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Drought-induced stress in leaves of Coix lacryma-jobi L. under exogenous application of proline and GABA amino acids

  • Biochemistry & Physiology - Original Article
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Abstract

Coix lacryma-jobi L. is an Asian plant widely used in traditional medicine. Drought conditions can lead to an impairment of photosynthesis which can be softened by the exogenous application of proline and γ-aminobutyric acid (GABA) to maintain the electron transport chain (ETC) and avoid reactive oxygen species-induced oxidative damage by inducing antioxidative enzymes. The aim of this study was to evaluate the effects of water deficit on C. lacryma-jobi leaves under the application of proline and GABA. Chlorophyll (Chl) a fluorescence emission, antioxidative enzyme activity (catalase, superoxide dismutase, ascorbate peroxidase and guaiacol peroxidase) and proline and GABA contents in leaf tissues were performed in plants subjected to 12 days of drought. Chl a fluorescence indicated impairments on photosynthetic apparatus due to water deficit that resulted into increased activity of antioxidant enzymes. The application of proline but not GABA was more efficient in alleviating the effects of water deficit, as evidenced by the maintenance of the dynamic dissipation of the photosynthetic energy, besides the greater accumulation of proline under these conditions. Water deficit induces alterations in the ETC, which is softened by the application of proline to cope with the deleterious effects of drought in C. lacryma-jobi plant leaves.

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Abbreviations

APX:

Ascorbate peroxidase

CAT:

Catalase

Chl:

Chlorophyll

ETC:

Electron transport chain

GABA:

γ-Aminobutyric acid

GPOD:

Guaiacol peroxidase

H2O2 :

Hydrogen peroxide

OEC:

Oxygen-evolving complex

PQ:

Plastoquinone

PQH2 :

Plastoquinol

PSI:

Photosystem I

PSII:

Photosystem II

QA :

Quinone A

ROS:

Reactive oxygen species

SOD:

Superoxide dismutase

References

  • Al-Quraan NA, Al-Share AT (2015) Characterization of the γ-aminobutyric acid shunt pathway and oxidative damage in Arabidopsis thaliana pop 2 mutants under various abiotic stresses. Biol Plant 60:132–138

    Article  Google Scholar 

  • Azevedo Neto AD, Prisco JT, Eneas Filho J, De Abreu CEB, Gomes Filho E (2006) Effect of salt stress on antioxidative enzymes and lipid peroxidation in leaves and roots of salt-tolerant and salt-sensitive maize genotypes. Environ Exp Bot 56:87–94

    Article  Google Scholar 

  • Bates LS, Waldren RD, Teare ID (1973) Rapid determination of free proline for water stress studies. Plant Soil 39:205–207

    Article  CAS  Google Scholar 

  • Ben Rejeb K, Abdelly C, Savouré A (2014) How reactive oxygen species and proline face stress together. Plant Physiol Biochem 80:278–284

    Article  CAS  Google Scholar 

  • Blokhina O, Fagerstedt KV (2010) Reactive oxygen species and nitric oxide in plant mitochondria: origin and redundant regulatory systems. Physiol Plant 138:447–462

    Article  CAS  Google Scholar 

  • Chaves MM, Flexas J, Pinheiro C (2009) Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Ann Bot 103:551–560

    Article  CAS  Google Scholar 

  • Corke H, Huang Y, Li JS (2016) Coix: overview. In: Wrigley C, Corke H, Seetharaman K, Faubion J (eds) Encyclopedia of food grains. Academic Press, Oxford, pp 184–189

    Chapter  Google Scholar 

  • Dodd IC, Ryan AC (2016) Whole-plant physiological responses to water-deficit stress. eLS. Wiley, Chichester, pp 1–9

    Google Scholar 

  • Flexas J, Bota J, Escalona JM, Sampol B, Medrano H (2002) Effects of drought on photosynthesis in grapevines under field conditions: an evaluation of stomatal and mesophyll limitations. Funct Plant Biol 29:461–471

    Article  Google Scholar 

  • Foyer CH, Ruban AV, Noctor G (2017) Viewing oxidative stress through the lens of oxidative signalling rather than damage. Biochem J 474:877–883

    Article  CAS  Google Scholar 

  • Gill SS, Tuteja N (2010) Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Biochem 48:909–930

    Article  CAS  Google Scholar 

  • Hsiao S, Chen S, Yang I, Chen C, Tsai C, Chuang Y, Wang F, Chen Y, Linc T, Lo Y (2010) Evaluation of plant seedling water stress using 41 dynamic fluorescence index with blue LED-based fluorescence imaging. Comput Electron Agric 72:127–133

    Article  Google Scholar 

  • Ivanov BN, Borisova-Mubarakhina MM, Kozuleva MA (2018) Formation mechanisms of superoxide radical and hydrogen peroxide in chloroplasts, and factors determining the signalling by hydrogen peroxide. Funct Plant Biol 45:102–110

    Article  CAS  Google Scholar 

  • Johnson BS, Singh NK, Cherry JH, Locy RD (1997) Purification and characterization of glutamate decarboxylase from cowpea. Phytochemistry 46:39–44

    Article  CAS  Google Scholar 

  • Karunamoorthi K, Jegajeevanram K, Vijayalakshmi J, Mengistie E (2013) Traditional medicinal plants: a source of phytotherapeutic modality in resource-constrained healthcare settings. J Evid Bas Complement Altern Med 18:67–74

    Article  Google Scholar 

  • Kim YH, Kwak SS (2010) The role of antioxidant enzymes during leaf development. In: Gupta SD (ed) Reactive oxygen species and antioxidants in higher plants. Science Publishers, Enfeld, pp 129–150

    Chapter  Google Scholar 

  • Lawlor DW, Cornic G (2002) Photosynthetic carbon assimilation and associated metabolism in relation to water deficits in higher plants. Plant Cell Environ 25:275–294

    Article  CAS  Google Scholar 

  • Li Y, Tian X, Li S, Chang L, Sun P, Lu Y, Yu X, Chen S, Wu Z, Xua Z, Kang W (2019) Total polysaccharides of adlay bran (Coix lacryma-jobi L.) improve TNF-α induced epithelial barrier dysfunction in Caco-2 cells via inhibition of the inflammatory response. Food Funct 10:2906–2913

    Article  CAS  Google Scholar 

  • Liang X, Zhang L, Natarajan SK, Becker DF (2013) Proline mechanisms of stress survival. Antioxid Redox Signal 19:998–1011

    Article  CAS  Google Scholar 

  • Liu X, Huang B (2008) Photosynthetic acclimation to high temperatures associated with heat tolerance in creeping bengrass. J Plant Physiol 165:1947–1953

    Article  CAS  Google Scholar 

  • Osakabe Y, Osakabe K, Shinozaki K, Tran LSP (2014) Response of plants to water stress. Front Plant Sci 5:86

    Article  Google Scholar 

  • Phukan UJ, Jeena GS, Shukla RK (2016) WRKY transcription factors: molecular regulation and stress responses in plants. Front Plant Sci 7:760

    Article  Google Scholar 

  • Renault H, Roussel V, Amrani A, Arzel M, Renault D, Boucherdeau A, Deleu C (2010) The Arabidopsis pop2-1 mutant reveals the involvement of GABA transaminase in salt stress tolerance. BMC Plant Biol 10:20

    Article  Google Scholar 

  • Ruminta NT, Wicaksono FY (2017) Growth and yield of job’s tears (Coix lacryma-jobi L.) response to different types of oldeman climate classification and row spacing in West Java Indonesia. J Agron 16:76–82

    Article  Google Scholar 

  • Shanti SS, Karl-Josef D (2006) The significance of amino acids and amino acid-derived molecules in plant responses and adaptation to heavy metal stress. J Exp Bot 57:711–726

    Article  Google Scholar 

  • Smirnoff N, Cumbes QJ (1989) Hydroxyl radical scavenging activity of compatible solutes. Phytochemistry 28:1057–1060

    Article  CAS  Google Scholar 

  • Sousa CAF, Sodek L (2003) Alanine metabolism and alanine aminotransferase activity in soybean (Glycine max) during hypoxia of the root system and subsequent return to normoxia. Environ Exp Bot 50:1–8

    Article  Google Scholar 

  • Stirbet A, Govindjee (2011) On the relation between the Kautsky effect (chlorophyll a fluorescence induction) and Photosystem II: basics and applications. J Photochem Photobiol B Biol 104:236–257

    Article  CAS  Google Scholar 

  • Strasser RJ, Tsimilli-Michael M, Srivastava A (2004) Analysis of the chlorophyll a fluorescence transient. In: Papageorgiou GC, Govindjee (eds) Chlorophyll a fluorescence: a signature of photosynthesis. Springer, Dordrecht, pp 321–362

    Chapter  Google Scholar 

  • Tsimilli-Michael M, Strasser RJ (2008) In vivo assessment of plants vitality: applications in detecting and evaluating the impact of Mycorrhization on host plants. In: Varma A (ed) Mycorrhiza, 3rd edn. Springer, Berlin, pp 679–703

    Chapter  Google Scholar 

  • Wang L, Sun J, Yi Q, Wang X, Ju X (2012) Protective effect of polyphenols extract of adlay (Coix lacryma-jobi L. var. ma-yuen Stapf) on hypercholesterolemia-induced oxidative stress in rats. Molecules 17:8886–8897

    Article  CAS  Google Scholar 

  • Yaish MW (2015) Proline accumulation is a general response to abiotic stress in the date palm tree (Phoenix dactylifera L.). Genet Mol Res 14:9943–9950

    Article  CAS  Google Scholar 

  • Yan K, Chen P, Shao H, Shao C, Zhao S, Brestic M (2013) Dissection of photosynthetic electron transport process in sweet sorghum under heat stress. PLoS ONE 8:62100

    Article  Google Scholar 

  • Yusuf MA, Kumar D, Rajwanshi R, Strasser RJ, Tsimilli-Michael M, Govindjee, Sarin NB (2010) Overexpression of γ-tocopherol methyl transferase gene in transgenic Brassica juncea plants alleviates abiotic stress: physiological and chlorophyll a fluorescence measurements. Biochem Biophys Acta (BBA) Bioenergy 1797:1428–1438

    Article  CAS  Google Scholar 

  • Zargar SM, Gupta N, Nazir MR, Malik FA, Sofi NR, Shikari AB, Salgrota RK (2017) Impact of drought on photosynthesis: molecular perspective. Plant Gene 11:154–159

    Article  CAS  Google Scholar 

  • Zhu JK (2016) Abiotic stress signaling and responses in plants. Cell 167:313–324

    Article  CAS  Google Scholar 

Download references

Acknowledgments

This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior—Brasil (CAPES)—Finance Code 001, Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ).

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RAF, JB, CMH, TBM and CRP contributed to the study conception and design. RAF, JB, CMH, ACBC, NPCC, DMC, RPB and CFP were involved in material preparation, data collection and analysis. The first draft of the manuscript was written by RAF, JB and CMH. All authors commented on previous versions of the manuscript, read and approved the final manuscript version.

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Correspondence to Junior Borella.

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Ferreira, R.A., Borella, J., Hüther, C.M. et al. Drought-induced stress in leaves of Coix lacryma-jobi L. under exogenous application of proline and GABA amino acids. Braz. J. Bot 43, 513–521 (2020). https://doi.org/10.1007/s40415-020-00637-0

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  • DOI: https://doi.org/10.1007/s40415-020-00637-0

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