Xyloglucan, galactomannan, glucuronoxylan, and rhamnogalacturonan I do not have identical structures in soybean root and root hair cell walls

Planta ◽  
2015 ◽  
Vol 242 (5) ◽  
pp. 1123-1138 ◽  
Author(s):  
Artur Muszyński ◽  
Malcolm A. O’Neill ◽  
Easwaran Ramasamy ◽  
Sivakumar Pattathil ◽  
Utku Avci ◽  
...  
2009 ◽  
Vol 152 (2) ◽  
pp. 541-552 ◽  
Author(s):  
Marc Libault ◽  
Andrew Farmer ◽  
Laurent Brechenmacher ◽  
Jenny Drnevich ◽  
Raymond J. Langley ◽  
...  

2000 ◽  
Vol 21 (1) ◽  
pp. 109-119 ◽  
Author(s):  
Joachim Goedhart ◽  
Mark A. Hink ◽  
Antonie J. W. G. Visser ◽  
Ton Bisseling ◽  
Theodorus W. J. Gadella

2003 ◽  
Vol 16 (10) ◽  
pp. 884-892 ◽  
Author(s):  
Joachim Goedhart ◽  
Jean-Jacques Bono ◽  
Ton Bisseling ◽  
Theodorus W. J. Gadella

Nod factors are signaling molecules secreted by Rhizobium bacteria. These lipo-chitooligosaccharides (LCOs) are required for symbiosis with legumes and can elicit specific responses at subnanomolar concentrations on a compatible host. How plants perceive LCOs is unclear. In this study, using fluorescent Nod factor analogs, we investigated whether sulfated and nonsulfated Nod factors were bound and perceived differently by Medicago truncatula and Vicia sativa root hairs. The bioactivity of three novel sulfated fluorescent LCOs was tested in a root hair deformation assay on M. truncatula, showing bioactivity down to 0.1 to 1 nM. Fluorescence microscopy of plasmolyzed M. truncatula root hairs shows that sulfated fluorescent Nod factors accumulate in the cell wall of root hairs, whereas they are absent from the plasma membrane when applied at 10 nM. When the fluorescent Nod factor distribution in medium surrounding a root was studied, a sharp decrease in fluorescence close to the root hairs was observed, visualizing the remarkable capacity of root hairs to absorb Nod factors from the medium. Fluorescence correlation microscopy was used to study in detail the mobilities of sulfated and nonsulfated fluorescent Nod factors which are biologically active on M. truncatula and V. sativa, respectively. Remarkably, no difference between sulfated and nonsulfated Nod factors was observed: both hardly diffuse and strongly accumulate in root hair cell walls of both M. truncatula and V. sativa. The implications for the mode of Nod factor perception are discussed.


Author(s):  
L. Goosen-de Roo ◽  
A. M. Mommaas-Kienhuis ◽  
J. W. Kijne

2012 ◽  
Vol 247 (1) ◽  
pp. 60-67 ◽  
Author(s):  
M. AKKERMAN ◽  
M.A.W. FRANSSEN-VERHEIJEN ◽  
P. IMMERZEEL ◽  
L.DEN HOLLANDER ◽  
J.H.N. SCHEL ◽  
...  

BIO-PROTOCOL ◽  
2015 ◽  
Vol 5 (7) ◽  
Author(s):  
Ling Bai ◽  
Yun Zhou ◽  
Pengtao Wang ◽  
Chun-Peng Song

1983 ◽  
Vol 61 (11) ◽  
pp. 2863-2876 ◽  
Author(s):  
Alison M. Berry ◽  
John G. Torrey

Structural and cell developmental studies of root hair deformation in Alnus rubra Bong. (Betulaceae) were carried out following inoculation with the soil pseudomonad Pseudomonas cepacia 85, alone or in concert with Frankia, and using axenically grown seedlings. Deformational changes can be observed in elongating root hairs within 2 h of inoculation with P. cepacia 85. These growing root hairs become branched or multilobed and highly modified from the single-tip growth of axenic root hairs. The cell walls of deformed hairs are histologically distinctive when stained with the fluorochrome acridine orange. Filtrate studies using P. cepacia 85 suggest that the deforming substance is not a low molecular weight compound. Root hair deformation and the associated wall histology are host specific in that Betula root hairs show none of these responses when grown and inoculated in the experimental conditions described. The bacterially induced changes in root hair cell walls during deformation may create a chemically and physically modified substrate for Frankia penetration, and the deformation itself may serve to entrap and enclose the filamentous organism, allowing wall dissolution and entry. Thus these events represent a complex host response as a precondition to successful nodulation.


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