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1.
杜鹃对SO2胁迫的抗氧化防护效应   总被引:3,自引:0,他引:3  
以SO2耐受性植物杜鹃(Rhododendron sp.)为材料,在2个高浓度SO2熏气后,检测了叶组织中丙二醛(MDA)、可溶性蛋白和叶绿素含量以及抗氧化酶活性.结果表明:40和80mg?m-3SO2熏气4h(1d)后,杜鹃叶片超氧化物歧化酶(SOD)活性和MDA含量均分别比对照显著增加了11.26%、11.86%和73.32%、76.43%;随熏气时间的延长,SOD、过氧化物酶(POD)、过氧化氢酶(CAT)活性持续增高,且SOD和CAT活性显著高于对照,MDA含量逐渐降至对照水平;SO2熏气导致叶片可溶性蛋白含量显著降低,但叶绿素含量却无显著改变.熏气后恢复期间,抗氧化酶活性相对降低,可溶性蛋白含量恢复至对照水平.研究发现,杜鹃对SO2的耐受性与细胞中抗氧化酶活性的诱导性增强有关,抗氧化能力增强是植物适应SO2胁迫的重要原因.  相似文献   

2.
小麦叶片的过氧化物酶活性随年龄增大而上升,同工酶谱也随不同叶层叶龄的增大而加强,并出现新的酶带。 SO_2熏气促进小麦叶片的过氧化物酶活性,不同层次叶片比较,幼嫩叶片促进程度比老叶大些。SO_2熏气对小麦叶片过氧化物酶同工酶的某些酶带有加强作用,并能诱导产生新的酶带。同一叶片的前半叶伤害比后半叶重,过氧化物酶活性也以前半叶为大,说明过氧化物酶活性的提高与伤害有一定关系。  相似文献   

3.
二氧化硫胁迫导致拟南芥防护基因表达改变   总被引:4,自引:0,他引:4  
仪慧兰  李利红  仪民 《生态学报》2009,29(4):1682-1687
研究SO2熏气对拟南芥细胞中mRNA和蛋白质表达的影响,分析植株对逆境胁迫的响应机制.结果表明,30 mg·m-3 SO2 熏气72 h后拟南芥地上组织中差异表达1倍以上的基因有494个,其中抗氧化酶、谷胱甘肽硫转移酶(GST)、硫氧还蛋白等多种与逆境生理关系密切的基因表达上调;2.5~30 mg·m-3 SO2 熏气可导致超氧化物岐化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GPX)和GST的活性诱导性增高,SOD、CAT同工酶谱带特征改变.研究结果表明,SO2 胁迫能够诱导拟南芥中防护基因在mRNA和蛋白质表达水平的改变,这些基因的差异性表达可能对逆境生理过程有益.  相似文献   

4.
研究了氮离子和氩离子注入萝卜种子对萝卜幼苗蛋白含量、过氧化物酶活性及过氧化物酶、淀粉酶和蛋白酶同工酶的影响。结果表明 :离子注入后 ,减低萝卜过氧化物酶活性和蛋白含量。萝卜不同生长时期同工酶变化不一样。在子叶时期 ,过氧化物酶同工酶谱带无明显变化 ,淀粉酶同工酶有酶带的消失 ;而在真叶时期 ,过氧化物酶在负极区减少一条酶带 ,Rf为 0 .2 2 ,正极区增加一条酶带 ,Rf为 0 .6 ,且随剂量增加 ,酶带着色增强 ;淀粉酶同工酶在注入剂量为 5× 10 5N+ / cm2 )时 ,有同工酶带增加 ,Rf为 0 .6 1。低剂量时蛋白酶活性增强 ,谱带增多 ,大剂量则减弱。因此 ,N+和 Ar+注入后 ,可影响萝卜过氧化物酶和淀粉酶的表达及蛋白质的合成或降解。  相似文献   

5.
受一定浓度SO_2熏气的大豆幼苗出现可见伤害以后,在继续熏气的过程中可见伤害程度不再进一步发展,表现出一定的适应性。与此相联系,膜透性增加和TTC还原力下降这两个SO_2伤害指标也得到一定程度的恢复,SO_2熏气使游离氨基酸含量增加,随着熏气时间延长,增加的游离氨基酸含量回到对照水平,提示受扰乱的代谢过程有所恢复。低浓度SO_2预处理提高了大豆对高浓度SO_2的抗性,与抗氧化有关的巯基(-SH)含量显著增加,超氧物歧化酶(SOD)活性也有所增强,同工酶谱分析显示有SOD同工酶带的酶量增加或新带出现。  相似文献   

6.
辐射对大麦过氧化物酶同工酶谱影响的初步研究*   总被引:8,自引:0,他引:8       下载免费PDF全文
γ射线处理大麦种子后其幼苗组织中过氧化物酶同工酶谱发生较大的变化。在偏负极端RfO.29-0.38出现新的酶带区,酶带数目随辐射剂量的增加而增加。低剂量辐射后在该区出现1-2条新同工酶带,以RfO.29 和Rf0.34酶带为主;较高剂量辐射后在该区出现2-3条新酶带,Rf为0.29、0.34或Rf0.29、0.34、0.38。研究结果表明这一带区的过氧化物酶同工酶谱与辐射损伤有一定的关系,其变化特点能反映出供试品种的辐射敏感性。  相似文献   

7.
干旱胁迫下内生真菌感染对黑麦草叶内几种同工酶的影响   总被引:11,自引:0,他引:11  
任安芝  高玉葆  陈悦 《生态学报》2004,24(7):1323-1329
以内生真菌感染(endophyte-infected,EI)与不感染(endophyte-free,EF)的黑麦草(Lolium perenne L.)种子建立实验种群,分别对其施加长时间不同强度的干旱胁迫,通过比较黑麦草体内过氧化物酶(POD)、超氧化物歧化酶(SOD)、多酚氧化酶(PPO)活性及其同工酶谱的变化以探讨保护酶系统在内生真菌——植物共生体的抗旱性方面所作的贡献。研究结果表明,水分胁迫和内生真菌对黑麦草3种酶的影响不仅表现在总量上而且表现在同工酶的酶谱及各区带的酶活力上。就总酶活力而言,EI和EF植株中POD、SOD和PPO的活性均随着干旱胁迫强度的增加而增加,进一步将EI和EF植株的酶活力进行比较,发现与EF植株相比,EI植株中POD和PPO的活性相对较低,而SOD的活性相对较高。从同工酶的谱带数量和强弱来看,POD同工酶各区带活力均随干旱胁迫强度的增加而增加,EI植株叶片增加的幅度高于EF叶片,而且EI叶片在重度胁迫下出现了1条新带SOD同工酶各区带活力在EI叶片中有随干旱胁迫增加而增加的趋势,而在EF叶片中有些区带酶活力增强,有些区带酶活力减弱,且EI叶片在中度胁迫下出现了1条新带;PPO同工酶随干旱胁迫的增强,EI和EF叶片均表现为有些区带酶活力增强,有些区带酶活力减弱。总之,内生真菌的感染虽然没有显著提高宿主植物黑麦草POD、SOD和PPO的活性,但使宿主黑麦草对干旱胁迫的反应更为迅速,其中既包括POD、SOD等酶活力的迅速升高,也包括新酶带的产生。  相似文献   

8.
南方红豆杉对二氧化硫胁迫的生理响应   总被引:1,自引:0,他引:1  
为探究南方红豆杉(Taxus chinensis var.mairei)对SO2污染的抗逆机理,本实验以1年生盆栽幼苗为材料,采用密闭箱静态熏气法,研究了不同质量浓度SO2(5、10、20和40mg·m-3)下对南方红豆杉主要逆境生理特性的影响。结果表明,随着SO2浓度的增加和熏气时间的延长,叶片受到不同程度的伤害,同时伴随着叶绿素a和叶绿素b的迅速下降,叶片质膜透性的急剧增加,丙二醛含量大幅度上升,可溶性糖和脯氨酸升高。在同一熏气时间下,随着SO2浓度的增加,SOD、POD、CAT、和APX活性呈现先升高后下降的趋势。在整个熏气时间段内,在5 mg·m-3SO2胁迫下,SOD和APX活性首先被诱导,而POD和CAT在10mg·m-3SO2下被诱导;在40 mg·m-3SO2浓度下,与对照相比,SOD、CAT、APX和POD活性显著下降。可以推断,在低于10 mg·m-3SO2浓度下,南方红豆杉通过自身的应激保护系统来提高对SO2的抗性,维持正常生长;南方红豆杉适用于SO2污染区的园林绿化。  相似文献   

9.
吴信忠  李树华 《动物学报》1998,44(3):286-292
采用同工酶电泳技术对三平正并殖吸虫童虫、早期成虫和后期成虫的葡萄糖磷酸变位酶、葡萄糖磷酸异构酶和葡萄糖-6-磷酸脱氢酶的同工酶进行了研究,结果显示三平正并殖吸虫由童虫向成熟期发育过程中,葡萄糖磷酸变位酶和葡萄糖磷酸异构酶的同工酶谱趋于复杂,酶带数目后期成虫〉早期成虫〉童虫;而葡萄糖-6-磷酸脱氢酶同工酶谱则趋于简单,童虫或未成熟虫体酶带数目较成熟虫体为多。三种酶系统的同工酶排列型式显示,吸虫由童虫  相似文献   

10.
多裂骆驼蓬提取物对玉米幼苗生长和细胞保护酶系的影响   总被引:5,自引:1,他引:4  
以不同浓度的多裂骆驼蓬提取液浸种处理玉米,研究对幼苗生长和细胞保护酶系的影响.结果表明,多裂骆驼蓬提取液浸种处理种子的萌发和种子中α-淀粉酶活性受到明显抑制,抑制作用随处理浓度提高而增强,随培养时间延长而减弱.随着培养时间的延长,浸种处理可显著提高幼苗根系活力和叶片硝酸还原酶活性,促进植株生长,根和茎叶生长量增加,根冠比增大.多裂骆驼蓬提取液浸种后显著降低叶片过氧化氢酶(CAT)、抗坏血酸氧化酶(ACO)活性,提高过氧化物酶(POD)活性,促进根系和叶片过氧化物同工酶谱的数量表达.  相似文献   

11.
二氧化硫对小麦的氧化胁迫及其某些信号分子的调节   总被引:11,自引:0,他引:11       下载免费PDF全文
通过在密闭的培养箱中一次性通入不同体积浓度的SO2气体,研究了小麦幼苗超氧自由基O2-含量和3种抗氧化酶活性的变化,探讨了信号分子水杨酸、乙烯和过氧化氢对SO2氧化胁迫的调节作用.结果表明,当通入10和40 μl·L-1 SO2时,小麦叶片中O2-含量递增,过氧化物酶(POD)和过氧化氢酶(CAT)活性增强,但超氧化物歧化酶(SOD)活性降低.当SO2浓度达到50 μl·L-1时,POD和CAT活性也开始降低,此时叶片尖端出现坏死,叶片绿色部位滋生大量真菌.用1 mmol·L-1水杨酸(SA)(pH6.5)浸泡小麦干种子6 h,或用10 mmol·L-1 H2O2浸泡幼苗,O2-含量低于对照植株,而3种酶的活性高于对照植株,均可有效地减轻SO2的氧化胁迫.在SO2熏蒸下,乙烯显著抑制3种酶的活力,提高O2-的形成速率.SA与乙烯同时使用时,SA几乎完全消除了乙烯的负面作用.  相似文献   

12.
(Na+ + K+)-ATPase activity of a dog kidney enzyme preparation was markedly inhibited by 10-30% (v/v) dimethyl sulfoxide (Me2SO) and ethylene glycol (Et(OH)2); moreover, Me2SO produced a pattern of uncompetitive inhibition toward ATP. However, K+-nitrophenylphosphatase activity was stimulated by 10-20% Me2SO and Et(OH)2 but was inhibited by 30-50%. Me2SO decreased the Km for this substrate but had little effect on the Vmax below 30% (at which concentration Vmax was then reduced). Me2SO also reduced the Ki for Pi and acetyl phosphate as competitors toward nitrophenyl phosphate but increased the Ki for ATP, CTP and 2-O-methylfluorescein phosphate as competitors. Me2SO inhibited K+-acetylphosphatase activity, although it also reduced the Km for that substrate. Finally, Me2SO increased the rate of enzyme inactivation by fluoride and beryllium. These observations are interpreted in terms of the E1P to E2P transition of the reaction sequence being associated with an increased hydrophobicity of the active site, and of Me2SO mimicking such effects by decreasing water activity: (i) primarily to stabilize the covalent E2P intermediate, through differential solvation of reactants and products, and thereby inhibiting the (Na+ + K+)-ATPase reaction and acting as a dead-end inhibitor to produce the pattern of uncompetitive inhibition; inhibiting the K+-acetylphosphatase reaction that also passes through an E2P intermediate; but not inhibiting (at lower Me2SO concentrations) the K+-nitrophenylphosphatase reaction that does not pass through such an intermediate; and (ii) secondarily to favor partitioning of Pi and non-nucleotide phosphates into the hydrophobic active site, thereby decreasing the Km for nitrophenyl phosphate and acetyl phosphate, the Ki for Pi and acetyl phosphate in the K+-nitrophenylphosphatase reaction, accelerating inactivation by fluoride and beryllium acting as phosphate analogs, and, at higher concentrations, inhibiting the K+-nitrophenylphosphatase reaction by stabilizing the non-covalent E2.P intermediate of that reaction. In addition, Me2SO may decrease binding at the adenine pocket of the low-affinity substrate site, represented as an increased Ki for ATP, CTP and 3-O-methylfluorescein phosphate.  相似文献   

13.
Plasmodium lophurae serine hydroxymethyltransferase (EC 2.1.2.1) was partially purified and characterized by (NH4)2SO4 fractionation and chromatography on Sephadex G-100. The enzyme, precipitated by 3.0.3.3 M (NH4)2SO4, had a molecular weight of 68,300 as estimated by exclusion chromatography on G-100. The pH optimum of the enzyme was 6.8-7.6 in sodium phosphate-citrate buffer. Citrate stabilized the enzyme during storage in phosphate buffer at 4 C. The Km was 4.3 X 10(-3) M for L-serine and 2.5 X 10(-4) M for tetrahydrofolate.  相似文献   

14.
Apparent carbonic anhydrase activity in leaf extracts, measured as the rate of H+ production associated with the CO2 hydration reaction, varied by as much as 25-fold when the assay buffer was varied. Highest activities were usually recorded in barbitone buffer, with lower activities in imidazole, Tricine, Hepes, Tris, and phosphate buffers. The greatest differences were observed with the enzyme isolated from leaves of the monocotyledonous plants Zea mays (maize) and Triticum aestivum (wheat). Smaller differences were observed with carbonic anhydrase from dicotyledonous species and there was no effect on the erythrocyte enzyme. Leaf carbonic anhydrase activity measured by the mass spectrometric procedure was unaffected by varying the assay buffer. The low activity in certain buffers observed with the former assay system was found to be due to inhibition of the enzyme-catalyzed reaction by higher concentrations of CO2. Carbonic anhydrase from some sources was also strongly inhibited by certain inorganic and organic anions.  相似文献   

15.
以小麦品种‘德抗961'为材料,用NO供体硝普钠(SNP)浸种研究外源NO对盐胁迫下小麦种子萌发的影响.结果表明:0.06 mmol/L的SNP浸种24 h后对盐胁迫下小麦种子发芽率、发芽指数、活力指数和吸胀速率的下调都有显著缓解作用;SNP浸种对盐胁迫下α-淀粉酶的活性无明显影响,但能显著提高盐胁迫下β-淀粉酶的活性;进一步研究表明,SNP浸种预处理对盐胁迫下的α-淀粉酶同工酶变浅的条带有所恢复(尤其是条带3),同时使盐胁迫下变浅的β-淀粉酶同工酶的条带有明显的恢复(尤其是d、e、f、g).并且SNP能显著降低盐胁迫下小麦地上部分和根中的Na^+含量,提高其K+含量,从而使K^+/Na^+显著提高.以上结果表明:SNP浸种预处理提高盐胁迫下小麦种子的萌发,主要是通过提高β-淀粉酶的活性来实现的.  相似文献   

16.
Horseradish peroxidase (HRP) has attracted intense research interest due to its potential applications in biotechnological fields. However, inadequate stability under prevalent conditions such as elevated temperatures and H(2)O(2) exposure, has limited its industrial application. In this study, stability of HRP was investigated in the presence of different buffer systems (potassium phosphate and Tris-HCl) and additives. It was shown that the concentration of phosphate buffer severely affects enzyme thermostability in a way that in diluted potassium phosphate buffer (10mM) half-life (from 13 to 35 min at 80 °C) and T(m) (from 73 to 77.5 °C) increased significantly. Among additives tested, trehalose had the most thermostabilizing effect. Exploring the role of glycosylation in stabilizing effect of phosphate buffer, non-glycosylated recombinant HRP was also examined for its thermal and H(2)O(2) stability in both diluted and concentrated phosphate buffers. The recombinant enzyme was more thermally stable in diluted buffer in accordance to glycosylated HRP; but interestingly recombinant HRP showed higher H(2)O(2) tolerance in concentrated buffer.  相似文献   

17.
Aims   总被引:2,自引:0,他引:2       下载免费PDF全文
 用He-Ne激光(5.23 mW·mm–2)处理经5%、10%、15% PEG6000胁迫的小麦幼苗, 分析了干旱胁迫条件下激光处理对小麦幼苗保护酶活性及脂质过氧化作用的影响。适度干旱胁迫的小麦幼苗经He-Ne激光辐照后, 丙二醛(MDA)含量和超氧自由基(O2–.)产生速率显著降低(p<0.05), 而过氧化物酶(POD)活性和抗坏血酸(AsA)、谷胱甘肽(GSH)含量却显著增加(p<0.05)。总体上看, 5%和10% PEG6000胁迫的小麦幼苗经激光辐照3 min后抗旱性增强。  相似文献   

18.
研究了根霉12号固体发酵产生纤溶酶的工艺条件。采用单因素试验、均匀设计方法对固体发酵培养基的碳源、氮源、碳氮比、初始pH、加水量、无机盐加量进行了优化;采用正交试验对发酵时间、接种量进行了研究。结果表明,实验范围内根霉12固体发酵产纤溶酶的适宜培养基组成为:麸皮∶豆粕=1∶2,初始pH5.0,加水量0.75ml/g物料, MnSO4H2O和 (NH4)2SO4加量分别为0.25%和 1.42%(对物料)。适宜培养条件为接种量107个孢子/g物料,培养时间72h。优化条件下的纤溶酶产量平均达791.81u/g物料。  相似文献   

19.
A proteinase from Pseudomonas aeruginosa exhibiting collagenolytic activity was purified 1575-fold with a recovery of 24% by use of chemical and chromatographic technics. The enzyme preparation appeared to be homogeneous when subjected to chromatographic, electrophoretic and ultracentrifugational analyses. A standard state sedimentation coefficient of 2.10 S was calculated and further analyses indicated that the enzyme had a molecular weight of 17 500 and dimerizes under certain conditions to yield an apparent molecular weight of 34 000. In addition to insoluble collagen, the enzyme catalyzed the hydrolysis of congocoll, azocoll, soluble collagen and casein, but did not attack orcein-elastin, azoalbumin, p-toluene eulfonyl-L-arginine methyl ester, benzoyl-L-tyrosine ethyl ester, and the hexapeptide N-benzyloxycarbonyl-glycyl-L-prolyglycylglycyl-L-prolyl-L-alanine. Enzymatic activity against congocoll was 6-fold greater at pH 7.5 in Tris with HCl than in phosphate buffer at the same ionic strength. Cobalt, and to a lesser extent, Zn2+ appeared to activate the enzyme, especially in phosphate buffer. NcCN and p-chloromercuribenzoate did not appreciably inhibit enzyme activity, while (NH4)2 SO4, EDTA and cysteine displayed a significant inhibitory effect under certain conditions.  相似文献   

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