APP N端片段的神经营养作用

APP是β－淀粉样肽的前体蛋白,由695－770个氨基酸经,春N端水解产物可分沁至细胞外环境。AP具有促进神经细胞生长作用,其中319－335肽段即APP17肽能提高动物的学习记忆能力。其他APP片段是否具有神经营养功能未见报道。本研究通过观察APP N端片段对人神经母细胞瘤株SY5Y生长的影响以及对实验性糖尿病动物行为的影响,希望APP促进神经细胞生长的其他肽段。用化学合肥APP N端多肽片段,以SY5Y细胞MTT代谢率、细胞计数、LDH漏出率和实验性糖尿病小鼠水迷宫试验结果为观察指标。结果APP64肽、29肽、11肽均有促进SY5Y细胞生长的作用,APP11肽可提高糖尿病动物水迷宫测试成绩,说明可溶性APP的N端可能具有神经营养作用,我们认为保持此作用的最短片段为APP11肽,此肽段的发现为进一步研究APP的构效关系奠定了基础。     

应用RNA干扰沉默猪内源性反转录病毒

目的:尝试应用RNA干扰(RNAi)沉默猪源PK-15细胞中的猪内源性反转录病毒(PERV),并通过反转录酶活性及pol基因相对荧光定量PCR检测沉默效果。方法:依据GenBank公布的PERV pol基因序列,采用Invitro-gen公司的BLOCK-iT RNAi Designer软件设计Stealth小干扰RNA(siRNA)序列;将合成的siRNA转染PK-15细胞,72 h后检测细胞上清PERV反转录酶活性及细胞内pol基因拷贝数并评价沉默效果。结果:反转录酶活性及pol基因拷贝数检测结果表明,设计的3条Stealth siRNA序列中,位于pol基因3272～3296 bp的序列能有效沉默PERV。结论:RNAi方法可有效使猪源PK-15细胞中的PERV沉默,为进一步研究天然抗病毒分子与PERV的相互作用提供了实验基础,同时也为猪源异种移植研究中去除PERV提供了一种可供尝试的方法。     

水稻品种与氮肥施用水平对田间褐飞虱发生的影响

于2010年在田间条件下研究了水稻品种和氮肥施用水平(250 kg/hm2有效氮,125 kg/hm2有效氮及不施氮肥的处理)对褐飞虱Nilaparvata tugens(St(a)l)发生的影响.结果表明,8月10日-9月10日期间,南粳44、宁粳1号、丙123、淮稻9号4个水稻品种上褐飞虱虫量显著低于感虫对照TN1...     

鸟苷发酵过程的多尺度问题研究

以鸟苷发酵为对象,在生物反应器中以多尺度问题的角度,对在线计算机数据进行相关分析,结合中间代谢物及有关酶活性的检测,建立了以代谢流为核心的多尺度调控方法;又通过与代谢流迁移有关的动态化学计量分析,实现了对批式发酵过程的时变系统估算,建立了主体代谢与产物形成的支路代谢间,包括能量与物质流的关系模型;最后,把具有不同生产能力菌株的关键基因与基因库数据进行了序列比较,发现了本文研究的菌株已具备高产能力,即编码sAMP合成酶的基因发生移码突变以及pur操纵子的多处突变,而中心代谢流迁移是过程优化的关键。对开展微生物功能基因组学的研究和工业过程优化的问题进行了探讨,作者提出有必要从生物反应器的系统生物学高度来认识和解决所面临的问题。     

Etiology and control of durian foliar blight and dieback caused by Rhizoctonia solani

Foliar blight and dieback of durian seedlings and trees in Peninsular Malaysia was found to be caused by Rhizoctonia solani (teleomorph - Thanatephoms cucumeris) The fungus grew well and produced abundant sclerotia at temperatures higher than 24°C with an optimum at 28°C. It grew poorly at 35°C and did not grow at 10°C. The strains studied were found to belong to the anastomosis group AG-1. They were pathogenic on durian, papaya, cucumber, long bean, Mikania weed, padi, musk melon, mung bean, Zoysia grass, Bermuda grass, and St Augustine grass. They were mildly pathogenic on groundnut, and non-pathogenic on maize, guava and Brassica‘pak choy’. The disease was effectively controlled by foliar sprays of pencycuron and benomyl; triadimefon and an antagonistic bacterium suspension treatment were less effective and quintozene-etridiazole mixture gave poor disease control.     

Growth Regulator Interactions in the Growth of the Shoot System of Avena sativa Seedling: II. THE GROWTH OF THE FIRST LEAF AND THE COLEOPTILE1

1. Studies have been made of the growth in culture medium of thecomponent parts of compositesegments excised from 3 to 7-day-oldAvena sativa seedlings and comprising portions of coleoptileand first leaf bases and various lengths of first internodetissue.
2. The effects of various concentrations of gibberellicacid (GA)and indole-3- acetic acid (IAA) alone and in combinationhavebeen studied on the growth of these organs.
3. Both GA andIAA stimulate the growth of coleoptile base tissuebut in combinationtheir joint effects are less than additive.No synergism occurs.
4. The growth of the first-leaf base is greatly stimulated byGAbut is inhibited by IAA. In combination, the stimulatoryeffectof GA (up to 1 0 p.p.m.) may be virtually eliminatedby evenlow concentrations of IAA (0.01 p.p.m.).
5. The inclusionof first internode tissue in the segments considerablyincreasesthe growth of first leaf base tissue but has no consistenteffecton the growth of coleoptile base tissue. The presenceof firstinternode tissue also greatly increases the degreeof growthstimulation invoked by GA but does not influence thedegreeof IAA inhibition. It is postulated that the first internodetissue is the source of an unknown growth factor necessary forGA action in the first leaf and potentiating the action of endogenousgibberellin.
6. Kinetin, adenine sulphate, glutarnine, glutarnicacid, asparagine,glycine, arginine, histidine, lysine, aneurin,and pyridoxinewill not simulate the effects of this unknowngrowth factorin the growth of leaf tissue. Like IAA, kinetinvirtually eliminatesthe GA stimulation of leaf growth.
7. Astudy of extracts of internode tissue in various solvents,analysedby paper partition chromatography and assayed by thegrowthof the first leaf base, has indicated the presence ofgrowthinhibitors and gibberellin-like substances but has failedtoisolate the postulated endogenous GA-synergist.
8. The implicationsof these results for growth correlations andthe hormone controlof shoot growth in Avena sativa seedlingsis discussed.

     

The Role of Anaerobic Respiration in Germinating Muskmelon Seeds: II. EFFECT OF ANOXIA TREATMENT AND ALCOHOL DEHYDROGENASE ACTIVITY

Exposing muskmelon (Cucumis melo L.) cultivar seedlots to N₂atmosphere created totally anaerobic conditions which stimulatedethanol production and accumulation in both high and low vigourseeds. However, accumulation of ethanol was consistently higherin the low vigour seeds than in the high vigour ones. In addition,CO₂ production under N₂ and in air suggests the presence ofan apparent ‘Pasteur effect’ in the low vigour seedsbut not in the high vigour seeds. Acetaldehyde production underN₂ was very low and did not seem to be associated with seedvigour, probably because of its nature as an intermediate inethanol production. The fast shift toward ethanol may be dueto the fact that alcohol dehydrogenase, the enzyme which catalyzesthe conversion of acetaldehyde to ethanol, exists in sufficientamounts in the imbibing seeds so that it is not a limiting factorin the conversion to ethanol. Alcohol dehydrogenase activitydid not appear to be related to seed vigour. Key words: Cucumis melo L., Anaerobic respiration, Germination, Seeds.     

转化生长因子TGF-1β1／结缔组织生长因子CTGF对骨创伤愈合的调控机理研究

转化生长N子TGF—β1和结缔组织生长因子CTGF是骨形成过程中不可或缺的重要生长因子。研究发现TGF-β1和CTGF具有协同生物效应,CTGF可能作为TGF-β1的下游信号发挥作用。本文对近年来TGF-β1／CTGF通路在骨发育与创伤愈合中相关信号转导调控及分子机制研究进行讨论。尤其是对成骨细胞增殖、分化和功能的调控机理进行综述。     

用于鉴定microRNA靶基因的新型双萤光素酶报告基因系统的构建及应用

目的:构建用于鉴定microRNA靶基因的报告基因系统。方法:在pGL3-Basic载体的luc基因上游插入CMV启动子,下游插入用于克隆靶基因3’UTR的多克隆位点,构建报告基因载体pMIR-luciferase;将pMIR-lu-ciferase载体的luc基因替换成Rluc基因,构建内参载体pMIR-control;将补体因子H(CFH)的3’UTR插入pMIR-luciferase载体的多克隆位点处,构建含有CFH 3’UTR的报告基因载体;用pIRES2-EGFP载体构建microRNA146a真核表达载体;将含有CFH 3’UTR的报告基因载体、microRNA146a真核表达载体及内参载体共转染HepG2细胞,进行报告基因的活性检测。结果:构建了报告基因载体、内参载体和microRNA146a真核表达载体,经酶切和测序鉴定正确;microRNA146a真核表达载体转染细胞72 h后,经荧光显微镜观察确认载体转染及表达;用实时定量PCR检测,microRNA146a的表达水平显著上调(P<0.01);用构建的报告基因系统检测,结果表明microRNA146a显著地抑制了含CFH 3’UTR的报告基因的活性(P<0.05)。结论:构建了一种新型的报告基因载体系统,该系统可用于miRNA靶基因的鉴定。