Physiological responses and P5CS gene expression of transgenic oil palm plantlet induced by drought stress

Authors

  • Turhadi TURHADI Indonesian Research Institute for Biotechnology and Bioindustry (IRIBB), Jalan Taman Kencana No.1, Bogor 16128, West Java, Indonesia
  • Hayati MINARSIH
  • Imron RIYADI
  • . PRIYONO
  • Asmini BUDIANI

DOI:

https://doi.org/10.22302/iribb.jur.mp.v88i2.386

Keywords:

carotenoids, chlorophyll, drought, drought tolerance, proline

Abstract

Drought is one of the limiting factors in crop cultivation, such as in oil palm (Elaeis guineensis Jacq.). The transgenic approaches are expected to increase plant tolerance to drought stress and minimize low productivity when drought occurs. Proline is an osmoprotectant compound in plants which its biosynthesis involved the P5CS gene. The objective of this study was to evaluate the tolerance level of P5CS-transgenic oil palm to drought stress induced by polyethylene glycol 6000 (PEG-6000). In this present study, the transgenic and non-transgenic oil palms were treated by  0, 2, and 4% PEG-6000 under in vitro conditions. The experiment was arranged as a factorial completely randomized design with three replications. The drought level score, total chlorophyll content, carotenoids, and proline content, as well as P5CS gene expression in leaf tissues were observed at 7 and 14 days after stress treatments. The result showed that transgenic plantlets had a lower drought level score than those of non-transgenic lines. A concentration of 4% PEG-6000 treatment reduced the total chlorophyll and carotenoids contents than that of 2% concentration in non-transgenic plantlets at 7 and 14 day after treatments (DAT). In addition, proline content and P5CS gene expression level in transgenic had been significantly increased during stress treatment. Based on these results, it can be concluded that the P5CS transgene increased the drought stress tolerance of oil palm.

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References

Abbas SR, SD Ahmad, SM Sabir & AH Shah (2014). Detection of drought tolerant sugarcane genotypes (Saccharum officinarum) using lipid peroxidation, antioxidant activity, glycine-betaine and proline contents. J Soil Sci Plant Nutr 14(1), 233-243.

Amanah DM, Nurhaimi-Haris & LP Santi (2019). Physiological responses of bio-silica-treated oil palm seedlings to drought stress. Menara Perkebunan 87(1), 20-30.

Ashraf M (2010). Inducing drought tolerance in plants: recent advances. Biotechnol Adv 28, 169-183.

Azzeme AM, SNA Abdullah, MA Aziz & PEM Wahab (2016). 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. Menara Perkebunan 2020, 88(2), 69-78.

Bandurska H, J Niedziela, Mał. Pietrowska-Borek, K Nuc, T Chadzinikolau & D Radzikowska (2017). Regulation of proline biosynthesis and resistance to drought stress in two barley (Hordeum vulgare L.) genotypes of different origin. Plant Physiol Biochem 118, 427-437.

Bates LS, RP Waldren & ID Teare (1973). Rapid determination of free proline for water-stress studies. Plant Soil 39, 205-207.

Borgo L, CJ Marur & LGE Vieira (2015). Effects of high proline accumulation on chloroplast and mitochondrial ultrastructure and on osmotic adjustment in tobacco plants. Acta Sci Agron 37(2), 191-199.

Badan Pusat Statistik (Indonesian Statistics) (2019). Indonesian Oil Palm Statistics 2018. Jakarta: Statistics Indonesia.

Budiani A, IB Nugroho, H Minarsih & I Riyadi (2019). Regeneration of P5CS-transformed oil palm plantlets mediated by Agrobacterium tumefaciens. Menara Perkebunan 87(2), 123-130.

Cha-um S, N Yamada, T Takabe & C Kirdmanee (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(3), 432-439.

Cha-um S, T Takabe & C Kirdmanee (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(39), 6509-6516.

Cha-um S, T Takabe & C Kirdmanee (2012). Physio-biochemical responses of oil palm (Elaeis guineensis Jacq.) seedlings to mannitol- and polyethylene glycol-induced iso-osmotic stresses. Plant Prod Sci 15(2), 65-72.

Corley RHV & PB Tinker (2016). The Oil Palm. Chichester: Blackwell Science.

Darlan NH, I Pradiko, Winarna & HH Siregar (2016). Dampak el niño 2015 terhadap performa tanaman kelapa sawit di Sumatera bagian tengah dan selatan. J Tanah dan Iklim 40(2), 35-42.

Das K & A Roychoudhury (2014). Reactive oxygen species (ROS) and response of antioxidants as ROS-scavengers during environmental stress in plants. Front Environ Sci. 2, 53.

Din J, SU Khan, I Ali & AR Gurmani (2011). Physiological and agronomic response of canola varieties to drought stress. J Anim Plant Sci, 21(1), 78-82.

Farooq M, M Hussain, A Wahid & KHM Siddique (2012). Drought Stress in Plants: An Overview. In: Aroca R (ed). Plant Responses to Drought Stress: From Morphological to Molecular Features. Berlin: Springer-Verlag.

Fauzi WR & ETS Putra (2019). Dampak pemberian kalium dan cekaman kekeringan terhadap serapan hara dan produksi biomassa bibit kelapa sawit (Elaeis gueenensis Jacq.). J Pen Kelapa Sawit 27(1), 41-56.

Fichman Y, SY Gerdes, H Kovács, L Szabados, A Zilberstein & LN Csonka (2015). Evolution of proline biosynthesis: enzymology, bioinformatics, genetics, and transcriptional regulation. Biol Rev Cambridge Philosophical Soc 90(4), 1065–1099.

Galeano E, TS Vasconcelos, PN de Oliveira & H Carrer (2019). Physiological and molecular responses to drought stress in teak (Tectona grandis L.f.). PLoS ONE 14(9): e0221571.

Ghobadi M, Taherabadi S, Ghobadi ME, Mohammadi GR & Jalali-Honarmand S (2013). Antioxidant capacity, photosynthetic characteristics and water relations of sunflower (Helianthus annuus L.) cultivars in response to drought stress. Ind Crops Prod 50, 29-38.

Indonesian Rice Research Institute (2002). Standart Evaluation System for Rice (SES). Manila: Indonesian Rice Research Institute.

Iskandar HM, D Widyaningrum & S Suhandono (2014). Cloning and characterization of P5CS1 and P5CS2 genes from Saccharum officinarum L under drought stress. J Tropical Crop Sci 1(1), 23-30.

Jazayeri SM, YD Rivera, JE Camperos-Reyes & HM Romero (2015). Physiological effects of water deficit on two oil palm (Elaeis guineensis Jacq.) genotypes. Agron Colomb 33(2), 164-173.

Kaur G & B Asthir (2017). Molecular responses to drought stress in plants. Biol Plant 61(2), 201-209.

Kishor PBK, S Sangam, RN Amrutha, PS Laxmi, KR Naidu, KRSS Rao, S Rao, KJ Reddy, P Theriappan & N Sreenivasulu (2005). Regulation of proline biosynthesis, degradation, uptake, and transport in higher plants: Its implication in plant growth and abiotic stress tolerance. Current Sci (88), 424-438.

Lichtenthaler HK (1987). Chlorophylls and carotenoid: pigments of photosynthetic biomembranes. Methods Enzymol 148, 350-382.

Lum MS, MM Hanafi, YM Rafii & ASN Akmar (2014). Effect of drought stress on growth, proline and antioxidant enzyme activities of upland rice. J Anim Plant Sci, 24(5), 1487-1493.

Man D, Bao YX & Han LB (2011). Drought tolerance associated with proline and hormone metabolism in two tall fescue cultivars. HortSci 46(7), 1027-1032.

Mibei EK, Ambuko J, Giovannoni JJ, Onyango AN & Owino WO (2017). Carotenoid profiling of the leaves of selected African eggplant accessions subjected to drought stress. Food Sci Nutr 5(1), 113-122.

Minarsih H, D Santoso & N Fitranti (2001). Identification of P5CS gene on sugarcane by PCR using heterologous primer. Menara Perkebunan 69(1), 1-9.

Minarsih H, D Subiyarti, I Riyadi, SM Putra & L Ambarsari (2015). Evaluasi varietas, sumber eksplan dan strain Agrobacterium terhadap keberhasilan transformasi tebu dengan gen P5CS. Menara Perkebunan 83(1), 1-9.

Moustakas M, I Sperdouli, T Kouna, CI Antonopoulou & I Therios (2011). Exogenous proline induces soluble sugar accumulation and alleviates drought stress effects on photosystem II functioning of Arabidopsis thaliana leaves. Plant Growth Regul 65(315), 1-10.

Pavei D, MC Gonçalves-Vidigal, AR Schuelter, I Schuster, ESN Vieira, ECG Vendruscolo & JP Poletine (2016). Response to water stress in transgenic (p5cs gene) wheat plants (Triticum aestivum L.). Australian J Crop Sci 10(6), 776-783.

Riduan A, H Aswidinnoor, Sudarsono, D Santoso & Endrizal (2010). Toleransi tembakau transgenik yang mengekspresikan gen P5CS terhadap stres kekeringan. J Pengkajian dan Pengembangan Teknologi Pertanian 13(2), 107-118.

Rivera-Mendes YD, JC Cuenca & HM Romero (2016). Physiological responses of oil palm (Elaeis guineensis Jacq.) seedlings under different water soil conditions. Agron Colomb 34(2), 163-171.

Schmittgen TD & KJ Livak (2008). Analyzing real-time PCR data by the comparative CT method. Nat Protoc 3, 1101-1108.

Talebi R, Ensafi MH, Baghebani N, Karami E & Mohammadi K (2013). Physiological responses of chickpea (Cicer arietinum) genotypes to drought stress. Environ Exp Bot 11, 9-15.

Todaka D, Y Zhao, T Yoshida, M Kudo, S Kidokoro, J Mizoi, KS Kodaira, Y Takebayashi, M Kojima, H Sakakibara, K Toyooka, M Sato, AR Fernie, K Shinozaki & K Yamaguchi-Shinozaki (2017). Temporal and spatial changes in gene expression, metabolite accumulation and phytohormone content in rice seedlings grown under drought stress conditions. Plant J 90, 61-78.

Toruan-Mathius N, T Liwang, I Danuwikarsa, G Suryatmana, H Djajasukanta, D Saodah & IGPW Astika (2004). Respons biokimia beberapa progeni kelapa sawit (Elaeis guineensis Jacq.) terhadap cekaman kekeringan pada kondisi lapang. Menara Perkebunan 72(2), 38-56.

Turhadi T, H Hamim, M Ghulamahdi & M Miftahudin (2019). Iron toxicity-induced physiological and metabolite profile variations among tolerant and sensitive rice varieties. Plant Signaling & Behav 14(12), e1682829.

Voronin PY, SN Maevskaya & MK Nikolaeva (2019). Physiological and molecular responses of maize (Zea mays L.) plants to drought and rehydration. Photosynthetica 57(3), 850-856.

Wang Y, X Jiang, K Li, M Wu, R Zhang, I Zhang & G Chen (2014). Photosynthetic responses of Oryza sativa L. seedlings to cadmium stress: physiological, biochemical and ultrastructural analyses. Biometals 27, 389-401.

Yehouessi LW, L Nodichao, H Adoukonou-Sagbadja & C Ahanhanzo (2019). Genotypic variability in oil palm (Elaeis guineensis Jacq.) towards drought damages in Benin (West Africa). Internat J Biol Chem Sci 13(3), 1737-1746.

Zarattini M & G Forlani (2017). Toward Unveiling the Mechanisms for Transcriptional Regulation of Proline Biosynthesis in the Plant Cell Response to Biotic and Abiotic Stress Conditions. Front Plant Sci 8, 927.

Zarei S, AA Ehsanpour & J Abbaspour (2012). The role of over expression of P5CS gene on proline, catalase, ascorbate peroxidase activity and lipid peroxidation of transgenic tobacco (Nicotiana tabacum L.) plant under in vitro drought stress. J Cell Molecular Res 4(1), 43-49.

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Submitted

09-06-2020

Accepted

11-09-2020

Published

30-10-2020

How to Cite

TURHADI, T., MINARSIH, H., RIYADI, I., PRIYONO, ., & BUDIANI, A. (2020). Physiological responses and P5CS gene expression of transgenic oil palm plantlet induced by drought stress. Menara Perkebunan, 88(2). https://doi.org/10.22302/iribb.jur.mp.v88i2.386

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