Studies on the mechanism of action of β-methylaspartic acid in the suppression of Aphanomyces root rot of pea

1970 ◽  
Vol 48 (3) ◽  
pp. 631-637
Author(s):  
R. D. Lumsden ◽  
G. C. Papavizas ◽  
W. A. Ayers

β-Methylaspartic acid (MAA) effectively reduced root rot of pea, caused by Aphanomyces euteiches, at concentrations as low as 4 p.p.m., and prevented disease at 15–20 p.p.m. The degree of methylation of pectic materials in healthy pea plants was not increased by MAA, which thus could not account for induced resistance to root rot. Further studies revealed that MAA in the absence of glutamic acid affected zoospore germination and inhibited growth of A. euteiches in vitro. Inhibition of growth and of root rot development was almost completely reversed by glutamic and aspartic acids, and partly reversed by several other amino acids. Studies of the mechanism of inhibition of growth of A. euteiches by MAA indicated that MAA did not affect glutamine synthetase or aspartate oxoglutarate transaminase, two amino acid metabolizing enzymes produced by A. euteiches, nor did it affect the uptake of 14C-labeled glutamic acid by mycelium of the fungus and the incorporation of glutamate into alcohol-insoluble material. It was concluded that MAA directly affects growth of A. euteiches and in this way controls root rot of pea.

Nature ◽  
1950 ◽  
Vol 166 (4217) ◽  
pp. 352-352 ◽  
Author(s):  
A. BACK ◽  
A. SADOVSKY ◽  
N. LICHTENSTEIN

1984 ◽  
Vol 11 (4) ◽  
pp. 296-300 ◽  
Author(s):  
JEAN-GUY BISAILLON ◽  
PIERRE TURGEON ◽  
DANIEL DUBREUIL ◽  
REJEAN BEAUDET ◽  
MICHEL SYLVESTRE ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Guillermo Gervasini ◽  
Maria J. Caballero ◽  
Juan A. Carrillo ◽  
Julio Benitez

The goal of this study was to assess in human liver microsomes the inhibitory capacity of commonly used antipsychotics on the most prominent CYP450 drug metabolizing enzymes (CYP1A2, CYP2C9, CYP2D6, and CYP3A). Chlorpromazine was the only antipsychotic that inhibited CYP1A2 activity (IC50=9.5 μM), whilst levomepromazine, chlorpromazine, and thioridazine significantly decreased CYP2D6-mediated formation of 1′-hydroxybufuralol (IC50 range, 3.5–25.5 μM). Olanzapine inhibited CYP3A-catalyzed production of 1′, and 4′-hydroxymidazolam (IC50=14.65 and 42.20 μM, resp.). In contrast, risperidone (IC50=20.7 μM) and levomepromazine (IC50=30 μM) showed selectivity towards the inhibition of midazolam 1′-hydroxylation reaction, and haloperidol did so towards 4′-hydroxylation (IC50 of 2.76 μM). Thioridazine displayed a Ki of 1.75 μM and an inhibitory potency of 1.57 on CYP2D6, suggesting a potential to induce in vivo interactions. However, with this exception, and given the observed Ki values, the potential of the assayed antipsychotics to produce clinically significant inhibitions of CYP450 isoforms in vivo seems limited.


2003 ◽  
Vol 93 (3) ◽  
pp. 329-335 ◽  
Author(s):  
Allen G. Xue

Pea root rot complex (PRRC), caused by Alternaria alternata, Aphanomyces euteiches, Fusarium oxysporum f. sp. pisi, F. solani f. sp. pisi, Mycosphaerella pinodes, Pythium spp., Rhizoctonia solani, and Sclerotinia sclerotiorum, is a major yield-limiting factor for field pea production in Canada. A strain of Clonostachys rosea (syn. Gliocladium roseum), ACM941 (ATCC 74447), was identified as a mycoparasite against these pathogens. When grown near the pathogen, ACM941 often was stimulated to produce lateral branches that grew directly toward the pathogen mycelium, typically entwining around the pathogen mycelium. When applied to the seed, ACM941 propagated in the rhizosphere and colonized the seed coat, hypocotyl, and roots as the plant developed and grew. ACM941 significantly reduced the recovery of all fungal pathogens from infected seed, increased in vitro seed germination by 44% and seedling emergence by 22%, and reduced root rot severity by 76%. The effects were similar to those of thiram fungicide, which increased germination and emergence by 33 and 29%, respectively, and reduced root rot severity by 65%. When soil was inoculated with selected PRRC pathogens in a controlled environment, seed treatment with ACM941 significantly increased emergence by 26, 38, 28, 13, and 21% for F. oxysporum f. sp. pisi, F. solani f. sp. pisi, M. pinodes, R. solani, and S. sclerotiorum, respectively. Under field conditions from 1995 to 1997, ACM941 increased emergence by 17, 23, 22, 13, and 18% and yield by 15, 6, 28, 6, and 19% for the five respective pathogens. The seed treatment effects of ACM941 on these PRRC pathogens were greater or statistically equivalent to those achieved with thiram. Results of this study suggest that ACM941 is an effective bioagent in controlling PRRC and is an alternative to existing chemical products.


1959 ◽  
Vol 101 (1) ◽  
pp. 145-147 ◽  
Author(s):  
A. R. Hennes ◽  
H. G. Muchmore ◽  
H. G. McClure ◽  
J. F. Hammarsten

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