水溶剂红花油合成共轭亚油酸研究——(I) 工艺优化研究

传统油脂共轭反应制备共轭亚油酸多采用有机溶剂,这种工艺存在溶剂残留等潜在问题。研究了红花油以水为溶剂的碱性异构化合成共轭亚油酸反应,考察了反应温度、时间、水油比、油碱比对共轭反应的影响,得到工艺条件的数学模型。反应的最佳条件为反应温度214℃,反应时间4.9h,水油比=4.3,油碱比=1.3。在此条件下,反应转化率可达到97.64%。     

Tachypnea and Antipyresis in Febrile Horses after Sedation with α2‐Agonists

Background: Signs of tachypnea after sedation of febrile horses with α₂‐agonists have been noted previously but have not been further investigated. Objectives: To examine the effects of xylazine and detomidine on respiratory rate and rectal temperature in febrile horses and to investigate if either drug would be less likely than the other to cause changes in these variables. Animals: Nine febrile horses and 9 healthy horses were included in the study. Methods: Horses were randomly assigned to sedation with xylazine 0.5 mg/kg or detomidine 0.01 mg/kg. Heart rate and respiratory rate were recorded before sedation and at 1, 3, and 5 minutes after injection. Hourly measurements of rectal temperature were performed starting before sedation. Results: All febrile horses experienced an episode of tachypnea and antipyresis after sedation. Rectal temperature in the febrile group was significantly lower at 1, 2, and 3 hours after sedation. In several measurements, the decrease was >1°C. Respiratory rate in the febrile group was significantly increased after sedation. All febrile horses were breathing >40 breaths/min and 3 horses >100 breaths/min 5 minutes after sedation. No differences were noted between the 2 treatments. No significant changes in respiratory rate or temperature were noted in the reference group. Conclusions and Clinical Importance: Febrile horses can become tachypneic after sedation with detomidine or xylazine. The antipyretic properties of α₂‐agonists need consideration when evaluating patients that have been sedated several hours before examination.     

南疆地区某猪场猪圆环病毒Ⅱ型的PCR检测

应用PCR技术对来自南疆某猪场的24例疑似病例进行猪圆环病毒Ⅱ检测,共检出PCV2阳性10份,阳性率为41.6%（10/24）。结果表明,该猪场存在PCV2的感染,且感染较为严重。     

漂白胶贮存性质的研究(一报)——漂白胶脱氯反应的研究

本文通过测定脱氯程度不同的漂白胶样品的结合氯含量、热寿命、软化点和颜色,研究了漂白胶脱氯反应的性质,结合氯含量与热寿命的关系以及软化点和颜色的变化规律。发现漂白胶的脱氯反应是一级反应,分为两段,前一段的反应常数为后一段的四倍,说明一部分氯容易脱除,而另一部分则比较难,后者留在漂白胶中对贮存性影响不大。此研究结果为解决漂白胶贮存性差这一难题提供了理论依据和基本途径。通过测定一批样品在多年存放期间热寿命的变化,证实了本研究结论的正确性。     

Application of polymerase chain reaction-denaturing gradient gel electrophoresis for comparison of direct and indirect extraction methods of soil DNA used for microbial community fingerprinting

 We used polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) to compare bacterial community patterns obtained with target DNA extracted from a soil by direct and indirect methods. For this purpose, two direct extraction methods, i.e. cell lysis by bead beating and cell disruption by grinding in liquid N, and two indirect methods, i.e. cell extraction followed by DNA extraction, and combined RNA/DNA extraction from the bacterial cell fraction, were performed. Crude extracts were purified and amplified using universal bacterial primers. PCR products were then analysed by DGGE, and similarity between the profiles obtained was determined by unweighted pair group with mathematical averages clustering. The results showed clear profiles that presumably represented the dominant bacterial fractions in the samples. The profiles generated by all four methods were similar, indicating that the methods were of approximately equal efficiency in the extraction of target DNA representative of the soil bacterial community. However, the patterns of clustering also indicated that different populations of bacteria could be detected in the same soil using different soil DNA extraction methods. The application of two dilution levels of DNA in PCR-DGGE showed that the most stable profile of the soil bacterial community could be generated by the direct methods. The indirect methods gave clustered profiles at both dilution levels. It is likely that these methods extracted DNA from a major, easily desorbed, bacterial fraction, consisting of low-density populations. PCR-DGGE was found to be a suitable technique with which to assess differences in methods for DNA extraction from soil, which can be further used for the determination of microbial community diversity at the molecular level. Received: 22 June 1999     

基于核酸适配体的PCR法检测溶藻弧菌及其灭活菌

溶藻弧菌(Vibrio alginolyticus)分布广,数量多,发病率高,是水产养殖中常见的条件致病菌,而对溶藻弧菌进行快速准确的识别鉴定是其病害防治的前提和基础。核酸适配体,因为具有较高的亲和特异性,在微生物的识别鉴定方面展现出了巨大的优势。本文利用核酸适配体和适配体筛选产物,通过结合、洗涤、加热分离、PCR扩增以及电泳检测等步骤,对溶藻弧菌进行了检测鉴定。结果表明,适配体和筛选产物都能对溶藻弧菌及其灭活菌进行较好的识别鉴定,适配体筛选产物对溶藻弧菌的检测下限为10~3cfu/mL,而对其灭活菌的检测下限为10~2cfu/mL,适配体对溶藻弧菌及其灭活菌的检测下限都可达到10 cfu/mL。该方法对溶藻弧菌有较好的亲和特异性,并能较好地区分溶藻弧菌与哈维氏弧菌等水产常见病原菌,在水产病害的检测中显示了较好的应用前景。     

对慢性心衰心阳虚证及其微观指标关系的思考

本文通过对慢性心力衰竭心阳虚证症候特点、病程变化机制、血流动力学、心功能分级、心脏负荷标志物、神经内分泌相关激素、炎症反应物等相关指标的关联整理,研究其诊断价值,为病证结合慢性心力衰竭心阳虚证提供辅助诊断依据,并对心衰心阳虚证微观辨证发展现状进行反思。     

Need for flagella for complete virulence of Pseudomonas syringae pv. tabaci: genetic analysis with flagella-defective mutants ?fliC and ?fliD in host tobacco plants

The flagellins purified from Pseudomonas syringae pv. tabaci induce a hypersensitive reaction in nonhost tomato cells. To investigate the role of flagella and flagellin in the compatible interaction, we generated two types of flagella-defective mutant. The fliC mutant lost the fliC gene that encodes flagellin protein, whereas the fliD mutant lost the fliD gene that encodes HAP2-capping protein. The two mutants had markedly reduced ability to cause disease symptoms in tobacco leaves. Furthermore, propagation of the mutants in tobacco leaves was less than that in wild-type pv. tabaci. Compared to the inoculation with wild-type pv. tabaci, inoculation with the two mutants did not markedly induce the expression of typical defense response-related genes such as PAL and hsr203J. Complementation of each fliC and fliD gene to the corresponding deficient mutant restored motility and virulence. These results indicate that flagella of P. syringae pv. tabaci are indispensable organelles for complete virulence on host tobacco plants.     

棕色化反应调控技术在烟草中的应用现状及展望

棕色化反应影响着烟叶及其烟草制品的外观和内在品质.对酶促褐变和非酶促褐变的反应杌理、调控技术研究和在烟草中的应用现状进行了综述,探讨了棕色化反应调控技术的发展前景.     

一种简单快速的DNA提取方法在水稻上的应用

采用了一种简单快速的DNA提取方法来提取水稻DNA,并用提取的DNA进行了PCR扩增。结果表明,该方法提取DNA不需要碾磨、离心等步骤,通过简单的加热、稀释等操作便能制备100个PCR反应的DNA模板,1h能提取96个样品的DNA。本研究成功地将该方法用于水稻SSR分析、白叶枯抗病基因Xa21的分子标记辅助育种和不育系纯度鉴定等方面。