1985
DOI: 10.1039/np9850200427
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Phytoalexins

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Cited by 101 publications
(45 citation statements)
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“…They have been described as antifungal agents and as phytoalexins. 16) The naturally-occurring aureusidin (4,6,3Ј,4Ј-tetrahydroxyaurone) was found to be a potent inhibitor of iodothyroninedeiodinase. 17 The binding of aurones to the purified C-terminal cytosolic domain of Pgp was measured by the quenching of protein intrinsic fluorescence, as previously described.…”
Section: Resultsmentioning
confidence: 99%
“…They have been described as antifungal agents and as phytoalexins. 16) The naturally-occurring aureusidin (4,6,3Ј,4Ј-tetrahydroxyaurone) was found to be a potent inhibitor of iodothyroninedeiodinase. 17 The binding of aurones to the purified C-terminal cytosolic domain of Pgp was measured by the quenching of protein intrinsic fluorescence, as previously described.…”
Section: Resultsmentioning
confidence: 99%
“…These antimicrobial metabolites may be either constitutive compounds, also called phytoanticipins (Osbourn, 1996), or biosynthesized de novo compounds such as phytoalexins (Brooks & Watson, 1985). The role of phytoalexins in resistance to pathogens has been well documented in the plant model Arabidopsis thaliana .…”
Section: Introductionmentioning
confidence: 99%
“…Réponse à deux niveaux Keen (1982Keen ( , 1986 (Doke et al, 1987) (Kiraly, 1980;Van Loon, 1982;Goodman et al, 1986;Ward, 1986 (Van Loon, 1982;Ward, 1986 Grisebach et Ebel (1978), Stoessl (1980Stoessl ( , 1983, Bailey (1982aBailey ( , 1982bBailey ( , 1983), Darvill et Albersheim (1984), Brooks et Watson (1985), Crute et al (1985), Kuc et Rush (1985), Ebel (1986), Keen (1986) (Cruickshank et Perrin, 1960Perrin, , 1963Perrin et Bottomley, 1962 (Paxton, 1981) (Coxon, 1982). La majeure partie des études concerne toutefois les seules légumineuses (Ingham, 1982) et solanacées (Kuc, 1982).…”
Section: Déterminisme Génétiqueunclassified
“…La plupart des espèces ne produisent que rarement des phytoalexines appartenant à plus de 2 ou 3 groupes de structure chimique différente et, dans une même classe de composés, les structures des phytoalexines produites sont, en général, très proches (Mansfield, 1983). Cependant, des composés présentant une même unité structurale (stilbènes par exemple) peuvent être détectés chez des espèces végétales très éloignées (Stoessl, 1983;Brooks et Watson, 1985 (Smith, 1982;Smith et Banks, 1986;Yoshikawa et al, 1987). Il existe toutefois des exemples où une action sur la respiration cellulaire est signalée (Yoshikawa et al, 1987).…”
Section: Déterminisme Génétiqueunclassified