分子标记在啤酒花种质资源研究中的应用

该论文利用分子生物学中常用的DNA分子标记对世界各地现存的野生和栽培的啤酒花种质资源遗传多样性研究的应用进展做一综述。通过查阅和研读20世纪90年代以来发表的各类文献进行归纳总结。发现DNA分子标记相比形态学标记和细胞学标记具有结果准确、稳定的特点,常用的分子标记技术有RAPD、RFLP、ISSR、SSR、AFLP、EST等;研究发现北美洲的啤酒花遗传多样性要高于欧洲的啤酒花,基因变异程度也相对较高;野生啤酒花的基因序列具有丰富的基因多样性,可在分子杂交遗传育种中作为一个种质去改善栽培品种的某些不良性状。因此,利用分子标记研究啤酒花的遗传多样性将对啤酒花的优良育种提供理论指导和技术支持,目前较为理想的技术是SSR和AFLP。     

安神健胃碑酒花

啤酒花(Humulus lupulus)又称忽布(英语俗名Hop的音译)和蛇麻。大麻科(艹律)草属多年生草质蔓生藤本。全球北温带地区广泛栽培或逸为野生。德国和美国是现今种植啤酒花的大国。 啤酒花雌雄异株,花单性。雌性球穗花序简称酒花,包含花茎、花轴、曲节和分枝轴以及前     

啤酒花的萃取

本文综述了使用啤酒花萃取物的优点以及啤酒花的超临界二氧化碳萃取和液态二氧化碳萃取的特点。     

啤酒花节间外植体再生体系的建立

在国内首次建立了两个啤酒花主栽品种（麒麟丰禄,青岛大花）的节间外植体再生体系。实验表明：啤酒花无菌苗的节间为适于不定芽再生韵外植体;适宜的再生培养基为Ms基本培养基＋B5维生素＋葡萄糖20g／L,附加IAA0．25mg／L＋TDZ2mg／L（麒麟丰禄）或IAA0．125mg／L＋TDZ1．5mg／L（青岛大花）,以7g／L琼脂固化,pH5．8;不定芽再生频率可达57％（麒麟丰禄）或16％（青岛大花）。啤酒花再生体系的建立,为利用植物基因工程技术培育抗病虫害啤酒花新品系奠定了基础。     

啤酒之魂 啤酒花

啤酒花是酿造啤酒的重要原料之一,它赋于啤酒一种独特的苦味和芳香。因此,啤酒酿造业称它为“啤酒之魂”。啤酒花(Humulus lupulus L)植物学名称是蛇麻,又叫忽布。大麻科植物,多     

啤酒花抗性机制的研究进展

酒花苦味酸是构成啤酒风味的重要组分,也是啤酒生产过程中的天然抑菌剂,酒花苦味酸通过降低pH梯度而抑制啤酒花敏感菌生长。研究发现,啤酒花抗性菌是通过膜上转运蛋白将酒花苦味酸泵出细胞外,以降低膜上的质子流速,维持了细胞内的pH梯度。结合近年来酒花抗性相关研究结果,讨论了细胞膜上酒花抗性相关组分与酒花抗性间的关系,提出了酒花抗性机制的模型。     

多效唑（MET）对啤酒花试管苗生长和移栽的影响

在培养基中加入0.1-0.2mg/L浓度的多效唑（MET）,啤酒花试管苗植株矮壮,单株生根数量增加、移栽成活率提高13％。0．5－2．0mg/L时,试管苗基部愈伤组织增多,枝叶失绿,生长受到抑制。初步发现多将唑对啤酒花试管苗的效力与葡萄糖用量呈正相关。     

啤酒花试管苗移栽过程中的某些生理生化特性变化

本文检测了接种后不同时期啤酒花(Humulus lupulus)试管苗和其移栽成活后以及实地二年生啤酒花生长过程中的叶绿素、还原糖、总糖、蛋白质含量和根系活性变化.实验材料有经过继代后培养15 d的啤酒花无菌苗叶片(ZY1)和根系(ZG1)、继代后培养30 d的无菌苗叶片(ZY2)和根系(ZG2)、外部移栽15 d初步成活苗的叶片(WY1)和根系(WG1)、外部移栽50 d完全成活苗的叶片(WY2)和根系(WG2)、外部移栽100 d完全成活苗的叶片(WY3)和根系(WG3)、实地二年生的叶片(CKY)和根部(CKG).     

江苏云台山野生珍稀濒危中药植物初步研究

通过查阅资料,访问及实地调查等方法,报道了云台山野生珍稀濒危中药植物24科37种,对它们的生长环境、药效及现在情况做了介绍,并分析了云台山野生中药植物资源被破坏的主要原因,提出了对云台山野生药用植物资源进行保护的具体措施。     

中国野生蜜蜂形态描述与地理分布概况

对2010年5月-9月采集的蜜蜂属Apis中野生蜜蜂进行鉴定,根据形态特征编制了中国蜜蜂属的分类检索表,并对各个种的主要形态特征进行了描述,同时对野生蜜蜂在我国及世界的分布情况进行了简要介绍。本文期望通过这次采样及基础研究推动对野生蜜蜂研究以及野生蜜蜂的保护工作的重视。     

Preliminary Observatiun of the Sex-Chromosomes of Rumex acetosa in China

The Rumex acetosa L. in China possesses sex-chromosomes 2n=12A+XX in female plant and 2n=12A+XY1Y2 in male plant. The sex-chromosomes of male plant exhibit a chain of trivalent (Y1-X-Y2) in diakinesis of PMC meiosis. At metaphase Ⅰ, they make a V-shaped or a ring configuration. Some of them may form a XY-bivalent and a Y-univalent. Finally two kinds of reale gametes e.g. 6A+X and .6A+YY, are produced. Monoecious plant may be found in R. acetosa and has 22 chromosomes (22=18A+ XX+YY). This is a triplont with sterility. Cells with different chromosome number in the same plant have also seen in R. acetosa, and such plant never blooms in its life.     

Karyology and Cytotaxonomy of the Genus Chrysolina Motschulsky (Coleoptera, Chrysomelidae)

Eight species of Chrysolina have been chromosomally studied in male individuals from Central Europe, South France and the Urals, in Russia. Ch. rufa had 2n = 23, Ch. purpurascens crassimargo 2n = 24 and a meioformula of 11 + Xy_p, Ch. globosa and Ch. bigorrensis 12 + Xy_p, Ch. umbratilis 2n = 30 and 14 + XY_p, a new non-chiasmate sex-chromosome system with both male sex-chromosomes of large size, Ch. cf. subcostata 12 + XY_p with large sex-chromosomes also, Ch. interstincta 2n = 40 and 19 + Xy_p, and Ch. obscurella 2n = 47. The taxonomic implications of these findings are discussed in relation with the current subgeneric classification of Chrysolina and principally that of the subgenera Colaphoptera, Sphaerochrysolina, Pleurosticha, Chalcoidea and Threnosoma.     

大麻染色体行为分析

以大麻不同性别的植株为材料,常规压片法观察细胞染色体行为规律。核型分析结果表明:大麻雌雄株的体细胞染色体数目均为2n=20,核型公式分别为雌株2n=2x=20=18m 2sm,雄株2n=2x=20=18m 2sm(1SAT)。雌株体细胞中有2条X染色体,而雄株只有一条X染色体和一条具有大随体的Y染色体。雌雄株核型均为2A型,为较对称核型。这一结果可为进一步研究大麻性别的分化机制提供细胞遗传学理论依据。     

七种药用植物的染色体研究

对山东７种药用植物的染色体进行了研究。结果表明：田旋花（ＣｏｎｖｏｌｖｕｌｕｓａｒｖｅｎｓｉｓＬ）的染色体数目为２ｎ＝７８;蜜柑草（ＰｈｙｌａｎｔｈｕｓｍａｔｓｕｍｕｒａｅＨａｖａｔａ）的染色体数目为ｎ＝８８;挂红灯（ＰｈｙｓａｌｉｓａｌｋｅｋｅｎｇｉＬｖａｒｆｒａｎｃｈｅｔｉ（Ｍａｓｔ）Ｍａｋｉｎｏ）的染色体数目为２ｎ＝２４,核型公式为Ｋ（２ｎ）＝２４＝２ｍ＋１８ｓｍ＋２ｓｔ＋２ｓｔ（ｓａｔ）,核型“２Ａ”型;无剌曼陀罗（ＤａｔｕｒａｓｔｒａｍｏｎｉｕｍＬｖａｒｉｎｅｒｍｉｓ（Ｊａｃｑ）ＳｃｈｉｎｚｅｔＴｈｅｌ）的染色体数目为２ｎ＝２４,核型公式为Ｋ（２ｎ）＝２４＝２０ｍ＋４ｓｍ,核型“１Ｂ”型;决明（ＣａｓｉａｔｏｒａＬ）的染色体数目为２ｎ＝２６,核型公式为Ｋ（２ｎ）＝２６＝２４ｍ＋２ｓｍ,核型“１Ａ”型;荔枝草（ＳａｌｖｉａｐｌｅｂｅｉａＲＢｒ）的染色体数目为２ｎ＝１６,核型公式为Ｋ（２ｎ）＝１６＝６ｍ＋１０ｓｍ,核型“２Ａ”型;车前（ＰｌａｎｔａｇｏａｓｉａｔｉｃａＬ）的染色体数目为２ｎ＝３６,核型公式为Ｋ（２ｎ）＝３６＝３２ｍ＋４ｓｍ,核型“１Ａ”型。     

Karyological notes on six beetle species from Armenia (Coleoptera: Tenebrionidae,Cerambycidae, Curculionidae)

Karyotypic details were studied in males of six beetle species from three families, viz. Tenebrionidae: Dailognatha pumila Bdy. (2n = 20, n(male) = 9 + Xy(p)), Pachyscelis musiva Ménétr. (2n = 18, n(male) = 8 + Xy(p)), Pimelia capito Kryn. (2n = 18, n(male) = 8 + Xy(p)); Cerambycidae: Agapanthia walteri Reitt. (2n = 20, n(male) = 9+Xy(p)), Agapanthia korostelevi Danilevsky (2n = 20, n(male) = 9 + Xy(p)); Curculionidae: Phyllobius caucasicus Stierl. (2n = 22, n(male) = 10 + Xy(p)). The chromosome number and sex determining system of all beetle species are described for the first time. Evolutionary trends in karyotypes of the studied beetle groups are briefly discussed.     

辽宁地区产6种乌头(Aconitum)的细胞分类学研究

对我国辽宁地区毛莨科(Ranunculaceae)乌头属(Aconitum) 6个种的染色体的数目和形态进行了研究,并进行了核型分析。其染色体基数为X=8,核型公式为:两色乌头:2n=2x=2m+10sm+4st;蛇岛乌头为:2n=4x=10m+20sm(SAT)+2st+2B;黄花乌头为:2n=4x=4m+12sm(SAT)+8st+1B;北乌头三倍体为:2n=3x=2M+4m+18sm;北乌头4倍体为2n=4x=4m+28sm。同时,对乌头属下某些种的分类学问题进行了探讨。     

Characterization of backcross generations obtained under field conditions from oilseed rape-wild radish F1 interspecific hybrids: an assessment of transgene dispersal

Gene flow from glufosinate-resistant transgenic oilseed rape to wild radish was studied over two backcross generations. Under field conditions,?seed production from oilseed rape-wild radish F₁ hybrids due to pollination by wild radish was always low: on average 0.12 and 0.78 seeds per 100 flowers and per plant, respectively. The cytogenetics of the resulting «BC₁» plants can be explained in the main by three different genomic constitutions: either ACRrRr, 2n=37, ACRr, 2n=28 (the same chromosome number as the mother plant), or by the amphidiploid AACCRrRr, 2n=56. The probability of gene exchange through chromosome pairing was high only in plants with 2n=28 or 37 chromosomes. Due to the viability of unreduced or partially reduced female gametes, most of the «BC₁» plants (81.9%) were Basta resistant whereas the analysis of oilseed rape specific loci indicated that their transmission varied with the locus. In spite of low male fertility (8.7%), an improvement of the female fertility over the F₁ hybrids was observed with an average production of 1.4 and 11 seeds per 100 flowers and per plant, respectively. At the following «BC₂» generation, the bar gene transmission (57.2% of Basta-resistant plants) decreased as did the chromosome number, with a majority of plants having between 24 and 27 chromosomes, with 10.5% similar to wild radish (2n=18). The lower the chromosome number, the better the fertility of the «BC₂» plants. On average, 7.9 and 229.3 seeds per 100 flowers and per plant were produced. Gene-flow assessment is discussed based on these data.     

山东10种植物的核型分析

对山东１０ 种植物进行了核型分析。茴茴蒜（ Ｒａｎｕｎｃｕｌｕｓｃｈｉｎｅｎｓｉｓ Ｂｇｅ－） 染色体数目２ｎ ＝１６ , 核型公式Ｋ（２ｎ） ＝ ２ｘ ＝ １６ ＝ ２ Ｍ ＋ ２ｍ ＋ ２ｓｍ ＋ １０ｓｔ, “３Ａ”类型; 五脉地椒（ Ｔｈｙｍｕｓｑｕｉｎｑｕｅｃｏｓｔａｔｕｓ Ｃｅｌａｋ－） 染色体数目２ｎ＝ ２６ , 核型公式Ｋ （２ｎ） ＝ ２ｘ＝ ２６ ＝ ８ Ｍ ＋ １８ｍ , “１Ａ”类型; 蛇床（ Ｃｎｉｄｉｕｍ ｍｏｎｎｉｅｒｉ（Ｌ－） Ｃｕｓｓ－） 染色体数目２ｎ＝ ２０ , 核型公式Ｋ （２ｎ） ＝ ２ｘ＝ ２０ ＝ ２Ｍ＋ １６ｍ ＋ ２ｓｍ , “２Ｂ”类型; 波斯菊（ Ｃｏｓｍｏｓ ｂｉｐｉｎｎａｔｕｓ Ｃａｖ－） 染色体数目２ｎ ＝ ２４ , 核型公式Ｋ（２ｎ） ＝ ２ｘ ＝ ２４ ＝ １６ｍ ＋ ２ｍ （ｓａｔ） ＋ ６ｓｍ , “２Ａ”类型; 白车轴草（ Ｔｒｉｆｏｌｉｕｍ ｒｅｐｅｎｓ Ｌ－） 染色体数目２ｎ＝ ３２ , 核型公式Ｋ （２ｎ） ＝ ４ｘ ＝ ３２ ＝ ３２ｍ , “１Ａ”类型; 铁苋菜（ Ａｃａｌｙｐｈａ ａｕｓｔｒａｌｉｓ Ｌ－）染色体数目２ｎ ＝ ３２ , 核型公式Ｋ （２ｎ） ＝ ２ｘ＝ ３２ ＝ ３２ｍ , “１Ｂ”类型; 地构叶（ Ｓｐｅｒａｎｓｋｉａ ｔ?     

白豆杉的核型和性染色体的研究

白豆杉pseudotaxus chienii(Cheng)Cheng是我国裸子植物特有属之一,雌雄异常,根尖 细胞染色体分析表明：雌株有一对异形性染色体,异配性别,属ZW型;雄株是同配性别,属ZZ型,雌株的型为2n=2x=24=22m(2SAT ZW) 2T,雄株的核型为2n=2x=24=22m(2SAT ZZ) 2T。Giemsa C-带,显示,Z染色体长短臂均具端带,W染色体不显带。     

Studies on Three Different Karyotypes of Wild Rice in China

In this paper three different karyotypes of wild rice species growing in China were examined, after the preparation of chromosome sample by wall degradation, hypotonic treatment and flame-drying method and stained with Giemsa, i.e., the karyotype of Oryza perennis: K(2n) = 24 =2Asm 20Bsm + 2tCsm; the karyotype of O. officinalis: K(2n) =24=4Am+18Bsm+2tCsm; the karyotype of O. meyeriana: K(2n)= 24= 6Am + 16Bsm + 2tCsm.