Response of Phaseolus vulgaris protoplasts to chemical components of fungal origin

1987 ◽  
Vol 65 (1) ◽  
pp. 63-68 ◽  
Author(s):  
Helen M. Griffiths ◽  
Anne J. Anderson

Colletotrichum lindemuthianum is the causal agent of anthracnose in Phaseolus vulgaris L. (French bean). The α and β races of the fungus were used in this study with French bean cultivar ‘Great Northern’. Whole plants inoculated with the α race developed brown lesions on the hypocotyls (susceptible response). The β race caused small limited lesions, indicating a more resistant interaction. Extracellular products and cell wall materials were isolated from β race cultures and extracellular products from α race cultures. The extracts were size fractionated. By using a cotyledon bioassay, elicitor activity was demonstrated on ‘Dark Red Kidney’ within fractions from the α race. Fractions from the β race had little activity on ‘Dark Red Kidney’ or ‘Great Northern’ cotyledons. Protoplasts were isolated from ‘Great Northern’ bean hypocotyl tissue and incubated with the fungal fractions. Even at low concentrations (0.01 μg glucose equivalent∙mL−1), the β race culture filtrate rapidly killed a greater percentage of protoplasts (30%) than the α race (15%). The β race wall extract had little effect upon protoplast viability. The proportion of nonviable protoplasts depended on the incubation period and the concentration of the fungal material. Heat treatment of the culture filtrates and wall extract did not decrease their lethal effects. The results suggest that protoplasts may be valuable in examining the nature of certain plant–pathogen interactions.

1985 ◽  
Vol 229 (3) ◽  
pp. 693-699 ◽  
Author(s):  
G P Bolwell ◽  
M P Robbins ◽  
R A Dixon

The enzyme prolyl hydroxylase (proline: 2-oxoglutarate dioxygenase, EC 1.14.11.12), induced in suspension-cultured cells of Phaseolus vulgaris L. (French bean) by treatment with an elicitor preparation from the phytopathogenic fungus Colletotrichum lindemuthianum, has been investigated. The enzyme, which catalyses the hydroxylation of poly-L-proline with the stoichiometric decarboxylation of 2-oxoglutarate, has been shown to be localized mainly in smooth endoplasmic reticulum. After solubilization from microsomal membranes, the hydroxylase was purified by ion-exchange chromatography and affinity chromatography on poly-L-proline-Sepharose 4B. The subunit Mr, as assessed by sodium dodecyl sulphate/poly-acrylamide-gel electrophoresis, was 65 000, the subunit apparently being recovered as a doublet: the subunits associate under non-denaturing conditions to give at least a tetramer. The bean hydroxylase has kinetic properties and cofactor requirements similar to those previously reported for the enzyme from other plants. Elicitor treatment of suspension-cultured bean cells leads to a rapid induction of prolyl hydroxylase activity concomitant with induction of a protein: arabinosyl-transferase and increased levels of an arabinosylated hydroxyproline-rich protein.


Planta ◽  
1994 ◽  
Vol 192 (2) ◽  
Author(s):  
ColinG. Smith ◽  
MatthewW. Rodgers ◽  
Alfred Zimmerlin ◽  
Dudley Ferdinando ◽  
G.Paul Bolwell

Planta ◽  
1994 ◽  
Vol 192 (2) ◽  
pp. 155-164 ◽  
Author(s):  
Colin G. Smith ◽  
Matthew W. Rodgers ◽  
Alfred Zimmerlin ◽  
Dudley Ferdinando ◽  
G. Paul Bolwell

1984 ◽  
Vol 222 (2) ◽  
pp. 427-435 ◽  
Author(s):  
G P Bolwell

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.


HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 481b-481
Author(s):  
A.E. Fiebig ◽  
J.T.A. Proctor ◽  
D. Murr ◽  
R. Releeder

Varying concentrations (500-4000 mg·L–1) of ethephon, an ethylene-releasing compound, were applied to 3-year-old ginseng (Panax quinquefolium L.) plants in fields of southern Ontario. The effects of this chemical on fruit removal, plant damage, infructescence morphology, and root mass were studied and compared to the normal practice of manual inflorescence removal. The highest concentrations had the highest rates of removal but also caused the greatest amount of damage to the whole plants when compared to the mid-range concentrations. The lowest concentrations showed less foliar damage but did not provide sufficient fruit removal to mimic hand removal. When individual inflorescences of the ethephon treatments were studied, the seed heads had fewer ripe berries and more unpollinated florets than the untreated controls. When root masses were compared, high and low concentrations showed lower masses than those of the standard production practice of hand removal. However, mid range concentrations showed similar root mass increase to manual removal. When all parameters were considered, the concentration range giving the best results was 1000-1500 mg·L–1. Multiple applications of ethephon, at weekly intervals, had an additive effect on flower removal and plant damage. Treatments having an additive concentration of over 2000 mg·L–1 had detrimental effects on all parameters. Those within the 1000–1500 mg·L–1 range showed the highest similarity to the hand removal benefits.


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