From Callus to Plantlet

unveiling the optimal hormonal synergy and sucrose supplementation for Zamioculcas zamiifolia micropropagation

Authors

DOI:

https://doi.org/10.1590/2447-536X.v31.e312953

Keywords:

callus, chlorophylls, micropropagation protocol, rooting, soluble carbohydrates

Abstract

Zamiifolia (Zamioculcas zamiifolia) is an important plant in ornamental markets, characterized by a slow growth rate and low propagation efficiency. To establish an efficient propagation protocol for this species, two experiments were conducted. The first experiment aimed to optimize the micropropagation of Zamiifolia through callus induction. The second experiment evaluated the effects of the callogenesis medium on the growth and performance of regenerated plants in greenhouse. Leaf explants were incubated on the half-strength Murashige and Skoog medium (½MS) containing different combinations of benzyladenine (0, 4.4, and 8.8 μM BA) and naphthalene acetic acid (0, 2.7, 5.4, and 10.8 μM) and sucrose (2.0% and 3.0%). The highest callus induction rate and weight were obtained using 0.0 μM BA+2.7 or 5.4 μM NAA+3.0% sucrose. The obtained calluses were incubated on ½MS medium supplemented with different combinations of BA (0.0, 2.2, and 8.8 μM) and NAA (0.0, 1.1, and 2.7 μM) for shoot regeneration , with the highest proliferation efficiency on medium containing 2.2 μM BA. Rooting of shoots evaluated in ½MS containing indole-3-butyric acid (0.0, 2.5 and 5.0, μM IBA) and NAA (0.0, 37.2, and 2.7 μM) and 2.5 μM IBA medium was suggested, respectively. In the second experiment, plantlets were regenerated from calli induced on the four most effective media, and their growth was evaluated under greenhouse conditions. The best growth and health of micropropagated plants were obtained from callogenesis medium containing 2.7 μM NAA+3.0% sucrose. Excessive cytokinin accumulation following BA treatment impaired root and overall growth of micropropagated plants.

Downloads

Download data is not yet available.

Author Biographies

Nafis Ashouri, University of Tehran

College of Aburaihan (Agricultural Technologies), Department of Horticultural Science, Pakdasht, Tehran, Iran.

Shirin Dianati Daylami, University of Tehran

College of Aburaihan (Agricultural Technologies), Department of Horticultural Science, Pakdasht, Tehran, Iran.

Soheil Karimi, University of Tehran

College of Aburaihan (Agricultural Technologies), Department of Horticultural Science, Pakdasht, Tehran, Iran.

References

An J, Almasaudi RA, Bouzayen M, Zouine M, Chervin C. Auxin and ethylene regulation of fruit set. Plant Sci. 2020;292:110381. https://doi.org/10.1016/j.plantsci.2019.110381

El-Gedawey HI, Abido AI, Gaber MK. Impact of kinetin and benzyladenine on growth performance of croton in vitro. Alexandria Sci. Exch. J. 2020;41:381-91. https://doi.org/10.21608/asejaiqjsae.2020.118280

Fathy M, Saad Eldin SM, Naseem M, Dandekar T, Othman EM. Cytokinins: wide-spread signaling hormones from plants to humans with high medical potential. Nutrients. 2022;14(7):1495. https://doi.org/10.3390/nu14071495

Karimi S, Karami H, Mokhtassi-Bidgoli A, Tavallali V, Vahdati K. Inducing drought tolerance in greenhouse grown Juglans regia by imposing controlled salt stress: the role of osmotic adjustment. Sci. Hortic. 2018;239:181-92. https://doi.org/10.1016/j.scienta.2018.05.029

Karimi S, Karami H, Vahdati K, Mokhtassi-Bidgoli A. Antioxidative responses to short-term salinity stress induce drought tolerance in walnut. Sci. Hortic. 2020;267:109322. https://doi.org/10.1016/j.scienta.2020.109322

Kharrazi M, Moradian M, Moghaddam ZS, Khadem A, Sharifi A. Micropropagation and ex vitro rooting of three ZZ plant (Zamioculcas zamiifolia Engl.) cultivars. In Vitro Cell. Dev. Biol. Plant. 2023;59(1):129-39. https://doi.org/10.1007/s11627-022-10323-3

Kristiansen K, Ørnstrup H, Brandt K. In vitro PPFD and media composition affect both in and ex vitro performance of Alstroemeria Butterfly-hybrids. Plant Cell Tissue Organ Cult. 1999;56:145-53. https://doi.org/10.1023/A:1006208119297

Li M, Kim C. Chloroplast ROS and stress signaling. Plant Commun. 2022;3(1):78-84. https://doi.org/10.1016/j.xplc.2021.100264

Martins JP, Rodrigues LC, Silva TD, Gontijo AB, Falqueto AR. Modulation of the anatomical and physiological responses of in vitro grown Alcantarea imperialis induced by NAA and residual effects of BAP. Ornam. Hortic. 2020;26(2):283-97. https://doi.org/10.1590/2447-536X.v26i2.2138

Nanda RM, Das P, Rout GR. In vitro clonal propagation of Acacia mangium and its evaluation of genetic stability through RAPD marker. Ann. For. Sci. 2004;61:381-6. https://doi.org/10.1051/forest:2004031

Nazir U, Gul Z, Shah GM, Khan NI. Interaction effect of auxin and cytokinin on in vitro shoot regeneration and rooting of endangered medicinal plant Valeriana jatamansi Jones through tissue culture. Am. J. Plant Sci. 2022;13(2):223-40. https://doi.org/10.4236/ajps.2022.132014

Ni K. Zamioculcas zamiifolia plant tissue culture method. Anhui Agric. Sci. Bull. 2015;10(6):56-63.

Nirmala KS, Prathibha BR, Anitha P, Chinnaswamy KP. Comparative evaluation of propagules and substrates for enhanced multiplication of Zamioculcas zamiifolia Engl. and its novel utility. Int. J. Chem. Stud. 2019;7(3):517-22. Available from: https://www.academia.edu/download/59211018/7-1-498-52720190511-12705-139aepo.pdf

Pourhassan A, Kaviani B, Kulus D, Miler N, Negahdar N. A complete micropropagation protocol for black-leaved Zamioculcas zamiifolia (Lodd.) Engl. ‘Dowon’. Horticulturae. 2023;9(4):422. https://doi.org/10.3390/horticulturae9040422

Roychoudhry S, Kepinski S. Auxin in root development. Cold Spring Harb. Perspect. Biol. 2022;14(4):a039933. https://doi.org/10.1101/cshperspect.a039933

Sahraie F, Jabbarzadeh Z, Amiri J. Fulvic acid improves morphophysiological traits and vase life in Alstroemeria ‘Orange Queen’ in soilless conditions. Ornam. Hortic. 2025;31:e312802. https://doi.org/10.1590/2447-536X.v31.e312802

Salam BB, Barbier F, Danieli R, Teper-Bamnolker P, Ziv C, Spíchal L, et al. Sucrose promotes stem branching through cytokinin. Plant Physiol. 2021;185(4):1708-21. https://doi.org/10.1093/plphys/kiab003

Sari YP, Kusumawati E, Saleh C, Kustiawan W, Sukartingsih S. Effect of sucrose and plant growth regulators on callogenesis and preliminary secondary metabolic of different explant Myrmecodia tuberosa. Nusantara Biosci. 2018;10(3):183-92. https://doi.org/10.13057/nusbiosci/n100309

Sayadi Nejad M, Sadeghi SM. Optimization of callus production and regeneration of Zamiifolia (Zamioculcas zamiifolia). J. Hortic. Sci. 2019;33(3):405-15. https://doi.org/10.22067/jhorts4.v33i3.73637

Shi H, Liang P. Plantlet regeneration from leaf explants of Zamioculcas zamiifolia. Acta Hortic. Sin. 2003;115:131-9. Available from: https://www.ahs.ac.cn/en/y2003/v30/i5/621

Thaneshwari CA. Effect of plant growth regulators and sucrose concentration on callus induction and shoot differentiation from ovary culture of marigold (Tagetes spp.). Int. J. Chem. Stud. 2018;6(1):618-23.

Van der Krieken WM, Breteler H, Visser MH, Mavridou D. The role of the conversion of IBA into IAA on root regeneration in apple: introduction of a test system. Plant Cell Rep. 1993;12(4):203-6. https://doi.org/10.1007/BF00237054

Vanize-Canton SD, Leonhardt KW. In vitro callus induction and plantlet regeneration protocol developed for the oryzalin treatment of Zamioculcas zamiifolia (Lodd.) Engl. (Araceae). Acta Hortic. 2009;813(26):201-8. https://doi.org/10.17660/ActaHortic.2009.813.26

Wahyuni DK, Huda A, Faizah S, Purnobasuki H, Wardojo BPE. Effects of light, sucrose concentration and repetitive subculture on callus growth and medically important production in Justicia gendarussa Burm. f. Biotechnol. Rep. 2020;27:e00473. https://doi.org/10.1016/j.btre.2020.e00473

Zayova E, Petrova M, Dimitrova L, Vasilevska-Ivanova R, Stoeva D. Effect of different auxins on in vitro rooting of Paulownia elongata propagated plants. Genet. Plant Physiol. 2014;4(9):155-62. Available from: http://www.bio21.bas.bg/ippg/bg/

Downloads

Published

2025-10-21

Issue

Section

Articles