Regular articlePhytoalexin elicitation in grape berries and their susceptibility toRhizopus stolonifer☆
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Genome-wide investigation and comparative expression profiling reveal R2R3-MYB genes involved in Sclerotinia sclerotiorum defence in tomato
2022, Physiological and Molecular Plant PathologyPterostilbene production of tomato transformed with resveratrol synthase and resveratrol O-methyltransferase genes
2022, Plant ScienceCitation Excerpt :This may be due to the high substrate level such as p-coumaryl CoA in tomatoes, or a new metabolic balance achieved by some type of regulation. Stilbene compounds can inhibit the growth of various fungi, including Downy mildew (Paolocci et al., 2014), B. cinerea, Powdery mildew (Romero-Pérez et al., 2001), Rhizopus gluteus (Sarig et al., 1997), and Aspergillus charcoal (Vezzulli et al., 2007). Zemova (Zernova et al., 2014) co-transformed peanut AhRS3 gene and grape VvROMT genes into soybean.
Resveratrol: from enhanced biosynthesis and bioavailability to multitargeting chronic diseases
2019, Biomedicine and PharmacotherapyCitation Excerpt :Apart from Plasmopora and Botrylis infection, Rhizopus stolonifer infection has also shown to augment synthesis of resveratrol. An exposure to the infection increases its content, which peaks after 24 h [21]. In another study to enhance the resistance of plants against fungal disease, Vitis vinifera was exposed to a combination of a soil bacterium B-781 (arrests fungal growth) and Botrytis cinerea.
High-Resolution Mass Spectrometry and Biological Properties of Grapevine and Wine Stilbenoids
2018, Studies in Natural Products ChemistryCitation Excerpt :Stilbenes are produced in soft tissues and act as phytoalexins when elicited by biotic and/or abiotic agents by activation of the stilbene synthase (STS) gene [2]. Several organisms, such as Botrytis cinerea [5–7], Plasmopara viticola [8], Erysiphe necator [9], esca disease fungi [10], Rhizopus stolonifer [11], and Aspergillus sp. [12,13] can induce the production of these phytoalexins. ɛ-Viniferin (E and Z isomers), ω-viniferin, and resveratrol oligomers (ampelopsin D, quadrangularin A, α-viniferin, E and Z miyabenol C, isohopeaphenol, ampelopsin H, vaticanol C-like) are found in vine leaves, roots, clusters, and stems [4]; E-ampelopsin E, eamurensin B, E-resveratroloside, E-3,5,4′-trihydroxystilbene 2-C-glucoside, Z-ampelopsin E, scirpusin A, E and Z vitisin B have all been identified in vine canes [14] (Table 5.1).
Pre-harvest hormetic doses of UV-C radiation can decrease susceptibility of lettuce leaves (Lactuca sativa L.) to Botrytis cinerea L.
2017, Scientia HorticulturaeCitation Excerpt :A large number of previously published works have shown that UV-C irradiation elicit defense responses in harvested horticultural crops (Charles et al., 2008a, 2008b, 2008c). The induction of disease resistance in post-harvest crops in response to UV-C appears to involve the elicitation and accumulation of phytoalexins (Ben-Yehoshua et al., 1992; Mercier et al., 1993b; Sarig et al., 1997; Charles et al., 2008a), the ultra-structural modification of the epicarp leading to the formation of physical barriers (Charles et al., 2008b), the reinforcement of the cell walls by phenolic compounds, lignin and suberin (Charles et al., 2008c), and the enhancement of constitutive and inducible β-1,3-glucanases and chitinases (Charles et al., 2009). We have recently shown that lettuce plants treated with a low dose of UV-C after harvest show increased resistance against B. cinerea and Sclerotinia minor (Ouhibi et al., 2015a, 2015b).
Physical treatments to control postharvest diseases of fresh fruits and vegetables
2016, Postharvest Biology and Technology