[1]常丽丽,彭存智,王丹,等.盐芥叶片应答盐胁迫的蛋白质组学分析[J].江苏农业学报,2022,38(01):49-64.[doi:doi:10.3969/j.issn.1000-4440.2022.01.006]
 CHANG Li-li,PENG Cun-zhi,WANG Dan,et al.Proteomics analysis of Eutrema salsugineum leaves in response to salt stress[J].,2022,38(01):49-64.[doi:doi:10.3969/j.issn.1000-4440.2022.01.006]
点击复制

盐芥叶片应答盐胁迫的蛋白质组学分析()
分享到:

江苏农业学报[ISSN:1006-6977/CN:61-1281/TN]

卷:
38
期数:
2022年01期
页码:
49-64
栏目:
遗传育种·生理生化
出版日期:
2022-02-28

文章信息/Info

Title:
Proteomics analysis of Eutrema salsugineum leaves in response to salt stress
作者:
常丽丽1彭存智1王丹1仝征1黄超1徐兵强12
(1.中国热带农业科学院热带生物技术研究所,海南海口571101;2.中国热带农业科学院海口实验站,海南海口571101)
Author(s):
CHANG Li-li1PENG Cun-zhi1WANG Dan1TONG Zheng1HUANG Chao1XU Bing-qiang12
(1.Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou 571101, China;2.Haikou Experimental Station, Chinese Academy of Tropical Agricultural Sciences, Haikou 571101, China)
关键词:
盐芥盐胁迫差异蛋白质iTRAQ
Keywords:
Eutrema salsugineumsalt stressdifferentially expressed proteinisobaric tags for relative and absolute quantification (iTRAQ)
分类号:
Q949.748.3;S591.2
DOI:
doi:10.3969/j.issn.1000-4440.2022.01.006
文献标志码:
A
摘要:
盐芥是研究耐盐机理的模式植物。为从蛋白质水平揭示盐芥响应盐胁迫的分子机制,本研究采用同位素标记相对和绝对定量(iTRAQ) 技术对不同NaCl浓度处理7 d的盐芥叶片进行差异蛋白质组学分析。结果表明,盐芥叶片中共鉴定到4 607个蛋白质,其中281个蛋白质的表达丰度显著增加,95个蛋白质的表达丰度显著降低。盐胁迫差异表达蛋白质的KEGG代谢通路和蛋白质互作网络分析结果表明,促进植株光合作用可帮助盐芥适应低盐环境;抑制叶绿素和支链氨基酸合成、调控应激反应基因的表达是盐芥应对中盐环境的重要因素;而有效清除活性氧、提高渗透物质积累量和增加能量供应可能是盐芥耐受高盐环境的关键。本研究结果为揭示盐芥应答盐胁迫的分子响应机制提供了理论基础。
Abstract:
Eutrema salsugineum is a model plant for salt tolerance study. To reveal the molecular mechanism of E. salsugineum in response to salt stress at protein level, isobaric tags for relative and absolute quantification (iTRAQ) technology was used to do differential proteomics analysis on E. salsugineum leaves treated under different NaCl concentrations for seven days. The results showed that, a total of 4 607 proteins were identified from leaves of E. salsugineum, among which the expressional abundance of 281 proteins were significantly up-regulated, while the expressional abundance of 95 proteins were significantly down-regulated. Results of KEGG metabolic pathway and protein-protein interaction network analysis for differentially expressed proteins under salt stress showed that, promotion of photosynthesis was helpful for E. salsugineum to adapt to environment with low salinity. Inhibition of chlorophyll and branched chain amino acids synthesis, as well as expression regulation of stress-responsive genes were important factors for E. salsugineum to survive in an environment with medium salinity. Moreover, the key points for E. salsugineum to tolerate high salinity condition might be effective elimination of reactive oxygen species (ROS), elevating accumulation of osmolytes and increasing energy supply. The results can provide theoretical basis for revealing molecular mechanism of E. salsugineum in response to salt stress.

参考文献/References:

[1]LIANG W J, MA X L, WAN P, et al. Plant salt-tolerance mechanism: a review[J]. Biochemical and Biophysical Research Communications, 2018, 495(1): 286-291.
[2]WARWICK S I, AL-SHEHBAZ I A, SAUDER C A. Phylogenetic position of Arabis arenicola and generic limits of Aphragmus and Eutrema (Brassicaceae) based on sequences of nuclear ribosomal DNA[J]. Canadian Journal of Botany-Revue Canadienne de Botanique, 2006, 84(2): 269-281.
[3]AMTMANN A, BOHNERT H J, BRESSAN R A. Abiotic stress and plant genome evolution. Search for new models[J]. Plant Physiology, 2005, 138(1): 127-130.
[4]BRESSAN R A, ZHANG C, ZHANG H, et al. Learning from the Arabidopsis experience. The next gene search paradigm[J]. Plant Physiology, 2001, 127(4): 1354-1360.
[5]ZHU J K. Plant salt tolerance[J]. Trends in Plant Science, 2001, 6(2): 66-71.
[6]TAJI T, SEKI M, SATOU M, et al. Comparative genomics in salt tolerance between Arabidopsis and Arabidopsis-related halophyte salt cress using Arabidopsis microarray[J]. Plant Physiology, 2004, 135(3): 1697-1709.
[7]PANG Q, CHEN S, DAI S, et al. Comparative proteomics of salt tolerance in Arabidopsis thaliana and Thellungiella halophila[J]. Journal of Proteome Research, 2010, 9(5): 2584-2599.
[8]ARBONA V, ARGAMASILLA R, GMEZ-CADENAS A. Common and divergent physiological, hormonal and metabolic responses of Arabidopsis thaliana and Thellungiella halophila to water and salt stress[J]. Journal of Plant Physiology, 2010, 167(16): 1342-1350.
[9]ZHOU Y J, GAO F, LI X F, et al. Alterations in phosphoproteome under salt stress in Thellungiella roots[J]. Chinese Science Bulletin, 2010, 55(32): 3673-3679.
[10]蔡小宁,杨平,贲爱玲,等. 盐芥ThHKT1基因的克隆[J], 江苏农业科学, 2006(6): 21-24.
[11]唐宁,杨平. 盐芥ThHKT1基因的生物信息学分析[J]. 药物生物技术, 2008, 15(6): 449-452.
[12]WU C, GAO X, KONG X Q, et al. Molecular cloning and functional analysis of a Na+/H+ antiporter gene ThNHX1 from a halophytic plant Thellungiella halophila[J]. Plant Molecular Biology Reporter, 2009, 27(1): 1-12.
[13]OH D H, GONG Q, ULANOV A, et al. Sodium stress in the halophyte Thellungiella halophila and transcriptional changes in a thsos1-RNA interference line[J]. Journal of Integrative Plant Biology, 2007, 49(10): 1484-1496.
[14]OH D H, LEIDI E, ZHANG Q, et al. Loss of halophytism by interference with SOS1 expression[J]. Plant Physiology, 2009, 151(1): 210-222.
[15]GAO F, GAO Q, DUAN X G, et al. Cloning of an H+-PPase gene from Thellungiella halophila and its heterologous expression to improve tobacco salt tolerance[J]. Journal of Experimental Botany, 2006, 57(12): 3259-3270.
[16]SUN Q H, GAO F, ZHAO L, et al. Identification of a new 130 bp cis-acting element in the TsVP1 promoter involved in the salt stress response from Thellungiella halophila[J]. BMC Plant Biology, 2010, 10(1): 90.
[17]LV S L, ZHANG K W, GAO Q, et al. Overexpression of an H+-PPase gene from Thellungiella halophila in cotton enhances salt tolerance and improves growth and photosynthetic performance[J]. Plant and Cell Physiology, 2008, 49(8): 1150-1164.
[18]ALEMN F, NIEVES-CORDONES M, MARTNEZ V, et al. Differential regulation of the HAK5 genes encoding the high-affinity K+ transporters of Thellungiella halophila and Arabidopsis thaliana[J]. Environmental and Experimental Botany, 2009, 65(2/3): 263-269.
[19]高秀华. 盐芥耐盐相关基因的功能研究[D]. 济南: 山东师范大学, 2006.
[20]XU X, ZHOU Y, WEI S, et al. Molecular cloning and expression of a Cu/Zn-containing superoxide dismutase from Thellungiella halophila[J]. Molecules and Cells, 2009, 27(4): 423-428.
[21]WANG X C, CHANG L L, WANG B C, et al. Comparative proteomics of Thellungiella halophila leaves from plants subjected to salinity reveals the importance of chloroplastic starch and soluble sugars in halophyte salt tolerance[J]. Molecular & Cellular Proteomics, 2013, 12(8): 2174-2195.
[22]CHANG L L, GUO A P, JIN X, et al. The beta subunit of glyceraldehyde 3-phosphate dehydrogenase is an important factor for maintaining photosynthesis and plant development under salt stress-Based on an integrative analysis of the structural, physiological and proteomic changes in chloroplasts in Thellungiella halophila[J]. Plant Science, 2015, 236: 223-238.
[23]WANG X C, SHI M J, LU X L, et al. A method for protein extraction from different subcellular fractions of laticifer latex in Hevea brasiliensis compatible with 2-DE and MS[J]. Proteome Science, 2010, 8(1): 35.
[24]BRADFORD M M. A rapid and sensitive method for the quantization of microgram quantities of protein using the principle of protein-dye binding[J]. Analytical Biochemistry, 1976, 72(1/2): 248-254.
[25]YAN M, LU Z L, LI B, et al. Comparative proteomics reveals new insights into the endosperm responses to drought, salinity and submergence in germinating wheat seeds[J]. Plant Molecular Biology, 2021, 105(3): 287-302.
[26]LI J, CUI J, CHENG D, et al. iTRAQ protein profile analysis of sugar beet under salt stress: different coping mechanisms in leaves and roots[J]. BMC Plant Biology, 2020, 20(1): 347.
[27]刘爱荣,赵可夫. 盐胁迫对盐芥生长及硝酸还原酶活性的影响[J]. 植物生理与分子生物学学报, 2005, 31(5): 469-476.
[28]KATSCHNIG D, BROEKMAN R, ROZEMA J. Salt tolerance in the halophyte Salicornia dolichostachya Moss: growth, morphology and physiology[J]. Environmental and Experimental Botany, 2013, 92: 32-42.
[29]YI X, SUN Y, YANG Q, et al. Quantitative proteomics of Sesuvium portulacastrum leaves revealed that ion transportation by V-ATPase and sugar accumulation in chloroplast played crucial roles in halophyte salt tolerance[J]. Journal of Proteomics, 2014, 99: 84-100.
[30]郭建荣,郑聪聪,李艳迪,等. NaCl处理对真盐生植物盐地碱蓬根系特征及活力的影响[J]. 植物生理学报, 2017, 53(1): 63-70.
[31]GOUSSI R, MANA A, DERBALI W, et al. Comparative analysis of salt stress, duration and intensity, on the chloroplast ultrastructure and photosynthetic apparatus in Thellungiella salsuginea[J]. Journal of Photochemistry and Photobiology B-Biology, 2018, 183: 275-287.
[32]PANG Q, CHEN S, DAI S, et al. Comparative proteomics of salt tolerance in Arabidopsis thaliana and Thellungiella halophila[J]. Journal of Proteome Research, 2010, 9(5): 2584-2599.
[33]LIU Z, ZOU L, CHEN C, et al. iTRAQ-based quantitative proteomic analysis of salt stress in Spica Prunellae[J]. Scientific Reports, 2019, 9(1): 9590.
[34]KUMARI M P, SEKAR K. Effect of plant growth regulators on chlorophyll and carotenoid content of salinity stressed okra seedlings[J]. Asian Journal of Horticulture, 2008, 3(1): 54-55.
[35]XING W, WANG J, LIU H, et al. Influence of natural saline-alkalistress on chlorophyll content and chloroplast ultrastructure of two contrasting rice(Oryza sativa L. japonica) cultivars[J]. Australian Journal of Crop Science, 2013, 7(2): 289-292.
[36]SAYYAD-AMIN P, JAHANSOOZ M R, BORZOUEI A, et al. Changes in photosynthetic pigments and chlorophyll-a fluorescence attributes of sweet-forage and grain sorghum cultivars under salt stress[J]. Journal of Biological Physics, 2016, 42(4): 601-620.
[37]SHOOLINGIN-JORDAN P M. Porphobilinogen deaminase and uroporphyrinogen Ⅲ synthase: structure, molecular biology, and mechanism[J]. Journal of Bioenergetics & Biomembranes, 1995, 27(2): 181-195.
[38]ELDER G H, ROBERTS A G. Uroporphyrinogen decarboxylase[J]. Journal of Bioenergetics & Biomembranes, 1995, 27(2): 207-214.
[39]SCHOEFS B, FRANCK F. Protochlorophyllide reduction: mechanisms and evolutions[J]. Photochemistry & Photobiology, 2003, 78(6): 543-557.
[40]ECKHARDT U, GRIMM B, HRTENSTEINER S. Recent advances in chlorophyll biosynthesis and breakdown in higher plants[J]. Plant Molecular Biology, 2004, 56(1): 1-14.
[41]IKEGAMI A, YOSHIMURA N, MOTOHASHI K, et al. The CHLI1 subunit of Arabidopsis thaliana magnesium chelatase is a target protein of the chloroplast thioredoxin[J]. Journal of Biological Chemistry, 2007, 282(27): 19282-19291.
[42]PRUZINSK A, TANNER G, ANDERS I, et al. Chlorophyll breakdown: pheophorbide a oxygenase is a Rieske-type iron-sulfur protein, encoded by the accelerated cell death 1 gene[J]. Proceedings of the National Academy of Sciences of the United States of America, 2003, 100(25): 15259-15264.
[43]TURAN S, TRIPATHY B C. Salt-stress induced modulation of chlorophyll biosynthesis during de-etiolation of rice seedlings[J]. Physiologia Plantarum, 2015, 153(3): 477-491.
[44]HU L, XIANG L, LI S, et al. Beneficial role of spermidine in chlorophyll metabolism and D1 protein content in tomato seedlings under salinity-alkalinity stress[J]. Physiologia Plantarum, 2016, 156(4): 468-477.
[45]GONG W, XU F, SUN J, et al. iTRAQ-based comparative proteomic analysis of seedling leaves of two upland cotton genotypes differing in salt tolerance[J]. Frontiers in Plant Science, 2017, 8: 2113.
[46]HILDEBRANDT T M, NUNES NESI A, ARAJO W L, et al. Amino acid catabolism in plants[J]. Molecular Plant, 2015, 8(11): 1563-1579.
[47]HUANG S P, ZENG Y L. Research progress on plant aldehyde dehydrogenase under adversity stresses[J]. Biotechnology Bulletin, 2015, 31(12): 8-14.
[48]HILDEBRANDT T M. Synthesis versus degradation: directions of amino acid metabolism during Arabidopsis abiotic stress response[J]. Plant Molecular Biology, 2018, 98(1/2): 121-135.
[49]LIU X, HAN Q, WANG J, et al. Two FgLEU2 genes with different roles in leucine biosynthesis and infection-related morphogenesis in Fusarium graminearum[J]. PLoS One, 2016, 11(11): e0165927.
[50]KOCHEVENKO A, FERNIE A R. The genetic architecture of branched-chain amino acid accumulation in tomato fruits[J]. Journal of Experimental Botany, 2011, 62(11): 3895-3906.
[51]HUANG T, JANDER G. Abscisic acid-regulated protein degradation causes osmotic stress-induced accumulation of branched chain amino acids in Arabidopsis thaliana[J]. Planta, 2017, 246(4): 737-747.
[52]CHEN D, MA X, LI C, et al. A wheat aminocyclopropane-1-carboxylate oxidase gene, TaACO1, negatively regulates salinity stress in Arabidopsis thaliana[J]. Plant Cell Reports, 2014, 33(11): 1815-1827.
[53]RAMADOSS N, GUPTA D, VAIDYA B N, et al. Functional characterization of 1-aminocyclopropane-1-carboxylic acid oxidase gene in Arabidopsis thaliana and its potential in providing flood tolerance[J]. Biochemical & Biophysical Research Communications, 2018, 503(1): 365-370.
[54]GUO Z, TAN J, ZHUO C, et al. Abscisic acid, H2O2 and nitric oxide interactions mediated cold-induced S-adenosylmethionine synthetase in Medicago sativa sub sp. falcata that confers cold tolerance through up-regulating polyamine oxidation[J]. Plant Biotechnology Journal, 2014, 12(5): 601-612.
[55]KIM S H, KIM S H, PALANIYANDI S A, et al. Expression of potato S-adenosyl-L-methionine synthase (SbSAMS) gene altered developmental characteristics and stress responses in transgenic Arabidopsis plants[J]. Plant Physiology and Biochemistry, 2015,87: 84-91.
[56]MA C, WANG Y, GU D, et al. Overexpression of S-adenosyl-l-methionine synthetase 2 from sugar beet M14 increased Arabidopsis tolerance to salt and oxidative stress[J]. International Journal of Molecular Sciences, 2017, 18(4): 847.
[57]APEL K, HIRT H. Reactive oxygen species: metabolism, oxidative stress, and signal transduction[J]. Annual Review of Plant Biology, 2004, 55(1): 373-399.
[58]MAY M J, VERNOUX T, LEAVER C, et al. Glutathione homeostasis in plants: implications for environmental sensing and plant development[J]. Journal of Experimental Botany,1998,49(321):649-667.
[59]CHOUDHURY F K, DEVIREDDY A R, AZAD R K, et al. Rapid accumulation of glutathione during light stress in Arabidopsis[J]. Plant & Cell Physiology, 2018, 59(9): 1817-1826.
[60]BELA K, HORVTH E, GALL , et al. Plant glutathione peroxidases: emerging role of the antioxidant enzymes in plant development and stress responses[J]. Journal of Plant Physiology, 2015, 176(1): 192-201.
[61]LABROU N E, PAPAGEORGIOU A C, PAVLI O, et al. Plant GSTome: structure and functional role in xenome network and plant stress response[J]. Current Opinion in Biotechnology, 2015, 32: 186-194.
[62]MILLA M, MAURER A, HUETE A R, et al. Glutathione peroxidase genes in Arabidopsis are ubiquitous and regulated by abiotic stresses through diverse signaling pathways[J]. The Plant Journal, 2003, 36(5): 602-615.
[63]XU J, TIAN Y S, XING X J, et al. Over-expression of AtGSTU19 provides tolerance to salt, drought and methyl viologen stresses in Arabidopsis[J]. Physiologia Plantarum, 2016, 156(2): 164-175.
[64]KANG S G, JEONG H K, SUH H S. Characterization of a new member of the glutathione peroxidase gene family in Oryza sativa[J]. Molecules & Cells, 2004, 17(1): 23-28.
[65]GALL , CSISZR J, SECENJI M, et al. Glutathione transferase activity and expression patterns during grain filling in ag leaves of wheat genotypes differing in drought tolerance: response to water deficit[J]. Journal of Plant Physiology, 2009, 166(17): 1878-1891.
[66]CSISZR J, GALL A, HORVTH E, et al. Different peroxidase activities and expression of abiotic stress-related peroxidases in apical root segments of wheat genotypes with different drought stress tolerance under osmotic stress[J]. Plant Physiology & Biochemistry, 2012, 52: 119-129.
[67]REZAEI M K, SHOBBAR Z S, SHAHBAZI M, et al. Glutathione S-transferase (GST) family in barley: identification of members, enzyme activity, and gene expression pattern[J]. Journal of Plant Physiology, 2013, 170(14): 1277-1284.
[68]CHAN C, LAM H M. A putative lambda class glutathione S-transferase enhances plant survival under salinity stress[J]. Plant and Cell Physiology, 2014, 55(3): 570-579.
[69]GAO F, CHEN J, MA T, et al. The glutathione peroxidase gene family in Thellungiella salsuginea: genome-wide identification, classification, and gene and protein expression analysis under stress conditions[J]. International Journal of Molecular Sciences, 2014, 15(2): 3319-3335.
[70]LI L J, LU X C, MA H Y, et al. Comparative proteomic analysis reveals the roots response to low root-zone temperature in Malus baccata[J]. Journal of Plant Research, 2018, 131(5): 865-878.
[71]JIA T, WANG J, CHANG W, et al. Proteomics analysis of E. angustifolia seedlings inoculated with arbuscular mycorrhizal fungi under salt stress[J]. International Journal of Molecular Sciences, 2019, 20(3): 788.
[72]CHEONG M, YUN D J. Salt-stress signaling[J]. Journal of Plant Biology, 2007, 50(2): 148-155.
[73]KHAN T A, YUSUF M, AHMAD A, et al. Proteomic and physiological assessment of stress sensitive and tolerant variety of tomato treated with brassinosteroids and hydrogen peroxide under low-temperature stress[J]. Food Chemistry, 2019, 289: 500-511.
[74]BANDURSKA H, NIEDZIELA J, PIETROWSKA-BOREK M, et al. Regulation of proline biosynthesis and resistance to drought stress in two barley (Hordeum vulgare L.) genotypes of different origin[J]. Plant Physiology And Biochemistry, 2017, 118: 427-437.
[75]尹秀,王俊,张二豪,等. PEG-6000浸种处理对甘青青兰种子萌发及幼苗抗旱性的影响[J].江苏农业科学,2020,48(13):168-172.
[76]殷世航,周赛,黄霄宇,等. 中蔗系列新品种对干旱胁迫的响应及抗旱性评价[J].南方农业学报,2020,51(6):1339-1345.
[77]任保兰,耿建建,吕亚,等. 辣木幼苗对淹水胁迫的生理响应及耐涝性综合评价[J].南方农业学报,2021,52(3):789-796.
[78]PREZ-ARELLANO I, CARMONA-ALVAREZ F, MARTNEZ A I, et al. Pyrroline-5-carboxylate synthase and proline biosynthesis: from osmotolerance to rare metabolic disease[J]. Protein Science, 2010, 19(3): 372-382.
[79]SINGH P, TIWARI A, SINGH S P, et al. Proline biosynthesizing enzymes (glutamate 5-kinase and pyrroline-5-carboxylate reductase) from a model cyanobacterium for desiccation tolerance[J]. Physiology and Molecular Biology of Plants, 2013, 19(4): 521-528.
[80]DEUSCHLE K, FUNCK D, HELLMANN H, et al. A nuclear gene encoding mitochondrial Δ1-pyrroline-5-carboxylate dehydrogenase and its potential role in protection from proline toxicity[J]. The Plant Journal, 2001, 27(4): 345-356.
[81]TIKHONOV A N. pH-dependent regulation of electron transport and ATP synthesis in chloroplasts[J]. Photosynthesis Research, 2013, 116(2/3): 511-534.
[82]WANG L X, PAN D Z, LI J, et al. Proteomic analysis of changes in the Kandelia candel chloroplast proteins reveals pathways associated with salt tolerance[J]. Plant Science, 2015, 231: 159-172.
[83]JI W, CONG R, LI S, et al. Comparative proteomic analysis of soybean leaves and roots by iTRAQ provides insights into response mechanisms to short-term salt stress[J]. Frontiers in Plant Science, 2016, 7: 573.
[84]LIU Z, ZOU L, CHEN C, et al. iTRAQ-based quantitative proteomic analysis of salt stress in Spica Prunellae[J]. Scientific Reports, 2019,9(1): 9590.

相似文献/References:

[1]韩金龙,李慧,蔺经,等.核黄素对盐胁迫下杜梨叶片抗氧化系统的影响[J].江苏农业学报,2015,(04):893.[doi:10.3969/j.issn.1000-4440.2015.04.029]
 HAN Jing-long,LI Hui,LIN Jing,et al.The regulatory role of riboflavin in antioxidant system of Pyrus betulaefolia in response to salt tolerance[J].,2015,(01):893.[doi:10.3969/j.issn.1000-4440.2015.04.029]
[2]安飞飞,简纯平,杨龙,等.木薯幼苗叶绿素含量及光合特性对盐胁迫的响应[J].江苏农业学报,2015,(03):500.[doi:10.3969/j.issn.1000-4440.2015.03.006]
 AN Fei-fei,JIAN Chun-ping,YANG Long,et al.Chlorophyll contents and photosynthetic characteristics of cassava seedlings in response to NaCl stress[J].,2015,(01):500.[doi:10.3969/j.issn.1000-4440.2015.03.006]
[3]刘金龙,辛寒晓,范学明,等.盐胁迫下鱼蛋白多肽对樱桃番茄种子发芽特性的影响[J].江苏农业学报,2017,(03):662.[doi:doi:10.3969/j.issn.1000-4440.2017.03.026]
 LIU Jin-long,XIN Han-xiao,FAN Xue-ming,et al.Effects of fish protein polypeptide on salt-stressed cherry tomato seed germination[J].,2017,(01):662.[doi:doi:10.3969/j.issn.1000-4440.2017.03.026]
[4]田礼欣,李丽杰,刘旋,等.外源海藻糖对盐胁迫下玉米幼苗根系生长及生理特性的影响[J].江苏农业学报,2017,(04):754.[doi:doi:10.3969/j.issn.1000-4440.2017.04.005]
 TIAN Li-xin,LI Li-jie,LIU Xuan,et al.Root growth and physiological characteristics of salt-stressed maize seedlings in response to exogenous trehalose[J].,2017,(01):754.[doi:doi:10.3969/j.issn.1000-4440.2017.04.005]
[5]黄芳,徐珍珍,孟珊,等.盐胁迫下棉花LTR-反转座子的转录激活及在耐盐相关基因发掘中的应用[J].江苏农业学报,2017,(06):1220.[doi:doi:10.3969/j.issn.1000-4440.2017.06.004]
 HUANG Fang,XU Zhen-zhen,MENG Shan,et al.The identification of long terminal repeat retrotransposons (LTR-RTs) with transcription activity under salt stress and its application in screening the candidate genes related to salt-tolerant in cotton[J].,2017,(01):1220.[doi:doi:10.3969/j.issn.1000-4440.2017.06.004]
[6]王旭明,赵夏夏,陈景阳,等.盐胁迫下水稻孕穗期SS和SPS活性与糖积累的响应及其相关性分析[J].江苏农业学报,2018,(03):481.[doi:doi:10.3969/j.issn.1000-4440.2018.03.001]
 WANG Xu-ming,ZHAO Xia-xia,CHEN Jing-yang,et al.The response and correlations between carbohydrate accumulation and activities of SPS, SS at booting stage of rice under salt stress[J].,2018,(01):481.[doi:doi:10.3969/j.issn.1000-4440.2018.03.001]
[7]李敏,郭聪,李玉娟,等.旱柳转录组测序及生物学分析[J].江苏农业学报,2019,(02):271.[doi:doi:10.3969/j.issn.1000-4440.2019.02.005]
 LI Min,GUO Cong,LI Yu-juan,et al.Transcriptome sequencing and biological analysis of willow (Salix matsudana)[J].,2019,(01):271.[doi:doi:10.3969/j.issn.1000-4440.2019.02.005]
[8]束晓春,李乃伟,汤兴利,等.NaCl处理对不同珊瑚菜种源光合生理和药用有效成分的影响[J].江苏农业学报,2019,(04):790.[doi:doi:10.3969/j.issn.1000-4440.2019.04.006]
 SHU Xiao chun,LI Nai wei,TANG Xing li,et al.Effects of NaCl stress on photosynthetic physiology and active component of different Glehnia littoralis provenance[J].,2019,(01):790.[doi:doi:10.3969/j.issn.1000-4440.2019.04.006]
[9]王馨,闫永庆,殷媛,等.外源γ-氨基丁酸(GABA)对盐胁迫下西伯利亚白刺光合特性的影响[J].江苏农业学报,2019,(05):1032.[doi:doi:10.3969/j.issn.1000-4440.2019.05.005]
 WANG Xin,YAN Yong-qing,YIN Yuan,et al.Effect of exogenous γ-aminobutyric acid(GABA) on photosynthetic characteristics of Nitraria sibirica pall under salt stress[J].,2019,(01):1032.[doi:doi:10.3969/j.issn.1000-4440.2019.05.005]
[10]石婧,刘东洋,张凤华.不同品种(品系)棉花对盐胁迫的生理响应及耐盐性评价[J].江苏农业学报,2020,(04):828.[doi:doi:10.3969/j.issn.1000-4440.2020.04.004]
 SHI Jing,LIU Dong-yang,ZHANG Feng-hua.Physiological responses of different cotton cultivars (strains) to salt stress and salt tolerance evaluation[J].,2020,(01):828.[doi:doi:10.3969/j.issn.1000-4440.2020.04.004]

备注/Memo

备注/Memo:
收稿日期:2021-04-19基金项目:中央级公益性科研院所基本科研业务费项目(1630052017008);海南省重点研发计划项目(ZDYF2018180)作者简介:常丽丽( 1984-) ,女,湖北荆门人,博士,助理研究员,主要从事热带作物蛋白质组学与分子生物学相关研究。(E-mail)tychang493875@126.com通讯作者:徐兵强,(E-mail)erger2002@163.com
更新日期/Last Update: 2022-03-04