用免疫分离法检测稻种上的白叶枯病菌

 免疫分离法是一种新型的、高度灵敏和准确的种菌带菌检验法,它结合了利用专化性抗血清的选择法吸附作用和活细菌可形成菌落的两方面的优点,从种苗材料中分离到目标细菌,用纯菌测试它的回收率为50~70%,最低检出率为50~100个菌/ml,人工喷接种和病田收获的病种带菌率达87%,平均每粒自然病种上的细菌数在100个左右。免疫分离所得菌落经致病性测定,大多数为白叶枯菌。     

2012年玉米大斑病重发原因和控制对策

玉米大斑病是由真菌引起的世界性玉米病害,常给生产造成严重损失。2012年玉米大斑病在东北、华北地区大流行,本文归纳了玉米大斑病全国发生概况、区域分布和各地病情。总结了2012年玉米大斑病发病时间早,流行速度快,品种间和地区间发病程度差异大等发生特点,分析了适宜天气条件、主栽品种不抗病、栽培管理措施不合理是导致大斑病重发的主要原因。并针对性地提出了重视玉米病害的预测预报、推荐种植抗病品种、加强病害综合防治的对策建议,旨在对今后进一步做好玉米大斑病测报工作,指导玉米病害防治、有效控制其危害、保障玉米生产有所裨益。     

代谢酶抑制剂PX对除草剂防除稗草的增效作用

为解决除草剂防除困难的问题,采用室内盆栽试验测定了PX、PM和Mn²⁺三种代谢酶抑制剂对精喹禾灵、莠去津、烟嘧磺隆、硝磺草酮和烯禾啶防除稗草Echinochloa crus-galli的增效作用,测定不同用量代谢酶抑制剂PX对这5种除草剂的增效作用及其与莠去津混用后稗草体内谷胱甘肽转移酶（glutathione S-transferase,GST）和细胞色素 P450（cytochrome P450,CYP450）活性的变化。结果显示,在3种代谢酶抑制剂中,代谢酶抑制剂PX对精喹禾灵、莠去津、烟嘧磺隆、硝磺草酮和烯禾啶5种除草剂的增效作用最显著。不同用量代谢酶抑制剂PX对不同除草剂的增效作用不同,其中75 g (a.i.)/hm²代谢酶抑制剂PX对莠去津的增效最佳,株防除效果和鲜重防除效果分别增加了35.33个百分点和37.33个百分点。莠去津与代谢酶抑制剂PX混用后,稗草体内GST和CYP450活性均较对照显著降低。表明除草剂与代谢酶抑制剂PX混用能增加除草剂对稗草的防除效果,可以达到减施除草剂的目的。     

Exploring the effectiveness of in ovo feeding of vitamin C based on the embryonic vitamin C synthesis and absorption in broiler chickensOA

Background: Many researches about in ovo feeding(IOF) of vitamin C(VC) are gradually carried out to explore physiological development in chicken, but little studies focus on VC synthesis capacity of the embryo itself, the selection of injection site and the effectiveness of IOF of VC. This study aims to explore the above problems.Results: Kidney and yolk sac were the main organs for VC synthesis and L-gulonolactone oxidase(GLO) expression was lower during pre-hatch development than that during p...     

Identification,Characteristics and Function of Phosphoglucomutase (PGM) in the Agar Biosynthesis and Carbon Flux in the Agarophyte Gracilariopsis lemaneiformis (Rhodophyta)

Agar is widely applied across the food, pharmaceutical and biotechnology industries, owing to its various bioactive functions. To better understand the agar biosynthesis in commercial seaweed Gracilariopsis lemaneiformis, the activities of four enzymes participating in the agar biosynthesis were detected, and phosphoglucomutase (PGM) was confirmed as highly correlated with agar accumulation. Three genes of PGM (GlPGM1, GlPGM2 and GlPGM3) were identified from the G. lemaneiformis genome. The subcellular localization analysis validated that GlPGM1 was located in the chloroplast and GlPGM3 was not significantly distributed in the organelles. Both the GlPGM1 and GlPGM3 protein levels showed a remarkable consistency with the agar variations, and GlPGM3 may participate in the carbon flux between (iso)floridoside, floridean starch and agar synthesis. After treatment with the PGM inhibitor, the agar and floridean starch contents and the activities of floridean starch synthase were significantly decreased; products identified in the Calvin cycle, the pentose phosphate pathway, the Embden-Meyerhof-Parnas pathway and the tricarboxylic acid cycle were depressed; however, lipids, phenolic acids and the intermediate metabolites, fructose-1,6-phosphate were upregulated. These findings reveal the essential role of PGM in regulating the carbon flux between agar and other carbohydrates in G. lemaneiformis, providing a guide for the artificial regulation of agar accumulation.     

联苯菊酯10%水乳剂的配方研究

本研究通过正交优化得到联苯菊酯10%水乳剂的最佳配方：联苯菊酯原药10%,二甲苯20%,农乳602#3.5%,Tween-20 2.5%,农乳500#2%,乙二醇4%,有机硅消泡剂0.2%,去离子水补足至100%。最佳生产工艺为：使用高速剪切机,剪切转速6 000r/min,剪切时间4min。该水乳剂pH值5.7～6.5,稀释100倍于（30±2）℃恒温水浴24h未出现浮油、沉油、沉淀,经（54±2）℃热贮14d,分解率〈2%,制剂表面张力低,倾倒性佳。     

咪鲜胺·抑霉唑混配制剂的反相离子对液相色谱分析

本文采用反相离子对色谱梯度洗脱外标法对咪鲜胺．抑霉唑乳油的2种有效成分进行一次性定量检测,采用C18色谱柱,以0．012mol／L庚烷磺酸钠(pH=2．5) 甲醇=30 70;20 80为流动相,流速1．5mL／min,二极管阵列检测器,检测波长：220nm。该方法中咪鲜胺和抑霉唑的标准偏差分别为0．065和0．024,变异系数分别为0．53％和1．13％．线性相关系数分别为0．9994和0．9995,平均回收率分别为99．4％、100．1％。     

通过考核认证提高警犬实战技能

2006年,辽宁省公安厅作为片区警犬资格认证的试点单位,分别于5月17日至6月12日、11月8日至9日,两次集中组织进行了警犬资格认证考核。全省公安机关共有133头警犬参加考核,占全省163     

羊绒与羊毛的PCR-RFLP识别方法

羊绒价格昂贵,在销售中时常出现掺假现象,最常见的是用羊毛,因此精确识别羊绒和羊毛纤维的方法非常重要。本试验采用聚合酶链式反应-限制性片段长度多态（PCR-RFLP）的技术方法,利用提取的羊绒和羊毛线粒体基因组,根据细胞色素b（Cytochrome b）基因已知的DNA序列设计引物,通过内切酶SspⅠ进行酶切,得到不同的片段长度,根据酶切图谱鉴别羊绒和羊毛样品,用来进行羊绒掺假试验的定性检测。     

含PRRS病毒ORF5的伪狂犬病病毒TK基因缺失转移载体的构建

提取伪狂犬病病毒（ＰＲＶ）ＢａｒｔｈａＫ６１株基因组ＤＮＡ,用限制性内切酶ＫｐｎＩ充分消化,回收５．９ｋｂ片段（Ｊ片段）,将其克隆于质粒ｐＵＣ１１９ ＫｐｎＩ位点上,获得ｐＢＫＪ。用两对针对ＰＲＶ ＴＫ基因的特异性引物对重组质粒进行ＰＣＲ鉴定,证明其中含有ＰＲＶ ＴＫ基因。然后用ＫｐｎＩ、ＰｓｔＩ和ＢａｍＨＩ等限制性内切酶对其进行酶切分析,确定了克隆片段的物理图谱。进一步研究证实ＴＫ基因位于其中的