‘品丽珠’葡萄不同营养系酚类物质差异分析

筛选山东蓬莱产区酿酒葡萄‘品丽珠’黄烷醇、花色素苷含量较高的优良营养系，以期为发挥其酿酒性能提供理论依据。以蓬莱产区品丽珠母本及3个芽变营养系（214、327、623）为试材，采用分光光度计法分析葡萄果皮和种子中总酚、总单宁、总花色素含量，利用高效液相色谱法分析酚酸类、黄酮醇类、黄烷醇类、花色苷单体及白藜芦醇含量。研究结果表明，黄烷醇是种子和果皮中主要的单体酚，其中儿茶素含量最高；二甲花翠素葡萄糖苷是果皮中主要的花色苷。在相同的栽培管理条件和自然条件下，品丽珠不同营养系间的酚类物质差异较明显，相同营养系不同年份间也有显著差异。其中营养系623果皮和种子的总酚、种子的单宁和黄烷醇以及果皮和种子中的酚酸类、单体花色苷含量显著高于其他营养系和母本。     

‘越心’草莓组培突变体着色差异的分子机理初探

初步探讨了在‘越心’草莓（Fragaria × ananassa‘Yuexin’）茎尖离体培养再生植株中发现的稳定变异突变体着色差异的分子机理。分析结果显示，突变体与‘越心’在植株形态、始花期、始果期、始熟期、单果质量、平均株产、果形、风味等方面均无明显差异；而突变体外果皮色泽较淡，L*值较高，a*值较低，H色度角值较大，颜色指数CIRG显著小，且果肉不着色（‘越心’果肉红色）。突变体果实总花青苷含量为‘越心’的13.2%，其中以天竺葵素–3–O–葡萄糖苷（Pg3G）含量差异最大，突变体Pg3G含量仅为‘越心’的12.9%。花青苷合成途径结构基因FaF3H、FaCHS、FaDFR、FaANS、FaCHI、Fa3GT的表达水平在突变体中显著降低，这可能是突变体成熟果实花青苷水平显著低于‘越心’的直接原因。FaMYB10和FaMYB1在突变体中的表达水平显著下降，且FaMYB10在几个主成分中的特征向量绝对值均显著较高，进一步证实了MYB10是草莓成熟过程中花青苷合成的类黄酮或苯丙烷类化合物途径主要调节因子之一。提取叶片基因组DNA进行基于KASP标记的基因分型结果显示，74对KASP引物在‘越心’草莓及其突变体中的基因分型不存在差异。本结果初步证实突变导致参与调控花青苷合成途径的关键基因表达发生显著下调从而使花青苷积累显著减少，果实着色变淡。     

不同花色牡丹品种花瓣色素含量及成分分析

以分属白、粉、红3个色系的6个牡丹品种花瓣为试材,采用薄层层析色谱法(TLC)、紫外-可见分光光度计(UV)和高效液相色谱仪-二极管阵列检测器(HPLC-DAD)研究不同花色牡丹品种花瓣中的色素含量,并进行了定性分析。结果表明:粉色和红色系牡丹中检测出2种花青苷,分别是矢车菊素-3,5-二葡糖苷和芍药花素-3,5-二葡糖苷,白色系牡丹中未检测到花青苷类物质,其中矢车菊素-3,5-二葡糖苷在粉色系牡丹中含量较高,而红色系中总黄酮和总花青苷的含量最高。     

高花青素洋葱品种"秀球赤玉"的选育与特征特性

“秀球赤玉”是以高花青素深紫皮不育系562A为母本，以高花青素深紫皮自交系2014-7-10-6为父本培育的中日照、早熟、高花青素三系杂交种。其表现：鳞茎大圆球形，花青素含量高达68.8 mg/g；洋葱鳞片从外至里均为深紫色，色泽亮，外观漂亮，商品率高；辣味轻，口感脆甜，可生食；植株长势强，抗病，耐抽薹，分球、裂球少；假茎细且收口紧，耐贮性好；平均单球质量600～1 000 g，667 m2产量8 000～12 000 kg；适宜在中日照地区推广，2019—2020年累计推广面积超过1 500 hm2。     

大白菜花青素含量及色差指标相关性研究

为了探寻大白菜花青素含量快速测定的方法,本文利用pH差计法和色差仪分别测定了‘城阳青’(普通大白菜)、‘秋宝黄’(黄心白菜)和‘彩凤’3个不同叶色大白菜品种花青素含量以及色差指标,并对6个色泽参数与花青素含量进行了相关和回归分析。结果表明:6个色泽参数均能反映白菜叶片间叶色的细微变化,‘城阳青’和‘秋宝黄’不含花青素,紫色白菜‘彩凤’的花青素主要分布于由外向内的第1～4层叶片。色泽参数L,b,h和C分别与花青素含量呈极显著或显著负相关关系(相关系数分别为-0.85**,-0.58**,-0.49*,-0.58**)。以色泽参数值L、a、h与花青素含量建立了多元回归方程:y=90.24-1.07x1+5.65x2-142.71x3(x1为L值,x2为a值,x3为h值,y为花青素含量),该回归方程相关系数为0.9629。通过色差计依据建立的回归方程可快速测定紫色大白菜花青素的含量。     

The study of introgressive lines of Triticum aestivum × Aegilops speltoides by in situ and SSR analyses

Fluorescence in situ hybridization (FISH) with a genome‐specific repeat, Spelt1, and wheat simple sequence repeat (SSR) markers were used to analyse the chromosome constitution of two Triticum aestivum×Aegilops speltoides introgressive lines. The lines 170/98i and 178/98i carried one and two subtelomeric regions of Ae. speltoides (per haploid genome), respectively, marked by Spelt1 repeats according to FISH data. SSR analysis detected homoeologous substitution of wheat chromosome 7D with Ae. speltoides chromosome 7S in the lines 178/98i and 170/98i as well as the assumed terminal translocation in the short arm of chromosome 3A in the line 178/98i. Anthocyanin pigmentation of the coleoptiles was found in the lines 170/98i and 178/98i and resulted from the 7S (7D) substitution. It was demonstrated that Spelt1 could be effectively used for the rapid identification (without DNA isolation) of terminal translocations of T. aestivum×Ae. speltoides introgressive lines as well as for further analysis of the stability of the hybrid plants.     

Detection of linkage between RFLP markers and genes affecting anthocyanin pigmentation in maize (Zea mays L.)

Summary Linkages between molecular markers and genes involved in the expression of agronomical traits have already been described in all of the major crops. In most cases, the genetic model underlying the Quantitative Traits Loci (QTL) is discussed. Here, Restriction Fragment Length Polymorphisms (RFLPs) and Mapmaker-QTL have been used to pinpoint seven regions of the genome significantly correlated with four pigmentation qualitative traits of maize (Zea mays L.). Two of these, located on chromosomes 2 and 10, explain most of the variation of these traits. The R and B gene loci known to be involved in the regulation of the anthocyanin pathway map to the same regions and we suggest that these loci could be the candidate genes involved in the correlations detected with RFLPs. This type of result is in accordance with the hypothesis of the candidate gene which supposes that, if we have a very high density map of randomly-selected cDNA clones, it should theoretically be possible to associate a cloned genic sequence with a phenotypic trait where correlations are found.     

芥蓝二氢黄酮醇4–还原酶基因BoaDFR的克隆与功能鉴定

以白花芥蓝‘四季粗条’为材料克隆了Boa DFR基因,Gen Bank登录号为MT472647,CDS序列长为1158 bp,编码385个氨基酸,与甘蓝型油菜、甘蓝和白菜等具有高度同源性。Boa DFR表达水平在芥蓝不同发育时期、不同器官中存在显著差异,随植株发育总体呈现先下降后上升的趋势,在幼嫩种子中表达量最高。芥蓝原生质体的亚细胞定位结果显示Boa DFR定位在细胞核上。构建了农杆菌介导的芥蓝瞬时过表达体系,将Boa DFR转入白花芥蓝‘四季粗条’和黄花芥蓝‘福州黄花’中,发现Boa DFR在两种芥蓝中均高水平表达,转基因植株叶片颜色明显变紫,花青素苷显著积累,总含量最高达461.43μg·g-1 FW,而野生型和转空载体芥蓝叶片中几乎检测不到花青素苷。通过HPLC在转基因植株叶片中共检测到8种花青素苷,均为矢车菊花青素苷,其中矢车菊–3–阿魏酰–丙二酰–槐糖苷–5–葡萄糖苷占比最高。