DOI QR코드

DOI QR Code

Physiological and molecular analysis of OsTPS30 by gamma irradiation

  • Kim, Se Won (Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute (KAERI)) ;
  • Jung, In Jung (Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute (KAERI)) ;
  • Kim, Sang Hoon (Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute (KAERI)) ;
  • Choi, Hong-Il (Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute (KAERI)) ;
  • Kang, Si-Yong (Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute (KAERI)) ;
  • Kim, Jin-Baek (Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute (KAERI))
  • 투고 : 2019.02.01
  • 심사 : 2019.03.29
  • 발행 : 2019.06.30

초록

Terpenes constitute a large class of secondary metabolites in plants. The Oryza sativa terpene synthase is a vital gene in plant defense response. In this study, the molecular and physiological functions of Oryza sativa terpene synthase 30 (OsTPS30, LOC_Os08g07080) were investigated after exposure of the seeds and plants to gamma-rays. The OsTPS30 expression was slightly induced at 200 Gray (Gy), but was significantly induced at 400 Gy. The total terpenoid was synthesized more in OsTPS30-overexpressing (OX-OsTPS30) Arabidopsisthaliana plants than in wild-type (WT) plants. The OX-OsTPS30 plants exhibited resistance to gamma-rays, as compared to WT. The OX-OsTPS30 plants had significantly increased height and weight after gamma irradiation. Additionally, the activity of antioxidant enzymes was increased more in OX OsTPS30 plants than in WT plants after gamma irradiation. Furthermore, the OsTPS30-GFP fusion protein was mostly localized in the chloroplast, suggesting that OsTPS30 is putative MEP pathway-related terpene synthase.

키워드

참고문헌

  1. Aharoni A, Giri AP, Deuerlein S, Griepink F, de-Kogel WJ, Verstappen FWA, Verhoeven HA, Jongsma MA, Schwab W, Bouwmeester HJ (2003) Terpenoid metabolism in wild type and transgenic Arabidopsis plants. Plant Cell 15:2866-2884 https://doi.org/10.1105/tpc.016253
  2. Arimura G, Matsui K, Takabayashi J (2009) Chemical and molecular ecology of herbivore-induced plant volatiles: proximate factors and their ultimate functions. Plant Cell Physiol 50:911-923 https://doi.org/10.1093/pcp/pcp030
  3. Baldwin IT, Halitschke R, Paschold A, Von Dahl CC, Preston CA (2006) Volatile signaling in plant-plant interactions: "Talking trees" in the genomics era. Science 311:812-815 https://doi.org/10.1126/science.1118446
  4. Bohlmann J, Martin D, Oldham NJ, Gershenzon J (2000) Terpenoid secondary metabolism in Arabidopsis thaliana: cDNA cloning, characterization, and functional expression of a myrcene/(E)-beta-ocimene synthase. Arch Biochem Biophys 375:261-269 https://doi.org/10.1006/abbi.1999.1669
  5. Bohlmann J, Meyer-Gauen G, Croteau R (1998) Plant terpenoid synthases: Molecular biology and phylogenetic analysis. Proc Natl Acad Sci USA 95:4126-4133 https://doi.org/10.1073/pnas.95.8.4126
  6. Bradford MM (1976), A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248-254 https://doi.org/10.1016/0003-2697(76)90527-3
  7. Chen F, Ro DK, Petri J, Gershenzon J, Bohlmann J, Pichersky E, Tholl D (2004) Characterization of a root-specific Arabidopsis terpene synthase responsible for the formation of the volatile monoterpene 1,8-cineole. Plant Physiol 135:1956-1966 https://doi.org/10.1104/pp.104.044388
  8. Chen F, Tholl D, Bohlmann J, Pichersky E (2011) The family of terpene synthases in plants: a mid-size family of genes for specialized metabolism that is highly diversified throughout the kingdom. Plant J 66:212-229 https://doi.org/10.1111/j.1365-313X.2011.04520.x
  9. Chen F, Tholl D, D'Auria JC, Farooq A, Pichersky E, Gershenzon J (2003) Biosynthesis and emission of terpenoid volatiles from Arabidopsis flowers. Plant Cell 15:481-494 https://doi.org/10.1105/tpc.007989
  10. Chen X, Chen H, Yuan JS, Kollner TG, Chen Y, Guo Y, Zhuang X, Chen X, Zhang YJ, Fu J, Nebenfuhr A, Guo Z, Chen F (2018) The rice terpene synthase gene OsTPS19 functions as an (S)-limonene synthase in planta, and its overexpression leads to enhanced resistance to the blast fungus Magnaporthe oryzae. Plant Biotechnol J 16:1778-1787 https://doi.org/10.1111/pbi.12914
  11. Cheng AX, Lou YG, Mao YB, Lu S, Wang LJ, Chen XY (2007) Plant terpenoids: Biosynthesis and ecological functions. J Integr Plant Biol 49:179-186 https://doi.org/10.1111/j.1744-7909.2007.00395.x
  12. Clough SJ, Bent AF (1998) Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J 16:735-743 https://doi.org/10.1046/j.1365-313x.1998.00343.x
  13. Copolovici LO, Filella I, Llusia J, Niinemets U, Penuelas J (2005) The capacity for thermal protection of photosynthetic electron transport varies for different monoterpenes in Quercus ilex. Plant Physiol 139:485-496 https://doi.org/10.1104/pp.105.065995
  14. Dudareva N, Negre F, Nagegowda DA, Orlova I (2006) Plant volatiles: recent advances and future perspectives. Crit Rev Plant Sci 25:417-440 https://doi.org/10.1080/07352680600899973
  15. Esnault MA, Legue F, Chenal C (2010) Ionizing radiation: advances in plant response. Environ Exp Bot 68:231-237 https://doi.org/10.1016/j.envexpbot.2010.01.007
  16. Falara V, Akhtar TA, Nguyen TT, Spyropoulou EA, Bleeker PM, Schauvinhold I, Matsuba Y, Bonini ME, Schilmiller AL, Last RL, Schuurink RC, Pichersky E (2011) The Tomato Terpene Synthase Gene Family. Plant Physiol 157:770-789 https://doi.org/10.1104/pp.111.179648
  17. Fares S, Loreto F, Kleist E, Wildt J (2008) Stomatal uptake and stomatal deposition of ozone in isoprene and monoterpene emitting plant. Plant Biol (Stuttg) 10:44-54 https://doi.org/10.1055/s-2007-965257
  18. Faldt J, Arimura G, Gershenzon J, Takabayashi J, Bohlmann J (2003) Functional identification of AtTPS03 as (E)-beta-ocimene synthase: a monoterpene synthase catalyzing jasmonate- and wound-induced volatile formation in Arabidopsis thaliana. Planta 216:745-751 https://doi.org/10.1007/s00425-002-0924-0
  19. Ghorai N, Chakraborty S, Gucchait S, Saha SK, Biswas S (2012) Estimation of total terpenoids concentration in plant tissues using a monoterpene, Linalool as standard reagent. Protocol Exchange Doi:10.1038/protex.2012.055
  20. Herde M, Gartner K, Kollner TG, Fode B, Boland W, Gershenzon J, Gatz C, Tholl D (2008) Identification and regulation of TPS04/GES, an Arabidopsis geranyl linalool synthase catalyzing the first step in the formation of the insect-induced volatile C16-homoterpene TMTT. Plant Cell 20:1152-1168 https://doi.org/10.1105/tpc.106.049478
  21. Irmisch S, Jiang Y, Chen F, Gershenzon J, Kollner TG (2014) Terpene synthases and their contribution to herbivore-induced volatile emission in western balsam poplar (Populus trichocarpa). BMS Plant Biol 14:270 https://doi.org/10.1186/s12870-014-0270-y
  22. Jenkins GI (2009) Signal transduction in responses to UV-B radiation. Annu Rev Plant Biol 60:407-431 https://doi.org/10.1146/annurev.arplant.59.032607.092953
  23. Keeling CI, Bohlmann J (2006) Genes, enzymes and chemicals of terpenoid diversity in the constitutive and induced defence of conifers against insects and pathogens. New Phytol 170: 657-675 https://doi.org/10.1111/j.1469-8137.2006.01716.x
  24. Kiryu M, Hamanaka M, Yoshitomi K, Mochizuki S, Akimitsu K, Gomi K (2018) Rice terpene synthase 18 (OsTPS18) encodes a sesquiterpene synthase that produces an antibacterial (E)-nerolidol against a bacterial pathogen of rice. J Gen Plant Pathol 84:221-229 https://doi.org/10.1007/s10327-018-0774-7
  25. Lee GW, Lee S, Chung MS, Jeong YS, Chung BY (2015) Rice terpene synthase 20 (OsTPS20) plays an important role in producing terpene volatiles in response to abiotic stresses. Protoplasma 252:997-1007 https://doi.org/10.1007/s00709-014-0735-8
  26. Lesburg CA, Zhai G, Cane DE, Christianson DW (1997) Crystal structure of pentalenene synthase: mechanistic insights on terpenoid cyclization reactions in biology. Science 277: 1820-1824 https://doi.org/10.1126/science.277.5333.1820
  27. Li G, Kollner GT, Yin Y, Jiang Y, Chen H, Xu Y, Gershenzon J, Pichersky E, Chen F (2012) Non-seed plant Selaginella moellendorfii has both seed plant and microbial types of terpene synthases. Proc Natl Acad Sci USA. 109:14711-14715 https://doi.org/10.1073/pnas.1204300109
  28. Loreto F, Forster A, Durr M, Csiky O, Seufert G (1998) On the monoterpene emission under heat stress and on the increased thermotolerance of leaves of Quercus ilex L. fumigated with selected monoterpenes. Plant Cell Environ 21:101-107 https://doi.org/10.1046/j.1365-3040.1998.00268.x
  29. Martin D, Faldt J, Bohlmann J (2004) Functional characterization of nine Norway spruce terpene synthase genes and evolution of gymnosperm terpene synthases of the TPS-d sub-family. Plant Physiol 135:1908-1927 https://doi.org/10.1104/pp.104.042028
  30. Mittler R, Zilinskas BA (1993) Detection of ascorbate peroxidase activity in native gels by inhibition of ascorbate dependent reduction of nitroblue tetrazolium. Anal Biochem 112:540-546 https://doi.org/10.1006/abio.1993.1366
  31. Moussa HR (2008) Gamma irradiation effects on antioxidant enzymes and G6PDH activities in Vicia Faba plant. J New Seeds 9:89-99 https://doi.org/10.1080/15228860701879364
  32. Park S, Moon JC, Park YC, Kim JH, Kim DS, Jang CS (2014) Molecular dissection of the response of a rice leucine-rich repeat receptor-like kinase (LRR-RLK) gene to abiotic stresses. J Plant Physiol 171:1645-1653 https://doi.org/10.1016/j.jplph.2014.08.002
  33. Peters RJ, Carter OA, Zhang Y, Matthews BW, Croteau RB (2003) Bifunctional abietadiene synthase: mutual structural dependence of the active sites for protonation-initiated and ionizationinitiated cyclizations. Biochemistry 42:2700-2707 https://doi.org/10.1021/bi020492n
  34. Putter J (1974) Peroxidase. In: H.U. Bergmeyer, Ed., Methods of enzymatic analysis. Verlag Chemie Weinhan 685-690
  35. Singh B, Sharma RA (2015) Plant terpenes: defense responses, phylogenetic analysis, regulation and clinical applications. 3 Biotech 5:129-151 https://doi.org/10.1007/s13205-014-0220-2
  36. Sun TP, Kamiya Y (1994) The Arabidopsis GA1 locus encodes the cyclase ent-kaurene synthetase A of gibberellin biosynthesis. Plant Cell 6:1509-1518 https://doi.org/10.2307/3869986
  37. Sun Y, Huang X, Ning Y, Jing W, Bruce TJ, Qi F, Xu Q, Wu K, Zhang Y, Guo Y (2017) TPS46, Rice terpene synthase conferring natural resistance to bird cherry-oat aphid, Rhopalosiphum padi (Linnaeus). Front Plant Sci 8:110
  38. Tholl D (2006) Terpene synthases and the regulation, diversity and biological roles of terpene metabolism. Curr Opin Plant Biol 9:297-304 https://doi.org/10.1016/j.pbi.2006.03.014
  39. Tholl D, Chen F, Petri J, Gershenzon J, Pichersky E (2005) Two sesquiterpene synthases are responsible for the complex mixture of sesquiterpenes emitted from Arabidopsis flowers. Plant J 42:757-771 https://doi.org/10.1111/j.1365-313X.2005.02417.x
  40. Tholl D, Lee S (2011) Terpene specialized metabolism in Arabidopsis thaliana. Arabidopsis Book 9:e0143 https://doi.org/10.1199/tab.0143
  41. Yamaguchi S, Sun TP, Kawaide H, Kamiya Y (1998) The GA2 locus of Arabidopsis thaliana encodes ent-kaurene synthase of gibberellin biosynthesis. Plant Physiol 116:1271-1278 https://doi.org/10.1104/pp.116.4.1271
  42. Yoshitomi K, Taniguchi S, Tanaka K, Uji Y, Akimitsu K, Gomi K (2016) Rice terpene synthase 24 (OsTPS24) encodes a jasmonate-responsive monoterpene synthase that produces an antibacterial ${\gamma}$-terpinene against rice pathogen. J Plant Physiol 191:120-126 https://doi.org/10.1016/j.jplph.2015.12.008
  43. Zhang P, Fuentes S, Siebert T , Krstic M, Herderich M, Barlowa ER, Howell K (2016) Comparison data of common and abundant terpenes at different grape development stages in Shiraz wine grapes. Data Brief 8:1127-1136 https://doi.org/10.1016/j.dib.2016.07.010