Inhibitory effect of cinnamaldehyde on Fusarium solani and its application in postharvest preservation of sweet potato

[Display omitted] •Cinnamaldehyde (CA) exhibited antifungal effect on Fusarium solani.•CA disrupted mitochondrial function and induced ROS accumulation.•ROS peroxidized mitochondrial cardiolipin and initiated apoptosis in F. solani.•CA holds promise as a preservative for postharvest storage of sweet...

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Veröffentlicht in:Food chemistry 2023-05, Vol.408, p.135213-135213, Article 135213
Hauptverfasser: Pan, Chao, Yang, Kunlong, Erhunmwunsee, Famous, Li, Yong-Xin, Liu, Man, Pan, Shenyuan, Yang, Dongjing, Lu, Guoquan, Ma, Daifu, Tian, Jun
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container_end_page 135213
container_issue
container_start_page 135213
container_title Food chemistry
container_volume 408
creator Pan, Chao
Yang, Kunlong
Erhunmwunsee, Famous
Li, Yong-Xin
Liu, Man
Pan, Shenyuan
Yang, Dongjing
Lu, Guoquan
Ma, Daifu
Tian, Jun
description [Display omitted] •Cinnamaldehyde (CA) exhibited antifungal effect on Fusarium solani.•CA disrupted mitochondrial function and induced ROS accumulation.•ROS peroxidized mitochondrial cardiolipin and initiated apoptosis in F. solani.•CA holds promise as a preservative for postharvest storage of sweet potato. Root rot caused by Fusarium solani is one of major postharvest diseases limiting sweet potato production. Antifungal effect and possible mode of action of cinnamaldehyde (CA) against F. solani were investigated. CA concentration of 0.075 g/L inhibited conidial viability of F. solani. CA vapor of 0.3 g/L in air completely controlled the F. solani development in sweet potatoes during storage for 10 days at 28 °C, and protected soluble sugar and starch in the flesh from depletion by the fungus. Further results demonstrated that CA induced reduction in mitochondrial membrane potential (Δψm), ROS accumulation, and cell apoptosis characterized by DNA fragmentation in F. solani. Moreover, CA facilitated decomposition of mitochondria-specific cardiolipin (CL) into its catabolites by the catalytic action of phospholipases. Altogether, the results revealed a specific antifungal mechanism of CA against F. solani, and suggest that CA holds promise as a preservative for postharvest preservation of sweet potato.
doi_str_mv 10.1016/j.foodchem.2022.135213
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Root rot caused by Fusarium solani is one of major postharvest diseases limiting sweet potato production. Antifungal effect and possible mode of action of cinnamaldehyde (CA) against F. solani were investigated. CA concentration of 0.075 g/L inhibited conidial viability of F. solani. CA vapor of 0.3 g/L in air completely controlled the F. solani development in sweet potatoes during storage for 10 days at 28 °C, and protected soluble sugar and starch in the flesh from depletion by the fungus. Further results demonstrated that CA induced reduction in mitochondrial membrane potential (Δψm), ROS accumulation, and cell apoptosis characterized by DNA fragmentation in F. solani. Moreover, CA facilitated decomposition of mitochondria-specific cardiolipin (CL) into its catabolites by the catalytic action of phospholipases. 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Root rot caused by Fusarium solani is one of major postharvest diseases limiting sweet potato production. Antifungal effect and possible mode of action of cinnamaldehyde (CA) against F. solani were investigated. CA concentration of 0.075 g/L inhibited conidial viability of F. solani. CA vapor of 0.3 g/L in air completely controlled the F. solani development in sweet potatoes during storage for 10 days at 28 °C, and protected soluble sugar and starch in the flesh from depletion by the fungus. Further results demonstrated that CA induced reduction in mitochondrial membrane potential (Δψm), ROS accumulation, and cell apoptosis characterized by DNA fragmentation in F. solani. Moreover, CA facilitated decomposition of mitochondria-specific cardiolipin (CL) into its catabolites by the catalytic action of phospholipases. 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Root rot caused by Fusarium solani is one of major postharvest diseases limiting sweet potato production. Antifungal effect and possible mode of action of cinnamaldehyde (CA) against F. solani were investigated. CA concentration of 0.075 g/L inhibited conidial viability of F. solani. CA vapor of 0.3 g/L in air completely controlled the F. solani development in sweet potatoes during storage for 10 days at 28 °C, and protected soluble sugar and starch in the flesh from depletion by the fungus. Further results demonstrated that CA induced reduction in mitochondrial membrane potential (Δψm), ROS accumulation, and cell apoptosis characterized by DNA fragmentation in F. solani. Moreover, CA facilitated decomposition of mitochondria-specific cardiolipin (CL) into its catabolites by the catalytic action of phospholipases. Altogether, the results revealed a specific antifungal mechanism of CA against F. solani, and suggest that CA holds promise as a preservative for postharvest preservation of sweet potato.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>36527924</pmid><doi>10.1016/j.foodchem.2022.135213</doi><tpages>1</tpages></addata></record>
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subjects air
Antifungal
Antifungal Agents - pharmacology
antifungal properties
Apoptosis
cardiolipins
Cinnamaldehyde
conidia
DNA fragmentation
food chemistry
fungi
Fusarium
Fusarium solani
Ipomoea batatas - microbiology
mechanism of action
membrane potential
metabolites
mitochondrial membrane
Nutrients
phospholipases
Postharvest
root rot
starch
sugars
Sweet potato
sweet potatoes
vapors
viability
title Inhibitory effect of cinnamaldehyde on Fusarium solani and its application in postharvest preservation of sweet potato
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