| 研究生: |
李石草 Ly, Thach-Thao |
|---|---|
| 論文名稱: |
鐮孢菌屬(Fusarium verticillioides)、產氣腸桿菌(Klebsiella aerogenes)產生的微生物揮發性氣味對水稻(Oryza sativa L.) 幼苗在植株生長和逆境耐受性的影響 The effect of microbial volatile produced by Fusarium verticillioides, Klebsiella aerogenes on plant growth and stress tolerance in rice (Oryza sativa L.) seedlings |
| 指導教授: |
黃浩仁
Huang, Hao-Jen |
| 共同指導教授: |
邱啟洲
Chiu, Chi-Chou |
| 學位類別: |
碩士 Master |
| 系所名稱: |
生物科學與科技學院 - 熱帶植物與微生物科學研究所 Institute of Tropical Plant Sciences |
| 論文出版年: | 2021 |
| 畢業學年度: | 109 |
| 語文別: | 英文 |
| 論文頁數: | 36 |
| 外文關鍵詞: | Fusarium verticillioides, Klebsiella aerogene, plant growth promotion, stress tolerance, abiotic stress |
| 相關次數: | 點閱:71 下載:11 |
| 分享至: |
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Global environmental change is becoming a serious problem worldwide, requires novel eco-friendly products that allow sustainable growth and commercial production following the needs of farmers and consumers. Hence, there are many studies have been done to discover eco-friendly alternatives, and volatile organic compounds emitted from microorganisms have emerged as effective, cheaper, and friendly with environment. Here, we studied the functional microbe-emitted volatiles in mediating plant growth promotion under stress and non-stress conditions, also the insight of molecular mechanisms related to growth promotion. Volatile compounds used in this study were produced by Fusarium verticillioides and Klebsiella aerogene. Shoot elongation in seedlings exposed to Fusarium and Klebsiella were increased but differ in root growth. There is adjusting expression of genes involved in hormone production resulted in the increased shoot growth. CKX1, CKX9 are responsible for degradation of cytokinin, was downregulated in exposed shoots result in the induction of cytokinin levels in shoot. High content of cytokinin may cause systemic acquired resistance process via induction of salicylic acid and PR1b protein activities. Interestingly, RR9, a cytokinin regulator, was induced the transcript levels in exposed plants meaning that there is negative feedback of cytokinin production within plant. Additionally, gibberellin 1 (GA1) production was triggered by down-expression levels of SAP11 (OsDOG), a negative regulator of GA. Fusarium not only induced the elongation of shoot but also enhanced the absorption of the nutrients by elevating the transcriptional levels of NAS2, one of genes in NAS family involve in metal transport. Furthermore, Fusarium and Klebsiella have been shown to increase the tolerance of plant to salt and copper stress, showed by reduction of ROS accumulation and cell death area on root tips. There are different impacts on antioxidant system between salt and copper stress led to the difference in antioxidant systems. Whereas, only SOD and POD-e,f isozymes still increase function in copper-stressed plant exposed to volatiles, almost isozyme of CAT, APX, POD and SOD were inducted activities in exposed plant stress by salt. Proline, member of ROS-scavengers, increased in exposed roots under both copper and salt stress.
Audrain, B., Farag, M. A., Ryu, C. M., & Ghigo, J. M. (2015). Role of bacterial volatile compounds in bacterial biology. FEMS Microbiology Reviews, 39(2), 222–233. https://doi.org/10.1093/femsre/fuu013
Bailly, A., Groenhagen, U., Schulz, S., Geisler, M., Eberl, L., & Weisskopf, L. (2014). The inter-kingdom volatile signal indole promotes root development by interfering with auxin signalling. Plant Journal, 80(5), 758–771. https://doi.org/10.1111/tpj.12666
Banchio, E., Xie, X., Zhang, H., & Paré, P. W. (2009). Soil bacteria elevate essential oil accumulation and emissions in sweet basil. Journal of Agricultural and Food Chemistry, 57(2), 653–657. https://doi.org/10.1021/jf8020305
Banu, A.N., Hoque, A., Watanabe-Sugimoto, M., Islam, M.M, Uraji, M., Matsuoka, & K., et al. (2010). Proline and glycinebetaine amelorated NaCl stress via scavenging of hydrogen peroxide and methylglyoxal but nit superoxide or nitric oxide in tobaco cultured cells. Bioscience, Biotechnology and Biochemistry, 74, 2043–2049.
Bockheim, J. G., & Gennadiyev, A. N. (2000). The role of soil-forming processes in the definition of taxa in Soil Taxonomy and the World Soil Reference Base. Geoderma, 95(1–2), 53–72. https://doi.org/10.1016/S0016-7061(99)00083-X
Castulo-Rubio, D. Y., Alejandre-Ramírez, N. A., Orozco-Mosqueda, M. del C., Santoyo, G., Macías-Rodríguez, L. I., & Valencia-Cantero, E. (2015). Volatile Organic Compounds Produced by the Rhizobacterium Arthrobacter agilis UMCV2 Modulate Sorghum bicolor (Strategy II Plant) Morphogenesis and SbFRO1 Transcription In Vitro. Journal of Plant Growth Regulation, 34(3), 611–623. https://doi.org/10.1007/s00344-015-9495-8
Charan Tripathy, B., & Oelmüller, R. (2012). Plant Signaling & Behavior Reactive oxygen species generation and signaling in plants. Plant Signaling & Behavior 1621 Plant Signaling & Behavior, 7, 1621–1633. https://doi.org/10.4161/psb.22455
Damanik, R. I., Marbun, P., & Sihombing, L. (2016). Antioxidant activity of seedling growth in selected soybean genotypes (Glycine max (L.) Merrill) responses of submergence. IOP Conference Series: Earth and Environmental Science, 41(1). https://doi.org/10.1088/1755-1315/41/1/012003
Escudero, V., Abreu, I., del Sastre, E., Tejada-Jiménez, M., Larue, C., Novoa-Aponte, L., Castillo-González, J., Wen, J., Mysore, K. S., Abadía, J., Argüello, J. M., Castillo-Michel, H., Álvarez-Fernández, A., Imperial, J., & González-Guerrero, M. (2020). Nicotianamine Synthase 2 Is Required for Symbiotic Nitrogen Fixation in Medicago truncatula Nodules. Frontiers in Plant Science, 10(January), 1–14. https://doi.org/10.3389/fpls.2019.01780
Gull, Audil & Lone, Ajaz & Wani, N. (2013). Biotic and Abiotic stresses in Plants. Intech, 32(July), 137–144. http://www.intechopen.com/books/trends-in-telecommunications-technologies/gps-total-electron-content-tec- prediction-at-ionosphere-layer-over-the-equatorial-region%0AInTec%0Ahttp://www.asociatiamhc.ro/wp-content/uploads/2013/11/Guide-to-Hydropower.pdf
Halliwell, B., Gutteridge, & J.M.C. (2007). Free Radicals in Biology and Medicine. Oxford University Press, New York.
Hamid, B., Zaman, M., Farooq, S., Fatima, S., Sayyed, R. Z., Ahmad Baba, Z., Sheikh, T. A., Reddy, M. S., Enshasy, H. El, Gafur, A., & Suriani, N. L. (2021). sustainability Bacterial Plant Biostimulants: A Sustainable Way towards Improving Growth, Productivity, and Health of Crops. https://doi.org/10.3390/su13052856
Hasanuzzaman, M., Bhuyan, M. H. M. B., Zulfiqar, F., Raza, A., Mohsin, S. M., Al Mahmud, J., Fujita, M., & Fotopoulos, V. (2020). Reactive oxygen species and antioxidant defense in plants under abiotic stress: Revisiting the crucial role of a universal defense regulator. Antioxidants, 9(8), 1–52. https://doi.org/10.3390/antiox9080681
Hoque, M. A., Banu, M. N. A., Okuma, E., Amako, K., Nakamura, Y., Shimoishi, Y., & Murata, Y. (2007). Exogenous proline and glycinebetaine increase NaCl-induced ascorbate-glutathione cycle enzyme activities, and proline improves salt tolerance more than glycinebetaine in tobacco Bright Yellow-2 suspension-cultured cells. Journal of Plant Physiology, 164(11), 1457–1468. https://doi.org/10.1016/j.jplph.2006.10.004
Inoue, H., Higuchi, K., Takahashi, M., Nakanishi, H., Mori, S., & Nishizawa, N. K. (2003). Three rice nicotianamine synthase genes, OsNAS1, OsNAS2, and OsNAS3 are expressed in cells involved in long-distance transport of iron and differentially regulated by iron. Plant Journal, 36(3), 366–381. https://doi.org/10.1046/j.1365-313X.2003.01878.x
Ito, Y., & Kurata, N. (2006). Identification and characterization of cytokinin-signalling gene families in rice. Gene, 382, 57–65. https://doi.org/10.1016/j.gene.2006.06.020
Jain, M., Tyagi, A.K., Khurana, & J.P. (2006). Molecular characterization and differential expression of cytokinin-responsive type-A response regulators in rice (Oryza sativa). BMC Plant Biology, 6, 1.
Ji, J., Yuan, D., Jin, C., Wang, G., Li, X., & Guan, C. (2020). Enhancement of growth and salt tolerance of rice seedlings (Oryza sativa L.) by regulating ethylene production with a novel halotolerant PGPR strain Glutamicibacter sp. YD01 containing ACC deaminase activity. Acta Physiologiae Plantarum, 42(4). https://doi.org/10.1007/s11738-020-3034-3
Jiang, C.-J., Shimono, M., Sugano, S., Kojima, M., Liu, X., Inoue, H., Sakakibara, H., & Takatsuji, H. (2013). Cytokinins Act Synergistically with Salicylic Acid to Activate Defense Gene Expression in Rice. / 287 MPMI, 26(3), 287–296. https://doi.org/10.1094/MPMI-06-12-0152-R
Kai, M., Haustein, M., Molina, F., Petri, A., Scholz, B., & Piechulla, B. (2009). Bacterial volatiles and their action potential. Applied Microbiology and Biotechnology, 81(6), 1001–1012. https://doi.org/10.1007/s00253-008-1760-3
Kanchiswamy, C. N., Malnoy, M., & Maffei, M. E. (2015a). Bioprospecting bacterial and fungal volatiles for sustainable agriculture. Trends in Plant Science, 20(4), 206–211. https://doi.org/10.1016/j.tplants.2015.01.004
Kanchiswamy, C. N., Malnoy, M., & Maffei, M. E. (2015b). Chemical diversity of microbial volatiles and their potential for plant growth and productivity. Frontiers in Plant Science, 6(MAR). https://doi.org/10.3389/fpls.2015.00151
Kiba, & T., et al. (2003). The type-A response regulator, ARR15, acts as a negative regulator in the cytokinin-mediated signal transduction in Arabidopsis thaliana. Plant Cell Physiol, 44, 868–874.
Kolbert, Z., Pető, A., Lehotai, N., Feigl, G., & Erdei, L. (2012). Long-term copper (Cu 2+ ) exposure impacts on auxin, nitric oxide (NO) metabolism and morphology of Arabidopsis thaliana L. Plant Growth Regulation, 68(2), 151–159. https://doi.org/10.1007/s10725-012-9701-7
Korpi, A., Järnberg, J., & Pasanen, A. L. (2009). Microbial volatile organic compounds. Critical Reviews in Toxicology, 39(2), 139–193. https://doi.org/10.1080/10408440802291497
Ledger, T., Rojas, S., Timmermann, T., Pinedo, I., Poupin, M. J., Garrido, T., Richter, P., Tamayo, J., & Donoso, R. (2016). Volatile-mediated effects predominate in Paraburkholderia phytofirmans growth promotion and salt stress tolerance of Arabidopsis thaliana. Frontiers in Microbiology, 7(NOV). https://doi.org/10.3389/FMICB.2016.01838
Lee, Samantha, Yap, M., Behringer, G., Hung, R., & Bennett, J. W. (2016). Volatile organic compounds emitted by trichoderma species mediate plant growth. Fungal Biology and Biotechnology, 3(1), 1–14. https://doi.org/10.1186/s40694-016-0025-7
Lee, Sichul, Persson, D. P., Hansen, T. H., Husted, S., Schjoerring, J. K., Kim, Y. S., Jeon, U. S., Kim, Y. K., Kakei, Y., Masuda, H., Nishizawa, N. K., & An, G. (2011). Bio-available zinc in rice seeds is increased by activation tagging of nicotianamine synthase. Plant Biotechnology Journal, 9(8), 865–873. https://doi.org/10.1111/j.1467-7652.2011.00606.x
Lemfack, M. C., Gohlke, B. O., Toguem, S. M. T., Preissner, S., Piechulla, B., & Preissner, R. (2018). MVOC 2.0: A database of microbial volatiles. Nucleic Acids Research, 46(D1), D1261–D1265. https://doi.org/10.1093/nar/gkx1016
Li, N., & Kang, S. (2018). Do volatile compounds produced by Fusarium oxysporum and Verticillium dahliae affect stress tolerance in plants? Mycology, 9(3), 166–175. https://doi.org/10.1080/21501203.2018.1448009
Li, Z. T., Janisiewicz, W. J., Liu, Z., Callahan, A. M., Evans, B. E., Jurick, W. M., & Dardick, C. (2019). Exposure in vitro to an environmentally isolated strain TC09 of Cladosporium sphaerospermum triggers plant growth promotion, early flowering, and fruit yield increase. Frontiers in Plant Science, 9(February), 1–19. https://doi.org/10.3389/fpls.2018.01959
Liu, Ya, Ren, X., Jeong, H. K., Wei, H., & Jeong, B. R. (2018). Growth and physiological responses of adenophora triphylla (Thunb.) A.DC. Plug seedlings to day and night temperature regimes. Agronomy, 8(9). https://doi.org/10.3390/agronomy8090173
Liu, Yaju, Xu, Y., Xiao, J., Ma, Q., Li, D., Xue, Z., & Chong, K. (2011). OsDOG, a gibberellin-induced A20/AN1 zinc-finger protein, negatively regulates gibberellin-mediated cell elongation in rice. Journal of Plant Physiology, 168(10), 1098–1105. https://doi.org/10.1016/j.jplph.2010.12.013
Livak, K. J., & Schmittgen, T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method. Methods, 25(4), 402–408. https://doi.org/10.1006/meth.2001.1262
Meena, M., Divyanshu, K., Kumar, S., Swapnil, P., Zehra, A., Shukla, V., Yadav, M., & Upadhyay, R. S. (2019). Regulation of L-proline biosynthesis, signal transduction, transport, accumulation and its vital role in plants during variable environmental conditions. Heliyon, 5(12), e02952. https://doi.org/10.1016/j.heliyon.2019.e02952
Minerdi, D., Bossi, S., Maffei, M. E., Gullino, M. L., & Garibaldi, A. (2011). Fusarium oxysporum and its bacterial consortium promote lettuce growth and expansin A5 gene expression through microbial volatile organic compound (MVOC) emission. FEMS Microbiology Ecology, 76(2), 342–351. https://doi.org/10.1111/j.1574-6941.2011.01051.x
Mitsuhara, I., Iwai, T., Seo, S., Yanagawa, Y., Kawahigasi, H., Hirose, S., Ohkawa, Y., & Ohashi, Y. (2008). Characteristic expression of twelve rice PR1 family genes in response to pathogen infection, wounding, and defense-related signal compounds (121/180). Mol Genet Genomics, 279, 415–427. https://doi.org/10.1007/s00438-008-0322-9
Mittler, R., Vanderauwera, S., Gollery, M., & Van Breusegem, F. (2004). Reactive oxygen gene network of plants. Trends in Plant Science, 9(10), 490–498. https://doi.org/10.1016/j.tplants.2004.08.009
Mondal, & K. et al. (2004). Antioxidants systems in ripening tomato fruits. Biol. Plantarum, 48, 49–53.
Niemann, M. C. E., Weber, H., Hluska, T., Leonte, G., Anderson, S. M., Novák, O., Senes, A., & Werner, T. (2018). The cytokinin oxidase/dehydrogenase CKX1 is a membrane-bound protein requiring homooligomerization in the endoplasmic reticulum for its cellular activity. Plant Physiology, 176(3), 2024–2039. https://doi.org/10.1104/pp.17.00925
Peñuelas, J., Asensio, D., Tholl, D., Wenke, K., Rosenkranz, M., Piechulla, B., & Schnitzler, J. P. (2014). Biogenic volatile emissions from the soil. Plant, Cell and Environment, 37(8), 1866–1891. https://doi.org/10.1111/pce.12340
Rehman, A. U., Bashir, F., Ayaydin, F., Kóta, Z., Páli, T., & Vass, I. (2021). Proline is a quencher of singlet oxygen and superoxide both in in vitro systems and isolated thylakoids. Physiologia Plantarum, 172(1), 7–18. https://doi.org/10.1111/ppl.13265
Ryu, C. M., Faragt, M. A., Hu, C. H., Reddy, M. S., Wei, H. X., Paré, P. W., & Kloepper, J. W. (2003). Bacterial volatiles promote growth in Arabidopsis. Proceedings of the National Academy of Sciences of the United States of America, 100(8), 4927–4932. https://doi.org/10.1073/pnas.0730845100
Sağlam, A., Yetişsin, F., Demiralay, M., & Terzi, R. (2015). Copper Stress and Responses in Plants. Plant Metal Interaction: Emerging Remediation Techniques, 21–40. https://doi.org/10.1016/B978-0-12-803158-2.00002-3
Schulz, S., & Dickschat, J. S. (2007). Bacterial volatiles: The smell of small organisms. Natural Product Reports, 24(4), 814–842. https://doi.org/10.1039/b507392h
Sharifi, R., & Ryu, C. M. (2018). Revisiting bacterial volatile-mediated plant growth promotion: Lessons from the past and objectives for the future. Annals of Botany, 122(3), 349–358. https://doi.org/10.1093/aob/mcy108
Sharma, P., Dubey, & R.S. (2005). Modulation of nitrate reductase activity in rice seedlings under aluminium toxicity and water stress: role of osmolytes as enzyme protectant. J Plant Physiol, 162, 854–864.
Siddiqui, M. H., Alamri, S., Al-Khaishany, M. Y., Nasir Khan, M., Al-Amri, A., Ali, H. M., Alaraidh, I. A., & Alsahli, A. A. (2019). Exogenous Melatonin Counteracts NaCl-Induced Damage by Regulating the Antioxidant System, Proline and Carbohydrates Metabolism in Tomato Seedlings. International Journal of Molecular Sciences Article Int. J. Mol. Sci, 20, 353. https://doi.org/10.3390/ijms20020353
Szabado, L., Savoure, & A. (2010). Proline: a multifunctional amino acid. Trends in Plant Science, 15, 89–97.
Thounaojam, T.C., Panda, P., Mazumdar, P., Kumar, D., Sharna, G.D., Sahoo, L., Sanjib, & P. (2012). Excess copper induced oxidative stress and response of antioxidants in rice. Plant Physiol. Bio, 53, 33–39.
Tyagi, S., Mulla, S.I., Lee, K.J., Chae, J.C., &Shukla, & P. (2018). VOCs-mediated hormonal signaling and crosstalk with plant growth promoting microbes. Critical Reviews in Biotechnology, 38, 1277–1296.
Wang, F., B, Z., Z, S., & C, Z. (n.d.). (2009). Relationship Between Proline and Hg 2+-Induced Oxidative Stress in a Tolerant Rice Mutant. Arch. Environ. Contam. Toxicol, 56, 723–731. https://doi.org/10.1007/s00244-008-9226-2
Wang, Y., Luo, Z., Du, R., Liu, Y., Ying, T., & Mao, L. (2013). Effect of nitric oxide on antioxidative response and proline metabolism in banana during cold storage. Journal of Agricultural and Food Chemistry, 61(37), 8880–8887. https://doi.org/10.1021/jf401447y
Yadav, Summy & Modi, Payal & Dave, Akanksha & Vijapura, Akdasbanu & Patel, Disha & Patel, M. (2013). Effect of Abiotic Stress con Crops. Intech, 32(July), 137–144.
Zaman, M., Kurepin, L. V., Catto, W., & Pharis, R. P. (2015). Enhancing crop yield with the use of N-based fertilizers co-applied with plant hormones or growth regulators. Journal of the Science of Food and Agriculture, 95(9), 1777–1785. https://doi.org/10.1002/jsfa.6938
Zhang, H., Sun, Y., Xie, X., Kim, M. S., Dowd, S. E., & Paré, P. W. (2009). A soil bacterium regulates plant acquisition of iron via deficiency-inducible mechanisms. Plant Journal, 58(4), 568–577. https://doi.org/10.1111/j.1365-313X.2009.03803.x
Zhao, S., Liu, Q., Qi, Y., Duo, & L. (2010). Responses of root growth and protective enzymes to copper stress in Turfgrass. Acta Biol. Cracov Ser. Bot, 52, 7–11.
Zou, C., Li, Z., & Yu, D. (2010). Bacillus megaterium strain XTBG34 promotes plant growth by producing 2-pentylfuran. Journal of Microbiology, 48(4), 460–466. https://doi.org/10.1007/s12275-010-0068-z