云南西双版纳勐腊并殖吸虫成虫扫描电镜观察

目的 是通过扫描电镜(SEM)观察勐腊并殖吸虫成虫体棘、口、腹吸盘．为鉴别其虫种提供资料。方法为直接从人工感染的猫体内解剖取出勐腊并殖吸虫成虫，用2．5％戊二醛和1％锇酸固定后，乙醇脱水，离子溅射仪镀金，JSM-820扫描电镜观察。结果表明云南西双版纳瑶瓦区阿括拿青(阿括拿青)虫体的体棘均为丛生型皮棘。新回宽寨老熊青(老熊青)虫体体棘在腹吸盘上方以单棘为主，偶见双棘。腹吸盘下方，为单双棘混合存在。结论认为从SEM形态观察发现勐腊两个不同点采集的勐腊并殖吸虫形态上不完全相同，存在一定的差异。     

用免疫荧光、酶标技术检测赭曲霉毒素A的研究

该项研究采用本课题组提纯的赭曲霉毒素A(Ochratoxin A·简称OA)和研制的兔抗OA抗体等,进行间接荧光法和ELISA间接法检测OA的试验。通过对不同浓度的OA纯品和含毒饲料浸提液及中毒死亡鸡内脏的间接荧光染色,均能检出分布均匀、大小有别的黄绿色荧光亮点;用OA为被检抗原和兔抗OA抗体与羊抗兔IgG-HRP进行ELISA间接法试验,对含不同浓度OA的试验孔和对照孔的检测,结果均正确稳定。研究结果证明,以上两种检测方法检测OA均具有灵敏、特异、快速等优点。     

Influence of death struggle on the structural changes in chub mackerel muscle during chilled storage

ABSTRACT: Chub mackerel (34–35 cm, approximately 500 g), which were caught by fishing with a rod and line at the Bungo Channel, Oita prefecture, were rested overnight in a fish preserve and either killed by decapitation (control group) or allowed to struggle in air for 30 min (struggled group). Muscle samples were excised every 4 h, and measurements on breaking strength and histological observations were done for both groups. The breaking strength of muscle in the control group was significantly higher than that in the struggled group, whereby a decrease in breaking strength was delayed for 12 h compared to the struggled group. Light microscopy showed space extension among muscle cells in association with a decrease in breaking strength. Especially in the struggled group, the extended area was larger and the difference in area was significant at the time when breaking strength showed a significant difference. Using electron microscopy, the extended area showed cut and/or disappeared collagen fibrils. From these results, it was demonstrated that struggling to death promoted the degradation of collagen fibrils and the weakening of connective tissue and, resultantly, led to the faster softening of muscle of chub mackerel.     

黄艾美球虫侵犯宿主组织的超微研究

利用透射电镜和扫描电镜相结合的技术对黄艾美球虫（E.flavescens）人工感染后的子孢子移动过程及被虫体寄生的宿主细胞形态学变化和粘膜形态学变化进行了观察。子孢子在进入小肠腺上皮过程中需白细胞介导，在白细胞内可发育成球形的滋养体，观察到有两个子孢子侵入同一白细胞的现象，但分别存在于各自的带虫空泡中，黄艾美球虫引起的肠粘膜损伤主要发生于感染177小时之后，其损伤主要表现在绒毛大片脱落，结缔组织裸露，表面可见到大量破损的孔洞及大量肠杆菌，被虫体寄生的腺上皮细胞基部膨胀，微绒毛脱落，细胞核膨大并部分包被虫体，有些细胞核裂解为二。     

几种芸香科植物花粉形态观察

应用扫描电子显微镜对佛手、代代、柚、柑橘和金橘等芸香科植物花粉进行形态观察。发现这几种植物的花粉在形态、大小、外壁纹饰、网孔等方面均有差异,其中3个佛手品种的花粉具网状纹饰,白衣秀士佛手和青衣童子佛手的网脊连续,而赤金王子佛手的网脊不连续,其他4种芸香科花粉具穴状纹饰,代代和柚的花粉比柑橘和金橘的花粉大,而代代和金橘的花粉表面孔穴密度比柚和柑橘的花粉表面孔穴密度大。这些花粉表面微观形态的差异将为上述品种鉴定提供依据。     

黄瓜幼叶细胞中钙调素的免疫胶体金定位

 采用免疫胶体金电镜技术对黄瓜幼叶叶肉细胞中的钙调素(CaM)进行定位。结果表明：适温下生长的黄瓜幼苗叶肉细胞中的CaM主要分布于细胞核和叶绿体内，细胞核中CaM主要存在于染色质和核仁上，叶绿体中CaM主要存在于类囊体膜上；线粒体中也有一定量的CaM分布；细胞质、液泡、液泡膜及质膜上只有少量CaM存在；而细胞壁和细胞间隙却很难发现显示CaM存在的金颗粒。     

鸭疫里氏杆菌形态特征的电镜观察

自鸭传染性浆膜炎的病死鸭中分离鉴定的鸭疫里氏杆菌(RA)Ⅰ、Ⅱ型两个菌株，用负染法和超薄切片法制备样品，于透射电镜下进行观察。结果观察到约占1／3的RA具有特殊的形态结构：在细菌的顶端或侧面有1～2个与菌体相连的芽状赘生物，有的也能从菌体上脱落下来。它在超薄切片中的大小约为菌体的1／3～1／5，能观察到其内部也具有类似菌体内部的结构。且具有类似菌体的“细胞壁”，类似于核体部分的结构位于“细胞壁”的一侧。而用相同的方法制作的鸭大肠杆菌(E．cozi)对照样品，却见不到这种特殊的形态结构。说明这种形态特征可能是RA特有的。     

不同固定条件对几种植物样品超微结构的影响

为比较几种固定条件对不同植物材料样品电镜超微结构图像清晰度的影响。以3个不同科属4种植物[油棕(Elaeis gineansis Jacq.)、拟南芥(Arabidopsis thaliana.)、花生(Arachis hypogaea Linn.)、柱花草(Stylosanthes guianensias Sw.)]为研究主体代表,探讨了2.5%戊二醛与4%戊二醛固定过夜、锇酸固定2 h及过夜的制备方法对其叶片超微结构的影响,并成功观察了柱花草接种胶苞炭疽野生型菌株CH008后的病菌侵入过程。结果表明:油棕、拟南芥、花生及柱花草叶片经4%戊二醛与1%锇酸固定液固定过夜,其组织成像的效果均较为理想,各种细胞器整体信息丰富、结构组织完好、线条清晰。表明,此制备方法能够较好的保存植物叶片和细胞组织,提高制样的成功率及观察分辨率。     

The Fluorescent Characterization and Analysis of Two Brucella Attenuated Vaccine Infecting Mouse Macrophagocyte

The experiment was conducted to discuss the difference of binding time of green fluorescent protein B.melitensis M5 (GFP-M5) and B.abortus S19 (GFP-S19) infecting the mouse macrophagocyte (RAW264.7),lysosome,endoplasmic reticulum and golgi body in the initial stage and compare the binding rate of GFP-M5,GFP-S19 with organelle in different timeline,respectively,by confocal laser scanning microscope (CLSM) and flow cytometry.The result showed that GFP-M5 and GFP-S19 were successfully constructed.The intracellular survival ability of Brucella M5,Brucella S19,GFP-M5 and GFP-S19 were not obvisouly affected after infecting RAW264.7.GFP-M5 and GFP-S19 could enter the macrophagocyte in 30 mins,and in 2 h the Brucella could reach lysosome,endoplasmic reticulum and golgi body.In addition,the binding time for two attenuated vaccine did not show differences in 1,2,3 and 4 h.The content of GFP⁺ cell produced by RAW264.7 infected by GFP-M5 and GFP-S19 did not show significant differences (P>0.05).Therefore,the two strains did not have significant differences in the invasion ability in the initial stage of infecting host cell.     

同步荧光法测定色氨酸

用同步荧光法测定了玉米、小麦、花粉等样品中的色氨酸.一般氨基酸分析用氨基酸分析仪和液相色谱仪,而色氨酸在酸解样品时被分解测不出.要测定色氨酸,需要重新制备样品,改变体系,比较繁杂.在多种氨基酸中仅有色氨酸、酪氨酸和苯丙氨酸有天然荧光,色氨酸的天然荧光最强,提供了直接测定的有利条件.用4N氢氧化钠碱解样品,在105℃时保温24小时,然后稀释,调pH为10.5—11之间,定容.最后用同步光谱扫描的办法测定,即激发波长和发射波长的单色器之间固定一定的波长差(Δλ=68nm),同时扫描,得到一个同步荧光光谱.其浓度和荧光强度有良好的线性关系,测定范围是0.01—0.20μg/ml.本方法弥补了在氨基酸测定中酸解样品时,色氨酸被分解测不出的不足,而且方法比较简单灵敏.