不同基因型北五味子资源的鉴定及离体再生体系的建立
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
北五味子是我国东北地区珍贵的道地药材,在国内外市场深受消费者的青睐。随着对北五味子开发利用的不断深入,其原料的需求量也逐年增加,但由于北五味子的人工栽培起步较晚,育成的优良品系较少,植株间的生物学特性和品质差异较大,丰产稳产性极差,严重制约了北五味子栽培产业的发展。为了更好地发挥北五味子的资源优势,本研究对不同基因型北五味子资源的果实表型和木脂素含量进行了鉴定分析,从而为北五味子种质资源评价提供参考;为了进行良种繁育,本研究以具有优良果实性状的北五味子的休眠芽为材料,建立了北五味子具有遗传稳定性的体细胞胚途径植株再生系统,并在此基础上针对内源激素的动态变化对其发生过程中各个阶段所产生的影响进行较全面的研究。主要研究成果如下:
     1.综合比较11份北五味子样本果实大小、果穗鲜果重、干果重、果实干鲜比、果穗长、果实数目以及紧实度,结果表明不同样本的这些表型存在广泛变异,并且这些表型在不同年份间存在差异。三种颜色的北五味子果实中,粉果的平均鲜果重、干果重、干鲜比和紧实度均最大,红果果粒直径最大。筛选出表型较好的种源编号为B、D、E、G、P1和P2。
     2.通过多次试验条件的摸索,本研究确立了北五味子总木脂素的最佳高效检测体系:Symmetry(?)C18色谱柱(4.6mm×250mm,5μm),流动相为乙腈-水梯度洗脱:0~15min,40:60→50:50;15~20min,50:50→75:25;20~25min,75:25→95:5;流速0.5mL·min-1,检测波长254nm,柱温:35℃,进样量20μL。本试验可在同一色谱条件下,可同时测定五味子甲素、五味子乙素、五味子丙素、五味子醇甲、五味子醇乙、五味子酯甲等六种木脂素类成分的含量,方法简便,且精密度高,重现性好。
     3.以11份北五味子果实样本为试材,对其六种主要木脂素含量进行了测定。七份红色北五味子样品在2011、2012年间除了五味子甲素含量相对稳定以外,五味子乙素、五味子丙素、五味子醇甲、五味子醇乙和五味子酯甲的含量均存在较大差异并呈现出不规律的变化,七份红色北五味子果实之间木脂素含量也存在一定差异。不同颜色北五味子果实木脂素含量存在较显著差异,红色北五味子果实六种木脂素总含量最高,白色果实次之,粉色果实最低。红色北五味子果实富含五味子醇甲、五味子乙素和五味子丙素,而白色北五味子果实中五味子醇乙和五味子甲素较高,粉色北五味子果实中五味子酯甲含量的平均值高于白果W和红果。通过果实表型以及果实品质两方面相结合,北五味子样品B,D,E的果实性状较好,适宜进行育种。
     4.利用筛选到的4对SRAP引物组合对七种北五味子样本A~G进行PCR扩增,共产生22个位点,其中有13个多态性位点,总的位点多态性比率为59.09%,说明这七种北五味子具有不同的基因型。
     5.本研究采用固液培养相结合的培养方式建立了高效稳定的北五味子植株再生系统,结果表明不同基因型的北五味子休眠芽愈伤组织诱导率不同,北五味子休眠芽在MS+3.0mg·L-12,4-D+0.2mg·L-1TDZ培养基上愈伤组织诱导率较高;将愈伤组织置于MS+1.0mg·L-1TDZ+0.2mg·L-1ZT+50mg·L-1AgNO3培养基中适宜胚性愈伤组织的产生;对胚性愈伤组织进行细胞悬浮培养,当50mLl/2MS培养基接种3g胚性愈伤组织时有利于球形胚的形成,将所获得的球形胚转入1/2MS固体培养基培养,能较好的完成后期分化;1/2MS+0.2mg·L-1IBA培养基最有利于北五味子再生植株根部的形成,将根系发达的北五味子小植株进行移栽,其移栽成活率为90%。本研究利用筛选到的4对SRAP引物组合对七株北五味子母本及再生植株进行PCR扩增,其产物均没有产生特异性条带,这说明本研究建立的北五味子离体再生体系遗传稳定,可以应用于北五味子再生植株的大量生产。
     6.本研究对内源激素的动态变化对北五味子体细胞胚的发生和发育所产生的影响进行了研究,结果表明在几种不同类型的愈伤组织中,胚性愈伤组织内源IAA、ABA、GA3含量均为最高,这与其胚性能力相关。北五味子体细胞胚发育过程中,内源IAA含量在球形胚时期达到最大值,内源ABA含量在子叶形胚阶段较高,内源GA3含量最高点出现在心形胚阶段,与球形胚阶段无显著性差异。在北五味子畸形胚中,内源IAA和GA3含量均显著高于正常体细胞胚,而ABA含量则显著低于正常体细胞胚。经过0.2mg·L-1IBA处理后的生根再生植株中,内源IAA含量显著上升,ABA和GA3含量均显著下降。
Schisandra chinensis (Turcz.) Baill. is the precious Chinese drugs in northeast China which favored by consumers in domestic and overseas. With the deepening of the development and utilization of S. chinensis, the demand for raw materials also increased in recent years. However, because of late start for artificial cultivation, less fine improved varieties, biological characteristics and quality diversity among the plants and poor yield stability seriously restrict the cultivation industry development of S. chinensis. In order to better utilize the resource advantage of S. chinensis, this research also studies the fruit phenotype and main lignan content in fruit of different genotypes, which provides foundation for the germplasm resources evaluation of S. chinensis. To breed improved variety, this study established a stable and efficient plant regeneration system for S. chinensis with good fruit characters via somatic embryogenesis, and the dynamic changes of endogenous hormones at various stages in this process are researched comprehensively. The main research results are as follows:
     1. Comprehensive comparison for11samples of S. chinensis, the fruit phenotype were extensive variation including size, average fresh and dry weight of fruit, dry-fresh ratio, cluster length, number of fruits and fruits compactness, moreover, these fruit phenotype were instable between two years. The average fres hweight, dry weight, the dry-fresh ratio and the compactness were greater in pink fruits than that in red fruits and white fruits. The size of red fruits was larger. The fruit phenotypes of B, D, E, G, P1and P2were better.
     2. A Symmetry(?) C18column (4.6×250mm,5μm) was maintained at35℃. Detection wavelength was set at254nm, The mobile phase consisted of acetonitrile (A) and water (B) at a flow-rate of0.5mL·min-1. The gradient programme was as follows:0~15min,40:60→50:50;15~20min,50:50→75:25;20~25min,75:25→95:5; injection volume:20μ L. schisandrin, schisantherin A, deoxyschizandrin, γ-schissandrin, schisandrol B and schisandrin C could be detected at the same time. This method was simple, repeatability and precision.
     3. We determined the contents of six lignans in11samples of S. chinensis, the results showed that most of the lignan contents varied between two years except the contents of deoxyschizandrin were relatively stable. The total contents of lignans in fruits with different colors presented large differences, which was found highest in red fruits and lowest in pink fruits. High contents of schizandrol, γ-schizandrin and schisandrin C in red fruits were observed while white fruit was rich in schisandrol B and deoxyschizandrin. The contents of schisantherin A in pink fruits were higher than that in W and the average contents in red fruits. Considering the factors of phenotype and fruit quality, fruit character of samples B, D and E were good and suitable for breeding.
     4. This study used4pairs of SRAP primer for PCR amplification of seven samples of S. chinensis, which produced22amplification bands and13bands were polymorphism. The results showed that the genotypes of these seven samples of S. chinensis were difference.
     5. This research adopted the combination of solid and liquid cultivation for the establishment of stable and efficient plant regeneration system for S. chinensis. Different genotype influenced the callus induction rate of S. chinensis. The callus induction rate was highest when the sterilized dormant bud of S. chinensis cultured on MS+3.0mg·L-12,4-D+0.2mg·L-1TDZ. MS+1.0mg·L-1TDZ+0.2mg·L-1ZT+5.0mgL-1AgN_3was beneficial to embryonic callus induction.3g embryonic callus cultured in50mLl/2MS liquid medium was suitable for the formation of globular embryo.1/2MS+0.2mg·L-1IBA was most favorable for the roots formation of the regeneration plant of S. chinensi and the survival rate was90%after2months transplanting. This study used4pairs of SRAP primer for PCR amplification of seven S. chinensis female parent and the regeneration plant via somatic embryogenesis system, and there were no specific bands produced by four pairs of primers, suggesting that the plant regeneration system we established in this study was stable and reliable, which could be applied to mass production for plant regeneration of S. chinensis.
     6. The effect of dynamic changes of endogenous hormones on the formation and development of somatic embryos was studied.The contents of endogenous IAA, ABA and GA3related to the embryonic ability,which were highest in embryonic callus among several different types of callus of S. chinensis. During the development of somatic embryos of S. chinensis, the content of endogenous IAA peaked in globular embryo period and the content of endogenous ABA was higher in cotyledon embryo phase. In the whole process, the content of endogenous GA3peaked at heart shaped embryo stage, but no significant difference with the content in globular embryo stage. The contents of endogenous IAA and GA3were significantly higher in malformed embryo of S. chinensis than that in normal somatic embryo, but the content of ABA in malformed embryo were significantly lower than that in normal somatic embryo. The content of IAA was increased significantly when the contents of ABA and GA3declined in rooted plant treated with0.2mg·L-1IBA.
引文
1. 艾军,王英平,张庆田,王振兴,李昌禹.2011.五味子种质资源果实性状的种内变异研究.北方园艺,(13):179-182.
    2. 蔡小东,张金晶,林丽君.2010.‘冰糖橙’畸形胚状体的生理生化特性研究.中国农学通报,26(20):259-262.
    3. 曹孜义,刘国民.1999.实用植物组织培养技术教程.兰州:甘肃科学技术出饭社.
    4. 陈建军,郝瑞.1990.北五味子一个新变种的发现及研究.吉林农业大学学报,12(4):65-69.
    5. 陈建军,王东升,李亚东.1996.北五味子丰产栽培经验.中药材,19(9):437438.
    6. 陈金慧,施季森,诸葛强,黄敏仁.2003.杂交鹅掌楸体细胞发生研究.林业科学,39(4):49-53.
    7. 陈业高,秦国伟,谢旅元.2001.五味子科植物的木脂素成分.武汉植物学研所,19(2):158.
    8. 陈以峰,周燮,汤日圣,张金榆,梅传生.1998.水稻体细胞培养中胚性细胞出现与IAA的关系.植物学报,40(5):472-477.
    9. 陈泽雄,胡凯,刘奕清.2013.灰毡毛忍冬工厂化快繁生产体系的建立及再生苗遗传稳定性的分子鉴定.园艺学报,40(12):2520-2526.
    10.陈志林.2007.木薯种质超低温保存及其再生植株遗传稳定性的研究.华南热带农业大学硕士学位论文.
    11.崔澄,桂耀林.1985.经济植物组织培养与快速繁殖.北京:农业出版社,231-238.
    12.崔凯荣,戴若兰.2001.植物体细胞胚发生的分子生物学.北京:科学出版社.
    13.崔凯荣,裴新梧,秦琳,王君健,王亚馥.1998.ABA对构祀体细胞胚发生的调节作用.试验生物学报,31(2):195-199.
    14.崔凯荣,邢更生,周功克.2002.植物激素对体细胞胚胎发生的诱导与调节.遗传,22(5):349-354.
    15.邓瑞宁,王沫,李再云,蔡明历,刘焰.2008.荆半夏遗传多样性的SRAP分析.农业生物技术学报,16(6):1070-1071.
    16.丁佐.2011.不同果型北五味子的木脂素含量比较.沈阳农业大学硕士学位论文.
    17.杜克久,郑均宝,徐振华,李际泉,王进茂.1998.体细胞胚胎发生的组织学及生理学研究.林业科学,34(6):99-104.
    18.丰先红,李健,罗孝贵.2010.植物组织培养中体细胞无性系变异研究.中国农学通报,26(14):70-73.
    19.冯雪松,刘雅茹,孟繁浩,吴立军.2006.五味子药材HPLC指纹图谱的研究.化学与生物工程,23(5):60-62.
    20.逢增玲.2007.北五味子的栽培技术.人参研究,19:3.
    21.高述民.2001.ABA和PEG对胡萝卜体细胞胚诱导和调控的影响.西北农林科技大学学报,29(2):12-16.
    22.葛会奇.2006.辽宁不同产地五味子中五味子乙素的含量测定.辽宁科技学院学报,8(6):45-46.
    23.耿立超,杨中林.2007.HPLC法测定不同产地五味子中木脂素的含量.中医药学报,35(2):47-48.
    24.巩檑,杨亚珺,周坚.2011.中国石蒜组培苗体细胞无性系变异的ISSR和SRAP检测.北方园艺,22:108-112.
    25.谷凤平,周春娥,路淑霞,姚换灵,王芳,段红英,周延清.2009.怀地黄SRAP分子标记体系的建立与DNA指纹图谱的构建.河南师范大学学报(自然科学版),37(3):175-178.
    26.官艳丽,曹沛,郁开北,廖循.2006.北五味子化学成分的研究.中草药,37(2):185-187.
    27.桂耀林,顾淑荣,徐廷玉.1984.罗汉果叶组织培养中的器官发生.植物学报,26(2):120-125.
    28.郭子彪.1997.内源激素IAA,ABA对大豆萌发子叶胚性愈伤组织诱导及其分化的调控.大豆科学,16(3):192-198.
    29.韩碧文,李颖章.1993.植物组织培养中器官建成的生理生化基础.植物学通报,10(2):1-6.
    30.何盛莲,崔党群,陈军营,陈新建,雷振生,吴政卿,方保停.2006.小麦幼胚培养特性对外源物质响应的研究.西北农业学报,15(2):49-53.
    31.何业华,罗吉,吴会桃,王瑞霞,高爱平,赵春香,余小玲,叶自行,王泽槐,韩景忠,刘和平.2007.菠萝叶基愈伤组织诱导体细胞胚.果树学报,24(1):59-63.
    32.胡央杰,陈建真,叶磊.2008.南、北五味子的化学成分和鉴别方法研究进展.现代中药研究与实践,22(4):59-62.
    33.黄健秋,卫志明.1995.针叶树体细胞胚胎发生研究进展.植物生理学通讯,31(2):85-90.
    34.黄锦文,梁康迳,梁义元,林文雄.2003.不同类型水稻籽粒灌浆过程中内源激素含量变化的研究.中国农业生态学报,11(2):11-13.
    35.黄璐,卫志明.1999.不同基因型玉米的再生能力和配型与非胚性愈伤组织DNA的差异.植物生理学报,25:332-338.
    36.贾定洪,王波,彭卫红.2011.23个金针菇菌株的SRAP分析.西南农业学报,24(5):1871-1874.
    37.可成友,高珍,康宏玲,吴晓芳,金常雪.2007.北五味子植物化学成分及其活性的研究进展.辽宁农业科学,(3):56-57.
    38.孔冬梅,沈海龙,冯丹丹,张莉杰.2006.水曲柳体细胞胚与合子胚发生的细胞学研究.林业科学,42(12):130-133.
    39.孔冬梅,沈海龙.2008.植物组织培养中畸形胚的发生和控制.植物生理学通讯,44:1018-1024.
    40.孔祥彬,张春庆,许子峰.2005.DNA指纹图谱技术在作物品种(系)鉴定与纯度分析中的应用.生物技术,(4):72-77.
    41.赖钟雄,陈春玲.2002.龙眼体细胞胚胎发生过程中的内源激素变化.热带作物学报,23(2)41-47.
    42.朗文香.2011.北五味子体细胞胚胎发生及植株再生的研究.沈阳农业大学硕士学位论文.
    43.李爱民,廉士起,宋婷婷,李昌禹.2005.北五味子主要育种性状的研究.特产研究,2:19-23.
    44.李爱民.2002.北五味子的育苗技术.特种经济动植物,5(1):33-34.
    45.李际红,邢世岩,姚培娟,谭起航,王海林.2012.欧石楠体细胞胚发生和植株再生.植物生理学报,48(11):1042-1049.
    46.李建军,肖层林,刘志坚,吴升高.2007.陆两优996种子纯度的SRAP指纹图谱鉴定.中国农学通报,6(23):112-114.
    47.李近雨,胡延杰.1992.北五味子种子休眠生理及催芽技术的初步研究.河北林学院学报,9(4): 289-294.
    48.李浚明.2002.植物组织培养教程.中国农业大学出版社.
    49.李廷春,樊洪泓,高正良,周应兵,杨华应.2008.丹参遗传多样性的SRAP标记分析.核农学报,22(5):576-580.
    50.李雪梅,刘熔山.1994.小麦幼穗胚性愈伤组织诱导和分化过程中内源激素的作用.植物生理学通讯,30(4):255-260.
    51.李宗霆,周燮.1996.植物激素及免疫检测技术.南京:江苏科学技术出版社.
    52.梁国经.1999.长白山区北五味子保护栽培技术的研究.中国林副特产,51(4):2-7.
    53.梁一池,杨华.2002.植物组织培养技术研究进展.福建林学院学报,22(1):93-96.
    54.廖祥儒,张会图.2000.甘露醇和AgNO3对小麦细胞再分化的影响.河北大学学报(自然科学版),20(3):263-265.
    55.林荣双,王庆华,梁丽现.2002.TDZ诱导花生幼叶的不定芽和体细胞胚胎发生.植物研究,23:169-172.
    56.林文学,王庆亚.2007.药用植物生态学研究.北京:中国林业出版社.
    57.刘公社,齐冬梅.2004.赖草属几种植物幼胚离体培养研究.草业学报,13(1):70-73.
    58.刘关君,李绪尧,由香玲,张静,赵颖慧,刘桂丰.2000.长白落叶松插穗内源激素变化与不定根产生的关系.东北林业大学学报,28(1):19-10.
    59.刘进平,郑成木,胡新文.2001.体细胞无性系变异研究进展.华南热带农业大学学报,7(2):22-29,34.
    60.刘琳,俞斌,黄鹏燕,贾军,赵华,彭俊华,陈鹏,彭良才.2013.芒不同基因型愈伤组织诱导及分化的差异.植物学报,48(2):192-198.
    61.刘清玮,余春粉,高延辉,王秀全.2009.北五味子主要性状的遗传参数及相关性研究.人参研究,(1):11-15.
    62.刘清玮.2005.北五味子群体变异及类型调查研究.吉林农业大学硕士学位论文.
    63.马丽.2007.玉米自交系幼胚高效再生系统的建立.西北农业学报,16(6):85-89.
    64.牛遇达.2007.北五味子体细胞胚发生的研究.东北林业大学硕士学位论文.
    65.齐力旺,韩一凡,李玲,韩素英.2000.应用最优回归设计研究ABA, PEG4000及AgNO3对落叶松体细胞胚发生数量的影响.生物工程学报,17(1):82-89.
    66.齐力旺.2000.华北落叶松体细胞胚胎发生及遗传转化系统的建立.中国林科院博士学位论文.
    67.钱丹,黄璐琦,崔光红,陈敏.2009.不同产地蒙古黄芪遗传关系的SRAP分析.中国中药杂志,34(4):382-385.
    68.乔琦,肖娅萍.2008.防风体细胞胚发生和发育的组织学研究.广西植物,28(1):113-116.
    69.邱婧.2008.霍山石斛不同继代次数试管苗遗传稳定性的研究.安徽农业大学硕士学位论文.
    70.曲绍轩,高山,黄晨阳.2007.SRAP、ISSR和RAPD分子标记技术在银耳菌株鉴别上的应用.食用菌学报,14(3):1-5.
    71.任步钧.1985.观赏花木栽培.北京:人民日报出版社.
    72.阮先乐.2008.马铃薯茎尖的超低温保存及再生植株的遗传稳定性分析.湖南农业大学硕士学位论文.
    73.沈文,叶正良,郭巧生.2010.东北不同产地五味子药材品质研究.中国中药杂志,35(22):3016-3020.
    74.宋万志.1982.中国五味子科药用植物及其木脂素成分.中草药,3(1):40-43.
    75.苏华,徐坤,刘伟.2007.大葱花芽分化过程中内源激素的变化.园艺学报,4(3):671-676.
    76.孙敬三,桂耀林.1995.植物细胞工程试验技术.北京科学出版社.
    77.孙敬爽,贾桂霞.2010.北美蓝云杉体细胞胚发生技术研究.北京林业大学学报,32(1):42-51.
    78.孙庆龙.2006.北五味子种质资源及评价研究.黑龙江中医药大学硕士学位论文.
    79.孙兴民,余智莹,张萌,董瑞奇,陶建敏.2012.葡萄未成熟胚诱导体细胞胚发生和植株再生与遗传鉴定.南京农业大学学报,35(3):13-18.
    80.汤国庆,李文安.1995.在离体条件下拐芹形成胚性愈伤组织和非胚性愈伤组织过程中几种内源激素的变化.试验生物学报,28(2):203-208.
    81.唐定台,徐民新,冯永红.1996.石竹试管花的诱导及其影响因子的研究.园艺学报,23(3):277-280.
    82.王傲雪,李景富.1992.植物体细胞胚状体的诱导研究及应用.黑龙江农业科学,2:39-41.
    83.王从彦,李晓慧,胡颖,郭二辉,田朝阳.2008SRAP分子标记分析芫花遗传多样性.河南科学,、26(5):552-556.
    84.王家福,刘月学.2000.枇杷胚性愈伤组织的诱导和保存.福建农业大学学报,29(3):305-310.
    85.王珂,童玉懿,宋万志.1990.五味子有效成分的薄层光密度法测定.药学学报,25(1):49-53.
    86.王丽,鲍晓明,黄百渠,郝水.1998.香雪兰外植体形态学极性决定的体细胞胚胎发生.植物学报,40(2):138-143.
    87.王丽薇,周长新,Bernd Schneider,赵昱.2006.五味子化学成分研究.中国现代应用药学,23(5):363-365.
    88.王义,赵又君,孙春玉,杨晶,蒋世翠,张美萍.2008.2,2-D,BA对人参体细胞胚胎发生过程的影响研究.中国生物工程杂志,28(10):106-112.
    89.王有菊,姜静,金顺玉,李慧玉.2007.北五味子遗传多样性的ISSR分析.林业科技.32(2):57-59.
    90.王勇锋,柴乖强,徐开杰,杨赛奇,孙风丽,刘曙东,吴亚军.2012.柳枝穆成熟胚愈伤组织诱导的影响因素.西北农林学报,21(6):140-145.
    91.王浴生.1983.中药药理与应用.北京:人民卫生出版社,177.
    92.武立丹.2009.北五味子组织培养研究.延边大学硕士学位论文.
    93.肖关丽,杨清辉,李富生.2001.甘蔗组培苗继代培养中内源激素与绿苗生根率关系研究.云南农业大学学报,6(4):271-273.
    94.谢海燕,毛碧增,单兰兰,陈毓荃.2004.狗牙根颖果胚性愈伤组织的诱导和胚性细胞的超微结构及植株再生.植物生理与分子生物学学报,30(2):209-215.
    95.谢芝馨,张玉喜,于元杰,杨龙,王希荣.2004.大葱试管苗玻璃化机理的探讨.分子植物育种,(2):71-75.
    96.邢登辉,赵云云,黄承芳.1999.皇冠草体细胞胚胎发生及其体胚发生过程中内源激素的变化.生物工程学报,15(1):98-103.
    97.徐华松,徐九龙,黄学林.1996.TDZ在植物组织培养中的作用.广西植物,16:77-80.
    98.徐佩贤.2009.东方杉嫩枝扦插繁殖技术及其生根机理研究.南京林业大学硕士学位论文.
    99.徐晓峰,黄学林.2003.TDZ:一种有效的植物生长调节剂.植物学通报,20(2):227-237.
    100.许晓岗,汤庚国,谢寅峰.2005.海棠果插穗的内源激素水平及其与扦插生根的关系.莱阳农学院学报,2(3):195-199.
    101.薛志强,徐道娜,张勇,马建祥,杨建强,侯沛,张显.2007.少籽西瓜内源激素含量变化与胚胎败育的关系.西北农业学报,16(3):182-187.
    102.闫伯前,王艇,胡理乐.2009.药用植物华中五味子的种群遗传多样性及遗传结构.生态学杂志,28(5):811-819.
    103.杨顺锦,詹儒林,赵艳龙,柳凤.2011.杧果畸形病茎部解剖结构及内源激素含量变化.果树学报,4:708-711.
    104.杨业正.1991.TDZ与植物细胞和组织培养.贵州农业科学,6:43-46.
    105.尹俊,徐妙云,贾小平,阚锐,李连国.2000.河套蜜瓜体胚发生及植株再生的研究.园艺学报,27(6):455-457.
    106.伊旭,刘权钢,李成录,金东淳,任范哲.2012.长白山区北五味子种质资源的遗传多样性分析.延边大学农学学报.34(4):304-308.
    107.于惠敏,石竹,杨俊杰.2007.番茄的不同基因型对组培植株再生能力的影响.山东师范大学学报(自然科学版),22(4):102-121.
    108.詹亚光,杨传平,金贞福,王玉成.2001.白桦扦插生根的内源激素和营养物质.东北林业大学学报,29(4):1-4.
    109.张东向,张崇浩,李杰芬.2000.玉米叶片胚性愈伤组织诱导及其与内源IAA和ABA关系的初步研究.作物学报,26(2):195-199.
    110.张兰杰,张维华,赵璐红.2002.五味子果实中多糖的提取与纯化研究.鞍山师范学院学报,4(1):58.
    111.张黎,翟彦.2005.不同基质不同部位对菊花扦插生根的影响.西北农林学报,14(6):112-114.
    112.张妮.2008.葡萄茎尖的超低温保存及再生植株的遗传稳定性分析.湖南农业大学硕士学位论文.
    113.张晓薇,夏媛,李凤兰,胡宝忠.2009.北五味子组织培养研究.安徽农业科学,9:3933-3935.
    114.赵福德,刘孝坤.2005.北五味子人工栽培技术.吉林林业科技,34(2):37-40.
    115.赵桂兰,艳芝,尹爱平.1998.大豆花药培养中胚状体萌发的研究.科学通报,43:1512-1516.
    116.赵艳玲,孔维军,山丽梅,肖小河,郭伟英.2008.HPLC法测定南北五味子中五味子甲素和五味子酯甲的含量.中药新药与临床药理,19(4):299-301.
    117.赵永德,崔惠玲,李娟.2005.五味子的药理作用及临床应用.药物与临床,(6):41-42.
    118.中国科学院中国植物志编委会.1979.中国植物志.北京:科学出版社.
    119.周俊彦,郭扶兴.1990.苯基腺衍生物的细胞分裂素活性.植物生理学通讯,4:7-13.
    120.周英,杨俊山,王立为.2003.五味子科植物三萜成分.中国药学杂志,38(2):81-83.
    121.朱俊义,刘雪莲,秦佳梅,顾地州.2006.北五味子组织培养中愈伤组织的诱导.东北林业大学学报,34(6):41-42.
    122.朱友银,赵德刚,冯怡,赵丰兰,钟德意,刘黔.2008.不同基因型玉米愈伤组织诱导与植株再生研究.生物技术,18(4):62-64.
    123.朱玉球,曾燕如,潘心平,斯金平,王祖良.1999.厚朴外观形状与内在品质的关系.浙江林学院学报,16(4):387.
    124.卓丽环,黄普华,金万昌,杨传平.1994.黑龙江省北五味子一新变种.植物研究,14(1):35-36.
    125. Ai Hua Chen, Jing Li Yang, Yu Da Niu.2010. High-frequency somatic embryogenesis from germinated zygotic embryos of Schisandra chinensis and evaluation of the effects of medium strength, sucrose, GA3 and BA on somatic embryo development. Plant Cell Tiss Org,102(3):357-364.
    126. Altman A, Goren R.1971. Promotion of Callus Forma-tion by Abscisic Acid in Citrus Bud Cultures. Plant Physiol,47:842-846.
    127. Al-Zahim M A, Ford-Lloyd B V, Newbury V J.1999. Detection of somaclonal variation in garlic(AIlium sativum L.) using RAPD and cytological analysis. Plant Cell Rep,18:473-477.
    128. Armstrong C L.1985. Establishment and main tenance of firable, embryogenic maize callus and the involvement of L-proline. Planta,164:207-214.
    129. Arndt, Rusch R, Stilfried H V.1976. A new cotton defoliant. Plant Physiol,57:99-104.
    130. Ashok K H G, Murthy H N, Peak K Y.2003. Embryogenesis and plant regeneration from another culture of Cucumis sativus L. Sci Hortic,98:213-222.
    131. Attree S M, Dunstan D I, Fowke L C.1989. Plantlet regeneration from embryogenic protoplasts of white soruce. Bio Technology,7:1060.
    132. Auboirn E, Carron M P, Nicole M F.1990. Atmospheric gazes and ethylene synthesis in somatic embryogenesis of Hevea brasiliensis. Plant Cell Tiss Org,21:31-37.
    133. Berry T A, Bewley J D.1992. A role for the surrounding fruit tissues in preventing germination of tomato seeds:a consideration of the osmotic environment and abscisic acid. Plant Physiol,100: 951-957
    134. Besse I, Verdeil J L, Duval I, Sotta B, Maldiney R, Miginiac E.1992. Oil palm Elaeis guimeensis Jaeq clonal didelity:endogenous cytokinins and indoleaeetie acid in embryogenic callus cultures. J ExP Bot, 44:983-989.
    135. Bhaskaren S, Smith R H.1990. Regeneration in cereal tissue culture:a review. Crop Sci,30: 1328-1336.
    136. Bingham E T, McCoy J T.1986. Somaclonal variation in alfalfa. Plant Breeding Rev,4:123-152.
    137. Broertjes C, Keen A.1980. Adventitious shoots:Do they develop from one ceil? Euphytica,29:73-87.
    138. Broertjes C.1969. Mutation of breeding of streptocarpus. Euphytica,18:333-339.
    139. Chen J T, Chang W C.2000. Efficient plant regeneration through somatic embryogenesis from callus of Oncidium (Orchidaceae). Plant Sci,160:87-93.
    140. Chengalrayan K, Mhaske V B, Hazra S.1997. High-frequency conversion of abnormal peanue somatic embryos. Plant Cell Rep,16:783-786.
    141. Chraibi K M, Iatche A, Roustan J P.1991. Stimulation of shoot regeneration from cotyledons of Helianthus annuns by the ethylene inhibitors silver and cobalt. Plant Cell Rep,10:202-207.
    142. Davis T D, Haissig B E.1994. Biology of Adventitious Root Fomation. New York:Plenum Press.
    143. Deng X X, Chen X H, Cheng W M,Shen Z D, Bi K S.2008. Simultaneous LC-MS Quantification of 15 lignans in Schisandra chinensis (Turcz.) Baill. Fruit. Chromatographia, (67):559.
    144. Epstein F, Koebba J, Neumann H.1977. Metabolism of indoleacetic acid by embryogenic and nonembryogenic callus lines of 《shamouti》 orange(Citrus sinensis OsB.). Z. Pflanzenphysiol,85: 263-268.
    145. Evans D A.1988. Applications of somaclonal variation. In:A Mizrahi (ed.). Biotechnology in agriculture. New York:Allan R. Liss.203-223.
    146. Feng N, Xue Q, Guo Q H, Zhao R, Guo M L.2009. Genetic diversity and population structure of Celosia argentea and related species revealed by SRAP. Biochem Genet,47(7-8):521-532.
    147. Ferriol M, Pico B, Nuez F.2003. Genetic diversity of a germplasm collection of Cucurbita pepo using SRAP and AFLP markers. Theor Genet,107:271-282.
    148. Ghosh A, Gadgil V N.1979. Shift in ploidy level of callus tissue:A function of growth substances. Indian J Exp Biol,17:562-564.
    149. Gould A R, King P J.1984. Control of the cell cycle in cultured plant cells. Crit Rev Plant Sci,1: 315-344.
    150. Higashi K, Daita M, Kobayashi T, Sasaki K, Harada H, Kamada H.1998. Inhibitory conditioning for carrot somatic embryogenesis in high-cell-density cultures. Plant Cell Rep,18:2-6.
    151. Hwang S C, Ko W H.1987. Somaclonal variation of bananas and screening for resistance to Fusarium wilt. Austral. ACIAR Proc,21:151-156.
    152. Jackson J A, Lyndon R F.1990. Habituation:Cultural curiosity or developmental determinant. Physiol Planta,79:579-583.
    153. Jimenez V M, Bangerth F.2001. Endogenous hormone levels in explants and in embryogenic and non-embryogenic cultures of carrot. Plant Physiol,111(3):389-395.
    154. Karp A.1992. The role of growth regulators in somaclonal variation. British Society for Plant Growth Regulation Annuan Bulletin,2:1-9.
    155. Kemq.1982. Physical and pharmacological properties of efficient components in traditional Chinese medicines. Changsha:Human Science and Technology Publishing House,541.
    156. Kim T D, Anbazhagan V R, Park J I.2005. Somatic embryogenesis Schisndra chinensis (TUR CZ.) BAILL. Intro Cell Dev Biol-Plant,41(3):253-257.
    157. Klotz K L, Lagrimini L M.1996. Phytohomone control of the tobacco anionic peroxidase pronoter. Plant Mol Biol,31:565-574.
    158. Kuo Y H, Wu M D, Hung C C.2005. Syntheses of C18 dibenzocyclooctadiene lignan derivatives as anti-HBsAg and anti-HBeAg agents. Bioorgan Med Chem,13:1555-1561.
    159. Lee H J, Kim C Y.2010. Simultaneous determination of nine lignans using pressurized liquid extraction and HPLC-DAD in the fruits of Schisandra chinensis. Food Chem,120:1222-1228.
    160. Li G, Quiros C F.2001. Sequence-related amplifiled polymorphism(SRAP), a new marker system based on a simple PCR reaction:its application to mapping and gene tagging in Brassica. Theor Appl Genet,103:455-461.
    161. Ma H L, Zhang C H, Xiao Z N, Yang B.1997. Effect of plant endogenous hormone levels on plant protoplast culture. Journal of Beijing Normal University. Natural Science,33(3):412-417.
    162. Marcotrigiano M.1990. Genetic mosaic and chimeras:Implications in biotechnology. Biotechnology in agriculture and forestry,11:85-111.
    163. McPheeters K, Skirvin R M.1983. Histogenic layer maniputation in chimera 'Thornless Evergreen' trailing blackberry. Euphytica,32:351-360.
    164. Mengoli M, Bagni N, Luccarini G.1989. Polymines and effect of Polmine biosynthesis inhibitors in the Preemfrygenic phase and different embryo stage. Plant Physiol,134:389.
    165. Murthy B N S, Saxena P K.1998. Somatic embryogenesis and plant regeneration of neem(Azadirachta inidica A. Juss). Plant Cell Rep,17:469-475.
    166. Osuga K, Kamada H, Komamine A.1993. Cell density is an important factor for synchronization of the latest age of somatic embryogenesis at high frequency. Plant Tiss Cult Lett,10:180-183.
    167. Perrin M, Gertz C, Masson J Z.2004. High efficiency initiation of regenerable embryogenic callus from anther filaments of 19-grapevine genotypes grown worldwide. Plant Science,167:1343-1349.
    168. Reinert J.1959. Uber die Kontrolle der Morphogenes and die Induktion von Adventive- embryonen an Gewebekulturen aus karotten. Plant,53:318-333.
    169. Riaz A, Li G, Quresh Z, Swati M S, Quiros C F.2001. Genetic diversity of oileed Brassica napus inbred lines based on sequence-related amplified polymorphism and its relation to hybrid performance. Plant Breeding,120(5):411-415.
    170. Ruiz J J, Gareia M S, Pieo B, Gao M, Quirs C F.2005. Genetic variability and relationship of closely related Spanish traditional cultivars of tomato as detected by SRAP and SSR markers. J Amer Soc Hort Sci,130:88-95.
    171. Sasakin K, Shimomura K, Kamada H, Harada H.1994. IAA metabolism in embryogenic and non-embryogenic carrot cells. Plant Cell Physiol,35:1159-1164.
    172. Smiskova A, Vlasinova H, Havel L.2005. Somatic embryogenesis from zygotic embryos of Schisndra chinensis. Biolgia PlanlaIum,49 (3):451-454.
    173. Steward F C, Mapes M O, Mears K.1958. Growth and organized development of cultured cells. Am J Bot,45(10):705-708.
    174. Tang Y L, Chen W E, Zhou X.1996. The changes of endogenous level of plant hormones during root and bud formation in tobacco leaf explants. Journal of Nanjing Agricultural University,19(2):12-16.
    175. Tao J, Zhan Y G, You X L,Yang C P, Liu Y X.1998. Study on tissue culture and regeneration system of Betula platyphyllrl Suks (Ⅲ):change of endogenous hormones in tissue culture. Journal of Northeast Forestry University,26(6):6-9.
    176. Turban H, Baser I.2004. Callus induction from mature embryo of inter wheat (Triticum aestivum L.). Asian Journal of Plant Sciences,3(1):17-19.
    177. Victor J M R, Murthy B N S, Murch S J, Saxena P K.1996. Role of endogenous purine metabolism in thidiazuron-induced somati embryogenesis of peanut (Arachis hypogaea L.). Plant Growth Regul,28: 41-47.
    178. Wilhel E.2000. Somatic embryogenesis in oak (Quercus spp). In Vitro Cell Dev-pl,36 (5):349-357.
    179. Xie X M, Chen X Y, Han L B.2001. Plant regeneration in Eucalyptus pellita. Forestry Studies China, 3:7-14.
    180. Xing D H, Wu Q S, Liu D J.1994. The crop cell culture-inducement and expression of the smaclones potential. The Biology Notification,29(7):1-31.
    181. Xu L J, Huang F, Chen S B, Zhang Q X, Li L N, Chen S L, Xiao P G 2006. New lignans and cytotoxic constituents from schisandra propinqua. Planta Med,2:169-174.
    182. Yadav J S, Rajam M V.1997. Partial distribution of free and eonjugaged polyamines in leaves of Solanum melongena L. assoeiated with differential morphogenetic capacity:effieient somatic embryogenesis with putreseine. J Exp Bot,48(313):1537-1545.
    183. Zhu M, Chen X S, Wang K X.2007. Variation of the Lignan Content of Schisandra chinensis (Turcz.) Baill. and Schisandra sphenanthera Rehd. et Wils. Chrommatographia,66:125-128.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700