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Sodium Hydrosulfide Induces Resistance Against Penicillium expansum in Apples by Regulating Hydrogen Peroxide and Nitric Oxide Activation of Phenylpropanoid Metabolism
As a multifunctional signaling molecule, hydrogen sulfide (H(2)S) has been reported to induce plant responses to a variety of abiotic stresses. However, there are no reports on H(2)S treatment inducing resistance in apples against Penicillium expansum, a biotic factor, and its possible mechanism of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440896/ https://www.ncbi.nlm.nih.gov/pubmed/34539612 http://dx.doi.org/10.3389/fmicb.2021.720372 |
Sumario: | As a multifunctional signaling molecule, hydrogen sulfide (H(2)S) has been reported to induce plant responses to a variety of abiotic stresses. However, there are no reports on H(2)S treatment inducing resistance in apples against Penicillium expansum, a biotic factor, and its possible mechanism of action. In this study, fumigating apples with 5 mM sodium hydrosulfide (NaHS), the exogenous donor of H(2)S, for 12 h reduced the diameter of lesions in fruit colonized by P. expansum. NaHS treatment markedly promoted the synthesis of endogenous H(2)S, hydrogen peroxide (H(2)O(2)), and nitrogen oxide (NO). In vivo NaHS treatment enhanced the activities of phenylalanine ammonia-lyase, cinnamate 4-hydroxylase, p-coumarate:coenzyme A ligase isoenzymes, caffeoyl-CoA-O-methyltransferase, caffeic acid-O-methyltransferase, ferulic acid-5-hydroxylase, cinnamyl-CoA reductase, and cinnamyl-alcohol dehydrogenase. The treatment also facilitated the production of specific phenolic acids, such as cinnamic acid, p-coumaric acid, caffeic acid, ferulic acid, and sinapic acid; total phenolic compounds; p-coumaryl alcohol; coniferyl alcohol; sinapyl alcohol; and lignin. NaHS treatment induced resistance against P. expansum in apples through H(2)O(2)- and NO-mediated activation of phenylpropanoid metabolism. |
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