发酵油茶饼粕饲喂荷斯坦牛的试验研究

试验采用发酵油茶饼粕代替部分豆粕饲喂泌乳期荷斯坦牛,旨在研究其对奶牛产奶量、乳品质和血液生化指标的影响。试验选取16头泌乳天数相近的荷斯坦牛,采用配对分组设计4个处理组：对照组饲喂基础日粮,试验组分别在基础日粮的精料中,用发酵油茶饼粕分别代替15％、30％和45％的豆粕。试验结果表明,发酵油茶饼粕代替部分豆粕饲喂泌乳期荷斯坦牛,对其产奶量、乳蛋白和乳脂率有一定的提升作用．且发酵油茶饼粕价格相对于豆粕有很大的优势;采用发酵油茶饼粕饲喂荷斯坦牛,能够有效降低饲养成本,值得推广应用。     

奶山羊乳房炎灭活疫苗的制备及免疫效果检测

为评估奶山羊乳房炎灭活疫苗的免疫效果,以大肠埃希菌、金黄色葡萄球菌、凝固酶阴性表皮葡萄球菌及产色葡萄球菌为材料,经甲醛37℃灭活,按照6∶1（V／V）与铝胶盐充分混匀,分别经腹股沟皮下、颈部皮下注射途径,免疫泌乳期奶山羊,免疫剂量均为2 mL,共免疫2次,每次间隔14 d。分别在免疫前及第1次免疫后10、24、60、180 d 采集血样和乳样,ELISA 测定抗体效价,用快速诊断液检测隐性乳房炎,统计患病奶山羊的数量。结果显示,与对照组相比,两次免疫后血液及乳汁中针对大肠埃希菌、金黄色葡萄球菌、凝固酶阴性表皮葡萄球菌及产色葡萄球菌的抗体效价含量均显著增加（P ＜0．05）,抗体维持时间长;颈部皮下免疫组免疫后180 d,腹股沟皮下免疫组免疫后的60 d,隐性乳房炎奶山羊数量均明显下降。结果表明,本研究制备的奶山羊乳房炎疫苗不仅能够刺激机体产生较好的体液免疫应答,而且还对隐性乳房炎有显著的治疗效果。     

农业科研单位大型仪器设备共享的研究与探讨——以中国热带农业科学院橡胶研究所为例

该文以中国热带农业科学院橡胶研究所大型仪器设备管理与共享的现状为例,对当前农业科研单位大型仪器设备购置、运行管理的专项基金、技术管理队伍建设、共享的相关规章制度、共享服务信息平台等方面存在的问题进行了探讨与分析,提出了加强大型仪器设备购置管理、设立大型仪器设备开放共享专项基金、加强大型仪器设备技术管理队伍建设、完善大型仪器设备共享管理相关规章制度服务信息平台功能等促进农业科研单位大型仪器设备共享的建议与途径     

氮素形态对紫花苜蓿盛花期生长及结瘤固氮的影响

在完全营养液条件下,采用砂培法,研究了3种氮素形态配比NO3--N,NH4+-N和NO3--N∶NH4+-N为1∶1和0、105、210mg/L 3个氮素水平对紫花苜蓿盛花期生长及结瘤固氮的影响。结果表明:不同形态氮素处理下紫花苜蓿的株高、生物量、根瘤数、根瘤重、固氮酶活性和全氮含量均显著高于CK。同一氮素水平下,株高表现为NO3--N和NH4+-N混合培养下效果最好,NO3--N培养下次之,NH4+-N培养下最低;生物量、根瘤数、根瘤重、固氮酶活性和全氮含量NO3--N和NH4+-N混合培养下效果最好,NH4+-N培养下次之,NO3--N培养下最低;茎叶比则是NO3--N培养下最大,NH4+-N培养下次之,NO3--N和NH4+-N混合培养下的最低,各氮素形态处理间差异显著(P0.05)。随着氮素水平的增加,各形态配比下紫花苜蓿的株高、生物量、根瘤数、根瘤重、固氮酶活性和全氮含量呈现增加的变化趋势,茎叶比呈现减小的变化趋势。NO3--N+NH4+-N的浓度为210mg/L时,紫花苜蓿的株高、生物量、根瘤数、固氮酶活性和全氮含量取得最大值,茎叶比取得最小值,根瘤重则在NO3--N+NH4+-N的浓度为105mg/L时取得最大值,紫花苜蓿在混合态氮培养下生长最好。     

光照对中国对虾稚虾3种消化酶活力的影响

在实验室条件下研究光照(光照周期、光照强度和光色)对中国对虾(Fenneropenaeus chinensis)稚虾3种消化酶(蛋白酶、淀粉酶和脂肪酶)活力的影响。在本实验条件下,主要结果如下:(1)4种光照周期下,对虾3种消化酶的活力差异不显著(P>0.05);(2)在完全黑暗、6μmol.m-2.s-1、30μmol.m-2.s-1和110μmol.m-2.s-1光照强度下,对虾蛋白酶的活力分别为0.361 U.mg-1(protein)、0.081 U.mg-1(protein)、0.088 U.mg-1(protein)和0.273 U.mg-1(protein),完全黑暗和110μmol.m-2.s-1下的活力显著高于其他两个光照强度(P<0.05),且两者间的差异达到显著水平(P<0.05);中国对虾淀粉酶的活力分别为0.386 U.mg-1(protein)、0.095 U.mg-1(protein)、0.111 U.mg-1(protein)和0.315 U.mg-1(protein),完全黑暗和110μmol.m-2.s-1条件下的活力显著高于其他两个光照强度(P<0.05),两者间的差异亦达到显著水平(P<0.05);对虾脂肪酶的活力分别为0.147×10-2U.mg-1(protein)、0.150×10-2U.mg-1(protein)、0.170×10-2U.mg-1(protein)和0.183×10-2U.mg-1(protein),完全黑暗和110μmol.m-2.s-1条件下的活力差异达到显著水平(P<0.05);(3)不同光色下,对虾蛋白酶和淀粉酶的活力差异不显著(P>0.05),脂肪酶的活力则存在一定的差异,蓝光和黄光下,对虾脂肪酶的活力分别为0.093×10-2U.mg-1(protein)和0.107×10-2U.mg-1(protein),显著高于白光和绿光下的活力(P<0.05),但蓝光组和黄光组间的差异不显著(P>0.05)。     

Role of ILK siRNA on expression of GSK-3β and β-catenin in human tubular epithelial cells stimulated by high glucose

AIM：To investigate the effects of siRNA targeting integrin-linked kinase (ILK) on the expression of glycogen synthase kinase 3β (GSK-3β) and β-catenin during epithelial-mesenchymal transition (EMT) in human kidney proximal tubular epithelial cell line HKC induced by high glucose. METHODS：HKC cells were divided into 4 groups:normal glucose (NG) group, high glucose (HG) group, HG+HK (a vector containing the non-specific siRNA designed as negative control) group and HG＋ILK siRNA group. The inverted fluorescence microscope was used to examine the expression of green fluorescent protein (GFP). The expression of ILK at mRNA and protein levels was detected by RT-PCR and Western blotting. The expression of p-GSK-3β and β-catenin was observed by immunocytochemical staining. The protein expression of total GSK-3β, p-GSK-3β, nuclear β-catenin, total β-catenin, E-cadherin and α-smooth muscle actin (α-SMA) was measured by Western blotting. RESULTS：GFP was observed in HKC cells, indicating that the transfection was successful. Both the protein and mRNA of ILK were down-regulated in HG＋ILK siRNA group compared with HG group and HG+HK group, but still higher than those in NG group. Silencing of ILK down-regulated the expression of p-GSK-3β and nuclear β-catenin. No difference of total GSK-3β or total β-catenin was observed among the 4 groups. CONCLUSION:These data support a functional role of ILK, GSK-3β and β-catenin in tubular EMT induced by high glucose. ILK may promote tubular EMT by regulating the activity of GSK-3β and β-catenin, the downstream effectors of the Wnt/β-catenin pathway.     

Expression of TMEM16A as a calcium-activated chloride channel in Fischer rat thyroid follicular epithelial cells and its electrophysiologic pro-perties

AIM：To investigate the expression of transmembrane protein 16A(TMEM16A) in Fischer rat thyroid follicular epithelial (FRT) cells and its electrophysiologic properties. METHODS：The eukaryotic expression vector of pUB6/V5-TMEM16A was constructed and transfected into FRT cells by liposome-mediated transfection. In order to obtain the high efficiency of gene transfection and expression, the quantity and ratio of lipid/DNA complexes were optimized. The FRT cells stably expressing TMEM16A were gained by the selection with blasticidin and confirmed by the techniques of RT-PCR and immunofluorescence. The expression and location of TMEM16A in the FRT cells were observed under an inverted fluorescence microscope. TMEM16A protein was associated with calcium-dependent chloride current, as measured with halide-sensitive fluorescent protein and patch-clamp technique. RESULTS：The results of double digestion and sequencing indicated that TMEM16A was cloned into pUB6/V5. The results of RT-PCR and immunofluorescence confirmed that TMEM16A was expressed in the FRT cells after transfection with TMEM16A. The classical calcium-activated chloride channel currents were recorded in the FRT cells stably expressing TMEM16A by the technique of patch-clamp and halide-sensitive fluorescent protein YFP-H148Q/I152L. CONCLUSION：The protein expression of TMEM16A in the FRT cells was observed. TMEM16A is the molecular identity of calcium-activated chloride channels.     

长沙市野生态动物园斑马蜱pcox1基因扩增及序列分析

为研究长沙市生态动物园引进的非洲肯尼亚斑马蜱的线粒体DNA的部分细胞色素C氧化酶第Ⅰ亚基(cytochrome coxidase subunit l,pcox1)基因序列的遗传变异情况,本研究对其线粒体pcox1基因序列进行PCR扩增,并使用DNAStar(V5.01)、Clustalx2.0及Phylip3.67进行分析。结果显示,几种斑马蜱为消色牛蜱、丽色扇头蜱和璃眼蜱属,种间差异为0.7%~20.2%,种内相似度较高,表明pcox1基因可作为蜱种间遗传变异研究的标记,研究结果为蜱的分类鉴定以及进一步的分子流行病学调查奠定了基础。     

以δc分析有机粪肥养鱼池中鱼类生长能源的初步研究

本文介绍了通过对鱼体、饵料、粪肥的δc值的分析来追踪碳元素的流向,从而研究施肥鱼池中鱼类生长能源的动力学过程的结果。研究表明,滤食性鱼类的生长能源主要来自自养生产系统;杂食性鱼类中的白鲫和鲤鱼,分别有三分之一以上和二分之一左右是来自自养生产系统,而其他部分的生长能源,则来自异养生产系统。