低温对不同耐寒力的黄瓜(Cucumic sativus)幼苗子叶各细胞器中超氧物歧化酶(SOD)的影响

黄瓜幼苗子叶SOD活性在细胞内的分布是细胞溶质部份最高(占总活性的85％左右),其次是线粒体(占10％)和叶绿体(约4％)。各细胞器的SOD同工酶酶谱均为三条同工酶活性带,迁移率较慢的一条是Mn-SOD同工酶,迁移率较快的二条为CuZn-SOD同工酶。各细胞器的SOD对低温的敏感程度不同,依次为:叶绿体>线粒体>细胞溶质部份。叶绿体和线粒体周工酶酶谱的CuZn-SOD活性带,随着处理温度的降低而减弱或接近消失。随着温度的降低,黄瓜幼苗子叶SOD活性的下降和电解质泄漏增加,幼苗逐渐呈现出伤害症状,而SOD活性的显著下降却比细胞电解质大量泄漏的出现要早。耐寒力不同的两个品种在SOD活性及电解质泄漏的变化上有差异。     

山楂叶螨危害对海棠叶片POD的影响

以人工接种的方法研究了山楂叶螨(Tetranychus viennensis Zacher)危害初期(9d内)对海棠(Malus zumi)叶片过氧化物酶(POD)的影响。结果表明,随危害时间延长和虫口密度增大,POD活性迅速升高,30头／叶危害9d和60头／叶危害6d时均约达对照的190％;PAGE分析结果显示叶螨危害使海棠叶片产生2种新的POD同工酶,受害植株的未接虫叶片的POD活性同时升高,并出现与接虫叶片相同的PAGE谱带,揭示叶螨危害对海棠叶片POD有系统诱导性。POD的变化可能是受害植株对叶螨危害的一种应激反应。     

大别山区六种黄精属植物的五种同工酶分析

采用聚丙烯酰胺凝胶电泳法对皖西大别山区六种黄精属植物的抗坏血酸氧化酶(AOD)、多酚氧化酶(PPO)、超氧化物歧化酶(SOD)、酯酶(EST)和过氧化物酶(POD)五种同工酶进行了比较分析。结果表明:(1)五种同工酶共显示出66条酶带,其中有3条是黄精属的特征酶带;并且来源于不同种的同一种酶的谱带数、相对迁移率、酶活性均不相同,呈现多样性;(2)五种同工酶谱的模糊聚类分析结果与形态学分类的结果一致,利用酶谱差异可以将六种黄精初步区分;(3)在六种黄精属植物中,湖北黄精、轮叶黄精、多花黄精和金寨黄精是较进化类型,玉竹和长梗黄精是较原始类型。     

3个桉树无性系过氧化氢酶活性及同工酶比较研究

本文研究杂交桉树(Eucalyptus urophylla×Eucalyptus camaldulensis)LH21无性系、LH22无性系和尾叶桉(Eucalyptus urophylla)U6无性系的过氧化氢酶(CAT)活性及同工酶的差异。结果表明,3个桉树无性系同一器官的CAT活性存在差异,同一个无性系中不同器官的CAT活性差异很显著。采用聚丙烯酰胺不连续凝胶垂直板电泳比较分析CAT同工酶,发现3个无性系的CAT同工酶存在着一定的差异,其中LH21和LH22叶片有相同的谱带,但根的谱带与叶片有差异;而U6各器官的CAT谱带与LH21和LH22有差异。3个无性系的CAT同工酶都在一定程度上具有器官的特异性。     

5种樱桃属植物的POD、CAT和SOD同工酶分析

采用聚丙烯酰胺垂直平板凝胶电泳技术对5种樱桃属植物的过氧化物酶(POD)同工酶、过氧化氢酶(CAT)同工酶和超氧化物歧化酶(SOD)同工酶的酶谱特征进行分析,结果表明:5种樱桃属植物共电泳出12条POD同工酶酶带、4条CAT同工酶酶带和8条SOD同工酶酶带;其中,POD同工酶酶谱具有5条共同谱带,CAT同工酶4条,SOD同工酶5条。冬季休眠期的樱桃属植物,POD与SOD同工酶谱带的多样性比较丰富,不同植物之间的谱带差异较大;而CAT同工酶谱带差异不明显。     

镧对鲤鱼五种组织超氧化物歧化酶同工酶及酶活性的影响

将鲤鱼暴露于不同浓度的氯化镧溶液120 d,研究稀土元素镧对鲤鱼脑、肝胰脏、肾、鳃、肌肉5种组织超氧化物歧化酶(SOD)同工酶及酶活性的长期影响,结果表明:镧对SOD的影响表现出一定的组织差异性.在实验浓度范围内(0.01～5 mg/L),镧对肝胰脏、鳃、肌肉SOD均有明显抑制作用,且与对照组相比相差显著或极显著(P< 0.05或P< 0.01),而脑、肾SOD活性与对照组相比无显著性差异(P>0.05).同工酶电泳实验结果表明:镧能使鲤鱼肝胰脏、脑、肾、肌肉、鳃SOD酶带活性强弱发生明显变化,还能使肝胰脏SOD同工酶酶带缺失.     

He-Ne激光处理不同时期蚕豆幼苗对抗氧化系统的影响

采用功率为3.50 mW/mm2的He-Ne激光处理不同时期蚕豆,研究其四叶期叶片中丙二醛(MDA)含量,超氧化物歧化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)活性及同工酶谱的变化。结果表明,与对照相比,He-Ne激光处理不同时期蚕豆,MDA含量均显著降低,且各处理间没有显著差异;SOD、POD、CAT酶活性有不同程度提高。SOD、POD同工酶的酶谱在浸种24小时和胚芽露头期经激光处理后改变,在一叶期处理后没有改变;CAT同工酶谱没有变化;在一叶期处理的三种同工酶谱都没有改变。     

摩西球囊霉对三叶鬼针草保护酶活性的影响

旱地农田入侵杂草三叶鬼针草(Bidens pilosa L.)与摩西球囊霉(Glomus mosseae)(AM真菌)经常形成长效的共生体,该霉菌对三叶鬼针草的入侵能力起到促进作用,但机理并不清楚。盆栽试验对正常浇水、中度干旱和重度干旱条件下接种AM真菌的三叶鬼针草植株与未接种植株之间叶片丙二醛(MDA)含量及超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、抗坏血酸氧化酶(ASP)和过氧化物酶(POD)等保护酶活性进行了比较研究。结果表明,干旱胁迫导致三叶鬼针草叶片内MDA含量升高,SOD、CAT、ASP和POD的活性升高;正常浇水条件下,接种G. mosseae 对MDA含量,SOD、ASP和CAT活性影响不显著;中度干旱条件下,接种没有显著影响ASP活性,但对SOD和CAT活性影响显著;在处理前期(7,14,21d)POD活性影响不显著,在处理后期(28,35d)接种植株显著低于未接种植株;重度干旱条件下,未接种植株MDA含量、CAT活性显著高于接种植株,POD活性差异不显著。ASP活性在21d前差异不显著,之后,未接种植株显著高于接种植株。因此,AM真菌G. mosseae 有效地降低了干旱胁迫对三叶鬼针草的伤害程度,随着土壤含水量的严重亏缺和胁迫时间的延长,摩西球囊霉对三叶鬼针草的保护作用逐渐减弱。由于三叶鬼针草和AM真菌之间普遍存在着共生关系,该共生关系可能是三叶鬼针草入侵能力强的关键生物因子之一。     

二斑叶螨刺吸胁迫对白三叶叶绿素含量和两种保护酶的影响

本文采用室内人工接螨法,研究了二斑叶螨Tetranychus urticae Koch不同虫口密度和不同为害时间对白三叶生理的影响。结果表明:在0、5和10头/小叶3个虫口密度下,二斑叶螨取食为害2、4、6和8 d后白三叶植株体内叶绿素含量、过氧化物酶(POD)和多酚氧化酶(PPO)活性有不同程度的变化。二斑叶螨为害后,在同一虫口密度下,随着为害天数的增加白三叶植株体内叶绿素含量呈下降的趋势、而POD和PPO活性呈上升趋势;在同一为害时间内,虫口密度越高,叶绿素含量下降的幅度越大,酶活力增加幅度越明显;方差分析表明,3个虫口密度下白三叶体内叶绿素含量、POD、PPO活性差异显著(P<0.05)。     

甘蓝幼苗受桃蚜危害后叶片中部分酶活性的变化

对桃蚜（Myzus persicae Sulzer）危害后甘蓝（Brassica oleracea L.）幼苗叶中多酚氧化酶（PPO）、苯丙氨酸解氨酶（PAL）、过氧化物酶（POD）活性及同工酶进行了研究。结果表明,随桃蚜危害时间延长,处理叶片PPO、PAL和POD的活性与对照相比均表现出升高的趋势,方差分析表明与对照之间差异显著。同工酶电泳结果表明,POD同工酶的部分谱带随危害时间而发生变化,但EST同工酶在接虫前后则无明显的变化。     

Effects of Cadmium on Antioxidant Enzyme Activities in Sugar Cane

Sugar cane (Saccharum officinarum L. cv. Copersucar SP80-3280) seedlings were grown in nutrient solution with varying concentrations (0, 2 and 5 mM) of cadmium chloride for 96 h. Leaves were analysed for catalase (CAT), glutathione reductase (GR) and superoxide dismutase (SOD) activities. Although a clear effect of CdCl₂ on plant growth was observed, the activity of SOD was not altered significantly. However, the CAT activity decreased as the concentration of CdCl₂ increased. GR exhibits a significant increase in activity at 2 and 5 mM CdCl₂. CAT and SOD isoenzymes were further characterised by analysis in non-denaturing PAGE. Activity staining for SOD revealed up to seven isoenzymes in untreated control and 2 mM CdCl₂ treated plants, corresponding to Cu/Zn-SOD isoenzymes. At 5 mM CdCl₂, only six Cu/Zn-SOD isoenzymes were observed. No Fe-SOD and Mn-SOD isoenzymes were detected. For CAT, one band of activity was observed.     

大豆黄酮对衰老小鼠脑组织SOD、LDH同工酶的影响

利用SOD和LDH同工酶电泳分析,研究大豆黄酮对衰老小鼠的抗氧化作用。结果显示大豆黄酮没有改变SOD和LDH同工酶谱的特征,但对因衰老引起的小鼠脑组织LDH和SOD同工酶活性、各组分的相对活性和比活力的变化有不同程度的改善作用,即LDH同工酶中LDH-2、LDH-3的活性明显下降,LDH-1的活性下降最为明显,而LDH-4的活性有所下降,但不显著,LDH-5的活性几乎没有变化,SOD同工酶的SOD-1和SOD-2的活性有不同程度的升高。这表明大豆黄酮是通过抑制LDH同工酶H亚基的合成来降低LDH的活性,而对M亚基的合成没有影响,并且能够促进SOD同工酶SOD-1和SOD-2的合成,不影响其遗传稳定性。     

二斑叶螨为害对草莓叶片H2O2、MDA含量以及部分防御酶活性的影响

本文旨在探究二斑叶螨Tetranychus urticae为害对草莓Fragaria×ananassa Duch.叶片内过氧化氢（H2O2）、丙二醛（MDA）含量以及部分防御酶活性的影响。在草莓苗上接种不同数量（5~25头）的二斑叶螨,分别在接种后的24 h、48 h和72 h取样,分析草莓叶片内H2O2、MDA的含量以及部分防御酶的活性。结果显示,二斑叶螨为害的草莓叶片内H2O2和MDA的含量以及超氧化物歧化酶（SOD）的活性随着时间的延长而呈现先升后降的趋势,在二斑叶螨持续为害草莓叶片24 h、48 h和72 h时,受损草莓叶片中H2O2的含量均显著高于对照（P<0.05）,不同密度二斑叶螨为害的草莓叶片中H2O2的含量均显著高于对照（P<0.05）,但与取食时间关系不大。当为害时间达到48 h时,MDA的含量和SOD的活性均达到最高峰,此时它们均与二斑叶螨的密度密切相关。当二斑叶螨为25头/叶时,MDA的含量和SOD的活性分别约是对照的3.6倍和10倍。过氧化物酶（POD）和过氧化氢酶（CAT）的活性随时间延长不断升高,均在二斑叶螨为害72 h时达到最高峰。同时,二斑叶螨的为害时间和为害密度之间存在一定的交互作用。以上结果表明草莓叶片主要通过调节其体内H2O2和MDA的含量以及各种防御酶活性的变化,对二斑叶螨的为害产生应激反应。     

Changes of antioxidant enzyme and phenylalanine ammonia-lyase activities during Chimonanthus praecox seed maturation

Changes in peroxidase (POD), superoxide dismutase (SOD), catalase (CAT) and phenylalanine ammonia-lyase (PAL) activities were studied during Chimonanthus praecox seed maturation. According to our findings the protein content increased steadily from 8 to 12 weeks after flowering, and thereafter decreased significantly. Similarly, SOD and POD activities increased gradually up to 12 weeks after flowering and then declined. PAL activity declined gradually during seed maturation. CAT activity, however, showed no changes during seed maturation. By means of polyacrylamide gel electrophoresis (PAGE), SOD and POD isoenzymes were observed during seed maturation. The staining intensities of SOD and POD isoenzymes correlated well with SOD and POD activities as obtained by an assay in solution. These findings suggest that POD, SOD and PAL may be involved in the growth and development during Chimonanthus praecox seed maturation.     

Comparison of antioxidant responses to cadmium and lead in Bruguiera gymnorrhiza seedlings

Seedlings of mangrove plant Bruguiera gymnorrhiza cultured in sand with Hoagland’s nutrient solution were treated with 1 to 30 mM Cd(NO₃)₂ or Pb(NO₃)₂ for 2 months. In all Cd/Pb treatments, the malondialdehyde content increased while the chlorophyll content declined. Peroxidase (POD) and superoxide dismutase (SOD) activities in roots increased at moderate Cd/Pb concentrations (1–10 mM), whereas decreased at higher concentrations (20–30 mM). Catalase (CAT) activity in roots was inhibited by 1–10 mM Cd but enhanced by 1–10 mM Pb. The activities of POD, SOD and CAT in leaves were less affected by Cd and Pb than in roots. A new SOD and three CAT isoenzymes were induced by Pb. In contrast, no additional SOD and CAT isoenzymes were induced by Cd.     

The Distribution and Cooperation of Antioxidant (Iso)enzymes and Antioxidants in Different Subcellular Compartments in Maize Leaves during Water Stress

The effects of mild water stress induced by polyethylene glycol (PEG) on the activities of antioxidant enzymes [superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX), and glutathione reductase (GR)] and their isoenzymes and the antioxidant content [ascorbate (ASC) and glutathione (GSH)] of different subcellular compartments were investigated in maize. For each subcellular compartment, the activities of almost all isoenzymes resolved on native PAGE increased after 4–12 h of exposure to water stress and declined after that, showing concomitant changes with the activities of their respective total enzymes and the antioxidant content. For each subcellular compartment, at least one isoform for the detected antioxidant enzymes was resolved, but different kinds of antioxidant isoenzymes in different subcellular compartments had different responses to water stress. The relative contribution of Fe–SOD in chloroplasts and Mn–SOD in mitochondria was higher than that in other subcellular compartments. However, in apoplasts the activities of Mn–SOD and Fe–SOD declined during the process of water stress, in contrast to those located in other subcellular compartments. The results from the activities of antioxidant (iso)enzymes demonstrated that all antioxidant enzymes in all subcellular compartments were mobilized in cooperation and responded synchronously under mild water stress, with the same trend of changes in their activity. This indicated their orchestrated effects in scavenging reactive oxygen species (ROS) in situ. Additionally, the results suggested that mitochondria and apoplasts, responding most actively, might be targets for improving plant performance under mild water stress.     

Identification of superoxide dismutase isoenzymes in tobacco pollen

We investigated the possible existence of superoxide dismutase (SOD; EC 1.15.1.1) isoenzymes in the pollen of Nicotiana tabacum (Petit Havana SR-1 cultivar). To detect SOD activity, crude extracts from tobacco pollen were subjected to native polyacrylamide gel electrophoresis followed by staining with nitroblue tetra-zolium (NBT). The presence of six SOD isoenzymes was detected in tobacco pollen. Treatment with SOD inhibitors indicated the presence of one manganese SOD (Mn SOD), five copper-zinc SOD (Cu/Zn SOD) isoenzymes, and the absence of iron SOD (Fe SOD).     

Identification of superoxide dismutase isoenzymes in tobacco pollen

We investigated the possible existence of superoxide dismutase (SOD; EC 1.15.1.1) isoenzymes in the pollen of Nicotiana tabacum (Petit Havana SR-1 cultivar). To detect SOD activity, crude extracts from tobacco pollen were subjected to native polyacrylamide gel electrophoresis followed by staining with nitroblue tetrazolium (NBT). The presence of six SOD isoenzymes was detected in tobacco pollen. Treatment with SOD inhibitors indicated the presence of one manganese SOD (Mn SOD), five copper-zinc SOD (Cu/Zn SOD) isoenzymes, and the absence of iron SOD (Fe SOD).     

Nickel elicits a fast antioxidant response in Coffea arabica cells.

The antioxidant responses of coffee (Coffea arabica L.) cell suspension cultures to nickel (Ni) were investigated. Ni was very rapidly accumulated in the cells and the accumulation could be directly correlated with the increase of NiCl(2) concentration in the medium. At 0.05 mM NiCl(2) growth was stimulated, but at 0.5 mM NiCl(2), the growth rate was reduced. An indication of alterations in the presence of reactive oxygen species was detected by an increase in lipid peroxidation at 0.5 mM NiCl(2). Catalase (CAT; EC 1.11.1.6), glutathione reductase (GR; EC 1.6.4.2), ascorbate peroxidase (APX; EC 1.11.1.11), guaiacol peroxidase (GOPX; EC 1.11.1.7) and superoxide dismutase (SOD; EC 1.15.1.1) activities were increased, particularly at earlier NiCl(2) exposure times and the activities were higher at 0.5 mM NiCl(2) for most of exposure times tested. Non-denaturing PAGE revealed one CAT isoenzyme, nine SOD isoenzymes and four GR isoenzymes. The SOD isoenzymes were differentially affected by NiCl(2) treatment and one GR isoenzyme was increased by NiCl(2). NiCl(2) at 0.05 mM did not induce lipid peroxidation and the main response appeared to be via the induction of SOD, CAT, GOPX and APX activities for the removal of the reactive oxygen species and through the induction of GR to ensure the availability of reduced glutathione.