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1.
NaCl胁迫对甘薯叶片叶绿体超微结构及一些酶活性的影响 总被引:36,自引:0,他引:36
随NaCl胁迫浓度的提高,甘薯叶片叶绿体数目逐渐减少,类囊体膜片层松散、扭曲、破裂及逐渐解体膜片层检叶绿素含量下降。与此同时,H2O2、MDA含量增加,ASP、SOD活性表现先上升后下降的趋势。耐盐品种在NaCl胁迫下能维持较强的H2O2清除能力和较低的MDA水平。 相似文献
2.
在0、100、300、500和700 mmol·L-1NaCl胁迫条件下比较了喷施0.1mmol·L-1亚精胺(Spd)对毕氏海蓬子(Salicomia bigelovii Torr.)幼苗叶绿素含量、净光合速率、气孔导度、胞间CO2浓度和叶绿体超微结构的影响.结果表明:毕氏海蓬子的叶绿素含量、净光合速率和气孔导度均呈低浓度条件下(0、100和300 mmol·L-1NaCl)升高、高浓度条件下(500和700 mmol·L-1NaCl)降低的趋势,在300 mmol·L-1 NaCl胁迫条件下达到最高值:胞间CO2浓度则呈低浓度NaCl胁迫条件下降低、500 mmol·L-1NaCl条件下升高、700 mmol·L-1NaCl条件下略降低的趋势;在0~500 mmol·L-1NaCl胁迫条件下叶绿素a/b值变化不明显,但在700 mmol·L-1NaCl条件下急剧降低.在低浓度NaCl胁迫条件下,叶绿体整体膨胀,类囊体片层结构松散,但叶绿体和类囊体结构仍保持完整;而经500和700mmol·L-1NaCl处理后,叶绿体超微结构被严重破坏,叶绿体膜结构破裂、类囊体结构松散呈放射状、有些叶绿体完全解体.而在相应的NaCl胁迫条件下喷施0.1 mmol·L-1Spd,毕氏海蓬子的叶绿素含量、净光合速率、气孔导度和胞间CO2浓度虽然也呈现出相同的变化趋势,但其数值均显著高于对照(未喷施Spd);且叶绿体超微结构的损伤程度也轻于对照.研究结果说明:喷施外源Spd能够减缓NaCl胁迫对毕氏海蓬子的伤害作用. 相似文献
3.
等渗NaCl、干旱胁迫对番茄幼苗光合特性及叶绿体超微结构的影响 总被引:1,自引:0,他引:1
为分析等渗盐分和水分胁迫对番茄叶片光合功能的影响,选用耐盐性不同的4种基因型番茄(小果型的辽园红玛瑙、野生醋栗番茄、大果型的金田粉冠、超402)进行等渗的140 mmol·L-1NaCl和15%PEG6000模拟盐分和水分胁迫.结果表明: 在光合特性方面,处理12 d后,两种胁迫导致4种不同基因型番茄的叶绿素含量(叶绿素a、叶绿素b、叶绿素总量)、光合速率、气孔导度、胞间CO2浓度、蒸腾效率降低,气孔限制值升高.两种胁迫导致的光合下降由气孔性因素所致.等渗的盐分胁迫对番茄的光合系统损伤大于水分胁迫,这是因为盐分胁迫除了渗透胁迫还会导致离子伤害.4种不同基因型番茄中,耐盐型的辽园红玛瑙具有高光合特性,金田粉冠光合效率最差.在叶绿体超微结构方面,两种胁迫会造成番茄叶片的气孔密度增加,气孔张开率降低,叶绿体长度增加,宽度变小,长宽比增大,叶绿体内基粒数减少,嗜锇颗粒数增多.盐分胁迫下两种番茄叶绿体结构的影响大于水分胁迫,耐盐种醋栗番茄气孔变化小于盐敏感品种金田粉冠. 相似文献
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5.
NaCl胁迫对5个引自北美的树种叶肉细胞超微结构的影响 总被引:1,自引:0,他引:1
为明确美国白蜡(Fraxinus americana L.)、茶条槭(Aceginnala Maxim.)、红桤木(Alnus rubra Bong.)、水紫树(Nyssa aquatica L.)和美国皂荚(Gleditsia triacanthos L.)5个引自北美的树种的耐盐性,采用水培方法、利用透射电镜技术对0(对照)、4和8 g·L-1 NaCl胁迫处理后5个树种1年生苗叶肉细胞超微结构的变化进行了观察和比较.观察结果表明:正常条件(0g·L-1NaCl)下,5个树种叶肉细胞在叶绿体形态、嗜锇颗粒数量等方面略有差异,但均未发生质壁分离现象.经NaCl胁迫处理后,5个树种叶肉细胞中的叶绿体和细胞核受到不同程度的损伤,表现为叶绿体膜消失,类囊体片层结构肿胀,叶绿体降解,嗜锇颗粒增大或增多,细胞核的核膜消失、核染色质凝聚;且随NaCl质量浓度的提高,损伤程度均逐渐加剧.4和8g·L-1NaC1胁迫条件下,美国皂荚、茶条槭和水紫树的叶肉细胞发生质壁分离现象,而红桤木、美国白蜡和水紫树的叶肉细胞内出现环状片层.根据观察结果,推测红桤木和美国白蜡对NaCl胁迫的耐性较强,美国皂荚和茶条槭也有一定的耐性,而水紫树的耐性最弱. 相似文献
6.
该研究以5个桂花品种为材料,以Hoagland培养液为对照,设计2个NaCl含量(70、100 mmol/L)处理10 d后利用透射电镜和扫描电镜观察各处理不同品种的叶片超微结构特征,以明确桂花品种对耐NaCl胁迫的解剖结构响应机制。结果显示:(1)透射电镜观察发现:随NaCl 胁迫程度的加强,5个桂花品种叶肉细胞中叶绿体结构受到不同程度地破坏;70 mmol/L NaCl处理后,5个品种的细胞核基本保持正常,而100 mmol/L NaCl处理后核内染色质发生降解;随着NaCl胁迫程度的加强,5个桂花品种的类囊体片层结构中嗜锇颗粒明显增多;在膜结构方面,大叶银桂的叶肉细胞被破坏程度最为严重,叶绿体膜被破坏,叶绿体形状基本不能辨认。(2)扫描电镜观察结果显示:随着NaCl浓度的增大,5个品种叶片表面的气孔密度不断增大,而张开气孔的密度却不断减小,且叶肉细胞体积均缩小;‘大叶银桂’、‘笑秋风’、‘晚籽银桂’的栅栏组织占叶厚的比重随NaCl胁迫浓度的增大而升高,‘潢川金桂’和‘紫梗籽银桂’的栅栏组织占叶厚的比重则随NaCl胁迫浓度的增大而呈先升高后降低的趋势。研究表明,NaCl胁迫对桂花叶片细胞叶绿体、细胞核等的超微结构会造成损伤,且NaCl胁迫浓度越高损伤越明显。该试验可初步判断‘大叶银桂’、‘笑秋风’、‘晚籽银桂’的耐盐性略高于‘潢川金桂’和‘紫梗籽银桂’。 相似文献
7.
干旱胁迫对5种植物叶绿体和线粒体超微结构的影响 总被引:3,自引:0,他引:3
应用温室盆栽方法,研究了土壤干旱胁迫对麻栎(Quercus acutissima Carruth)、黄檀(Dalbergia hupeana Hance)、黄连木(Pistacia chinensis)、湿地松(Pinus elliottii)、朴树(Celtis sinesis Pers)5个树种叶肉细胞超微构的影响。结果表明:正常水分条件下,叶肉细胞中各细胞器结构完整。轻度干旱胁迫下,湿地松的叶片超微结构未受损伤。麻栎线粒体无明显变化,叶绿体有扩张现象。黄连木与黄檀线粒体外膜有降解现象,叶绿体膨胀。朴树线粒体与叶绿体受损明显。重度胁迫下,湿地松和麻栎的线粒体内部出现降解,叶绿体受损。黄连木与黄檀出现质壁分离,叶绿体与线粒体受到严重损伤。朴树细胞内部受损最严重。可将5个树种分为3种不同的抗旱等级:湿地松与麻栎抗旱性较强,黄连木与黄檀抗旱性中等,朴树抗旱性较弱。 相似文献
8.
温室条件下,分别用浓度为150、300、350 mmol/L的NaCl和Na2SO4处理‘石头扁桃’和‘桃扁桃’实生苗植株,处理10 d后分别测定其叶片叶绿素含量、净光合速率、气孔导度、细胞间隙CO2浓度,并观察叶绿体超微结构的变化。研究发现:(1)盐胁迫下,‘石头扁桃’和‘桃扁桃’chl a、chl b均在低浓度盐区含量最高,而在高浓度盐区含量最低,Na2SO4处理区chl a、chl b含量均低于NaCl处理区;(2)‘石头扁桃’和‘桃扁桃’叶片净光合速率随盐浓度的增加而下降,‘石头扁桃’下降的幅度较大;(3)‘桃扁桃’叶片细胞间隙CO2浓度随盐浓度的增加而升高,但‘石头扁桃’叶片细胞间隙的CO2浓度变化没有稳定的规律;(4)2个品种的叶片气孔导度均随盐浓度的增加而降低;(5)盐胁迫后,叶绿体基粒、基质片层扭曲,类囊体肿胀;随盐浓度的增加,形变加剧,叶绿体由椭圆形肿胀成圆形,叶绿体膜解体,且‘石头扁桃’叶绿体对盐胁迫比较敏感。综合分析发现,2种盐胁迫对植物造成伤害的机理不同,‘石头扁桃’的耐盐能力较差。 相似文献
9.
间作套种是我国主要的花生(Arachis hypogaea)种植方式之一。然而, 与单作相比, 在间作套种体系中, 花生截获的光能较少, 生长发育差, 产量低, 研究不同品种耐阴机理对选择适宜间作套种的花生品种具有重要意义。该研究用耐阴性不同的两个花生品种‘花育22号’ (强耐阴性)和‘白沙1016’ (弱耐阴性)为材料, 在大田条件下采用不同透光率遮阴网设置50%自然光强(中度弱光胁迫)和15%自然光强(严重弱光胁迫) 2个弱光处理, 从出苗期开始遮阴40天, 以自然光强为对照, 研究了弱光胁迫对花生功能叶片RuBP羧化酶活性和叶绿体超微结构的影响。结果表明: 光强为自然光照50%和15%的处理, ‘花育22号’ RuBP羧化酶活性与对照相比虽有降低, 但差异不显著, 而‘白沙1016’分别比对照低40.1%和59.4%, 显著低于对照。与对照相比, 50%自然光强下‘花育22号’叶绿体数不变, 叶绿体基粒数和基粒片层数显著增多, 叶绿体变长且发育完好, 15%自然光强下, 叶绿体数、基粒数和淀粉粒数显著减少, 叶绿体膜和基粒片层出现破损, 但叶绿体变长, 基粒片层数增加; ‘白沙1016’在50%自然光强下, 叶绿体数目和超微结构变化同‘花育22号’相似, 在15%自然光强下叶绿体变圆, 基粒数的降幅和基粒片层破损程度大于‘花育22号’且基粒片层数减少, 淀粉粒数增多。因此, 弱光胁迫特别是严重弱光胁迫条件下, 功能叶RuBP羧化酶活性降低幅度小、叶绿体超微结构受损程度低是‘花育22号’耐阴的光合生理基础。 相似文献
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11.
Intact chloroplasts isolated from sulphur dioxide fumigatedHardwickia binata leaves showed inhibition of PS II electron transport activity without any significant effect on photosystem I. Sulphur dioxide
exposed leaves accumulated more hydrogen peroxide than those from non-fumigated plants and this was caused by increase in
superoxide radical production. Hydrogen peroxide formation was inhibited by addition of cytochrome C and superoxide disrnutase.
In sulphur dioxide fumigated leaves, increase in superoxide dismutase activity showed resistance to sulphite toxicity. The
localization of ascorbate peroxidase, glutathione reductase and dehydroascorbate reductase activities in chloroplasts provide
evidence for the photogeneration of ascorbate. The scavenging of hydrogen peroxide in chloroplast due to ascorbate regenerated
from DHA by the system: PS I → Fd → NADP → glutathione. The system can be considered as a means for preliminary detoxification
of sulphur dioxide by chloroplasts 相似文献
12.
The involvement of enzymic antioxidant system, superoxide dismutase, guaiacol peroxidase, ascorbate peroxidase in defense
reaction to environmental stress evoked by air and soil pollution, was seasonally studied on three populations of Scots pine
(Pinus sylvestris L.) growing on experimental areas close two industrial objects in Poland. The first of them (Luboón) is localised near a
phosphate fertiliser factory, the second (Głogów) near a copper foundry, and control stand is placed in Kórnik. Głogów is
the most polluted site, where in 1998 monthly mean daily concentrations was: SO2 - 17 μg·m−3, NOx- 12 μg·m−3 and dust containing heavy metals (Cu, Pb, Cd) - 29 μg·m−3. Trees in Luboń were influenced for many years by high concentration of SO2 and fluor compounds. Few years ago emissions were markedly reduced, but changes in the soil (low pH and high concentration
of aluminium ions) still influence the growth of trees. In needles of two populations: 3 (Russia) and 8 (Poland), from the
polluted sites Głogów and Luboń, activities of superoxide dismutase (SOD) and guaiacol peroxidase (PO) were significantly
higher compared to Kórnik. However, in one population (16 - Slovakia), such dependance was not evident. Activity of ascorbate
peroxidase (AP) measured in winter was also higher in needles from polluted sites. The results indicated that the sensitivity
of free radical scavenging system in Scots pine needles differs among populations. 相似文献
13.
Chilling Induced Oxidative Stress in Germinating Wheat Grains as Affected by Water Stress and Calcium 总被引:1,自引:0,他引:1
Wheat (Triticum aestivum L.) plants were subjected to mild water stress during grain filling at milk (early, medium, and late) and dough (early, soft, hard) stages. The grains harvested from stressed plants were subjected to low temperature stress of 10 °C for 24 h in presence or absence of 1 mM CaCl2, and embryos were examined for oxidative injury. The embryos of grains water stressed at milk and soft dough stages showed lowest contents of H2O2 and malondialdehyde and highest membrane stability index, ascorbic acid content, and activities of catalase, ascorbate peroxidase, and superoxide dismutase as compared to control embryos or water-stressed at other stages. Presence of Ca2+ in the medium reduced H2O2 and malondialdehyde content and increased ascorbic acid content, and catalase, ascorbate peroxidase and superoxide dismutase activities. 相似文献
14.
The enzymes of hydrogen peroxide metabolism have been investigated in the cestodes H. diminuta and M. expansa. Neither catalase, lipoxygenase, glutathione peroxidase, NADH peroxidase nor NADPH peroxidase could be detected in homogenates of either species. However, both H. diminuta and M. expansa possessed a peroxidase which had a high affinity for reduced cytochrome c. The peroxidase was characterized by substrate and inhibitor studies and cell fractionation showed the enzyme to be located in the mitochondrial membrane fraction. The peroxidase could act as a substitute for catalase, by destroying metabolic hydrogen peroxide. Appreciable superoxide dismutase activity was found in M. expansa and H. diminuta and it is possible that this enzyme is the source of helminth hydrogen peroxide. 相似文献
15.
The present study was carried out to study the effect of salt stress on cell membrane damage, ion content and antioxidant
enzymes in wheat (Triticum aestivum) seedlings of two cultivars salt-tolerant KRL-19 and salt-sensitive WH-542. Seedlings (4-d-old) were irrigated with 0, 50
and 100 mM NaCl. Observations were recorded on the 3rd and 6th day after salt treatment and 2nd day after salt removal. The relative water content declined with induction of salt stress, more in WH-542 than in cv. KRL-19.
K+/Na+ ratio in KRL-19 was higher than in WH-542. WH-542 suffered greater damage to cellular membranes due to lipid peroxidation
as indicated by higher accumulation of H2O2, MDA and greater leakage of electrolytes than KRL-19. The activities of catalase, peroxidase and ascorbate peroxidase and
glutathione reductase increased with increase in salt stress in both the cultivars, however, superoxide dismutase activity
declined. Upon desalanization, partial recovery in the activities of these enzymes was observed in KRL-19 and very slow recovery
in WH-542. 相似文献
16.
Kozi Asada 《Physiologia plantarum》1992,85(2):235-241
Ascorbate peroxidase is a hydrogen peroxide-scavenging enzyme that is specific to plants and algae and is indispensable to protect chloroplasts and other cell constituents from damage by hydrogen peroxide and hydroxyl radicals produced from it. In this review, first, the participation of ascorbate peroxidase in the scavenging of hydrogen peroxide in chloroplasts is briefly described. Subsequently, the phylogenic distribution of ascorbate peroxidase in relation to other hydrogen peroxide-scavenging peroxidases using glutathione, NADH and cytochrome c is summarized. Chloroplastic and cytosolic isozymes of ascorbate peroxidase have been found, and show some differences in enzymatic properties. The basic properties of ascorbate peroxidases, however, are very different from those of the guaiacol peroxidases so far isolated from plant tissues. Amino acid sequence and other molecular properties indicate that ascorbate peroxidase resembles cytochrome c peroxidase from fungi rather than guaiacol peroxidase from plants, and it is proposed that the plant and yeast hydrogen peroxide-scavenging peroxidases have the same ancestor. 相似文献
17.
Our previous research suggests that interspecific variation in stress tolerance in intertidal Fucus spp. (Phaeophyceae) is partially mediated by differences in the production of, or ability to detoxify, reactive oxygen. Here we report on the content of antioxidants (ascorbate, glutathione, carotenoids, and tocopherols) and protective enzymes (catalase, superoxide dismutase, ascorbate peroxidase, and glutathione reductase) involved in reactive oxygen metabolism in three species of intertidal brown algae— Fucus spiralis L., F. evanescens C. Ag., and F. distichus L.—that differ in stress tolerance and position in the intertidal zone. Contents of the major antioxidants were similar in the three species and were not correlated with stress tolerance. The least stress tolerant species, F. distichus, had the lowest activity of reactive-oxygen-scavenging enzymes, although F. spiralis, the species with the highest stress tolerance, and F. evanescens contained similar activities of antioxidant enzymes on a fresh-weight basis. However, the activities of superoxide dismutase and ascorbate peroxidase in F. evanescens are lower than those of F. spiralis when expressed on the basis of chlorophyll. These data show that the ratio between reactive oxygen protection and production might be more important than the absolute content of antioxidants and protective enzymes. It also shows the importance of localization of detoxifying mechanisms and avoidance of oxidative stress. 相似文献
18.
Efficiency of pretreatment as foliar spray of indole-3-acetic acid, gibberellic acid and kinetin, each ranging from 0.1 to 10.0 μM concentration, in restoring the metabolic alterations imposed by NaCl salinity was investigated in Vigna radiata (L.) Wilczek. Glycolate oxidase, superoxide dismutase, catalase and peroxidase activities increased under stress in leaves and roots also. Malondialdehyde content and total peroxide content also increased under stress. All the three hormones used were able to overcome to variable extents the adverse effects of stress imposed by NaCl to these parameters. This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
19.
Anionic sweet potato peroxidase (SPP; Ipomoea batatas) was shown to efficiently catalyse luminol oxidation by hydrogen peroxide, forming a long-term chemiluminescence (CL) signal. Like other anionic plant peroxidases, SPP is able to catalyse this enzymatic reaction efficiently in the absence of any enhancer. Maximum intensity produced in SPP-catalysed oxidation of luminol was detected at pH 7.8-7.9 to be lower than that characteristic of other peroxidases (8.4-8.6). Varying the concentrations of luminol, hydrogen peroxide and Tris buffer in the reaction medium, we determined favourable conditions for SPP catalysis (100 mmol/L Tris-HCl buffer, pH 7.8, containing 5 mmol/L hydrogen peroxide and 8 mmol/L luminol). The SPP detection limit in luminol oxidation was 1.0 x 10(-14) mol/L. High sensitivity in combination with the long-term CL signal and high stability is indicative of good promise for the application of SPP in CL enzyme immunoassay. 相似文献
20.
Tethering the N-terminus of the prion protein compromises the cellular response to oxidative stress 总被引:4,自引:0,他引:4
The role of the N-terminal half of the prion protein (PrPC) in normal cellular function and pathology remains enigmatic. To investigate the biological role of the N-terminus of PrP, we examined the cellular properties of a construct of murine PrP, PrP-DA, in which the N-terminus is tethered to the membrane by an uncleaved signal peptide and which retains the glycosyl-phosphatidylinositol anchor. Human neuroblastoma SH-SY5Y cells expressing PrP-DA were more susceptible to hydrogen peroxide and copper induced toxicity than wtPrP expressing cells. The PrP-DA expressing cells had an increased level of intracellular free radicals and reduced levels of superoxide dismutase and glutathione peroxidase as compared to the wtPrP expressing cells. The membrane topology, cell surface location, lipid raft localisation, intracellular trafficking and copper-mediated endocytosis of PrP-DA were not significantly different from wtPrP. However, cells expressing PrP-DA accumulated an N-terminal fragment that was resistant to proteinase K. The data presented here are consistent with the N-terminal region of PrPC having a role in the cellular response to oxidative stress, and that tethering this region of the protein to the membrane compromises this function through the accumulation of a protease-resistant N-terminal fragment, similar to that seen in some forms of human prion disease. 相似文献