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紫外光促进苦荞中黄酮类化合物积累的分子机制探究 被引量:4
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作者 朱智慧 温东 +7 位作者 张栋 晁二昆 董刚强 杜伟 孙伟 Krzysztof Dziedzic 师玉华 薛建平 《中草药》 CAS CSCD 北大核心 2021年第5期1448-1453,共6页
目的研究紫外光对苦荞Fagopyrumtataricum幼苗中黄酮类化合物的影响及其分子机制。方法采用中波紫外光紫外线B(Ultraviolet Radiation B,UVB)处理苦荞幼苗,通过超高效液相色谱仪检测紫外光处理前后苦荞中芦丁等黄酮类化合物含量变化,同... 目的研究紫外光对苦荞Fagopyrumtataricum幼苗中黄酮类化合物的影响及其分子机制。方法采用中波紫外光紫外线B(Ultraviolet Radiation B,UVB)处理苦荞幼苗,通过超高效液相色谱仪检测紫外光处理前后苦荞中芦丁等黄酮类化合物含量变化,同时采用实时荧光定量PCR(qRT-PCR)检测苦荞中黄酮类化合物合成途径中关键酶基因的表达量。结果紫外光处理后苦荞中芦丁、儿茶素和表儿茶素3种黄酮类化合物的含量均显著增加,其中芦丁含量是黑暗处理对照组的1.5倍。同时通过qRT-PCR检测发现苦荞中黄酮类化合物合成途径中苯丙氨酸解氨酶(phenylalanine ammonia lyase,PAL)、肉桂酸-4-羟化酶(cinnamate-4-hydroxylase,C4H)、黄烷酮-3-羟化酶(flavanone-3-hydroxylase,F3H)、二氢黄酮醇-4-还原酶(dihydroflavonol-4-reductase,DFR)等11个关键酶基因的表达量均有不同程度升高。结论UVB通过正调控多个黄酮合成关键酶基因的表达促进苦荞中黄酮类化合物的积累,为阐明UVB对苦荞中黄酮类化合物的调控机制奠定基础。 展开更多
关键词 苦荞麦 紫外光处理 芦丁 黄酮 生物合成途径
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苦荞芽和苗中黄酮类化合物含量差异及关键基因表达分析 被引量:1
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作者 钱广涛 晁二昆 +7 位作者 孙伟 杨维 董刚强 杜伟 陈庆富 朱智慧 盛玮 薛建平 《中国实验方剂学杂志》 CAS CSCD 北大核心 2020年第13期174-180,共7页
目的:研究新资源食品苦荞芽和苦荞苗中黄酮类化合物儿茶素、表儿茶素、芦丁和槲皮素的含量差异及相关基因表达情况,揭示苦荞麦种子发芽过程中黄酮类次生代谢产物及相关基因表达的动态变化趋势,为苦荞芽苗菜的品质选择提供科学依据。方法... 目的:研究新资源食品苦荞芽和苦荞苗中黄酮类化合物儿茶素、表儿茶素、芦丁和槲皮素的含量差异及相关基因表达情况,揭示苦荞麦种子发芽过程中黄酮类次生代谢产物及相关基因表达的动态变化趋势,为苦荞芽苗菜的品质选择提供科学依据。方法:运用超高效液相色谱-串联四级杆质谱(UPLC-ESI-QQQ-MS)对苦荞芽和苦荞苗中儿茶素、表儿茶素、芦丁和槲皮素进行含量检测,并通过实时荧光定量聚合酶链式反应(Real-time PCR)技术检测苦荞芽和苗中有关黄酮类化合物合成相关基因的表达水平。结果:通过多反应MRM模式检测发现苦荞芽和苦荞苗中儿茶素、表儿茶素、芦丁、槲皮素的相对含量及合成路径中相关基因FtPAL,FtC4H,Ft4CL,FtCHS,FtCHI,FtF3H,FtF3’H,FtFLS,FtDFR,FtLAR,FtANS,FtANR的表达量均存在差异,苦荞芽中黄酮类化合物含量和相关基因表达量均高于苦荞苗。结论:苦荞芽中黄酮类次生代谢物的更多积累可能和苦荞麦种子萌发初始阶段抵御外界环境有关。从应用角度来看,苦荞芽中的黄酮类化合物含量高于苦荞苗,具有更高的营养价值。 展开更多
关键词 苦荞芽 苦荞苗 黄酮类化合物 基因表达 发芽过程 动态变化
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Identification of processed Chinese medicinal materials using DNA mini-barcoding 被引量:7
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作者 SONG Ming dong gang-qiang +2 位作者 ZHANG Ya-Qin LIU Xia SUN Wei 《Chinese Journal of Natural Medicines》 SCIE CAS CSCD 2017年第7期481-486,共6页
Most of Chinese medicinal herbs are subjected to traditional processing procedures, including stir-frying, charring, steaming, boiling, and calcining before they are released into dispensaries. The marketing and ident... Most of Chinese medicinal herbs are subjected to traditional processing procedures, including stir-frying, charring, steaming, boiling, and calcining before they are released into dispensaries. The marketing and identification of processed medicinal materials is a growing issue in the marketplace. However, conventional methods of identification have limitations, while DNA mini-barcoding, based on the sequencing of a short-standardized region, has received considerable attention as a new potential means to identify processed medicinal materials. In the present study, six DNA barcode loci including ITS2, psb A-trn H, rbc L, mat K, trnL(UAA) intron and its P6 loop, were employed for the authentication of 45 processed samples belonging to 15 species. We evaluated the amplification efficiency of each locus. We also examined the identification accuracy of the potential mini-barcode locus, of trnL(UAA) intron P6 loop. Our results showed that the five primary barcode loci were successfully amplified in only 8.89%——20% of the processed samples, while the amplification rates of the trnL(UAA) intron P6 loop were higher, at 75.56% successful amplification. We compared the mini-barcode sequences with Genbank using the Blast program. The analysis showed that 45.23% samples could be identified to genus level, while only one sample could be identified to the species level. We conclude that trnL(UAA) p6 loop is a candidate mini-barcode that has shown its potential and may become a universal mini-barcode as complementary barcode for authenticity testing and will play an important role in medicinal materials control. 展开更多
关键词 DNA barcoding trnL(UAA)intron P6 loop IDENTIFICATION PROCESSED MEDICINAL MATERIALS Mini-barcode
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