A NEW EULOPHID PARASITIZING LITCHI GALL MIDGE FROM CHINA (HYMENOPTERA: CHALCIDOIDEA)

Abstract  Mangocharis litchii sp. nov. is described from south China as a parasitoid of Mayetiola sp. on leaf of litchi tree. The gall midge is a serious pest of the fruit tree in south China. The biology of the new chalcidoid is also dealt with. The genus Mangocharis is new to China.     

重组人IL6／2融合蛋白对6.5Gy照射小鼠造血功能恢复的影响

观察了ｈＦＰＩＬ６／２对６．５Ｇｙγ线照射ＮＩＨ小鼠第１０天造血功能恢复的影响。结果表明：照射小鼠连续４ｄ给予ｈＦＰＩＬ６／２２５０μｇ·ｋｇ－１·ｄ－１,其脾重、ＣＦＵ－８、骨髓有核细胞数及ＣＭ－ＣＦＵ分别比对照组增加５９．０％、２７８．５％、５７．９％和１３８．２％,统计学处理均有显著差异;对此四项指标的改善也明显优于２５μｇ组。另外,２５０μｇ剂量组小鼠外周血象３０ｄ的动态观察结果表明,ｈＦＰＩＬ６／２不但能明显提高红细胞和血红蛋白的最低值,而且能使血小板的恢复提前。提示ｈＦＰＩＬ６／２在促进血小板生成和促进红系造血方面可能具有良好的应用前景。     

天然吸附剂—壳聚糖吸附性能的研究

本文通过研究天然吸附剂—壳聚糖对古龙酸、缬氨酸、水杨酸和谷氨酸等物质的吸附性能,主要研究了吸附容量随时间变化,吸附容量与pH值的关系以及它们的饱和吸附容量,从而为这种天然吸附剂的应用提供了基础。     

果树介壳虫寄生蜂资源的研究

介壳虫是果树的重要害虫,研究利用寄生蜂的自然控制作用是果树介壳虫生物防治和综合治理的重要途径。本论述了果树介壳虫寄生蜂资源的研究,报道了小蜂总科寄生蜂5科25属63种。     

显脉獐牙菜的单萜环烯醚甙

近年来,肝炎发病率高,青叶胆(Swertia mileensis)因此被大量采挖,野生青叶胆资源逐年减少。为发掘新药源,我们对云南产狭叶獐牙菜(S.angustifolia)和显脉獐牙菜(S.nervasa)的化学成分进行了研究。本文报道从中分离鉴定的4个单萜环烯醚甙Ⅰ—Ⅳ。Ⅰ、Ⅲ、Ⅳ分别为维哥罗甙(vegeloside)、獐牙菜甙(sweroside)和獐牙菜苦甙(swertiamarin),Ⅱ是Ⅰ的同分异构体,命名为显脉獐牙菜甙(nervoside)。显脉獐牙菜甙(Ⅱ)白色无定形粉末,味极苦。UVλ-_(max)~(EtOH):243nm(log ε-3.89)。IR v_(max)~(KBr) cm~(-1):3400、1700和1610,显示单萜环烯醚的特征吸收峰显脉獐牙菜;显脉獐牙菜甙;单萜环烯醚甙     

Investigations of interaction mechanism and conformational variation of serum albumin affected by artemisinin and dihydroartemisinin

In this work, binding interactions of artemisinin (ART) and dihydroartemisinin (DHA) with human serum albumin (HSA) and bovine serum albumin (BSA) were investigated thoroughly to illustrate the conformational variation of serum albumin. Experimental results indicated that ART and DHA bound strongly with the site I of serum albumins via hydrogen bond (H-bond) and van der Waals force and subsequently statically quenched the intrinsic fluorescence of serum albumins through concentration-dependent manner. The quenching abilities of two drugs on the intrinsic fluorescence of HSA were much higher than the quenching abilities of two drugs on the intrinsic fluorescence of BSA. Both ART and DHA, especially DHA, caused the conformational variation of serum albumins and reduced the α-helix structure content of serum albumins. DHA with hydrophilic hydroxyl group bound with HSA more strongly, suggesting the important roles of the chemical polarity and the hydrophilicity during the binding interactions of two drugs with serum albumins. These results reveal the molecular understanding of binding interactions between ART derivatives and serum albumins, providing vital information for the future application of ART derivatives in biological and clinical areas.