Effect of flavonoids on mycelial growth of Verticillium albo-atrum

Picman, Anna K.; Schneider, Edward F.; Picman, Jaroslav

doi:10.1016/0305-1978(95)00081-x

Cited by 46 publications

(46 citation statements)

References 14 publications

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“…Their fungicidal action is related to the damage to the plasmalemma, a rapid blockage of cytoplasmic movement, and disorganization of cell organelles. Moreover, they disturb fungal respiration and nutrient uptake (Weidenbörner et al 1990;Picman et al 1995). The high level of isoflavonoid glycosides particularly genistein-7-O-glucoside and free isoflavonoid aglycones (i.e., genistein, wighteone, and luteone) constituted an important element of resistance of tissues nourished with sucrose against infections.…”

Section: Involvement Of Sugars In Plant Defense Responses During Infementioning

confidence: 99%

The role of sugar signaling in plant defense responses against fungal pathogens

2014

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Section: Involvement Of Sugars In Plant Defense Responses During Infementioning

confidence: 99%

The role of sugar signaling in plant defense responses against fungal pathogens

2014

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“…Simmonds (2001Simmonds ( , 2003 studied the bioactivity of different flavonoids and confirmed that these compounds could modulate the feeding and oviposition behavior of insects. Also, flavonoids inhibited the mycelial growth of a crop pathogen, Verticillium albo-atrum (Picman, 1995).…”

Section: Introductionmentioning

confidence: 99%

Impact of Flavonoids against Woolly Apple Aphid, Eriosoma lanigerum (Hausmann) and Its Sole Parasitoid, Aphelinus mali (Hald.)

Ateyyat¹,

Abu-Romman²,

Abu-Darwish³

et al. 2012

JAS

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Cut-shoot bioassay test was used to study the significance of three flavonoids as aphicides against the woolly apple aphid (WAA), Eriosoma lanigerum (Hausmann). The used flavonoids were two flavanols that are quercetin dehydrate and rutin hydrate, but rutin hydrate is a glycoside of quercetin dehydrate. In addition to one flavanone that was naringine. These flavonoids were used at three concentrations; 100 ppm, 1000 ppm and 10,000 ppm. Results showed that the three tested flavonoids were active as aphicides against the target species and that mortality to nymphs was higher than that obtained against apterous adults. Increasing the concentration of the flavonoids resulted in a remarkable increase in nymphs mortality. However, rutin hydrate is more toxic to WAA than quercetin dehydrate and naringin.The three flavonoids had slight effect on the sole parasitoid of WAA, Aphelinus mali compared with effect caused by imodacloprid insecticide. Quercetin dehydrate, rutin hydrate and naringine can be used as botanical insecticides and incorporated into integrated management programs of the aphid.

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“…* (Bassam et al, 1988) 5,7-dihydroxy-6-methoxyflavanone Beta vulgaris Rhizoctonia solani (Takahashi et al, 1987) 7,3´-dihydroxy-4´-methoxyflavanone Vicia sativa Rhizobium leguminosarum* (Zaat et al, 1989) eriodictyol commercial agent Rhizobium leguminosarum* (Firmin et al, 1986;Zaat et al, 1989), Rhizobium meliloti* (Peters & Long, 1988) eriodictyol 7-O-glucoside commercial agent Rhizobium leguminosarum* (Zaat et al, 1989) flavanone commercial agent Verticillium albo-atrum (Picman et al, 1995), Aspergillus spp. (Weidenbörner et al, 1990b) hesperetin commercial agent Verticillium albo-atrum (Picman et al, 1995), Aspergillus spp. (Weidenbörner et al, 1990b), Rhizobium leguminosarum* (Firmin et al, 1986;Zaat et al, 1989) hesperetin 7-O-rutinoside commercial agent Verticillium albo-atrum (Picman et al, 1995) homoeriodictyol commercial agent Rhizobium leguminosarum* (Zaat et al, 1989) isosakuranetin commercial agent Rhizobium leguminosarum* (Zaat et al, 1989) naringenin Prunus cerasus (Rosaceae), Vigna angularis (Leguminosae), commercial agent Verticillium albo-atrum (Picman et al, 1995), Aspergillus spp.…”

Section: (2s3s)-( )-Taxifolin 3-o-glucosidementioning

confidence: 99%

“…(Weidenbörner et al, 1990b) Flavanone betagarin Beta vulgaris Cercospora beticola (Johnson et al, 1976;Martin, 1977;Geigert et al, 1973), Rhizoctonia solani (Takahashi et al, 1987) liquiritigenin Medicago sativa, commercial agent Rhizobium meliloti* Maxwell et al, 1989), Rhizobium spp. * (Bassam et al, 1988) 5,7-dihydroxy-6-methoxyflavanone Beta vulgaris Rhizoctonia solani (Takahashi et al, 1987) 7,3´-dihydroxy-4´-methoxyflavanone Vicia sativa Rhizobium leguminosarum* (Zaat et al, 1989) eriodictyol commercial agent Rhizobium leguminosarum* (Firmin et al, 1986;Zaat et al, 1989), Rhizobium meliloti* (Peters & Long, 1988) eriodictyol 7-O-glucoside commercial agent Rhizobium leguminosarum* (Zaat et al, 1989) flavanone commercial agent Verticillium albo-atrum (Picman et al, 1995), Aspergillus spp. (Weidenbörner et al, 1990b) hesperetin commercial agent Verticillium albo-atrum (Picman et al, 1995), Aspergillus spp.…”

Section: (2s3s)-( )-Taxifolin 3-o-glucosidementioning

confidence: 99%

“…(Weidenbörner et al, 1990b) hesperetin commercial agent Verticillium albo-atrum (Picman et al, 1995), Aspergillus spp. (Weidenbörner et al, 1990b), Rhizobium leguminosarum* (Firmin et al, 1986;Zaat et al, 1989) hesperetin 7-O-rutinoside commercial agent Verticillium albo-atrum (Picman et al, 1995) homoeriodictyol commercial agent Rhizobium leguminosarum* (Zaat et al, 1989) isosakuranetin commercial agent Rhizobium leguminosarum* (Zaat et al, 1989) naringenin Prunus cerasus (Rosaceae), Vigna angularis (Leguminosae), commercial agent Verticillium albo-atrum (Picman et al, 1995), Aspergillus spp. (Weidenbörner et al, 1990b), Cystospora persoonii (Geibel, 1995), Rhizobium leguminosarum* (Firmin et al, 1986;Zaat et al, 1989), Cephalosporium gregatum (Abe et al, 1987), Rhizobium spp.…”

Section: (2s3s)-( )-Taxifolin 3-o-glucosidementioning

confidence: 99%

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Flavonoid Function and Activity to Plants and Other Organisms

Iwashina

2003

Biol. Sci. Space

151

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Flavonoid compounds distribute widely in vascular plants and Bryophytes, and ca. 5,000 kinds have been reported as naturally occurring substances. Many biological activities of the flavonoids were found until now. They include pollinator attractants, oviposition stimulants, feeding attractants and deterrents, allelopathy and phytoalexins. This paper reviews function and activity of flavonoids against plants and other organisms.Key words: flavonoids, pollinator attractants, feeding attractants and deterrents, allelopathy, phytoalexins di-P-coumaroylglucoside) and quercetin 3-O-(3´´,6´´-di-P-coumaroylglucoside) in Pinus sylvestris (Pinaceae) (Jungblut et al., 1995), quercetin 3-O-galactoside, myricetin 3-O-rutinoside and two P-coumaroyl kaempferol 3-Oglucoside in Quercus ilex (Fagaceae) (Skaltsa et al., 1994), and glycosides of quercetin, apigenin and luteolin in Olea europea (Oleaceae) (Karabourniotis et al., 1992) The occurrence of anthocyanins as pollinator attractants is well-known as a function of the flavonoids in plants. Additionally, it is known that flavones and flavonols, which can hardly see by human eyes, also act as pollinator attractants in addition to visible anthocyanins. Recently, other functions, oviposition stimulants, feeding attractants, feeding deterrents, allelopathy and phytoalexins of naturally occurring flavonoids, were found by many authors.In this paper, the flavonoid function and activity to plants and other organisms are reviewed.

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Effect of flavonoids on mycelial growth of Verticillium albo-atrum

Cited by 46 publications

References 14 publications

The role of sugar signaling in plant defense responses against fungal pathogens

The role of sugar signaling in plant defense responses against fungal pathogens

Impact of Flavonoids against Woolly Apple Aphid, Eriosoma lanigerum (Hausmann) and Its Sole Parasitoid, Aphelinus mali (Hald.)

Flavonoid Function and Activity to Plants and Other Organisms

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