斜板上流式厌氧污泥床处理低浓度有机废水的试验研究

本文报告了用１６．１升斜板上流式厌氧污泥床在常温下处理低浓度有机废水的启动和运行试验研究。试验使用稀释酒精废水为模拟处理基质，启动阶段仅用７７天时间，装置水力负荷达到２ｍ３／（ｍ３．ｄ），ＣＯＤ去除率达到７８．９％，此时进水ＣＯＤ浓度为７６７．８ｍｇ／Ｌ。在第二阶段试验中，仅用一天时间，装置就恢复了时隔半年的正常运行。以后在温度１２℃以上，ＨＲＴ为１２小时，进水ＣＯＤ浓度在６６０．０～９８２．０ｍｇ／Ｌ范围的１２９天稳定运行中，平均ＣＯＤ去除率为７６．１％。结果表明：采用该工艺处理低浓度有机废水在技术上是可行的，具有启动快，运行稳定，工艺控制简便的优点。水浸没的成组浅层斜板在ＵＡＳＢ／ＩＴＳ反应器中有良好的污泥截留能力和稳流效果，容易生成大颗粒污泥。颗粒污泥最大粒径可达５ｍｍ，ＳＶＩ为１８．２ｍｌ／ｇ。颗粒污泥中以甲烷丝菌为优势菌。     

基于Pro/E的装配体三维设计

介绍了使用Pro/E计算机软件作为计算机设计绘图工具，建立3D实体模型，然后根据零件间的位置关系将所涉及的零件逐个地进行装配；并简单阐述了其工程图的制作及齿轮三维造型的方法。     

Mechanism of Fuzilizhong decoction alleviating inflammatory damage of rats with non-alcoholic fatty liver disease

AIM To observe the effect of Fuzilizhong decoction on the inflammatory damage of non-alcoholic fatty liver disease （NAFLD） rats and to explore its mechanism. METHODS SPF male SD rats were randomly divided into 6 groups： control group, model group, high dose （20 mg·kg^-1·d^-1）, middle dose （10 mg·kg^-1·d^-1）, low dose （5 mg·kg^-1·d^-1） Fuzilizhong decoction group and Yishanfu （30 mg·kg^-1·d^-1）group, 8 rats in each group. A NAFLD rat modelwas established by intragastric administration of fat emulsion for 4 weeks. Then the drug was given for 4 weeks in each treatment group. HE staining was performed to observe the histopathological changes of the rat liver.The serum levels of interleukin-2（IL-2）, IL-6 and tumor necrosis factor-α（TNF-α） were measured by ELISA. The expression of toll like receptor 4（TLR4） and NF-κB p65 in liver tissues at mRNA and protein levels was determined by RT-qPCR and Western bolt,respectively. RESULTS Compared with control group, the inflammatory damage of liver tissue was more serious, the serum levels of IL-2, IL-6 and TNF-α, the mRNA expression TLR4 and NF-κB p65 in liver tissues were significantly increased in model group（P<0.05）. However, compared with model group, the liver pathological changes in each treatment group were significantly relieved, the serum levels of IL-2, IL-6 and TNF-α, the mRNA expression of TLR4 and NF-κB p65 in liver tissues were significantly reduced（P<0.05）.In addition, the changes of TLR4 and p-NF-κB p65 protein levels in liver tissue were consistent with the changes of TLR4 and NF-κB p65 mRNA. CONCLUSION Fuzilizhong decoction attenuates the inflammatory damages of NAFLD in rats by inhibiting TLR4/NF-κB p65 signaling pathway.     

p300/p53/Smad3 pathway involved in aging-related atrial fibrosis in human atrial fibroblasts

AIM To investigate the role of p300 in aging-related atrial fibrosis in human atrial fibroblasts （HAFs） and its potential mechanism. METHODS HAFs were obtained from human left atrial tissue, and the senescence model was established by cell passage. Senescence-associated β-galactosidase （SA-β-Gal） staining was used to detect the cell senescence, and Western blot was used to determine the protein levels of p300, p53, Smad3 and other senescence and fibrosis associated proteins in HAFs. RESULTS Compared to passage 3 HAFs, the proportion of senescent cells, and the protein levels of p300, p53, p-Smad3 and other senescence and fibrosis associated proteins were increased in HAFs at passage 7 and 11 （P<0.05）. After treated with curcumin （a p300 inhibitor） or transfection with p300 small-hairpin （sh） RNA plasmid, the protein levels of p300, and the senescence and fibrosis associated proteins were decreased in HAFs at passage 7（P<0.05）. Up-regulation of p300 by transfection with p300 over-expression plasmid increased the protein levels of p53, Smad3 and MMP-2 in HAFs at passage 3 （P<0.05）. CONCLUSION p300/p53/Smad3 signaling pathway plays an important role in aging-related atrial fibrosis in HAFs.     

博落回急性及亚慢性毒性试验

博落回对小鼠经口急性毒性和对大鼠腹腔注射慢性毒性试验结果表明：博落回生物碱硫酸盐对昆明系小鼠的急性毒性为：水溶液ＬＤ５０＝９００ｍｇ·ｋｇ＾－１，水混悬液ＬＤ５０＝１０４３ｍｇ·ｋｇ＾－１，均属低毒级。博落回注射液对Ｗｉｓｔａｒ大鼠亚慢性毒作用的靶器官主要为肝，长时间或大剂量接毒引起肝细胞变性，增生，使雄性动物肝／体比明显增高，而血清谷－丙转氯酶下降。     

Synthesis and Anthelmintic Activity of 7-Hydroxy- 5-oxo-5H-thieno[3,2-b]pyran-6-carboxanilides and -6-thiocarboxanilides

7-Hydroxy-5-oxo-5H-thieno[3,2-b]pyran-6-carboxanilides and -6-thio-carboxanilides represent a novel series of anthelmintic compounds, with broad-spectrum activity against important parasitic nematodes in sheep and dogs. In particular, an improved efficacy against Trichostrongylus colubriformis in sheep over the related 3-carbamoyl-4-hydroxycoumarins has been noted. New synthetic routes to the key intermediate, 7-hydroxythieno[3,2-b]pyran-5-one, have been developed.     

天女木兰的物候及生长过程

对生长于北华大学林学院树木园内的天女木兰进行物候观测,并将物候与气象因子紧密结合,揭示了天女木兰的物候规律。同时通过对天女木兰的树干解析,找出了野生天女木兰树木的生长规律,从而为天女木兰的保育和开发利用提供了科学依据。     

利杂犊牛小肠各段长度与黏膜结构的发育学变化

利用图像分析法研究1月龄,4月龄和6月龄健康利杂犊牛小肠结构的发育形态变化。结果显示,犊牛小肠各段在不同的月龄,其长度变化差异显著(P<0.05);不同月龄犊牛的十二指肠、空肠、回肠的黏膜厚度、肌层厚度不同程度的增加且差异极显著(P<0.01);从1月龄至6月龄,十二指肠、回肠绒毛长度分别增加45.7%和8.0%;而空肠的绒毛以4月龄最长(392.48μm),绒毛高度/隐窝深度(V/C)值以4月龄的最大(2.63),且与1月龄和6月龄时比较差异极显著(P<0.01),但1月龄与6月龄相比较差异不显著(P>0.05)。结果提示,6月龄前犊牛小肠黏膜结构变化较大,犊牛断奶合理日龄应进一步研究。     

Characterization of Bioactivities and Biosynthesis of Angucycline/Angucyclinone Derivatives Derived from Gephyromycinifex aptenodytis gen. nov., sp. nov.

Strain NJES-13^T is the type strain and currently the only species of the newly established actinobacteria genera Aptenodytes in the family Dermatophilaceae isolated from the gut microbiota of the Antarctic emperor penguin. This strain demonstrated excellent bioflocculation activity with bacteria-derived exopolysaccharides (EPSs). Moreover, it produced bioactive angucycline/angucyclinone derivatives (ADs) and contained one type III polyketide synthase (T3PKS), thus demonstrating great potential to produce novel bioactive compounds. However, the low productivity of the potential new AD metabolite was the main obstacle for its chemical structure elucidation. In this study, to increase the concentration of targeted metabolites, the influence of cellular morphology on AD metabolism in strain NJES-13^T was determined using glass bead-enhanced fermentation. Based on the cellular ultra-structural observation driven by bacterial EPSs, and quantitative analysis of the targeted metabolites, the successful increasing of the productivity of three AD metabolites was achieved. Afterward, a new frigocyclinone analogue was isolated and then identified as 2-hydroxy-frigocyclinone, as well as two other known ADs named 2-hydroxy-tetrangomycin (2-HT) and gephyromycin (GPM). Three AD metabolites were found to demonstrate different bioactivities. Both C-2 hydroxyl substitutes, 2-hydroxy-tetrangomycin and 2-hydroxy-frigocyclinone, exhibited variable inhibitory activities against Staphylococcus aureus, Bacillus subtilis and Candida albicans. Moreover, the newly identified 2-hydroxy-frigocyclinone also showed significant cytotoxicity against three tested human-derived cancerous cell lines (HL-60, Bel-7402 and A549), with all obtained IC₅₀ values less than 10 µM. Based on the genetic analysis after genomic mining, the plausible biogenetic pathway of the three bioactive ADs in strain NJES-13^T was also proposed.