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Biophys J, November 2000, p. 2382-2390, Vol. 79, No. 5


*Department of Plant Pathology and
Department of
Mathematics, University of California, Riverside, California 92521 USA;
Department of Botany and Plant Pathology, Purdue
University, West Lafayette, Indiana 47907-1057 USA; and
§Centro de Biotecnología, Instituto
Tecnológico y de Estudios Superiores, 64849 Monterrey, N. L. México
By computer-enhanced videomicroscopy, we mapped the
trajectory of external and internal cell surface markers in growing
fungal hyphae to determine the pattern of cell wall expansion during apical growth. Carbon particles (India ink) were chosen as external markers for tip expansion of Rhizoctonia solani hyphae.
Irregularities in the growing apical walls of R. solani
served as internal markers. Marker movement was traced in captured
frames from the videotaped sequences. External and internal markers
both followed orthogonal trajectories; i.e., they moved perpendicular
to the cell surface regardless of their initial position in the hyphal
apex. We found no evidence that the tip rotates during elongation. The
discovery that the cell wall of a growing hypha expands orthogonally
has major repercussions on two fronts: 1) It supports the long-held view that turgor pressure is the main force driving cell wall expansion. 2) It provides crucial information to complete the mathematical derivation of a three-dimensional model of hyphal morphogenesis based on the vesicle supply center concept. In three dimensions, the vesicle gradient generated by the vesicle supply center
is insufficient to explain shape; it is also necessary to know the
manner in which the existing surface is displaced during wall expansion.
Biophys J, November 2000, p. 2382-2390, Vol. 79, No. 5
© 2000 by the Biophysical Society 0006-3495/00/11/2382/09 $2.00
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