转cry1Ab基因水稻中毒蛋白的表达、分泌及其在土壤中的残留

研究了转cry1Ab基因水稻(克螟稻)中Cry1Ab毒蛋白的表达、根系分泌及其在土壤中的残留规律.结果表明,分蘖始期至成熟期,克螟稻地上部和根部中的Cry1Ab毒蛋白的表达量(FW)分别为3.23～8.22 μg/g和0.68～0.89 μg/g.生育期间克螟稻根系分泌的Cry1Ab毒蛋白含量仅为1.66～48.02 ng/(株·d).试验证实,克螟稻根际土中的Cry1Ab毒蛋白残留含量低于检测限(<0.5ng/g 干燥土).生物测定还表明,克螟稻根际土及其提取液对棉铃虫初孵幼虫和3龄幼虫不产生致死性效应.相对于Cry1Ab毒蛋白的根系分泌转移,克螟稻秸秆还田对土壤环境的影响应引起重视.     

九畹溪大桥大跨度钢管拱分段整体吊装施工安全措施探讨

在进行缆索吊装大跨度双肋钢管拱悬拼施工中,过去多采用空中焊接横联作业,该项施工难度大,尤其在桥高、风大、两岸地形陡峭、施工条件困难的情况下,施工安全和施工质量难以保证。是否能将空中焊接作业转化成地面作业,本文详细介绍缆索吊装大跨度双肋钢管拱进行悬拼施工新技术,并结合九畹溪大桥施工实例,探讨缆索吊装双肋悬拼钢管拱施工中工艺程序、质量控制、安全措施等工程施工新方法及施工效果。     

张北地震序列的尾波Qc值研究

采用尾波单次散射模型,选取张北地震序列70条波形记录,计算了张北地区t=58.88s时的尾波QC值:QC(f)=132.6±20f0.96±0.14。研究中发现,随流逝时间的增加QC逐渐增大,当流逝时间>120s时,出现逆转,QC迅速减小。文中采用频率域方法计算QC值,尾波功率谱计算自t>2ts开始,选用垂直向波形记录,取时间窗长为5.12s,步长2.56s向前滑动,每个时间窗两端5%的数据与余弦函数相乘,然后做FFT变换,分别计算9个中心频点各时间窗的能量密度谱,尾波流逝时间取各时间窗的中心点。当信号的能量密度<4倍的背景噪声能量密度时,尾波能量密度取值结束。求得能量密度谱后,线性拟合可求得不同流逝时间各频点的QC值。     

纳米氧化镍颗粒对长牡蛎(Crassostreagigas)抗氧化防御体系的影响

纳米氧化镍(nNiO)作为一种广泛使用的纳米颗粒,其水生毒理效应研究还很有限。为探索n Ni O对海洋贝类的毒性机制,本研究将长牡蛎(Crassostrea gigas)置于不同浓度(0、1、10、100 mg·L~(-1))的n Ni O中暴露96 h,分别测定鳃和消化腺组织的丙二醛(MDA)含量和超氧化物歧化酶(SOD)、过氧化物酶(POD)以及过氧化氢酶(CAT)活性,并通过实时荧光定量PCR技术测定了鳃和消化腺中应激蛋白HSP70和AOX基因的表达变化。结果显示:在100 mg·L~(-1)n Ni O处理下,2种组织中MDA含量均显著性升高(P0.01),显示纳米颗粒造成了长牡蛎的脂质过氧化,并可能引起相应的氧化损伤。同时,n Ni O暴露也诱导了长牡蛎抗氧化酶(SOD、CAT和POD)活性的改变。其中,SOD和CAT活性在10 mg·L~(-1)浓度处理组达到最高,而POD活性在1 mg·L~(-1)浓度组即达最高值。在高浓度n Ni O(100 mg·L~(-1))胁迫下,3种抗氧化酶的活性均比低浓度(1和10 mg·L~(-1))处理组降低,表明抗氧化酶的保护作用在较低浓度暴露下更有效;而热激蛋白(hsp70)和交替氧化酶(aox)基因却分别在长牡蛎消化腺和鳃组织中上调表达(P0.01),并表现出一定的组织差异。说明高浓度纳米颗粒暴露中主要是应激蛋白发挥了作用。本文结果为纳米氧化镍对海洋双壳贝类的毒性机制研究及生态风险评估提供了基础数据。     

磷酸三苯酯(TPP)和磷酸三(2-氯异丙基)酯(TCPP)诱导人胚肾细胞HEK293凋亡的机制研究

磷系阻燃剂对人体的潜在毒性作用引起了国内外研究者的广泛关注。肾脏是机体重要的排毒器官,若肾脏细胞受损,可能影响肾脏功能的正常发挥。本研究以人胚肾细胞HEK293为研究对象,结合传统毒理学实验,筛选出磷酸三苯酯(TPP)及磷酸三(2-氯异丙基)酯(TCPP)诱导人胚肾细胞HEK293凋亡的关键靶标基因p53。在此基础上采用分子对接模拟和光谱法分析发现,TPP和TCPP分别以嵌插方式和沟槽方式结合p53-DNA,改变基因片段的框架结构,启动分子起始事件,通过影响相关基因(Bax、Hrk、Bcl-2和Bad)的表达量,导致线粒体途径释放cyt c,最终激活Caspase 7实现细胞凋亡。研究结果阐明了此类污染物诱导凋亡的作用机制,为毒害化学品的污染防控提供理论依据。     

Using mRNA to investigate the effect of low-pressure ultraviolet disinfection on the viability of E. coli

UV can induce damages on mRNA consistently among different genes. SOS response was more active after UV treatment. Programmed cell death was not found to be more active after UV treatment. The efficacy of ultraviolet (UV) disinfection has been analyzed and validated by numerous studies using culture-based methods, yet the discovery of the viable but nonculturable state necessitates the investigation of UV disinfection based on viability parameters. Paired regulators of the SOS response system, recA-lexA, and the programmed cell death system, mazEF, in Escherichia coli were chosen as the target genes, and the effect of UV irradiation on the mRNAs of the four genes was studied. This research showed that, after UV irradiation, the responses of the mRNAs were highly consistent, with reduction percentages of approximately 60% at 20 mJ/cm², 70% at 40 mJ/cm², and 90% at 80 mJ/cm², and these reductions were believed to be the result of direct UV damage to nucleic acids. After 24 h of dark incubation, recA and lexA were both upregulated but to a lesser extent for repressor lexA; and mazE and mazF were both downregulated. This result implies that UV irradiation induces the dark repair system more actively, and the cells will proceed to death at a rate similar to that associated with natural decay.     

Higher-efficiency for combined photovoltaic-thermoelectric solar power generation

Solar energy application in a large spectrum has the potential for high-efficiency energy conversion. Though, solar cells can only absorb photon energy of the solar spectrum near their band-gap energy, and the remaining energy will be converted into thermal energy. The use of the thermoelectric generator becomes a necessity for convert this thermal energy dissipated so as to increase efficiency conversion.

This paper analyses the feasibility of photovoltaic-thermoelectric hybrid system and reviews their performance in order to optimize harvested energy. Regarding the thermoelectric effect, a new method of the ambient energy harvesting is presented. This method combines thermoelectric generators and the effects of heat sensitive materials associated to photovoltaic cells in phase change for generating both energy day and night. Experimental measures have been conducted primarily in laboratory conditions for a greater understanding of hybridization phenomena under real conditions and to test the actual performance of devices made. Results show that the hybrid system can generate more power than the simple PV and TEG in environmental conditions. This hybrid technology will highlight the use of renewable energies in the service of the energy production.     

加卸荷条件下岩石力学特性与声发射特征

为了探究真三轴复杂应力变化条件下岩石强度及破坏模式,通过真三轴卸荷扰动测试系统对砂岩试件进行不同第二主应力加卸荷试验,讨论在加卸荷过程中岩石的力学特性及声发射特征。试验结果表明:第二主应力的增加对试件的承载能力起到先增强后弱化的效果;不同第二主应力加卸荷声发射能量及累计振铃计数变化趋势大体一致,耗散能量比在载荷达到岩石损伤强度时突增;声发射能量峰值提前于试件轴向应力跌落,声发射能量和累计振铃计数大幅突增可作为岩石破坏的前兆;在低载荷下岩石中活动主要是裂隙压密与发育,在达到岩石损伤强度后岩石中的活动主要是裂纹贯通形成破裂面,砂岩试件声发射定位点集中区域与试件主要破裂面基本吻合。     

水稻精细胞差异表达基因RSG6的克隆和抗体制备

选用在水稻精细胞和二细胞花粉的差减文库中获得的在精细胞中表达量显著增强且可能代表新基因的EST之一 (BF4 75 2 0 7)为探针 ,筛选水稻精细胞cDNA文库 ,得到一全长为 1176bp的序列 ,其开放读码框编码 2 81个氨基酸 ,与已知蛋白质无明显同源性 ,属于一新发现的基因 ,GenBank登录号为AF4 4 2 4 90 .这是第 1次从高等植物精细胞中分离到的全长基因 .RT PCR结果证明该基因在根、叶、二细胞花粉、成熟花粉、授粉子房和精细胞中均有表达 ,但在精细胞中的表达量要高得多 ,是精细胞差异表达基因 .将此基因命名为RSG6 (ricespermgene6 ) .将RSG6的编码区克隆到表达载体pQE30上 ,构建重组质粒 .经IPTG诱导后 ,在E .coliM15 (pREP4 )中表达出了N端融合了 6×His的融合蛋白 .用纯化的融合蛋白免疫家兔 ,制得高效价、高特异性的抗体     

三价钇对紫露草的遗传毒性研究

用紫露草四分体微核试验法和紫露草雄蕊毛细胞突变法研究了稀土元素三价钇的遗传毒性．结果表明：Y3＋能引起紫露草四分体微核率显著升高，提示Y3＋是诱变剂或纺锤丝毒剂；Y3＋能引起雄蕊毛细胞突变率显著升高，进一步明确Y3＋是诱变剂．