一条卡瓦胡椒特异RAPD带转化成SCAR标记的研究

采用27份不同来源的胡椒属(Piper)材料和1份不同属的草胡椒(Peperomia pellucida)材料用引物OPQ-03扩增得到一条约400碱基对(bp)卡瓦胡椒特异片段。对该片段进行了克隆和序列分析,并根据序列分析结果将上述RAPD分子标记转化为重复性和特异性更好的SCAR(sequence characterized amplifiedre-gions,序列特征化扩增区)分子标记。本研究设计出了1对卡瓦胡椒特异SCAR引物P7.1(5′-GGT CAC CTC ACC GCA GCA GGA TGA ACG-3′)和P7.2(5′-GGT CAC CTC AAT GAC ATG GGA TGA ATC-3′),用这对特异引物对本次试验的28份材料进行PCR扩增,结果只有不同属的草胡椒材料无任何扩增,其它材料均扩增出了预期大小440bp的特异带。     

卡瓦胡椒SCAR标记的研究

目的：采用6份卡瓦胡椒材料、21份栽培胡椒和野生胡椒材料、1份不同属的草胡椒材料共计28份试验材料,开发1对特异SCAR引物。方法：在对它们进行了RAPD研究的基础上,通过克隆、测序和引物设计进行了SCAR分子标记研究。结果：本研究开发了1对特异SCAR引物P10．1和P10．2,用这对特异引物对本次试验的28份材料进行PCR扩增,结果显示,6份卡瓦胡椒材料扩增出了三条带,三条带离的较近,中间一条为预期494bp特异片段。其它胡椒属材料均扩增出一条494bp的特异带,而不同属的草胡椒无任何扩增。结论：这说明引物P10．1和P10．2适用于卡瓦胡椒的分子鉴定(三条带),也可用于胡椒属植物的分子鉴定(一条带),这对卡瓦胡椒种质资源的真伪鉴定及胡椒属植物的分子分类有一定帮助。     

卡瓦胡椒及胡椒的RAPD聚类分析

目的：通过RAPD分析搞清楚卡瓦胡椒与胡椒及胡椒属其它近缘野生种的亲缘关系。方法和结果：采用随机引物80条进行筛选,用从80条随机引物中入选的20条引物,对卡瓦胡椒和胡椒属共计28份材料进行RAPD扩增,均能产生清晰的扩增谱带。重复1—2次,结果稳定可靠。20个引物共扩增出170个条带,其中多态性条带有20条,占总扩增条带数的12％。RAPD分析结果显示在相似系数0．36处对28份种质可划分为6个类型,其中卡瓦胡椒被单独聚为一类,说明卡瓦胡椒与胡椒及其它近缘野生种的亲缘关系有一定的距离。     

卡瓦胡椒SCAR分子标记的研究

目的:采用6份卡瓦胡椒材料、21份栽培胡椒和野生胡椒材料1、份不同属的草胡椒材料共计28份试验材料,开发1对特异SCAR引物。方法:在对它们进行了RAPD研究的基础上,通过克隆、测序和引物设计进行了SCAR分子标记研究。结果:研究开发了1对卡瓦胡椒特异SCAR引物P4.1和P4.2,用这对特异引物对试验的28份材料进行PCR扩增,结果只有6份卡瓦胡椒材料扩增出了预期大小562bp的特异带,其它材料均无任何扩增。结论:这说明引物P4.1和P4.2为卡瓦胡椒特异SCAR引物,可用于卡瓦胡椒的分子鉴定,这对卡瓦胡椒种质资源的真伪鉴定有一定帮助。     

神奇的热带特异资源——卡瓦胡椒

介绍了卡瓦胡椒的发现、起源、化学成分及药理作用.近年来卡瓦胡椒在欧洲和美国开始为人们所接受,1990年,德国联邦卫生局批准卡瓦胡椒制剂WS1490用于治疗焦虑症,卡瓦胡椒成为德国销售量最大的20味草药之一.1992年卡瓦胡椒根被美国食品、药品检验局(FDA)认证为"精神健康"食品.1998年,卡瓦胡椒被美国人称为"植物药之星".1999年卡瓦胡椒又在美国创下年销售额50亿美元的奇迹.2001年,卡瓦胡椒的引种、适应性和生物技术的研究项目被列为我国"十五"科技攻关项目.     

卡瓦胡椒RAPD反应体系的建立

卡瓦胡椒RAPD分子标记的研究,目前国内外尚未见有报道。该试验通过CTAB法提取卡瓦胡椒基因组DNA,通过对模板DNA用量、Mg^2＋浓度、退火温度、电泳上样量等几个单因子试验来建立RAPD稳定扩增体系和反应条件,RAPD扩增结果重复性好,稳定可靠,为卡瓦胡椒RAPD分子标记的研究打下基础。     

芽孢杆菌TS02特异RAPD标记的SCAR标记转化和验证

利用自主分离的蜡状芽孢杆菌菌株TS02, 采用RAPD方法对TS02及其同源性相近的5株芽孢杆菌(地衣芽孢杆菌、枯草芽孢杆菌、凝结芽孢杆菌、巨大芽孢杆菌、短小芽孢杆菌) 进行了RAPD条带特异性分析, 从TS02基因组中筛选获得了一个533 bp的特异RAPD标记TSR1。TSR1克隆、测序后, 根据其序列设计出一对特异引物P1/P2进行扩增, 结果只在TS02中扩增得到目的片段, 而其余对照菌株扩增为阴性, 从而证明试验得到了在种水平上对该菌种进行准确鉴定的特异SCAR标记。     

芽孢杆菌TS02特异RAPD标记的SCAR标记转化和验证

利用自主分离的蜡状芽孢杆菌菌株TS02,采用RAPD 方法对TS02及其同源性相近的5株芽孢杆菌(地衣芽孢杆菌、枯草芽孢杆菌、凝结芽孢杆菌、巨大芽孢杆菌、短小芽孢杆菌)进行了RAPD条带特异性分析,从TS02基因组中筛选获得了一个533 bp的特异RAPD标记TSR1.TSR1克隆、测序后,根据其序列设计出一对特异引物P1/P2进行扩增,结果只在TS02中扩增得到目的片段,而其余对照菌株扩增为阴性,从而证明试验得到了在种水平上对该菌种进行准确鉴定的特异SCAR标记.     

大麻性别的RAPD和SCAR分子标记

利用随机扩增多态性DNA（random amplified polymorphic DNA,RAPD)技术获得与大麻性别连锁的分子标记,将10株雄性大麻或10株雌性麻的单个DNA样品等量混合分别组成雄性或雌性DNA池（DNApool),以提供具有相同遗传背景的雄,雄性DNA样品。每个随机引物分别用三个不同的循环程序进行PCR扩增,在30个随机引物中,用引物S401扩增得到一条约2．5kb雄性多态性片段,对该片段进行了克隆和序列分析 ,并根据序列分析结果将上述RAPD分子标记转化为重复性和特异性更好的SCAR（Sequence characterized amplified regions)分子标记。     

利用RAPD特异标记分析东北猬草染色体组成

选用5个染色体组特异的RAPD引物(St、H、Ns、Ee、Eb),对东北猬草[Hystrix komarovii (Roshev.) Ohwi]等5个猬草属及其8个近缘属物种进行PCR扩增,以探讨东北猬草的染色体组组成.结果显示:Hy.komarovii具有Ns染色体组特异的RAPD标记,而没有St、H、Ee和Eb特异的RAPD标记.表明Hy.komarovii含有Ns染色体组,而不含St和H染色体组,认为其染色体组组成可能与Hy.duthiei、Hy.coreana和Leymus arenarius一样,具有NsXm染色体组.根据染色体组分类原理,支持将东北猬草归于赖草属中.     

Study on the RAPD Specific Band of Kava ( Piper,Piperaceae) Transferring to the SCAR Molecular Marker

This paper studied on 28 pepper materials, including 16 cultivated papper materials, 3 wild pepper materials, 2 wild relatives of pepper materials , 6 kava ( Piper methysticum) materials, and 1 Peperomia pellucida materials. According to RAPD analysis, we generate SCAR marker for identifying Kava ( Piper, Piperaceae ) . A Kava-associated fragment with a length ofabout 400 bp was generated with OPQ-03 primer . The fragment was cloned and sequenced . PCR amplification with the specific primers P7 . 1 ( 5′-GGT CAC CTC ACC GCA GCA GGA TGA ACG-3′) and P7 .2 (5′-GGT CAC CTC AAT GAC ATG GGA TGA ATC-3′) was performed to 28 materials , which 27 materials amplified the 440 bp specific band except for Peperomia pellucida Kunth .     

Floristic Geography of Piper (Piperaceae) in China

Piper is the largest genus and important Pantropical components of the Piperaceae family with approximately 1000-2000 species in the world. China is in the northern verge of its natural distribution. In this study, floristic geography of the Piper genus in China was analyzed to reveal its botanical characteristic, origins of speciation and its dispersal channels. The study results showed Yunnan province is one of the very important distribution regions for Piper species, served as the center of the Piper species dispersal toward to the eastern and northern regions of China with gradually reduced species numbers. The similarity level appeared to be low for its species among different provinces, and the Piper distribution regions could be approximately clustered into three clades: tropical clade, subtropical clade and Taiwan clade. Cladistically, Piper species found in China have the highest proportions which were endemic to China, and then followed by Piper species distributed in Tropical Asia, only few species belonged to Pantropical and East Asia areal types. The floristic geography of Piper genus in China is related to that of Indo Chinese Peninsula, Java Islands and Indian Peninsula in some degrees, but not closely related. This study revealed Yunnan province is one of the central of origins for the Piper species, and or one of the central of regions for its species diversification, and the Piper species of Taiwan mainly came from Philippine islands and further diversified into Taiwan clade. Our study results presented a useful method for the systematic studying of Piper genus taxonomy and the evolution of Piper speciation.     

Areas of endemism and distribution patterns for Neotropical Piper species (Piperaceae)

Aim The study aimed to establish areas of endemism and distribution patterns for Neotropical species of the genus Piper in the Neotropical and Andean regions by means of parsimony analysis of endemicity (PAE) and track‐compatibility analysis. Location The study area includes the Neotropical region and the Northern Andean region (Páramo‐Punan subregion). Methods We used distribution information from herbarium specimens and recent monographic revisions for 1152 species of Piper from the Neotropics. First, a PAE was attempted in order to delimit the areas of endemism. Second, we performed a track‐compatibility analysis to establish distribution patterns for Neotropical species of Piper. Terminology for grouping Piper is based on recent phylogenetic analyses. Results The PAE yielded 104 small endemic areas for the genus Piper, 80 of which are in the Caribbean, Amazonian and Paranensis subregions of the Neotropical region, and 24 in the Páramo‐Punan subregion of the Andean region. Track‐compatibility analysis revealed 26 generalized tracks, one in the Páramo‐Punan subregion (Andean region), 19 in the Neotropical region, and six connecting the Andean and Neotropical regions. Both the generalized tracks and endemic areas indicate that distribution of Piper species is restricted to forest areas in the Andes, Amazonia, Chocó, Central America, the Guayana Shield and the Brazilian Atlantic coast. Main conclusions Piper should not be considered an Andean‐centred group as it represents two large species components with distributions centred in the Amazonian and Andean regions. Furthermore, areas of greater species richness and/or endemism are restricted to lowland habitats belonging to the Neotropical region. The distribution patterns of Neotropical species of Piper could be explained by recent events in the Neotropical region, as is the case for the track connecting Chocó and Central America, where most of the species rich groups of the genus are found. Two kinds of event could explain the biogeography of a large part of the Piper taxa with Andean–Amazonian distribution: pre‐Andean and post‐Andean events.     

Taxonomic notes on the genus Piper (Piperaceae)

Sixteen lectotypifications of Asian Piper species are provided. Piper argyrites, P. baccatum, P. leptostachyum, P. majusculum, P. peepuloides, P. quinqueangulatum and P. sulcatum are accepted as species and many new synonyms are proposed. Useful diagnostic characters are described and geographical distribution data of each species are provided.