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Benzaldehyde as a new class plant growth regulator on Brassica campestris

  • Choi, Geun-Hyoung (Chemical Safety Division, National Institute of Agricultural Science, Rural Development Administration) ;
  • Ro, Jin-Ho (Chemical Safety Division, National Institute of Agricultural Science, Rural Development Administration) ;
  • Park, Byoung-Jun (Chemical Safety Division, National Institute of Agricultural Science, Rural Development Administration) ;
  • Lee, Deuk-Yeong (Division of Applied Life Science (BK21 plus program), Institute of Agriculture and Life Science, Gyeongsang National University) ;
  • Cheong, Mi-Sun (Division of Applied Life Science (BK21 plus program), Institute of Agriculture and Life Science, Gyeongsang National University) ;
  • Lee, Dong-Yeol (Division of Applied Life Science (BK21 plus program), Institute of Agriculture and Life Science, Gyeongsang National University) ;
  • Seo, Woo-Duck (Crop Foundation Division, National Institute of Crop Science, Rural Development Administration) ;
  • Kim, Jin Hyo (Division of Applied Life Science (BK21 plus program), Institute of Agriculture and Life Science, Gyeongsang National University)
  • Received : 2016.02.19
  • Accepted : 2016.04.06
  • Published : 2016.06.30

Abstract

Plant growth regulator is an essential pesticide to date while the available active ingredient is not well understood unlike fungicide, insecticide and herbicide. This study was aimed to evaluate a new chemical class of plant growth regulator, and the total of 92 benzene derivatives were screened for their germination and early stage of the root growth regulation on Brassica campestris. Thirty benzaldehydes, nine acids, one amide, and one ester showed potent root growth inhibitory activity (>70 % inhibition) while only salicylaldehyde showed potent germination inhibition ($IC_{50}=81.2mg/L$) suggesting that benzaldehyde was a key module candidate for the growth inhibition. Benzaldehydes were further evaluated for root growth inhibition. 2,3-Dihydroxybenzaldehyde and salicylaldehyde showed $IC_{50}$ values of 8.0 and 83.9 mg/L, respectively. On the other hand, salicylaldehyde, and 2,4,5-trihydroxybenzaldehyde were found to have root growth promotion effects less than 10 mg/L. This result suggests that the benzaldehyde is a new class candidate for plant growth regulator.

Keywords

References

  1. Alam MN, Bristi NJ, Rafiquzzaman M (2013) Review on in vivo and in vitro methods evaluation of antioxidant activity. Saudi Pharm J 21: 143-152 https://doi.org/10.1016/j.jsps.2012.05.002
  2. Czarnota MA, Paul RN, Dayan FE, Nimbal CI, Weston LA (2001) Mode of action, localization of production, chemical nature, and activity of sorgoleone: A potent PSII inhibitor in Sorghum spp. root exudates. Weed Tech 15: 813-825 https://doi.org/10.1614/0890-037X(2001)015[0813:MOALOP]2.0.CO;2
  3. Foti MC, Daquino C, Mackie ID, DiLabio GA, Ingold KU (2008) Reaction of phenols with the 2,2-diphenyl-1-picrylhydrazyl radical. Kinetics and DFT calculations applied to determine ArO-H bond dissociation enthalpies and reaction mechanism. J Org Chem 73: 9270-9282 https://doi.org/10.1021/jo8016555
  4. Gonzalez VM, Kazimir J, Nimbal C, Weston LA, Cheniae GM (1997) Inhibition of a photosystem II electron transfer reaction by the natural product sorgoleone. J Agric Food Chem 45: 1415-1421 https://doi.org/10.1021/jf960733w
  5. Hayat Q, Hayat S, Irfan M, Ahmad A (2010) Effect of exogenous salicylic acid under changing environment: a review. Environ Exp Bot 68: 14-25 https://doi.org/10.1016/j.envexpbot.2009.08.005
  6. Hristea EN, Hillebrand M, Caproiu MT, Caldararu H, Constantinescu T, Balaban AT (2002) Scavenging the hydroxyl radical by 2,2-diphenyl-1-picrylhydrazyl. Arkivoc ii: 123-132
  7. Inderjit (1996) Plant phenolics in allelopathy. Bot Rev 62: 186-202 https://doi.org/10.1007/BF02857921
  8. KCPA (2014) Agrochemicals use guide book-2014. Eds. Korea crop protection association (KCPA). Seoul, Republic of Korea. May 2014. pp 1176-1213
  9. Kim JB (2005) Pathogen, insect and weed control effects of secondary metabolites from plants. J Kor Soc Appl Biol Chem 48: 1-15
  10. Kim JH, Kim JY, Ryu SJ, Choi GH, Kim WI, Kim SR, Park BJ, Cho NJ (2014) Effect of ethanol extract of herbal medicine on crop growth inhibitor. Kor J Environ Agric 33: 69-72 https://doi.org/10.5338/KJEA.2014.33.2.69
  11. Lee JH, Park KH, Lee MH, Kim HT, Seo WD, Kim JY, Baek IY, Jang DS, Ha TJ (2013) Identification, characterisation, and quantification of phenolic compounds in the antioxidant activity-containing fraction from the seeds of Korean perilla (Perilla frutescens) cultivars. Food Chem 136: 843-852 https://doi.org/10.1016/j.foodchem.2012.08.057
  12. Lee S, Kim SG, Park CM (2010a) Salicylic acid promotes seed germination under high salinity by modulating antioxidant activity in Arabidopsis. New Phytol 188: 626-637 https://doi.org/10.1111/j.1469-8137.2010.03378.x
  13. Lee, SE, Yun MS, Yeon BR, Choi JS, Cho NK, Hwang KH, Wang HY, Kim S (2010b) Herbicidal activity of benzaldehyde in Cajuput (Melaleuca cajeputi) essential oil. Kor J Weed Sci 30: 191-198 https://doi.org/10.5660/KJWS.2010.30.3.191
  14. Li ZH, Wang QA, Ruan XA, Pan CD, Jiang DA (2010) Phenolics and plant allelopathy. Molecules 15: 8933-8952 https://doi.org/10.3390/molecules15128933
  15. Loake G, Grant M (2007) Salicylic acid in plant defence-the players and protagonists. Curr. Opin Plant Biol 10: 466-472 https://doi.org/10.1016/j.pbi.2007.08.008
  16. Mu J, Uehara T, Furuno T (2006) Regulation effect of Phyllostachys pubescens methanol extractives on growth of seed plants. J Wood Sci 52: 367-371 https://doi.org/10.1007/s10086-005-0768-x
  17. Rani PU (2008) Allelochemical stress induced biochemical changes in the leaves and plant growth regulation in Ricinus communis L. Allelopathy J 22: 79-91
  18. Raskin I (1992) Role of salicylic acid in plants. Annu Rev Plant Physiol Plant Mol Biol 43: 439-463 https://doi.org/10.1146/annurev.pp.43.060192.002255
  19. Reigosa MJ, Pazos-Malvido E (2007) Phytotoxic effects of 21 plant secondary metabolites on Arabidopsis thaliana germination and root growth. J Chem Ecol 33: 1456-1466 https://doi.org/10.1007/s10886-007-9318-x
  20. Reynolds T (1978) Comparative effects of aromatic compounds on inhibition of lettuce fruit germination. Ann Bot 42: 419-427 https://doi.org/10.1093/oxfordjournals.aob.a085475
  21. Singh HP, Batish DR, Kohli RK (2003) Allelopathic interactions and allelochemicals: New possibilities for sustainable weed management. Crit Rev Plant Sci 22: 239-311 https://doi.org/10.1080/713610858
  22. Weir TL, Bais HP, Vivanco JM (2003) Intraspecific and interspecific interactions mediated by a phytotoxin, (-)-catechin, secreted by the roots of Centaurea maculosa (spotted knapweed). J Chem Ecol 29: 2397-2412 https://doi.org/10.1023/A:1026313031091
  23. Weir TL, Park SW, Vivanco JM (2004) Biochemical and physiological mechanisms mediated by allelochemicals. Curr Opin Plant Biol 7: 472-479 https://doi.org/10.1016/j.pbi.2004.05.007
  24. Yoshioka T, Inokuchi T, Fujioka S, Kimura Y (2004) Phenolic compounds and flavonoids as plant growth regulators from fruit and leaf of Vitex rotundifolia. Z Naturforsch C-A J Biosci 59: 509-514
  25. Zeng RS, Luo SM, Shi YH, Shi MB, Tu CY (2001) Physiological and biochemical mechanism of allelopathy of secalonic acid F on higher plants. Agron J 93: 72-79 https://doi.org/10.2134/agronj2001.93172x

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