离子交换层析结合反向色谱纯化聚二氨基丙酸

ε-聚赖氨酸生产菌株Streptomyces albulus PD-1可合成一种新型非蛋白质氨基酸均聚物聚二氨基丙酸,采用离子交换层析和反向色谱,对聚二氨基丙酸的分离纯化进行研究。离子交换层析柱选用DEAE-Sepharose Fast Flow填料,50 mmol/L磷酸盐缓冲液(p H 7.5)平衡上样,含0.5 mol/L Na Cl的磷酸盐缓冲液(p H 7.5)洗脱,收集洗脱液用分子筛Sephadex G-25除去磷酸盐缓冲液。然后用C18反相色谱进一步纯化,流动相为V(甲醇)/V(0.1%磷酸)=5/95。经过离子交换层析和反向色谱,纯化得到聚二氨基丙酸纯品,回收率为39.8%,样品纯度达98.4%,为后续的聚二氨基丙酸的深入研究奠定基础。     

Localization of human mononuclear cell interleukin 1

The detection and localization of interleukin (IL) 1 in human monocytes was carried out by flow cytometry using monoclonal antibodies to IL-1 alpha and IL-1 beta proteins. IL-1 alpha was detected on the surface of monocytes and the surface expression increased following lipopolysaccharide activation. No demonstrable IL-1 beta protein could be observed on the cell surface by antibody staining, while both IL-1 alpha and IL-1 beta could be visualized intracellularly by the appropriate monoclonal antibodies following acetone permeabilization of the monocytes. Further experiments with cell associated IL-1 revealed that most of the biological activity of human monocytes could be inhibited by affinity purified polyclonal antibodies to IL-1 alpha protein, whereas no inhibitory activity was observed with IL-1 beta specific antibodies. These data support the hypothesis that a differential localization of IL-1 alpha and IL-1 beta exists within human blood-derived monocytes.     

高效液相色谱法在脱氧核糖核酸酶解动力学研究中的应用

为了更好地对脱氧核糖核酸酶解动力学过程进行研究,建立脱氧核糖核酸（DNA）酶解液中4种脱氧核苷酸（腺嘌呤脱氧核苷酸（dAMP）、鸟嘌呤脱氧核苷酸（dGMP）、胞嘧啶脱氧核苷酸（dCMP）、胸腺嘧啶脱氧核苷酸（dTMP））的高效液相测定方法,能将酶解液中4种脱氧核苷酸完全分离并准确定量。在此基础上,对DNA酶解的动力学进行初步研究,其反应机理为不存在底物和产物抑制的双底物顺序反应,动力学方程为x=1／bin（1＋abt）（其中a=0．3723p0—0．974;b=-0．0493p0^2＋1．1150p0-1．1103）,该方程可以很好地描述DNA酶解过程,误差仅为3．31％.     

The murine interleukin-4 receptor: molecular cloning and characterization of secreted and membrane bound forms

Receptors for interleukin-4 (IL-4) are expressed at low levels on a wide variety of primary cells and cultured cell lines. Fluorescence-activated sorting of CTLL-2 cells resulted in the isolation of a subclone, CTLL 19.4, which expressed 10(6) IL-4 receptors per cell. These cells were used for the purification of IL-4 receptor protein and to prepare a hybrid-subtracted cDNA probe for isolation of cDNA clones. Three classes of IL-4 receptor cDNA were identified. The first encoded a 140 kd membrane bound IL-4 receptor containing extracellular, transmembrane, and cytoplasmic domains. The second class lacked the cytoplasmic region, and the third encoded a secreted form of the receptor. All cDNA clones expressed in COS-7 cells had IL-4 binding properties comparable to the native IL-4 receptor. The soluble form of the IL-4 receptor blocked the ability of IL-4 to induce CTLL cell proliferation and may represent a regulatory molecule specific for IL-4-dependent immune responses.     

Expression of cell type-specific markers during pancreatic development in the mouse: implications for pancreatic cell lineages

Summary The islet cells of the mammalian pancreas are comprised of four different endocrine cell types, each containing a specific hormone. Islet cells also contain two enzymes of the catecholamine biosynthetic pathway: tyrosine hydroxylase (TH) and aromatic L-amino acid decarboxylase (AADC). The cell lineage relationships of these different cell types have not been examined and it is not known whether, during development, they originate from the same or from different precursor populations. In this study we used immunocytochemical procedures to determine whether developing pancreatic cells express markers common to endocrine and exocrine cell types. We found that acinar cell precursors express AADC prior to the appearance of an exocrine marker and that the expression of AADC in acinar cells persists throughout embryogenesis to the first month of postnatal life. At this time, acinar cells do not contain AADC. We also found that exocrine cells containing AADC never express other islet-cell markers. These findings suggest that while acinar and islet cells both arise from precursor cells containing AADC, these progenitor cells do not express a combined endocrine-exocrine phenotype.     

上海公园水体夏季浮游植物群落与环境因子的关系

为了解公园水体浮游植物群落状况,分析浮游植物物种分布和环境因子之间的关系,揭示浮游植物物种对生态环境的需求,于2008年7月和9月对上海市11个公园水体浮游植物群落进行了调查,对获得的浮游植物数据和环境因子数据进行典范相关分析(CCA),并绘制了物种与环境因子关系的二维排序图。结果表明：调查期间共鉴定出浮游植物384种,隶属于8门,浮游植物密度范围为2.01×10⁵～57.60×10⁵ cells·L^-1;群落组成以蓝藻、裸藻、硅藻和绿藻为主,主要优势种有细微颤藻、无常蓝纤维藻、尾裸藻、颗粒直链藻、梅尼小环藻、普通小球藻、四尾栅藻等;7月影响浮游植物分布的主要环境因子依次为铵态氮、溶解氧、水温和总磷,而9月的pH值、水温、溶解氧、透明度和总氮含量对浮游植物的分布产生影响较大;其中,透明度和浮游动物量是影响隐藻、甲藻和硅藻藻类生物量的主要环境因子,而蓝藻、裸藻、绿藻主要受水体氮磷营养盐浓度和溶解氧的影响。     

中国森林生态资产价值评估

森林资源是支撑人类社会发展的重要生态资产,探索森林生态资产价值的评估方法,对合理利用和有效保护森林资源具有重要意义。运用净现值法计算了中国森林生态资产总价值为698.5万亿元,其中直接价值为7.5万亿元,包括林木价值4.5万亿元和林下产品价值3.0万亿元;间接价值为691万亿元,其中,气候调节价值量最高,占间接价值的48%;水源涵养价值量次之,占间接价值的27%。从森林生态资产总价值的分布来看,广西省、广东省和云南省位于全国前列,分别占森林生态资产总价值的10%、9%和9%。单位面积森林生态资产价值表现为海南省、浙江省和广东省较高,分别为954万元/hm2,915万元/hm2和888万元/hm2。森林生态资产价值研究为我国编制自然资源资产负债表提供理论依据,因此全面的估算中国森林生态资产价值很有意义。     

低温驯化对布氏田鼠小肠黏膜结构和黏膜免疫相关细胞的影响

环境温度的变化影响野生啮齿动物的消化道形态与功能。小肠是吸收营养成分的主要部位,其结构和功能具有可塑性。为了解小肠黏膜的结构和功能对环境温度变化的响应机制,以布氏田鼠为研究对象,比较了低温组和常温组动物小肠黏膜的组织结构和小肠黏膜免疫相关细胞的数目。结果显示：（1）低温组布氏田鼠的十二指肠、空肠和回肠的绒毛长度及绒毛长度与隐窝深度的比值均高于对照组;（2）低温驯化使布氏田鼠小肠上皮内淋巴细胞的数量增加;（3）低温驯化使布氏田鼠十二指肠、空肠和回肠的杯状细胞数量均显著增加。结果表明,在低温环境下布氏田鼠的小肠黏膜结构和免疫细胞的数量发生了可塑性变化,这可能与低温环境下的高能量需求和免疫功能的变化有关。