Changes in oxygen-scavenging systems and membrane lipid peroxidation during maturation and ripening in blackberry

Maturation and ripening of blackberry (Rubus sp.) fruit was accompanied by decreased activities of oxygen-scavenging enzymes [superoxide dismutase (EC 1.15.1.1), glutathione-peroxidase (EC 1.11.1.9), catalase (EC 1.11.1.6)] and enzymes in the ascorbate-glutathione cycle [ascorbate peroxidase (EC 1.11.1.11), monodehydroascorbate reductase (EC 1.6.5.4), dehydroascorbate reductase (EC 1.8.5.1), and glutathione reductase (EC 1.6.4.2)]. Nonenzyme components in the ascorbate-glutathione cycle such as ascorbate (AsA), dehydroascorbate (DHAsA), glutathione (GSH), and oxidized glutathione (GSSG) and the ratios of AsA/DHAsA, GSH/GSSG were also decreased. These decreases in antioxidant capacity were correlated with increases in the ratios of saturated to unsaturated fatty acid of polar lipids and free sterols to phospholipids, thus contributing to decreased fluidity, enhanced lipid peroxidation, and membrane deterioration, which may be associated with ripening and senescence in blackberry fruit.     

Elevated carbon dioxide increases contents of antioxidant compounds in field-grown strawberries

The effects of elevated CO2 concentrations on the antioxidant capacity and flavonoid content in strawberry fruit (Fragaria x ananassa Duch.) were studied under field conditions. Increased CO(2) (300 and 600 micromol mol(-1) above ambient) concentrations resulted in increases in ascorbic acid (AsA), glutathione (GSH), and ratios of AsA to dehydroascorbic acid (DHAsA) and GSH to oxidized glutathione (GSSG), and a decrease in DHAsA in strawberry fruit. High anthocyanin and phenolic content were also found in fruit of CO(2) treated plants. Growing strawberry plants under CO(2) enrichment conditions significantly enhanced fruit p-coumaroylglucose, dihydroflavonol, quercetin 3-glucoside, quercetin 3-glucuronide, and kaempferol 3-glucoside contents, as well as cyanidin 3-glucoside, pelargonidin 3-glucoside, and pelargonidin 3-glucoside-succinate content. Fruit of strawberry plants grown in the CO(2) enrichment conditions also had high oxygen radical absorbance activity against ROO(*), O(2)(*-), H(2)O(2), OH(*), and (1)O(2) radicals.     

Manipulation of plant methylglyoxal metabolic and signaling pathways for improving tolerance to drought stress

Drought stress is considered one of the major constraints to crop production with devastating effects worldwide. Methylglyoxal (MG) homeostasis plays an essential role in promoting plant growth, development, metabolic adaptation, signal transduction, and thereby responses to drought stress. Manipulation of genes encoding aldose-aldehyde reductases (ALRs), aldo– keto reductases (AKRs), genes that are involved in maintaining high ascorbate:glutathione (AsA:GSH), glutathione:glutathione disulfide (GSH:GSSG) contents and ratios, as well as jasmonic acid (JA) biosynthesis are of critical importance for improving MG detoxification, and thereby tolerance to drought stress. MG detoxification by maintaining optimal abscisic acid (ABA), JA, salicyclic acid (SA), and brassinosteroid (BR) homeostasis and crosstalk is also essential to optimize plant performance under both normal and drought stress conditions.     

The Cd‐tolerant rice mutant cadH‐5 is a high Cd accumulator and shows enhanced antioxidant activity

To investigate the mechanism of cadmium (Cd) detoxification in rice (Oryza sativa L.), a Cd‐tolerant mutant cadH‐5, obtained by an Agrobacterium tumefaciens‐based gene‐delivery system, was used for a Cd‐tolerance and accumulation study. After 15 d of exposure to 0.75 mM CdCl₂, significant phenotypic differences were observed between the wild type (WT) and cadH‐5. When exposed to 0.5 mM CdCl₂, higher Cd levels were accumulated in cadH‐5 root cell wall, root cytosol, and membranes than those in WT. However, Cd concentrations in root tissues varied in both WT and cadH5. No significant difference of hydrogen peroxide (H₂O₂) concentrations was observed between WT and cadH‐5, while contents of cell‐wall polysaccharides and phytochelatins (PCs) in the mutant were higher compared to WT. The ratios of reduced glutathione to oxidized glutathione (GSH : GSSG) and ascorbate to dehydroascorbate (ASC : DHA) were lower in WT than in cadH‐5, while the NADPH : NADP⁺ ratio was different to the ratios of GSH : GSSG and ASC : DHA; the ascorbate peroxidase (APX, EC 1.11.1.11), glutathione peroxidase (GR, EC 1.6.4.2), dehydroascorbate reductase (DHAR, EC 1.8.5.1), and monodehydroascorbate reductase (MDHAR, EC 1.6.5.4) activities were lower in WT compared to cadH‐5. Our results indicate that under long‐term Cd stress, cadH‐5 plants can accumulate more Cd with more PC. Also, the redox status of ASC‐GSH cycle was more inhibited in WT than in cadH‐5 plants, rendering WT less able to scavenge reactive oxygen species (ROS). The cadH‐5 mutant maintains relatively high ASC, GSH, and NADPH concentrations, ratios of ASC : DHA, GSH : GSSG, and NADPH : NADP⁺, as well as antioxidative enzymatic activities and PC concentrations. Thus, it is tolerant of relatively high Cd accumulation.     

Simultaneous determination of oxidized and reduced glutathione in eel's (Monopterus albus) plasma by transient pseudoisotachophoresis coupled with capillary zone electrophoresis

Both the reduced form of glutathione (GSH) and the oxidized form of glutathione (GSSG) in eel's ( Monopterus albus) plasma were for the first time determined by transient pseudoisotachophoresis coupled with capillary zone electrophoresis. The method of transient pseudoisotachophoresis coupled with capillary zone electrophoresis has been thoroughly optimized and adequately evaluated for the simultaneous determination of GSH and GSSG in eel's plasma. The detection limits (S/N = 3) of the method developed were 0.2 and 0.05 micromol/L for GSH and GSSG, respectively. The linearity of the calibration curves was valid in the range of 0-10 micromol/L GSH and 0-0.70 micromol/L GSSG. The method was simple, fast, and reproducible. It was found that the respective concentrations of GSH and GSSG were in the range of 9.1-14.5 and 0.31-0.58 micromol/L in the adult eel's plasma, and 10.8-17.9 and 0.49 - 0.68 micromol/L in the juvenile eel's plasma of the three populations determined. Each blood sample was a composite of five eels. For each of the three populations, the concentrations of GSH and GSSG in the adult eel's plasma were lower than those in the juvenile eel's plasma, and the concentrations of GSH and GSSG in the plasma of population 1 (deep yellow finless eels) were higher than those in populations 2 (light yellow finless eels) and 3 (green finless eels) for either the adult or the juvenile eels.     

Correlation of antioxidant capacities to oxygen radical scavenging enzyme activities in blackberry

The activities of the oxygen radical scavenging enzymes [glutathione-peroxidase (GSH-POD), superoxide dismutase (SOD), and guaiacol peroxidase (G-POD)], hydrogen peroxide scavenging enzymes in the ascorbate-glutathione cycle [ascorbate peroxidase (AsA-POD), monodehydroascorbate reductase (MDAR), dehydroascorbate reductase (DHAR), and glutathione reductase (GR)], the nonenzyme components [ascorbate (AsA), dehydroascorbate (DHAsA), glutathione (GSH), and oxidized glutathione (GSSG)], and their antioxidant capacity [oxygen radical absorbance capacity (ORAC)] were measured in the juice of six different thornless blackberry (Rubus sp.) cultivars. The 'Hull Thornless' cultivar contained the highest levels, whereas 'Black Satin' consistently had the lowest activities for all the enzymes tested in this study. ORAC values were also the highest in 'Hull Thornless' and lowest in 'Black Satin'. The highest levels of AsA and DHAsA were in the juice of 'Hull Thornless' blackberries with 1. 09 and 0.15 micromol/g fresh wt, respectively. 'Hull Thornless' also had the highest ratio of AsA/DHAsA among the six blackberry cultivars studied. The 'Smoothstem' cultivar contained the lowest amounts of AsA and DHAsA. 'Hull Thornless' had the highest GSH content with 78.7 nmol/g fresh wt, while 'Chester Thornless' contained the largest amount of GSSG. The highest GSH/GSSG ratio was 4.90 which was seen in the 'Hull Thornless' cultivar. The correlation coefficient between ORAC values and AsA/DHAsA ratios was as high as 0.972. A correlation (r = 0.901) was also detected between ORAC values and GSH content. The antioxidant activity in blackberry juice was positively correlated to the activities of most antioxidant enzymes (r = 0.902 with SOD; r = 0.858 with GSH-POD; r = 0.896 with ASA-POD; and r = 0.862 with GR).     

Compost as a soil supplement increases the level of antioxidant compounds and oxygen radical absorbance capacity in strawberries

Compost as a soil supplement significantly enhanced levels of ascorbic acid (AsA) and glutathione (GSH) and ratios of AsA/dehydroascorbic acid (DHAsA) and GSH/oxidized glutathione (GSSG) in fruit of two strawberry (Fragaria x ananassa Duch.) cultivars, Allstar and Honeoye. The peroxyl radical (ROO(*)) as well as the superoxide radical (O(2)(*)(-)), hydrogen peroxide (H(2)O(2)), hydroxyl radical (OH(*)), and singlet oxygen ((1)O(2)) absorbance capacity in strawberries increased significantly with increasing fertilizer strength and compost use. The planting medium (compost) x fertilizer interaction for phenolics and flavonoids was significant. Fruit from plants grown in full-strength fertilizer with 50% soil plus 50% compost and 100% compost yielded fruit with the highest levels of phenolics, flavonol, and anthocyanin content. A positive relationship between antioxidant activities and contents of AsA and GSH and ratios of AsA/DHAsA and GSH/GSSG existed in fruit of both strawberry cultivars. Correlation coefficients for the content of antioxidant components versus antioxidant activity [against ROO(*), O(2)(*)(-), H(2)O(2), OH(*), or (1)O(2)] ranged from r( )()= 0.7706 for H(2)O(2) versus GSH/GSSH in cv. Allstar to r = 0.9832 for O(2)(*)(-) versus total flavonoids in cv. Allstar.     

Distribution of Glutathione in Millstreams and Relationships to Chemical and Baking Properties of Flour

Fourteen millstream flours, a straight‐run flour, bran, pollard, and germ were prepared separately from two Australian and two New Zealand wheat cultivars using a 650 kg/hr pilot roller mill. Glutathione (GSH) and oxidized glutathione (GSSG) were measured in all samples. The Australian cultivars had higher levels of GSH and GSSG than the New Zealand cultivars, and in all cultivars the levels in pollard and germ were considerably higher than in flour samples. Generally, the early break flours and early reduction flours had lower GSSH/GSSG levels than the tail‐end break and reduction flours. There was a strong correlation between GSH/GSSG and ash content in millstream flours, which indicated that much of the GSH/GSSG in the flour was likely to have derived from contamination by bran, aleurone (pollard), and germ. There were also moderate to strong correlations between GSH/GSSG and the cysteine content of all proteins in flour. GSH/GSSG correlated strongly with the albumin and globulin content of flour but not with gliadin and glutenin. The volume and crumb texture properties of bread made with millstream flours in the absence of ascorbic acid (AA) were negatively correlated with GSH/GSSG. The change in bread volume and texture properties when AA was added to dough (baking improver effect of AA), however, were poorly correlated with GSH/GSSG.     

Modulation of hepatic drug metabolizing enzymes and oxidative status by rooibos (Aspalathus linearis) and Honeybush (Cyclopia intermedia), green and black (Camellia sinensis) teas in rats

Rooibos and honeybush teas significantly (P < 0.05) enhanced the activity of cytosolic glutathione S-transferase alpha. A significant (P < 0.05) to marginal (P < 0.1) increase in the activity of the microsomal UDP-glucuronosyl transferase was obtained with unprocessed rooibos and honeybush teas, respectively. Oxidized glutathione (GSSG) levels were significantly (P < 0.05) reduced in the liver of all tea treated rats while reduced glutathione (GSH) was markedly increased in the liver of the herbal tea treated rats. These changes resulted in a significant (P < 0.05) increase in the GSH/GSSG ratio by the unprocessed, processed rooibos and unprocessed honeybush teas. Green and black teas markedly to significantly decreased the oxygen radical absorbance capacity in liver homogenates, respectively. Modulation of phase II drug metabolizing enzymes and oxidative status in the liver may be important events in the protection against adverse effects related to mutagenesis and oxidative damage.     

外源谷胱甘肽喷施对缺硫胁迫下小白菜谷胱甘肽代谢的影响

[目的]硫是植物生长发育过程中所必需的营养元素,缺硫会阻碍植物生长发育,研究外源谷胱甘肽(GSH)对缺硫胁迫下小白菜GSH代谢的影响,为利用外源GSH减轻缺硫胁迫对植物造成的伤害提供理论依据.[方法]以小白菜为试验材料,采用营养液栽培方法,设正常供硫并喷施蒸馏水对照(CK)、缺硫喷施蒸馏水(H2O)、缺硫喷施25 mg...     

Reduced-Oxidized Glutathione Status as a Potential Index of Oxidative Stress in Mature Cereal Grain

The purpose of this study was to examine the reduced and oxidized glutathione status of selected cereal grains as a potential index of balance between oxidative stress and antioxidant systems, and the contribution of reduced glutathione to the total antioxidant status in cereal grain extracts. Wheat cultivars Almari and Henika, barley cultivars Gregor and Mobek, rye cultivar Dañkowskie Złote, oat cultivar Sławko, and buckwheat cultivar Kora were used. Total antioxidant status (TAS) was measured by the ABTS (2,2'-azinobis(3-ethyl-benzothiazoline-6-sulphonate)) method. Contents of total phenolic compounds were also determined. Reduced (GSH) and oxidized glutathione (GSSG) (γ-glutamyl-cysteinyl-glycine) were assayed using the spectrofluorimetric method, and results were confirmed by the enzyme recycling method. Correlation coefficient for the GSH/GSSG ratio was r = 0.79. Correlation between TAS and the total phenolic compound content was r = 0.81. Correlation between GSH/GSSG ratio and TAS values was r= 0.46, depending on the extraction system used. The GSH/GSSG ratio may indicate a hierarchy among different cultivars and variance of cereal grains against damage caused by reactive oxygen species. For the main water-soluble antioxidants, our data indicate a potential hierarchy of resistance in investigated cereals against oxidative stress (buckwheat > wheat > barley ≈ rye > oat). This hierarchy was confirmed by the ability of investigated cereal extracts to scavenge superoxide anion radicals in vitro. The reduced-oxidized glutathione status in different cereal grains can be applied as a potential index of balance between oxidative stress and antioxidant systems.     

Impact of food disinfection on beneficial biothiol contents in strawberry

In this study, the impact of four food disinfectants including hydrogen peroxide, free chlorine, and gaseous- and aqueous-phase ozone with industrial doses on the concentration of biothiol compounds gamma-glutamylcysteinylglycine (GSH) and cystein (CYS) in strawberry was investigated for 1, 5, 15, 30, and 60 or 120 min. Additionally, the amount of oxidized glutathione (GSSG) was analyzed for calculation of the GSH/GSSG ratio as an indicator of oxidative stress. After this treatment, thiol contents of strawberry samples were examined using high-performance liquid chromatography (HPLC) technique. According to the results of measurements, free chlorine treatment for only 60 min significantly decreased CYS content in strawberry (p < 0.05). A significant decline in the GSH/GSSG ratio was also observed when H2O2 was applied for all time intervals except for 1 min (p < 0.05). However, aqueous-phase ozone treatment did not significantly affect the thiol levels (p < 0.05). In conclusion, this study may provide optimum disinfection methods for strawberry to minimize loss of beneficial biothiols.     

烟嘧磺隆胁迫对甜玉米幼苗活性氧积累、抗氧化系统及相关基因表达的影响

为减轻烟嘧磺隆对甜玉米(Zea mays L. seccharata Sturt)的药害作用,探究甜玉米幼苗抗氧化系统对烟嘧磺隆胁迫的响应机制,本研究以一对甜玉米姊妹系(对烟嘧磺隆表现耐药性的甜玉米自交系HK301和对烟嘧磺隆表现敏感的甜玉米自交系HK320)为试材,研究烟嘧磺隆胁迫对不同耐药性甜玉米品种氧化压力、抗氧化酶、抗氧化系统非酶类物质和抗氧化酶关键基因表达量的影响。结果表明,烟嘧磺隆胁迫后,与对照(HK301-CK)相比,HK301的超氧阴离子自由基( {\mathrm{O}}_2^{\frac{-}{·}} )产生速率、过氧化氢(H₂O₂)含量和丙二醛(MDA)含量先增加后减少,超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、抗坏血酸过氧化物酶(APX)、单脱氢抗坏血酸还原酶(MDHAR)、脱氢抗坏血酸还原酶(DHAR)、谷胱甘肽还原酶(GR)活性均呈先升高后降低的趋势,抗坏血酸(AsA)含量、脱氢抗坏血酸(DHA)、还原型谷胱甘肽(GSH)含量先增加后减少,氧化型谷胱甘肽(GSSG)含量持续增加,抗坏血酸氧化还原状态(AsA/DHA比值)显著降低,谷胱甘肽氧化还原状态(GSH/GSSG比值)无显著差异。与对照(HK320-CK)相比,HK320的 {\mathrm{O}}_2^{\frac{-}{·}} 产生速率和H₂O₂含量显著增加, CAT、APX、DHAR、GR活性先升高后下降,SOD、MDHAR活性和GSH含量、GSH/GSSG 比值、AsA/DHA 比值呈下降趋势,DHA含量持续增加,GSSG含量无显著差异。烟嘧磺隆胁迫后,相较于HK320,HK301显著上调了SOD、CAT、APX、MDHAR、DHAR和GR基因的相对表达量。综合分析显示,不同耐药性甜玉米幼苗通过调节体内抗氧化物质含量和酶活性来清除活性氧,从而提高幼苗对除草剂的耐药性。本研究为揭示烟嘧磺隆胁迫下甜玉米幼苗抗氧化系统的代谢机制提供了理论依据。     

Effect of diallyl sulfide on in vitro and in vivo Nrf2-mediated pulmonic antioxidant enzyme expression via activation ERK/p38 signaling pathway

Increasing oxidative stress is intimately involved in the pathogenesis of lung failure. Nuclear factor-erythroid 2 related factor 2 (Nrf2) is a key element in redox homeostasis. Nrf2 regulates antioxidant-associated genes that are often the target of phytochemicals in chemoprevention. This study evaluated the effect of diallyl sulfide (DAS), which is present in garlic, on the expression of antioxidant enzymes in the rat lung and the Nrf2 modulation in MRC-5 lung cells. DAS increased the activities of glutathione S-transferase, glutathione reductase, and catalase as well as the GSH/GSSG ratio compared with the lung of untreated control rats (p < 0.05). The pulmonic superoxide dismutase, glutathione peroxidase, NAD(P)H:quinone oxidoreductase 1, and catalase mRNA levels were also significantly increased (p < 0.05) after DAS treatment. Following DAS treatment, DAS level was measured in the plasma after 7 days of oral administration, and the C(max) value was 15 ± 4.2 μM. The total amount of pulmonic Nrf2 and the nuclear translocation of Nrf2 were elevated in DAS-treated rats, clarifying the effect of DAS on the modulation of antioxidant enzymes. Furthermore, DAS could induce nuclear translocation of Nrf2 via ERK/p38 signaling pathway in lung MRC-5 cells. This study demonstrates that DAS administration can significantly induce the activity of antioxidant enzymes in rat lungs and suggests a possible use for DAS as a dietary preventive agent against oxidative stress-induced lung injury.     

Urinary and plasma levels of resveratrol and quercetin in humans, mice, and rats after ingestion of pure compounds and grape juice

The present study investigates the bioavailability of resveratrol and quercetin in humans, mice, and rats after oral ingestion of grape juice preparations or pure aglycones. Oral administration of resveratrol and quercetin to humans yielded detectable levels of resveratrol, quercetin, and their derivatives in the plasma and urine. Urinary levels of resveratrol, quercetin, and their metabolites were observed in human subjects receiving 600 and 1200 mL of grape juice, whereas quercetin metabolites were identified in urine samples even after receiving 200 mL of grape juice. The cumulative amounts of resveratrol and quercetin excreted in the urine of mice receiving concentrated grape juice for 4 days were 2.3 and 0.7% of the ingested doses, respectively. After i.g. administration of resveratrol to rats (2 mg/kg), up to 1.2 microM resveratrol was observed in the plasma. The study demonstrates that the glycoside forms of resveratrol and quercetin in grape juice are absorbed to a lesser extent than the aglycones.     

Effect of ethanol and red wine on ochratoxin a-induced experimental acute nephrotoxicity

Ochratoxin A (OTA), is a nephrotoxic mycotoxin present in wine, which is nephrotoxic in humans. Our working hypothesis is that natural substances in wine may counteract OTA toxicity. Thirty-six rats were randomized to OTA dissolved in saline, red wine, or 13.5% ethanol or to OTA-free wine, ethanol, or saline. OTA (289 microg/kg of body weight/48 h) was administered by gastric gavage for 2 weeks. Serum creatinine, tubular enzymuria, renal lipohydroperoxides (LOOH), reduced (GSH) and oxidized (GSSG) glutathione, and renal superoxide dismutase activity (SOD) were determined in renal tissue. OTA alone produced significant increases in renal lipoperoxides and significant decreases in SOD and GSH/GSSG ratio. In red wine or ethanol, OTA was less nephrotoxic, reducing oxidative damage as revealed by LOOH. In OTA-wine and OTA-ethanol groups, SOD activity was higher than in the OTA-treated one, suggesting that both ethanol and nonalcoholic fractions may preserve antioxidant reserve. GSH/GSSG ratio was significantly preserved only in the OTA-wine group and not in OTA-ethanol. Red wine may exert a protective effect against OTA nephrotoxicity by limiting oxidative damage. The ostensible protection afforded by ethanol deserves further investigation.     

Effect of ascorbic acid in dough: reaction of oxidized glutathione with reactive thiol groups of wheat glutelin

The reactions of oxidized glutathione generated from endogenous glutathione by the addition of ascorbic acid (AA) prior to dough mixing on free thiol groups of gluten proteins have been investigated. A small amount of (35)S-labeled glutathione was added as a tracer to identify the reaction products of GSSG and free protein thiols by radioactivity measurement. First, gluten was isolated from the dough, then the gliadins were extracted, and residual glutenin was partially hydrolyzed with thermolysin. After preseparation by gel permeation chromatography, the fractions with the highest radioactivity were separated by high-performance liquid chromatography. Radioactive peptides were identified, isolated, sequenced, and assigned to amino acid sequences of gluten protein components. The isolated peptides contained exclusively the cysteine residues C(b) and C(x) of low molecular weight subunits of glutenin, which are supposed to be highly reactive in forming intermolecular disulfide bonds. From these results it can be assumed that the cysteine residues C(b) and C(x) of the low molecular weight subunits of glutenin are at least partly present in the thiol form in flour. During dough mixing they are converted to protein-protein disulfides or glutathione-protein mixed disulfides by thiol/disulfide interchange reactions. Oxidized glutathione necessary for this reaction is generated from glutathione by the action of AA. These results are in accordance with the major hypothesis about the mechanism of action of AA.     

胁迫对菜用大豆种子抗坏血酸-谷胱甘肽循环的影响

采用蛭石栽培,在100 mmol/L NaCl 胁迫下,对耐盐性不同的两个菜用大豆［Glycine max (L.)Merr.］品种种子的过氧化氢（H2O2）含量及抗坏血酸-谷胱甘肽（AsA-GSH）循环进行了研究。结果显示,NaCl胁迫显著增加了菜用大豆种子的H2O2含量,但耐盐品种 绿领特早的增幅低于盐敏感品种理想高产95-1。NaCl胁迫期间,绿领特早种子中抗坏血酸过氧化物酶（APX）、脱氢抗坏血酸还原酶（DHAR）、谷胱甘肽还原酶（GR）活性,AsA、GSH含量以及AsA/DHA值和GSH/GSSG值的增幅高于同期的理想高产95-1,或降幅低于同期的理想高产95-1; 脱氢抗坏血酸（DHA）、氧化型谷胱甘肽（GSSG）含量的增幅低于同期的理想高产95-1。表明 绿领特早种子在胁迫期间能够保持较高的AsA-GSH循环效率,可有效地抑制H2O2的积累,这可能是其耐盐性较强的重要原因之一。     

硒镉伴生对富硒土壤柑橘生长及生理代谢的影响

为保障富硒柑橘的安全生产,明确富硒土壤硒镉伴生现象对柑橘生长、硒镉吸收转运和抗氧化能力的影响,采用盆栽试验,以一年生大雅柑橘为试验材料,研究添加硒代蛋氨酸(SeMet,CK,模拟富硒土壤)和添加SeMet与镉(模拟富硒土壤硒镉伴生)对富硒土壤柑橘的生长指标、硒镉含量、叶片还原型抗坏血酸-谷胱甘肽(AsA-GSH)循环效率的影响。结果表明,与CK相比,富硒土壤中,硒镉伴生增加了柑橘叶片叶绿素a+b、叶绿素a、叶绿素b和类胡萝卜素含量,但对株高、新梢长度、新梢数量以及根茎叶的干物质量影响不显著;在富硒土壤中,硒镉伴生显著增加了大雅柑橘硒含量和硒的富集系数(BCF),降低了硒的转运系数(TF);硒和镉主要分布在根系,其次是叶片和茎;在AsA-GSH循环中,硒镉伴生使过氧化氢(H₂O₂)和还原型抗坏血酸(AsA)含量显著上升,脱氢抗坏血酸(DHA)含量上升但未达到显著水平,抗坏血酸过氧化物酶(APX)、谷胱甘肽还原酶(GR)活性和脱氢抗坏血酸还原酶(DHAR)活性显著上升,而GSH和氧化型谷胱甘肽(GSSG)含量下降,AsA/(AsA+DHA)和GSH/(GSH+GSSG)比值降低,谷胱甘肽过氧化物酶(GPX)活性显著降低。本研究为阐明镉胁迫对富硒土壤柑橘的生理影响机制提供了理论依据。     

耐盐和非耐盐大麦幼苗叶片抗氧化及抗坏血酸–谷胱甘肽循环系统对 NaCl 胁迫的反应差异

【目的】研究NaCl胁迫下,耐盐和非耐盐品系大麦幼苗叶片抗氧化系统及抗坏血酸–谷胱甘肽循环的反应差异。【方法】以耐盐品系12pj-118和非耐盐品系12pj-045为材料进行了水培试验。营养液中设定了6个NaCl浓度:0、100、200、300、400、500 mmol/L。在大麦苗生长至3叶1心时,取样分析测定叶片中活性氧代谢、抗氧化酶活性以及抗坏血酸–谷胱甘肽循环变化。【结果】随着NaCl胁迫的增加,2个品系的O_2~-产生速率、H_2O_2含量和MDA含量均逐渐增加,耐盐品系12pj-118的增幅均小于非耐盐品系12pj-045;SOD、POD、CAT、APX、GR活性、As A含量、GSH含量和As A/DHA比值均呈先上升后下降的趋势。12pj-118的SOD、POD、CAT活性在各NaCl浓度胁迫下的增幅大于12pj-045,降幅小于12pj-045;12pj-118的APX、GR活性在同一盐浓度胁迫下的增幅均大于非耐盐品系12pj-045,降幅小于12pj-045;在各NaCl浓度下,12pj-118的As A含量和As A/DHA比值较对照增幅均大于12pj-045;GSH/GSSG比值呈波状变化,12pj-118在较高NaCl浓度下,仍能够维持较高的GSH含量和GSH/GSSG比值。显示12pj-118较12pj-045有较强的耐盐性。【结论】耐盐和非耐盐品系大麦叶片抗氧化及抗坏血酸–谷胱甘肽循环系统在NaCl胁迫下的反应不同。在一定范围内,随着盐胁迫增强,耐盐品系12pj-118叶片SOD、POD、CAT、APX和GR活性、As A和GSH含量增幅均大于非耐盐品系12pj-045,降幅小于12pj-045,表明叶片抗氧化及抗坏血酸–谷胱甘肽循环系统与大麦幼苗抗盐性密切相关。