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利用共聚焦显微镜对豆科植物根瘤发育进行快速分析。

Rapid analysis of legume root nodule development using confocal microscopy.

作者信息

Haynes Janine G, Czymmek Kirk J, Carlson Carol A, Veereshlingam Harita, Dickstein Rebecca, Sherrier D Janine

机构信息

Department of Plant and Soil Sciences, University of Delaware, Newark, DE 19717, USA.

Delaware Biotechnology Institute, Newark, DE 19711, USA.

出版信息

New Phytol. 2004 Sep;163(3):661-668. doi: 10.1111/j.1469-8137.2004.01138.x.

Abstract

•  A rapid method for detailed analysis of nodule formation has been developed. •  Inoculated root tissues were stained with SYTO 13, a cell-permeant fluorescent nucleic acid-binding dye, and visualized using confocal laser scanning microscopy (CLSM). Structures with high concentrations of DNA and RNA, such as plant cell nuclei and bacteria, labeled strongly. The autofluorescent properties of cell walls made it possible to use CLSM to visualize both plant and rhizobial structures and generate a three-dimensional reconstruction of the root and invading bacteria. •  This method allowed clear observation of stages and structures important in nodule formation, such as rhizobial attachment to root hairs, hair deformation, infection thread ramification, nodule primordium development and nodule cell invasion. Bacteroid structures were easily assessed without the need for fixation that might alter cellular integrity. Plant nodulation mutants with phenotypic differences in thread growth, cellular invasion and plant defense response were also documented. •  Multiple samples can be assessed using detailed microscopy without the need for extensive preparative work, labor-intensive analysis, or the generation of genetically modified samples.

摘要

• 已开发出一种用于详细分析根瘤形成的快速方法。

• 对接种的根组织用SYTO 13进行染色,SYTO 13是一种可穿透细胞的荧光核酸结合染料,然后使用共聚焦激光扫描显微镜(CLSM)进行观察。含有高浓度DNA和RNA的结构,如植物细胞核和细菌,会被强烈标记。细胞壁的自发荧光特性使得利用CLSM观察植物和根瘤菌结构并生成根和入侵细菌的三维重建成为可能。

• 该方法能够清晰观察根瘤形成过程中重要的阶段和结构,如根瘤菌附着在根毛上、根毛变形、侵染线分支、根瘤原基发育以及根瘤细胞入侵。无需进行可能改变细胞完整性的固定处理,就可以轻松评估类菌体结构。还记录了在侵染线生长、细胞入侵和植物防御反应方面具有表型差异的植物结瘤突变体。

• 使用详细的显微镜可以评估多个样本,无需进行大量的准备工作、劳动密集型分析或生成转基因样本。

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