, 张成武. 利用平板反应器大量培养高产油绿藻——尖状栅藻的生长和油脂积累规律[J]. 中国生物工程杂志, 2014, 34(11): 91-99.