surfaces can often extend storage by creating a hostile environment for nonacid-tolerant organisms ( Hobbs, 1986 ). Pao and Petracek (1997) were able to extend shelf life of peeled and cut oranges with 0.5% and 1% citric acid when fruit were stored at 4
Simona Pinnavaia, Emilio Senesi, Anne Plotto, Jan A. Narciso and Elizabeth A. Baldwin
L. Zhang, J.R. Livingstone, Y. Tarui and E. Hirasawa
CA did not survive after 20 weeks under the low-illumination conditions. In contrast, treatment with acetic acid instead of CA completely failed to suppress defoliation of the plant (data not shown). Fig. 1. Effects of citric acid in mineral nutrition
Martin P.N. Gent, Zakia D. Parrish and Jason C. White
Exudation of organic acids by roots has been implicated in uptake of minerals from soil. Three cultivars within each of two subspecies of summer squash (Cucurbita pepo ssp. ovifera D. S. Decker var. ovifera and C. pepo ssp. pepo var. pepo) were grown in the field. Plants of ssp. pepo had higher concentrations of K, P, and Zn than those of ssp. ovifera. These same cultivars were grown under P sufficient and depleted conditions in hydroponics, to measure exudation of organic acids from roots. When grown in hydroponics, tissues of ssp. ovifera had similar or higher concentrations of nutrients than ssp. pepo. Therefore, differences in tissue composition of field-grown plants are likely due to differences in nutrient uptake ability, not inherent differences in tissue composition between subspecies. Phosphorus nutrition played a significant role in exudation of organic acids into the hydroponics solution. For both subspecies, P depletion resulted in exudation of more citric and succinic acid, and less oxalic and tartaric acid. Under P depletion, ssp. pepo exuded more citric acid than ssp. ovifera. When soil was eluted with solution containing root exudates, the exudates from ssp. pepo eluted more K, Mg, Fe, and Zn than did those from ssp. ovifera. Among subspecies of C. pepo, exudation of organic acids, particularly exudation of citric acid in response to P depletion, is associated with the plant's ability to accumulate more inorganic nutrients when grown in the field.
Victor M. Gallegos-Cedillo, Juan E. Álvaro, Th. Capatos, T. Luan Hachmann, Gilda Carrasco and Miguel Urrestarazu
Si and citric acid are active substances accepted in organic farming in Europe ( DOUE, 2008 ) and the United States ( USDA Organic, 2015 ). Although blueberry is a clearly acidophilic plant, there is no possibility of using nitric or other inorganic
Iftikhar Ahmad and John M. Dole
metabolic processes and continued flower opening during vase life. Among acidifiers, citric acid is the most common compound and is used to lower the pH of the preservative solutions and control microbial proliferation. Citric acid has been found effective
Hisashi Kato-Noguchi and Alley E. Watada
Avi Sadka, Bracha Artzi, Lydia Cohen, Esther Dahan, David Hasdai, Eliezer Tagari and Yair Erner
Arsenic compounds generate diverse effects in all living organisms. In citrus (Citrus L. sp.), they reduce acidity and improve fruit quality by unknown mechanisms. The major organic acid in citrus fruit is citric acid, which begins accumulating early in fruit development, reaches a peak in middle-sized fruit and then, in most species, declines as the fruit matures. In an attempt to understand the basis of the effect of arsenite, it was applied to `Minneola' tangelo (Citrus paradisi Macf. × C. reticulata Blanco) ≈6 weeks postanthesis, and a detailed analysis of total titratable acidity and citric acid concentration was performed throughout fruit growth. Within 35 days after arsenite application, total acid content and citrate concentration were slightly lower compared with the controls, and this difference persisted throughout fruit development. The concentrations of other organic acids were not reduced by the treatment. Sodium arsenite reduced the citrate concentration in `Eurieka' lemon callus [Citrus limon (L.) Burm.] also, without affecting tissue growth. Extractable activity of citrate synthase in treated fruit was inhibited within 1 day following arsenite spray, but recovered to a normal level a few days later. In contrast, gene expression was remarkably induced 1 day following treatment, which might explain the recovery in enzyme activity. Data suggest that reduction in acid accumulation may not be related to the initial inhibition of citrate synthase activity.
Yosef Burger, Uzi Sa'ar, Asaph Distelfeld, Nurit Katzir, Yelena Yeselson, Shmuel Shen and Arthur A. Schaffer
The sweet cultivars of Cucumis melo are characterized by high sucrose levels, together with low acid levels in the mature fruit flesh. The trait of high sugar accumulation in C. melo fruit is determined by a single recessive gene, suc. High acid content, conferred by a single dominant gene, So, is found only in C. melo varieties that do not accumulate high levels of sugar and are used for nondessert purposes. We combined the genetic traits of high acid content (low pH) and high sugar levels by crossing the nonsweet, high acid C. melo var. flexuosus, `Faqqous' (So/So, Suc/Suc), with high sugar, low acid C. melo genotypes (so/so, suc/suc) and generating the recombinant genotype So/—, suc/suc. Segregating F2 populations derived from the cross between `Faqqous' and a standard high sugar, low acid line showed that the traits of high sugar and low pH were inherited independently of each other. The accumulation of acid and sugar in the developing fruit of a recombinant high acid, high sugar breeding line, A6, were also temporally independent, with acid accumulation preceding the rise in sucrose levels. The low pH of A6 was correlated with the developmental increase in titratable acidity and particularly of citric acid levels. The combination of increased acidity and high sugar provides the melons with a unique taste due to a sugar to acid ratio not present in sweet C. melo cultivars. These results are discussed in terms of the evolution under domestication of C. melo.
Rafael Alique, José P. Zamorano, Ma Luisa Calvo, Carmen Merodio and José L. De la Plaza
`Fino de Jete' cherimoya fruit were stored at 20, 10, 8, or 6C, 80% relative humidity. Two rises of CO2 production and an ethylene rise following the first peak of respiration were obtained in fruit held at 20C. The ripe stage coincided with the onset of the second respiratory rise. Soluble sugar and organic acid concentration were maximal, and flesh firmness was 18 N in ripe fruit. Lower temperature reduced respiration rate and ethylene production; however, some stimulation of ethylene synthesis was observed at 10C. Cherimoyas ripened to edible condition during 6 days at 10C, but fruit maintained at 8C for up to 12 days required transfer to 20C to ripen properly. Our results suggest that high increases in CO2 are not sufficient to complete cherimoya fruit ripening without the concurrent rise in ethylene production. Citric acid accumulation, inhibition of ethylene synthesis, and reduced accumulation of sucrose were observed during storage at 6C. Removal to 20C after 12 days at 6C resulted in no ripening, almost complete inhibition of ethylene synthesis, and severe skin browning. Thus, 8C is the lowest tolerable temperature for prolonged cold storage of cherimoya `Fino de Jete'. Fruit can be held at 8C for up to 12 days without damage from chilling injury.
A. Belakbir, J.M. Ruiz and L. Romero
To test the effectiveness of different bioregulators in enhancing bell pepper (Capsicum annuum L.) yield and fruit quality, the commercial bioregulators CCC, NAA, GA3, and Biozyme® were sprayed on plants at flower initiation, followed by two additional applications at 30-day intervals. Biozyme produced a significant increase in total yield but ≈40% of the fruit were not marketable. Treatment with NAA produced the highest yield of marketable fruit. Treatments did not affect fruit firmness compared to the control. Gibberellic acid increased fruit ascorbic acid and citric acid concentrations and Biozyme, GA3, and CCC increased fruit soluble solids content. Biozyme treatment increased fruit fructose, sucrose, carotenoid, and lycopene concentration. Treatments had no effect on fruit calcium concentration or pH. Chemical names used: chlormequat chloride (CCC); naphthaleneacetic acid (NAA), gibberellic acid (GA3); GA3 + IAA (indoIe-3-acetic acid) + zeatine + micronutrients (Biozyme®).