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作 者:覃思颖 罗燕 张禾 胡君 廖菊够[3] Siying Qin;Yan Luo;He Zhang;Jun Hu;Jugou Liao(School of Life Sciences,Peking University,Beijing 100871,China;School of Advanced Agricultural Sciences,Peking University,Beijing 100871,China;School of Ecology and Environmental Science,Yunnan University,Kunming 650500,China)
机构地区:[1]北京大学生命科学学院,北京100871 [2]北京大学现代农学院,北京100871 [3]云南大学生态与环境学院,昆明650500
出 处:《植物学报》2024年第5期783-791,共9页Chinese Bulletin of Botany
基 金:国家自然科学基金(No.32060175,No.32060043);云南省基础研究计划重点项目(No.202201AS070014)。
摘 要:原子力显微技术是研究植物细胞壁超微结构与力学性质的重要表征手段,良好的样品制备是获得可靠数据的前提。花粉管作为微米级别的植物样品,是研究细胞壁结构与功能的典型实验材料,但是制样过程中活性生理状态下的花粉管与基底黏附不牢固,难以获得活性生理状态下的花粉管原子力显微镜观测数据。该文以烟草(Nicotiana tabacum)花粉管为材料,对花粉管原子力显微样品制备和观测方法进行优化,采用固体培养基薄层作为花粉管与基底之间的黏附剂,花粉管在萌发和生长的同时完成与基底的黏附。与常规的干燥-复水法相比,优化的液下黏附法,可在液体环境下直接观测,无需经过干燥处理,避免了干燥-复水过程对花粉管造成的形貌皱缩与力学性质改变,能够获得活性生理状态下花粉管细胞壁原位的高分辨率原子力显微镜观测数据。该方法可应用于不同种属及不同尺寸花粉管的原子力显微镜观测。Atomic force microscopy(AFM)is a powerful tool for studying the ultrastructure and mechanical properties of plant cell walls,while good sample preparation is essential for AFM data acquisition.As micron-scale plant samples,pollen tubes are typical experimental materials for studying the structure and function of cell walls.Due to the difficulty in sample preparation,it is hard to obtain in situ AFM data in physiological state of pollen tubes as pollen tubes are hard to attach to the substrate firmly in fluid.In this study,the AFM preparation and detection methods are optimized using Nicotiana tabacum pollen tubes as the experimental materials.Thin solid medium is used as the adhesive,thereby pollen tubes are attached to the glass slide during germination and elongation in fluidic environment.Compared with the conventional drying-rehydration method,the optimized liquid-attaching method allows observation directly in fluid without drying treatment,which avoids the shrinkage and denaturation of pollen tubes caused by drying-rehydration process.Accordingly,liquid-attaching method can be applied for pollen tubes of different species and sizes,providing support to obtain high-resolution in situ AFM data of pollen tube cell walls in native physiological state under aqueous conditions.
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