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广藿香毛状根多倍体诱导及其植株再生
引用本文:施和平,余武,张国鹏,曾宝强,周卓辉.广藿香毛状根多倍体诱导及其植株再生[J].生物工程学报,2014,30(8):1235-1246.
作者姓名:施和平  余武  张国鹏  曾宝强  周卓辉
作者单位:1 华南师范大学生命科学学院 广东省植物发育生物工程重点实验室,广东 广州 510631;1 华南师范大学生命科学学院 广东省植物发育生物工程重点实验室,广东 广州 510631;1 华南师范大学生命科学学院 广东省植物发育生物工程重点实验室,广东 广州 510631;2 香港教育学院科学与环境学系,香港 新界;2 香港教育学院科学与环境学系,香港 新界
基金项目:广东省科技计划项目 (No. 2008B020200005) 资助。
摘    要:为了提高药用植物广藿香的次生物质广藿香醇含量,采用秋水仙素人工诱导染色体加倍技术,进行了广藿香毛状根多倍体诱导及其植株再生、倍性鉴定和挥发油组分广藿香醇含量的测定。结果表明,广藿香毛状根多倍体诱导的最佳条件为0.05%秋水仙素处理36 h,其多倍体诱导率可达40%以上;经秋水仙素加倍的广藿香毛状根在MS+6-BA 0.2 mg/L+NAA 0.1 mg/L培养基中培养60 d后可获得毛状根多倍体再生植株。与对照(二倍体植株)相比,广藿香毛状根多倍体再生植株根系更发达、茎更粗、节间变短、叶片的长度、宽度和厚度均较二倍体明显增大。根尖细胞染色体压片观察证实,所获得的广藿香毛状根多倍体再生植株为四倍体,其根尖细胞染色体数约为128;同时,其叶片的气孔保卫细胞体积及其叶绿体数目均约为对照的两倍;但其气孔密度则随着倍性增加而下降,二倍体植株叶片的气孔密度约为四倍体植株叶片的1.67倍。GC-MS测定结果表明,广藿香毛状根多倍体再生植株的广藿香挥发油组分广藿香醇的含量为4.25 mg/g干重,约为二倍体植株的2.30倍。该结果证实毛状根多倍体化可提高药用植物广藿香的广藿香醇含量。

关 键 词:广藿香  秋水仙素  多倍体  再生植株
收稿时间:2013/10/22 0:00:00

Induction of polyploid hairy roots and its plant regeneration in Pogostemon cablin
Heping Shi,Wu Yu,Guopeng Zhang,Pokeung Eric Tsang and Cheuk Fai Stephen Chow.Induction of polyploid hairy roots and its plant regeneration in Pogostemon cablin[J].Chinese Journal of Biotechnology,2014,30(8):1235-1246.
Authors:Heping Shi  Wu Yu  Guopeng Zhang  Pokeung Eric Tsang and Cheuk Fai Stephen Chow
Institution:1 Guangdong Key Laboratory of Biotechnology for Plant Development, College of Life Science, South China Normal University, Guangzhou 510631, Guangdong, China;1 Guangdong Key Laboratory of Biotechnology for Plant Development, College of Life Science, South China Normal University, Guangzhou 510631, Guangdong, China;1 Guangdong Key Laboratory of Biotechnology for Plant Development, College of Life Science, South China Normal University, Guangzhou 510631, Guangdong, China;2 Department of Science and Environmental Studies, The Hong Kong Institute of Education, New Territories, Hong Kong, China;2 Department of Science and Environmental Studies, The Hong Kong Institute of Education, New Territories, Hong Kong, China
Abstract:In order to enhance the content of secondary metabolites patchouli alcohol in Pogostemon cablin, we induced polyploid hairy roots and their plant regeneration, and determined the content of patchouli alcohol through artificial chromosome doubling with colchicine. The highest rate of polyploidy induction was more than 40% when hairy roots were treated with 0.05% colchicine for 36 h. The obtained polyploid hairy roots formed adventitious shoots when cultured in an MS medium with 6-BA 0.2 mg/L and NAA 0.1 mg/L for 60 d. Compared with the control diploid plants, the polyploid hairy root-regenerated plants of P. cablin had more developed root systems, thicker stems, shorter internodes and longer, wider and thicker leaves. Observation of the chromosome number in their root tip cells reveals that the obtained polyploid regenerated plants were tetraploidy, with 128 (4n=128) chromosomes. The leaves contained around twice as many stomatal guard cells and chloroplasts as the controls, but the stomatal density declined with increasing ploidy. The stomatal density in diploid plants was around 1.67 times of that in polyploid plants. GC-MS analysis shows that the content of patchouli alcholol in the hairy root-derived polyploid plants was about 4.25 mg/g dry weight, which was 2.3 times of that in diploid plants. The present study demonstrates that polyploidization of hairy roots can stimulate the content of patchouli alcholol in medicinal plant of P. cablin.
Keywords:Pogostemon cablin (Blanco) Benth  colchicines  polyploidy  plant regeneration
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