绿色荧光蛋白基因(GFP)在抗虫转基因植物研究中的应用(英文)

用合成的cry1Ac基因与绿色荧光蛋白基因 (GFP)构成融合蛋白基因 ,然后和改造的GNA基因构建双价抗虫基因植物表达载体pBGbfg ,经根癌农杆菌介导转化了烟草。在紫外灯照射下 ,观察到转基因植株叶片中有较强的绿色荧光 ;经抗虫试验、PCR、Southernblot和Westernblot等检测 ,表明该重组植物表达载体能够在转基因植物中有效表达外源基因 ,转基因植株绿色荧光的表型与其抗虫性密切相关。从而成功地建立了以绿色荧光蛋白基因与抗虫基因组成的融合基因转化系统 ,简化了抗虫转基因植物筛选程序 ,有助于快速获得双价抗虫转基因植株。     

秋茄KcRD22基因的克隆与功能分析

本文以用200 mmol/L NaCl处理24 h后的秋茄幼苗为材料提取秋茄叶片总RNA,利用RT-PCR方法克隆获得KcRD22基因的全长cDNA,通过构建pCAMBIA-2300-KcRD22过表达载体,利用农杆菌侵染的方式获得过表达KcRD22的烟草转基因株系,并对转基因株系的耐盐性做出初步分析.实验结果显示:KcRD22基因的ORF长1 131 bp,编码1个等电点为9.07、分子量为39.8 kD、由375个氨基酸组成的蛋白.PCR及RT-PCR鉴定结果表明,KcRD22基因已经分别整合到8株烟草的染色体中,并在两个株系中获得表达.对转基因烟草进行光合作用测定,结果显示100 mmol/L NaCl处理显著降低了野生型烟草的净光合速率,而转基因植株叶片的光合作用受到的影响较小.盐浓度达到200 mmol/L时,转基因植株及野生型烟草净光合速率都明显降低,但盐胁迫解除后,转基因烟草光合作用的恢复情况明显好于野生型烟草,说明KcRD22的过表达提高了烟草的抗盐性.本文初步确定了KcRD22基因对植物耐盐性的贡献,这为进一步深入研究该基因在耐盐机制中的功能奠定了良好基础.     

转MhGlu基因烟草灰霉病抗性及光合特性研究

以湖北海棠盆栽及组培苗叶片为材料,经NaCl、PEG-6000及4℃下ABA处理后,通过RT-PCR技术克隆了湖北海棠β-1,3-葡聚糖酶基因MhGlu;构建MhGlu基因的植物表达载体,通过农杆菌介导法将MhGlu基因转入烟草中,并通过PCR和RT-PCR检测,成功获得了4个转基因株系T6、T8、T11和T18;以转基因烟草株系T6及T8和非转基因对照植株为材料,对MhGlu基因的功能进行了进一步分析。结果显示:(1)半定量qRT-PCR显示,NaCl、PEG-6000及4℃下ABA处理均可以诱导湖北海棠盆栽及组培苗叶片MhGlu基因的表达;NaCl和PEG-6000处理48h内MhGlu基因的表达随处理时间延长逐渐增强,4℃下ABA处理的MhGlu基因表达量在4h时开始上调,12h时略降低,48h时又达到最大。(2)半定量RT-PCR检测转基因烟草植株几个病程相关基因PRs的表达量,表明过表达的MhGlu基因诱导并增强了烟草病程相关基因NtPR1、NtPR3和NtPR5的表达。(3)用灰霉病侵染烟草叶片,转基因烟草株系T6、T8均表现出较强的抗灰霉病特性。(4)测定烟草植株光合特性参数,转MhGlu基因烟草株系的净光合速率(Pn)、蒸腾速率(Tr)和气孔导度(Gs)较对照组均显著提高,且T8的净光合速率和蒸腾速率均显著高于T6,而T8与T6的气孔导度差异不显著。MhGlu基因在烟草中的过量表达能诱导病程相关基因PRs的表达,激活了烟草的光合特性保护机制,提高了转MhGlu基因烟草植株的灰霉病抗性。     

绿色荧光蛋白基因（G卯）在抗虫转基因植物研究中的应用

用合成的crylAc基因与绿色荧光蛋白基因(GFP)构成融合蛋白基因,然后和改造的GNA基因构建双价抗虫基因植物表达载体pBGbfg,经根癌农杆菌介导转化了烟草。在紫外灯照射下,观察到转基因植株叶片中有较强的绿色荧光;经抗虫试验、PCR、Southern blot和Western blot等检测,表明该重组植物表达载体能够在转基因植物中有效表达外源基因,转基因植株绿色荧光的表型与其抗虫性密切相关。从而成功地建立了以绿色荧光蛋白基因与抗虫基因组成的融合基因转化系统,简化了抗虫转基因植物筛选程序,有助于快速获得双价抗虫转基因植株。     

小黑杨PsnHB22基因在烟草中的遗传转化研究

HD-Zip转录因子在光信号转导、非生物胁迫、叶片发育等方面发挥重要的作用，HB22转录因子是HD-ZipⅠ亚家族的成员之一。为研究PsnHB22基因的功能，从小黑杨（Populus simonii×P.nigra）cDNA中克隆PsnHB22基因并构建植物表达载体进行烟草（Nicotiana tabacum）的遗传转化，以获得该基因过量表达的转基因株系。对转基因株系进行PCR、qRT-PCR分子检测后观察表型，结果显示在营养生长时期，转基因烟草叶片窄小并且株高显著低于野生型对照。测定转基因烟草及野生型叶片的叶绿素含量，发现转基因烟草叶绿素含量显著高于野生型。由此推测PsnHB22基因在植株高生长、光合作用及叶片的形态建成等过程中起着重要的作用。     

利用双T-DNA载体系统培育无选择标记转基因烟草

建立了一种利用双T-DNA载体培育无选择标记转基因植物的方法.通过体外重组构建了双T-DNA双元载体pDLBRBbarm.载体中,选择标记nptⅡ基因和另一代表外源基因的bar基因分别位于2个独立的T-DNA.利用农杆菌介导转化烟草(Nicotiana tabacum L.),在获得的转化植株中,同时整合有nptⅡ基因和bar基因的频率为59.2%.对4个同时整合有nptⅡ和bar基因植株自交获得的T1代株系进行检测分析,发现在3个T1代株系2个T-DNA可以发生分离,其中约19.5%的转基因T1代植株中只存在bar基因而不带选择标记nptⅡ.这一结果说明双T-DNA载体系统能有效地用于培育无选择标记的转基因植物.研究还利用位于2个不同载体上的nptⅡ基因与 bar基因通过农杆菌介导共转化烟草,获得共转化植株的频率为20.0%～47.4%,低于使用双T-DNA转化的共转化频率.     

利用转基因烟草表达人胰高血糖素样肽1的研究

人胰高血糖素样肽1(hGLP1)是一种短肽激素,是近年来备受关注的治疗糖尿病最有前景的候选药物。在设计合成hGLP1基因并构建植物表达载体的基础上,通过农杆菌介导将hGLP1基因导入烟草基因组中,获得转化再生植株,经过PCR扩增和Southern blot分析,证实hGLP1基因已整合进入6个株系的烟草基因组中。GUS组织化学染色表明,与目的基因融合的报告基因在转基因烟草中获得表达。Western blot检测表明,其中2个株系转基因烟草叶片中能够检测到hGLP1融合蛋白的表达。初步的动物试验表明该融合蛋白具有一定的降血糖生物活性。     

转OsMAPK4基因烟草的抗旱性研究与遗传分析

以低温处理的水稻辽盐241植株叶片总RNA为模板, 用OsMAPK4基因特异引物通过RT-PCR扩增出OsMAPK4基因, 构建了由E12启动子调控的OsMAPK4基因植物表达载体pBME12。通过农杆菌介导法将OsMAPK4基因导入烟草, 筛选获得25株转基因植株。抗旱性研究结果表明, OsMAPK4基因的超量表达提高了T1代转基因植株的抗旱性。卡那霉素抗性在T1代转基因植株中的分离情况表明, 大多数转基因株系符合单基因遗传规律。     

转拟南芥ICE1基因增强烟草抗寒性的研究

ICE1是CBF冷响应通道的上游转录调控因子,通过与CBF启动子中MYC顺式作用元件的结合激活CBF3基因表达.采用RT-PCR方法,从拟南芥获得AtICE1基因,将AtICE1导入pCAMBIA1301构建35S:AtICE1植物表达载体.通过根癌农杆菌GV3101,将AtICE1基因导人烟草,T1代植株经潮霉素抗性筛选,PCR、RT-PCR检测,结果表明AtICE1基因已经整合到烟草基因组中,并在转录水平表达;在正常生长条件下,转基因烟草与对照烟草的生长未见明显区别,而在瞬时低温冻害下,转基因烟草存活率明显高于对照烟草植株,说明Atl-CEI基因可以提高低温敏感作物的耐寒性.     

沙柳SpsLAS基因超表达对拟南芥营养生长的影响

用沙柳SpsLAS基因构建35S∷SpsLAS超表达载体并转化野生型拟南芥,对转基因拟南芥进行表型观察,利用荧光定量PCR,对分枝、生长素及细胞分裂素相关基因进行表达分析。结果显示:(1)成功构建35S∷SpsLAS超表达载体,并获得9株纯合转基因株系,且转基因株系的萌芽速率快于野生型(对照),生活周期也较长;其中7个株系表现为生长迅速、株高增加、莲座叶叶片增大、分枝增加,2个株系表现为矮化、分枝增加、育性降低等一系列变化。(2)荧光定量PCR显示,与对照相比24h时转基因株系幼苗生长素及细胞分裂素途径关键基因无明显变化,4d时各基因在各转基因株系呈上调趋势;30d时分枝相关基因RAX1、RAX3表达量均上调,而MAX1、MAX3、REV、AXR1无明显变化。研究表明,SpsLAS基因过表达对拟南芥株型、莲座叶有明显影响,该研究结果为进一步研究该基因对分枝调控机制奠定了基础。     

红豆越桔活性成分研究及开发利用

红豆越桔是一种新兴的水果,其果实根茎叶中含有丰富的活性物质——花青素、黄酮、有机酸等。这些活性物质具有抗氧化损伤、清除氧自由基、抑制癌细胞、提高视力等多种作用。本文综述了国内外近年来对红豆越桔活性物质的研究概况,以及对红豆越桔产品的开发现状,并对进一步的研究提出了展望。     

高效液相色谱法分析测定越桔果渣中的黄酮甙元

采用高效液相色谱法对越桔果渣中黄酮甙元进行定性和定量分析.用甲醇和水（60：40）以0.8 mL/min流速进行洗脱,368 nm波长检测越桔果渣水解液中黄酮类成分并测定其含量.结果：越桔果渣中黄酮甙元主要有杨梅素和槲皮素,其含量分别为：0.0206%和0.0686%.该方法测定样品简单易行,分离效果佳,灵敏度高,重现性好,结果准确可靠.     

分布尼泊尔至台湾的少齿越桔组(越桔属)

对越桔属Vaccinium中曾经被认为属于越桔组sect.Vitis-idoea的种或与之相关的76个运算上的分类单位进行数值分析,并记录了44个特片,解析如下:Vaccinium sect.Vitis-idoea应是局限于越桔V.vitis-idaca这个种而言;5个喜马拉雅的分类单位:V.nummularia,V.paucicrenatum,V．delavayi,V.retusum,V.moupinense,有2个表面上类似V.vitis-idaea的分类单位,运算上部是聚类在一起都被归入少齿越桔组scet.Aethopus.其余20个操作分类单位(OTU)包含10个分类单位,每个都十分特殊,但没有显著的片段的祥式可分辨。     

大兴安岭北部林区野果资源及保护利用

调查了大兴安岭北部林区野生果树种质资源及其开发利用现状。记录到该地区野生肉果类10科,15属,29种。其中越桔和笃斯越桔是大兴安岭北部林区资源极其丰富的野果。蔷薇科有16种,为该地区野生果树的优势科。介绍了11种具有重要经济价值的野果。大兴安岭北部林区的野果资源已得到初步开发利用,越桔、笃斯越桔、山刺玫等数种野果已进入产业化阶段。提出了合理保护和利用对策。     

Contrasting strategies for UV-B screening in sub-Arctic dwarf shrubs

The content and distribution of UV-absorbing phenolic compounds was investigated in leaves of three species of Vaccinium co-existing at a site in north Sweden. Vaccinium myrtillus L., Vaccinium vitis-idaea L., and Vaccinium uliginosum L. exhibit markedly different strategies, in terms of localization and content of leaf phenolics and in their responses to UV-B enhancement. Plants were exposed to either ambient radiation or to enhancement of UV-B corresponding to 15% (clear sky) depletion of stratospheric ozone for approximately 10 years prior to commencement of this study. Vaccinium myrtillus contained the highest concentration of methanol-extractable UV-B-absorbing compounds, which was elevated in plants exposed to enhanced UV-B. Fluorescence and confocal laser scanning microscopy showed that these compounds were distributed throughout the leaf, and were particularly concentrated in chlorophyll-containing cells. In V. vitis-idaea, most phenolic compounds were cell wall-bound and concentrated in the walls of the epidermis; this pool increased in response to UV-B enhancement. It is suggested that these two plants represent extreme forms of two divergent strategies for UV-B screening, the different responses possibly being related to leaf longevity in the two species. The response of V. uliginosum was intermediate between the other two, with high concentrations of cell wall-bound phenolics in the epidermis but with this pool decreasing, and the methanol-soluble pool tending to increase, after exposure to enhanced UV-B. One explanation for this response is that this plant is deciduous, like V. myrtillus, but has leaves that are structurally similar to those of V. vitis-idaea.     

Leaf habit influences nitrogen remobilization in Vaccinium species.

The effect of N supply on plant growth and leaf demography of a deciduous and an evergreen Ericaceae was studied in relation to their internal cycling of N. Mature ramets of Vaccinium myrtillus (deciduous) and Vaccinium vitis-idaea (evergreen) were established in sand culture for 1 year with an adequate supply of a balanced nutrient solution. During one growing season, the plants were given two levels of N supply enriched with 15N and eight sequential destructive harvests were taken. Recovery of unlabelled N in the new shoot was used to determine the remobilization of N from storage. Initially, growth was unaffected by N supply. After May, High N enhanced growth for both species but the nature of their growth response differed. For both species, new shoot biomass and leaf number increased but root biomass production was affected for V. myrtillus only. Whole plant biomass production was similar for both species under High N, but was greater for V. vitis-idaea under Low N. The amount of N remobilized to support new shoot growth was similar for the two species and was independent of N current supply. N was remobilized predominantly from previous year leaves for V. vitis-idaea and from previous year stems and roots for V. myrtillus. The contribution of remobilization to new shoot N was similar for the two species, but depended on N supply. Remobilization was faster in V. myrtillus, but lasted longer in V. vitis-idaea. The results are discussed in relation to species growth in N-poor environments, focusing on the extent to which species-differences in the dynamic of N remobilization and growth may explain their adaptation to constant and/or changeable N supply.     

Late Holocene deforestation of a tree line site: estimation of pre-fire vegetation composition and black spruce cover using soil charcoal

Anatomical identification of soil charcoal fragments was used to reconstruct the pre-fire vegetation composition of a tree line site that burned ca 930 cal. AD in northern Québec, Canada. Soil charcoal was also used as a proxy to estimate black spruce Picea mariana palaeo-cover. The site (a low-elevated hilltop) is presently devoid of spruce trees and dominated by dwarf birch Betula glandulosa , lichens, ericaceous shrubs ( Ledum decumbens , Vaccinium vitis-idaea ) and sedges. In contrast, black spruce dominated before the fire with an understory of Empetrum nigrum and Vaccinium vitis-idaea . Pre-fire black spruce cover was estimated at 32%, giving an indication of the potential for warming-induced natural reforestation of the forest-tundra.     

Effects of water and mineral nutrient supply on a deciduous and an evergreen dwarf shrub: Vaccinium uliginosum L. and V. vitisidaea L.

The effects of irrigation and fertilization on nutrient content, shoot growth and photosynthetic rate of the deciduous Vaccinium uliginosum L. and the evergreen V. vitis-idaea L. were studied in a field experiment at Abisko, Swedish Lapland. V. vitis-idaea responded to fertilization with a greater increase in leaf nitrogen, phosphorus and potassium concentrations, as well as with a relatively greater change in shoot growth than V. uliginosum . Also to irrigation did V. vitis-idaea respond more strongly. Decreased leaf longevity was indicated in both irrigated and fertilized plants of V. vitis-idaea . It is concluded that no general response pattern for evergreen and deciduous plants can be expected to emerge unless one also takes other plant characteristics, and also site characteristics, into consideration.     

大豆fad基因反义表达载体构建及转化烟草研究

使用PCR方法从大豆基因组DNA中扩增出大豆油酸脱饱和酶基因fad2-1,连接到pMD18-T载体中,转化大肠杆菌JM109菌株.测序后,用DNAstar软件进行同源性比对.然后将正确的序列反向克隆到表达载体pBt,并转化农杆菌菌株LBA4404,经双酶切鉴定和PCR扩增检测,获得具有该基因反向序列的农杆菌工程菌,转化...