Microfibril Organization Is Altered in Elongating Cells of kob1-1.
FESEM of cryosectioned roots of the wild type (Ws) ([A], [D], [F], and [H]), kob1-1 ([B], [E], [G], [I], and [K]), and pom1 ([C] and [J]) at low magnification (×100) ([A] to [C]) and ×25,000 magnification of hypochlorite-treated samples ([D] to [G] and [J]) and ×50,000 magnification of hypochlorite-pectolyase–treated samples ([H] and [I]). Microfibrils are parallel and oriented transversely to the elongation axis in cells in the division zone (D) and the elongation zone (F) in the wild type. In kob1-1, microfibrils are indistinguishable from those of the wild type in the division zone (E); however, in the elongation zone (G), only amorphous material can be seen. This is primarily pectic material, because pectolyase treatment of the same cells reveals microfibrils in kob1-1 (I). These remaining microfibrils are disordered, as opposed to the ordered microfibrils seen in the wild type treated in the same way (H). This microfibril defect is unlikely an indirect effect of reduced cell elongation in kob1-1, because in pom1, a mutant with a comparable cell elongation defect in the root (C), microfibrils are indistinguishable from those of the wild type (J). In contrast to the findings in elongating cells, in secondary thickenings in xylem cells of kob1-1 roots, microfibrils show a normal parallel orientation (K). Bars = 100 μm in (A) to (C), 1 μm in (D) to (G) and (J), and 500 nm in (H) and (I).