Elicitor-binding proteins and signal transduction in the activation of a phytoalexin defense response

1995 ◽  
Vol 73 (S1) ◽  
pp. 506-510 ◽  
Author(s):  
Jürgen Ebel ◽  
Markus Feger ◽  
Ulrich Kissel ◽  
Axel Mithöfer ◽  
Tom Waldmüller ◽  
...  

Inducible plant defenses against potential pathogens are thought to be activated by signal compounds released during early stages of the infection process. In the incompatible interaction between soybean (Glycine max L.) and the oomycete Phytophthora megasperma f.sp. glycinea (= Phytophthora sojae) a rapid, localized phytoalexin response is activated at the level of transcription. The phytoalexin response is also stimulated in various soybean tissues, including cultured cells, following treatment with an elicitor derived from the cell walls of the fungus. The best characterized elicitors of P. megasperma for soybean are the branched (1→3)- and (1→6)-linked β-glucans, structural polysaccharides of the hyphal walls. The glucans are naturally released during the early stages of germination of the fungal cysts in a host-independent manner. Cyclic β-glucans of Bradyrhizobium japonicum USDA 110, a symbiont of soybean, arc not active in inducing phytoalexin production in soybean. When tested in combination, B. japonicum β-glucans inhibited stimulation of phytoalexin accumulation by the fungal glucans. Surface-localized glucan-binding proteins exist in soybean cells that display high affinity and specificity for the fungal β-glucans, including an elicitor-active hepta-β-glucoside fragment derived from the polysaccharide, suggesting that elicitor action involves a transmembrane signalling process. The main component of the soybean β-glucan binding sites appears to be a 70-kDa protein. Hepta-β-glucoside binding sites exist in several other legumes, such as bean (Phaseolus vulgaris L.), pea (Pisum sativum L.), and lupine (Lupinus albus L.). The signalling process initiated by the β-glucan elicitor, which leads to the activation of the phytoalexin defense response in soybean, involves changes in the permeability of the plasma membrane to Ca2+ and H+. Chloride channel antagonists are more efficient than calcium channel antagonists in inhibiting both the phytoalexin response and the inducible ion fluxes. The results present evidence that the observed permeability changes of the plasma membrane are primary events in the transduction of the elicitor signal(s) by the challenged soybean cells. Key words: soybean (Glycine max), Phytophthora megasperma f.sp. glycinea, β-glucan elicitor, elicitor-binding proteins, phytoalexins, Ca2+.

1996 ◽  
Vol 74 (5) ◽  
pp. 800-802 ◽  
Author(s):  
Mark Gijzen ◽  
Helga Förster ◽  
Michael D. Coffey ◽  
Brett Tyler

The F2 progeny resulting from a cross of Phytophthora sojae race 2 (avirulent on Rps4 and Rps6) and race 7 (virulent on Rps4 and Rps6) were tested for their ability to cause disease on soybean plants carrying the Rps4 or the Rps6 resistance genes. Of 55 F2 progeny analyzed, 41 individuals were avirulent on both of these genes and 14 were virulent on Rps4 and Rps6, indicating that avirulence on Rps4 and Rps6 is dominant and linked. These results support the suggestion that the soybean–Phytophthora relationship is a gene for gene interaction and that the presumptive Avr4 and Avr6 genes are either tightly linked or identical. Keywords: avirulence, genetic mapping, Glycine max, incomplete dominance, Phytophthora megasperma f.sp. glycinea.


1983 ◽  
Vol 38 (7-8) ◽  
pp. 578-582 ◽  
Author(s):  
Michael G. Hahn ◽  
Hans Grisebach

Abstract cAMP levels were monitored in soybean (Glycine max) infected with race 1 of Phytophthora megasperma f. sp. glycinea and in soybean cell suspension cultures treated with a glucan elicitor from P. megasperma. While cAMP could be readily detected in soybean hypocotyls using a radio ­ immunoassay, no correlation was observed between infection and cAMP levels. No cAMP was detected in suspension cultured soybean cells. These results suggest that cAMP does not play a significant role in the plant's response to fungal attack, or the response of suspension cultured cells to elicitor.


1978 ◽  
Vol 40 (02) ◽  
pp. 212-218 ◽  
Author(s):  
P Massini ◽  
R Käser-Glanzmann ◽  
E F Lüscher

SummaryThe increase of the cytoplasmic Ca-concentration plays a central role in the initiation of platelet activation. Four kinds of movements of Ca-ions are presumed to occur during this process: a) Ca-ions liberated from membranes induce the rapid shape change, b) Vesicular organelles release Ca-ions into the cytoplasm which initiate the release reaction, c) The storage organelles called dense bodies, secrete their contents including Ca-ions to the outside during the release reaction, d) At the same time a rearrangement of the plasma membrane occurs, resulting in an increase in its permeability for Ca-ions as well as in an increase in the number of Ca-binding sites.Since most processes occurring during platelet activation are reversible, the platelet must be equipped with a mechanism which removes Ca-ions from the cytoplasm. A vesicular fraction obtained from homogenized platelets indeed accumulates Ca actively. This Ca- pump is stimulated by cyclic AMP and protein kinase; it may be involved in the recovery of platelets after activation.It becomes increasingly clear that the various manifestations of platelet activation are triggered by a rise in the cytoplasmic Ca2+-concentration. The evidence for this and possible mechanisms involved are discussed in some detail in the contributions by Detwiler et al. and by Gerrard and White to this symposium. In this article we shall discuss four different types of mobilization of Ca-ions which occur in the course of the activation of platelets. In addition, at least one transport step involved in the removal of Ca2+ must occur during relaxation of activated platelets.


2013 ◽  
Vol 8 (7) ◽  
pp. 1934578X1300800 ◽  
Author(s):  
Kei Shimoda ◽  
Manabu Hamada ◽  
Hatsuyuki Hamada ◽  
Mai Takemoto ◽  
Hiroki Hamada

Incubation of cultured cells of Glycine max with trans-resveratrol gave its 3-O-β-D- and 4′- O-β-D-glucosides. Cultured Gossypium hrsutum cells glycosylated trans-resveratrol to its 3-O-β-D-, 4′- O-β-D- and 3,4′- O-β-D-diglucosides. On the other hand trans-resveratrol was converted into cis-resveratrol 4′- O-β-D-glucoside together with trans-resveratrol 3- O-β-D-glucoside and trans-resveratrol 4′- O-β-D-glucoside by Eucalyptus perriniana.


2015 ◽  
Vol 471 (3) ◽  
pp. 403-414 ◽  
Author(s):  
M. Florencia Rey-Burusco ◽  
Marina Ibáñez-Shimabukuro ◽  
Mads Gabrielsen ◽  
Gisela R. Franchini ◽  
Andrew J. Roe ◽  
...  

Necator americanus fatty acid and retinol-binding protein-1 (Na-FAR-1) is an abundantly expressed FAR from a parasitic hookworm. The present work describes its tissue distribution, structure and ligand-binding characteristics and shows that Na-FAR-1 expands to transport multiple FA molecules in its internal cavity.


1985 ◽  
Vol 33 (8) ◽  
pp. 837-839 ◽  
Author(s):  
A Messing ◽  
A Stieber ◽  
N K Gonatas

The resolution of indirect immunoperoxidase methods for localizing antigens on the surface of plasma membranes of cultured cells was tested using dissociated monolayer cultures of ciliary ganglion neurons prelabeled with cationic ferritin. Clusters of ferritin were produced on the cell surface by warming the cells to 37 degrees C after the ferritin, rabbit anti-ferritin, and goat anti-rabbit immunoglobulin coupled to horseradish peroxidase had all been applied. Intense 3,3'-diaminobenzidine tetrahydrochloride (DAB) staining was limited to the regions immediately surrounding the ferritin clusters. The lateral spread of the DAB reaction product beyond the outer ferritin particles in each cluster averaged 54-81 nm in four experiments. A second type of increased density, coinciding with the thickness of the plasma membrane, was also seen. These stained plasma membranes extended 161-339 nm from the ferritin clusters.


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