Amelioration of chilling stress by triadimefon in cucumber seedlings

Cucumber (Cucumis satvus L.) seeds were imbibed in distilled water (control) and 10 mg l^–1 triadimefon (TDM) for 10 h and then grown in a plant growth chamber with a light/dark temperature of 28/20 °C and a photoperiod of 14 h with a light intensity of 60 µmol m^–2 s^–1. 14-day-old seedlings were exposed to chilling stress with a light/dark temperature of 6/3 °C for 4 d. TDM improved the growth rate of cucumber seedling subjected to chilling stress and increased photosynthetic pigments contents and relative water content compared with the control at the end of chilling stress. Chilling stress decreased protein content and the activities of SOD, CAT and POD, but it increased proline, H₂O₂ and MDA accumulation, and relative electrical conductivity. TDM ameliorated the injury caused by chilling stress by preventing decreases in protein content and the activities of SOD, CAT and POD and by inhibiting increases in proline, H₂O₂ and MDA contents, and relative electrical conductivity, which suggested that TDM ameliorated the negative effect of chilling stress.     

A double enhancement of greening in the cotyledons of cucumber seedlings by excision and red light

Cotyledons excised without the hypocotyl hook from 6-day-old etiolated cucumber ( Cucumis sativus L. var. Elem) seedlings accumulated a significantly higher amount of chlorophyll than cotyledons excised with hooks or intact cotyledons. It was found that maximum ehancement of greening was achieved after 2 h of dark incubation following excision. Pretreatments with red light effected an additive rise in chlorophyll level in subsequent white light after a dark incubation, suggesting that the effects of excision and phytochrome on greening act independently. Etiolated seedlings were variously dissected before greening and it was found that enhancement occurred only when cotyledons were excised at the level of the hypocotyl hook or above it. Similar results were obtained when the dissected plants were pre-treated with red light.     

Induction of chilling tolerance in cucumber (Cucumis sativus) seedlings by endogenous and applied ethanol

Five-day-old etiolated cucumber ( Cucumis sativus L.) seedlings cv. Marketmore held at 2°C for 72 h developed chilling injury, resulting in desiccation and collapse of the hypocotyl tissue and eventual plant death. Hypoxia-induced accumulation of ethanol and acetaldehyde led to tolerance of subsequent chilling, as evidenced by continued hypocotyl growth and freedom from injury. Attenuated accumulation of volatiles by applied bisulfite reduced the development of hypoxia-induced chilling tolerance in seedlings. In seedlings held in normoxia cold tolerance was induced by applied ethanol vapors, whereas acetaldehyde had a marginal effect, suggesting that hypoxia-induced cold tolerance may arise from the accumulation and activity of ethanol. Cold tolerance was also induced by exposure of seedlings to volatile anesthetics including n -propanol, n -butanol, chloroform and halothane, suggesting that ethanol activity may result from fluidization of membrane lipids. This view is consistent with results which showed that ethanol activity was not associated with lipid metabolism. However, development of cold tolerance in ethanol-enriched tissues was time dependent, indicating that ethanol activity probably also entails biosynthetic event(s).     

高温胁迫下外源褪黑素对黄瓜幼苗活性氧代谢的影响

以黄瓜品种‘津春4号’为试材,用叶面喷施的方法,研究了高温胁迫条件下外源褪黑素(melatonin,MT)对黄瓜幼苗活性氧（ROS）代谢的影响.结果表明：外源MT能显著降低高温胁迫下黄瓜叶片超氧阴离子自由基（O₂^-.）产生速率、过氧化氢（H₂O₂）含量、电解质漏渗率（relative electric conductivity, REC）及丙二醛(MDA)含量,增强黄瓜幼苗叶片中超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、过氧化物酶(POD)活性,提高抗坏血酸（AsA）、谷胱甘肽（GSH）及可溶性蛋白质含量.说明MT预处理能抑制高温胁迫条件下黄瓜幼苗体内ROS的产生,提高抗氧化酶系的活性及抗氧化物质的含量,降低膜质过氧化水平,保护脂膜的完整性,减少电解质的外渗,减轻高温胁迫对幼苗造成的伤害,提高幼苗抗高温胁迫的能力.     

Homeostasis in cucumber plants during low temperature stress

Shoots, roots and whole plants of Cucumis sativus L. cv. Inspektowy Warszawski were subjected to different temperatures. The magnitude and direction of alterations of growth depended on the organ that was submitted to stress conditions. Changes in soluble protein level in leaves and in roots were inversely correlated with changes of total organic nitrogen level in both organs. In spite of differentiated temperature conditions between plant organs, the allometric coefficients and the ratio between maintenance respiration in shoot and in roots remained constant. Such constancy may be treated as an indicator of homeostasis of the whole-plant system. The results point to the importance of both shoot and roots in the response of the plant to temperature stress.     

Biosynthesis of stress ethylene in soybean seedlings: Similarities to endogenous ethylene biosynthesis

The similarity of stress ethylene biosynthesis in whole plants to endogenous ethylene biosynthesis was investigated using two inhibitors of ethylene biosynthesis, aminoethoxyvinylglycine (AVG) and cobalt chloride (Co²⁺); and the intermediates, methionine, S -adenosylmethionine (SAM), and 1-aminocyclopropane-1-carboxylic acid (ACC), of basal ethylene biosynthesis. Stress ethylene production induced by ozone, cadmium, or 2,4-dichlorophenoxyacetic acid was inhibited in hydroponically-grown soybean seedlings in a concentration-dependent manner by both AVG and CO²⁺. The ethylene intermediates evoked responses in intact seedlings similar to that described for endogenous ethylene production in isolated vegetative tissue. The addition of SAM to the hydroponic system relieved AVG inhibition of stress ethylene production. Feeding ACC to the seedlings resulted in increased ethylene production independent of stress application or prior AVG inhibition. Cobalt inhibition of stress ethylene production was relieved by increasing concentrations of ACC. A short lag period of 12–18 min was observed in stress ethylene production following a 30-min ozone exposure. Addition of cycloheximide partially inhibited ozone-induced ethylene production.
These results suggest a common pathway in whole plants for stress ethylene production and endogenous ethylene biosynthesis.     

Phytochrome-mediated control of respiratory activities of mitochondria in cotyledons of dark-grown cucumber seedlings

Mitochondria isolated from cotyledons of dark-grown cucumber ( Cucumber sativus L., cv. Shimotsuki-Aonaga) seedlings after illumination with continuous far-red light showed an increased capacity for oxidation of malate or α-ketoglutarate, as compared with those from cotyledons of non-illuminated seedlings. This increase is supposed to be caused by phytochrome action (high irradiance response). Exogenous NAD⁺ had no effect on the rate of the oxidation of α-ketoglutarate or malate by mitochondria isolated from far-red light-treated cotyledons, but it enhanced the oxidation rate of mitochondria from control cotyledons to the level of mitochondria from light-treated ones. The NAD (NAD⁺+ NADH) content was higher in mitochondria isolated from continuously far-red light-treated cotyledons than in mitochondria from controls. The NAD content was also increased by the treatment with a red light pulse and this response was reversed by a subsequent far-red light pulse. It is proposed that phytochrome controls respiratory activities of cucumber mitochondria by changing the size of the NAD pool in the mitochondria.     

Photooxidative damage to the photosynthetic apparatus during chilling

Short periods of chilling in the presence of light (up to 6 h: 1°C; 270 W/m²) decreased the subsequent apparent photosynthesis and chlorophyll fluorescence of leaf discs of Cucumis sativus L. cv. Kleine Groene Scherpe. The extent of the injury depended on the duration of the chilling pretreatment. After 6 h the subsequent apparent photosynthesis even reached a negative value, and it increased only slightly during the next 2 1/2 h. The decrease of apparent photosynthesis was not a consequence of increased dark respiration but was of photooxidative origin since the presence of both light and oxygen was required. Preincubation in the light for 2 h at 20°C sensitized leaf discs to subsequent photooxidation during chilling. Prompt and delayed chlorophyll fluorescence decreased simultaneously after chilling and light treatment. The corresponding decrease of photosynthesis and chlorophyll fluorescence is discussed in relation to primary photooxidative damage to the photosystems in the chloroplast membrane.     

Phytochrome-mediated development of glycine oxidation by mitochondria in cucumber cotyledons

The development of glycine oxidation activity in mitochondria in etiolated cucumber ( Cucumis sativus L., cv. Shinfushinari) cotyledons is regulated by phytochrome. This conclusion is based on two lines of evidence. 1. The oxidation activity was increased by continuous illumination of far-red light. 2. It was also increased by brief red light pulses, the effect of which was reversed by brief far-red light pulses. The light-induced increase in glycine oxidation and in glycine decarboxylase (EC 2.1.2.10) activity in the cotyledons was inhibited by cycloheximide, but not by chloramphenicol. While glycine oxidation activity continued to increase during light-illumination for 20 h, malate oxidation activity increased for 6 to 8 h after illumination and decreased thereafter. This transient increase in the activity of malate oxidation was also induced by red light pulses and the effect of the red light was reversed by far-red light pulses.     

Uptake and translocation of calcium in cucumber

Uptake and translocation of Ca²⁺(⁴⁵Ca) were compared with water translocation in 12-day old intact plants and excised roots of cucumber ( Cucumis sativus L. var. Cilla), which had been cultivated in nutrient solution. No immediate reduction of Ca²⁺ uptake was found when water translocation was reduced by excision of the shoot. In the presence of 2,4-dinitrophenol Ca²⁺ translocation was reduced in the intact plants while water translocation was unchanged. It is suggested that regulation of Ca²⁺ uptake is primarily achieved in the root. The DNP-sensitive mechanism of Ca²⁺ uptake was associated with the root and probably represented transport through the endodermis into the stele.     

Responses of ethylene biosynthesis to saline stress in seedlings of eight plant species

The effect of salinity (100 mM NaCl) on ethylene metabolism in the early phase of vegetative development of several plant species has been investigated. The effects of saline treatment on shoot and root growth, ranged in sensitivity with respect to species: pepper (Capsicum annum L. cv Pairal) > tomato (Lycopersicon esculentum Mill. cv Malpica) > broccoli (Brassica oleraceae L. var. Italica Plenk. cv Marathon F1) ≅ lettuce (Lactuca sativa var. longifolia Lam. cv Inverna) ≅ melon (Cucumis melo L. cv Ruano F1, Roche type) > bean (Phaseolus vulgaris L. cv. Gator Green 15) ≅ spinach (Spinacia oleracea L. cv Boeing) > beetroot (Beta vulgaris L. var. crassa (Alef.) J. Helm. cv Detroit). After saline treatment, ethylene production increased 4.2-fold in pepper shoots. Significant increases were also found in shoots of tomato, broccoli and bean. In contrast, salinity decreased shoot ethylene production rate in melon, spinach, and beetroot. In roots, the general effect of salinity was a decrease in ethylene production, especially in broccoli and bean, except in tomato root, in which a sharp increase in ethylene production occurred. In general, saline treatment increased total ACC concentration in both shoot and root in most of the plant species examined, which was related to plant sensitivity to salinity. For example, pepper shoot was the most sensitive to saline treatment, showing the highest fresh weight inhibition and the highest increase in total ACC concentration (8.5-fold), while, beetroot was less affected by salinity and showed no effect on total ACC concentration in response to saline treatment.     

Role of thermal dissipation in the photoprotection in cucumber plants after exposure to a chill stress

Experiments were carried out to investigate the changes in CO₂ assimilation, photon allocation, and photosynthetic electron flux in leaves of cucumber (Cucumis sativus L.) plants after chilling stress. Chilling significantly decreased CO₂ assimilation, the energy flux via linear electron transport (J _PS2) and non-constitutive thermal dissipation (J _NPQ) but increased fluorescence and constitutive thermal dissipation (J _f,D) in chilling-sensitive genotype Jinyan No. 4. In contrast, chilling had little effects on J _NPQ and J _f,D although CO₂ assimilation and J _PS2 were inhibited in chilling-tolerant genotype Jinchun No. 3. In parallel with the reduction in J _PS2, electron flux to oxygenation and carboxylation by ribulose-1,5-bisphosphate carboxylase/oxygenase all significantly decreased while electron flux to O₂ significantly increased, especially in chilling-sensitive genotype. Thermal and fluorescence dissipation were the main energy dissipation pathways whilst water-water cycle was an important electron sink when photosynthetic carbon reduction was suppressed after chilling. Chilling sensitivity of the photosynthetic apparatus was related to the operation of different photoprotection mechanisms.     

Modulation of enzyme activities and expression of genes related to primary and secondary metabolism in response to UV-B stress in cucumber (Cucumis sativus L.)

Abstract

Exposure to UV-B at ambient or enhanced levels is known to trigger a variety of responses in all living organisms, including higher plants. Here we show that in Cucumis sativus L. UV-B radiation affects enzyme activity of key oxydative pentose phosphate pathway (OPPP) enzymes glucose-6-phosphate dehydrogenase (G6P-DH) and 6-phosphogluconate dehydrogenase (6-PGlu-DH), of key phenolic compounds enzyme phenylalanine ammonia lyase (PAL) as well as erythrose-4-phosphate, tryptophan and tyrosine levels. Furthermore, we found an increased activity of antioxidant enzymes such as peroxidase (POX) and catalase (CAT) in treated plants, with respect to the controls. In order to confirm the biochemical results, we isolated total RNA from both controls and UV-B treated plants to be used for gene expression analysis. We demonstrated that UV-B increases the gene expression level of peroxidase (POX), catalase (CAT) and phenylalanine ammonia lyase (PAL). Finally, our results are useful for understanding protective strategies against UV-B radiation and for elucidating what components are involved in stress-induced signals within the plant.     

外源硝酸钙对盐胁迫下黄瓜幼苗叶片抗氧化系统及膜质子泵活性的影响

采用营养液水培法,以较耐盐黄瓜品种"新泰密刺"为试验材料,研究了叶面喷施硝酸钙对盐胁迫(NaCl65mmol·L-1)下黄瓜幼苗活性氧、谷胱甘肽-抗坏血酸循环(GluAsA)中抗氧化酶和抗氧化物质及膜质子泵活性的影响。结果表明:叶面喷施硝酸钙能够显著降低盐胁迫下黄瓜幼苗叶片超氧阴离子(O.2-)产生速率和丙二醛(MDA)含量;显著提高盐胁迫下黄瓜幼苗叶片抗坏血酸过氧化物酶(APX)和脱氢抗坏血酸还原酶(DHAR)等酶活性、抗氧化物质抗坏血酸(AsA)含量、AsA/DHA和GSH/GSSG比值及质膜和液泡膜H+-ATPase和H+-PPase活性。表明外源硝酸钙通过提高Glu-AsA抗氧化系统和膜质子泵活性,降低活性氧对叶片的伤害,增强了植株抗氧化能力和对离子的区域化,进而提高植株盐胁迫耐性。     

Photomorphogenic effects of UV-B radiation on hypocotyl elongation in wild type and stable-phytochrome-deficient mutant seedlings of cucumber

Hypocotyl elongation responses to ultraviolet-B (UV-B) radiation were investigated in glasshouse studies of de-etiolated seedlings of a long-hypocotyl mutant ( lh ) of cucumber ( Cucumis sativus L.) deficient in stable phytochrome, its near isogenic wild type (WT), and a commercial cucumber hybrid (cv. Burpless). A single 6- or 8-h exposure to UV-B applied against a background of white light inhibited hypocotyl elongation rate by ca 50% in lh and WT seedlings. This effect was not accompanied by a reduction in cotyledon area expansion or dry matter accumulation. Plants recovered rapidly from inhibition and it was possible to stimulate hypocotyl elongation in plants exposed to UV-B by application of gibberellic acid. In all genotypes inhibition of elongation was mainly a consequence of UV-B perceived by the cotyledons; covering the apex and hypocotyl with a filter that excluded UV-B failed to prevent inhibition. These results indicate that reduced elongation does not result from assimilate limitation or direct damage to the apical meristem or elongating cells, and strongly suggest that it is a true photomorphogenic response to UV-B. The fact that UV-B fluences used were very low in relation to total visible light, and the similarity in the responses of lh and wild-type plants, are consistent with the hypothesis that UV-B acts through a specific photoreceptor. It is argued that, given the weak correlation between UV-B and visible-light levels in most natural conditions, the UV-B receptor may play an important sensory function providing information to the plant that cannot be derived from light signals perceived by phytochrome or blue/UV-A sensors.     

Electrophysiological evidence for a role for calcium in temperature sensing by roots of cucumber seedlings

Abstract. Rapid-cooling pulses to non-stressful temperatures cause strong, transient depolarizations in cortical cells of cucumber roots. The amplitudes of these electrical responses are graded according to the rate and amplitude of the cooling pulse. Such graded potentials are typical of sensory processes and indicate that plants possess the ability to sense temperature change. La³⁺, a blocker of Ca²⁺ channels, and ethylene glycol bis-(β-aminoethyl ether) N,N,N',N'-acetic acid (EGTA), a Ca²⁺ chelator, inhibit the electrical responses elicited by rapid-cooling pulses. High external [Ca²⁺] enhances them. These results indicate the involvement of a plasma membrane-associated Ca²⁺ channel in the process of temperature sensing by plants. Calmodulin antagonists prolong the repolarization phase of the electrical responses, suggesting a role for calmodulin in the recovery from stimulation.     

Differential gene expression in cucumber plants in response to brief daily cold treatments

The mechanisms of plant responses to short-term cold treatments applied daily in the period of active growth remain unknown. Cucumber (Cucumis sativus L.) plants were subjected to brief drops of temperature (2 h, 12°C) at the end of each night over a 6-day period (DROP treatment) and to prolonged (6 days) cooling at 12°C (permanent low-temperature treatment, PLT). The plants exposed to cold treatments and control plants grown at 20°C were compared in terms of cold resistance and changes in gene expression. Cold resistance of plants was determined on the basis of LT₅₀ temperature. The response of cucumber genetic machinery was assessed by means of a differential display method based on polymerase chain reaction (PCR). The changes in mRNA pool in cells of cucumber plants subjected to permanent and periodic chilling were assessed after comparing the populations of PCR fragments of cDNA. In both types of chilling protocols, the cold resistance started to increase from the 2nd day of low temperature treatment. At the end of the experiment (on the 6th day), the increment in cold resistance was three times larger for DROP compared to PLT treatment. Analysis of mRNA pool showed that the numbers of amplified fragments were nearly identical in both types of low-temperature treatment. The higher level of cold resistance under DROP conditions was assumed to depend on features of metabolism.