Acta Prataculturae Sinica ›› 2023, Vol. 32 ›› Issue (6): 186-202.DOI: 10.11686/cyxb2022303
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Wen-juan WANG(), Shang-li SHI(), Long HE, Bei WU, Chan-chan LIU
Received:
2022-07-26
Revised:
2022-09-01
Online:
2023-06-20
Published:
2023-04-21
Contact:
Shang-li SHI
Wen-juan WANG, Shang-li SHI, Long HE, Bei WU, Chan-chan LIU. Accumulation and functions of polyamines in plants under drought stress[J]. Acta Prataculturae Sinica, 2023, 32(6): 186-202.
物种 Species | 干旱条件 Drought conditions | 胁迫时间 Stress times | 3种多胺含量的变化 Changes in the content of the three polyamines | 参考文献 References |
---|---|---|---|---|
小麦 T. aestivum | 停止灌溉Stop irrigation | 12,24,36,48 h | Put、Spd和Spm含量先迅速升高而后下降,较高的Spd和Spm含量有利于增强小麦幼苗的抗旱性。 Put, Spd and Spm contents increased rapidly and then decreased, and higher Spd and Spm contents were beneficial to enhance the drought resistance of wheat seedlings. | [ |
小麦 T. aestivum | 停止灌溉Stop irrigation | 11 d | Put和Spm含量升高,Spd含量下降,其中Put的增加可能有利于Spm的进一步积累,从而抵抗干旱胁迫。 Put and Spm contents increased and Spd content decreased, in which the increase of Put might be beneficial to the further accumulation of Spm, thus resisting drought stress. | [ |
黑麦草 | 停止灌溉Stop irrigation | 20 d | Put、Spd和Spm含量上升,其中Spd和Spm上升幅度更大,与抗旱性关系密切。Put, Spd and Spm contents increased, among which Spd and Spm increased more and were closely related to drought resistance. | [ |
车前草 C. plantagineum | 停止灌溉Stop irrigation | 1,2,4,8,24,72,96 h | 在干旱处理的前24 h内,Spd和Spm含量增加,Put含量逐渐降低。Spd and Spm content increased and Put content gradually decreased during the first 24 h of drought treatment. | [ |
水稻 O. sativa | 土壤含水量为田间持水量的50%。Soil water content is 50% of field water holding capacity. | 18 d | Put 和Spd含量下降,Spm含量显著增加,Spm有利于增强植株抗旱性。Put and Spd content decreased and Spm content increased significantly, and Spm was beneficial to enhance the drought resistance of plants. | [ |
紫花苜蓿 | 土壤含水量为田间持水量的(55±5)%和(35±5)%。Soil water content is (55±5)% and (35±5)% of field water holding capacity. | 1,3,5,7 d | Put、Spd和Spm含量先上升后下降。 Put, Spd and Spm content increased and then decreased. | [ |
油菜 | 土壤含水量为田间持水量的50%、30%和10%。Soil water content is 50%, 30% and 10% of field water holding capacity. | 7 d | Put和Spm含量增加。Put and Spm content increased. | [ |
大马士革玫瑰 R. damascena | 土壤含水量为田间持水量的50%和25%。Soil water content is 50% and 25% of field water holding capacity. | 1,3,6,12 d | Put含量降低,Spd和Spm含量增加。 Put content decreased and Spd and Spm content increased. | [ |
李 | 对叶片喷清水,盆内不浇水。Spray water on the leaves and keep the pots unwatered. | 60 d | Put、Spd和Spm含量明显增加。 Put, Spd and Spm contents were significantly increased. | [ |
毛竹 | 5%、15%和25% PEG 6000模拟干旱胁迫。5%, 15% and 25% PEG 6000 simulated drought stress. | 20 d | Put含量显著下降、Spd和Spm含量逐渐上升,Put向Spd和Spm的转化有利于增强抗旱性。Put content decreased significantly and Spd and Spm content increased gradually, and the conversion of Put to Spd and Spm was beneficial to enhance drought resistance. | [ |
鹰嘴豆 C. arietinum | -0.6 MPa PEG 6000模拟干旱胁迫。 -0.6 MPa PEG 6000 to simulate drought stress. | 1,2,3,4,5,6,7 d | Put、Spd和Spm含量升高,其中Spd含量的显著增加在抵抗干旱胁迫中发挥着重要作用。Put, Spd and Spm contents increased, among which the significant increase in Spd content played an important role in the resistance to drought stress. | [ |
番茄 L. esculentum | 10% PEG 6000模拟干旱胁迫。10% PEG 6000 simulated drought stress. | 6,12,24,36,48 h | Put、Spd和Spm含量不断增加,其中Spd和Spm的积累量均高于Put,Spm和Spd维持其抗旱性。 Put, Spd and Spm contents increased continuously, where both Spd and Spm accumulated more than Put, and Spm and Spd maintained their drought resistance. | [ |
Table 1 The accumulation of polyamines in different species under drought stress
物种 Species | 干旱条件 Drought conditions | 胁迫时间 Stress times | 3种多胺含量的变化 Changes in the content of the three polyamines | 参考文献 References |
---|---|---|---|---|
小麦 T. aestivum | 停止灌溉Stop irrigation | 12,24,36,48 h | Put、Spd和Spm含量先迅速升高而后下降,较高的Spd和Spm含量有利于增强小麦幼苗的抗旱性。 Put, Spd and Spm contents increased rapidly and then decreased, and higher Spd and Spm contents were beneficial to enhance the drought resistance of wheat seedlings. | [ |
小麦 T. aestivum | 停止灌溉Stop irrigation | 11 d | Put和Spm含量升高,Spd含量下降,其中Put的增加可能有利于Spm的进一步积累,从而抵抗干旱胁迫。 Put and Spm contents increased and Spd content decreased, in which the increase of Put might be beneficial to the further accumulation of Spm, thus resisting drought stress. | [ |
黑麦草 | 停止灌溉Stop irrigation | 20 d | Put、Spd和Spm含量上升,其中Spd和Spm上升幅度更大,与抗旱性关系密切。Put, Spd and Spm contents increased, among which Spd and Spm increased more and were closely related to drought resistance. | [ |
车前草 C. plantagineum | 停止灌溉Stop irrigation | 1,2,4,8,24,72,96 h | 在干旱处理的前24 h内,Spd和Spm含量增加,Put含量逐渐降低。Spd and Spm content increased and Put content gradually decreased during the first 24 h of drought treatment. | [ |
水稻 O. sativa | 土壤含水量为田间持水量的50%。Soil water content is 50% of field water holding capacity. | 18 d | Put 和Spd含量下降,Spm含量显著增加,Spm有利于增强植株抗旱性。Put and Spd content decreased and Spm content increased significantly, and Spm was beneficial to enhance the drought resistance of plants. | [ |
紫花苜蓿 | 土壤含水量为田间持水量的(55±5)%和(35±5)%。Soil water content is (55±5)% and (35±5)% of field water holding capacity. | 1,3,5,7 d | Put、Spd和Spm含量先上升后下降。 Put, Spd and Spm content increased and then decreased. | [ |
油菜 | 土壤含水量为田间持水量的50%、30%和10%。Soil water content is 50%, 30% and 10% of field water holding capacity. | 7 d | Put和Spm含量增加。Put and Spm content increased. | [ |
大马士革玫瑰 R. damascena | 土壤含水量为田间持水量的50%和25%。Soil water content is 50% and 25% of field water holding capacity. | 1,3,6,12 d | Put含量降低,Spd和Spm含量增加。 Put content decreased and Spd and Spm content increased. | [ |
李 | 对叶片喷清水,盆内不浇水。Spray water on the leaves and keep the pots unwatered. | 60 d | Put、Spd和Spm含量明显增加。 Put, Spd and Spm contents were significantly increased. | [ |
毛竹 | 5%、15%和25% PEG 6000模拟干旱胁迫。5%, 15% and 25% PEG 6000 simulated drought stress. | 20 d | Put含量显著下降、Spd和Spm含量逐渐上升,Put向Spd和Spm的转化有利于增强抗旱性。Put content decreased significantly and Spd and Spm content increased gradually, and the conversion of Put to Spd and Spm was beneficial to enhance drought resistance. | [ |
鹰嘴豆 C. arietinum | -0.6 MPa PEG 6000模拟干旱胁迫。 -0.6 MPa PEG 6000 to simulate drought stress. | 1,2,3,4,5,6,7 d | Put、Spd和Spm含量升高,其中Spd含量的显著增加在抵抗干旱胁迫中发挥着重要作用。Put, Spd and Spm contents increased, among which the significant increase in Spd content played an important role in the resistance to drought stress. | [ |
番茄 L. esculentum | 10% PEG 6000模拟干旱胁迫。10% PEG 6000 simulated drought stress. | 6,12,24,36,48 h | Put、Spd和Spm含量不断增加,其中Spd和Spm的积累量均高于Put,Spm和Spd维持其抗旱性。 Put, Spd and Spm contents increased continuously, where both Spd and Spm accumulated more than Put, and Spm and Spd maintained their drought resistance. | [ |
物种 Species | 取样部位 Sampling area | 抗旱类型 Types of drought resistance | 多胺含量的变化Changes in polyamine content | 参考文献 References | ||
---|---|---|---|---|---|---|
Put | Spd | Spm | ||||
小麦T. aestivum | 叶片Leaf | 耐旱型Drought tolerant | ↑ | ↑ | ↑ | [ |
敏感型Drought sensitive | ↑↑ | - | - | |||
玉米Z. mays | 叶片Leaf | 耐旱型Drought tolerant | ↑ | ↑↑ | ↑↑ | [ |
敏感型Drought sensitive | ↑↑ | ↑ | ↑ | |||
大豆G. max | 叶片Leaf | 耐旱型Drought tolerant | ↑ | ↑↑ | ↑↑ | [ |
敏感型Drought sensitive | ↑↑ | ↑ | ↑ | |||
番茄S. lycopersicum | 叶片Leaf | 耐旱型Drought tolerant | - | ↑ | ↑ | [ |
敏感型Drought sensitive | - | ↓ | ↓ | |||
番茄L. esculentum | 果实Fruit | 耐旱型Drought tolerant | ↓ | ↑ | ↓ | [ |
敏感型Drought sensitive | ↑ | - | - |
Table 2 The accumulation differences of three polyamines in different drought-resistant varieties under drought stress
物种 Species | 取样部位 Sampling area | 抗旱类型 Types of drought resistance | 多胺含量的变化Changes in polyamine content | 参考文献 References | ||
---|---|---|---|---|---|---|
Put | Spd | Spm | ||||
小麦T. aestivum | 叶片Leaf | 耐旱型Drought tolerant | ↑ | ↑ | ↑ | [ |
敏感型Drought sensitive | ↑↑ | - | - | |||
玉米Z. mays | 叶片Leaf | 耐旱型Drought tolerant | ↑ | ↑↑ | ↑↑ | [ |
敏感型Drought sensitive | ↑↑ | ↑ | ↑ | |||
大豆G. max | 叶片Leaf | 耐旱型Drought tolerant | ↑ | ↑↑ | ↑↑ | [ |
敏感型Drought sensitive | ↑↑ | ↑ | ↑ | |||
番茄S. lycopersicum | 叶片Leaf | 耐旱型Drought tolerant | - | ↑ | ↑ | [ |
敏感型Drought sensitive | - | ↓ | ↓ | |||
番茄L. esculentum | 果实Fruit | 耐旱型Drought tolerant | ↓ | ↑ | ↓ | [ |
敏感型Drought sensitive | ↑ | - | - |
1 | Fan Z Q. Molecular adaptation mechanism of plants under drought environmental stress and its applications. Shanghai: Fudan University, 2004. |
樊正球. 干旱环境胁迫下的植物分子适应机理及其应用研究. 上海: 复旦大学, 2004. | |
2 | Liu J H, Wang W, Wu H, et al. Polyamines function in stress tolerance: From synthesis to regulation. Frontiers in Plant Science, 2015, 6: 827. |
3 | Chen D D, Shao Q S, Yin L H, et al. Polyamine function in plants: Metabolism, regulation on development, and roles in abiotic stress responses. Frontiers in Plant Science, 2019, 9: 1945. |
4 | Liu H P, Dong B H, Zhang Y Y, et al. Relationship between osmotic stress and the levels of free, conjugated and bound polyamines in leaves of wheat seedlings. Plant Science, 2004, 166(5): 1261-1267. |
5 | Luo J, Fuell C, Parr A, et al. A novel polyamine acyltransferase responsible for the accumulation of spermidine conjugates in Arabidopsis seed. The Plant Cell, 2009, 21(1): 318-333. |
6 | Martin-Tanguy J. Conjugated polyamines and reproductive development: Biochemical, molecular and physiological approaches. Physiologia Plantarum, 1997, 100(3): 675-688. |
7 | Igarashi K, Kashiwagi K. Modulation of protein synthesis by polyamines. IUBMB Life, 2015, 67(3): 160-169. |
8 | Jankovska-Bortkevič E, Gavelienė V, Jurkonienė S. Physiological roles and signaling of polyamines in plants under stressed conditions//Aftab T, Naeem M. Emerging plant growth regulators in agriculture. New York: Academic Press, 2022: 303-316. |
9 | Tiburcio A F, Altabella T, Bitrián M, et al. The roles of polyamines during the lifespan of plants: From development to stress. Planta, 2014, 240(1): 1-18. |
10 | Hussain S S, Ali M, Ahmad M, et al. Polyamines: Natural and engineered abiotic and biotic stress tolerance in plants. Biotechnology Advances, 2011, 29(3): 300-311. |
11 | Groppa M D, Benavides M P, Tomaro M L. Polyamine metabolism in sunflower and wheat leaf discs under cadmium or copper stress. Plant Science, 2003, 164(2): 293-299. |
12 | Rider J E, Hacker A, Mackintosh C A, et al. Spermine and spermidine mediate protection against oxidative damage caused by hydrogen peroxide. Amino Acids, 2007, 33(2): 231-240. |
13 | Yamaguchi K, Takahashi Y, Berberich T, et al. A protective role for the polyamine spermine against drought stress in Arabidopsis. Biochemical and Biophysical Research Communications, 2007, 352(2): 486-490. |
14 | Duan J, Li J, Guo S, et al. Exogenous spermidine affects polyamine metabolism in salinity-stressed Cucumis sativus roots and enhances short-term salinity tolerance. Journal of Plant Physiology, 2008, 165(15): 1620-1635. |
15 | Cuevas J C, López-Cobollo R, Alcázar R, et al. Putrescine is involved in Arabidopsis freezing tolerance and cold acclimation by regulating abscisic acid levels in response to low temperature. Plant Physiology, 2008, 148(2): 1094-1105. |
16 | Shen H J, Xie Y F. Polyamines (PAs) and several stress responses in plants. Journal of Nanjing Forestry University, 1997, 21(4): 28-32. |
沈惠娟, 谢寅峰. 多胺(PAs)与植物的几种胁迫反应. 南京林业大学学报, 1997, 21(4): 28-32. | |
17 | Watson M B, Malmberg R L. Regulation of Arabidopsis thaliana (L.) Heynh arginine decarboxylase by potassium deficiency stress. Plant Physiology, 1996, 111(4): 1077-1083. |
18 | Watson M B. Isolation and characterization of a second arginine decarboxylase cDNA from Arabidopsis (Accession No. AF009647). Plant Physiology, 1997, 114: 1569. |
19 | Hanzawa Y, Imai A, Michael A J, et al. Characterization of the spermidine synthase-related gene family in Arabidopsis thaliana. FEBS Letters, 2002, 527(1/2/3): 176-180. |
20 | Franceschetti M, Hanfrey C, Scaramagli S, et al. Characterization of monocot and dicot plant S-adenosyl-l-methionine decarboxylase gene families including identification in the mRNA of a highly conserved pair of upstream overlapping open reading frames. Biochemical Journal, 2001, 353(2): 403-409. |
21 | Hashimoto T, Tamaki K, Suzuki K, et al. Molecular cloning of plant spermidine synthases. Plant and Cell Physiology, 1998, 39(1): 73-79. |
22 | Urano K, Yoshiba Y, Nanjo T, et al. Characterization of Arabidopsis genes involved in biosynthesis of polyamines in abiotic stress responses and developmental stages. Plant, Cell & Environment, 2003, 26(11): 1917-1926. |
23 | Urano K, Hobo T, Shinozaki K. Arabidopsis ADC genes involved in polyamine biosynthesis are essential for seed development. FEBS Letters, 2005, 579(6): 1557-1564. |
24 | Hanzawa Y, Takahashi T, Michael A J, et al. ACAULIS5, an Arabidopsis gene required for stem elongation, encodes a spermine synthase. The EMBO Journal, 2000, 19(16): 4248-4256. |
25 | Panicot M, Minguet E G, Ferrando A, et al. A polyamine metabolon involving aminopropyl transferase complexes in Arabidopsis. The Plant Cell, 2002, 14(10): 2539-2551. |
26 | Janowitz T, Kneifel H, Piotrowski M. Identification and characterization of plant agmatine iminohydrolase, the last missing link in polyamine biosynthesis of plants. FEBS letters, 2003, 544(1/2/3): 258-261. |
27 | Piotrowski M, Janowitz T, Kneifel H. Plant CN hydrolases and the identification of a plant N-carbamoylputrescine amidohydrolase involved in polyamine biosynthesis. Journal of Biological Chemistry, 2003, 278(3): 1708-1712. |
28 | Allen K D. Assaying gene content in Arabidopsis. Proceedings of the National Academy of Sciences, 2002, 99(14): 9568-9572. |
29 | Hanfrey C, Sommer S, Mayer M J, et al. Arabidopsis polyamine biosynthesis: Absence of ornithine decarboxylase and the mechanism of arginine decarboxylase activity. The Plant Journal, 2001, 27(6): 551-560. |
30 | Cona A, Rea G, Angelini R, et al. Functions of amine oxidases in plant development and defence. Trends in Plant Science, 2006, 11(2): 80-88. |
31 | Moschou P N, Paschalidis K A, Delis I D, et al. Spermidine exodus and oxidation in the apoplast induced by abiotic stress is responsible for H2O2 signatures that direct tolerance responses in tobacco. The Plant Cell, 2008, 20(6): 1708-1724. |
32 | Planas-Portell J, Gallart M, Tiburcio A F, et al. Copper-containing amine oxidases contribute to terminal polyamine oxidation in peroxisomes and apoplast of Arabidopsis thaliana. BMC Plant Biology, 2013, 13(1): 1-13. |
33 | Petřivalský M, Brauner F, Luhová L, et al. Aminoaldehyde dehydrogenase activity during wound healing of mechanically injured pea seedlings. Journal of Plant Physiology, 2007, 164(11): 1410-1418. |
34 | Møller S G, McPherson M J. Developmental expression and biochemical analysis of the Arabidopsis atao1 gene encoding an H2O2-generating diamine oxidase. The Plant Journal, 1998, 13(6): 781-791. |
35 | Groß F, Rudolf E E, Thiele B, et al. Copper amine oxidase 8 regulates arginine-dependent nitric oxide production in Arabidopsis thaliana. Journal of Experimental Botany, 2017, 68(9): 2149-2162. |
36 | Takahashi Y, Ono K, Akamine Y, et al. Highly-expressed polyamine oxidases catalyze polyamine back conversion in Brachypodium distachyon. Journal of Plant Research, 2018, 131(2): 341-348. |
37 | Hao Y W, Huang B B, Jia D Y, et al. Identification of seven polyamine oxidase genes in tomato (Solanum lycopersicum L.) and their expression profiles under physiological and various stress conditions. Journal of Plant Physiology, 2018, 228(5): 1-11. |
38 | Federico R, Ercolini L, Laurenzi M, et al. Oxidation of acetylpolyamines by maize polyamine oxidase. Phytochemistry, 1996, 43(2): 339-341. |
39 | Tavladoraki P, Cona A, Federico R, et al. Polyamine catabolism: Target for antiproliferative therapies in animals and stress tolerance strategies in plants. Amino Acids, 2012, 42(2): 411-426. |
40 | Yu Z, Jia D, Liu T. Polyamine oxidases play various roles in plant development and abiotic stress tolerance. Plants, 2019, 8(6): 184. |
41 | Liu Y, Wang Y, Long C, et al. Metabolic pathway of polyamines in plants: A review. Chinese Journal of Biotechnology, 2011, 27(2): 147-155. |
刘颖, 王莹, 龙萃, 等. 植物多胺代谢途径研究进展. 生物工程学报, 2011, 27(2): 147-155. | |
42 | Moschou P N, Wu J, Cona A, et al. The polyamines and their catabolic products are significant players in the turnover of nitrogenous molecules in plants. Journal of Experimental Botany, 2012, 63(14): 5003-5015. |
43 | Angelini R, Cona A, Federico R, et al. Plant amine oxidases “on the move”: An update. Plant Physiology and Biochemistry, 2010, 48(7): 560-564. |
44 | Tavladoraki P, Rossi M N, Saccuti G, et al. Heterologous expression and biochemical characterization of a polyamine oxidase from Arabidopsis involved in polyamine back conversion. Plant Physiology, 2006, 141(4): 1519-1532. |
45 | Moschou P N, Sanmartin M, Andriopoulou A H, et al. Bridging the gap between plant and mammalian polyamine catabolism: A novel peroxisomal polyamine oxidase responsible for a full back-conversion pathway in Arabidopsis. Plant Physiology, 2008, 147(4): 1845-1857. |
46 | Kamada-Nobusada T, Hayashi M, Fukazawa M, et al. A putative peroxisomal polyamine oxidase, AtPAO4, is involved in polyamine catabolism in Arabidopsis thaliana. Plant and Cell Physiology, 2008, 49(9): 1272-1282. |
47 | Fincato P, Moschou P N, Spedaletti V, et al. Functional diversity inside the Arabidopsis polyamine oxidase gene family. Journal of Experimental Botany, 2011, 62(3): 1155-1168. |
48 | Ahou A, Martignago D, Alabdallah O, et al. A plant spermine oxidase/dehydrogenase regulated by the proteasome and polyamines. Journal of Experimental Botany, 2014, 65(6): 1585-1603. |
49 | Kim D W, Watanabe K, Murayama C, et al. Polyamine oxidase 5 regulates Arabidopsis growth through thermospermine oxidase activity. Plant Physiology, 2014, 165(4): 1575-1590. |
50 | Moschou P N, Paschalidis K A, Roubelakis-Angelakis K A. Plant polyamine catabolism: The state of the art. Plant Signaling & Behavior, 2008, 3(12): 1061-1066. |
51 | Pál M, Szalai G, Janda T. Speculation: Polyamines are important in abiotic stress signaling. Plant Science, 2015, 237(8): 16-23. |
52 | Kusano T, Kim D W, Liu T, et al. Polyamine catabolism in plants//Kusano T, Suzuki H. Polyamines. Tokyo: Springer, 2015: 77-88. |
53 | Sequera-Mutiozabal M, Tiburcio A F, Alcázar R. Drought stress tolerance in relation to polyamine metabolism in plants//Hossain M A, Wani S H, Bhattacharjee S, et al. Drought stress tolerance in plants. Cham: Springer, 2016: 267-286. |
54 | Martin-Tanguy J. Metabolism and function of polyamines in plants: Recent development (new approaches). Plant Growth Regulation, 2001, 34(1): 135-148. |
55 | Velikova V, Yordanov I, Edreva A. Oxidative stress and some antioxidant systems in acid rain-treated bean plants: Protective role of exogenous polyamines. Plant Science, 2000, 151(1): 59-66. |
56 | Arasimowicz-Jelonek M, Floryszak-Wieczorek J, Kubiś J. Interaction between polyamine and nitric oxide signaling in adaptive responses to drought in cucumber. Journal of Plant Growth Regulation, 2009, 28(2): 177-186. |
57 | Yamasaki H, Cohen M F. NO signal at the crossroads: Polyamine-induced nitric oxide synthesis in plants? Trends in Plant Science, 2006, 11(11): 522-524. |
58 | Alcázar R, Altabella T, Marco F, et al. Polyamines: Molecules with regulatory functions in plant abiotic stress tolerance. Planta, 2010, 231(6): 1237-1249. |
59 | Kusano T, Yamaguchi K, Berberich T, et al. Advances in polyamine research in 2007. Journal of Plant Research, 2007, 120(3): 345-350. |
60 | Pottosin I, Shabala S. Polyamines control of cation transport across plant membranes: Implications for ion homeostasis and abiotic stress signaling. Frontiers in Plant Science, 2014, 5: 154. |
61 | Kusano T, Berberich T, Tateda C, et al. Polyamines: Essential factors for growth and survival. Planta, 2008, 228(3): 367-381. |
62 | Richards F J, Coleman R G. Occurrence of putrescine in potassium-deficient barley. Nature, 1952, 170(4324): 460. |
63 | Yang J, Zhang J, Liu K, et al. Involvement of polyamines in the drought resistance of rice. Journal of Experimental Botany, 2007, 58(6): 1545-1555. |
64 | Zhang F, Zou Y N, Wu Q S, et al. Arbuscular mycorrhizas modulate root polyamine metabolism to enhance drought tolerance of trifoliate orange. Environmental and Experimental Botany, 2020, 171: 103926. |
65 | Xing G S, Zhou G K, Li Z X, et al. Studies of polyamine metabolism and β-N-oxalyl-L-α, β-diaminopropionic acid accumulation in grass pea (Lathyrus sativus) under water stress. Journal of Integrative Plant Biology, 2000, 42(10): 1039-1044. |
66 | Chen K M, Zhang C L. Polyamine content in the spring wheat leaves and their velations to drought resistance. Acta Phytophysiologica Sinica, 2000, 26(5): 381-386. |
陈坤明, 张承烈. 干旱期间春小麦叶片多胺含量与作物抗旱性的关系. 植物生理学报, 2000, 26(5): 381-386. | |
67 | Nayyar H, Chander S. Protective effects of polyamines against oxidative stress induced by water and cold stress in chickpea. Journal of Agronomy and Crop Science, 2004, 190(5): 355-365. |
68 | Do P T, Drechsel O, Heyer A G, et al. Changes in free polyamine levels, expression of polyamine biosynthesis genes, and performance of rice cultivars under salt stress: A comparison with responses to drought. Frontiers in Plant Science, 2014, 5: 182. |
69 | Ebeed H T, Hassan N M, Aljarani A M. Exogenous applications of polyamines modulate drought responses in wheat through osmolytes accumulation, increasing free polyamine levels and regulation of polyamine biosynthetic genes. Plant Physiology and Biochemistry, 2017, 118: 438-448. |
70 | Guan J F, Liu H L, Li G M. Changes of polyamines content and polyamine oxidase activity of roots and leaves during drought stress in wheat seedlings. Acta Phytophysiologica Sinica, 2003, 27(5): 655-660. |
关军锋, 刘海龙, 李广敏. 干旱胁迫下小麦幼苗根、叶多胺含量和多胺氧化酶活性的变化. 植物生态学报, 2003, 27(5): 655-660. | |
71 | Xu C, Wu X Q, Zhang H Y. Impact of D-Arg on drought resistance and endogenous polyamines in mycorrhizal Pinus massoniana. Journal of Nanjing Forestry University (Natural Science Edition), 2009, 33(4): 19-23. |
徐超, 吴小芹, 张红岩. D-精氨酸对菌根化马尾松植株内源多胺和抗旱能力的影响. 南京林业大学学报(自然科学版), 2009, 33(4): 19-23. | |
72 | Alcázar R, Bitrián M, Bartels D, et al. Polyamine metabolic canalization in response to drought stress in Arabidopsis and the resurrection plant Craterostigma plantagineum. Plant Signaling & Behavior, 2011, 6(2): 243-250. |
73 | Zhou Q, Yu B. Changes in content of free, conjugated and bound polyamines and osmotic adjustment in adaptation of vetiver grass to water deficit. Plant Physiology and Biochemistry, 2010, 48(6): 417-425. |
74 | An Z F, Li C Y, Zhang L X, et al. Role of polyamines and phospholipase D in maize (Zea mays L.) response to drought stress. South African Journal of Botany, 2012, 83: 145-150. |
75 | Zhang C M, Huang Z. Effects of endogenous abscisic acid, jasmonic acid, polyamines, and polyamine oxidase activity in tomato seedlings under drought stress. Scientia Horticulturae, 2013, 159: 172-177. |
76 | Adamipour N, Khosh-Khui M, Salehi H, et al. Role of genes and metabolites involved in polyamines synthesis pathways and nitric oxide synthase in stomatal closure on Rosa damascena Mill. under drought stress. Plant Physiology and Biochemistry, 2020, 148: 53-61. |
77 | Wu Q. Effects of polyamine on drought resistance of perennial ryegrass. Beijing: Beijing Forestry University, 2014. |
吴情. 多胺对多年生黑麦草抗旱性的影响. 北京: 北京林业大学, 2014. | |
78 | Do P T, Degenkolbe T, Erban A, et al. Dissecting rice polyamine metabolism under controlled long-term drought stress. The Public Library of Science, 2013, 8(4): e60325. |
79 | Liu Y, Zhang C M, Xie X R, et al. Effect of drought stress on polyamine metabolism in the leaves and roots of alfalfa. Acta Prataculturae Sinica, 2012, 21(6): 102-107. |
刘义, 张春梅, 谢晓蓉, 等. 干旱胁迫对紫花苜蓿叶片和根系多胺代谢的影响. 草业学报, 2012, 21(6): 102-107. | |
80 | Chen J, Xiong W D, Yang W W, et al. Effects of drought stress on polyamine metabolism in rapeseed. Seeds, 2009(12): 74-76. |
陈健, 熊王丹, 杨伟伟, 等. 干旱胁迫对油菜多胺代谢的影响. 种子, 2009(12): 74-76. | |
81 | Wang S K, Du H Y. Effects of polyamines and their inhibitor on photosynthesis and free polyamines in plum ‘Qiuji’ leaves under drought stress. Journal of Anhui Agricultural University, 2016, 43(5): 815-819. |
王尚堃, 杜红阳. 多胺及其抑制剂对干旱胁迫下李幼苗叶片光合作用和游离态多胺含量的影响. 安徽农业大学学报, 2016, 43(5): 815-819. | |
82 | Ying Y Q. Study on the drought control mechanism of polyamines on moso bamboo seedlings. Beijing: Beijing Forestry University, 2013. |
应叶青. 多胺对毛竹幼苗抗旱调控机理的研究. 北京: 北京林业大学, 2013. | |
83 | Lee T M. Polyamine regulation of growth and chilling tolerance of rice (Oryza sativa L.) roots cultured in vitro. Plant Science, 1997, 122(2): 111-117. |
84 | Hatmi S, Gruau C, Trotel-Aziz P, et al. Drought stress tolerance in grapevine involves activation of polyamine oxidation contributing to improved immune response and low susceptibility to Botrytis cinerea. Journal of Experimental Botany, 2015, 66(3): 775-787. |
85 | Kasukabe Y, He L, Nada K, et al. Overexpression of spermidine synthase enhances tolerance to multiple environmental stresses and up-regulates the expression of various stress-regulated genes in transgenic Arabidopsis thaliana. Plant and Cell Physiology, 2004, 45(6): 712-722. |
86 | Santa-Cruz A, Perez-Alfocea F, Caro M, et al. Polyamines as short-term salt tolerance traits in tomato. Plant Science, 1998, 138(1): 9-16. |
87 | Hu B Y, Niu M G, Wang Q M, et al. Relationship between osmotic stress and polyamine content of soybean seedling leaves. Journal of Plant Nutrition and Fertilizer, 2006, 12(6): 881-886. |
胡炳义, 牛明功, 王启明, 等. 渗透胁迫与大豆幼苗叶片多胺含量的关系. 植物营养与肥料学报, 2006, 12(6): 881-886. | |
88 | Liu H P, Ji X E, Liu T X, et al. Effect of osmotic stress on the contents of different form polyamines in leaves of maize seedlings. Acta Agronomica Sinica, 2006, 32(10): 1430-1436. |
刘怀攀, 纪秀娥, 刘天学, 等. 渗透胁迫对玉米幼苗叶片不同形态多胺含量的影响. 作物学报, 2006, 32(10): 1430-1436. | |
89 | Montesinos-Pereira D, Barrameda-Medina Y, Romero L, et al. Genotype differences in the metabolism of proline and polyamines under moderate drought in tomato plants. Plant Biology, 2014, 16(6): 1050-1057. |
90 | Sánchez-Rodríguez E, Romero L, Ruiz J M. Accumulation of free polyamines enhances the antioxidant response in fruits of grafted tomato plants under water stress. Journal of Plant Physiology, 2016, 190: 72-78. |
91 | Groppa M D, Benavides M P. Polyamines and abiotic stress: Recent advances. Amino Acids, 2008, 34(1): 35-45. |
92 | Capell T, Bassie L, Christou P. Modulation of the polyamine biosynthetic pathway in transgenic rice confers tolerance to drought stress. Proceedings of the National Academy of Sciences, 2004, 101(26): 9909-9914. |
93 | DiTomaso J M, Shaff J E, Kochian L V. Putrescine-induced wounding and its effects on membrane integrity and ion transport processes in roots of intact corn seedlings. Plant Physiology, 1989, 90(3): 988-995. |
94 | Walden R, Cordeiro A, Tiburcio A F. Polyamines: Small molecules triggering pathways in plant growth and development. Plant Physiology, 1997, 113(4): 1009-1013. |
95 | Nilsen E T, Orcutt D M. The physiology of plants under stress: Abiotic factors. The Quarterly Review of Biology, 1997, 72(4): 476. |
96 | Xiang Y R, Shi D F, Feng H Z, et al. Advances in the responding mechanism of polyamines to the abiotic stresses of plant. Hunan Agricultural Sciences, 2014(2): 19-22. |
向玥如, 史端甫, 冯怀章, 等. 多胺参与植物逆境响应过程的作用机理研究进展. 湖南农业科学, 2014(2): 19-22. | |
97 | Sergiev I, Todorova D, Shopova E, et al. Exogenous auxin type compounds amend PEG-induced physiological responses of pea plants. Scientia Horticulturae, 2019, 248: 200-205. |
98 | Todorova D, Katerova Z, Alexieva V, et al. Polyamines-possibilities for application to increase plant tolerance and adaptation capacity to stress. Genetics and Plant Physiology, 2015, 5(2): 123-144. |
99 | Xu H. Effect of polyamines on seed germination of wheat under drought and mechanism research. Xianyang: Northwest A & F University, 2016. |
许红. 干旱胁迫下多胺对小麦种子萌发的影响及其机理研究. 咸阳: 西北农林科技大学, 2016. | |
100 | Wei X K, Jing Y Q, He J X, et al. Alleviation effect of exogenous spermidine on drought stress in flue-cured tobacco seedlings. Crops, 2022, 38(3): 143-148. |
魏晓凯, 景延秋, 何佶弦, 等. 外源亚精胺对烤烟幼苗干旱胁迫的缓解效应研究. 作物杂志, 2022, 38(3): 143-148. | |
101 | Tian J Y. The study on the effect of exogenous spermidine on alleviation of drought stress in seedlings of Hordeum jubatum. Harbin: Northeast Forestry University, 2020. |
田静瑶. 外源亚精胺对芒颖大麦草苗期干旱胁迫缓解作用的研究. 哈尔滨: 东北林业大学, 2020. | |
102 | Fujita M, Shinozaki K. Polyamine transport systems in plants// Kusano T, Suzuki H. Polyamines. Tokyo: Springer, 2015: 179-185. |
103 | Tabart J, Franck T, Kevers C, et al. Effect of polyamines and polyamine precursors on hyperhydricity in micropropagated apple shoots. Plant Cell, Tissue and Organ Culture, 2015, 120(1): 11-18. |
104 | Doneva D, Pál M, Brankova L, et al. The effects of putrescine pre-treatment on osmotic stress responses in drought-tolerant and drought-sensitive wheat seedlings. Physiologia Plantarum, 2021, 171(2): 200-216. |
105 | Chang N, Zhou Z W, Li Y Y, et al. Exogenously applied Spd and Spm enhance drought tolerance in tea plants by increasing fatty acid desaturation and plasma membrane H+-ATPase activity. Plant Physiology and Biochemistry, 2022, 170: 225-233. |
106 | Satish L, Rency A S, Ramesh M. Spermidine sprays alleviate the water deficit-induced oxidative stress in finger millet (Eleusine coracana L. Gaertn.) plants. 3 Biotech, 2018, 8(1): 1-11. |
107 | Shi J, Fu X Z, Peng T, et al. Spermine pretreatment confers dehydration tolerance of citrus in vitro plants via modulation of antioxidative capacity and stomatal response. Tree Physiology, 2010, 30(7): 914-922. |
108 | Minocha R, Majumdar R, Minocha S C. Polyamines and abiotic stress in plants: A complex relationship. Frontiers in Plant Science, 2014, 5: 175. |
109 | Berberich T, Sagor G H M, Kusano T. Polyamines in plant stress response//Alcázar R, Tiburcio A F. Polyamines. Tokyo: Springer, 2015: 155-168. |
110 | Romero F M, Maiale S J, Rossi F R, et al. Polyamine metabolism responses to biotic and abiotic stress//Alcázar R, Tiburcio A F. Polyamines. New York: Humana Press, 2018: 37-49. |
111 | Pál M, Szalai G, Gondor O K, et al. Unfinished story of polyamines: Role of conjugation, transport and light-related regulation in the polyamine metabolism in plants. Plant Science, 2021, 308: 110923. |
112 | Prabhavathi V R, Rajam M V. Polyamine accumulation in transgenic eggplant enhances tolerance to multiple abiotic stresses and fungal resistance. Plant Biotechnology, 2007, 24(3): 273-282. |
113 | Momtaz O A, Hussein E M, Fahmy E M, et al. Expression of S-adenosyl methionine decarboxylase gene for polyamine accumulation in Egyptian cotton Giza 88 and Giza 90. Genetically Modified Crops, 2010, 1(4): 257-266. |
114 | Zhou C, Sun Y, Ma Z, et al. Heterologous expression of EsSPDS1 in tobacco plants improves drought tolerance with efficient reactive oxygen species scavenging systems. South African Journal of Botany, 2015, 96: 19-28. |
115 | Jiang X, Zhan J, Wang Q, et al. Overexpression of the pear PbSPMS gene in Arabidopsis thaliana increases resistance to abiotic stress. Plant Cell, Tissue and Organ Culture, 2020, 140(2): 389-401. |
116 | Yan M. Seed priming stimulate germination and early seedling growth of Chinese cabbage under drought stress. South African Journal of Botany, 2015, 99: 88-92. |
117 | Jaleel C A, Manivannan P, Wahid A, et al. Drought stress in plants: A review on morphological characteristics and pigments composition. International Journal of Agriculture and Biology, 2009, 11(1): 100-105. |
118 | Alcázar R, Bueno M, Tiburcio A F. Polyamines: Small amines with large effects on plant abiotic stress tolerance. Cells, 2020, 9(11): 2373. |
119 | Hussain S, Farooq M, Wahid M A, et al. Seed priming with putrescine improves the drought resistance of maize hybrids. International Journal of Agriculture & Biology, 2013, 15(6): 1349-1353. |
120 | Li Z, Peng Y, Zhang X Q, et al. Exogenous spermidine improves seed germination of white clover under water stress via involvement in starch metabolism, antioxidant defenses and relevant gene expression. Molecules, 2014, 19(11): 18003-18024. |
121 | Naz R, Sarfraz A, Anwar Z, et al. Combined ability of salicylic acid and spermidine to mitigate the individual and interactive effects of drought and chromium stress in maize (Zea mays L.). Plant Physiology and Biochemistry, 2021, 159: 285-300. |
122 | Berahim Z, Dorairaj D, Omar M H, et al. Spermine mediated improvements on stomatal features, growth, grain filling and yield of rice under differing water availability. Scientific Reports, 2021, 11(1): 1-15. |
123 | Shi H T, Ye T T, Chan Z L. Comparative proteomic and physiological analyses reveal the protective effect of exogenous polyamines in the bermudagrass (Cynodon dactylon) response to salt and drought stresses. Journal of Proteome Research, 2013, 12(11): 4951-4964. |
124 | Krishnan S, Merewitz E B. Polyamine application effects on gibberellic acid content in creeping bentgrass during drought stress. Journal of the American Society for Horticultural Science, 2017, 142(2): 135-142. |
125 | Kotakis C, Theodoropoulou E, Tassis K, et al. Putrescine, a fast-acting switch for tolerance against osmotic stress. Journal of Plant Physiology, 2014, 171(2): 48-51. |
126 | Khosrowshahi Z T, Ghassemi-Golezani K, Salehi-Lisar S Y, et al. Changes in antioxidants and leaf pigments of safflower (Carthamus tinctorius L.) affected by exogenous spermine under water deficit. Biologia Futura, 2020, 71(3): 313-321. |
127 | Hassan N, Ebeed H, Aljaarany A. Exogenous application of spermine and putrescine mitigate adversities of drought stress in wheat by protecting membranes and chloroplast ultra-structure. Physiology and Molecular Biology of Plants, 2020, 26(2): 233-245. |
128 | Hassan F A S, Ali E F, Alamer K H. Exogenous application of polyamines alleviates water stress-induced oxidative stress of Rosa damascena Miller var. trigintipetala Dieck. South African Journal of Botany, 2018, 116: 96-102. |
129 | Fang Y, Xiong L. General mechanisms of drought response and their application in drought resistance improvement in plants. Cellular and Molecular Life Sciences, 2015, 72(4): 673-689. |
130 | Gupta S, Agarwal V P, Gupta N K. Efficacy of putrescine and benzyladenine on photosynthesis and productivity in relation to drought tolerance in wheat (Triticum aestivum L.). Physiology and Molecular Biology of Plants, 2012, 18(4): 331-336. |
131 | Mustafavi S H, Shekari F, Maleki H H. Influence of exogenous polyamines on antioxidant defence and essential oil production in valerian (Valeriana officinalis L.) plants under drought stress. Acta Agriculturae Slovenica, 2016, 107(1): 81-91. |
132 | Li Z, Jing W, Peng Y, et al. Spermine alleviates drought stress in white clover with different resistance by influencing carbohydrate metabolism and dehydrins synthesis. Public Library of Science, 2015, 10(4): e0120708. |
133 | Sadeghipour O. Polyamines protect mung bean [Vigna radiata (L.) Wilczek] plants against drought stress. Biologia Futura, 2019, 70(1): 71-78. |
134 | Slabbert M M, Krüger G H J. Antioxidant enzyme activity, proline accumulation, leaf area and cell membrane stability in water stressed Amaranthus leaves. South African Journal of Botany, 2014, 95: 123-128. |
135 | Zhao J Q, Wang X F, Pan X B, et al. Exogenous putrescine alleviates drought stress by altering reactive oxygen species scavenging and biosynthesis of polyamines in the seedlings of Cabernet sauvignon. Frontiers in Plant Science, 2021, 12: 767992. |
136 | Islam M J, Uddin M J, Hossain M A, et al. Exogenous putrescine attenuates the negative impact of drought stress by modulating physio-biochemical traits and gene expression in sugar beet (Beta vulgaris L.). Public Library of Science, 2022, 17(1): e0262099. |
137 | Abid G, Ouertani R N, Ghouili E, et al. Exogenous application of spermidine mitigates the adverse effects of drought stress in faba bean (Vicia faba L.). Functional Plant Biology, 2022, 49(4): 405-420. |
138 | Jia T, Hou J R, Iqbal M Z, et al. Overexpression of the white clover TrSAMDC1 gene enhanced salt and drought resistance in Arabidopsis thaliana. Plant Physiology and Biochemistry, 2021, 165: 147-160. |
139 | Liu Y, Sun G, Zhong Z H, et al. Overexpression of SAMDC gene from Salvia miltiorrhiza enhances drought tolerance in transgenic tobacco (Nicotiana tabacum). Journal of Agricultural Biotechnology, 2017, 25(5): 729-738. |
140 | Wi S J, Kim S J, Kim W T, et al. Constitutive S-adenosylmethionine decarboxylase gene expression increases drought tolerance through inhibition of reactive oxygen species accumulation in Arabidopsis. Planta, 2014, 239(5): 979-988. |
141 | Wang B, Chen M D, Lin L, et al. Signal pathways and related transcription factors of drought stress in plants. Acta Botanica Boreali-Occidentalia Sinica, 2020, 40(10): 1792-1806. |
王彬, 陈敏氡, 林亮, 等. 植物干旱胁迫的信号通路及相关转录因子研究进展. 西北植物学报, 2020, 40(10): 1792-1806. | |
142 | Shi H T, Chan Z L. Improvement of plant abiotic stress tolerance through modulation of the polyamine pathway. Journal of Integrative Plant Biology, 2014, 56(2): 114-121. |
143 | Espasandin F D, Maiale S J, Calzadilla P, et al. Transcriptional regulation of 9-cis-epoxycarotenoid dioxygenase (NCED) gene by putrescine accumulation positively modulates ABA synthesis and drought tolerance in Lotus tenuis plants. Plant Physiology and Biochemistry, 2014, 76: 29-35. |
144 | Lau S E, Hamdan M F, Pua T L, et al. Plant nitric oxide signaling under drought stress. Plants, 2021, 10(2): 360. |
145 | Montilla-Bascón G, Rubiales D, Hebelstrup K H, et al. Reduced nitric oxide levels during drought stress promote drought tolerance in barley and is associated with elevated polyamine biosynthesis. Scientific Reports, 2017, 7(1): 1-15. |
146 | Li Z, Zhang Y, Peng D D, et al. Polyamine regulates tolerance to water stress in leaves of white clover associated with antioxidant defense and dehydrin genes via involvement in calcium messenger system and hydrogen peroxide signaling. Frontiers in Physiology, 2015, 6: 280. |
147 | Peng D D, Wang X J, Li Z, et al. NO is involved in spermidine-induced drought tolerance in white clover via activation of antioxidant enzymes and genes. Protoplasma, 2016, 253(5): 1243-1254. |
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