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1.
Plant Cell Environ ; 39(10): 2185-97, 2016 10.
Artículo en Inglés | MEDLINE | ID: mdl-27351898

RESUMEN

Physiological, biochemical and morpho-anatomical traits that determine the phenotypic plasticity of plants under drought were tested in two Arundinoideae with contrasting habitats, growth traits and metabolism: the fast-growing Arundo donax, which also is a strong isoprene emitter, and the slow-growing Hakonechloa macra that does not invest on isoprene biosynthesis. In control conditions, A. donax displayed not only higher photosynthesis but also higher concentration of carotenoids and lower phenylpropanoid content than H. macra. In drought-stressed plants, photosynthesis was similarly inhibited in both species, but substantially recovered only in A. donax after rewatering. Decline of photochemical and biochemical parameters, increased concentration of CO2 inside leaves, and impairment of chloroplast ultrastructure were only observed in H. macra indicating damage of photosynthetic machinery under drought. It is suggested that volatile and non-volatile isoprenoids produced by A. donax efficiently preserve the chloroplasts from transient drought damage, while H. macra invests on phenylpropanoids that are less efficient in preserving photosynthesis but likely offer better antioxidant protection under prolonged stress.


Asunto(s)
Butadienos/metabolismo , Ácidos Cumáricos/metabolismo , Sequías , Ecosistema , Hemiterpenos/metabolismo , Pentanos/metabolismo , Poaceae/metabolismo , Ácido Abscísico/metabolismo , Apigenina/metabolismo , Carotenoides/metabolismo , Clorofila/metabolismo , Cloroplastos/ultraestructura , Deshidratación/metabolismo , Luteolina/metabolismo , Fotosíntesis , Poaceae/crecimiento & desarrollo , Poaceae/ultraestructura , Agua/metabolismo
2.
Plants (Basel) ; 12(11)2023 May 27.
Artículo en Inglés | MEDLINE | ID: mdl-37299104

RESUMEN

In recent years, light emitting diodes (LEDs), due to their low energy consumption, low heat emission and specific wavelength irradiation, have become an alternative to fluorescent lamps (FLs) in plant tissue culture. The aim of this study was to investigate the effects of various LED light sources on the in vitro growth and rooting of plum rootstock Saint Julien (Prunus domestica subsp. insititia). The test plantlets were cultivated under a Philips GreenPower LEDs research module illumination system with four spectral regions: white (W), red (R), blue (B) and mixed (W:R:B:far-red = 1:1:1:1). The control plantlets were cultivated under fluorescent lamps (FL) and the photosynthetic photon flux density (PPFD) of all treatments was set at 87 ± 7.5 µmol m-2 s-1. The effect of light source on the selected physiological, biochemical and growth parameters of plantlets was monitored. Additionally, microscopic observations of leaf anatomy, leaf morphometric parameters and stomata characteristics were carried out. The results showed that the multiplication index (MI) varied from 8.3 (B) to 16.3 (R). The MI of plantlets grown under mixed light (WBR) was 9, lower compared to the control (FL) and white light (W), being 12.7 and 10.7, respectively. In addition, a mixed light (WBR) favored plantlets' stem growth and biomass accumulation at the multiplication stage. Considering these three indicators, we could conclude that under the mixed light, the microplants were of better quality and therefore mixed light (WBR) was more suitable during the multiplication phase. A reduction in both net photosynthesis rate and stomatal conductance in the leaves of plants grown under B were observed. The quantum yield (Yield = FV/FM), which represents the potential photochemical activity of PS II, ranged from 0.805 to 0.831 and corresponded to the typical photochemical activity (0.750-0.830) in the leaves of unstressed healthy plants. The red light had a beneficial effect on the rooting of plum plants; the rooting was over 98%, significantly higher than for the control (FL, 68%) and the mixed light (WBR, 19%). In conclusion, the mixed light (WBR) turned out to be the best choice during the multiplication phase and the red LED light was more suitable during the rooting stage.

3.
J Plant Physiol ; 169(10): 955-64, 2012 Jul 01.
Artículo en Inglés | MEDLINE | ID: mdl-22575055

RESUMEN

Extreme low temperatures cause plants multiple stresses, among which oxidative stress is presumed to be the major component affecting the resultant recovery rate. Plants of Hypericum perforatum L., which are known especially for the photodynamic activities of hypericins capable of producing reactive oxygen species under exposure to visible light, were observed to display a substantial increase and persistence in active oxygen production at least two months after recovery from cryogenic treatment. In an effort to uncover the causative mechanism, the individual contributions of wounding during explant isolation, dehydration and cold were examined by means of antioxidant profiling. The investigation revealed activation of genes coding for enzymatic antioxidant catalase and superoxide dismutase at both the transcript and protein levels. Interestingly, plants responded more to wounding than to either low-temperature associated stressor, presumably due to tissue damage. Furthermore, superoxide dismutase zymograms showed the Cu/Zn isoforms as the most responsive, directing the ROS production particularly to chloroplasts. Transmission electron microscopy revealed chloroplasts as damaged structures with substantial thylakoid ruptures.


Asunto(s)
Antioxidantes/metabolismo , Frío , Hypericum/fisiología , Estrés Oxidativo , 3,3'-Diaminobencidina/metabolismo , Catalasa/genética , Catalasa/metabolismo , Cloroplastos/ultraestructura , Criopreservación , Fluoresceínas/metabolismo , Regulación de la Expresión Génica de las Plantas , Genotipo , Peróxido de Hidrógeno/metabolismo , Hypericum/enzimología , Hypericum/genética , Hypericum/ultraestructura , Isoenzimas/genética , Isoenzimas/metabolismo , Estrés Oxidativo/genética , Células Vegetales/ultraestructura , Brotes de la Planta/enzimología , Brotes de la Planta/genética , Especies Reactivas de Oxígeno/metabolismo , Coloración y Etiquetado , Estrés Fisiológico/genética , Superóxido Dismutasa/genética , Superóxido Dismutasa/metabolismo , Factores de Tiempo
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