The distribution and localization of the stage-specific GP31 antigen from infective Ostertagia circumcincta larvae.

The 31,000 mol. wt glycoprotein (GP31) antigen of infective third-stage (L3) Ostertagia circumcincta larvae was shown, by surface labelling experiments and immunofluorescent antibody staining of whole larvae and larval sections, to be distributed internally. When transverse sections of L3 O. circumcincta, taken from the anterior pharyngeal region, were further examined by electron microscopy, after immunogold staining with rabbit anti-GP31 antiserum, the GP31 antigen was found to be specifically located in 'secretory organelles' within the cells of the oesophageal glands. By in vitro culturing L3 O. circumcincta in medium supplemented with 35S-methionine and then analysing the excretory-secretory material released by the larvae, it was found that the GP31 molecule was one of the major components of the excretory-secretory complex. The purified GP31 molecule had no detectable proteolytic activity in protein degradation assays. On examination of Triton X-100 extracts of infective larvae from other nematode parasite species, a predominant antigen similar to GP31 was found in Trichostrongylus colubriformis and Haemonchus contortus, but in Toxocara canis a minor component corresponding in mol. wt to GP31 was also detected. Based on these results the possible role of GP31 as a candidate antigen for a broad spectrum molecular vaccine against gastrointestinal nematode parasites in sheep is discussed.     

Characteristics of the interaction of calcium with casein submicelles as determined by analytical affinity chromatography

Interaction of calcium with casein submicelles was investigated in CaCl2 and calcium phosphate buffers and with synthetic milk salt solutions using the technique of analytical affinity chromatography. Micelles that had been prepared by size exclusion chromatography with glycerolpropyl controlled-pore glass from fresh raw skim milk that had never been cooled, were dialyzed at room temperature against calcium-free imidazole buffer, pH 6.7. Resulting submicelles were covalently immobilized on succinamidopropyl controlled-pore glass (300-nm pore size). Using 45Ca to monitor the elution retardation, the affinity of free Ca2+ and calcium salt species was determined at temperatures of 20 to 40 degrees C and pH 6.0 to 7.5. Increasing the pH in this range or increasing the temperature strengthened the binding of calcium to submicelles, similar to previous observations with individual caseins. However, the enthalpy change obtained from the temperature dependence was considerably greater than that reported for alpha s1- and beta-caseins. Furthermore, the elution profiles for 45Ca in milk salt solutions were decidedly different from those in CaCl2 or calcium phosphate buffers and the affinities were also greater. For example, at pH 6.7 and 30 degrees C the average dissociation constant for the submicelle-calcium complex is 0.074 mM for CaCl2 and calcium phosphate buffers, vs 0.016 mM for the milk salt solution. The asymmetric frontal boundaries and higher average affinities observed with milk salts may be due to binding of calcium salts with greater affinity in addition to the binding of free Ca2+ in these solutions.     

Decay of the tryptophan fluorescence anisotropy in bacteriorhodopsin and its modified forms.

In this work we study the decay of the polarization of the Trp fluorescence in native bacteriorhodopsin (bR), deionized bR (dlbR), and the retinal-free form of bR, bacterioopsin (bO), using picosecond laser/streak camera system. Two types of depolarization processes are observed, one around 250 ps, which is temperature independent around room temperature, and the other in the 1-3-ns range, which is sensitive to temperature and certain bR modifications. This suggests the presence of at least two different environments for the eight Trp molecules in bR. Native bR and deionized bR gave the same depolarization decay times, suggesting that the removal of metal cations does not change the microenvironment of the emitting Trp molecules. The slow component is faster in bO than in bR, suggesting a change in the environment of the Trp molecules upon the removal of the retinal chromophore. All these results are discussed in terms of the different mechanisms of Trp fluorescence depolarization. A comparison between the depolarization decay in rhodopsin and bR is made.     

Genetics of glucosephosphate isomerase in Aedes togoi (Diptera: Culicidae)

The genetics of glucosephosphate isomerase (E.C. 5.3.1.9) in two strains (Malaysian and Taiwan) of Aedes togoi is reported. Three electrophoretic phenotypes were present in both sexes. The zymogram patterns were identical in both strains of A. togoi. The phenotypes were governed by a pair of codominant alleles. The allele frequency of the slow-moving band was 0.63 in the Malaysian strain and was 0.86 and 0.82 in F161 and F169 generations, respectively, of the Taiwan strain. The sample studied was in good accord with Hardy-Weinberg expectations.     

多源空间数据整合视角下的城市开发强度研究

城市开发强度能直观表征人类活动强度,对指导城市规划与管理、促进城市可持续发展具有重要价值。采用社会-经济-生态系统耦合视角构建城市开发强度的多维测度体系,整合多源空间数据,测度了杭州市主城及3个副城的开发强度并揭示了其空间分布特征。结果表明,杭州城市开发强度由主城向副城呈波动降低,高强度开发过度集中于主城,主城的功能疏散有待加强;各副城开发强度不一,江南城与主城呈现跨江融合,临平城、下沙城空间上较为独立;各开发维度中,建筑强度、功能强度及效益强度热点区分布基本一致,环境响应高强度区则集聚于主副城交界处,表现出空间异质性。多维测度体系可较好表征城市开发强度,对城市规划及精细化管理具有一定的应用价值。     

一株产纤溶酶菌株的分离、鉴定及其酶活特征的初步研究

[目的]分离筛选并鉴定产纤溶酶的菌株.[方法]采用血粉培养基富集,琼脂糖-纤维蛋白平板筛选,从自然界中分离筛选出一株产纤溶活性物质的菌株.通过形态学特征、生理生化特征研究,并结合16S rRNA基因序列分析及分子系统发育树的构建结果,确定菌株的种类.[结果]从自然界分离筛到一株产纤溶酶的菌株EF608,经鉴定该菌株为粪肠球菌(Enterococcus faecalis). SDS-PAGE和纤维蛋白自显影表明该纤溶酶的分子量为37 kD,最适反应温度和pH分别为35℃和7.5,EDTA能完全抑制其纤溶活性,而PMSF对其活性无抑制作用.菌株EF608发酵液不仅可以直接水解纤维蛋白,而且具有体外溶栓的作用,对血红细胞没有溶解作用.[结论]筛选到一株具有纤溶活性的粪肠球菌——EF608,为获取新型纤溶酶提供了一种的新的菌源.     

基于碳排放核算的中国区域旅游业生态效率测度及比较研究

旅游业作为国民经济发展的战略性支柱产业在区域发展中具有重要作用。借鉴生态效率的基本思想,考虑区域能源消费结构差异,使用自下而上的方法将旅游交通、旅游住宿与游憩活动碳排放进行加总估算出2000—2013年中国旅游业碳排放量;接着运用单一比值法计算出2000—2013年中国及各地区旅游业生态效率值,利用变异系数、莫兰指数对测度结果进行分析并与可持续发展生态效率值进行比较。研究结果表明:(1)2000—2013年,中国旅游业碳排放量不断增加,从2000年的1202.71万t增加到2013年的4151.57万t。旅游业部门之间碳排放量差异较大,尤其是旅游交通部门占到旅游业碳排放量的90%左右;(2)得益于2000—2013年旅游业发展的促进政策,中国及各地区旅游业生态效率总体上呈现不断改善的趋势,中国旅游业生态效率由2000年0.1193 kgCO_2-e/$下降到0.0309 kgCO_2-e/$。(3)时间维度上,中国旅游业生态效率的区域不平衡问题仍然存在,相比于2000年旅游业生态效率变异系数0.7114,2013年的变异系数反而增加到0.7483;空间维度上,各地区旅游业生态效率聚集模式发生了明显变化,莫兰指数由0.3036减少到0.0278。(4)通过将测度结果进行比较,中国旅游业自2000年开始进入可持续发展阶段,中国旅游业的整体可持续水平要优于其他产业,各地区的旅游业在2010年全部进入可持续发展状态。最后,对结果进行了讨论并提出旅游业生态效率的优化应从旅游收入增加与旅游业减排两方面进行。     

大豆过氧化物酶在毕赤酵母中功能表达

【目的】大豆过氧化物酶(SBP)作用底物广泛、比活高、热稳定性好,使其在免疫检测、工业污染废水处理领域有着广泛的应用潜力。现有的生产方法主要是从大豆壳中提取,这种方法产量低,成本高,远不能满足于工业应用要求,本研究希望实现在毕赤酵母中高效表达有功能活性的大豆过氧化物酶。【方法】将大豆过氧化物酶基因以及C末端截短20个氨基酸的基因克隆pPIC-9K载体中,并在毕赤酵母X-33中诱导表达。同时还将糖基化位点的天冬酰胺突变成为谷氨酰胺,研究糖基化位点对表达的影响。【结果】全长SBP在毕赤酵母中表达是无活性的,只有截短的SBP△20在试管发酵的表达活力达23.5 U/mL,经过糖基化位点的突变表明130、144、185、197对酶活非常重要,不能突变;211和216位点去糖基化突变对酶活有所提高。【结论】经过发酵条件的优化,在5 L的发酵罐中发酵液上清最高酶活力达510 U/mL,是目前报道的最高水平。     

北方风沙区生态修复的科学原理、工程实践和恢复效果

北方风沙区位于欧亚草原的东部,是我国生态环境最为脆弱的地区之一,其在北方生态安全屏障和丝绸之路经济带建设中具有十分重要的战略地位。在国家一系列生态保育工程的支持下,该地区的生态环境得到明显改善。但是,由于受人类活动和全球气候变化的影响,该地区仍然面临着严峻的环境压力。在中国科学院科技服务网络计划(STS计划)等项目支持下,开展了北方风沙区土地沙化成因及退化土地空间分布研究,集成了北方风沙区重点脆弱区生态恢复的理论和技术体系,以内蒙古中部的阴山北麓地区、内蒙古浑善达克沙地和蒙辽交界的科尔沁沙地为重点研究区域,进行了高效人工草地建植、天然草地恢复和管理、沙化草地治理等相关工程技术的示范,开展生态恢复模式的效果跟踪监测和生态效益评估,确定生态恢复技术和模式的技术参数和指标,明确不同集成技术与模式在北方风沙区的适用区域和范围,为技术模式的推广应用提供科学依据。通过上述研究,可以为中央和地方政府制定生态系统管理和退化生态系统恢复政策、建立我国北方生态安全屏障提供决策依据,为生态修复产业提供技术指南,为相关研究提供全面系统的基础数据支撑。     

滇西北退化高寒草甸植物群落结构对刈割的响应

为探究滇西北不同退化级别高寒草甸植物群落结构对外界干扰的响应敏感性,以香格里拉市的典型高寒草甸为研究对象,于2018-2020年在三个退化梯度上（严重退化,S1;中度退化,S2;轻度退化,S3）开展控制刈割实验,进而分析草甸植物物种丰富度、群落组成相似性、群落复杂度和关键种的变化规律。结果表明：（1）刈割后,S1的物种丰富度显著增加（P<0.05）,S2和S3的物种丰富度未发生显著变化（P>0.05）;（2）相较于S2和S3,S1梯度的植物群落组成变化最大;（3） S1、S2和S3的植物群落复杂度在刈割后均呈先下降后增加的趋势,但S1的植物群落复杂度变化幅度高于S2和S3;（4）刈割导致各退化草甸植物群落的关键种发生了变化,2018、2019和2020年S1梯度的关键种在豆科（Leguminsae）和蔷薇科（Rosaceae）之间变化,S2梯度的关键种在禾本科（Gramineae）和菊科（Compositae）之间变化,S3梯度的关键种在蔷薇科（Rosaceae）、菊科（Compositae）和禾本科（Gramineae）之间转变。研究表明,滇西北高寒草甸植物物种丰富度、群落组成和群落复杂度对外界干扰响应的敏感性可能随退化加剧而上升,但群落关键种的响应过程较复杂。