Botanical Research
Vol. 09  No. 03 ( 2020 ), Article ID: 35732 , 7 pages
10.12677/BR.2020.93028

The Role of Nitric Oxide in Plant Immune Response

Zhenchao Li

College of Chemistry and Life Science, Zhejiang Normal University (ZJNU), Jinhua Zhejiang

Received: Apr. 10th, 2020; accepted: May 18th, 2020; published: May 25th, 2020

ABSTRACT

Reactive oxygen species (ROS) is an important component of the signalling network that plants use for responding to environmental challenges. NO has an important function as a key signalling molecule in plant growth, development, and senescence, and reactive nitrogen species (RNS), like reactive oxygen species (ROS), also play an important role as signalling molecules in the response to biotic stressc. Similarly, NO is a key mediator, in co-operation with ROS, in the defence response to pathogen attacks in plants. NO regulates diverse cellular signaling through S-nitrosylation of specific Cys residues of target proteins. The intracellular level of S-nitrosoglutathione (GSNO), a major bioactive NO species, is regulated by GSNO reductase 1 (GSNOR1), a key enzyme that regulates cellular homeostasis of S-nitrosylation across kingdoms. GSNOR1 also plays an important role in plant immune defense response. Here we review the research progress of the role of NO in plant defense responses.

Keywords:Nitric Oxide, S-Nitrosoglutathione Reductase, Programmed Cell Death, Disease Resistance

一氧化氮在植物免疫反应中的作用

李贞超

浙江师范大学化学与生命科学学院,浙江 金华

收稿日期:2020年4月10日;录用日期:2020年5月18日;发布日期:2020年5月25日

摘 要

活性氧(Reactive Oxygen Species, ROS)是植物响应外界胁迫信号通路中的重要组分。一氧化氮(Nitric Oxide, NO)是植物生长、发育和衰老中的关键信号分子。与ROS一样,活性氮(Reactive Nitrogen Species, RNS)在植物应对生物胁迫中发挥着重要的作用。此外,NO可以和ROS协同应对病原菌的侵袭。NO通过调控特定靶蛋白半胱氨酸残基的S-亚硝基化来进行信号转导,而亚硝基谷胱甘肽(S-nitrosoglutathione, GSNO)是生物体内具有生物活性的NO形式。亚硝基谷胱甘肽还原酶1 (S-nitrosoglutathione reductase 1, GSNOR1)可以特异性还原GSNO以达到植物体内亚硝基化水平稳态平衡。GSNOR1在植物免疫防御反应中同样具有重要的作用。在这里我们就NO在植物防御反应中的作用的研究进展进行了综述。

关键词 :一氧化氮,亚硝基谷胱甘肽还原酶,细胞程序性死亡,免疫反应

Copyright © 2020 by author(s) and Hans Publishers Inc.

This work is licensed under the Creative Commons Attribution International License (CC BY 4.0).

http://creativecommons.org/licenses/by/4.0/

1. 引言

一氧化氮(Nitric oxide, NO)是参与动物和植物各种发育过程和胁迫响应的关键信号分子 [1]。通过对催化NO合成的酶以及NO调控靶蛋白的不断研究,NO信号转导机制越来越明了 [2] [3]。动物中NO不仅来自亚硝酸盐,还来自L-精氨酸(L-Arg),L-Arg是动物NO合成的主要底物 [4]。而在植物中NO不仅可以在体内产生还可以从周围的环境或土壤中获得 [4]。

NO通过调控特定靶蛋白半胱氨酸残基的S-亚硝基化来进行信号转导 [5] [6]。近年来,植物中大量蛋白质被鉴定为S-亚硝基化的靶标,蛋白质亚硝基化可以直接或间接的影响植物细胞程序性死亡(Programmed cell death, PCD) [7]。在植物应对生物和非生物胁迫响应中,ROS和NO的爆发及其相互调节对于早期信号转导至关重要。GSNO是植物体内主要的具有生物活性的NO形式 [6]。GSNO可以被保守的亚硝基谷胱甘肽还原酶1 (GSNOR1)特异性降解,从而使植物体内亚硝基化水平可以保持稳态平衡 [8]。NO及其信号网络组分的改变都会对植物免疫产生重要影响。

2. 植物一氧化氮产生及ROS信号转导

NO是活性氮(Reactive nitrogen species, RNS)种类之一 [9],它在植物生长、发育、应对生物和非生物胁迫以及细胞程序性细胞死亡(PCD)中具有重要作用 [10] [11]。动物中NO主要由一氧化氮合成酶(Nitric oxide synthase, NOS)产生 [1]。植物中产生NO有两种不同的酶途径:硝酸盐/亚硝酸盐依赖途径和L-精氨酸依赖的合成途径。第一个途径涉及硝酸还原酶(Nitrate reductase, NR)和根特异性质膜亚硝酸盐还原酶(Nitrite-NO reductase, Ni-NOR) [1] [12]。在植物体内的研究多认为NR可能调控多种植物叶和根中NO产生 [13] [14] [15]。在拟南芥中研究发现,NR是NO产生的关键酶,NR介导的NO的产生是ABA信号转导途径中的关键组分 [16] [17]。除了NR外,Ni-NOR也可以催化亚硝酸盐形成NO,但是只限在根中合成,NR可以将硝酸盐还原成亚硝酸盐,Ni-NOR可以与NR相协调共同调控NO的合成 [18]。另外Ni-NOR还参与一系列根的生理过程 [19],但是除此之外我们对于Ni-NOR知之甚少。

在植物发育过程中不同酶或细胞器中可以产生一些过氧化物 [10] [20],尤其是羟基自由基(Hydroxyl radical)和单线态氧(Singlet oxygen),都是非常强的氧化剂 [21] [22]。因此,为了防止氧化应激的产生,植物细胞产生了一系列的酶和非酶抗氧化剂来清除过量的氧化物。以上是植物生物学中之前关于氧化胁迫的普遍观点,而现在这一观点慢慢向氧化信号转导转变。这意味着,原本被认为有害的ROS其实是植物用来发育和应对外界胁迫的重要信号分子。植物体内高效的抗氧化系统很可能是植物细胞为避免氧化胁迫,并利用这些活性物质作为信号转导媒介所产生的 [23]。在不利环境条件下的细胞响应过程其实是由ROS的持续产生和不同的抗氧化系统之间的平衡来实现的 [24]。因此,除了ROS单独增加外,抗氧化酶的下调也可能参与了植物胁迫过程中的信号转导。

3. ROS与RNS协同参与植物免疫

在植物免疫反应过程中,ROS和RNS都会迅速过量产生,两者协同在植物防御反应中起着重要的作用 [23] [25]。NO和ROS可以调控植物应对病原菌侵袭产生的超敏反应(Hypersensitive reaction, HR),但是这一过程更依赖于NO和ROS之间的紧密平衡,而不是仅仅依赖于单一分子的调控。例如,用双芳基甲烷酮激发子(NUBS-4190)可以使本生烟草单独产生一氧化氮从而增强植物免疫,但是却观察不到ROS依赖的HR的发生 [26]。

NPR1是系统获得性抗性(System acquired resistance, SAR)必须的,防御反应中NO和ROS信号之间的交互可以从对NPR1的影响上体现出来。NPR1的寡聚化是植物防御相关基因表达所必需的,然而这一过程需要S-亚硝基化的调控 [6]。另一方面NPR1转移到细胞核的过程也受到胞浆内过氧化氢浓度的影响 [27]。由此可以看出,NO和ROS均会影响NPR1的功能,从而展现了两者之间复杂的调控机制。NO和ROS的相互影响还体现在NO可以调控ROS的产生。AtRBOHD可以在病原菌侵染植物后产生ROS,但是其活性却可以被S-亚硝基化所抑制 [28] [29]。不过与此相反的是,糖醛酸(Hyaluronic Acid, HA)要想完全诱导拟南芥ROS的产生还需要NO的参与 [30]。这些结果的发现同样也说明了NO和ROS信号转导之间的复杂关系。S-亚硝基谷胱甘肽是生物体内重要的NO流动库 [31],在O2存在的情况下,NO可以通过S-亚硝基化反应与还原型谷胱甘肽(GSH)反应形成S-亚硝基谷胱甘肽(GSNO)。过氧亚硝酸盐(ONOO)是由NO和O− 2之间的快速反应形成的一种强氧化剂/硝化物质 [32]。由于植物组织中存在NO和GSNO,再加上ONOO的产生,使得S-亚硝基化和蛋白质硝化这些重要的共价翻译后修饰(PTM)可以在自然或胁迫条件下发生 [33]。尽管目前已经公认ROS和RNS在细胞间和细胞内分子通讯中起着关键作用,但是关于ROS信号的启动、传感和响应机制以及生产与清除之间的微妙平衡是如何实现的,仍有许多问题需要我们去解决。

4. NO可以介导植物免疫过程中的PCD

病原菌诱导的HR、植物衰老、及非生物胁迫等都可以诱导细胞程序性死亡(PCD) [34],NO和ROS是PCD信号中的关键调节因子 [35]。抗坏血酸过氧化物酶(APX)可以调节细胞中过氧化氢(H2O2)的水平 [36]。当用NO处理烟草悬浮细胞的时候能够明显抑制APX的活性,说明NO可能通过抑制APX的活性来参与防御反应 [37]。另有报道指出APX重组蛋白的亚硝基化可以增强其酶活性 [38]。抛去这两者结果的矛盾不管,S-亚硝基化确实可以通过影响APX酶的活性来调控H2O2介导的防御反应。抗氧化蛋白(Peroxiredoxins, Prxs)具有巯基催化活性,几乎存在于所有生物体内,根据它们的结构不同可以将Prxs分为6类。Prx5是植物中最具多样性和分布最广的Prx亚族,包括PrxII-E和PrxII-F [39]。在植物防御反应期间,PrxII-E的亚硝基化不仅抑制了其对过氧化物的解毒能力,同时也降低了该酶对过氧亚硝酸盐(ONOO)的解毒能力,从而促进了PCD的发生 [40]。PrxII-F的S-亚硝基化可以促进柠檬酸合酶(Citrate (Si)-synthase, CS)和PrxII-F之间的相互作用,从而使植物免受氧化和亚硝化胁迫的影响 [41]。由此可以看出PrxII-E和PrxII-F的S-亚硝基化对于植物PCD过程以及在植物应对外界胁迫的各种响应中都具有重要作用。

水杨酸(Salicylic acid, SA)是植物应对病原菌侵袭的一类重要激素,SA可以和植物体内免疫防御相关的多种蛋白质结合,从而调节它们的活动诱导HR的产生 [42] [43]。水杨酸结合蛋白3 (SABP3)表现出和SA很高的亲和性,并且在线粒体中表现出碳酸酐酶(Carbonic Anhydrase, CA)的活性 [44]。AtSABP3在Cys280处的S-亚硝基化可以抑制AtSABP3的SA亲和能力和CA活性,从而负调控植物免疫反应 [45]。NPR1是另外一种与SA相关的蛋白,它可以和SA结合并且在免疫应答中激活SA信号途径中相关防御基因的表达 [46]。植物可以通过S-亚硝基化调控NPR1的稳态从而影响其与TGACG基序结合因子1 (TGA1)相互作用参与调控植物免疫 [47]。

5. GSNOR1在植物NO免疫信号通路中具有重要的作用

GSNO是植物体内NO主要的运输形式,尽管NO和GSNO并不总是与相同的靶蛋白相互作用 [48]。但作为一氧化氮的缓冲剂,GSNO可以维持蛋白质的S-亚硝基化稳态平衡 [8]。GSNOR1作为GSNO的特异性还原酶在RNS的代谢中起着关键作用,它可以维持细胞内NO的稳态变化和控制S-亚硝基化蛋白与GSNO之间的反式亚硝化平衡 [48] [49]。GSNOR1是NO介导的植物免疫信号分子中的重要调控者,这已经在拟南芥GSNOR1功能丧失的突变体(AtGSNOR1-3)中得到了证实,该突变体体内S-NOs水平增加,SA积累减少,并伴随着基础和非宿主抗性受损 [49]。拟南芥GSNOR1等位基因突变体hot5也显示出相似的表型特征,说明S-NOs稳态在调节生物、非生物胁迫反应中具有重要作用 [50]。除上述作用外,由GSNOR1/HOT5调节的细胞内NO水平变化是否参与其他细胞活动很大一部分仍然是未知的。

系统获得性抗性(SAR)在GSNOR1反义沉默植株中增强,在超表达植株中降低,与系统获得性抗性一致,植株中的S-NOs的水平也发生了相应的变化 [51]。另有报道指出GSNO和SA可以在SAR中起到协同作用 [49]。但是报道中也有与此相反的结果,即GSNOR1在病原菌侵染植物早期具有正向调控植物免疫的作用。当敲除AtGSNOR1之后,植物的基础抗性减弱,并且伴随着SA依赖的抗病基因表达量的减少 [49],之后在向日葵 [52],以及黄瓜中也发现了类似的结果 [53]。抛去以上矛盾之处,这些证据也进一步证实了GSNOR1在植物免疫防御中的重要作用。

植物免疫反应过程中,GSNOR1在NO/GSNO介导的化学修饰中也具有重要的作用。GSH可以促进烟草BY-2细胞GSNOR1及水杨酸依赖基因NPR1显著上调 [54]。GSNO还可以诱导拟南芥NPR1的表达和SA的积累从而增强拟南芥对Pst DC3000的抗性 [6]。研究表明NO可以诱导GSH的产生,而GSH是SA积累和NPRI诱导所必需的,但是在拟南芥NO过表达突变体(nox1)中SA的生物合成以及依赖SA表达的基因都有所降低 [55]。之后通过不同的双突变体nox1/AtGSNOR1-1 (植物过表达GSNOR1)或nox1/AtGSNOR1-3 (GSNOR1敲除的植物)发现NO或GSNO可以通过调控独立的或者重叠的靶标来对细胞进行调控。这就说明了GSNOR1调控的GSNO/NO信号通路在植物免疫过程中具有高度的复杂性 [56]。

GSNOR1还可以参与植物免疫反应过程中的PCD。当用Pst DC3000侵染AtGSNOR1-3时,突变体叶片较野生型中出现了更严重的细胞死亡;但是在AtGSNOR1-3/sid2 (水杨酸缺乏突变体),AtGSNOR1-3/AtRBOHD或AtGSNOR1-3/rbohF (缺乏活性氧中间体)双突变体植株中却没有观察到死亡减轻的现象,说明在没有SA和活性氧中间体合成的情况下植物体内升高的S-NOs就可以促进HR的发生 [28]。前面我们讲到NO可以和ROS协同调控植物死亡,但需要注意的是,当S-NOs浓度升高时,一氧化氮介导的AtRBOHD的S-亚硝基化形成一个反馈回路抑制了超敏反应的发生 [28]。百草枯(Paraquat, PQ)是一种研究PCD的重要试剂,它可以诱导绿色植物产生大量活性氧,从而促使植物死亡。但是当用PQ处理拟南芥GSNOR1等位基因突变体par2-1时,该突变体却表现出对百草枯诱导死亡增强的抗性 [57]。以上可以看出GSNOR1在不同条件下可以起到正负调控细胞死亡的功能。

6. 结语

S-亚硝基化是植物NO信号通路中的重要组成部分。GSNOR1作为调控蛋白质亚硝基化、去亚硝基化以及GSNO稳态的关键酶,在植物免疫反应中扮演着重要的角色,但是关于GSNOR1的体内调控机制还有很大一部分是未知的。虽然有大量的证据表明NO和ROS在植物免疫信号转导之间存在着串扰,但是S-亚硝基化如何参与其中还需要我们去进一步探索。此外NO来源的鉴定,以及植物中不同亚细胞区间中NO介导S-亚硝基化的产生依然是研究的重点。最后我们期望能够通过模式植物对NO调控免疫信号通路中的相关基因进行研究,从而将已有知识扩展到经济作物,增强作物抗逆性和提高作物产量。

文章引用

李贞超. 一氧化氮在植物免疫反应中的作用
The Role of Nitric Oxide in Plant Immune Response[J]. 植物学研究, 2020, 09(03): 240-246. https://doi.org/10.12677/BR.2020.93028

参考文献

  1. 1. Besson-Bard, A., Pugin, A. and Wendehenne, D. (2008) New Insights into Nitric Oxide Signaling in Plants. Annual Review of Plant Biology, 59, 21-39. https://doi.org /10.1146/annurev.arplant.59.032607.092830

  2. 2. Urushitani, M. and Shimohama, S. (2001) The Role of Nitric Oxide in Amyotrophic Lateral Sclerosis. Amyotrophic Lateral Scle-rosis and Other Motor Neuron Disorders, 2, 71-81. https://doi.org /10.1080/146608201316949415

  3. 3. Kone, B.C., Kuncewicz, T., Zhang, W. and Yu, Z.Y. (2003) Protein Interactions with Nitric Oxide Synthases: Controlling the Right Time, the Right Place and the Right Amount of Nitric Oxide. American Journal of Physiology-Renal Physiology, 285, F178-F190. https://doi.org /10.1152/ajprenal.00048.2003

  4. 4. Sahay, S. and Gupta, M. (2017) An Update on Nitric Oxide and Its Benign Role in Plant Responses under Metal Stress. Nitric Oxide, 67, 39-52. https://doi.org /10.1016/j.niox.2017.04.011

  5. 5. Kneeshaw, S., Gelineau, S., Tada, Y., Loake, G.J. and Spoel, S.H. (2014) Selective Protein Denitrosylation Activity of Thioredoxin-h5 Modulates Plant Immunity. Molecular Cell, 56, 153-162. https://doi.org /10.1016/j.molcel.2014.08.003

  6. 6. Tada, Y., Spoel, S.H., Pajerowska-Mukhtar, K., Mou, Z., Song, J., Wang, C. and Dong, X. (2008) Plant Immunity Requires Conformational Changes of NPR1 via S-Nitrosylation and Thioredoxins. Science, 321, 952-956. https://doi.org /10.1126/science.1156970

  7. 7. Huang, D., Huo, J., Zhang, J., Wang, C., Wang, B., Fang, H. and Liao, W. (2019) Protein S-Nitrosylation in Programmed Cell Death in Plants. Cellular and Molecular Life Sciences, 76, 1877-1887. https://doi.org /10.1007/s00018-019-03045-0

  8. 8. Liu, L., Hausladen, A., Zeng, M., Que, L., Heitman, J. and Stamler, J.S. (2001) A Metabolic Enzyme for S-Nitrosothiol Conserved from Bacteria to Humans. Nature, 410, 490-494. https://doi.org /10.1038/35068596

  9. 9. Mata-Perez, C., Sanchez-Calvo, B., Padilla, M.N., Bega-ra-Morales, J.C., Valderrama, R., Corpas, F.J. and Barroso, J.B. (2017) Nitro-Fatty Acids in Plant Signaling: New Key Mediators of Nitric Oxide Metabolism. Redox Biology, 11, 554-561. https://doi.org /10.1016/j.redox.2017.01.002

  10. 10. Baxter, A., Mittler, R. and Suzuki, N. (2014) ROS as Key Players in Plant Stress Signalling. Journal of Experimental Botany, 65, 1229-1240. https://doi.org /10.1093/jxb/ert375

  11. 11. Gupta, D.K., Inouhe, M., Rodriguez-Serrano, M., Romero-Puertas, M.C. and Sandalio, L.M. (2013) Oxidative Stress and Arsenic Toxicity: Role of NADPH Oxidases. Chemosphere, 90, 1987-1996. https://doi.org /10.1016/j.chemosphere.2012.10.066

  12. 12. Yamasaki, H. and Sakihama, Y. (2000) Simultaneous Production of Nitric Oxide and Peroxynitrite by Plant Nitrate Reductase: In Vitro Evidence for the NR-Dependent Formation of Active Nitrogen Species. FEBS Letters, 468, 89-92. https://doi.org /10.1016/S0014-5793(00)01203-5

  13. 13. Lea, U.S., Ten Hoopen, F., Provan, F., Kaiser, W.M., Meyer, C. and Lillo, C. (2004) Mutation of the Regulatory Phosphorylation Site of Tobacco Nitrate Reductase Results in High Nitrite Excretion and NO Emission from Leaf and Root Tissue. Planta, 219, 59-65. https://doi.org /10.1007/s00425-004-1209-6

  14. 14. Rockel, P., Strube, F., Rockel, A., Wildt, J. and Kaiser, W.M. (2002) Regulation of Nitric Oxide (NO) Production by Plant Nitrate Reductase in Vivo and in Vitro. Journal of Experimental Botany, 53, 103-110. https://doi.org /10.1093/jexbot/53.366.103

  15. 15. Vanin, A.F., Svistunenko, D.A., Mikoyan, V.D., Serezhenkov, V.A., Fryer, M.J., Baker, N.R. and Cooper, C.E. (2004) Endogenous Superoxide Production and the Nitrite/Nitrate Ra-tio Control the Concentration of Bioavailable Free Nitric Oxide in Leaves. The Journal of Biological Chemistry, 279, 24100-24107. https://doi.org /10.1074/jbc.M312601200

  16. 16. Bright, J., Desikan, R., Hancock, J.T., Weir, I.S. and Neill, S.J. (2006) ABA-Induced NO Generation and Stomatal Closure in Arabidopsis Are Dependent on H2O2 Synthesis. The Plant Journal, 45, 113-122. https://doi.org /10.1111/j.1365-313X.2005.02615.x

  17. 17. Desikan, R., Cheung, M.K., Bright, J., Henson, D., Hancock, J.T. and Neill, S.J. (2004) ABA, Hydrogen Peroxide and Nitric Oxide Signalling in Stomatal Guard Cells. Journal of Experimental Botany, 55, 205-212. https://doi.org /10.1093/jxb/erh033

  18. 18. Stohr, C., Strube, F., Marx, G., Ullrich, W.R. and Rockel, P. (2001) A Plasma Membrane-Bound Enzyme of Tobacco Roots Catalyses the Formation of Nitric Oxide from Nitrite. Planta, 212, 835-841. https://doi.org /10.1007/s004250000447

  19. 19. Stohr, C. and Stremlau, S. (2006) Formation and Possible Roles of Nitric Oxide in Plant Roots. Journal of Experimental Botany, 57, 463-470. https://doi.org /10.1093/jxb/erj058

  20. 20. Sun, L.R., Zhao, Z.J. and Hao, F.S. (2019) NADPH Oxidases, Essential Players of Hormone Signalings in Plant Development and Response to Stresses. Plant Signaling and Behavior, 14, 1657343. https://doi.org /10.1080/15592324.2019.1657343

  21. 21. Anjum, N., Amreen, A., Tantray, A.Y., Khan, N.A. and Ahmad, A. (2019) Reactive Oxygen Species Detection-Approaches in Plants: Insights into Genetically Encoded FRET-Based Sensors. Journal of Biotechnology, 308, 108-117. https://doi.org /10.1016/j.jbiotec.2019.12.003

  22. 22. Foyer, C.H. and Noctor, G. (2005) Redox Homeostasis and Antioxidant Signaling: A Metabolic Interface between Stress Perception and Physiological Responses. Plant Cell, 17, 1866-1875. https://doi.org /10.1105/tpc.105.033589

  23. 23. Mittler, R., Vanderauwera, S., Suzuki, N., Miller, G., Tognetti, V.B., Vandepoele, K. and Van Breusegem, F. (2011) ROS Signaling: The New Wave? Trends in Plant Science, 16, 300-309. https://doi.org /10.1016/j.tplants.2011.03.007

  24. 24. Bailey-Serres, J. and Mittler, R. (2006) The Roles of Reactive Oxygen Species in Plant Cells. Plant Physiology, 141, 311. https://doi.org /10.1104/pp.104.900191

  25. 25. Airaki, M., Leterrier, M., Mateos, R.M., Valderrama, R., Chaki, M., Barroso, J.B. and Corpas, F.J. (2012) Metabolism of Reactive Oxygen Species and Reactive Nitrogen Species in Pepper (Capsicum an-nuum L.) Plants under Low Temperature Stress. Plant Cell Environment, 35, 281-295. https://doi.org /10.1111/j.1365-3040.2011.02310.x

  26. 26. Monjil, M.S., Shibata, Y., Takemoto, D. and Kawakita, K. (2013) BiS-Aryl Methanone Compound Is a Candidate of Nitric Oxide Producing Elicitor and Induces Resistance in Nicotiana bentha-miana against Phytophthora Infestans. Nitric Oxide, 29, 34-45. https://doi.org /10.1016/j.niox.2012.12.004

  27. 27. Peleg-Grossman, S., Melamed-Book, N., Cohen, G. and Levine, A. (2010) Cytop-lasmic H2O2 Prevents Translocation of NPR1 to the Nucleus and Inhibits the Induction of PR Genes in Arabidopsis. Plant Signaling & Behavior, 5, 1401-1406. https://doi.org /10.4161/psb.5.11.13209

  28. 28. Yun, B.W., Feechan, A., Yin, M., Saidi, N.B., Le Bihan, T., Yu, M. and Loake, G.J. (2011) S-Nitrosylation of NADPH Oxidase Regulates Cell Death in Plant Immunity. Nature, 478, 264-268. https://doi.org /10.1038/nature10427

  29. 29. Suzuki, N., Miller, G., Morales, J., Shulaev, V., Torres, M.A. and Mittler, R. (2011) Respiratory Burst Oxidases: The Engines of ROS Sig-naling. Current Opinion in Plant Biology, 14, 691-699. https://doi.org /10.1016/j.pbi.2011.07.014

  30. 30. Rasul, S., Dubreuil-Maurizi, C., Lamotte, O., Koen, E., Poinssot, B., Alcaraz, G. and Jeandroz, S. (2012) Nitric Oxide Production Mediates Oligogalacturonide-Triggered Immunity and Resistance to Botrytis Cinerea in Arabidopsis thaliana. Plant Cell Environment, 35, 1483-1499. https://doi.org /10.1111/j.1365-3040.2012.02505.x

  31. 31. Ortega-Galisteo, A.P., Rodriguez-Serrano, M., Pazmino, D.M., Gupta, D.K., Sandalio, L.M. and Romero-Puertas, M.C. (2012) S-Nitrosylated Proteins in Pea (Pisum sativum L.) Leaf Peroxisomes: Changes under Abiotic Stress. Journal of Experimental Botany, 63, 2089-2103. https://doi.org /10.1093/jxb/err414

  32. 32. Radi, R. (2013) Protein Tyrosine Nitration: Biochemical Mechanisms and Structural Basis of Functional Effects. Accounts of Chemical Research, 46, 550-559. https://doi.org /10.1021/ar300234c

  33. 33. Romero-Puertas, M.C., Rodriguez-Serrano, M. and Sandalio, L.M. (2013) Protein S-Nitrosylation in Plants under Abiotic Stress: An Overview. Frontiers in Plant Science, 4, 373. https://doi.org /10.3389/fpls.2013.00373

  34. 34. Kotak, S., Larkindale, J., Lee, U., von Koskull-Doring, P., Vierling, E. and Scharf, K.D. (2007) Complexity of the Heat Stress Response in Plants. Current Opinion in Plant Biology, 10, 310-316. https://doi.org /10.1016/j.pbi.2007.04.011

  35. 35. Hess, D.T. and Stamler, J.S. (2012) Regulation by S-nitrosylation of Protein Post-Translational Modification. The Journal of Biological Chemistry, 287, 4411-4418. https://doi.org /10.1074/jbc.R111.285742

  36. 36. Kaya, C., Ashraf, M., Alyemeni, M.N. and Ahmad, P. (2019) The Role of Endogenous Nitric Oxide in Salicylic Acid-Induced Up-Regulation of Ascorbate-Glutathione Cycle Involved in Salinity Tolerance of Pepper (Capsicum annuum L.) Plants. Plant Physiology and Biochemistry, 147, 10-20. https://doi.org /10.1016/j.plaphy.2019.11.040

  37. 37. Clark, D., Durner, J., Navarre, D.A. and Klessig, D.F. (2000) Nitric Oxide Inhibition of Tobacco Catalase and Ascorbate Peroxidase. Molecular Plant-Microbe Interactions, 13, 1380-1384. https://doi.org /10.1094/MPMI.2000.13.12.1380

  38. 38. de Pinto, M.C., Locato, V., Sgobba, A., Romero-Puertas Mdel, C., Gadaleta, C., Delledonne, M. and De Gara, L. (2013) S-Nitrosylation of Ascorbate Peroxidase Is Part of Pro-grammed Cell Death Signaling in Tobacco Bright Yellow-2 Cells. Plant Physiology, 163, 1766-1775. https://doi.org /10.1104/pp.113.222703

  39. 39. Brehelin, C., Meyer, E.H., de Souris, J.P., Bonnard, G. and Meyer, Y. (2003) Resemblance and Dissemblance of Arabidopsis Type II Peroxiredoxins: Similar Sequences for Divergent Gene Expression, Protein Localization and Activity. Plant Physiology, 132, 2045-2057. https://doi.org /10.1104/pp.103.022533

  40. 40. Romero-Puertas, M.C., Laxa, M., Matte, A., Zaninotto, F., Finkemeier, I., Jones, A.M. and Delledonne, M. (2007) S-Nitrosylation of Peroxiredoxin II E Promotes Peroxynitrite-Mediated Tyrosine Nitration. Plant Cell, 19, 4120-4130. https://doi.org /10.1105/tpc.107.055061

  41. 41. Camejo, D., Ortiz-Espín, A., Lázaro, J. J., Romero-Puertas, M. C., Lázaro-Payo, A., Sevilla, F. and Jiménez, A. (2015) Experimental Evidences of the NO Action on a Recombinant PrxII F from Pea Plant and Its Effect Preventing the Citrate Synthase Aggregation. Data in Brief, 3, 108-112. https://doi.org /10.1016/j.dib.2015.02.009

  42. 42. Slaymaker, D.H., Navarre, D.A., Clark, D., del Pozo, O., Martin, G.B. and Klessig, D.F. (2002) The Tobacco Salicylic Acid-Binding Protein 3 (SABP3) Is the Chloroplast Carbonic Anhydrase, which Exhibits Antioxidant Activity and Plays a Role in the Hypersensitive Defense Response. Proceed-ings of the National Academy of Sciences of the United States of America, 99, 11640-11645. https://doi.org /10.1073/pnas.182427699

  43. 43. Kumar, D. and Klessig, D.F. (2003) High-Affinity Salicylic Acid-Binding Protein 2 Is Required for Plant Innate Immunity and Has Salicylic Acid-Stimulated Lipase Activity. Proceedings of the National Academy of Sciences of the United States of America, 100, 16101-16106. https://doi.org /10.1073/pnas.0307162100

  44. 44. Guerra, D., Ballard, K., Truebridge, I. and Vierling, E. (2016) S-Nitrosation of Con-served Cysteines Modulates Activity and Stability of S-Nitrosoglutathione Reductase (GSNOR). Biochemistry, 55, 2452-2464.

  45. 45. Wang, Y.Q., Feechan, A., Yun, B.W., Shafiei, R., Hofmann, A., Taylor, P. and Loake, G.J. (2009) S-Nitrosylation of AtSABP3 Antagonizes the Expression of Plant Immunity. The Journal of Biological Chemistry, 284, 2131-2137. https://doi.org /10.1074/jbc.M806782200

  46. 46. Wu, Y., Zhang, D., Chu, J.Y., Boyle, P., Wang, Y., Brindle, I.D. and Despres, C. (2012) The Arabidopsis NPR1 Protein Is a Receptor for the Plant Defense Hormone salicylic Acid. Cell Reports, 1, 639-647. https://doi.org /10.1016/j.celrep.2012.05.008

  47. 47. Mou, Z., Fan, W. and Dong, X. (2003) Inducers of Plant Sys-temic Acquired Resistance Regulate NPR1 Function through Redox Changes. Cell, 113, 935-944. https://doi.org /10.1016/S0092-8674(03)00429-X

  48. 48. Frungillo, L., Skelly, M.J., Loake, G.J., Spoel, S.H. and Salgado, I. (2014) S-Nitrosothiols Regulate Nitric Oxide Production and Storage in Plants through the Nitrogen Assimilation Pathway. Nature Communications, 5, 5401. https://doi.org /10.1038/ncomms6401

  49. 49. Feechan, A., Kwon, E., Yun, B.W., Wang, Y., Pallas, J.A. and Loake, G.J. (2005) A Central Role for S-Nitrosothiols in Plant Disease Resistance. Proceedings of the National Academy of Sciences of the United States of America, 102, 8054-8059. https://doi.org /10.1073/pnas.0501456102

  50. 50. Lee, U., Wie, C., Fernandez, B.O., Feelisch, M. and Vierling, E. (2008) Modulation of Nitrosative Stress by S-Nitrosoglutathione Reductase Is Critical for Thermotolerance and Plant Growth in Arabidopsis. Plant Cell, 20, 786-802. https://doi.org /10.1105/tpc.107.052647

  51. 51. Rustérucci, C., Espunya, M.C., Díaz, M., Chabannes, M. and Martínez, M.C. (2007) S-Nitrosoglutathione Reductase Affords Protection against Pathogens in Arabidopsis, both Locally and Systemically. Plant Physiology, 143, 1282-1292. https://doi.org /10.1104/pp.106.091686

  52. 52. Chaki, M., Fernández-Ocaña, A.M., Valderrama, R., Carreras, A., Esteban, F.J., Luque, F. and Barroso, J.B. (2009) Involvement of Reactive Nitrogen and Oxygen Species (RNS and ROS) in Sunflower-Mildew Interaction. Plant and Cell Physiology, 50, 665-679. https://doi.org /10.1093/pcp/pcp039

  53. 53. Kubienova, L., Ticha, T., Jahnova, J., Luhova, L., Mieslerova, B. and Petrivalsky, M. (2014) Effect of Abiotic Stress Stimuli on S-Nitrosoglutathione Reductase in Plants. Planta, 239, 139-146. https://doi.org /10.1007/s00425-013-1970-5

  54. 54. Kovacs, I., Durner, J. and Lindermayr, C. (2015) Crosstalk between Nitric Oxide and Glutathione Is Required for Nonexpressor of Pathogenesis-Related Genes 1 (NPR1)-Dependent Defense Signaling in Arabidopsis thaliana. The New phytologist, 208, 860-872. https://doi.org /10.1111/nph.13502

  55. 55. Yun, B.-W., Skelly, M., Yin, M., Yu, M., Mun, B.-G., Lee, S.-U. and Loake, G. (2016) Nitric Oxide and S-Nitrosoglutathione Function Additively during Plant Immunity. The New phytologist, 211, 516-526. https://doi.org /10.1111/nph.13903

  56. 56. Jahnová, J., Luhová, L. and Petřivalský, M. (2019) S-Nitrosoglutathione Reductase-The Master Regulator of Protein S-Nitrosation in Plant NO Signaling. Plants, 8, 48. https://doi.org /10.3390/plants8020048

  57. 57. Chen, R. Q., Sun, S.L., Wang, C., Li, Y.S., Liang, Y., An, F. Y. and Zuo, J.R. (2009) The Arabidopsis PARAQUAT RESISTANT2 Gene Encodes an S-Nitrosoglutathione Reductase that Is a Key Regulator of Cell Death. Cell Research, 19, 1377-1387. https://doi.org /10.1038/cr.2009.117

期刊菜单