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1.
【背景】马克斯克鲁维酵母(Kluyveromyces marxianus)具有完整的木糖代谢途径,可以高效利用木质纤维素中的木糖,因此对其糖转运蛋白基因的研究或可有效解决酵母木糖转运的相关问题。【目的】根据马克斯克鲁维酵母DMKU3-1042中KLMA_70145和KLMA_80101基因位点的功能预测,获得马克斯克鲁维酵母GX-UN120相应的糖转运蛋白基因序列并探究其功能。【方法】将转运蛋白基因分别克隆表达至酿酒酵母EBY.VW4000中考察重组菌株生长特性,以此间接评价对应转运蛋白的转运能力。【结果】Km_SUT2基因编码的糖转运蛋白可有效提高宿主细胞转运木糖、阿拉伯糖、山梨糖、核糖、乳糖和葡萄糖的能力,但却不能转运甘露糖、果糖、蔗糖和半乳糖。类似地,Km_SUT3基因编码的糖转运蛋白可提高细胞转运木糖、阿拉伯糖、山梨糖、半乳糖、核糖、乳糖和葡萄糖的能力,但却不能转运甘露糖和果糖。然而在葡萄糖存在的条件下,重组菌株对各种碳源的利用均受抑制,但Km_SUT3转运木糖和核糖过程中受葡萄糖的抑制作用较小。【结论】马克斯克鲁维酵母GX-UN120中转运蛋白Km_SUT2和Km_SUT3可...  相似文献   
2.
地衣芽胞杆菌有效的基因编辑工具有限,为了拓展和丰富其基因编辑手段,在地衣芽胞杆菌中构建一个抗性标记可重复使用的FLP/FRT基因编辑系统,并通过敲除α-淀粉酶基因amyL、蛋白酶基因aprE及敲入外源透明颤菌血红蛋白基因vgb对该系统进行初步验证。首先以温敏质粒pNZT1为载体分别构建amyL和aprE基因敲除质粒pNZTT-AFKF和pNZTT-EFKF,两个敲除质粒各自包含针对目标基因的同源臂、抗性基因及同向的FRT位点;将敲除质粒转化地衣芽胞杆菌并经过两次同源交换过程实现目标基因的敲除;最后导入一个FLP重组酶表达质粒通过FLP/FRT系统的重组作用介导抗性基因的回收。为进一步验证本系统的实用性及编辑效率,构建了包含透明颤菌血红蛋白编码基因vgb表达盒及基因组丙酮酸甲酸裂解酶编码基因pflB敲除盒的重组质粒pNZTK-PFTF-vgb,并以此进行外源基因vgb在基因组上的定向敲入。结果显示,成功敲除amyL及aprE并回收了抗性标记卡那霉素基因,敲除后淀粉酶活和蛋白酶活分别减少95.3%和80.4%;vgb基因成功整合入基因组pflB位点并回收了抗性标记四环素基因,并利用荧光定量PCR技术检测到vgb的整合表达。文中首次建立了一个适用于地衣芽胞杆菌的、抗性标记可重复使用的FLP/FRT基因编辑系统,并进行了基因敲除及基因敲入验证,为地衣芽胞杆菌遗传改造提供了良好的方法参考。  相似文献   
3.
几种控释氮肥减少氨挥发的效果及影响因素研究   总被引:25,自引:4,他引:21  
采用“静态吸收法”和“土柱淋溶法”、室内模拟试验,研究几种控释氮肥施入土壤后的氨挥发损失情况、N溶出速率、土壤脲酶活性及pH值变化的关系.结果表明,施氮450mg·kg^-1土时,3种控释氮肥氨挥发损失氮总量分别比普通尿素减少49.7%、28.0%和71.2%;施氮600mg·kg^-1土时,3种控释氮肥氨挥发损失氮总量分别比普通尿素减少34.6%、12.3%和69.9%.控释氮肥能显著降低土壤氨挥发量,减少因施肥而引起的大气环境污染.控释氮肥氨挥发量与不同氮肥引起的土壤脲酶活性、pH值、土壤中氮溶出速率密切相关.土壤的氨挥发总量与肥料在土壤中溶出总量的相关系数达到0.9533,在肥料施入的前期土壤氨挥发量同土壤脲酶活性、pH值的相关系数达到0.9533和0.9908。  相似文献   
4.
Crystal growth regulation has become an effective solution to reduce the defects at grain boundaries (GBs) and surfaces of perovskite films for better photovoltaic performances. Oxime acid materials are maturely used as selective collectors in the flotation separation of oxide minerals. Such materials, showing a strong coordination effect and high selectivity with lead, may have great potential in controlling the crystal growth and passivating the defect of perovskite film, which are rarely applied in perovskite solar cells (PerSCs). Herein, an oxime acid-based material with multi-coordination sites, ethyl 2-(2-aminothiazole-4-yl)-2-hydroxyiminoacetate (EHA), is incorporated into the PbI2 precursor solution to fabricate high-performance PerSCs using a two-step method. The multidentate coordination effect of EHA can link and integrate the PbI2 colloidal clusters to achieve pre-aggregation in the PbI2 precursor solution, facilitating the sequent crystal growth progress of perovskite film. Meanwhile, EHA can connect grains and fill GBs, which is favorable for charge transfer and passivating both Pb-I anti-site and iodine vacancy defects. As a result, the optimal devices show an enhanced efficiency of 24.1% and excellent humidity and thermal stability. This work affords a promising strategy to fabricate efficient and stable PerSCs via multidentate coordination-induced crystallization control and GB passivation.  相似文献   
5.
Intracellular polyamines(putrescine, spermidine, and spermine) have emerged as important molecules for viral infection;however, how viruses activate polyamines biosynthesis to promote viral infection remains unclear. Ornithine decarboxylase 1(ODC1) and its antienzyme 1(OAZ1) are major regulators of polyamine biosynthesis in animal cells. Here, we report that rice yellow stunt virus(RYSV), a plant rhabdovirus, could activate putrescine biosynthesis in leafhoppers to promote viral propagation by inhibiting OAZ1 expression. We observed that the reduction of putrescine biosynthesis by treatment with difluormethylornithine(DFMO), a specific nontoxic inhibitor of ODC1, or with in vitro synthesized dsRNAs targeting ODC1 mRNA could inhibit viral infection. In contrast, the supplement of putrescine or the increase of putrescine biosynthesis by treatment with ds RNAs targeting OAZ1 mRNA could facilitate viral infection. We further determined that both RYSV matrix protein M and ODC1 directly bind to the ODC-binding domain at the C-terminus of OAZ1. Thus, viral propagation in leafhoppers would decrease the ability of OAZ1 to target and mediate the degradation of ODC1, which finally activates putrescine production to benefit viral propagation. This work reveals that polyamine-metabolizing enzymes are directly exploited by a vector-borne virus to increase polyamine production, thereby facilitating viral infection in insect vectors.  相似文献   
6.
荞麦起源于我国, 演化形成了丰富的物种和遗传多样性。为了有效研究和利用荞麦及其野生种资源, 以从四川、甘肃、贵州等地采集的荞麦属(Fagopyrum)10个种(含变种、亚种和复合体种)共71份材料为对象, 通过ITS和叶绿体ndhF-rpl32序列分析, 利用MEGA5.0构建系统进化树, 探讨了荞麦种内及种间亲缘关系。结果表明, 在ITS序列矩阵中, 序列长度为725 bp, 信息位点为150个, 占序列总长度的20.7%; 在ndhF-rpl32序列矩阵中, 序列长度为940 bp, 信息位点为158个, 占序列总长度的16.8%。由ITS序列和ndhF-rpl32序列构建的两个进化树都可以将71份材料分为大粒荞麦种组和小粒荞麦种组; 其中, 大粒荞麦种组包括栽培苦荞和米苦荞(F. tataricum)、金荞复合体(F. cymosum complex)、栽培甜荞(F. esculentum)和野生甜荞(F. esculentum ssp. ancestralis); 小粒荞麦种组包括齿翅野荞(F. gracilipes var. odontopterum)、疏穗小野荞(F. leptopodum var. grossii)、小野荞(F. leptopodum)、密毛野荞(F. densovillosum)、细柄野荞(F. gracilipes)和硬枝万年荞(F. urophyllum)。而ndhF-rpl32序列构建的系统发育树还能区分栽培甜荞和野生甜荞, 具有更好的聚类效果。另外, 与栽培甜荞相比, 金荞复合体与栽培苦荞的亲缘关系更近。该研究为荞麦属种的分类和条形码研究提供了一定的科学依据。  相似文献   
7.
以魔芋生粉为唯一碳源的筛选培养基,从魔芋废渣中分离筛选出一株可以降解魔芋生粉的细菌菌株,编号为LS-6。根据16SrDNA序列和生理生化特性,将该菌株鉴定为枯草芽孢杆菌Bacillus subtilis。胞内外葡甘露聚糖酶酶活分析结果表明,LS-6产生的葡甘聚糖酶为胞外酶。LS-6产生葡甘聚糖酶的最佳培养基组分和条件是:1%魔芋生粉,0.5%酵母粉,0.5%NaCl,培养基初始pH为6.0,最佳发酵条件是25℃,摇床转速200r/min,培养48h。酶解产物的高效液相色谱分析结果表明,LS-6粗酶液的酶解产物主要为葡萄糖和甘露糖。LS-6的分离为进一步克隆常温葡甘聚糖酶基因和产酶工程菌的构建奠定了基础。  相似文献   
8.
广州地区晚稻田CH4和N2O的排放通量及其影响因素   总被引:23,自引:3,他引:23  
用密闭箱法同时研究了广州地区晚稻田CH4和N2 O的排放通量。结果表明 ,连续淹水、常规连作和水旱轮作等 3种处理的CH4平均排放通量分别为 1 7 63、2 84和0 36mg·m- 2 ·h- 1 ,而N2 O的平均排放通量分别为 6 74、1 1 69和 55 0 7μgN2 O N·m- 2 ·h- 1 ,表明稻田连续淹水显著增加CH4的排放而降低N2 O的排放。水旱轮作降低CH4排放而提高N2 O的排放 ,说明稻田CH4和N2 O排放之间存在着消长关系。讨论了这 2种温室气体排放的影响因素 ,并初步分析了它们对温室效应的相对贡献。  相似文献   
9.
菠萝-甘蔗轮作的土壤生态效应   总被引:8,自引:0,他引:8  
郑超  廖宗文  谭中文  刘可星 《生态科学》2003,22(3):248-249,274
通过2000~2002年进行菠萝-甘蔗轮作田间试验,研究了菠萝、甘蔗轮作对甘蔗土壤生态的影响。结果表明:菠萝甘蔗轮作田与甘蔗连作田比较,能明显地改善土壤的通气和蓄水性,加速速效性养分的释放;增强土壤酶活性;增加土壤微生物总量(一般好气性细菌、真菌、放线菌);有益的氨化细菌和硝化细菌成倍增加,而无益的厌氧性细菌、反硝化细菌则受到抑制;固氮菌数量小且变化不大。菠萝-甘蔗轮作对甘蔗土壤生态环境的改善其实质在于:菠萝、甘蔗轮作后,由于其作物种类的不同导致土壤结构的改善和土壤微生物种类和数量增多,土壤生物活性增强,并导致土壤速效养分的增加。  相似文献   
10.
This paper demonstrates a new magnetophoretic position detection method for multiplexed immunoassay using colored microspheres as an encoding tool in a microchannel. Colored microspheres conjugated with respective capture molecules are incubated with a mixture of target analytes, followed by reaction with the probe molecules which had been conjugated with superparamagnetic nanoparticles (SMNPs). Under the magnetic field gradient, the resulting microspheres are deflected from their focused streamlines in a microchannel, and respective colored microspheres are detected using color charge-coupled device (CCD) in a specific detection region of the microchannel. The color and position of respective colored microspheres are automatically decoded and analyzed by MATLAB program, and the position was correlated with the concentration of corresponding target analytes. As a proof-of-concept, we attempted to assay simultaneously three types of biotinylated immunoglobuline Gs (IgGs), such as goat, rabbit and mouse IgGs, using colored microspheres (red, yellow and blue, respectively). As the capture molecules, corresponding anti-IgGs were employed and target analytes were probed using streptavidin-modified superparamagnetic nanoparticles. As a result, three analytes were simultaneously assayed using colored microspheres with high accuracy, and detection limits of goat IgG, rabbit IgG and mouse IgG were estimated to be 10.9, 30.6 and 12.1fM, respectively. In addition, with adjustment of the flow rate and detection zone, the dynamic range could be controlled by more than one order of magnitude.  相似文献   
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