Specificity in the immobilisation of cell wall proteins in response to different elicitor molecules in suspension-cultured cells of French bean (Phaseolus vulgaris L.)

1995 ◽  
Vol 28 (6) ◽  
pp. 1075-1087 ◽  
Author(s):  
Przemys?aw Wojtaszek ◽  
Jonathan Trethowan ◽  
G. Paul Bolwell
Keyword(s):  
Cell Wall ◽  
Phaseolus Vulgaris ◽  
Cultured Cells ◽  
French Bean ◽  
Cell Wall Proteins ◽  
Phaseolus Vulgaris L ◽  
Suspension Cultured Cells

scholarly journals Synthesis of dehydrogenation polymers of ferulic acid with high specificity by a purified cell-wall peroxidase from French bean (Phaseolus vulgaris L.)

1994 ◽  
Vol 299 (3) ◽  
pp. 747-753 ◽  
Author(s):  
A Zimmerlin ◽  
P Wojtaszek ◽  
G P Bolwell
Keyword(s):  
Cell Wall ◽  
Phaseolus Vulgaris ◽  
Ferulic Acid ◽  
Cultured Cells ◽  
Gel Filtration ◽  
High Specificity ◽  
French Bean ◽  
Good Evidence ◽  
Ionization Mass ◽  
Phaseolus Vulgaris L

A cationic (pI 8.3) wall-bound peroxidase has been purified to homogeneity from suspension-cultured cells of French bean (Phaseolus vulgaris L.). The enzyme was a glycoprotein and its M(r) was 46,000 as determined by SDS/Page and h.p.l.c. gel filtration. It was localized biochemically to microsomes and the cell wall, and the latter subcellular distribution was confirmed by immunogold techniques. The native enzyme showed absorption maxima at 403, 500 and 640 nm, with an RZ (A405/A280) of 3.3. The peroxidase oxidized guaïacol and natural phenolic acids. By desorption-chemical-ionization mass spectrometry the enzyme was found to oxidize the model compound, ferulic acid, into dehydrodiferulic acid. Kinetics studies indicated an apparent Km of 113.3 +/- 22.9 microM and a Vmax of 144 mumol.min-1.nmol-1 of protein at an H2O2 concentration of 100 microM. In comparison with a second French-bean peroxidase (FBP) and horseradish peroxidase, as a model, it acted with a 6-10-fold higher specificity in this capacity. It is a member of the peroxidase superfamily of bacterial, fungal and plant haem proteins by virtue of its highly conserved amino acid sequence within the proximal and distal haem-binding sites. This is good evidence that this particular FBP may function in constructing covalent cross-linkages in the wall during development and response to pathogens.

scholarly journals Cell-Wall Proteins Induced by Water Deficit in Bean (Phaseolus vulgaris L.) Seedlings

1995 ◽  
Vol 107 (4) ◽  
pp. 1119-1128 ◽  
Author(s):  
A. A. Covarrubias ◽  
J. W. Ayala ◽  
J. L. Reyes ◽  
M. Hernandez ◽  
A. Garciarrubio
Keyword(s):  
Cell Wall ◽  
Phaseolus Vulgaris ◽  
Water Deficit ◽  
Cell Wall Proteins ◽  
Phaseolus Vulgaris L

scholarly journals Cell wall polysaccharide biosynthesis and related metabolism in elicitor-stressed cells of French bean (Phaseolus vulgaris L.)

1995 ◽  
Vol 306 (3) ◽  
pp. 745-750 ◽  
Author(s):  
D Robertson ◽  
B A McCormack ◽  
G P Bolwell
Keyword(s):  
Cell Wall ◽  
Phaseolus Vulgaris ◽  
Time Course ◽  
Glucose Dehydrogenase ◽  
French Bean ◽  
Primary Cell Wall ◽  
Cell Wall Polysaccharide ◽  
Phaseolus Vulgaris L ◽  
Glucan Synthase ◽  
Elicitor Treatment

Enzyme activities involved in quantitative and qualitative flux of sugars into cell wall polysaccharides were determined following elicitor treatment of suspension cultured cells of French bean (Phaseolus vulgaris L.). Two subsets of activities were examined: the first were involved in synthesis and metabolism of UDP-glucose and the provision of the pool of UDP-sugars, and the second a selection of membrane-bound glycosyltransferases involved in the synthesis of pectins, hemicelluloses and glucans of the primary cell wall. Of the first group, only UDP-glucose dehydrogenase (EC 1.1.1.22) showed any significant induction in response to elicitor treatment, sucrose synthase (EC 2.4.1.13), UDP-glucuronate decarboxylase (EC 4.1.1.35), UDP-glucose and UDP-xylose 4-epimerases (EC 5.1.3.2 and EC 5.1.3.5 respectively) did not change in activity significantly over the time course. In contrast, enzymes of the second group showed a more complex response. Callose synthase (glucan synthase II, EC 2.4.1.12) increased in activity, as has been shown in other systems, while arabinan synthase (EC 2.4.1.-), xylan synthase (EC 2.4.1.72), xyloglucan synthase (EC 2.4.1.72) and glucan synthase I (EC 2.4.1.12) activities were rapidly depleted from membranes within 3 h following elicitor action. This rapid turnover of activity was striking, indicating that the half-life of such enzymes can be short and that elicitor action causes substantial perturbation of some membrane activities. Glucan synthase I activity appears to increase in the later stages over the time period measured, indicating some recovery of this metabolism.

Interactions of the nonhost French bean plant (Phaseolus vulgaris) with parasitic and saprophytic fungi. III. Cytologically detectable responses

1989 ◽  
Vol 67 (3) ◽  
pp. 676-686 ◽  
Author(s):  
Myriam R. Fernandez ◽  
Michèle C. Heath
Keyword(s):  
Cell Wall ◽  
Phaseolus Vulgaris ◽  
General Feature ◽  
Fungal Spores ◽  
French Bean ◽  
Cell Necrosis ◽  
Phaseolus Vulgaris L ◽  
Fungal Cell ◽  
Parasitic Fungi ◽  
Nonhost Plant

Cytologically detectable responses of the nonhost French bean (Phaseolus vulgaris L. cv. Pinto) to saprophytic and parasitic fungi were examined when fungal spores were introduced into heated or unheated leaves via wounds or by injection. Although similar types of responses were observed in interactions with all the fungi, some of these responses were characteristic of each group (saprophytes vs. parasites) in the frequency and (or) extent with which they were elicited. Differences in responses between and within each of these groups of fungi were more related to their degree of adaptation for parasitism than to their taxonomic relationships. Certain responses that were typically elicited by the saprophytes occurred to a lesser extent in tissue responding to the parasites, suggesting that the ability to not trigger, or suppress, these responses may be a general feature of parasitic fungi. None of the fungi elicited significant levels of plant cell necrosis, and for two of the saprophytes, dead spores elicited a lower frequency of responses than live ones. The data indicate that many of the responses of a nonhost plant to living fungi may be the result of reactions to fungal activity rather than to constitutive recognition molecules such as components of the fungal cell wall.

scholarly journals Differential patterns of arabinosylation by membranes of suspension-cultured cells of Phaseolus vulgaris (French bean) after subculture or elicitation

1984 ◽  
Vol 222 (2) ◽  
pp. 427-435 ◽  
Author(s):  
G P Bolwell
Keyword(s):  
Phaseolus Vulgaris ◽  
Cultured Cells ◽  
Initial Period ◽  
French Bean ◽  
Colletotrichum Lindemuthianum ◽  
Fungal Elicitor ◽  
Arabinogalactan Protein ◽  
Suspension Cultured Cells

Suspension-cultured cells of Phaseolus vulgaris (French bean) incorporated [1-3H] arabinose in vivo into high-Mr polymers that could be separated into glycoprotein and polysaccharide. Microsomal membranes from suspension-cultured cells of beans incorporated arabinose from UDP-beta-L-arabinose in vitro into both polysaccharide and glycoprotein. The enzyme involved in arabinan synthesis, arabinan synthase, appeared to be immunologically distinct from the protein:arabinosyltransferase system. Both these activities are inducible, but behave differently with either plant-growth-regulator or fungal-elicitor treatments. After subculture of cells entering the stationary growth phase the arabinan synthase activity reaches much higher values than does that of the protein transferase system during the initial period of cell division and growth, whereas after elicitation at the same growth stage, all the increased incorporation of arabinose occurs into glycoprotein of Mr higher than 200 000 and to a greater extent into a specific glycoprotein of Mr 42 500. Preliminary characterization of these glycoproteins prepared under non-reducing conditions and after acid and alkaline hydrolysis suggests that the high-Mr glycoprotein material is similar to arabinogalactan protein, whereas the lower-Mr material may be a hydroxyproline-rich protein existing as a dimer and that specifically increases during the hypersensitive response of the cells to the fungal elicitor from Colletotrichum lindemuthianum.

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