黑胫病菌（Leptosphaeria biglobosa）在油菜叶片和茎中的侵染过程观察     

史志丹  宋培玲  郝丽芬  皇甫海燕  燕孟娇  杨永青  吴晶  赵丽丽  李子钦 《中国油料作物学报》2021,43(2):286-292

为明确黑胫病菌（Leptosphaeria biglobosa）在甘蓝型油菜叶片和茎中的侵染及扩展过程，利用绿色荧光蛋 白（GFP）标记的黑胫病菌株接菌油菜叶片，利用激光共聚焦显微镜观察菌株在油菜叶片和茎中的侵染过程。结果 表明，接种油菜叶片7 h后，分生孢子萌发并长出芽管；17 h后，芽管侵入气孔；24 h后，分生孢子全部萌发；36 h后萌 发的芽管形成菌丝；120 h后，菌丝在叶片表皮细胞间隙蔓延，并侵入叶肉细胞。13 d后，菌丝侵入茎部皮层组织； 15 d后，菌丝在皮层细胞间隙蔓延，并侵染至茎表皮；21 d后，菌丝侵染至维管组织；23 d后，菌丝侵染至茎韧皮部； 25 d后，茎导管被侵染，并向木质部扩展。本研究发现的L. biglobosa 在油菜叶片和茎中的侵染过程，可为油菜与黑 胫病菌互作的研究、黑胫病致病机理及防治提供参考。  相似文献   

肾俞穴,后三里穴与子宫相关的神经基础   总被引：7，自引：0，他引：7  

陈树林  李育良 《中国兽医学报》1997,17(5):505-507

应用辣根过氧化物酶（ＨＲＰ）法和荧光素双标记法，研究了家兔子宫与肾俞穴、后三里穴的外周神经联系。结果显示，支配子宫与肾俞穴、后三里穴的初级传入神经元及交感节后神经元分布节段部分重叠，在腰１（Ｌ１）脊神经节有少量的荧光素双标记细胞，约占该节荧光素标记细胞总数的２．６％，表明Ｌ１脊神经节有一些初级传入神经元，其周围突分支分布于肾俞穴和子宫，提示子宫与肾俞穴除通过中枢途径联系外，还可通过外周突分支投射的感觉神经元直接相联系；在胸１２～荐３（Ｔ１２～Ｓ３）交感神经节出现大量分别支配子宫和后三里穴的标记细胞，这两种细胞紧密相邻，提示支配子宫和后三里穴的交感节后神经元之间，可能还存在直接或间接联系。上述结果为穴位－内脏相关机理提供了形态学证据。  相似文献   

应用FA及PPA-ELISA技术对猪瘟的检测   总被引：3，自引：0，他引：3  

潘树德  何利昆  李学俭  马兴元 《动物医学进展》2003,24(5):114-116

用免疫荧光抗体诊断技术及单克隆抗体纯化酶联免疫吸附试验诊断技术对疑为猪瘟病毒感染猪进行了检测 ,重点阐述了 2种方法的技术原理和操作过程。通过用免疫荧光抗体诊断技术检测了 5份病料 ,其中有 2份为阳性 ,阳性率为 40 % ;用单克隆抗体纯化酶联免疫吸附试验诊断技术检测了猪瘟血清抗体 ,在 40头母猪血清样品中 ,猪瘟弱毒抗体效价 OD值较高 ,有 1 0 0 %的保护率 ,但是发现母猪群中有 1 0 %隐性猪瘟感染 ,其强毒抗体效价 OD值大于 0 .5,体内带有猪瘟病毒。结果及过程表明此两种诊断方法检测快速、鉴别准确、分辨率高  相似文献   

BR农用荧光灯补光育苗的研究     

王羽梅  赵清岩  底升琪 《内蒙古农业大学学报(自然科学版)》1991,(1)

对黄瓜、番茄在育苗前期进行短时间的人工补光有明显促进生长的效果。农用荧光灯(BR)的补光效果优于日光型荧光灯(W)。早春育苗进行人工补光的时间以下午自然光照强度稍高于光补偿点、叶片气孔尚未关闭之前为好,呼和浩特、包头3月份16:00、4月份17:00开始补光为宜。补光的光强度在500～800lx 效果明显。光源距幼苗的距离以10cm 为宜。  相似文献   

北疆棉花不同品种叶绿素荧光特性的研究   总被引：8，自引：3，他引：5  

汤照云  万国强  刘彤  王志勇 《棉花学报》2004,16(3):166-169

测定了北疆6个不同棉花品种田间叶片的净光合作用、荧光参数的变化。结果表明:晴天棉花叶片的光化学效率(Fv/Fm)随着光强上升而下降,到14∶00左右降到最低值,之后又随光强的减弱逐渐回升;非光化学猝灭系数(qN)则与此相反。棉叶在晴天易发生光抑制,可能会引发反应中心的降解等破坏反应。产量较高的新陆早8号和新陆早10号的Fv/Fm、光化学猝灭系数(qP)均高,且正午过后Fv/Fm恢复较快,不仅能较强地吸收光能,同时还具有较高的PSII的活性和光能转化效率,从而将所吸收的光能有效地转化为化学能,提高光合电子传递速度,形成更多的ATP和ENADPH,为光合碳同化提供充分的能量和还原能力。  相似文献   

Development of a semi-selective medium and an immunofluorescence colony-staining procedure for the detection of Clavibacter michiganensis subsp. sepedonicus in cattle manure slurry     

N. J. M. Roozen  J. W. L. Van Vuurde 《European journal of plant pathology / European Foundation for Plant Pathology》1991,97(5):321-334

Various compounds and basal media were tested for their suitability to create a semi-selective medium for isolation ofClavibacter michiganensis subsp.sepedonicus (Cms) from cattle manure slurry containing c. 10⁸ colony forming units (cfu) per ml.Plating efficiency of Cms in yeast glucose mineral medium (YGM) was 104% compared with yeast peptone glucose medium. Nalidixic acid, polymyxin B sulphate and the experimental disinfectant S-0208 inhibited colony growth of cattle slurry bacteria as compared with Cms in YGM. The optimal concentration of these inhibitors in combination was determined by modified agar diffusion tests and by pour plating in 24-well tissue culture plates. The semi-selective medium YGMI consisted of YGM supplemented with nalidixic acid (2 mg/l), polymyxin B sulphate (30 mg/l) and S-0208 (125 mg/l). Plating efficiency varied for Cms between 50.9 and 69.6%, for cattle slurry bacteria between 1.8 and 2.5% and for saprophytes from potato heel end extracts between 11.5 and 27.4%.Differentiation of Cms colonies from other colonies was based on their small and bluish colony morphology in pour plates and on immunofluorescence colony-staining (IFC). IFC of a pure culture of micro colonies of Cms in YGM was possible after one day incubation (colonies c. 5 cells). Green background fluorescence in the agar gels was prevented by addition of Tween 20 (0.1%) to the washing buffer and the use of 1% agar gels. IFC of macro colonies of Cms in YGMI, visible with 4x objective magnification, was possible after 4 days. The detection level of the target organism in artificially inoculated cattle slurry in YGMI based on colony morphology varied between 1.4×10³ and 2.3×10⁴ cfu per ml of cattle slurry. Miniaturized plating combined with IFC, using wells in tissue culture plates (=16 mm), proved suitable for detection, but was c. 30 times les sensitive. The recovery of Cms was negatively correlated with the number of saprophytic colonies in the agar plates (R ²=0.74).  相似文献   

根癌农杆菌介导绿色荧光蛋白基因转化印度酸桔的研究   总被引：14，自引：0，他引：14  

石玮  李东栋  邓秀新  伊华林 《园艺学报》2002,29(2):109-112

 通过根癌农杆菌介导将绿色荧光蛋白基因转入印度酸桔的胚性愈伤组织中, 经潮霉素筛选,获得抗性愈伤组织, 并再生植株。对这些植株进行GUS 染色、PCR 分析、绿色荧光检测和Sourthern 杂交验证, 结果表明绿色荧光蛋白已经在转基因植株中表达。  相似文献   

农杆菌介导的蝴蝶兰基因转化系统的建立   总被引：9，自引：1，他引：9  

柴明良  金斗焕 《园艺学报》2004,31(4):537-540

 针刺后的蝴蝶兰‘White Hikaru’的类原球茎(PLB)，与含绿色荧光蛋白基因( )和潮霉素磷酸转移酶基因(^p￡)的pCAMBIA 1300一SmGFP的根瘤农杆菌LBA4404 共培养，培育出了转基因的蝴蝶兰。经绿色荧光蛋白检测和Southern印迹，证实了再生植株中含cop基因和hpt基因。  相似文献   

芽孢杆菌绿色荧光蛋白标记及其在小麦体表定殖的初探   总被引：17，自引：0，他引：17  

田涛  亓雪晨  王琦  梅汝鸿 《植物病理学报》2004,34(4):346-351

 将来自质粒pAD4412的启动子和绿色荧光蛋白基因gfpmut3a插入大肠杆菌-枯草芽孢杆菌穿梭载体pBE2,构建成芽孢杆菌表达载体pGF P4412,用其转化野生型生防芽孢杆菌83-6和A-47等8个菌株,均得到良好的发光表型。质粒稳定性实验表明重组质粒pG FP4412稳定性为92%。借助荧光显微镜对gfp标记的菌株A-47-gfp在小麦体表的定殖进行初步的研究。结果表明:A-47-gfp能够在小麦根际及小麦体表定殖(包括根表和茎叶表面);相对于在茎叶表面定殖的A-47-gf p在根表定殖的菌体与根的结合更为牢固;从根基到根尖A-47-gfp的定殖量有明显的减少趋势。  相似文献   

Effect of EGFP gene transfection on the cell cycle distribution of primary cultured human chondrocytes     

JIANG Xun  ZENG Yao-ying  HE Xian-hui  XU Li-hui  DI Jing-fang  FENG Zheng  ZHAO Jing-xian  WANG Qing  WANG Tong  SHI Jian-bo 《园艺学报》2004,20(6):924-928

AIM: To investigate the effect of enhanced green fluorescence protein (EGFP) gene transfection on the cell cycle distribution of primary cultured human chondrocytes in order to establish a tracking method of cultured human nasoseptal chondrocytes. METHODS: pEGFP-N1 plasmid was amplified in E.coli, and purified by high purity kit. Primary cultured human chondrocytes,which were initially obtained from the nasoseptal cartilage, were cultured in vitro and transferred with pEGFP-N1 by means of electroporation with Amaxa nucleofector device. Transfering process and transient expression were evaluated by laser scanning confocal microscope (LSCM), the transfer efficiency and the cell cycle distribution were evaluated by flow cytometry. RESULTS: There was significant expression of EGFP at 24 h after transferring. The transfection efficiency of pEGFP-N1 into primary cultured human chondrocytes reached 35.37％ at 48 h. It didn't affect the process of cell adherance and had no effect on the cell cycle distribution. CONCLUSION: Primary cultured human chondrocytes, which were transfected with pEGFP, are alive in vitro, and the transferring process doesn't affect the cell cycle distribution. These results suggest that pEGFP-N1 is an ideal transient expression vector for primary cultured human chondrocytes and it might be a well tracer in construction tissue engineered cartilage.  相似文献