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Changes in amino acid levels and their effects on parthenocarpic fruit formation in young Barhi date palms Phoenix dactylifera L. derived from tissue culture

Authors

DOI:

https://doi.org/10.14719/pst.3982

Keywords:

essential amino acids, HPLC analysis, flowering, phenotypes, methionine

Abstract

This research aims to analyse the quantities of non-essential amino acids (histidine, arginine, alanine, cysteine and tyrosine) and essential amino acids (aspartic, glutamine, serine, glycine, phenylalanine, threonine, valine, isoleucine, leucine, methionine and lysine) in the leaves of three different date palm phenotypes. These phenotypes are derived through tissue culture from and parthenocarpic fruits (shees) produces, normal fruits (normal) produce and propagated by offshoots of normal fruits (vegetal) produces. This study focuses on three distinct stages: pre-flowering, flowering and fruiting. The amino acid levels were determined using HPLC. Results of this study indicate that the shees phenotype has the lowest levels of amino acids compared with the normal and vegetal phenotypes. Most amino acids exhibit a consistent trend throughout the examined stages, with levels declining from the pre-flowering stage to the flowering stage, but show an increase in the fruiting stage compared with the preceding stage. In addition, the results reveal that methionine is absent in the shees phenotype during all stages of the study but present at high levels in the vegetal and normal phenotypes. These results indicate that the metabolism of amino acids varies among different phenotypes of date palms. This variation directly or indirectly affects the development of parthenocarpic fruits in date palms of the Barhi cultivar derived from tissue culture during the juvenile period.

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References

Suhim AA, Awad KM, Jaffer ON, Abass MH. The impact of salicylic and jasmonic acid in mitigating salinity stress on date palm Phoenix dactylifera L. Barhi Cv. Basrah Journal of Agricultural Sciences,36(1):120-30. https://doi.org/10.37077/25200860.2023.36.1.10

Mondal S, Chowdhury A, Basu SK, Chowdhury M. In vivo seed germination and seedling morphology of Phoenix dactylifera L. and Phoenix sylvestris (L) Roxb.. NBU Journal of Plant Sciences, 10(1): 45-48. https://doi.org/10.55734/NBUJPS.2016.v10i01.004

Al-Mahmoudi SJF, Alnajjar MAH, Alpresem WFF. Effect of Fluraton and male cultivar on embryonic development of flowers of date palm (Phoenix dactylifera L.) CV ‘Barhee’. J Glob Innov. Agric. Sci., 11(4):649-655

Heidarpoor M, Kalantar M, Khosroshaheli M, Hervan EM. Investigation on the direct shoot regeneration in date palm CV. Pyarum and possible genetics changes in induced shoots. Nexo Scientific Journal. 2020;33(02):423-30. https://doi.org/10.5377/nexo.v33i02.10781

Tisserat B. (1979). Tissue culture of the date palm. J Hered, 70(3), 221-22. https://doi.org/10.1093/oxfordjournals.jhered.a109241

Ghailan SA, Suhim AA, Awad KM. A hormonal study of the phenomenon of parthenocarpic fruits in the date palm Phoenix dactylifera L. of the Barhi cultivar derived from tissue culture. Journal of Wildlife and Biodiversity.7 (Special Issue):262-76. https://doi.org/10.5281/ZENODO.10212278

Kaeppler SM, Kaeppler HF, Rhee Y. (2000) Epigenetic aspects of somaclonal variation in plants. Plant Mol Biol 43: 179-88. https://doi.org/10.1023/A:1006423110134

Ali-Dinar H, Mohammed M, Munir M. Effects of pollination interventions, plant age and source on hormonal patterns and fruit set of date palm (Phoenix dactylifera L.). Horticulturae. 2021, 7(11):427. https://doi.org/10.3390/horticulturae7110427

Salomón-Torres R, Krueger R, García-Vázquez JP, Villa-Angulo R, Villa-Angulo C, Ortiz-Uribe N, Sol-Uribe JA, Samaniego-Sandoval L. Date palm pollen: Features, production, extraction and pollination methods. Agronomy (Basel. Switzerland), 2021, 11(3):504. https://doi.org/10.3390/agronomy11030504

Cheruth AJ, Kurup SS, Subramaniam S. Variations in hormones and antioxidant status in relation to flowering in early, mid, and late varieties of date palm (Phoenix dactylifera) of United Arab Emirates. The Scientific World Journal. 2015; 2015(1):846104. https://doi.org/10.1155/2015/846104

Hadi S, Swaleh Al-Khalifah N, Abdo Moslem M. (2015). Hormonal basis of ‘shees’ fruit abnormality in tissue culture derived plants of date palm. Int J Agric Biol. 17(3): 607-612. https://doi.org/10.17957/ijab/17.3.14.088

Kelen M, Demiralay EC, ?EN S, ALSANCAK GÖ. Separation of abscisic acid, indole-3-acetic acid, gibberellic acid in 99 R (Vitis berlandieri x Vitis rupestris) and rose oil (Rosa damascena Mill.) by reversed phase liquid chromatography. Turkish Journal of Chemistry. 2004; 28(5):603-10.

Cohen Y, Korchinsky R, Tripler E. Flower abnormalities cause abnormal fruit setting in tissue culture-propagated date palm (Phoenix dactylifera L.). The Journal of Horticultural Science and Biotechnology. 2004; 79(6):1007-13. https://doi.org/10.1080/14620316.2004.11511853

Hildebrandt TM, Nesi AN, Araújo WL, Braun HP. Amino acid catabolism in plants. Molecular plant. 2015; 8(11):1563-79. https://doi.org/10.1016/j.molp.2015.09.005

Bajguz A, Piotrowska-Niczyporuk A. Biosynthetic pathways of hormones in plants. Metabolites. 2023 Jul:13(8):884. https://doi.org/10.3390/metabo13080884

Borghi M, Fernie AR. Floral metabolism of sugars and amino acids: implications for pollinators’ preferences and seed and fruit set. Plant Physiology. 2017; 175(4):1510-24. https://doi.org/10.1104/pp.17.01164

Palanivelu R, Brass L, Edlund AF, Preuss D. Pollen tube growth and guidance is regulated by POP2, an Arabidopsis gene that controls GABA levels. Cell. 2003; 114(1):47-59.https://doi.org/10.1016/s0092-8674(03)00479-3

Winter G, Todd CD, Trovato M, Forlani G, Funck D. Physiological implications of arginine metabolism in plants. Front. Plant Sci, 2015; 6:534. https://doi.org/10.3389/fpls.2015.00534

Hiscock SJ, Allen AM. Diverse cell signalling pathways regulate pollen?stigma interactions: the search for consensus. New Phytol. 2008; 179(2):286-317. https://doi.org/10.1111/j.1469-8137.2008.02457.x

Campbell K, Vowinckel J, Keller MA, Ralser M. Methionine metabolism alters oxidative stress resistance via the pentose phosphate pathway. Antioxidants and Redox Signaling, 24(10): 543-47. https://doi.org/10.1089/ars.2015.6516

Bloom AJ. The increasing importance of distinguishing among plant nitrogen sources. Curr Opin. Plant Biol. 2015; 25:10-16. https://doi.org/10.1016/j.pbi.2015.03.002

Jain BK, Patel VA. Pre and post pollination changes in amino acids and mineral compositions of anther and stigma in Solanum surattense burm.F. Journal of Pure and Applied Sciences, 20:19-23. https://www.spuvvn.edu/publication/prajna/prajna_2012/bioscience/4-BK%20Jain.pdf

Baqir HA, Zeboon NH, Al-Behadili AAJ. The role and importance of amino acids within plants: A review. Plant Archives. 2019; 19(2):1402-10. http://plantarchives.org/SPL%20ISSUE%20SUPP%202,2019/244%20(1402-1410).pdf

Published

08-08-2024

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How to Cite

1.
Salah AG, Aqeel AS, Khairullah MA. Changes in amino acid levels and their effects on parthenocarpic fruit formation in young Barhi date palms Phoenix dactylifera L. derived from tissue culture. Plant Sci. Today [Internet]. 2024 Aug. 8 [cited 2024 Nov. 21];. Available from: https://horizonepublishing.com/journals/index.php/PST/article/view/3982

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Research Articles