Biological control of Sclerotinia sclerotiorum on aerial parts of plants by the hyperparasite Coniothyrium minitans

1982 ◽  
Vol 78 (3) ◽  
pp. 521-529 ◽  
Author(s):  
Peter Trutmann ◽  
Philip J. Keane ◽  
Peter R. Merriman
2004 ◽  
Vol 26 (21) ◽  
pp. 1649-1652 ◽  
Author(s):  
Junling Shi ◽  
Yin Li ◽  
Huali Qian ◽  
Guocheng Du ◽  
Jian Chen

1974 ◽  
Vol 140 (1) ◽  
pp. 47-55 ◽  
Author(s):  
David Jones ◽  
Alex. H. Gordon ◽  
John S. D. Bacon

1. Two fungi, Coniothyrium minitans Campbell and Trichoderma viride Pers. ex Fr., were grown on autoclaved crushed sclerotia of the species Sclerotinia sclerotiorum, which they parasitize. 2. in vitro the crude culture filtrates would lyse walls isolated from hyphal cells or the inner pseudoparenchymatous cells of the sclerotia, in which a branched β-(1→3)-β-(1→6)-glucan, sclerotan, is a major constituent. 3. Chromatographic fractionation of the enzymes in each culture filtrate revealed the presence of several laminarinases, the most active being an exo-β-(1→3)-glucanase, known from previous studies to attack sclerotan. Acting alone this brought about a limited degradation of the glucan, but the addition of fractions containing an endo-β-(1→3)-glucanase led to almost complete breakdown. A similar synergism between the two enzymes was found in their lytic action on cell walls. 4. When acting alone the endo-β-(1→3)-glucanase had a restricted action, the products including a trisaccharide, tentatively identified as 62-β-glucosyl-laminaribiose. 5. These results are discussed in relation to the structure of the cell walls and of their glucan constituents.


Author(s):  
Nyckle J. Fokkema ◽  
Matthijs Gerlagh ◽  
Jürgen Köhl

2002 ◽  
Vol 80 (8) ◽  
pp. 892-898 ◽  
Author(s):  
G Q Li ◽  
H C Huang ◽  
S N Acharya

Assays on mycelial growth and spore germination were carried out to determine the sensitivity of the biocontrol agents Ulocladium atrum and Coniothyrium minitans and the plant pathogen Sclerotinia sclerotiorum to benomyl and vinclozolin. Ulocladium atrum was more tolerant to these fungicides than C. minitans and S. sclerotiorum. The 50% effective concentration (EC50) of U. atrum based on the mycelial growth inhibition was 1467.3 µg active ingredient (a.i.)/mL for benomyl and 12.6 µg a.i./mL for vinclozolin, and the maximum inhibition concentration was higher than 4000 µg a.i./mL for both fungicides. For C. minitans and S. sclerotiorum, however, the EC50 based on mycelial growth inhibition was lower than 1 µg a.i./mL. After incubation for 24 h at 20°C, the germination rate of U. atrum conidia was 90–99% on potato dextrose agar (PDA) amended with benomyl at 100–500 µg a.i./mL or vinclozolin at 10–500 µg a.i./mL. At these concentrations, germ tubes of U. atrum developed into long, branched hyphae in benomyl treatments, but they remained short and clustered in vinclozolin treatments. Pycnidiospores of C. minitans and ascospores of S. sclerotiorum germinated on PDA amended with benomyl at 100–500 µg a.i./mL, but the germ tubes did not grow further. Spore germination of C. minitans and S. sclerotiorum was less than 3.2% on PDA amended with vinclozolin at 10–500 µg a.i./mL after 24 h. This is the first report on the sensitivity of U. atrum and C. minitans to benomyl and vinclozolin. The results suggest that it is possible to control S. sclerotiorum using a combination of U. atrum and benomyl or vinclozolin.Key words: fungicides, mycelial growth, spore germination, integrated pest management.


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