水杨酸对水分胁迫黄瓜幼苗叶片生理过程的影响

研究了外源水杨酸 salicylic acid,SA 对水分胁迫下黄瓜幼苗叶片主要生理过程的影响 . 1m mol/L 的 SA处理黄瓜幼苗 2 4 h后 ,叶片中 POD活性剧增 ,SOD活性增加不明显 ,H2 O2 清除酶 CAT和 APX活性受抑制 ,H2 O2 含量上升引起膜脂过氧化产物 MDA含量上升 ,造成轻度氧化胁迫 ;在随后水分胁迫过程中 ,经 SA预处理积累的 H2 O2 诱导 APX和 CAT活性上升并清除产生的 H2 O2 ;SA预处理后 ,叶片中 Rubisco含量及其基因转录水平明显高于对照 ,光合作用受影响较小 .这表明 SA使黄瓜幼苗生理活性有较大改善 ,增强了植株对水分胁迫的抗性     

虫害对不同水分条件胡杨披针形叶活性氧代谢的影响

在不同土壤水分条件下,研究了胡杨披针形叶叶片遭受虫害胁迫时活性氧释放和抗氧化酶活性的变化．结果表明,单纯的土壤水分亏缺并不导致O2·^-、H2O2的释放增加以及SOD、CAT活性上升;但土壤水分亏缺条件下的虫害胁迫却导致胡杨披针形叶叶片O2·^-、H2O2的释放增加,SOD、CAT活性上升．在人工灌溉生境下,虫害胁迫却使二者均呈下降趋势．可以认为,土壤水分亏缺条件下的虫害胁迫是造成胡杨枯死亡的主要原因之一．     

叶片喷施甲醇对铝胁迫下黑大豆抗氧化酶活性的影响

在营养液水培条件下,分析叶片预喷施5％ (V/V)甲醇对50μmol·L-1的AlCl3胁迫下黑大豆叶和根中H2O2和MDA含量以及抗氧化酶SOD、POD和CAT活性的影响,为进一步研究甲醇及抗氧化酶在响应铝胁迫应答中的调控机制奠定基础.结果显示:(1)在铝胁迫下,随着铝处理浓度的升高根尖吸收的铝越多,且根的生长被抑制越严重.(2)铝胁迫能诱导黑大豆叶和根中可溶性总蛋白、H2O2和MDA含量的增加,POD和CAT活性增强,但SOD活性变化不明显.(3)当叶片喷施5％甲醇预处理后再进行50 μmol·L1 AlCl3胁迫,随着处理时间增加黑大豆叶和根中可溶性总蛋白含量及POD和CAT活性显著增加,而H2O2和MDA含量显著下降,SOD活性变化亦不显著.研究结果表明,在铝胁迫下叶片喷施5％甲醇能够增强黑大豆叶和根中POD和CAT活性,降低H2O2和MDA的积累,这可能是甲醇通过抗氧化酶参与铝胁迫应答的一种重要机制.     

水杨酸对水分胁迫黄瓜幼苗叶片生理过程的影响

研究了外源水杨酸(salicylic acid,SA)对水分胁迫下黄瓜幼苗叶片主要生理过程的影响。1mmol／L的SA处理黄瓜幼苗24h后,叶片中POD活性剧增,SOD活性增加不明显,H2O2清除酶CAT和APX活性受抑制,H2O2含量上升引起膜脂过氧化产物MDA含量上升,造成轻度氧化胁迫;在随后水分胁迫过程中,经SA预处理积累的H2O2诱导APX和CAT活性上升并清除产生的H2O2;SA预处理后,叶片中Rubisco含量及其基因转录水平明显高于对照,光合作用受影响较小。这表明SA使黄瓜幼苗生理活性有较大改善,增强了植株对水分胁迫的抗性。     

水杨酸调节决明根系铝诱导的氧化胁迫

水杨酸(Salicylic acid,SA)在调节生物和非生物胁迫,诱导植物氧化胁迫中起着重要的作用,但对铝诱导的氧化胁迫的调节作用尚不清楚.本文研究了SA对决明(Cassiatora L.)根系铝诱导的H2O2和O2-含量变化,包括抗氧化酶活性以及细胞质膜过氧化胁迫变化的影响.介质中20 μmol/L铝处理增加质膜透性,导致MDA含量上升及根尖细胞Evans blue染色加重(测定细胞死亡),而外源供给5 μmol/L SA能缓解铝诱导的氧化胁迫.SA处理能明显降低根尖H2O2和O2-的含量,但两者含量与CAT、APX和GR的活性变化没有相关性,而与POD活性增加有关.水杨酸诱导H2O2含量的下降与抑制O2积累和SOD活性有关.结果表明,SA可能激活一条由H2O2介导的、依赖于POD的抗氧化机制来缓解脂质的过氧化作用.     

微囊藻毒素缓解过氧化氢胁迫下铜绿微囊藻损伤的初步研究

过氧化氢可抑制藻类生长, 同时会导致微囊藻毒素(Microcystins, MCs)的释放, 实验设置4个处理组探讨了外源微囊藻毒素MC-LR对H2O2胁迫下铜绿微囊藻生理生化变化的影响。结果表明: 在H2O2胁迫下, 微囊藻的生长和光合活性受到显著抑制, 藻细胞存活率降低, ROS含量明显增加, SOD活性上升。与单独H2O2胁迫相比, 加入MC-LR能增加微囊藻细胞的存活率。250 mol/L H2O2处理24h和48h后, 在培养基中加入200 ng/mL MC-LR可以缓解H2O2对铜绿微囊藻光合系统PSII活性的抑制作用。当微囊藻暴露于250 mol/L H2O2环境中时, 添加了MC-LR处理组藻细胞中的ROS含量明显减少(P0.05)。在相同浓度H2O2且加入了外源MC-LR后藻细胞SOD活性下降(P0.05)。因此, 微囊藻毒素MC-LR可缓解250 mol/L H2O2引起的氧化损伤并增强微囊藻自身的生存能力。研究结果有利于阐明H2O2胁迫影响产毒蓝藻生长代谢的途径及MCs生物学意义。       

H2O2和ABA对干旱高温复合胁迫诱导的玉米叶片sHSPs表达的影响

以玉米脱落酸(ABA)缺失突变体vp5及其野生型Vp5的叶片为材料,分别采用ABA、碘化钾(H2O2清除剂)、钨酸钠(ABA抑制剂)预先处理,对干旱+高温复合胁迫下玉米叶片小热休克蛋白(sHSPs)基因表达进行研究,以确定H2O2和ABA对干旱+高温复合胁迫诱导的玉米叶片sHSPs基因表达的影响。结果显示:(1)与对照和干旱相比,高温、干旱+高温复合胁迫显著诱导了sHSP16.9、sHSP17.2、sHSP17.4、sHSP17.5、sHSP22和sHSP26等6种sHSPs的表达。(2)H2O2清除剂KI和ABA抑制剂钨酸钠预处理,仅略微抑制高温、干旱+高温复合胁迫诱导的6种sHSPs表达。(3)与未用100μmol/L ABA预处理的vp5相比,100μmol/L ABA预处理仅略微提高了高温、干旱+高温复合胁迫诱导的6种sHSPs的表达水平。研究表明,在干旱+高温复合胁迫条件下H2O2和ABA参与了干旱+高温复合胁迫诱导的玉米叶片sHSPs表达,但并无显著影响,暗示了H2O2和ABA不是干旱+高温复合胁迫诱导sHSPs表达的重要调控因子。     

拟南芥CEO1基因在氯化镉诱导的氧化胁迫中的作用

以拟南芥ceo1、突变体为材料,研究CEO1（clone eight-one）在镉胁迫条件下作用的结果表明,与野生型植株相比,150μmol·L^-1的CdCl2处理10d后,拟南芥ceo1突变体表现为植株生长矮小,叶片卷曲发黄,根系短小。镉处理后,拟南芥突变体幼苗叶中H2O2的积累较多;镉处理1h后的突变体中抗坏血酸过氧化物酶（APX）活性明显上升,至2h时又开始下降,而镉处理2h后,野生型APX活性才开始增加。镉处理2h后的野生型的谷胱甘肽还原酶（GR）显著增加,而突变体无明显变化。两种类型拟南芥的超氧化物歧化酶（SOD）与过氧化氢酶（CAT）的活性没有明显差异。     

草酸诱导黄瓜幼苗对霜霉病的抗性与H2O2的关系

以长春密刺黄瓜幼苗为材料,对经草酸处理或霜霉菌接种后黄瓜叶片的过氧化物酶(POD)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性及H2O2含量的变化进行了研究.结果表明:草酸处理或霜霉菌接种均可诱导黄瓜幼苗叶片H2O2含量显著增加,且草酸预处理后接种的叶片比相应对照叶片能更快地积累H2O2;草酸处理后叶片SOD和POD活性均升高,而CAT活性却受到一定程度的抑制.研究发现,H2O2参与了幼苗对霜霉病的抗性诱导;叶片H2O2含量的增加与其SOD、POD活性升高、CAT活性下降有关;通过调节黄瓜叶片H2O2的含量来调控有关黄瓜霜霉病抗性的防御基因表达是草酸诱导抗性的机制之一.     

过氧化氢预处理增强敏感型黑豆抗铝能力的生理机制

以铝敏感型黑豆(简称SB)幼苗为实验材料,在水培条件下进行不同浓度过氧化氢(H2O2)和AlCl3处理,考察其生长和相关生理指标变化,探讨H2 O2预处理缓解黑豆铝毒害的生理以及分子机理.结果显示:(1)黑豆幼苗根的相对生长量在0.1和1.0 μmol·L-1 H2O2处理下始终得到显著促进,并以后者效果更好,而在10.0和100.0 μmol·L1 H2O2处理下先表现促进后受到显著抑制.(2)经过1.0 μmol·L-1 H2O2预处理的SB幼苗在不同程度Al3+胁迫(50～400 μmol·L 1)3周后,其叶片和根中总蛋白含量分别显著增加了16.7％～41.2％和10.0％～25.0％,MDA含量减少了近50％;而其同期的SOD和POD活性显著增加.(3) H2 O2预处理可诱导SB根和叶中的SOD基因(Mg/Fe-SOD和Mn-SOD)的表达水平明显提高.研究表明,低浓度H2O2能显著促进铝胁迫下铝敏感型黑豆幼苗生长,且主要是通过增加植株抗氧化酶活性和相关基因表达水平来提高其对铝胁迫的抗性.     

Species and Organ Diversity in the Effects of Hydrogen Peroxide on Superoxide Dismutase Activity In Vitro

Superoxlde dlsmutase （SOD） is ubiquitous in aerobic organisms and constitutes the first link In the enzyme scavenging system of reactive oxygen species. In the present study, species and organ diversity of SOD activity In a solution and In an in-gel assay system, as well as the effects of hydrogen peroxide （H202） on SOD activity, were Investigated. In a solution assay system, SOD activity of jackfruIt root, shoot, leaves, axes, and cotyledons, of maize embryos and endosperms, of mung bean leaves and seeds, of sacred lotus axes and cotyledons, and of rice and wheat leaves was Increased by 1-15 mmol/L H2O2. However, SOD activity In rice root and seeds, maize roots and leaves, mung bean roots and shoots, and wheat seeds was decreased by 1-15 mmol/L H2O2. The SOD activity of wheat root and soybean roots, leaves, axes, and cotyledons was Increased by 1-4 mmol/L H2O2, but was decreased by concentrations of H2O2 〉4 mmol/L. The SOD activity of soybean shoots was not affected by 1-15 mmol/L H2O2. The SOD activity In crude mltochondrla of jackfruIt, maize, and upas seeds, as well as In purified mitochondria of jackfruIt, was also Increased by 1-15 mmol/L H2O2. In the In-gel assay system, the SOD In jackfruIt cotyledons was comprised of Mn-SOD, Cu/Zn-SOD, and Fe-SOD, the crude mltochondria of jackfruit seeds and maizes embryo was comprised of Mn-SOD and Cu/ Zn-SOD, and the crude mltochondria of maize seeds was comprised of Mn-SOD only. In the present study, H2O2 markedly Inhibited Cu/Zn-SOD and Fe-SOD activity.     

Nitric oxide reduces hydrogen peroxide accumulation involved in water stress-induced subcellular anti-oxidant defense in maize plants

Nitric oxide （NO） is a bioactive molecule involved in many biological events, and has been reported as pro-oxidant as well as anti-oxidant in plants. In the present study, the sources of NO production under water stress, the role of NO in water stress-induced hydrogen peroxide （H2O2） accumulation and subcellular activities of anti-oxidant enzymes in leaves of maize （Zea mays L.） plants were investigated. Water stress induced defense increases in the generation of NO in maize mesphyll cells and the activity of nitric oxide synthase （NOS） in the cytosolic and microsomal fractions of maize leaves. Water stress-induced defense increases in the production of NO were blocked by pretreatments with inhibitors of NOS and nitrate reductase （NR）, suggesting that NO is produced from NOS and NR in leaves of maize plants exposed to water stress. Water stress also induced increases in the activities of the chloroplastic and cytosolic anti-oxidant enzymes superoxide dismutase （SOD）, ascorbate peroxidase （APX）, and glutathione reductase （GR）, and the increases in the activities of anti-oxidant enzymes were reduced by pretreatments with inhibitors of NOS and NR. Exogenous NO increases the activities of water stress-induced subcellular anti-oxidant enzymes, which decreases accumulation of H2O2. Our results suggest that NOS and NR are involved in water stress-induced NO production and NOS is the major source of NO. The potential ability of NO to scavenge H2O2 is, at least in part, due to the induction of a subcellular anti-oxidant defense.     

Evaluation of oxidative stress tolerance in maize (Zea mays L.) seedlings in response to drought

Seedlings of selected six genotypes of maize (Zea mays L.) differing in their drought sensitivity (LM5 and Parkash drought-tolerant and PMH2, JH3459, Paras and LM14 as drought-sensitive) were exposed to 72 h drought stress at two leaf stage. Alterations in their antioxidant pools combined with activities of enzymes involved in defense against oxidative stress were investigated in leaves. Activities of some reactive oxygen species (ROS)-scavenging enzymes, catalase (CAT) and ascorbate peroxidase (APX) were enhanced in tolerant genotypes in response to drought stress. Superoxide dismutase (SOD) activity was significantly decreased in sensitive genotypes, but remained unchanged in tolerant genotypes under stress. Peroxidase (POX) activity was significantly induced in tolerant, as well as sensitive genotypes. Imposition of stress led to increase in H2O2 and malondialdehyde (MDA, a marker for lipid peroxidation) content in sensitive genotypes, while in tolerant genotypes no change was observed. Significant increase in glutathione content was observed in sensitive genotypes. Ascorbic acid pool was induced in both tolerant and sensitive genotypes, but induction was more pronounced in tolerant genotypes. Significant activation of antioxidative defence mechanisms correlated with drought-induced oxidative stress tolerance was the characteristic of the drought tolerant genotypes. These studies provide a mechanism for drought tolerance in maize seedlings.     

马缨丹叶提取液对水葫芦叶片中超氧物歧化酶活性和过氧化氢积累的影响

水葫芦[Eichhornia crassipes（Mart）Solms]是世界上繁殖最快、危害最严重的多年生水生杂草之一。为了避免化学除草剂对水体的污染,生物防治已成为当前水葫芦治理的重要方向。马缨丹（Lantana camara）是马鞭草科的一种植物,其叶片提取物对水葫芦有很强的毒性。研究结果表明：经马缨丹叶提取液处理的水葫芦叶片中,超氧物歧化酶（SOD）活性与H2O2浓度均显著升高,但过氧化氢酶的活性受到抑制,膜脂过氧化程度明显增加。H2O2的组织化学染色结果表明H2O2在气孔细胞中有异常高的积累,H2O2过量产生同时导致水葫芦叶片失绿与细胞死亡。因此,氧胁迫可能是马缨丹提取液对水葫芦毒害的主要原因之一。     

Effects of Exogenous Spermidine on Antioxidant System Responses of Typha latifolia L. Under Cd^2＋ Stress

The effects of foliar spraying with spermidine (Spd), ranging in concentration from 0.25 to 0.50 mmol/L, on the antioxidant system under Cd^2 stress (range 0.1- 0.2 mmol/L Cd^2 ) in Typha latifolia L. grown hydroponically were investigated in order to offer a referenced evidence for an understanding of the mechanism by which polyamines (PAs) relieve the damage to plants by heavy metal and improve the phytoremediation efficiency of heavy metal-contaminated water. The results showed that Cd^2 stress induced oxidative injury, as evidenced by an increase in the generation of superoxide anion (O2), as well as the hydrogen peroxide (H2O2) and malondialdehyde (MDA) contents in both leaves and caudices. With the exception of superoxide dismutase (SOD) activity in the leaves, an increase in the activities of catalase (CAT), guaiacol peroxidase (GPX), and glutathione reductase (GR) was observed in both leaves and caudices, SOD activity was increased in caudices, and ascorbate peroxidase (APX) activity was increased in leaves following Cd^2 treatment. The reduced glutathione (GSH) content in both leaves and caudices and the reductive ascorbate content in leaves was obviously increased, which were prompted by the application of exogenous Spd. Spraying with Spd increased the activity of GR and APX in both leaves and caudices, whereas the activity of SOD, CAT, and GPX was increased only in caudices following spraying with Spd. The generation of O2 and the H2O2 and MDA content in both leaves and caudices decreased after spraying with Spd. The decrease in MDA was more obvious following the application of 0.25 than 0.50 mmol/L Spd. It is supposed that exogenous Spd elevated the tolerance of T. latifolia under Cd^2 stress primarily by increasing GR activity and the GSH level.     

Involvement of Protein Phosphorylation in Water Stress-induced Antioxidant Defense in Maize Leaves

Using pharmacological and biochemical approaches, the role of protein phosphorylation and the interrelationship between water stress-enhanced kinase activity, antioxidant enzyme activity, hydrogen peroxide (H2O2) accumulation and endogenous abscisic acid in maize (Zea mays L.) leaves were investigated. Water-stress upregulated the activities of total protein phosphorylation and Ca2+ -dependent protein kinase, and the upregulation was blocked in abscisic acid-deficient vp5 mutant. Furthermore, pretreatments with a nicotinamide adenine dinucleotide phosphate oxidase inhibitor and a scavenger of H2O2 significantly reduced the increased activities of total protein kinase and Ca2+-dependent protein kinase in maize leaves exposed to water stress. Pretreatments with different protein kinase inhibitors also reduced the water stress-induced H2O2 production and the water stress-enhanced activities of antioxidant enzymes such as superoxide dismutase, catalase, ascorbate peroxidase and glutathione reductase. The data suggest that protein phosphorylation and H2O2 generation are required for water stress-induced antioxidant defense in maize leaves and that crosstalk between protein phosphorylation and H2O2 generation may occur.     

Abscisic acid is a key inducer of hydrogen peroxide production in leaves of maize plants exposed to water stress

The histochemical and cytochemical localization of water stress-induced H(2)O(2) production in the leaves of ABA-deficient vp5 mutant and wild-type maize (Zea mays L.) plants were examined, using 3,3-diaminobenzidine and CeCl(3) staining, respectively, and the roles of endogenous ABA in the production of H(2)O(2) induced by water stress were assessed. Water stress induced by polyethylene glycol resulted in the accumulation of H(2)O(2) in mesophyll cells, bundle-sheath cells and vascular bundles of wild-type maize leaves, and the accumulation was substantially blocked in the mutant maize leaves exposed to water stress. Pre-treatments with several apoplastic H(2)O(2) manipulators abolished the majority of H(2)O(2) accumulation induced by water stress in the wild-type leaves. The subcellular localization of H(2)O(2) production was demonstrated in the cell walls, xylem vessels, chloroplasts, mitochondria and peroxisomes in the leaves of wild-type maize plants exposed to water stress, and the accumulation of H(2)O(2) induced by water stress in the cell walls and xylem vessels, but not in the chloroplasts, mitochondria and peroxisomes, was arrested in the leaves of the ABA mutant or the ABA biosynthesis inhibitor (tungstate)-pre-treated maize plants. Pre-treatments with the apoplastic H(2)O(2) manipulators also blocked the apoplastic but not the intracellular H(2)O(2) accumulation induced by water stress in the leaves of wild-type plants. These data indicate that under water stress, the apoplast is the major source of H(2)O(2) production and ABA is a key inducer of apoplastic H(2)O(2) production. These data also suggest that H(2)O(2) generated in the apoplast could not diffuse freely into subcellular compartments.     

水杨酸对镉胁迫下玉米幼苗质膜透性和保护酶活性的影响

在Cd^2＋胁迫下,添加外源水杨酸（SA）的培养液中生长的玉米幼苗叶中超氧化物歧化酶（SOD）、过氧化物酶（POD）和过氧化氢酶（CAT）的活性均提高,质膜透性降低,丙二醛（MDA）的积累减少,显示SA对Cd^2＋胁迫具有一定的缓解效应。     

C3和C4植物叶片对光氧化响应的日变化

田间生长的C3植物花生和C4植物玉米分别于晴天上午9：00、中午12：00、下午15：00取样。中午12：00花生叶片的Fv／Fm较早上9：见下降16％,出现了光抑制现象,玉米叶片的Fv／Fm则未下降。不同时间取样的花生和玉米叶片经甲基紫精（MV） 强光的人为光氧化处理,叶绿素和类胡萝卜素出现不同程度的氧化降解,中午12：00降解幅度最大,15时降幅最小。植物叶片的抗氧化能力与其SOD活性相关,而与PEPCase的活性没有明显的相关性。光氧化处理后,花生和玉米的叶绿素荧光参数FV／Fm、qp、pSII都下降,花生在12：00的降幅最小,玉米的降幅最大。光氧化引起花生的qN和热耗散系数（KD）上升,玉米则都下降．结果显示C3植物花生和C4植物玉米对光氧化的响应可能存在不同的机制。     

Effects of Exogenous Spermidine on Antioxidant System Responses of Typha latifolia L. Under Cd2+ Stress

The effects of foliar spraying with spermidine (Spd), ranging in concentration from 0.25 to 0.50mmol/L, on the antioxidant system under Cd2 stress (range 0.1- 0.2 mmol/L Cd2 ) in Typha latifolia L.grown hydroponically were investigated in order to offer a referenced evidence for an understanding of the mechanism by which polyamines (PAs) relieve the damage to plants by heavy metal and improve the phytoremediation efficiency of heavy metal-contaminated water. The results showed that Cd2 stress inhydrogen peroxide (H2O2) and malondialdehyde (MDA) contents in both leaves and caudices. With theexception of superoxide dismutase (SOD) activity in the leaves, an increase in the activities of catalase (CAT), guaiacol peroxidase (GPX), and glutathione reductase (GR) was observed in both leaves and caudices,SOD activity was increased in caudices, and ascorbate peroxidase (APX) activity was increased in leaves following Cd2 treatment. The reduced glutathione (GSH) content in both leaves and caudices and the reductive ascorbate content in leaves was obviously increased, which were prompted by the application of exogenous Spd. Spraying with Spd increased the activity of GR and APX in both leaves and caudices,whereas the activity of SOD, CAT, and GPX was increased only in caudices following spraying with Spd.with Spd. The decrease in MDA was more obvious following the application of 0.25 than 0.50 mmol/L Spd.It is supposed that exogenous Spd elevated the tolerance of T. latifolia under Cd2 stress primarily by increasing GR activity and the GSH level.