Abstract:Brief exposure of etiolated pea (Pisum sativum cv. Alaska) seedlings to red light enhances subsequent development of geotropic curvature of the stem. Both this response and inhibition of ethylene production by red light become maximal 8 hours after illumination. Very low concentrations of applied ethylene inhibit development of geotropic curvature, whereas hypobaric treatment enhances geotropic sensitivity by removing endogenous ethylene. Increased geotropic sensitivity after illumination is accompanied by inc… Show more
“…It has recently been reported that light inhibits ethylene production in segments of green oat leaves but not in etiolated leaves (7). The experiments dealing with the effect of monochromatic light on plant tissues suggest an inhibitory effect of red light as compared to darkness on the rate of ethylene production (8,11,12,18). However, Janes et al (10) found no effect of red light on the rate of ethylene production in the intact lettuce seedlings.…”
High CO2 concentration (0.5%) increased the rate of ethylene production, measured in a continuous flow system, in intact sunflower (Helianthus auwus L.) plants. However, the rate of ethylene production subsided to near control levels after approximately 24 hours. The effect of high CO2 could only be observed in light. Although high CO2 concentration had no effect on the rate of ethylene production in darkness, prolonged exposure (approximately 16 hours) of plants to high CO2 in the dark prevented the increase in ethylene production when the plants were exposed to light and high C02.The interactions between CO2 and ethylene are of interest both for their role in the basic understanding of ethylene action in plants and for their use in preservation of produce, flowers, and fruits, etc. Little work has been done to study the effect of CO2 on the rate of ethylene production in plants. Aharoni and Lieberman (2) have reported recently that CO2 stimulates the ethylene production of tobacco leaf discs senescing in the dark. In an earlier report by Imaseki et al. (9), it was shown that the removal of CO2 from the atmosphere surrounding sweet potato tuber sections infected by black rot fungus decreased the rate of ethylene production. CO2 has been reported either to inhibit (15,20) or to have no effect (4) on ethylene production in ripening fruit but the results are difficult to interpret because of the possible effects of ethylene on its own production in these tissues (13).In most of the above cases, the experiments were done with excised plant parts sealed in closed systems. Numerous possible sources of error inherent in such techniques have already been pointed out (3,6). Further, with such systems it is not feasible to study the exact relationship between CO2 concentration and the rate of ethylene production on a temporal basis since the tissue is sealed for a considerable duration before sufficient amount of ethylene can accumulate to permit accurate analysis.Techniques have been developed in our laboratory that allow measurement of rate of ethylene production by the intact shoots of plants in a continuous flow system (3,6). Using these techniques, we have recently reported that an increase in the concentration of CO2 in the atmosphere surrounding the sunflower plants increased the rate of ethylene production (5). The change in rate of ethylene production was evident within the first few minutes of the carbon dioxide treatment. All the experiments reported in that paper were done in continuous light.The present study was undertaken to further explore the rela-'Financial assistance from the Natural Sciences and Engineering Re- MATERIALS AND METHODS The seedlings of sunflower (Helianthus annus L.) were started in trays containing vermiculite, in a constantly lit controlled environment growth chamber. The temperature in the growth chamber was maintained at 27 ± 1°C and the RH at 75%. After 7 d, the seedlings were transplanted to individual pots containing sand:vermiculite:peat moss (1:1:1).A 2-week-old plant ...
“…It has recently been reported that light inhibits ethylene production in segments of green oat leaves but not in etiolated leaves (7). The experiments dealing with the effect of monochromatic light on plant tissues suggest an inhibitory effect of red light as compared to darkness on the rate of ethylene production (8,11,12,18). However, Janes et al (10) found no effect of red light on the rate of ethylene production in the intact lettuce seedlings.…”
High CO2 concentration (0.5%) increased the rate of ethylene production, measured in a continuous flow system, in intact sunflower (Helianthus auwus L.) plants. However, the rate of ethylene production subsided to near control levels after approximately 24 hours. The effect of high CO2 could only be observed in light. Although high CO2 concentration had no effect on the rate of ethylene production in darkness, prolonged exposure (approximately 16 hours) of plants to high CO2 in the dark prevented the increase in ethylene production when the plants were exposed to light and high C02.The interactions between CO2 and ethylene are of interest both for their role in the basic understanding of ethylene action in plants and for their use in preservation of produce, flowers, and fruits, etc. Little work has been done to study the effect of CO2 on the rate of ethylene production in plants. Aharoni and Lieberman (2) have reported recently that CO2 stimulates the ethylene production of tobacco leaf discs senescing in the dark. In an earlier report by Imaseki et al. (9), it was shown that the removal of CO2 from the atmosphere surrounding sweet potato tuber sections infected by black rot fungus decreased the rate of ethylene production. CO2 has been reported either to inhibit (15,20) or to have no effect (4) on ethylene production in ripening fruit but the results are difficult to interpret because of the possible effects of ethylene on its own production in these tissues (13).In most of the above cases, the experiments were done with excised plant parts sealed in closed systems. Numerous possible sources of error inherent in such techniques have already been pointed out (3,6). Further, with such systems it is not feasible to study the exact relationship between CO2 concentration and the rate of ethylene production on a temporal basis since the tissue is sealed for a considerable duration before sufficient amount of ethylene can accumulate to permit accurate analysis.Techniques have been developed in our laboratory that allow measurement of rate of ethylene production by the intact shoots of plants in a continuous flow system (3,6). Using these techniques, we have recently reported that an increase in the concentration of CO2 in the atmosphere surrounding the sunflower plants increased the rate of ethylene production (5). The change in rate of ethylene production was evident within the first few minutes of the carbon dioxide treatment. All the experiments reported in that paper were done in continuous light.The present study was undertaken to further explore the rela-'Financial assistance from the Natural Sciences and Engineering Re- MATERIALS AND METHODS The seedlings of sunflower (Helianthus annus L.) were started in trays containing vermiculite, in a constantly lit controlled environment growth chamber. The temperature in the growth chamber was maintained at 27 ± 1°C and the RH at 75%. After 7 d, the seedlings were transplanted to individual pots containing sand:vermiculite:peat moss (1:1:1).A 2-week-old plant ...
“…Although most reports related that white or red light inhibited ethylene production (5,8,17,19), one report observed that red light promoted ethylene production in the shoot of pea seedling (16). It (2,5,9). Possible involvement of phytochrome in inhibiting ethylene formation in these etiolated hook region by promoting ACC malonylation is currently under investigation.…”
Section: Methodsmentioning
confidence: 99%
“…However, light did not cause any significant increase in the extractable ACC-malonyltransferase activity. A number of reports have shown that light regulated ethylene production which in turn modified plant growth (4,5,9,18,19 m-2 s-'), red light or far-red light. The red and far-red light sources were from a projector equipped with a 650 nm and 730 nm filter, respectively.…”
Section: Abstracitmentioning
confidence: 99%
“…A number of reports have shown that light regulated ethylene production which in turn modified plant growth (4,5,9,18,19). Depending on the tissues and conditions employed, light promoted (16,18) and inhibited (2)(3)(4)(5)(6)(7)(8)(9)(10)20) ethylene production.…”
mentioning
confidence: 99%
“…Depending on the tissues and conditions employed, light promoted (16,18) and inhibited (2)(3)(4)(5)(6)(7)(8)(9)(10)20) ethylene production. Since the plant tissues used in these earlier studies normally contained low level of endogenous ACC,3 the effects of light on the changes in ACC levels in relation to ethylene production were not examined.…”
ABSTRACITWhile light-grown wheat leaves produced ethylene at a low rate of <0.1 nanomoles per gram per hour and contained 1-aminocyclopropane-1-carboxylic acid (ACC) at low levels of <2.5 nanomoles per gram, etiolated wheat leaves produced ethylene at a rate of 2 nanomoles per gram per hour and accumulated concentrations of ACC at levels of 40 nanomoles per gram. Upon illumination of 8-day-old etiolated wheat seedlings with white light, the ethylene production rate increased initially, due to the activation of ethylene-forming activity, but subsequently declined to a low level (0.1 nanomoles per gram per hour) at the end of the 6-hour illumination. This light-induced decline in ethylene production rate resulted from a decline (more than 35 nanomoles per gram) in ACC level, which was accompanied by a corresponding increase in 1-malonylamino)cyclopropane-l-carboxylic acid content. These data indicate that illumination promoted ACC malonylation, resulting in reduced ACC level and consequently reduced ethylene production. However, light did not cause any significant increase in the extractable ACC-malonyltransferase activity. A number of reports have shown that light regulated ethylene production which in turn modified plant growth (4,5,9,18,19 m-2 s-'), red light or far-red light. The red and far-red light sources were from a projector equipped with a 650 nm and 730 nm filter, respectively. For the red light treatment, tubes were exposed to red light with intensity of 12 ,uE m-2 s-' for 5 min; for far-red treatment, tubes were exposed to far-red light with intensity of0.85 uE m-2 s-' for 10 min. Tubes were returned to darkness for the subsequent measurements.Determination of Ethylene Production. Leaf segments in tube were flushed with air and sealed with a rubber serum cap after each sampling. At indicated time intervals, 1 ml gas samples were drawn from the tubes and injected into a gas chromatograph equipped with an alumina column and a FID detector at 90°C.Determination of ACC and MACC. Samples were extracted twice with 5 ml of 80% ethanol at 55°C for 10 min. The ethanol extract was evaporated under vacuum at the same temperature. The residue was dissolved in 2 ml water and the pigment was removed by the addition of 0.5 ml chloroform. ACC content in 0.2 ml aliquots of the aqueous solutions was determined according to the method of Lizada and Yang (14). The quantitation of MACC in the extract was carried out first by passing 0.2 ml extract through a Dowex 50 (H+-form) resin column with 0.5 ml bed volume to removed ACC. The effluent solution containing MACC was hydrolyzed in 2 N HCl for 3 h as described previously (13). Following neuralization with NaOH, the resulting hydrolysate was assayed for ACC content, which was taken as the amount of MACC in the extract.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.