Competitive enzyme-linked immunoassay for sialoglycoprotein of edible bird's nest in food and cosmetics

The proliferation of fake and inferior edible bird's nest (EBN) products has recently become an increasingly serious concern. To identify and classify EBN products, a competitive enzyme-linked immunoassay (ELISA) was developed to quantitate sialoglycoprotein in EBN used in food and cosmetic applications. The characteristic sialoglycoprotein in EBN was found, extracted, purified, and analyzed. Sialoglycoprotein, considered the main carrier of sialic acid in EBN, consisted of 106 and 128 kDa proteins. A monoclonal antibody that could recognize both proteins was prepared. The heat-treated process did not change the affinity of sialoglycoprotein with the antibody. An optimized ELISA method was established with a cross-reactivity of less than 0.1% and an IC(50) of 3.3 μg/mL. On the basis of different food and cosmetic samples, the limits of detection (LOD) were 10-18 μg/g. Recoveries of fortified samples at levels of 20 and 80 μg/g ranged from 81.5 to 96.5%, respectively. The coefficients of variation were less than 8.0%.     

Synchronizing rock clocks of Earth history

Calibration of the geological time scale is achieved by independent radioisotopic and astronomical dating, but these techniques yield discrepancies of approximately 1.0% or more, limiting our ability to reconstruct Earth history. To overcome this fundamental setback, we compared astronomical and 40Ar/39Ar ages of tephras in marine deposits in Morocco to calibrate the age of Fish Canyon sanidine, the most widely used standard in 40Ar/39Ar geochronology. This calibration results in a more precise older age of 28.201 +/- 0.046 million years ago (Ma) and reduces the 40Ar/39Ar method's absolute uncertainty from approximately 2.5 to 0.25%. In addition, this calibration provides tight constraints for the astronomical tuning of pre-Neogene successions, resulting in a mutually consistent age of approximately 65.95 Ma for the Cretaceous/Tertiary boundary.     

Valuing Potential Benefits of Research into the Biological Control of Californian Thistle （Cirsium arvense）： A Bioeconomic Model

The present research developed a bioeconomic model for control of Californian thistle （Cirsium arvense L. Scop.） in intensive, lowland sheep pastures in New Zealand. Production costs included two control methods： herbicides and defoliation, with defoliation encompassing both physical means and biocontrol measures. The model was used to examine the economic value of a research programme into biological control of the weed, given several different future scenarios. These scenarios were high herbicide prices, a price premium for lamb raised without chemical herbicides, and development of herbicide resistance. The model results were used to estimate national impacts. If the only change in the agricultural sector was the cost of the biocontrol to the nation＇s farmers, the research programme to find an effective biocontrol agent had little economic impact. If other factors changed, such as the price of petroleum or levels of herbicide resistance in the weed. the model＇s results suggested that intensive sheep farming could grow or shrink by as much as NZ$219 million dollars over five years. In the latter case, having an alternative control method reduced potential losses and increased potential gains, resulting in a net benefit of between NZ$81 million and NZ$153 million. This work extended prior research in several ways. First. Californian thistle reproduces via root buds, which affected the modelling of weed behaviour. Secondly, the model allowed optimistation over continuous levels of weed control for two different methods. Thirdly, the model accounted for both weed control and damage to nitrogen-fixing clover from herbicide use. Finally, the research investigated optimal weed control in several different alternative future states.     

牛附睾和附睾液分析与牛附睾尾精子在模拟附睾液中存活试验

[目的]新鲜精液在离开生殖腺后存活时间很短.相关研究表明副睾液为精子的存活提供了特殊的环境.试验探讨和研究牛附睾精子在体外模拟附睾液中的存活试验的各因素的影响.[方法]试验对公牛附睾头部和尾部的摩尔渗透压和蛋白质浓度进行了分析,牛附睾尾部精子在不同蛋白浓度的CEP-2溶液中,在4℃条件下孵育120h.每24h做一次精子活力检测.[结果]5 d后精子活力仍然超过60;.附睾头、尾部的渗透压分别为(287.0±13.7)mOsm和(310.8±17.0)mOsm.蛋白浓度分别为(37.43±12.55)mg/mL和(50.58±11.08)mg/mL.[结论]附睾尾精子在蛋白浓度为40mg/mL,渗透压为345 mOsm时,精子存活率最高.     

土壤保持耕作——全球农业可持续发展优先领域

 从农业活动对全球变化以及对农业可持续发展的影响进而导致全球性土壤保持需求的迫切性增加出发，追踪了国外土壤保持耕作领域的研究和发展动态；对中国该领域研究发展现状和研究水平，从时间、深度、方法、生产应用等方面与国外进行了比较分析。中国是一个水土流失和耕地退化严重的农业大国，而从全球统计数字来看，中国土壤保持耕作面积目前仅占全球保持耕作面积的0.2%，仅占全国耕地面积的0.1%， 其现状与中国耕地资源和环境的继续退化以及对土壤保持耕作需求的增加极不相符。加强中国土壤保持耕作系统研究和土壤保持耕作"节能固碳"长期建设不仅对中国而且对全球变化及农业可持续发展具有重大意义。鉴于中国土壤保持耕作领域研究和发展所存在的不足和所面临的更大挑战，以及该领域研究涉及到复杂的农业系统"耕作管理-生物过程-环境变化"相互作用及其系统能流-碳流循环过程，尤其农业生态系统碳汇/源估量尚存在诸多不确定性因素等科学问题，有必要运用综合的系统性研究分析方法，借助国外长期试验和理论研究经验，以及系统模型模拟研究手段等多学科和交叉学科知识，加速提升中国土壤保持耕作领域的科研实力和水平，为实现碳汇/源科学调控管理、减缓农业对温室效应贡献、促进农业可持续发展提供科学依据。     

多糖和寡糖的体外发酵特性及其对鸡盲肠微生物菌群的影响

本研究采用体外累积发酵产气法和16SrDNA指纹图谱鉴定技术研究了来自香菇、银耳和黄芪的天然免疫活性多糖(LenE,TreE和AstE)及酵母胞壁甘露寡糖(MOS)对鸡肠道微生物菌群及其发酵特性的影响。结果表明,三种多糖提取物的总糖含量均占干物质的60%以上,而MOS总糖含量在90%以上。多糖和寡糖具有不同的发酵模式;MOS、AstE和LenE三种糖的发酵模式相似,呈一阶段发酵模式;TreE呈两阶段的发酵模式。三种糖中,MOS和AstE发酵速度较TreE快。MOS和AstE在发酵后总VFA产量最高,pH最低;黄芪多糖发酵后产生较多的直链脂肪酸和较低的氨。这些多糖和寡糖提取物影响肠道微生物的活性和组成成分,体现在发酵模式和发酵终产物的显著改变上。以上研究结果表明,来自香菇、银耳和黄芪的天然免疫活性多糖(LenE,TreE和AstE)及酵母胞壁甘露寡糖(MOS)在体外发酵后,均具有显著改变鸡盲肠微生物发酵终产物的含量和盲肠微生物活性的作用。     

糊状饲料热加工过程中清除嗜温性细菌的挤出条件的优化

饲料和环境中会滋生沙门氏菌和其他感染畜禽的病原微生物。因此有必要采取措施控制动物沙门氏菌感染,以改善食品安全和减少生产损失。本研究旨在研究将替代饲料基质内细菌减少的挤出条件的优化。用单螺杆挤出机来处理饲料,用嗜热性脂肪芽孢杆菌12980(美国典型菌种收藏所,莱斯顿,弗吉尼亚州)人工接种饲料。初步实验表明在中度挤出强度(每kg糊状饲料含水分285g,挤出机出桶温度为83℃,挤出机桶保留时间为7S)条件下,可以从饲料中清除鼠伤寒沙门氏菌(鼠伤寒NALr),因此,还需要研究更耐热生物体。将B型嗜热性脂肪杆菌12980的芽孢接种到替代饲料基质上,基质中组成分别为玉米粉600g/kg,豆粕300g/kg,动物蛋白质100g/kg,用来研究三个挤压变量对杀菌的影响。三个变量为挤出机出桶温度(T),糊状饲料水分含量(MC),和饲料在挤出机桶的平均保留时间(Rt)。每个旋转中心复合设计使用三个自变量和五个水平。用计算孢子数的二次响应面模型来预测最大限度杀菌的挤出条件。响应面证实在设计区的平稳点是一个鞍点。最大杀菌的估测峰表明,在挤出机设置为T=110℃,Mc=245g/kg和Rt=11s时,会发生最高1.03个数量级的减幅,由于在中度强度条件(T=83℃,Mc=285g/kg和Rt=7s)下,可以完全清除测试饲料中可检出的鼠伤寒沙门氏菌,可见在中央复合设计区,所有鼠伤寒沙门细胞和所有耐热的嗜温生物体在多数挤出条件下会被清除。     

禽类味觉系统研究进展

文章基于哺乳动物的味觉系统,分析了家禽味觉的结构和功能,着重从不同类型的味觉受体的研究进展进行了综述,并指出了今后禽类味觉的研究方向。     

大麦黄矮病毒(BYDV) cDNA的合成、克隆及初步应用

 以大麦黄矮病毒二叉蚜和麦长管蚜专化株的病毒核酸为模板,以小牛胸腺DNA为引物,合成cDNA的第一条链,再用缺口翻译法合成第二条链,然后采用加装BamH₁人工接头的方法将ds-cDNA插入到质粒载体pUC₈中,重组质粒于大肠杆菌JM—83中进行克隆,以克隆的颜色变化选择含有外源DNA的克隆,再用病毒核酸制备的探针筛选真正病毒cDNA插入的克隆。重组质粒中ds-DNA的插入长度在300—1600bp之间。用缺口翻译法制备质粒DNA分子探针检测同源病毒液,反应灵敏度在100pg-1ng之间。应用cDNA探针检测不同病毒和病毒株系,从中筛选出黄矮病毒株系专化克隆系,黄矮病毒专化克隆系和黄矮病毒组专化克隆系.