农村建设中太阳能路灯综合效益评价研究

我国新农村建设中太阳能利用取得了快速发展,本文简要介绍了太阳能路灯系统的工作原理,结合某市循环经济示范村太阳能路灯系统的使用现状,采用费用-效益评价指标从经济、环境和社会效益3个方面对太阳能路灯系统进行综合评价与分析,得到太阳能路灯与普通路灯相比较,在经济上是可行的;安装太阳能路灯系统减少了对环境的污染,提高了可再生能源的利用价值,对于该旅游区的环境保护具有重大意义;对新农村建设新能源的利用,起到了很好的引导作用,为太阳能路灯系统大力推广提供一定的实践依据。     

几种苹果矮化砧木的抗寒性研究

以71-3-150、GM256、SH6及M9 4种苹果(Malus)矮化砧木的1年生枝条为试材,进行-20℃、-25℃、-30℃、-35℃、-40℃低温处理,用电导法配合Logistic方程,求得拐点温度(LT50)即半致死温度,并对其电导率、可溶性蛋白含量和POD酶活性等指标进行了测定比较。结果表明:测得的电解质渗出率呈典型的S型曲线,与相应的低温呈极显著负相关;71-3-150、GM256、SH6及M9的半致死温度分别为-40.63℃、-39.29℃、-34.10℃、-30.10℃;抗寒性强的71-3-150和GM256能保持较高的可溶性蛋白含量和POD酶活性。     

健康家兔肠道中乳酸菌的分离鉴定

本试验选用MRS、MRS+10%家兔硬粪浸出液和MRS+10%泡菜汁3种选择培养基,对健康家兔肠道的乳酸菌群分别进行需氧和厌氧培养,根据可培养细菌菌落特征、染色特性、显微镜形态观测,共分离出7株乳酸菌株,其中需氧菌2株,厌氧菌5株。结合生化试验初步鉴定,需氧菌株分别为乳酸乳球菌和短乳杆菌,厌氧菌株分别为嗜酸乳杆菌,嗜粪乳杆菌,肠乳杆菌,乳酸乳杆菌和弯曲乳杆菌。本实验为弄清健康家兔肠道的有益菌群,以便下一步制作更易于在畜禽的肠道中定植存活的复合动物微生态制剂做准备。     

鱼肠道弧菌免疫检测方法的研究

采用灭活的鱼肠道弧菌作为抗原,制备兔抗血清,建立了鱼肠道弧菌的间接荧光抗体检测技术(indirect im-munofluorescence assay test,IFAT)、Western-blotting免疫印迹检测技术。IFAT结果显示阳性信号覆盖整个菌体,明亮,清晰,荧光信号呈长弧形且两端钝圆,与鱼肠道弧菌形状一致。Western-blotting结果显示共10条蛋白带发生免疫反应,其中6条蛋白带结果较清晰,显示出较强的特异性免疫反应,阴性对照组无条带。IFAT和Western-blotting结果说明所建立检测方法能够准确、快速的检测出鱼肠道弧菌。     

基于图像处理与GUI的大蒜切脐的研究

本课题采用数字图像处理技术,通过研究适合于大蒜切脐定位的专用算法,通过GUI界面编程编写出大蒜切脐软件系统,实现对切脐位置的自动、精确定位。结果表明,该程序能够很好的将大蒜根须与蒜体区分,为大蒜切脐机械化的实现提供了技术支持。     

大白菜花青素含量及色差指标相关性研究

为了探寻大白菜花青素含量快速测定的方法,本文利用pH差计法和色差仪分别测定了‘城阳青’(普通大白菜)、‘秋宝黄’(黄心白菜)和‘彩凤’3个不同叶色大白菜品种花青素含量以及色差指标,并对6个色泽参数与花青素含量进行了相关和回归分析。结果表明:6个色泽参数均能反映白菜叶片间叶色的细微变化,‘城阳青’和‘秋宝黄’不含花青素,紫色白菜‘彩凤’的花青素主要分布于由外向内的第1～4层叶片。色泽参数L,b,h和C分别与花青素含量呈极显著或显著负相关关系(相关系数分别为-0.85**,-0.58**,-0.49*,-0.58**)。以色泽参数值L、a、h与花青素含量建立了多元回归方程:y=90.24-1.07x1+5.65x2-142.71x3(x1为L值,x2为a值,x3为h值,y为花青素含量),该回归方程相关系数为0.9629。通过色差计依据建立的回归方程可快速测定紫色大白菜花青素的含量。     

不同抗热应激添加剂对热应激小鼠精液品质的影响

为探讨抗热应激添加剂对热应激状态下小鼠精液品质的影响,选取年龄和健康状况相近的成年雄性鼠150只,按照常温、热应激、添加剂处理后热应激的方式进行分组试验,对各组精液品质等指标进行统计分析。结果表明,3组热应激添加剂在缓解热应激小鼠的精液品质的影响效果上存在显著差异,其中效果最好的为中药组,其次是电解质组,最后是维生素组。从Hsp70mRNA表达量上来看,抗热应激添加剂组明显高于常温对照组。但与热应激组比较,维生素组与电解质组表达量低,而中药组表达量高。     

人工塑石假山在现代园林中的应用

对当前塑石假山工程现状及存在的问题进行了分析,并结合塑石假山的特点提出了若干建议,以期为创造精品塑石假山景观提供更好的借鉴。     

Role of translationally controlled tumor protein in PRL-3-promoted metastasis of colon cancer cells

AIM: To study the role of translationally controlled tumor protein (TCTP) in the proliferation, migration and invasion of phosphatase of regenerating liver-3(PRL-3)-promoted colon cancer cells.METHODS: The vectors pAcGFP-C3 and pAcGFP-C3-PRL-3 were constructed and transfected into the colon cancer cell line LoVo.LoVo-PRL-3 cells stably expressing PRL-3 and LoVo-control cells were established. The expression levels of PRL-3 and TCTP in both cells were detected by Western blotting and real-time PCR. The specific siRNA sequence for TCTP mRNA and control-siRNA were synthesized and transfected into the LoVo-PRL-3 cells. TCTP expression at mRNA and protein levels in LoVo-PRL-3 was detected by Western blotting and real-time PCR 24 h, 48 h and 72 h after transfection. The proliferation, migration and invasion abilities of LoVo-control cells, LoVo-PRL-3 cells, TCTP-siRNA and control-siRNA cells were detected by CCK-8 assay and the method of Transwell cell culture chambers.RESULTS: The expression of TCTP at mRNA and protein levels in LoVo cells was significantly increased after PRL-3 transfection (P<0.05). TCTP mRNA was significantly inhibited 24 h, 48 h and 72 h after transfection of TCTP-siRNA (P<0.01). TCTP protein was also significantly inhibited 48 h and 72 h after transfection (P<0.01). Compared with LoVo-control cells, the proliferation, migration and invasion abilities of LoVo-PRL-3 cells were significantly enhanced (P<0.05). However, lowering the up-regulated expression of TCTP in LoVo-PRL-3 cells inhibited the proliferation, migration and invasion abilities (P<0.05). CONCLUSION: PRL-3 promotes proliferation, migration and invasion of colon cancer cells by up-regulating the TCTP expression. siRNA targeting TCTP may be an effective method for prevention and treatment of colon cancer cell metastasis.     

Lenalidomide alone or combined with bortezomib inhibits growth and induces apoptosis in KM3 cells

AIM: To investigate the effects of lenalidomide alone or combined with bortezomib on induction of apoptosis in multiple myeloma(MM) KM3 cells.METHODS: The KM3 cells were treated with lenalidomide alone or combined with bortezomib. The number of viable cells was determined by trypan blue exclusion. Apoptotic cells were simultaneously stained with annexin V-FITC and PI and determined by flow cytometry. RT-PCR was used to examine the level of p65 mRNA. Western blotting was used to examine the protein levels of P65, pP65, caspase-3,-8, -9, and poly (ADP-ribose) polymerase (PARP). RESULTS: Lenalidomide-inhibited the cell growth and induced apoptosis of KM3 cells. The mechanism responsible for lenalidomide-mediated inhibition was via NF-κB and activation of caspase-mediated induction of apoptosis. A synergistic effect was observed when combination of lenalidomide with bortezomib was used. CONCLUSION: Lenalidomide inhibits the growth and induces apoptosis in KM3 cells. There is a synergistical effect when combination of lenalidomide with bortezomib is in use.