欢迎访问作物学报,今天是

作物学报 ›› 2011, Vol. 37 ›› Issue (01): 177-181.doi: 10.3724/SP.J.1006.2011.00177

• 研究简报 • 上一篇    下一篇

外源一氧化氮供体SNP对水稻叶片中由硒引起的脂质过氧化的调节作用

肖强1,杨曙1,郑海雷2,*   

  1. 1 湖北民族学院 / 生物资源保护与利用湖北省重点实验室, 湖北恩施445000; 2 厦门大学生命科学学院, 福建厦门361005
  • 收稿日期:2010-05-10 修回日期:2010-09-19 出版日期:2011-01-12 网络出版日期:2010-11-16
  • 基金资助:

    本研究由国家自然科学基金项目(30670317), 湖北省教育厅中青年人才项目(Q20092901), 国家民委科研项目(09HB02), 湖北民族学院博士启动基金项目和湖北民族学院校内青年科研项目(MYQ2006032)资助。

Effects of Exogenous Nitric Oxide Donor SNP on Lipid Peroxidation Caused by Selenium in Rice Seedlings

XIAO Qiang1,YANG Shu1,ZHENG Hai-Lei2,*   

  1. 1 Key Laboratory of Biological Resources Protection and Utilization of Hubei Province / Hubei Institutes for Nationalities, Enshi 445000, China; 2 School of Life Sciences, Xiamen University, Xiamen 361005, China
  • Received:2010-05-10 Revised:2010-09-19 Published:2011-01-12 Published online:2010-11-16

摘要: 一氧化氮(nitric oxide, NO)是植物中一种重要的信号分子, 在诱导种子萌发, 影响植物生长发育, 促进植物细胞衰亡等方面发挥着重要作用。然而对于外源NO是否参与了Se诱导的脂质过氧化调节过程仍不为人知。我们研究了0.2 μmol L-1和20 μmol L-1Na2SeO3及一氧化氮供体硝普钠(sodium nitroprusside, SNP)处理对水稻叶片叶绿素、H2O2和硫代巴比妥酸反应产物(Thiobarbituric Acid Reactive Substances, TBARS)含量, 愈创木酚过氧化物酶(guaiacol peroxidase, GPX)、超氧化物歧化酶(superoxide dismutase, SOD)、过氧化氢酶(catalase, CAT)以及抗坏血酸过氧化物酶(ascorbate peroxidase, APX)活性等生理生化指标的影响。结果表明, 1 μmol L-1SNP处理促进GPX、APX和CAT活性, 缓解膜脂过氧化, 降低TBARS含量; 显著提高0.2 μmol L-1Na2SeO3处理下水稻叶片中叶绿素含量。在20 μmol L-1Na2SeO3处理下, 外加1 μmol L-1SNP更加显著促进GPX和CAT活性, 与此同时明显降低20 μmol L-1Na2SeO3处理引起的H2O2含量上升, 并降低TBARS含量。NO对植物中由Se引起的脂质过氧化具有调节作用。

关键词: 水稻, SNP, 脂质过氧化

Abstract: Nitric oxide (NO) is a bioactive molecule that has been suggested to act as a signaling molecular in plants. It induces germination, affects plant growth and development, and promotes plant cell death. NO is also involved in plant response to heat, salinity, ultraviolet-B, and heavy metal stresses. It is known that some effects of NO may relate to the regulation of reactive oxygen species (ROS) metabolism by means of affecting activities of catalase (CAT) with hemachrome iron, and/or guaiacol peroxidase (GPX) with none-hemachrome iron. However, whether NO regulates lipid peroxidation in rice seedlings induced by selenium is not yet understood. In this article, we reported some regulative  effects of exogenous nitric oxide donor SNP on oxidative stresses induced by selenium in rice seedlings. The contents of chlorophyll, H2O2, TBARS and the activities of GPX, superoxide dismutase (SOD), CAT and ascorbate peroxidase (APX) in rice seedlings treated with a varying concentrations of seleniumand 1 μmol L-1SNP were investigated. The results showed that the content of chlorophyll increased by treatment with SNP in 0.2 μmol L-1Na2SeO3 group. SNP alleviated significantlythe lipid peroxidation in rice seedlings via promoting GPX, APX and CAT activities in rice leaf. In 20 μmol L-1Na2SeO3 treated rice seedlings, SNPalleviated significantlyTBARScontent and the increase of H2O2 content that resulted from high selenium stress via promoting GPX, especially APX and CAT activities. Taken together, our results suggested that NO regulates lipid peroxidation caused by selenium in rice seedlings.

Key words: Oryza sativa, Selenium, Sodium nitroprusside, Lipid peroxidation

[1]Neill S J, Desikan R, Hancock J T. Nitric oxide signaling in plants. New Phytol, 2003, 159: 11–35
[2]Clark D, Durner J, Navarre D A, Klessig D F. Nitric oxide inhibition of tobacco catalase and ascorbate peroxidase. Mol Plant-Microbe Interact, 2000, 13: 1380–1384
[3]Cheng F Y, Hsu S Y, Kao C H. Nitric oxide counteracts the senescence of detached rice leaves induced by dehydration and polyethylene glycol but not by sorbitol. Plant Growth Regul, 2002, 38: 265–272
[4]Kopyra M, Gwózdz E A. Nitric oxide stimulates seed germination and counteracts the inhibitory effect of heavy metals and salinity on root growth of Lupinus luteus. Plant Physiol Biochem, 2003, 41: 1011–1017
[5]Besson-Bard A, Gravot A, Richaud P, Auroy P, Duc C, Gaymard F, Taconnat L, Renou J P, Pugin A, Wendehenne D. Nitric oxide contributes to cadmium toxicity in Arabidopsis by promoting cadmium accumulation in roots and by up-regulating genes related to iron uptake. Plant Physiol, 2009, 149: 1302–1315
[6]Xiao Q, Ru Q M, Wu F H, Huang X, Pei Z M, Zheng H L. Nitric oxide alleviates oxidative stress caused by lanthanum in rice leaves. J Rare Earths, 2007, 25: 631–636
[7]Xue Q-L(薛秦麟), Hou S-F(侯少范), Tan J-A(谭见安), Liu G-L(刘更另). Antioxidant effect of Se in higher plants. Chin Sci Bull (科学通报), 1993, 38(3): 274–277 (in Chinese)
[8]Sors T G, Ellis D R, Salt D E. Selenium uptake, translocation, assimilation and metabolic fate in plants. Photosynth Res, 2005, 86: 373–389
[9]Rios J J, Blasco B, Cervilla L M, Rosales M A, Sanchez-Rodriguez E, Romero L, Ruiz J M. Production and detoxification of H2O2 in lettuce plants exposed to selenium. Ann Appl Biol, 2009, 154: 107–116
[10]Liu K-L(刘开力), Han H-R(韩航如), Xu Y-J(徐颖洁), Ling T-F(凌腾芳), Liu Z-B(刘志兵), Sun Y-G(孙永刚), Hua R(花榕), Shen W-B(沈文飚). Exogenous nitric oxide alleviates salt stress-induced membrane lipid peroxidation in rice seedling roots. Chin J Rice Sci (中国水稻科学), 2005, 19(4): 333–337 (in Chinese with English abstract)
[11]Arnon D I. Copper enzymes in isolated chloroplasts: polyphenol oxidase in Beta vulgaris. Plant Physiol, 1949, 24: 1–15
[12]Mukherjee S P, Choudhuri M A. Implications of water stress induced changes in the levels of endogenous ascorbic acid and hydrogen peroxide in vigna seedlings. Physiol Plant, 1983, 58: 166–170
[13]Dhindsa R S, Plumb-Dhindsa P, Thorpe T A. Leaf senescence: Correlated with increased levels of membrane permeability and lipid peroxidation, and decreased levels of superoxide dismutase and catase. J Exp Bot, 1981, 32: 93–101
[14]Bradford M M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Anal Biochem, 1976, 72: 248–254
[15]Beauchamp C, Fridovich I. Superoxide dismutase, improved assays and an assay applicable to acrylamide gels. Anal Biochem, 1971, 44: 276–287
[16]Ruan H H, Shen W B, Ye M B, Xu L L. Protective effects of nitric oxide on salt stress-induced oxidative damages to wheat (Triticum aestivum L.) leaves. Chin Sci Bull, 2002, 47: 677–681
[17]Chance B, Maehly A. Assay of catalases and peroxidase methods. Method Enzymol, 1955, 2: 764–775
[18]Parida, A K, Das A B, Mohanty P. Defense potentials to NaCl in a mangrove, Bruguiera parviflora: differential changes of isoforms of some antioxidative enzymes. J Plant Physiol, 2004, 161: 531–542
[19]Lin K-F(林匡飞), Xu X-Q(徐小清), Jin X(金霞) , Shao Z-H(邵志慧), Xiang Y-L(项雅玲). Eco-toxicological effects of selenium and its critical value on Oryza sativa. Chin J Appl Ecol (应用生态学报), 2005, 16(4): 678–682 (in Chinese with English abstract)
[20]Delledonne M, Xia Y J, Dixon R A, Lamb C. Nitric oxide functions as a signal in plant disease resistance. Nature, 1998, 394: 585–588
[21]Lum H K, Lee C H, Butt Y K C, Lo S C L. Sodium nitroprusside affects the level of photosynthetic enzymes and glucose metabolism in Phaseolus aureus (mung bean). Nitric Oxide, 2005, 12: 220–230
[22]Takahashi S, Yamasaki H. Reversible inhibition of photophosphorylation in chloroplasts by nitric oxide. FEBS Lett, 2002, 512: 145–148
[23]Wu Y-Y(吴永尧), Lu X-Y(卢向阳), Peng Z-K(彭振坤), Luo Z-M(罗泽民). Effect of Se on physiological and biochemical characters of paddy rice. Sci Agric Sin (中国农业科学), 2000, 33(1): 100–103 (in Chinese with English abstract)
[24]Laxalt A M, Beligni M V, Lamattina L. Nitric oxide preserves the level of chlorophyll in potato leaves infected by Phytophthora infestans. Eur J Plant Pathol, 1997, 103: 643–651
[25]Beligni M V, Lamattina L. Nitric oxide counteracts cytotoxic processes mediated by reactive oxygen species in plant tissues. Planta, 1999, 208: 337–344
[26]Jasid S, Simontacchi M, Bartoli C G, Puntarulo S. Chloroplasts as a nitric oxide cellular source-effect of reactive nitrogen species on chloroplastic lipids and proteins. Plant Physiol, 2006, 142: 1246–1255
[1] 胡赵, 钱润, 谢丰璞, 应素平. 水稻SPX基因家族鉴定及响应磷处理的表达分析[J]. 作物学报, 2026, 52(6): 1902-1912.
[2] 邹仪妹, 徐敏, 汪海洋, 姚辉, 王加峰, 刘浩, 任代胜. 两系不育系水稻幼苗根系响应盐胁迫的转录因子调控网络鉴定[J]. 作物学报, 2026, 52(6): 1728-1742.
[3] 闫安, 蒋昆炜, 王蓉圆, 田林, 张璐, 王韵, 徐建龙. 水稻剑叶小维管束数基因SVN7的鉴定与克隆[J]. 作物学报, 2026, 52(5): 1364-1372.
[4] 陈伟, 卫万娟, 赵其兵, 常东伟, 余凌波, 翟鹏飞, 冯志明, 陈宗祥, 任仰涛, 杨鹏, 刘海浪, 李珍富, 杨永乐, 金彦刚, 左示敏. 利用CRISPR/Cas9编辑Hd6基因创制优质早熟水稻新种质[J]. 作物学报, 2026, 52(4): 1046-1056.
[5] 石少阶, 刘凯, 陈姿夷, 王卉颖, 李三和, 周雷, 游艾青. 水稻矮化多分蘖基因DMT1的克隆与功能分析[J]. 作物学报, 2026, 52(4): 1022-1034.
[6] 田红丽, 杨扬, 范亚明, 易红梅, 郭丹丹, 王凤格, 赵久然. 适于玉米品种鉴定的一套三等位变异SNP新型标记组合[J]. 作物学报, 2026, 52(4): 993-1005.
[7] 覃奕琰, 付瑶, 苏畅, 李娜, 徐静茹, 程笑然, 张琪, 赵明辉. OsST41调控水稻苗期耐盐性的功能分析[J]. 作物学报, 2026, 52(3): 802-812.
[8] 叶凡, 李帅, 李思宇, 陈云, 窦超银, 刘立军. 不同节水灌溉方式对东北稻区水稻产量和群体质量的影响[J]. 作物学报, 2026, 52(3): 895-907.
[9] 李云香, 郭千纤, 侯万伟, 张小娟. 引进ICARDA小麦苗期根系抗旱性状的全基因组关联分析[J]. 作物学报, 2025, 51(9): 2387-2398.
[10] 王婵, 吴莹莹, 李文奇, 李霞, 王芳权, 周彤, 杨杰. 基于HRM技术开发水稻抗条纹叶枯病基因STV11功能标记[J]. 作物学报, 2025, 51(9): 2547-2556.
[11] 陈惠莹, 何嘉欣, 朱斌, 黄士轩, 周星佑, 伍君权, 杨美艳. 水稻黄单胞菌噬菌体vB_XaS_HDB2的全基因组分析和生物学特性研究[J]. 作物学报, 2025, 51(8): 2087-2099.
[12] 杨海洋, 吴林宣, 李博纹, 石翰峰, 袁禧龙, 刘金朝, 蔡海荣, 陈诗怡, 郭涛, 王慧. 基于QTL定位发现的OsWRI3调控水稻种子的落粒性[J]. 作物学报, 2025, 51(7): 1712-1724.
[13] 雷松翰, 范骏扬, 车艳奕, 代永东, 郑雨萌, 田维江, 桑贤春, 王晓雯. 水稻内卷叶突变体acl3的鉴定及调控基因的功能分析[J]. 作物学报, 2025, 51(6): 1467-1479.
[14] 李福媛, 杨奕, 马继琼, 许明辉, 林良斌, 孙一丁. 水稻OsPUB4基因克隆、激素诱导表达分析与互作蛋白筛选[J]. 作物学报, 2025, 51(6): 1690-1700.
[15] 王琼, 邹丹霞, 陈兴运, 张威, 张红梅, 刘晓庆, 贾倩茹, 魏利斌, 崔晓艳, 陈新, 王学军, 陈华涛. 大豆开花时间和成熟期性状全基因组关联分析与候选基因预测[J]. 作物学报, 2025, 51(6): 1558-1568.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!