Use of 1-Methylcyclopropene in Ornamentals: Carnations as a Model System for Understanding Mode of Action

• Published in: HortScience Vol. 43; no. 1; pp. 95 - 98
• Main Authors: Reid, M.S, Çelikel, F.G
• Format: Journal Article Conference Proceeding
• Language: English
• Published: Alexandria, VA American Society for Horticultural Science 01-02-2008
• Subjects: 1-methylcyclopropene; Agronomy. Soil science and plant productions; application rate; application timing; binding sites; Biological and medical sciences; chemical structure; corolla; cut flowers; enzyme activity; ethylene; Fundamental and applied biological sciences. Psychology; inhibitors; mechanism of action; plant growth substances; postharvest physiology; protein structure; vase life; Senescence; Temperature; flower senescence; Horticulture; Cycloalkene; Ornamental crop; Binding site; Physical environment; Modeling; System; Unsaturated compound; petal inrolling; Dicotyledones; Angiospermae; Mechanism of action; Corolla; Organic compounds; Flower; Use; Metabolic inhibitor; Dianthus caryophyllus; Caryophyllaceae; Cyclic compound; Flower crop; Spermatophyta; Models
• DOI: 10.21273/HORTSCI.43.1.95
• EISSN: 2327-9834
• ISSN: 0018-5345

The first commercial use of 1-methylcyclopropene (1-MCP) was with cut flowers and potted plants, and treatment with this compound is still the preferred strategy for protection of most ethylene-sensitive crops. Research is continuing into optimum treatment conditions and strategies for efficient application in commerce. In studies using carnation ( Dianthus caryophyllus L. ‘White Sim’) petals to determine the optimal conditions for commercial treatment, we noted some aspects of the inhibition response that were not consistent with the current competitive inhibition model of 1-MCP action. Our data are better explained by an alternative model in which 1-MCP binds to a site that is exposed during the allosteric changes that accompany the enzymatic activities of the binding site in the absence of ethylene.