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Oil palm leaves and roots differ in physiological response, antioxidant enzyme activities and expression of stress-responsive genes upon exposure to drought stress

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Abstract

The seedling stage is a critical period for survival under drought stress. To identify biochemical and molecular drought response changes, oil palm seedlings were exposed to different levels of drought severity. Total chlorophyll, total soluble protein and total proline content were measured while expression of stress responsive genes was quantified using qPCR. The diminishing total chlorophyll (chl) content and the ratio of chla to chlb (chla:chlb) were observed to be significant. The significant reduction of chla was closely related to photosystem II deficiency. Based on the effects of drought on chlorophyll content, the samples can be categorised into mild (7 days of water withholding; DWW), moderate (14 DWW) and severe (21, 28 and 35 DWW). Sample at 21 DWW was used to represent the severe stage. Genes encoding ethylene responsive binding protein, late embryogenesis abundant (LEA), dehydrin (DHN), cold-induced, heat shock protein 70 and metallothionein type 2 were differentially up-regulated in the leaves, while in the roots only LEA and DHN were up-regulated. The proline content increased gradually in both vegetative tissues, while the total soluble protein content was affected by increasing drought severity. The activity of catalase was highest in the roots at the severe drought stage, while guaicol peroxidase activity was shown to be highest in the leaves under mild drought. These findings provide new insights into stress tolerance mechanisms of oil palm seedlings and can be used to develop stress tolerant oil palm through classical breeding and genetic engineering.

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References

  • Ahmad MA, Murali PV, Panneerselvam R (2013) Drought stress induced biochemical alterations in two varieties of Paspalum scrobiculatum L. Int J Curr Sci 7:80–96

    Google Scholar 

  • Ananthi K, Vijayaraghavan H (2012) Soluble protein, nitrate reductase activity and yield responses in cotton genotypes under water stress. Insight Biochem 2:1–4

    Article  Google Scholar 

  • Anjum SA, Farooq M, Xiea X, Liu X (2012) Antioxidant defense system and proline accumulation enables hot pepper to perform better under drought. Sci Hortic 140:66–73

    Article  CAS  Google Scholar 

  • Ashraf M, Foolad MR (2007) Roles of glycine, betaine and proline in improving plant abiotic stress resistance. Environ Exp Bot 59:206–216

    Article  CAS  Google Scholar 

  • Augustine SM, Narayan JA, Syamaladevi DP, Appunu C, Chakravarthi M, Ravichandran V, Subramonian N (2015) Erianthus arundinaceus HSP70 (EaHSP70) overexpression increases drought and salinity tolerance in sugarcane (Saccharum spp. hybrid). Plant Sci 232:23–34

    Article  PubMed  CAS  Google Scholar 

  • Bates LS (1973) Rapid determination of free proline for water-stress studies. Plant Soil 39:205–207

    Article  CAS  Google Scholar 

  • Beguerisse-Diaz M, Hern’andez-G’omez MC, Lizzul AM, Barahona M, Desikan R (2012) Compound stress response in stomatal closure: a mathematical model of ABA and ethylene interaction in guard cells. BMC Syst Biol 6:1–15

    Article  CAS  Google Scholar 

  • 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

    Article  PubMed  CAS  Google Scholar 

  • Cao H, Sun C, Shao H, Lei X (2011) Effects of low temperature and drought on the physiological and growth changes in oil palm seedlings. Afr J Biotechnol 10:2630–2637

    CAS  Google Scholar 

  • Caulet R-P, Gradinariu G, Iurea D, Morariu A (2014) Influence of furostanol glycosides treatments on strawberry (Fragaria × ananassa Duch.) growth and photosynthetic characteristics under drought condition. Sci Hortic 169:179–188

    Article  CAS  Google Scholar 

  • Cha-um S, Takabe T, Kirdmanee C (2010) Osmotic potential, photosynthetic abilities and growth characters of oil palm (Elaeis guineensis Jacq.) seedlings in responses to polyethylene glycol-induced water deficit. Afr J Biotechnol 9:6509–6516

    CAS  Google Scholar 

  • Cha-um S, Yamada N, Takabe T, Kirdmanee C (2011) Mannitol-induced water deficit stress in oil palm (Elaeis guineensis Jacq.) seedlings. J Oil Palm Res 23:1193–1201

    CAS  Google Scholar 

  • Cha-um S, Yamada N, Takabe T, Kirdmanee C (2013) Physiological features and growth characters of oil palm (Elaeis guineensis Jacq.) in response to reduced water-deficit and rewatering. Aust J Crop Sci 7:432–439

    CAS  Google Scholar 

  • Chen LM, Zhou XA, Li WB, Chang W, Zhou R, Wang C, Sha AH, Shan ZH, Zhang CJ, Qiu DZ, Yang ZL, Chen SL (2013) Genome-wide transcriptional analysis of two soybean genotypes under dehydration and rehydration conditions. BMC Genom 14:1–19

    Article  Google Scholar 

  • Chutia J, Borah SP (2012) Water stress effects on leaf growth and chlorophyll content but not the grain yield in traditional rice (Oryza sativa Linn.) genotypes of Assam, India II. Protein and proline status in seedlings under PEG induced water stress. Am J Plant Sci 3:971–980

    Article  CAS  Google Scholar 

  • Cohen D, Bogeat-Triboulot MB, Tisserant E, Balzergue S, Martin-Magniette M-L, Lelandais G, Ningre N, Renou J-P, Tamby J-P, Thiec DL, Hummel I (2010) Comparative transcriptomics of drought responses in Populus: a meta-analysis of genome-wide expression profiling in mature leaves and root apices across two genotypes. BMC Genom 11:1–21

    Article  CAS  Google Scholar 

  • Cominelli E, Galbiati M, Tonelli C (2010) Transcription factors controlling stomatal movements and drought tolerance. Biochem Soc Symp 1:41–45

    Google Scholar 

  • Ding H, Zhang ZM, Qin FF, Dai LX, Li CJ, Ci DW, Song WW (2014) Isolation and characterization of drought-responsive genes from peanut roots by suppression subtractive hybridization. Electron J Biotechnol 17:304–310

    Article  CAS  Google Scholar 

  • Du H, Zhou P, Huang B (2013) Antioxidant enzymatic activities and gene expression associated with heat tolerance in a cool-season perennial grass species. Environ Exp Bot 87:159–166

    Article  CAS  Google Scholar 

  • Farooq M, Wahid A, Kobayashi N, Fujita D, Basra SMA (2009) Plant drought stress: effects, mechanisms and management. Agron Sustain Dev 29:185–212

    Article  Google Scholar 

  • Gao C, Liu Y, Wang C, Zhang K, Wang Y (2014) Expression profiles of 12 late embryogenesis abundant protein genes from Tamarix hispida in response to abiotic stress. Sci World J 2014:1–9. doi:10.1155/2014/868391

    Google Scholar 

  • Gulli M, Salvatori E, Fusaro L, Pellacani C, Manes F, Marmiroli N (2015) Comparison of drought stress response and gene expression between a GM maize variety and a near-isogenic non-GM variety. PLoS ONE 10:1–21

    Article  CAS  Google Scholar 

  • Hadi NAA, Abdullah SNA, Azzeme AM, Al-Shanfari A, Saud HM (2015) Effects of over-expressing ethylene responsive transcription factor on expression of selected fruit ripening-related genes in Oil Palm (Elaeis guineensis Jacq.) mesocarp. J Trop Agric Sci 38:143–159

    Google Scholar 

  • Hao L, Wang Y, Zhang J, Xie Y, Zhang M, Duan L, Li Z (2010) Coronatine enhances drought tolerance via improving antioxidative capacity to maintaining higher photosynthetic performance in soybean. Plant Sci 210:1–9

    Article  CAS  Google Scholar 

  • Harb A, Krishnan A, Ambavaram MMR, Pereira A (2010) Molecular and physiological analysis of drought stress in Arabidopsis reveals early responses leading to acclimation in plant growth. Plant Physiol 154:1254–1271

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Harborne JB (1973) Phytochemical methods. Chapman & Hall, London

    Google Scholar 

  • Hillel D, Rosenzweig C (2002) Desertification in relation to climate variability and change. Adv Agron 77:1–38

    Article  Google Scholar 

  • Huseynova IM (2012) Photosynthetic characteristics and enzymatic antioxidant capacity of leaves from wheat cultivars exposed to drought. Biochim Biophys Acta 1817:1516–1523

    Article  PubMed  CAS  Google Scholar 

  • Ishida H, Yoshimoto K, Izumi M, Reisen D, Yano Y, Makino YO, Hanson MR, Mae T (2008) Mobilization of rubisco and stroma-localized fluorescent proteins of chloroplast to the vacuole by an ATG gene-dependent autophagic process. Plant Physiol 148:142–155

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Jebara S, Jebara M, Limam F, Aouani ME (2005) Changes in ascorbate peroxidase, catalase, guaiacol peroxidase and superoxide dismutase activities in common bean (Phaseolus vulgaris) nodules under salt stress. J Plant Physiol 162:929–936

    Article  PubMed  CAS  Google Scholar 

  • Kazuoka T, Oeda K (1992) Heat stable COR cold-regulated proteins associated with freezing tolerance in spinach. Plant Cell Physiol 33:1107–1114

    CAS  Google Scholar 

  • Kazuoka T, Oeda K (1994) Purification and characterization of COR85-oligomeric complex from cold-acclimated spinach. Plant Cell Physiol 35:601–611

    CAS  Google Scholar 

  • Khan MS, Ahmad D, Khan MA (2015) Utilization of genes encoding osmoprotectants in transgenic plants for enhanced abiotic stress tolerance. Electron J Biotechnol 18:257–266

    Article  CAS  Google Scholar 

  • Liu M, Shi J, Lu C (2013) Identification of stress-responsive genes in Ammopiptanthus mongolicus using ESTs generated from cold- and drought-stressed seedlings. BMC Plant Biol 13:1–14

    Article  Google Scholar 

  • Liu J, Li J, Su X, Xia Z (2014) Grafting improves drought tolerance by regulating antioxidant enzyme activities and stress-responsive gene expression in tobacco. Environ Exp Bot 107:173–179

    Article  CAS  Google Scholar 

  • Martignone RA, Guiamot JJ, Nakayama F (1987) Nitrogen partitioning and leaf senescence in soybean as related to nitrogen supply. Field Crops Res 17:17–20

    Article  Google Scholar 

  • Massacci A, Pietrosanti L, Nematov SK, Chernikova TN, Thor K, Leipner J (2008) Response of the photosynthetic apparatus of cotton (Gossypium hirsutum) to the onset of drought stress under field conditions studied by gas-exchange analysis and chlorophyll fluorescence imaging. Plant Physiol Biochem 46:189–195

    Article  PubMed  CAS  Google Scholar 

  • Mirzaee M, Moieni A, Ghanati F (2013) Effects of drought stress on the lipid peroxidation and antioxidant enzyme activities in two canola (Brassica napus L.) cultivars. J Agric Sci Technol 15:593–602

    CAS  Google Scholar 

  • Nishimura S, Tatano S, Miyamato Y, Ohtani K, Fukumoto T, Gomi K, Tada Y, Ichimura K, Akimitsu K (2013) A zinc-binding citrus protein metallothionein can act as a plant defense factor by controlling host-selective ACR-toxin production. Plant Mol Biol 81:1–11

    Article  PubMed  CAS  Google Scholar 

  • Nodichao L, Chopart J-L, Roupsard O, Vauclin M, Ake S, Jourdan C (2011) Genotypic variability of oil palm root system distribution in the field. Consequences for water uptake. Plant Soil 341:505–520

    Article  CAS  Google Scholar 

  • Omidvar V, Abdullah SNA, Ho CL, Mahmood M, Al-Shanfari AB (2012) Isolation and characterization of two ABRE-binding proteins: EABF and EABF1 from the oil palm. Mol Biol Rep 39:8907–8918

    Article  PubMed  CAS  Google Scholar 

  • Omidvar V, Abdullah SNA, Ho CL, Mahmood M (2013) Isolation and characterization of an ethylene-responsive element binding protein (EgEREBP) from oil palm (Elaeis guineensis). Aust J Crop Sci 7:219–226

    CAS  Google Scholar 

  • Ozturk L, Demir Y (2002) In vivo and in vitro protective role of proline. Plant Growth Regul 38:259–264

    Article  CAS  Google Scholar 

  • Prescot A, Martin C (1987) A rapid method for the quantitative assessment of levels of specific mRNAs in plants. Plant Mol Biol Rep 4:219–224

    Article  Google Scholar 

  • Rakic T, Gajic G, Lazarevic M, Stevanovic B (2015) Effects of different light intensities, CO2 concentrations, temperatures and drought stress on photosynthetic activity in two paleoendemic resurrection plant species Ramonda serbica and R. nathaliae. Environ Exp Bot 109:63–72

    Article  CAS  Google Scholar 

  • Ranjan A, Pandey N, Lakhwani D, Dubey NK, Pathre UV, Sawant SV (2012) Comparative transcriptomic analysis of roots of contrasting Gossypium herbaceum genotypes revealing adaptation to drought. BMC Genom 13:1–22

    Article  CAS  Google Scholar 

  • Ricardi F, Gazeau P, de Vienne D, Zivy M (1998) Protein changes in response to progressive water deficit in maize. Plant Physiol 117:1253–1263

    Article  Google Scholar 

  • Rodrigo M-J, Alquezar B, Zacarias L (2006) Cloning and characterization of two 9-cis-epoxycarotenoid dioxygenase genes, differentially regulated during fruit maturation and under stress conditions, from orange (Citrus sinensis L. Osbeck). J Exp Bot 57:633–643

    Article  PubMed  CAS  Google Scholar 

  • Sasaki K, Christov NK, Tsuda S, Imai R (2013) Identification of a novel LEA protein involved in freezing tolerance in wheat. Plant Cell Physiol 55:136–147

    Article  PubMed  CAS  Google Scholar 

  • Sekmen AH, Ozgur R, Uzilday B, Turkan I (2014) Reactive oxygen species scavenging capacities of cotton (Gossypium hirsutum) cultivars under combined drought and heat induced oxidative stress. Environ Exp Bot 99:141–149

    Article  CAS  Google Scholar 

  • Shao R, Wang K, Shangguan Z (2010) Cytokinin-induced photosynthetic adaptability of Zea mays L. to drought stress associated with nitric oxide signal: probed by ESR spectroscopy and fast OJIP fluorescence rise. J Plant Physiol 167:472–479

    Article  PubMed  CAS  Google Scholar 

  • Smith AM, Stitt M (2007) Coordination of carbon supply and plant growth. Plant, Cell Environ 30:1126–1149

    Article  CAS  Google Scholar 

  • Sun C, Cao H, Shao H, Lei X, Xiao Y (2011) Growth and physiological responses to water and nutrient stress in oil palm. Afr J Biotechnol 10:10465–10471

    Article  CAS  Google Scholar 

  • Tanaka Y, Sano T, Tamaoki M, Nakajima N, Kondo N, Hasezawa S (2005) Ethylene inhibits abscisic acid-induced stomatal closure in Arabidopsis. Plant Physiol 138:2337–2343

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Vaseva II, Anders I, Feller U (2014) Identification and expression of different dehydrin subclasses involved in the drought response of Trifolium repens. J Plant Physiol 171:213–224

    Article  PubMed  CAS  Google Scholar 

  • Wang Q, Wu J, Lei T, He B, Wu Z, Liu M, Mo X, Geng G, Li X, Zhou H, Liu D (2014) Temporal-spatial characteristics of severe drought events and their impact on agriculture on a global scale. Quatern Int 349:10–21

    Article  Google Scholar 

  • Wanner LA, Junttila O (1999) Cold-induced freezing tolerance in Arabidopsis. Plant Physiol 120:391–399

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Zhang J-Y, de Carvalho C, Torres-Jerez I, Kang Y, Allen SN, Huhman DV, Tang Y, Murray J, Sumner LW, Udvardi MK (2014) Global reprogramming of transcription and metabolism in Medicago truncatula during progressive drought and after rewatering. Plant, Cell Environ 37:2553–2576

    Article  Google Scholar 

  • Zhu J, Alvarez S, Marsh EL, LeNoble ME, Cho I-J, Sivaguru M, Chen S, Nguyen HT, Wu Y, Schachtman DP, Shar RE (2007) Cell wall proteome in the maize primary root elongation zone. II. Region-specific changes in water soluble and lightly ionically bound proteins under water deficit. Plant Physiol 145:15331548

    Google Scholar 

  • Zivcak M, Kalaji HM, Shao H-B, Olsovska K, Br M (2014) Photosynthetic proton and electron transport in wheat leaves under prolonged moderate drought stress. J Photochem Photobiol B 137:107–115

    Article  PubMed  CAS  Google Scholar 

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Acknowledgments

We thank Universiti Putra Malaysia for providing the research grant.

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Correspondence to Siti Nor Akmar Abdullah.

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Communicated by Y Wang.

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Azzeme, A.M., Abdullah, S.N.A., Aziz, M.A. et al. Oil palm leaves and roots differ in physiological response, antioxidant enzyme activities and expression of stress-responsive genes upon exposure to drought stress. Acta Physiol Plant 38, 52 (2016). https://doi.org/10.1007/s11738-016-2073-2

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  • DOI: https://doi.org/10.1007/s11738-016-2073-2

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