We investigated the role of nano-silver (NAg) and the bacterial strain Enterobacter cloacae in increasing the vase life of cut carnation flowers 'Omea.' NAg treatment extended vase life of the flowers by increasing relative fresh weight, antioxidant activities, and expression level of the cysteine proteinase inhibitor gene (DcCPi), and by suppressing bacterial blockage in stem segments, ethylen...

The main object of this study is to investigate the effect of plant growth regulators on the prolongation of vase life of two kinds of cut carnation under normal and ethylene. Carnation is one of the most popular flowers that has a short life due to its sensitivity to ethylene. Also, the effect of plant growth regulators on several physiological traits under ethylene stress and normal condition...

The phytohormone ethylene is essential for senescence in many fruits and flowers. In the biosynthesis of ethylene in plants, the conversion of S-adenosyl methionine (SAM) to 1-aminocyclopropane1-carboxylic acid (ACC) and the conversion of ACC to ethylene are catalyzed by ACC synthase (ACS) and ACC oxidase (ACO), respectively (Adams and Yang, 1979). Using a cDNA clone representing carnation ACO ...

Wu, M.J., Zacarias, L. and Reid. M.S., 1991. Variation in the senescence of carnation (Dianthus cao,ophyllus L.) cultivars. II. Comparison o f sensitivity to exogenous ethylene and of ethylene binding. Scientia Hortic., 48:109-116. Flowers o f the 'Sandra' and "Chinera" cultivars o f carnation (Dianthus caryophyllus L. ) last about twice as long ( 14 days) as those o f 'Whi te Sim' cultivar (7 ...

The effect of leaf extracts of Psidium guajava and Piper betle on prolonging vase life of cut carnation flowers was studied. "Carola" and "Pallas Orange" carnation flowers, at bud stage, were pulsed 24 hours with a floral preservative. Then, flowers were placed in a vase solution containing sprite and a "germicide" (leaf extracts of P. guajava and P. betle, 8-HQC, or a copper coin). Flowers tre...

Doubled haploids of carnation (Dianthus caryophyllus L.) were obtained by pseudofertilized ovule culture. Emasculated ̄ower buds of carnation were pollinated with pollen inactivated by Xray irradiation. After 2±3 weeks, the ovaries were explanted and were cultured on solid MS medium containing 2 mM NAA, 2 mM BAP and 6% sucrose. Regenerated plants(R0) were morphologically different from the moth...