不同产地人参种质资源RAPD和SSR分析

以15个产地人参种质资源为试材,采用RAPD和SSR分子标记技术对其遗传多样性进行分析。结果表明:2种分子标记均能揭示不同地区人参种质间的遗传多样性。共筛选出11条RAPD随机引物,平均每条引物可扩增出3~17条DNA片段,共扩增出104条清晰条带,多态性条带100条,多态性百分率为96.15%,揭示供试材料间遗传相似系数(GS)为0.505 3~0.989 5,平均值为0.760 4。筛选出5对SSR引物,平均每对引物可扩增出1~8条DNA片段,共扩增出38条清晰条带,多态性条带35条,多态性百分率为92.11%,揭示供试材料间遗传相似系数(GS)为0.400 0~0.960 0,平均值为0.742 1。RAPD和SSR标记的聚类分析在分类上稍有差异,但总体趋势一致,RAPD、SSR及RAPD+SSR均将样品聚为三大类,均能揭示它们之间的亲缘关系,为人参种质资源的收集与利用奠定了基础。     

应用SSR荧光标记法构建22个柚类品种的分子身份证

【目的】应用荧光SSR分子标记构建柚类种质分子身份证，用于品种资源鉴定。【方法】收集22份柚类材料，筛选SSR荧光标记引物，采用荧光毛细管电泳检测技术分析扩增条带分子质量和等位基因，获得相应的扩增带型，从而对每份柚材料进行标记。采用个位阿拉伯数字和小写英文字母对不同等位基因分子质量大小进行编码，再按照引物扩增带型数由大到小顺序将各位点赋值编码的数字串联排序，构建供试样品的分子身份证。【结果】筛选出4对多态性较好的引物，使用这4对引物共检测到49个扩增带型和41个SSR等位位点，平均每对引物的有关带型数12.25个、位点数10.25个。【结论】通过扩增带型分析，构建了22份柚类种质的分子身份证，包括12条信息独特的身份证。遗传聚类与分子身份证分析结果一致，为柚类品种鉴定和保护提供了重要依据。     

十二份杧果种质亲缘关系的SRAP分析

以12份杧果种质为试材,利用SRAP分子标记技术对其进行遗传多样性研究。结果表明:从36对引物中筛选出22对多态性好的引物,共扩增出251条DNA条带,其中多态性谱带181条,平均每对引物扩增得到15.08条多态性谱带,多态性比率为72.11%。UPGMA聚类表明,所有供试品种(系)之间的亲缘关系都比较近,相似系数在0.77~0.89;如果以相似系数0.78为标准,可将供试的12个品种(系)分为3类。表明利用SRAP技术能较好的区分杧果的亲缘关系;SRAP分子标记适合杧果的DNA遗传多样性分析,可作为杧果种质鉴定依据之一。     

萱草部分野生种和栽培品种亲缘关系的AFLP分析

 借助AFLP标记对35份萱草野生种和栽培品种进行亲缘关系研究, 结果表明, 7对引物组合对萱草共扩增出条带380条, 其中多态性条带357条, 平均多态性达到93.39% , 单对引物扩增条带19～85条, 平均每对引物组合扩增多态性条带51条。7对引物扩增出的多态性条带均超过90.0%。种质资源相似系数为0.3822～0.9656, 平均相似系数为0.7039。UPGMA聚类结果将供试材料分为3类, 即早花、中花和晚花类, 同一产地的品种基本能聚在一起。AFLP标记技术能较好地从分子水平揭示萱草种质资源的亲缘关系。     

葡萄种质遗传多样性的SSR分析及指纹库构建

以取自郑州果树研究所的45个葡萄品种为试材,利用SSR标记技术对其进行了遗传多样性分析.结果表明:利用19对基本核心引物对位于不同染色体上的SSR位点进行PCR扩增,共扩增出76条带,其中包括74条多态性条带.每对引物可检测到等位位点数为2～5个,多态率为66.7％～100％.通过聚类分析结果表明,在遗传距离为0.41处,45份葡萄材料可分为三大类群.对供试葡萄品种的不同引物的扩增产物进行检测,得到了每个品种在一组位于不同染色体的SSR位点上的基因型图谱,从而初步建立一个供试葡萄品种的SSR基因型指纹库.这为利用SSR标记鉴定葡萄品种或品系提供了基础数据.     

苹果品种的SSR分析

 利用SSR方法对苹果25个品种进行了基因组多态性分析, 从20对引物中筛选出10对多态性引物用于正式扩增, 一共扩增出97个位点, 平均每对引物扩增出917个位点, 扩增条带的多态性百分率在56.4%～100%之间。用两对引物(GD142和02b1) 即可区分全部供试品种。根据SSR 分析结果, 应用NTSYS软件进行相似性系数计算, 利用UPGMA法构建聚类树状图。其结果表明, 供试苹果品种分为4个类群, 与传统系谱基本一致。     

中国马铃薯部分栽培品种遗传多样性的AFLP分析

 采用AFLP方法分析中国各地79个马铃薯栽培品种, 获得了8对引物组合的扩增谱带, 为马铃薯品种的鉴定提供了分子依据。8对引物组合扩增结果共获得801条带, 平均每对引物组合产生100.13条带。其中493条为多态性条带, 平均多态性检出率为61.2% , 引物组合E11 /M51扩增的多态性比率最高。聚类分析将材料分成3类, 聚类结果与地域无明显相关。     

豆瓣菜种质资源遗传多样性的RAPD和ISSR分析

以8个豆瓣菜的品种为试材，用筛选出的79个RAPD引物和34个ISSR引物对这8个品种的基因组DNA进行扩增，分别扩增出361条和179条谱带，每个引物扩增出的带在3～10条之间，平均每个引物扩增出约5条带。根据所得的条带进行聚类分析，两种标记产生的聚类图存在一些差异，但它们都可以较好地将8个品种按亲缘关系的远近划分为3个不同的类群。Mantel测试得出相关系数r=0．58155，表明RAPD和ISSR两种分子标记技术的相关度很低。     

寒地李和杏遗传多样性SSR分析

以27份适宜北方生长的李、杏品种为试材,采用SSR分子标记技术对其进行遗传多样性分析,并运用UPGMA聚类分析法,分析了27份试材的亲缘关系,为寒地李、杏种质资源保存和品种选育提供分子生物学依据。结果表明:筛选的25对SSR多态性引物共扩增等位位点245个,其中多态性位点240个,多态性比率为97.96%。每对引物的等位基因数量为4~13,平均值为9.8。有效等位基因数平均值为2.740 5,Shannon′s信息指数平均值为1.052 0,多态性信息含量平均值为0.595 5,表明试材具有较高的遗传多样性。聚类分析结果表明,在遗传相似系数0.612处,27份试材可以分为李和杏两大类群。     

利用荧光标记SSR构建百合种质资源分子身份证

以96份百合种质资源为材料,使用SSR标记进行百合种质分子身份证构建试验。从172对百合SSR引物中筛选出20对多态性好的核心引物,采用四重荧光毛细管电泳技术检测扩增条带分子量的方法对百合资源进行标记分析,获得供试样品相应的扩增带型。采用个位数字和小写英文字母对不同带型进行编码,按照20对引物扩增带型数由少到多顺序串联排序的方式构建供试样品的分子身份证。结果显示：20对SSR引物共检测到69个SSR等位位点和170个带型,平均每对引物对品种扩增的等位位点3.45个,带型8.50个。对带型进行编码的结果表明：96份百合种质资源的SSR分子身份证互不相同,可以将材料完全区分开。     

Identification of S-haplotypes of European cultivars of sour cherry

The sour cherry is known to exhibit the phenomenon of gametophytic self-incompatibility which prevents self-fertilization. In sour cherry, besides self-incompatible cultivars, there often occur self-compatible cultivars. This is due to the occurrence of natural mutations of the S-RNase or SFB genes and, consequently, loss of functionality of S-alleles. Here we present the results of the identification of S-haplotypes of 21 cultivars of sour cherry from various regions of Europe. The analyses were performed using methods based on the amplification of intron I and intron II of the S-RNase gene and fragments specific to the individual alleles of the S-RNase or SFB genes. The tested cultivars were found to contain 15 S-haplotypes: S₁, S_1?, S₄, S₆, S_6m, S_6m2, S₉, S₁₂, S₁₃, S_13?, S₂₆, S₃₅, S_36a, S_36b, and S_36b2. The most frequently occurring S-haplotypes were S_13? (61.9%), S_36a (57.1%), and S₂₆ (47.6%). On the basis of the results, 17 of the 21 cultivars were deduced to be self-compatible. The results will be of use in the production of sour cherry fruit by facilitating the selection of suitable pollinating cultivars. The results are also expected to be useful in the breeding of new cultivars of sour cherry when selecting genotypes for crosses.     

化学药剂对香椿休眠解除的影响及其机理

 采用五元二次正交旋转组合设计, 探索6-BA、GA₃ 、(NH₂) ₂CS、ZnSO₄ 、KNO₃ 对香椿休眠解除的影响, 5 种化学药剂解除休眠的作用依次为ZnSO4 > (NH₂) ₂CS > GA₃ > 6-BA > KNO₃ 。打破香椿休眠的最佳药剂组合是: 6-BA 20 mg/L + GA₃ 180 mg/L + (NH₂) ₂CS 1 % + ZnSO4 0.5 % + KNO₃ 2 %。用上述药剂处理可以使香椿提早23 d 萌芽。     

Ozone forming potential of tropical plant species of the Vidarbha region of Maharashtra state of India

Volatile organic compounds (VOC) are emitted by many plants. In this study, sixty common plant species of the Vidarbha region of Maharashtra, India were examined for VOC (isoprene and monoterpene) emissions. Plant species VOC emission rates ranged from undetectable to 75.2 μg g^?1 h^?1. Dalbergia sissoo exhibited a maximum VOC emission rate of 75.2 μg g^?1 h^?1. Ozone forming potentials (OFP) of the sixty plant species were also estimated using the method of Benjamin and Winer (1998). Maximum ozone forming potential of 77 g O₃ (tree)^?1 d^?1 was observed in the case of Mangifera indica. Out of 60 species, 26 species (43.3%) had low OFP (less than 1 g O₃ (tree)^?1 d^?1), 18 species (30%) had medium OFP (less than 1–10 g O₃ (tree)^?1 d^?1) and 16 species (26.7%) had high OFP (more than 10 g O₃ (tree)^?1 d^?1).     

京白梨等品种S 基因型鉴定及新基因S28 和S30 的核苷酸序列分析

 根据梨S基因高度保守区C1和C3区, 设计1对引物P1和P2, 对梨品种的基因组DNA进行S基因特异扩增、克隆、测序, 并在GenBank中BLAST比较, 确定S 基因特异性片段, 对京白梨等6个供试自交不亲和品种的S基因型比对结果为: 白梨中的‘库尔勒香梨’为S₂₁ S₂₈ , ‘苹果梨’为S₁₇S₁₉ ; 砂梨中的‘台湾蜜梨’为S₁₁ S₂₂ ; 西洋梨中的‘葫芦梨’为S_a S_b; 秋子梨中的‘京白’为S₁₆ S₃₀ , ‘早梨18’为S₄ S₂₈。其中S₂₈和S₃₀为首次登录的新S 基因, 在GenBank的登录号分别为AY562394 (库尔勒香梨) 和AY876945 (京白) 。     

The effect of organic supplementation of solarized soil on the quality of tomato fruit

Soil solarization, used to control weeds and soil-borne pathogens in hot climates, has not yet been widely adapted as a commercial practice because of its lack of efficacy. Experiments were carried out in southern Italy over two growing seasons to study the effect of three levels (0, 0.35 and 0.7 kg m⁻²) of organic supplementation of the soil prior to solarization on soil mineral availability and fruit quality attributes. Soil temperature and chemical properties were monitored, together with changes in the physical characteristics and chemical composition of tomato fruits grown under commercial greenhouse conditions. Organic supplementation increased the soil temperature achieved through solarization by 3.9 to 5.5 °C. Organic supplementation increased (P ≤ 0.05) the soil concentration of NO₃⁻-N, exchangeable K₂O, Ca²⁺, Na⁺ and Mg²⁺ and the level of electrical conductivity in the soil extract. Physical characteristics of tomato fruits were improved by supplementation, with fresh and dry weight enhanced up to 11 and 21%, respectively, mesocarp thickness up to 19%, firmness up to 36% and skin redness (a^*/b^* ratio) up to 24%. As the supplementation rate was raised from 0 to 0.7 kg m⁻², the fruit content of reducing sugars increased (P ≤ 0.01) from 1.75 to 2.14 g per 100 g f.w., ash from 0.49 to 0.62%, soluble solid from 5.12 to 6.18 °Brix, titratable acidity from 0.16 to 0.19%, and ascorbic acid from 25.1 to 32.5 mg 100 mL⁻¹. We concluded that organic supplementation appears to be a valuable and environmentally friendly way to improve the mineral availability in the soil and improve fruit quality of tomato.     

金嘴蝎尾蕉切花苞片褐变的控制

 研究了金嘴蝎尾蕉切花最佳采收时期和对其苞片褐变具有良好控制效果的预处理保鲜液及瓶插方法。结果表明: 金嘴蝎尾蕉以中蕾期采收最佳; 整个花枝水平放置, 完全浸泡于500 mg·L ^{- 1} H₃BO₄或500 mg·L ^{- 1} MgSO₄中1 h后, 结合2 mg·L ^{- 1} 6-BA + 200 mg·L ^{- 1} Al₂ ( SO₄ ) 3瓶插保鲜及0.1%聚乙烯醇喷洒花枝, 可显著控制苞片褐变, 保持组织较低水平pH值, 减缓膜透性的上升。其瓶插寿命分别达12 d和11.5 d, 显著高于对照的4 d。     

Comparison of anthocyanins in non-blotches and blotches of the petals of Xibei tree peony

A comparison in non-blotches and blotches of 35 cultivars of Xibei tree peony was investigated to explore flower coloration of Xibei tree peony (the second cultivar group in Chinese tree peony). With high performance liquid chromatography (HPLC) analysis, six anthocyanins including peonidin 3,5-di-O-glucoside (Pn3G5G), peonidin 3-O-glucoside (Pn3G), cyanidin 3,5-di-O-glucoside (Cy3G5G), cyanidin 3-O-glucoside (Cy3G), pelargonidin 3,5-di-O-glucoside (Pg3G5G), and pelargonidin 3-O-glucoside (Pg3G) were detected in non-blotches and blotches of petals. Total anthocyanins (TA), total flavones and flavonols (TF), and the copigmentation index (CI) were also analyzed. Cyanidin-based glycosides, which accumulated abundantly at the basal petal, resulted in blotch formation. Some peculiar cultivars with only one kind of anthocyanins or without anthocyanins in non-blotches were found in this study. For example, ‘Feng Zi Xiu Se’, ‘Ou Duan Si Lian’, and ‘Xi Wang’ contained only Pn3G5G; ‘Bing Shan Cang Yu’ and ‘Jin Bo Dang Yang’ contained only Cy3G; while no anthocyanins were found in ‘Bing Shan Xue Lian’. Several cultivars were rich in Pg-based glycosides, such as ‘Ni Hong Huan Cai’, and ‘Ju Yuan Shao Nv’. These cultivars would be excellent parents for creating new cultivars with novel flower color in the future.     

Analyses of pollen-tube growth and biological action of S-RNase in the style of self-compatible Japanese pear

The Japanese pear ‘Osa-Nijisseiki’ (S₂S₄^SM) (SM = stylar-part mutant) is a self-compatible bud mutant that originated from self-incompatible ‘Nijisseiki’ (S₂S₄). The S₄-allele of the pear is deleted and it shows unilateral incompatibility to cultivar with an S₂S₄ genotype. However, when pollen-tube growth was compared between cross-compatible [‘Osa-Nijisseiki’ × ‘Okusankichi’ (S₅S₇)], unilateral-compatible [‘Osa-Nijisseiki’ × ‘Kikusui’ (S₂S₄)], self-compatible (‘Osa-Nijisseiki’ × ‘Osa-Nijisseiki’), and unilateral-incompatible pollination (‘Kikusui’ × ‘Osa-Nijisseiki’), pollen-tube growth clearly showed the following order: cross-compatible > unilateral-compatible > self-compatible > unilateral-incompatible. This indicates that the ‘Osa-Nijisseiki’ style produces specific inhibitor(s) not only to S₂- and S₄-pollen but also “self-pollen”, because the phenotype of S₄^SM-pollen is the same as S₄-pollen. Stylar protein analysis demonstrated that ‘Osa-Nijisseiki’ produces S₂-RNase (RNase associated with S₂-allele) together with a small amount of S₄-RNase. The purified S₄-RNase possessed almost the same inhibitory action on the growth of S₄-pollen-tubes in vitro at 1 μg μl⁻¹ as that from original ‘Nijisseiki’. These results suggest that the depressed growth of unilateral-compatible and self-pollen-tubes in ‘Osa-Nijisseiki’ is due to this biologically active S₄-RNase. Growth of self-pollen-tubes may also be depressed by inhibitor(s) specific to “self-pollen” unrelated to S-alleles.     

Cross-compatibility of apple cultivars possessing S-RNase alleles of similar sequence

Summary

We investigated the functional differences in three pairs of S-RNase alleles having similar sequences. It was confirmed using pollination tests that S₁₉ and S₂₈ behaved as different alleles, while S₁₇ and S₁₉ appeared to be the same allele. Our previous new allele designation of S_6b in place of S₁₇ and S₁₉, and not S₁₉ and S₂₈, from S-RNase sequence analyses was therefore confirmed. The deduced amino acid sequences of S₃ and S₁₀, although showing high similarity (94%), were functionally distinct.     

DNA profiling of Capsicum landraces of Manipur

Seven chilli landraces of Manipur belonging to three cultivated species of Capsicum (Capsicum annuum, Capsicum frutescens, and Capsicum chinense) form economically important food crops of the region. The genotypes were characterized using ten random amplified polymorphic DNA (RAPD) markers. The cluster analysis based on Jaccard's similarity coefficient calculated by UPGMA method differentiated the genotypes into two main cluster groups. One cluster represented the C. annuum genotypes while the other cluster represented the C. frutescens and the C. chinense genotypes. C. chinense genotypes were more close to C. frutescens genotypes. Genetic variation between the C. frutescens genotypes was more than among the C. annuum genotypes and the C. chinense genotypes were the least similar ones.