Plant Physiology 60:247-254 (1977)
© 1977 American Society of Plant Biologists
Articles
Cell Growth Pattern and Wall Microfibrillar Arrangement
Experiments with Nitella
Edith T. Gertel1 and
Paul B. Green2
a Department of Biological Sciences, Stanford University, Stanford, California 94305
In cylindrical cells growing throughout their length, over-all transverse reinforcement of the wall by microfibrils is believed to be required for cell elongation. The multinet theory states that in such cells microfibrils are deposited at the inner surface of the wall with transverse orientation and are then passively reoriented toward the longitudinal direction by the predominant longitudinal strain (surface expension). In the present study young Nitella cells were physically forced to grow in highly abnormal patterns: in length only, in girth only, or with localized suppression of growth. Subsequent gradients of microfibrillar arrangement within the wall cross-section were measured with polarized light and interference microscopes. The novel wall structures produced were in all cases explainable by passive reorientation, i.e. by the multinet theory. The study also showed that orientation of synthesis remains insensitive to several of the physical manipulations that strongly influence the passive behavior of wall microfibrils. Only the localized complete suppression of surface growth led to the deposition of nontransverse cellulose. These results suggest that the presence of strain is needed for continued oriented synthesis, but that the directional aspect of strain is not an "instructional" agent continuously guiding the orientation of synthesis, once this orientation has been established.
1 Present address: Cátedra de Fisiologiá Vegetal, Instituto de Ciencias Agrónomicas, Universidad Nacional de Córdoba, Ciudad Universitaria, Córdoba, Argentina.
2 Supported by National Science Foundation Grant BMX 73-01459-A01. To whom reprint requests should be sent.
This article has been cited by other articles:

|
 |

|
 |
 
I. Burgert and P. Fratzl
Plants control the properties and actuation of their organs through the orientation of cellulose fibrils in their cell walls
Integr. Comp. Biol.,
July 1, 2009;
49(1):
69 - 79.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. Kwiatkowska
Structural integration at the shoot apical meristem: models, measurements, and experiments
Am. J. Botany,
September 1, 2004;
91(9):
1277 - 1293.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. M. DONALD, F. S. BAKER, A. C. SMITH, and K. W. WALDRON
Fracture of Plant Tissues and Walls as Visualized by Environmental Scanning Electron Microscopy
Ann. Bot.,
July 1, 2003;
92(1):
73 - 77.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. C. Gardiner, J. D. I. Harper, N. D. Weerakoon, D. A. Collings, S. Ritchie, S. Gilroy, R. J. Cyr, and J. Marc
A 90-kD Phospholipase D from Tobacco Binds to Microtubules and the Plasma Membrane
PLANT CELL,
September 1, 2001;
13(9):
2143 - 2158.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. J. Whittaker and B. A. Triplett
Gene-Specific Changes in alpha -Tubulin Transcript Accumulation in Developing Cotton Fibers
Plant Physiology,
September 1, 1999;
121(1):
181 - 188.
[Abstract]
[Full Text]
|
 |
|

|
 |

|
 |
 
D. D. Fisher and R. J. Cyr
Extending the Microtubule/Microfibril Paradigm . Cellulose Synthesis Is Required for Normal Cortical Microtubule Alignment in Elongating Cells
Plant Physiology,
March 1, 1998;
116(3):
1043 - 1051.
[Abstract]
[Full Text]
|
 |
|
|
|