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The results of mycelium growth rate showed that the value of EC50 against Bipolaria maydis, Macrophoma kawatsukai, Fusanrium oxysporum, Fusarium solaid and Fusarium oxysporium were 0.979, 0.505, 1.733, 0.425 and 0.849mL/L. The result of spore germination proved that the value of EC50 against Alternaria longipes, Exserohilum trucicum, Fulua fulua and Fusarium solani were 1.709, 0.375, 0.445 and 1.333mL/L.

该菌株发酵液对玉米小斑病菌、苹果轮纹病菌、棉花枯萎病菌、马铃薯干腐病菌和西瓜枯萎病菌菌丝的生长抑制中浓度(EC50)分别为0.979，0.505，1.733，0.425和0.849mL/L，对玉米大斑病菌、番茄叶霉病菌、马铃薯干腐病菌和烟草赤星病菌的孢子萌发抑制中浓度(EC50)分别为1.709，0.375，0.445和1.333mL/L。

Precocene could induce macropter, the more macropterous adult were found the higher titer of preconece was applied to the larvae, and the macropter inducement was more effective at the 3rd instar than at the 4th instar, the macropterous adults rates were 100% or 86.67% respectively when S. furcifera were treated by 10μg/μl or 100ng/μl preconece at the 3rd instar.

早熟素具有明显的长翅化效应，随着处理浓度的增高，被处理的白背飞虱若虫形成的长翅型成虫数也逐渐增加，且早熟素在3龄期处理对白背飞虱长翅诱导作用强于在4龄期进行的处理，如在3龄期处理时，10μg/μl和100ng/μl的处理组长翅型成虫比率分别高达100%和86.67%。

The result of anaerobic baffled reactor treating low strength wastewater on mesophilic condition indicates that on the condition of influent CODCr concentration of about 500 mg/L,HRT 3～12 h,the reactor was efficient in the removal of CODCr,viz above 84%,effluent CODCr concentration of 75 mg/L.

对厌氧折流板反应器在中温条件下处理低浓度废水的试验结果表明：在进水CODCr浓度为500mg/L、水力停留时间为3～12h时，CODCr的平均去除率可达84%，出水CODCr浓度可降至75mg/L。

The main gluconeogenic precursor in kidney is thought to be lactate; however, less is emphasized enantiomerically. L-lactate is a glycolysis end-product, but D-lactate is formed after detoxification of methylglyoxal, which is the main source of advanced glycation end-products.

乳酸为肾脏糖质新生的主要来源，其含有一不对称碳，故具有D-、L-乳酸两种镜相异构物，而D-、L-乳酸两者之生成相当不同，L-乳酸是糖解作用之终产物，D-乳酸为体内一醣化终产物(advanced glycation end-products)─甲基乙二醛进行去毒化反应所生成，目前缺乏对乳酸镜像异构物与肾脏糖质新生间相关的探讨。

Firstly, callus induction and subculture for Mikania micrantha were studied systematically. The research on callus induction showed that: Shoot tip has higher induction rate than other explants ; At 25℃ and dark regime, the callus was better cultivated on Murashige and Skoog medium (pH5.8) containing 2.0mg/L 2,4-D and 1.0mg/L KT.

首先，对微甘菊愈伤组织诱导和继代增殖培养进行系统研究，愈伤组织诱导研究表明：外植体中芽尖诱导率最高，在含2，4-D2.0mg／L、KT1.0mg／L、pH5.8的MS培养基上25℃黑暗条件下愈伤组织诱导效果较好。

And the conditions in cell suspension culture of Mikania micrantha were studied. The results showed that sucrose was the compatible carbon sucrose, and 30g/L sucrose concentration can satisfy the growth of Mikania micrantha cell; ammonium was absorbed under different sucrose concentration that haven't demonstrated significant specificity, and was completely absorbed on the lag phase and the early logarithmic phase; while nitrate was mainly absorbed on logarithmic phase. The density-dependent of Mikania micrantha cell starting to grow and density-inhibited of cell growth were proposed, the fittest inoculating quantity of Mikania micrantha in cell suspension culture was 40g/L.

并对微甘菊细胞悬浮培养条件进行研究，结果表明，微甘菊细胞生长适宜的碳源是蔗糖，并且较合适的蔗糖浓度为30g／L；在不同蔗糖浓度下氨基氮的吸收差别不大，氨基氮在迟滞期和对数期前期已基本消耗完毕，对数期生长主要利用硝基氮，因而提出，在微甘菊细胞液体悬浮培养中，氮源可以采用初始低氨基氮浓度，对数期中间维持高硝基氮，而且对数期中逐步流加少量的氨基氮；微甘菊细胞迟滞期分裂启动存在密度依赖现象，对数期生长存在密度抑制现象，最适接种量为40g／L。

PCC6803. In the enclosed photobioreactor, after 58. 5h mixotrophic cultivation, 2. 50g/L cell density, 1. 0g/L. d productivity, 15. 3μg/ml chlorophyll concentration and 25. 3%energy efficiency were achieved, which were respectively 8. 9 times, 11times, 2. 3 times and 4. 9 times as much as those in photoautotrophic culture.

在封闭式光生物反应器中，混合营养培养58.5小时，集胞藻6803藻细胞密度达到2.50g/L，是同期光自养的9倍，藻细胞产率为1.0g／L.d，是光自养培养的11倍，叶绿素浓度为15.3μg／ml，是光自养的2.3倍，能量得率为25.3％，是光自养培养过程的5倍。

Detection the early stage apoptosis cells by flow cytornetry Incubating SCL-1 cells in 6-well culture medium with 1×10~6/well, after 12～48hculture with the concentration of imiquimod 0μg/mL and 150μg/mL, gathering cellsgrowing along the wall and making monocellular suspension, washing in PBS for 2times, and then add 5μL Annexin V/FITC and 10μL PI solutions, reaction for 15min avoiding light, detection the early stage apoptosis cells by flow cytometry.

流式细胞仪测定细胞早期凋亡 SCL-1细胞以1×10~6个／孔接种于6孔培养板中，使用含0μg／mL、150μg／mL咪喹莫特的培养液培养12～48h，收集贴壁生长的细胞制成单细胞悬液，PBS洗两次，分别加入5μL Annexin V／FITC和10μL浓度20μg／mL的PI溶液，混匀后室温避光孵育15min，流式细胞仪检测，结果用Cell Quest软件分析。

METHODS: Fetal liver was obtained sterilely. Monoplast suspension was collected by collagenase digestion and mechanical separation, and then centrifuged using 1.070 g/mL Percoll separating medium and 1.077 g/mL Ficoll separating medium. Cells achieved from the interface of separatory liquids were cultured in DMEM/F12 medium, supplemented with 0.1 volume fraction of fetal bovine serum, 20 μg/L hepatocyte growth factor and 40 μg/L epidermal growth factor, for 9 days.

无菌状态下取出胎儿肝脏，以胶原酶消化法和机械分离法获得胎儿肝脏来源单细胞悬液，分别采用1.070 g/mL Percoll分离液和1.077 g/mL Ficoll分离液进行密度梯度离心，吸取界层细胞，添加含体积分数为0.1 FBS、20 μg/L肝细胞生长因子、40 μg/L表皮生长因子的DMEM/F12新鲜培养基诱导9 d。

Results: At the concentrations of 0.1, 1 and 10 μmol/L, berberine dose-dependently suppressed the formation of TRAP-positive multinucleated cells, the TRAP activity and the osteoclastic bone resorption. The strongest inhibitory effect was exhibited at the concentration of 10 μmol/L, with the inhibiting rate of 60.45%, 42.12% and 72.69% respectively.

结果：小檗碱在0.1~10μmol/L范围内，浓度依赖性地抑制TRAP阳性多核破骨细胞的形成和TRAP活性，减少破骨性骨吸收陷窝的面积；在10μmol/L浓度下，对破骨细胞的抑制作用最强，对TRAP阳性多核破骨细胞的形成和TRAP活性的抑制率分别达到了60.45%和42.12%，骨吸收陷窝面积减少72.69%。

And Pharaoh spoke to Joseph, saying, Your father and your brothers have come to you.

47：5 法老对约瑟说，你父亲和你弟兄们到你这里来了。

Additionally, the approximate flattening of surface strip using lines linking midpoints on perpendicular lines between geodesic curves and the unconditional extreme value method are discussed.

提出了用测地线方程、曲面上两点间短程线来计算膜结构曲面测地线的方法，同时，采用测地线间垂线的中点连线和用无约束极值法进行空间条状曲面近似展开的分析。