Phylogenetic relationships between rice dwarf phytoreovirus isolates from five countries

Rice dwarf virus isolates were collected from several locations in Japan, the Philippines, China, Nepal and Korea. Genomic dsRNA segment profiles in polyacrylamide gel electrophoresis differed among the isolates. There were less differences in the profiles between isolates from Japan and Korea than in those between these two Countries and others. Nucleic acid hybridization was used to examine the extent of genomic variation. Full-length cDNAs to all genomic segments encoding non-structural proteins (S4, S6, S9, S10, S11 and S12) were synthesized from two Japanese isolates, and were used for dot-blot hybridization. Hybridizations using probes generated from the full-length cDNA clones failed to differentiate isolates from different geographical areas. However, cDNA probes covering a variable region of S12 were able to distinguish Japanese and Korean isolates from those of other countries. Phylogenetic tree analysis based on the amino acid sequence of P12 encoded by S12 grouped Japanese and Korean isolates together. The Chinese isolates from two different locations (Yunnan and Fujian) were closely related to each other, and were the most distantly related to Japanese and Korean isolates.     

棉酚和单宁酸对棉铃虫幼虫生长和消化生理的影响

作者利用昆虫人工饲料测试了棉酚和单宁酸对棉铃虫幼虫生长、营养指标以及中肠主要蛋白酶活力的影响。结果表明,棉酚和单宁酸均能显著地抑制幼虫的生长,但二者之间无交互作用,其中单宁酸的作用较棉酚强。含3％棉酚或单宁酸的人工饲料,饲喂4龄幼虫48h后,可引起幼虫近似消化率减小和食物转化率增大,但食物利用率无显著变化。棉酚在离体条件下对类胰蛋白酶和类胰凝乳蛋白酶活力有不同程度的抑制作用,但在活体条件下,上述酶活力无显著变化,仅有中肠总蛋白酶活力下降。单宁酸在离体条件下对类胰蛋白酶有抑制作用,而对类胰凝乳蛋白酶活力无作用:在活体条件下,仅总蛋白酶活力和弱碱性类胰蛋白酶活力显著下降。由此可知,棉酚和单宁酸对棉铃虫的生长抑制作用与幼虫中肠蛋白酶活力和食物消化率的降低有关。     

差量法测定猪回肠AA的真消化率及内源AA的排泄量

本文探讨了采用差量法测定猪对豆粕氨基酸(AA)的消化率和内源氨基酸排泄量的可行性.试验测得豆粕在16%、10%日粮蛋白水平上的表观氨基酸消化率分别为81.84%、78.59%,以差量法求得真消化率为87.87%.研究结果表明,差量法可以作为测定猪氨基酸真消化率和内源氨基酸排泄量的新方法.     

酸益(SI)在断奶仔猪日粮中的应用比较

选用杂种仔猪杜×(长×川白)24头,于28±2日龄断奶,以玉米-豆粕型日粮饲喂,进行为期30d的饲养试验,研究日粮中添加0.1%复合酸化剂-酸益SI、0.1%复合酸化剂FD和降低1.5%乳清粉用量对断奶仔猪生产性能、日粮酸和力及肠道大肠杆菌数的影响.结果表明,添加复合酸化剂-酸益(SI)可明显提高仔猪日增重,改善料肉比,大幅度降低腹泻率,降低乳清粉用量与饲料成本.其料肉比、日增重与使用进口产品FD差异不显著(P＞0.05).     

利用体外培养法建立饲料营养成分与瘤胃丙酸产量的回归模型

根据美国康乃尔净碳水化合物和蛋白质体系 (CNCPS) ,分析测定了 4类 2 4种饲料的营养成分 ,利用体外批次培养技术测定了它们在体外培养一定时间后的丙酸产量 ,并由此建立了饲料中产丙酸的营养成分和瘤胃丙酸产量的回归方程     

按不同氨基酸模式配制肉鸭日粮的比较研究

试验比较了不同氨基酸模式对肉鸭生产性能的影响。将320只1日龄的樱桃谷鸭随机分为4组,每组80只,设4个重复,每个重复20只,公母各半,分别饲喂四种日粮(按四种氨基酸模式配制),试验期21天。结果表明:日粮的氨基酸模式为Lys∶Met∶Trp∶Thr=100∶45∶21∶62时,其2周和3周体重高于其它各组,但差异不显著(P>0.05),且F/G和血清尿酸水平最低。     

苯丙烯酸对黄瓜幼苗光合作用和细胞超微结构的影响

 通过基质栽培研究不同浓度的苯丙烯酸对黄瓜幼苗光合作用和超微结构的影响。结果表明，苯丙烯酸浓度在80 µmol·L 时显著地降低了黄瓜幼苗的叶面积、叶绿素a含量、光合速率、蒸腾速率、根系活力和气孔张开数(P<0.05)；叶绿体和线粒体等超微结构也受到破坏，而浓度在150 µmol·L 时显著减少了全株干质量和气孔总数，细胞器出现解体现象。     

草酸对重寄生真菌盾壳霉分生孢子萌发和菌丝生长的影响

 本文研究了草酸对核盘菌的重寄生真菌盾壳霉(Coniothyrium minitans)分生孢子萌发和菌丝生长的影响。结果表明:草酸对盾壳霉分生孢子萌发没有明显促进作用,在酸碱性非缓冲基质(水琼脂)和酸碱性缓冲基质中,抑制盾壳霉分生孢子萌发的最低浓度分别为150和700μg/mL。在马铃薯葡萄糖琼脂培养基中,当草酸浓度为100~2000μg/mL时,盾壳霉菌丝能够生长,且浓度为300~500μg/mL的草酸对盾壳霉的菌丝生长具有明显的促进作用。在以草酸为唯一碳源的合成培养基中,在酸碱性非缓冲的条件下,当草酸浓度为100~2000μg/mL时,盾壳霉菌丝能够生长,且草酸浓度为500μg/mL时对盾壳霉菌丝生长具有促进作用,而当草酸浓度为2500μg/mL时,盾壳霉菌丝则停止生长。在酸碱性缓冲的合成基质中,草酸浓度为100~4000μg/mL时,盾壳霉菌丝能够生长,且草酸浓度为1500~2500μg/mL时对盾壳霉菌丝生长具有促进作用。在含草酸钙的混浊培养基(以草酸为唯一碳源)上,盾壳霉菌落区域形成了透明圈。上述结果说明盾壳霉能忍耐一定浓度的草酸而进行分生孢子萌发及菌丝生长,且这种真菌可能对草酸分子具有分解作用。     

不同地域环境对枸杞蛋白质和药用氨基酸含量的影响

根据2000～2001年我国北方六省(区)多点枸杞采样资料和田间试验资料,利用K-均值聚类方法和非线性回归方法,对比分析了宁杞1号枸杞蛋白质和9种药用氨基酸含量的差异和特点,以及生态因子对它们的影响。分析结果表明,不同地域栽种的宁杞1号枸杞蛋白质和9种药用氨基酸含量的变异系数分别为16.58%和16.22%,除品种因子的决定作用以外,环境条件对枸杞蛋白质含量有一定作用,其中土壤水解氮含量对蛋白质和氨基酸合成有一定作用,二者呈对数关系。     

Expression of cyclooxygenase-2 in IL-1β-stimulated mesangial cells is medicated by NF-κB/IκB signal pathway

AIM: To investigate the role of NF-κB/IκB signal pathway in the regulation of cyclooxygenase-2 (COX-2) expression in human mesangial cells (HMC). METHODS: The PGE₂ concentration in supernatants of HMC was measured by radioimmunoassay. COX-2 mRNA and protein expression were determined by RT-PCR and Western blot. Electrophoretic mobility shift assay (EMSA) and Western blot were used to detect the activity of NF-κB and degradation of IκB. RESULTS: IL-1β significantly upregulated COX-2 expression and PGE₂ production in HMC. Significant up-regulation of NF-κB activation, nuclear translocation of p65 subunit, and degradation of IκB α and IκB β were observed in IL-1β-induced HMC. CONCLUSION: Expression of COX-2 in IL-1β-induced HMC is mediated by NF-κB/IκB signal pathway.