In vitro rooting development and ex vitro acclimatization for Rosa damascena Mill. plant regeneration using auxin treatments
DOI:
https://doi.org/10.14719/pst.3758Keywords:
acclimatization, IAA, IBA, NAA, rooting induction, R. damascena MillAbstract
R. damascena, renowned for its aromatic essence, holds immense significance in various industries, including perfumery and cosmetics. However, its propagation presents challenges due to its recalcitrant nature. This study aimed to investigate micropropagation in vitro from single nodes as an alternative to traditional cutting methods, focusing on enhancing plant material preservation. Nodal explants were subjected to different auxin treatments (Indole-3-butyric-acid at T1:0.1, T2:0.5, and T3:1 mg/L; Indole-3-acetic-acid at T4:0.1, T5:0.5, and T6:1 mg/L; and 1-Naphthaleneacetic-acid at T7:0.5, T8:1, and T9:1.5 mg/L) to assess rooting efficiency and subsequent plant development. Results revealed a significant increase in rooting rate, with the highest rooting rate observed in the T3 treatment (97.22%) with 1 mg/L of IBA after 12 weeks of incubation. Moreover, the mortality rate varied significantly among treatments, with the highest rate observed in the control group (55.56%). The bud break rate was significantly higher in the T3 treatment compared to other treatments (100%). Correlations between morphological traits unveiled intricate relationships, highlighting the influence of auxin type and concentration on various parameters such as mortality and bud break rate. During the acclimatization process, a substrate composed of perlite, peat, and sand in a ratio of 3:1:1 (v/v/v) was utilized. The IBA-treated plants demonstrated superior growth, with an average apical growth of (2.84 cm) and a leaf area of (20.95 cm²) after 6 weeks. Our findings provide valuable insights into optimizing micropropagation techniques for R. damascena, thereby contributing to sustainable cultivation practices and meeting the increasing demand for this prized botanical resource.
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References
Nunes HS, Miguel MG. R. damascena essential oils: a brief review about chemical composition and biological properties. 2017.
Ivanova T, Ganeva-Raichev? V, Bosseva Y, Dimitrova D. Singing the nature-?thnobotanical knowledge in Bulgarian folk songs. Botanical Sciences. 2021;99(2):321-41.
El Malahi S, Irahoui L, Mokhtari W, Ennami M, Taimourya H, Zim J, et al. Exploring the synergistic effect of rose distillation waste and biostimulant beside other organic amendments on R. damascena seedlings’ growth. Int J Recyc Organic Waste Agri [Internet]. 2024 Jan 7 [cited 2024 Jan 8]; Available from: https://ijrowa.isfahan.iau.ir/article_709016.html
Azadi P, Beyrami ZE, Otang NV. A simple protocol for somatic embryogenesis in Rosa hybrida L. cv. Apollo. The J Horti Sci Biotechnol. 2013;88(4):399-402.
Rusanov K, Kovacheva N, Dobreva A, Atanassov I. Rosa x damascena Mill. (Rose). Medicinal, aromatic and stimulant plants. 2020;467-500.
Seyed HH, Azizi S, Aghaee A, Karakus S, Kaya O. Nano-silicone and Ascophyllum nodosum-based biostimulant down-regulates the negative effect of in vitro induced-salinity in R. damascena. BMC Plant Biology. 2023;23(1):560.
Biotech B. Effects of culture medium and concentration of different growth regulators on organogenesis damask rose (R. damascena Mill). J Plant Bioinfo Biotechnol. 2021;1(1).
Rezanejad F, Abarian M, Abdirad S. Shoot and root induction and growth of single nodes of R. damascena in different culture media. J Plant Physiol Breed. 2021;11(2):97-108.
El Malahi S, Sbah N, Zim J, Ennami M, Zakri B, Mokhtari W, et al. Enhancing rooting efficiency and nutrient uptake in R. damascena Mill. cuttings: insights into auxin and cutting type optimization. Plant Science Today. 2024 Jan 1;11(1):119-31.
Abbas MM, Ahmad S, Anwar R. Effect of growth retardants to break apical dominance in R. damascena. Pak J Agri Sci. 2007; 44:524-28.
Ginova A, Tsvetkov I, Kondakova V. R. damascena Mill. -an overview for evaluation of propagation methods. Bulg J Agri Sci (Bulgaria). 2012.
Musavi AM, Ahmadi N, Dehestani-Ardakani M. Putrescine and IBA enhanced the adventitious root formation in Damask rose (Rosa× damascena Mill.) under in vivo and in vitro conditions. J Horti Posthar Res. 2023;383-96.
Nasri F, Fadakar A, Saba MK, Yousefi B. Study of indole butyric acid (IBA) effects on cutting rooting improving some of wild genotypes of damask roses (R. damascena Mill.). J Agri Sci Belgrade. 2015;60(3):263-75.
Mirshahi H, Mahdinezhad N, Soloki M, Samiei L. Effect of plant growth adjuvants on direct regeneration of Mohammadi flower (R. damascena Mill.) using thin cell layering technique. Acta Sci Polo Hort Cultus. 2020;19(3).
Zhao Y. Essential roles of local auxin biosynthesis in plant development and in adaptation to environmental changes. Ann Rev Plant Biol. 2018;69:417-35.
Pikaard CS, Scheid OM. Epigenetic regulation in plants. Cold Spring Harbor perspectives in biology. 2014;6(12):a019315.
Amal AI, Abdelghani TA, Latifa AZ, Amina IH, Mimoun MO. Effects of cutting origin and exogenous auxin treatment on the rooting of R. damascena (Mill) cuttings from the M’goun-Dades valleys in Morocco. Arab J Medi Arom Plants. 2022 Feb 10;8(1):134-54.
Tharwat SK, Hafiz MM, Mazen AN. The effect of IBA (Indol-3-Butyric Acid) treatment on ?rooting of some Damask rose (R. damascena Mill.) ?rootstock genotypes. Syrian J Agri Res. 2019;7(2):69-78.
Bashir MA, Anjum MA, Chaudhry Z, Rashid H. Response of Jojoba (Simmondsia chinensis) cuttings to various concentrations of auxins. Pak J Bot. 2009 Dec 1;41(6):2831-40.
Hu S, Zhang M, Yang Y, Xuan W, Zou Z, Arkorful E, et al. A novel insight into nitrogen and auxin signaling in lateral root formation in tea plant [Camellia sinensis (L.) O. Kuntze]. BMC Plant Biology. 2020;20(1):1-17.
Neves M, Correia S, Cavaleiro C, Canhoto J. Modulation of organogenesis and somatic embryogenesis by ethylene: An overview. Plants. 2021 Jun 14;10(6):1208.
Sotelo M, Cuadrado B, Sainz M, Piriz S, Borsani O. Root growth adaptation under water deficit. 2021.
Kaviani B, Deltalab B, Kulus D, Khoddamzadeh AA, Roque-Borda CA. In Vitro shoot multiplication and rooting of ‘Kashan’and ‘Hervy Azerbaijan’Damask rose (R. damascena Mill.) genotypes for cosmetic and ornamental applications. Plants. 2024 May 14;13(10):1364.
Pati PK, Prakash O, Sharma M, Sood A, Ahuja PS. Growth performance of cuttings raised from in vitro and in vivo propagated stock plants of R. damascena Mill. Biologia Plantarum. 2004;48:609-11.
Pati PK, Rath SP, Sharma M, Sood A, Ahuja PS. In vitro propagation of rose-a review. Biotechnology Advances. 2006;24(1):94-114.
Aslam M, Raina PA, Rafiq RU, Siddiqi TO, Reshi ZA. Adventitious root formation in branch cuttings of Taxus wallichiana Zucc.(Himalayan yew): A clonal approach to conserve the scarce resource. Current Botany. 2017; 8:127-35.
García M, De María D. Aplicación exógena de poliaminas en la mejora de cultivos agrícolas frente al estrés. 2021.
Abdelaal K, Alsubeie MS, Hafez Y, Emeran A, Moghanm F, Okasha S, et al. Physiological and biochemical changes in vegetable and field crops under drought, salinity and weeds stresses: control strategies and management. Agriculture. 2022;12(12):2084.
Monteiro MV, Blanuša T, Verhoef A, Hadley P, Cameron RW. Relative importance of transpiration rate and leaf morphological traits for the regulation of leaf temperature. Aus J Bot. 2016;64(1):32-44.
Shekhaliya K, Tank JG. Changes in growth physiology of Vigna unguiculata in hydroponic system. In: Proceedings of the National Conference on Innovations in Biological Sciences (NCIBS); 2020.
Etesami H, Glick BR. Bacterial indole-3-acetic acid: A key regulator for plant growth, plant-microbe interactions and agricultural adaptive resilience. Microbiological Research. 2024;127602.
Monteuuis O, Bon MC. Influence of auxins and darkness on in vitro rooting of micropropagated shoots from mature and juvenile Acacia mangium. Plant Cell Tissue and Organ Culture. 2000 Dec;63(3):173-77.
Abdalla N, El-Ramady H, Seliem MK, El-Mahrouk ME, Taha N, Bayoumi Y, et al. An academic and technical overview on plant micropropagation challenges. Horticulturae. 2022;8(8):677.
Corral-Martínez P, Seguí-Simarro JM. Refining the method for eggplant microspore culture: effect of abscisic acid, epibrassinolide, polyethylene glycol, naphthaleneacetic acid, 6-benzylaminopurine and arabinogalactan proteins. Euphytica. 2014;195:369-82.
Hakman I, Hallberg H, Palovaara J. The polar auxin transport inhibitor NPA impairs embryo morphology and increases the expression of an auxin efflux facilitator protein PIN during Picea abies somatic embryo development. Tree Physiology. 2009;29(4):483-96.
Mondal M, Das S, Chandra I. Effect of individual plant growth regulators on modulation of secondary metabolites production in an important medicinal plant Gloriosa superba L. Plant Cell Tissue and Organ Culture (PCTOC). 2024;156(1):28.
Leftley N, Banda J, Pandey B, Bennett M, Voß U. Uncovering how auxin optimizes root systems architecture in response to environmental stresses. Cold Spring Harbor Perspectives in Biology. 2021;13(11):a040014.
Wang Y, Khan MA, Zhu Z, Hai T, Sang Z, Jia Z, et al. Histological, morpho-physiological and biochemical changes during adventitious rooting induced by exogenous auxin in Magnolia wufengensis cuttings. Forests. 2022;13(6):925.
Kim SH, Zebro M, Jang DC, Sim JE, Park HK, Kim KY, et al. Optimization of plant growth regulators for in vitro mass propagation of a disease-free ‘Shine Muscat’Grapevine cultivar. Curr Issues Mol Biol. 2023;45(10):7721-33.
Dubey SM, Serre NB, Oulehlová D, Vittal P, Fendrych M. No time for transcription—rapid auxin responses in plants. Cold Spring Har Persp Biol. 2021;13(8):a039891.
Kaushik S, Shukla N. A review on effect of IBA and NAA and their combination on the rooting of stem cuttings of different ornamental crops. J Pharmacog Phytochem. 2020;9(3):1881-85.
Akhiyarova G, Veselov D, Ivanov R, Sharipova G, Ivanov I, Dodd IC, et al. Root ABA accumulation delays lateral root emergence in osmotically stressed barley plants by decreasing root primordial IAA accumulation. Int J Plant Biol. 2023;14(1):77-90.
Voothuluru P, Wu Y, Sharp RE. Not so hidden anymore: Advances and challenges in understanding root growth under water deficits. The Plant Cell. 2024;koae055.
Qiao L, Zhang T, Yang H, Yang S, Wang J. Overexpression of a SHORT-ROOT transcriptional factor enhances the auxin mediated formation of adventitious roots and lateral roots in poplar trees. Plant Science. 2022;323:111408.
Ludwig-Mueller J. Synthesis and hydrolysis of auxins and their conjugates with different side-chain lengths: Are all products active auxins? Spiridion Brusina lecture. Periodicum Biologorum. 2020;(3-4):81-96.
Abshahi M, García-Morote FA, Zarei H, Zahedi B, Nejad AR. Improvement of rooting performance in stem cuttings of savin juniper (Juniperus sabina L.) as a function of IBA pretreatment, substrate and season. Forests. 2022;13(10):1705.
Bai T, Dong Z, Zheng X, Song S, Jiao J, Wang M, et al. Auxin and its interaction with ethylene control adventitious root formation and development in apple rootstock. Frontiers in Plant Science. 2020;11:574881.
Li SW. Molecular bases for the regulation of adventitious root generation in plants. Frontiers in Plant Science. 2021;12:614072.
Prakash V, Vishwakarma K, Singh VP, Rai P, Ramawat N, Tripathi DK, et al. NO and ROS implications in the organization of root system architecture. Physiologia Plantarum. 2020;168(2):473-89.
Datta SK. Rose. In: Floriculture and Ornamental Plants. Springer; 2022. p. 153-80.
George E, Marschner H. Nutrient and water uptake by roots of forest trees. Zeitschrift für Pflanzenernährung und Bodenkunde. 1996;159(1):11-21.
Doussan C, Pagès L, Pierret A. Soil exploration and resource acquisition by plant roots: an architectural and modelling point of view. Sustainable Agriculture. 2009;583-600.
Cavallaro V, Pellegrino A, Muleo R, Forgione I. Light and plant growth regulators on in vitro proliferation. Plants. 2022;11(7):844.

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Copyright (c) 2025 EL MALAHI Soumia, GANOUDI Matike, ENNAMI Mounia , TAIMOURYA Houda , LAMHAMDI Mostafa, EL KHAL Fatima Ezzahrae, MOKHTARI Mimoun, HMOUNI Driss, IDRISSI HASSANI Lalla Mina

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