科尔沁沙地东南缘大青沟自然保护区土壤水分的时空分布特征

用TDR分层对科尔沁沙地东南缘大青沟国家级自然保护区土壤水分进行定位观测,采用多重比较等方法,对土壤水分与环境因子关系的差异进行分析,通过Kriging插值法用Surfer软件绘制土壤水分等值线图,研究结果表明:土壤含水率在不同的生长季节上变化,表现为夏季>秋季>春季,各层间没有显著差异;月均(5、7、9月)土壤含水率的变异系数坡向>植被类型>坡位;层均(0~60cm)土壤含水率变异系数坡位>植被类型>坡向>样带。月均土壤含水率从高到低依次为:阔叶林>矮林>樟子松林>疏林草原>灌丛,不同植被类型各层月均土壤含水率总体上差异极显著,阔叶林远远高于其它植被类型;层均土壤含水率,各植被类型各月份间总体差异极显著,总体趋势从高到低为:阔叶林>矮林>樟子松林>灌丛>疏林草原,阔叶林明显高于其它类型。月均土壤含水率坡向间总体上差异显著,层间无显著差异;东、西坡与北坡有显著差异,东西坡高于南北坡;层均土壤含水率,同一月份各个坡向间差异不明显,7月明显高于其它月份;各月总体表现为:东>西>南>北坡。月均土壤含水率除31~45cm外,3个坡位间各层均有极显著差异,下坡位明显高于上坡位与中坡位;中坡位各层月均土壤含水率差异极显著;层均土壤含水率各月份各坡向间差异极显著,下坡位远大于上坡位与中坡位。该区从沟底到坡顶的植被变化逐渐由湿生-中生-旱生逐渐过度,垂直分布明显,这类天然残遗植被与土壤水分及其与环境因子的关系,对于促进周边沙地植被恢复具有重要的参照意义,据此建议了大青沟周边沙地植被恢复模式相应的最低土壤水分阈值,沙地0~30cm土层土壤含水率9.1%~11.5%、8.1%~9.0%、6.0%~8.0%;沙地31~60cm土层土壤含水率11.1%~13%、8.5%~11%、6.0%~8.4%,分别适合恢复为疏林、灌丛、半灌丛。     

Electrochemical detection of nucleic base mismatches with ferrocenyl naphthalene diimide

Electrochemical detection of nucleic base mismatches was attempted successfully with ferrocenyl naphthalene diimide (FND) in a model system with 20-meric double-stranded oligonucleotides with or without a mismatch(es). Thus, dA(20) or a 20-meric sequence of the lac Z gene was immobilized on a gold electrode and complementary oligonucleotides with different numbers of mismatches were allowed to hybridize in the presence of FND to give rise to an electrochemical signal. The signal intensity varied depending on the number of unpaired bases on the DNA duplex. From experiments with a quartz crystal microbalance, eight molecules of FND were found to bind to the 20-meric double-stranded oligos and this number decreased as the number of mismatches increased. These findings were further supported by matrix-assisted laser desorption ionization time-of-flight mass spectroscopy. This novel method will be useful for the analysis of single-nucleotide polymorphisms present on human genes.     

基于CRISPR/Cas系统的生物传感策略研究进展

CRISPR/Cas9系统是继锌指核酸内切酶、类转录激活因子效应物核酸酶之后的第三代基因组定点编辑工具,因其具有特异性切割双链DNA的能力,被广泛应用于基因编辑、生物传感等领域。Cas12a(Cpf1)、Cas13a(C2c2)等蛋白"附属切割"活性的发现,拓展了CRISPR/Cas系统在生物传感中的应用。近年来,研究人员开发出一系列快速、超敏、高特异性的生物传感系统用于分子检测,如SHERLOCK,DETECTR等。本文主要综述了基于CRISPR/Cas系统的生物传感策略的研究进展,并展望了其未来发展的方向。     

鼠脑微透析液痕量氨基酸的激光诱导荧光检测

使用自制微透析探针和活动体位生化取样装置以及自行组装的毛细管电泳-增强型电荷耦合器件-激光诱导荧光系统,对鼠脑透析液中的痕量氨基酸以异硫氢酸荧光黄(FITC)进行柱前衍生后进行了分离和检测. 鼠脑海马CA₃区微透析液中游离氨基酸的浓度为10^-8～10^-6 mol/L, 并将其用于学习与记忆的研究, 为无损伤研究活体脑内神经递质和其他痕量生化物质的动态变化提供了一种新方法.     

基于免疫纳米颗粒强化的压电免疫传感器检测大肠杆菌O157︰H7

摘要：【目的】结合纳米技术建立检测大肠杆菌（Escherichia coli）O157︰H7高灵敏检测技术。【方法】采用化学共沉淀法制备出核心粒径约为10 nm的免疫纳米磁颗粒,柠檬酸钠还原法制备粒径约为20 nm的免疫胶体金。压电免疫传感器通过金黄色葡萄球菌蛋白A（Protein A from Staphylococcus aureus SPA）法将抗体固定于石英晶振上,两种免疫纳米颗粒借助不同的抗体连接于传感器上对检测频率信号进行放大。【结果】SPA在石英晶振上的最佳固定浓度和时间为1.2 mg/mL和40 min,抗体的最佳固定浓度和时间为1.0 mg/mL和60 min。压电免疫传感器通过两种免疫纳米颗粒的放大作用,使其对大肠杆菌O157︰H7的检测限从104 cfu/mL提高到101 cfu/mL。【结论】免疫纳米颗粒强化对压电免疫传感器的检测频率信号具有很好的放大效应,可以明显提高其检测灵敏度。     

The chemiluminescence immunoassay for aflatoxin B1 based on functionalized magnetic nanoparticles with two strategies of antigen probe immobilization

A rapid and sensitive chemiluminescence immunoassay (CLIA) based on magnetic nanoparticles (MNPs) was developed to detect aflatoxin B1 (AFB1), which is a potent carcinogen in nature. We prepared monodisperse MNPs (300 nm in diameter) according to the solvothermal synthesis reaction and the MNPs were coated with silica by the Stöber method. Triethox was used as a one‐step carboxylation reagent, and 3‐aminopropyltriethoxysilane (APTES) an amination reagent, to modify the MNPs. We prepared two types of solid phase antigens using the above synthesized functionalized MNPs coupled with the later prepared AFB1‐oxime active ester and the purchased BSA–AFB1 respectively. 2′,6′‐dimethylcarbonylphenyl‐10‐sulfopropylacridinium‐9‐carboxylate 4′‐N‐hydroxysuccinimide (4′‐NHS) ester (NSP–DMAE–NHS), as a novel luminescent reagent, was used to label anti‐AFB1 antibodies. The two CLIA calibration curves based on the two types of solid phase antigens were obtained and compared. The acquired limit of detection (LOD) was about 0.001 ng/mL for the two functionalized MNPs‐based immunoassays, and the half maximal inhibitory concentration (IC₅₀) was 0.51 ng/mL for the MNPs–AFB1‐based method and 0.72 ng/mL for the MNPs–BSA–AFB1‐based method.     

单核苷酸多态性检测分析技术

单核苷酸多态性(SNP)作为第三代遗传标记已经广泛用于基因作图、疾病相关性分析、群体遗传学及药物研究等领域。 文中系统地介绍了目前国内外主要的SNP检测技术,任何一种SNP的检测方法都可将之看成由两部分组成,即区分SNP位点的原理方法和数据的检测分析手段,文章对这两部分做了较详细的介绍,并对SNP检测技术的发展进行了展望。 Abstract :As the third generation of genetic markers SNPs（single nucleotide polymorphisms）has been used extentively in gene mapping,disease-correlativity analysis ,population genetics and drug research.Here methods for detection are reviewed.Most SNP genotyping are a combination of method for interrogating SNPs and analysis tecnique.It described both parts and give a outlook for detection.     

基于SD的生态安全指标阈值的确定及应用——以上海崇明岛为例

结合区域复合生态系统的特点,建立由经济、人口、资源、环境和生态5个子系统71个参数构成的上海崇明岛区域生态安全的系统动力学模型,并以变量"净GDP"为参考依据,通过情景仿真进行生态安全趋势分析和方案比较,确定生态安全的指标阈值;通过系统模拟对阈值进行验证,认为阈值在反映系统动态发展趋势上,是一定发展模式下的生态安全的特征参照系。这一尝试克服了目前生态安全指标阈值的研究中以参照法为主的静态性缺憾。将确定的阈值应用于崇明岛生态安全的评价和因子分析中,发现由于崇明岛生态岛的定位和生态保障措施的实施,近几年生态安全综合得分呈现逐步提高的特点,但目前(2007年)得分为0.523,仍处于中等水平;并以阈值为标准的因子检验发现各主要安全因子差异较大,主要的制约因子主要体现为环境治污水平和能源利用等方面。     

质粒pCAMBIA1301的检测

用引物延伸芯片法实现对转基因水稻中 生物芯片技术是生物技术和微制造技术的融合, 已广泛用于生命科学的研究及实践、医学科研及临床、药物设计、环境保护、农业、军事等各个领域。而基因芯片是生物芯片中的一种,是指将大量基因探针分子固定于支持物上,然后与标记的样品进行杂交,所以一次可对大量核酸分子进行检测分析,从而解决了传统核酸印迹杂交技术操作复杂、自动化程度低、检测目的分子数量少、效率低等不足。文章探讨了用基因芯片这一新的检测手段对转基因植物的初步检测,采用一种新的反应机制－引物延伸芯片法（arrayed primer extension）,实现了样品扩增和杂交的一步化,而在传统的基因芯片检测中要需要两步来完成,从而为目前基因芯片中大片段样品的检测提供了一种可能性。 Abstract: Biochip technology which had emerged from the fusion of biotechnology and micro/nanofabrication technology at the end of 1980s has been widely used in life science ,medicine,clinical diagnosis,durg design,agricμLture,envioment pretection and strategics. DNA microarray (also call gene chip,DNA chip),one kind of biochips,is small chip containing many oligonucleotide probe .It can hybridize with labelled sample which makes it possible to detect large numbers of oligonucleotides at one time.So DNA microarray can overcome the disadvantage of traditional hybridization technology such as complexity,low automatization,poor efficiency and amount of detcting molecμLes. This paper describes a new method to detect transgenic plant with gene chip.We have developed a novel arrayed-primer extension technique. It combines hybridization and PCR at one step, while two separate steps are needed in the ordinary DNA microarray, therefore our method provide a feasibility to detect long DNA fragment .