Journal: Plant Methods
Article Title: FE-SEM visualization of cortical microtubules in plant cells using freeze-fracture techniques
doi: 10.1186/s13007-026-01510-z
Figure Lengend Snippet: Cryo-FE-SEM images of freeze-knife-fractured faces of young branches of ginkgo ( Ginkgo biloba ). Cryo-FE-SEM images of freeze-knife-fractured faces of young branches of gingko ( G. biloba ). A , B Low-magnification images. Boxed areas indicate the location of the phloem axial parenchyma cells, as shown in B – D . C Numerous cortical microtubules (CMTs) were observed on the protoplasmic fracture face (PF) of phloem axial parenchyma cells. The CMTs were generally oriented nearly perpendicular to the direction of cell elongation, with most exhibiting a meandering pattern across the cytoplasm. However, some CMTs were aligned nearly parallel to the direction of elongation. D High-magnification image of the PF. In regions where CMTs were bundled, ladder-like structures connecting adjacent microtubules were observed (boxed area). The ladder-like structures bridged two microtubules with an inter-microtubule spacing of approximately 20–40 nm. E , F In the PF of the epidermal parenchyma cells, the CMT bundles were arranged at an angle of approximately 45 ° relative to the direction of elongation. Each CMT bundle consisted of 3–4 microtubules. Black arrows = direction of cell elongation; White arrows = CMTs; CW = cell wall. Scale bars = 50 μm ( A ), 5 μm ( B ), 1 μm ( C , E ), 500 nm ( D , F )
Article Snippet: Observations were made using an FE-SEM device (JSM-7900F, JEOL) at an accelerating voltage of 1 kV, and the images were acquired using a secondary electron detector.
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