排序方式： 共有193条查询结果，搜索用时 15 毫秒
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基材是影响门窗节能性的重要因素之一,从国内外相关学者对木塑复合材料的原料利用、制备工艺以及制品性能检测等方面的研究入手,系统阐述了木塑复合材料的研究现状,着重分析了木塑门窗的设计方法,可为节能环保型木塑门窗的制作提供理论依据. 相似文献
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以一株侧孢芽孢杆菌(Brevibacillus laterosporus)为试验菌株,研究其对铜绿微囊藻(Microcystis aeruginosa)的抑制效应,并将其应用于水产养殖富营养化水体中,进行蓝藻水华的生态控制。结果表明,侧孢芽孢杆菌可以抑制铜绿微囊藻的生长,使其叶绿素a的含量显著下降,从而抑制了其光合作用的活性,达到限制铜绿微囊藻细胞增殖的目的。这种抑制作用与侧孢芽孢杆菌的细菌含量成正比,初始接种的菌体浓度越高,抑制作用越强,且这种限制作用在菌藻接触后的8~10 d较为显著。将活菌数≥108个/mL的侧孢芽孢杆菌按0.50、1.00 mg/L的用量加入淡水池塘养殖的富营养水体,在60 d内不仅可使养殖水体中的TN、TP和高锰酸盐指数有所下降,同时还可显著抑制藻类的数量,增加藻类的种类,提高养殖水体中藻类的Shannon-Weaver多样性指数,较好地调节藻类群落结构。研究显示,侧孢芽孢杆菌因具有较强的抑藻能力,在生物修复养殖富营养化水体的水生生态系统方面有着良好的应用前景。 相似文献
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小麦淀粉糊化特性是评价小麦加工品质和品质育种的重要指标之一。对不同年份和地点5个环境生长的矮孟牛姊妹系及其衍生系共109份材料的RVA参数(峰值黏度、低谷黏度、稀澥值、最终黏度、回生值和糊化温度)观测, 并利用混合线性模型分析其与覆盖小麦全基因组的971个DArT (Diversity Array Technology)标记的关联性。结果表明, 分布于19条染色体上的70个DArT标记与上述RVA参数显著关联(P≤0.001), R2值范围是0.2%~23.3%。2A、2B和2D染色体上标记与多个RVA参数都有关联, 且效应值较大。这为淀粉湖化特性的分子标记辅助选择提供了重要的信息。 相似文献
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LIU Yun-bo HU Peng-fei WANG Hai-long ZHANG Jin-you LI Chang-sheng ZHANG Gui-xue* 《东北农业大学学报(英文版)》2005,12(1):68-73
Research on development of fetal ovary was traced to late 70 s. Histological study on fetal horse ovarian germinal epithelium was conducted[1], followed research on germcell proliferation was carried out[2]. In the late 80s,development of 37-118 dfetalrhesus ovaries were studied through continuous ultrathin sec-tion [3]. Histological study on late fetal rhesus ovaries were conducted [4]. It was believed that fetal ovaries had ability to biosynthesis estrogen and response to gonadotrophin after… 相似文献
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REN Gui-ping QU Juan-juan PEI Fu-cheng LI Jing-peng LIU Xiang-yu LI Lu WANG Jun-wei* 《东北农业大学学报(英文版)》2005,12(1):11-13
To obtain the protein of duck interferon alpha and study its biological activities, the prokaryotic ex-pression vector of DuIFN-α was constructed and expressed in BL21 (DE3) plysS. Using PCR technique, the proteingene of DuIFN-α was cloned from pMD-18-duIFN-α recombinant. The gene was then inserted to pGEM-T vectorand identified by restriction endonuclease analysis and sequencing. DuIFN-α was ligated with the prokaryotic expres-sion vector of pET30 a, then transformed into BL21 (DE3) plysS. The best inducing time and IPTG concentration for the expression of this recombinant protein was tested through the expression of the positive recombinant with differ-ent time span and different IPTG concentration. Lots of the protein of DuIFN-α were expressed in BL21 (DE3)plysS with 1 mmol·L-1 IPTG for 4 hours and its molecular weight for 34 000. 相似文献
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