An Academic and Technical Overview on Plant Micropropagation Challenges
Open accessAbstract
The production of micropropagated plants in plant-tissue-culture laboratories and nurseries is the most important method for propagation of many economic plants. Micropropagation based on tissue-culture technology involves large-scale propagation, as it allows multiplication of a huge number of true-to-type propagules in a very short time and in a very limited space, as well as all year round, regardless of the climate. However, applying plant-tissue-culture techniques for the commercial propagation of plants may face a lot of obstacles or troubles that could result from technical, biological, physiological, and/or genetical reasons, or due to overproduction or the lack of facilities and professional technicians, as shown in the current study. Moreover, several disorders and abnormalities are discussed in the present review. This study aims to show the most serious problems and obstacles of plant micropropagation, and their solutions from both scientific and technical sides. This review, as a first report, includes different challenges in plant micropropagation (i.e., contamination, delay of subculture, burned plantlets, browning, in vitro rooting difficulty, somaclonal variations, hyperhydricity, shoot tip necrosis, albino plantlets, recalcitrance, shoot abnormalities, in vitro habituation) in one paper. Most of these problems are related to scientific and/or technical reasons, and they could be avoided by following the micropropagation protocol suitable for each plant species. The others are dominant in plant-tissue-culture laboratories, in which facilities are often incomplete, or due to poor infrastructure and scarce funds.
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Micropropagation has expanded to include various crops, fruit plants, vegetables, trees, medicinal and aromatic plants, and is now a multibillion-dollar industry worldwide.
“Micropropagation, initially applied to ornamental plants [5], has expanded to include various crops, fruit plants, vegetables, trees, and medicinal and aromatic plants, and is now a multibillion-dollar industry worldwide [6].”
From Somaclonal Variation and Clonal Fidelity in Commercial Micropropagation: Challenges and Perspectives (2025) · cites this paper as [5]
The paper discusses micropropagation across diverse plants, including fruit crops, trees, and medicinal plants (References; Section 4.4), and describes its commercial use (General Discussion). It does not give a worldwide market value or say the industry is worth multiple billions of dollars. The separate claim about its initial use in ornamentals is attached to [5], not this source. (LLM, conf=0.84)
Experimental — accuracy not yet measuredPlant tissue culture is an alternative method of conventional vegetative propagation.
“Thus, plant tissue culture is an alternative method of conventional vegetative propagation [4,5].”
From Somaclonal Variation and Clonal Fidelity in Commercial Micropropagation: Challenges and Perspectives (2025) · cites this paper as [5]
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References 148 · Cited by 177
Research works printed but not linked: 106
- Bridgen, M.; Van Houtven, W.; Eeckhaut, T. Plant Tissue Culture Techniques for Breeding. In Ornamental Crops, Handbook of Plant Breeding; Van Huylenbroeck, J., Ed.; Springer International Publishing AG: Cham, Switzerland, 2018; pp. 127-144.
- Neumann, K.-H.; Kumar, A.; Imani, J. Plant Cell and Tissue Culture-A Tool in Biotechnology Basics and Application, 2nd ed.; Springer Nature Switzerland AG: Cham, Switzerland, 2020; pp. 1-11.
- Viana, C.M.; Freire, D.; Abrantes, P.; Rocha, J.; Pereira, P. Agricultural land systems importance for supporting food security and sustainable development goals: A systematic review. Sci. Total Environ. 2022, 806, 150718. [CrossRef] [PubMed] · DOI
- Bidabadi, S.S.; Jain, S.M. Cellular, Molecular, and Physiological Aspects of In Vitro Plant Regeneration. Plants 2020, 9, 702. [CrossRef] [PubMed] · DOI
- Rani, A.; Donovan, N.; Mantria, N. Review: The future of plant pathogen diagnostics in a nursery production system. Biosens. Bioelectron. 2019, 145, 111631. [CrossRef] [PubMed] · DOI
- Pe, P.P.W.; Naing, A.H.; Soe, M.T.; Kang, H.; Park, K.I.; Kim, C.K. Establishment of meristem culture for virus-free and genetically stable production of the endangered plant Hosta capitata. Sci. Hortic. 2020, 272, 109591. [CrossRef] · DOI
- Kumar, M.K.; Sandeep, B.V.; Rao, S.P. Development of salt tolerant callus cultures by somatic hybridization between Oryza sativa and mangrove grass Myriostachya wightiana. Ann. Agrar. Sci. 2018, 16, 396-404. [CrossRef] · DOI
- Wang, M.; Ji, Y.; Feng, S.; Liu, C.; Xiao, Z.; Wang, X.; Wang, Y.; Xia, G. The non-random patterns of genetic variation induced by asymmetric somatic hybridization in wheat. BMC Plant Biol. 2018, 18, 244. [CrossRef] [PubMed] · DOI
- Park, S. Plant Tissue Culture Techniques and Experiments, 5th ed.; Academic Press: Cambridge, MA, USA; Elsevier Inc.: London, UK, 2021; pp. 1-23.
- Naing, A.H.; Adedeji, O.S.; Kim, C.K. Protoplast technology in ornamental plants: Current progress and potential applications on genetic improvement. Sci. Hortic. 2021, 283, 110043. [CrossRef] · DOI
- Sánchez, M.A.; Coronado, Y.M.; Coronado, A.C.M. Androgenic studies in the production of haploids and doubled haploids in Capsicum spp. Rev. Fac. Nac. Agron. Medellín 2020, 73, 9047-9056. [CrossRef] · DOI
- Dhiman, K.M.; Sharma, L.; Singh, A.; Sharma, M.M. Ex situ Conservation Using In vitro Methods of an Endangered Plant Sterculia urens Roxb.: A High Volume Trade Plant for Gum. Ind. Crops Prod. 2020, 158, 113015. [CrossRef] · DOI
- Karakas, F.P.; Bozat, B.G. Fluctuation in secondary metabolite production and antioxidant defense enzymes in in vitro callus cultures of goat's rue (Galega officinalis) under different abiotic stress treatments. Plant Cell Tissue Organ Cult. 2020, 142, 401-414. [CrossRef] · DOI
- Soleimani, S.H.; Bernard, F.; Amini, M.; Khavari-Nezhad, R.A. Cadmium accumulation and alkaloid production of Narcissus tazetta plants grown under in vitro condition with cadmium stress. Plant Physiol. Rep. 2020, 25, 51-57. [CrossRef] · DOI
- Fortini, E.A.; Batista, D.S.; Mamedes-Rodrigues, T.C.; Felipe, S.H.S.; Correia, L.N.F.; Chagas, K.; Silva, P.O.; Rocha, D.I.; Otoni, W.C. Gas exchange rates and sucrose concentrations affect plant growth and production of favonoids in Vernonia condensata grown in vitro. Plant Cell Tissue Organ Cult. 2021, 144, 593-605. [CrossRef] · DOI
- Kyzioł, A.; Łukasiewicz, S.; Sebastian, V.; Kustrowski, P.; Kozieł, M.; Majda, D.; Cierniak, A. Towards plant-mediated chemistry- Au nanoparticles obtained using aqueous extract of Rosa damascena and their biological activity in vitro. J. Inorg. Biochem. 2021, 214, 111300. [CrossRef] [PubMed] · DOI
- Gregorio, N.; Herbohn, J.; Harrison, S. Small-scale Forestry Development in Leyte, Philippines: The Central Role of Nurseries. Small-Scale For. 2004, 3, 337-351. [CrossRef] · DOI
- Degrande, A.; Tadjo, P.; Takoutsing, B.; Asaah, E.; Tsobeng, A.; Zac Tchoundjeu, Z. Getting Trees In to Farmers' Fields: Success of Rural Nurseries in Distributing High Quality Planting Material in Cameroon. Small-Scale For. 2013, 12, 403-420. [CrossRef] · DOI
- Marshall, M.; Sutherland, R.; Hulme, P.E. Assessing the role of plant trade networks in the vulnerability of forest nurseries to plant pathogens. Australas. Plant Pathol. 2021, 50, 671-681. [CrossRef] · DOI
- Seliem, M.K.; Abdalla, N.A.; El-Ramady, H.R. Response of Phalaenopsis Orchid to Selenium and Bio-NanoSelenium: In Vitro Rooting and Acclimatization. Env. Biodiv. Soil Secur. 2020, 4, 277-290. [CrossRef] · DOI
- Pandey, S.; Sundararajan, S.; Ramalingam, S.; Pant, B. Effects of sodium nitroprusside and growth regulators on callus, multiple shoot induction and tissue browning in commercially important Valeriana jatamansi Jones. Plant Cell Tissue Organ Cult. 2020, 142, 653-660. [CrossRef] · DOI
- Teixeira da Silva, J.A.; Nezami-Alanagh, E.; Barreal, M.E.; Kher, M.M.; Wicaksono, A.; Gulyás, A.; Hidvégi, N.; Magyar-Tábori, K.; Mendler-Drienyovszki, N.; Márton, L.; et al. Shoot tip necrosis of in vitro plant cultures: A reappraisal of possible causes and solutions. Planta 2020, 252, 47. [CrossRef] · DOI
- Pawełkowicz, M.E.; Skarzy ńska, A.; Mróz, T.; Bystrzycki, E.; Pl ąder, W. Molecular insight into somaclonal variation phenomena from transcriptome profiling of cucumber (Cucumis sativus L.) lines. Plant Cell Tissue Organ Cult. 2021, 145, 239-259. [CrossRef] · DOI
- Ranghoo-Sanmukhiya, V.M. Somaclonal Variation and Methods Used for Its Detection. In Propagation and Genetic Manipulation of Plants; Siddique, I., Ed.; Springer Nature: Singapore, 2021; pp. 1-18.
- Thakur, M.; Rakshandha; Sharma, V.; Chauhan, A. Genetic fidelity assessment of long term in vitro shoot cultures and regenerated plants in Japanese plum cvs Santa Rosa and Frontier through RAPD, ISSR and SCoT markers. S. Afr. J. Bot. 2020, 140, 428-433. [CrossRef] · DOI
- FAO/IAEA. Low-Cost Options for Tissue Culture Technology in Developing Countries. In Proceedings of the Technical Meeting Organized by the Joint FAO/IAEA Division of Nuclear Techniques in Food and Agriculture, Vienna, Austria, 26-30 August 2002; Available online: https://www-pub.iaea.org/mtcd/publications/pdf/te_1384_web.pdf (accessed on 14 June 2022).
- Loyola-Vargas, V.M.; Ochoa-Alejo, N. An Introduction to Plant Tissue Culture: Advances and Perspectives. In Plant Cell Culture Protocols, Methods in Molecular Biology; Loyola-Vargas, V.M., Ochoa-Alejo, N., Eds.; Springer Nature: New York, NY, USA, 2018; Volume 1815, pp. 3-13.
- Singh, C.R. Review on problems and its remedy in plant tissue culture. Asian J. Biol. Sci. 2018, 11, 165-172. [CrossRef] · DOI
- Gangopadhyay, M.; Nandi, S.; Roy, S.K.B. An efficient ex plant sterilization protocol for reducing microbial contamination of Solanum tuberosum CV. 'Kufri jyoti for establishing micropropagation in rainy season. J. Basic Appl. Plant Sci. 2017, 1, 25.
- Jugreet, B.S.; Mahomoodally, M.F. Essential oils from 9 exotic and endemic medicinal plants from Mauritius shows in vitro antibacterial and antibiotic potentiating activities. S. Afr. J. Bot. 2020, 132, 355-362. [CrossRef] · DOI
- Bhatia, S.; Sharma, K.; Dahiya, R.; Bera, T. Modern Applications of Plant Biotechnology in Pharmaceutical Sciences; Academic Press: Cambridge, MA, USA; Elsevier: London, UK, 2015; pp. 31-107.
- Taha, H.; Ghazy, U.M.; Gabr, A.M.M.; EL-Kazzaz, A.A.A.; Ahmed, E.M.M.; Haggag, K.M. Optimization of in vitro culture conditions affecting propagation of mulberry plant. Bull. Natl. Res. Cent. 2020, 44, 60. [CrossRef] · DOI
- Carvalho, S.D.; Ortega, M.; Orellana, M.; Rodríguez, M.; Folta, K.M.; Torres, M.L. In vitro propagation of the Amazonian medicinal plant guayusa (Ilex guayusa) and effects of light in the growth and development of this shade tolerant plant. Plant Cell Tissue Organ Cult. 2021, 147, 503-517. [CrossRef] · DOI
- Molinari, L.V.; Souza, D.M.S.C.; Avelar, M.L.M.; Fernandes, S.B.; Gonçalves, D.S.; Faria, J.C.T.; de Carvalho, D.; Brondani, G.E. Effects of chemical sterilization of the culture media, porous membranes and luminosity on in vitro culture of Eucalyptus grandis × Eucalyptus urophylla. J. For. Res. 2021, 32, 1587-1598. [CrossRef] · DOI
- Andújar, I.; González, N.; García-Ramos, J.C.; Bogdanchikova, N.; Pestryakov, A.; Escalona, M.; Concepción, O. Argovit™ silver nanoparticles reduce contamination levels and improve morphological growth in the in vitro culture of Psidium friedrichsthalianum (O. Berg) Nied. SN Appl. Sci. 2020, 2, 2110. [CrossRef] · DOI
- Nartop, P. Green Sterilization of Rosmarinus officinalis L. Stem Surfaces with Silver Nanoparticles Synthesized Using Rubia tinctorum L. Cell Culture Extracts. Iran J. Sci. Technol. Trans. A Sci. 2018, 42, 411-414. [CrossRef] · DOI
- Ahmed, N.; Mohamed, H.F.; Xu, C.; Lin, X.; Huang, L. A novel surface sterilization method using Artemisia dracunculus extract for tissue culturing of endangered species Sargassum fusiforme. Plant Cell Tissue Organ Cult. 2022, 149, 135-145. [CrossRef] · DOI
- Ahmadpoor, F.; Zare, N.; Asghari, R.; Sheikhzadeh, P. Sterilization protocols and the effect of plant growth regulators on callus induction and secondary metabolites production in in vitro cultures Melia azedarach L. AMB Express 2022, 12, 3. [CrossRef] [PubMed] · DOI
- Urtiga, C.D.C.; Silva-Cardoso, I.M.D.A.; Figueiredo, S.A. Low sodium isocyanurate concentrations as a substitute to medium autoclaving in plant tissue culture. Plant Cell Tissue Organ Cult. 2019, 139, 601-604. [CrossRef] · DOI
- Rency, A.S.; Pandian, S.; Ramesh, M. Influence of adenine sulphate on multiple shoot induction in Clitoria ternatea L. and analysis of phyto-compounds in in vitro grown plants. Biocatal. Agric. Biotechnol. 2018, 16, 181-191. [CrossRef] · DOI
- Kendon, J.P.; Rajaovelona, L.; Sandford, H.; Fang, R.; Bell, J.; Sarasan, V. Collecting near mature and immature orchid seeds for ex situ conservation: 'in vitro collecting' as a case study. Bot. Stud. 2017, 58, 34. [CrossRef] [PubMed] · DOI
- El-Banna, A.N.; El-Mahrouk, M.E.; Dewir, Y.H.; Farid, M.A.; Abou Elyazid, D.M.; Schumacher, H.M. Endophytic Bacteria in Banana In Vitro Cultures: Molecular Identification, Antibiotic Susceptibility, and Plant Survival. Horticulturae 2021, 7, 526. [CrossRef] · DOI
- Seliem, M.K.; El-Mahrouk, M.E.; El-Banna, A.N.; Hafez, Y.M.; Dewir, Y.H. Micropropagation of Philodendron selloum: Influence of copper sulfate on endophytic bacterial contamination, antioxidant enzyme activity, electrolyte leakage, and plant survival. S. Afr. J. Bot. 2021, 139, 230-240. [CrossRef] · DOI
- Abdalla, N.A.; Ragab, M.E.; El-Miniawy, S.M.; Arafa, N.M.; Taha, H.S. A New Aspect for In vitro Propagation of Jerusalem Artichoke and Molecular Assessment Using RAPD, ISSR and SCoT Marker Techniques. Egypt. J. Bot. 2021, 61, 203-218. [CrossRef] · DOI
- Abou Elyazid, D.M.A.; Salama, A.-M.; Zanaty, A.M.E.; Abdalla, N. In Vitro Propagation and Acclimatization of Banana Plants: Antioxidant Enzymes, Chemical Assessments and Genetic Stability of Regenerates as a Response to Copper Sulphate. Plants 2021, 10, 1853. [CrossRef] · DOI
- Ray, S.S.; Ali, N. Biotic Contamination and Possible Ways of Sterilization: A Review with Reference to Bamboo Micropropagation. Braz. Arch. Biol. Technol. 2016, 59, e160485. [CrossRef] · DOI
- Alagarsamy, K.; Shamala, L.F.; Wei, S. Influence of media supplements on inhibition of oxidative browning and bacterial endophytes of Camellia sinensis var. sinensis. 3 Biotech 2018, 8, 356. [CrossRef] · DOI
- Neri, D.; Cioccolanti, T.; Zuccherelli, G.; Navacchi, O.; Giorgi, V.; Lodolini, E.M. Micropropagation Effects on Juvenile Traits, Flower Differentiation, and Tree Architecture in Young Olive Trees. Agronomy 2020, 10, 1742. [CrossRef] · DOI
- Naing, A.H.; Kim, S.H.; Chung, M.Y.; Park, S.K.; Kim, C.K. In vitro propagation method for production of morphologically and genetically stable plants of different strawberry cultivars. Plant Methods 2019, 15, 36. [CrossRef] [PubMed] · DOI
- Malhotra, E.V.; Kamalapriya, M.; Bansal, S.; Meena, D.P.S.; Agrawal, A. Improved protocol for micropropagation of genetically uniform plants of commercially important cardamom (Elettaria cardamomum Maton). In Vitro Cell. Dev. Biol. Plant. 2021, 57, 409-417. [CrossRef] · DOI
- Sirikonda, A.; Jogam, P.; Ellendula, R.; Kudikala, H.; Mood, K.; Allini, V.R. In vitro micropropagation and genetic fidelity assessment in Flemingia macrophylla (Willd.) Merr: An ethnomedicinal plant. Vegetos 2020, 33, 286-295. [CrossRef] · DOI
- El-Mahrouk, M.E.; El-Shereif, A.R.; Hafez, Y.M.; Abdelaal, K.A.; El-Hendawy, A.S.; Migdadi, H.; Al-Obeed, R.S. Micropropagation of Banana: Reversion, Rooting, and Acclimatization of Hyperhydric Shoots. HortScience 2019, 54, 1384-1390. [CrossRef] · DOI
- Mendonça, E.G.; Batista, T.R.; Stein, V.C.; Balieiro, F.P.; de Abreu, R.J.; Pires, M.F.; de Souza, P.A.; Paiva, L.V. In vitro serial subculture to improve rooting of Eucalyptus urophylla. New Forest 2020, 51, 801-816. [CrossRef] · DOI
- Siddique, I.; Javed, S.B.; Al-Othman, M.R.; Anis, M. Stimulation of in vitro organogenesis from epicotyl explants and successive micropropagation round in Cassia angustifolia Vahl.: An important source of sennosides. Agrofor. Syst. 2013, 87, 583-590. [CrossRef] · DOI
- Khamushi, M.; Ardakani, M.D.; Zarei, A.; Aliabad, K.K. An efficient protocol for micropropagation of old cypress of Abarkuh (Cupressus sempervirens var. horizontalis [Mill.]) under in vitro condition. Plant Cell Tissue Organ Cult. 2019, 138, 597-601. [CrossRef] · DOI
- Vujović, T.; Ružić, D.J.; Cerović, R. In vitro shoot multiplication as influenced by repeated subculturing of shoots of contemporary fruit rootstocks. Hort. Sci. 2012, 39, 101-107. [CrossRef] · DOI
- Norton, M.E.; Norton, C.R. Change in shoot proliferation with repeated in vitro subculture of shoots of woody species of Rosaceae. Plant Cell Tissue Organ Cult. 1986, 5, 187-197. [CrossRef] · DOI
- Remphrey, W.R.; Palmer, C.E.; Blouw, M.J. In vitro branching in relation to repeated subculture in two cultivars of Potentilla fruticosa. Plant Cell Tissue Organ Cult. 1993, 32, 235-240. [CrossRef] · DOI
- Hamad, A.M.; Taha, R.M. Effect of sequential subcultures on in vitro proliferation capacity and shoot formation pattern of pineapple (Ananas comosus L. Merr.) over different incubation periods. Sci. Hortic. 2008, 117, 329-334. [CrossRef] · DOI
- Peng, X.; Zhang, T.-T.; Zhang, J. Effect of subculture times on genetic fidelity, endogenous hormone level and pharmaceutical potential of Tetrastigma hemsleyanum callus. Plant Cell Tissue Organ Cult. 2015, 122, 67-77. [CrossRef] · DOI
- Hassanein, A.M.; Salem, J.M.; Faheed, F.A.; El-nagish, A. Effect of anti-ethylene compounds on isoenzyme patterns and genome stability during long term culture of Moringa oleifera. Plant Cell Tissue Organ Cult. 2018, 132, 201-212. [CrossRef] · DOI
- Zhao, S.; Wang, H.; Liu, K.; Li, L.; Yang, J.; An, X.; Li, P.; Yun, L.; Zhang, Z. The role of JrPPOs in the browning of walnut explants. Plant Biol. 2021, 21, 9. [CrossRef] · DOI
- Dobránszki, J.; Jámbor-Benczúr, E.; Hudák, I.; Magyar-Tábori, K. Model experiments for establishment of in vitro culture by micrografting in apple. Int. J. Hortic. Sci. 2005, 1, 47-49. [CrossRef] · DOI
- Dobránszki, J.; Teixeira da Silva, J.A. Micropropagation of apple-A review. Biotechnol. Adv. 2010, 28, 462-488. [CrossRef] · DOI
- Teixeira da Silva, J.A.; Guly, A.; Magyar-Tabori, K.; Wang, M.R.; Wang, Q.-W.; Dobránszki, J. In vitro tissue culture of apple and other Malus species: Recent advances and applications. Planta 2019, 249, 975-1006. [CrossRef] · DOI
- Li, J.; Gao, C.; Miao, Y.; Liu, Z.; Cui, K. Development of a highly efficient callus induction and plant regeneration system for Dendrocalamus sinicus using hypocotyls as explants. Plant Cell Tissue Organ Cult. 2021, 145, 117-125. [CrossRef] · DOI
- Magyar-Tábori, K.; Dobránszki, J.; Hudák, I. Effect of cytokinin content of the regeneration media on in vitro rooting ability of adventitious apple shoots. Sci. Hortic. 2011, 129, 910-913. [CrossRef] · DOI
- Dewir, Y.H.; Murthy, H.N.; Ammar, M.H.; Alghamdi, S.S.; Al-Suhaibani, N.A.; Alsadon, A.A.; Paek, K.Y. In vitro Rooting of Leguminous Plants: Difficulties, Alternatives, and Strategies for Improvement. Hortic. Environ. Biotechnol. 2016, 57, 311-322. [CrossRef] · DOI
- Shaik, N.M.; Arha, M.; Nookaraju, A.; Gupta, S.K.; Srivastava, S.; Yadav, A.K.; Kulkarni, P.S.; Abhilash, O.U.; Vishwakarma, R.K.; Singh, S.; et al. Improved method of in vitro regeneration in Leucaena leucocephala. Physiol. Mol. Biol. Plants 2009, 15, 311-318. [CrossRef] [PubMed] · DOI
- Zayova, E.; Petrova, M.; Nikolova, M.; Dimitrova, L. Effect of Medium Salt Strength on the Micropropagation, Phenolic Content and Antioxidant Activity of Arnica montana L., Threatened Plant Species. Bio. Bulletin. 2016, 2, 6-13.
- Rezali, N.I.; Sidik, N.J.; Saleh, A.; Osman, N.I.; Adam, N.A.M. The effects of different strength of MS media in solid and liquid media on in vitro growth of Typhonium flagelliforme. Asian Pac. J. Trop. Biomed. 2017, 7, 151-156. [CrossRef] · DOI
- Dewir, Y.H.; Aldubai, A.A.; Kher, M.M.; Alsadon, A.A.; El-Hendawy, S.; Al-Suhaibani, N.A. Optimization of media formulation for axillary shoot multiplication of the red-peeled sweet potato (Ipomoea batatas [L.] Lam.) 'Abees. Chil. J. Agric. Res. 2020, 80, 3-10. [CrossRef] · DOI
- Dewir, Y.H.; El-Mahrouk, M.E.; Murthy, H.N.; Yoeup, H.P. Micropropagation of Cattleya: Improved in vitro rooting and acclimati- zation. Hortic. Environ. Biotechnol. 2015, 56, 89-93. [CrossRef] · DOI
- Nayak, N.R.; Rath, S.P.; Patnaik, S. In vitro propagation of three epiphytic orchids, Cymbidium aloifolium (L.) Sw., Dendrobium aphyllum (Roxb.), Fisch. and Dendrobium moschatum (Buch-Ham) Sw. through thidiazuron-induced high frequency shoot proliferation. Sci. Hortic. 1997, 71, 243-250. [CrossRef] · DOI
- Alghamdi, S.S.; Dewir, Y.H.; Khan, M.A.; Migdadi, H.; EL-Harty, E.H.; Aldubai, A.A.; Al-Aizari, A.A. Micropropagation and germplasm conservation of four chickpea (Cicer arietinum L.) genotypes. Chil. J. Agric. Res. 2020, 80, 487-495. [CrossRef] · DOI
- Hasançebi, S.; Kara, N.T.; Çakir, Ö.; Ari, Ş. Micropropagation and root culture of Turkish endemic Astragalus chrysochlorus (Leguminosae). Turk. J. Botany 2011, 35, 7. [CrossRef] · DOI
- Isutsa, D.K.; Pritts, M.P.; Mudge, K.W. A protocol for rooting and growing apple rootstock microshoots. Fruit Var. J. 1998, 52, 107-116.
- Dobránszki, J.; Magyar-Tábori, K.; Jámbor-Benczúr, E.; Lazányi, J.; Bubán, T.; Szalai, J. Influence of aromatic cytokinins on shoot multiplication and their post-effects on rooting of apple cv. Húsvéti rozmaring. Int. J. Hortic. Sci. 2000, 6, 84-87.
- Rescalvo-Morales, A.; Monja-Mio, K.; Robert, M.L.; Sánchez-Teyer, L.F. Telomere length in Agave tequilana Weber plants during the in vitro to ex vitro transition. Plant Cell Tissue Organ Cult. 2019, 136, 133-140. [CrossRef] · DOI
- Dev, R.; Singh, S.K.; Dayal, V.; Kumar, K.; Singh, T. Standardization of in vitro Hardening Strategies for Tissue Cultured Wine Grape (Vitis vinifera L) Genotypes. Int. J. Curr. Microbiol. App. Sci. 2019, 8, 2108-2117. [CrossRef] · DOI
- Teixeira da Silva, J.A.; Hossain, M.M.; Sharma, M.; Dobránszki, J.; Cardoso, J.C.; Songjun, Z. Acclimatization of in Vitro-derived Dendrobium. Hortic. Plant J. 2017, 3, 110-124. [CrossRef] · DOI
- Shah, S.; Thapa, B.B.; Chanda, K.; Pradhan, S.; Singh, A.; Varma, A.; Thakur, L.S.; Joshi, P.; Pant, B. Piriformospora indica promotes the growth of the in-vitro-raised Cymbidium aloifolium plantlet and their acclimatization. Plant Signal. Behav. 2019, 14, e1596716. [CrossRef] [PubMed] · DOI
- Cantabella, D.; Dolcet-Sanjuan, R.; Casanovas, M.; Solsona, C.; Torres, R.; Teixido, N. Inoculation of in vitro cultures with rhizosphere microorganisms improve plant development and acclimatization during immature embryo rescue in nectarine and pear breeding programs. Sci. Hortic. 2020, 273, 109643. [CrossRef] · DOI
- De Araújo, R.C.; Rodrigues, F.A.; Nadal, M.C.; Ribeiro, M.D.; Antonio, C.A.C.; Rodrigues, V.A.; de Souza, A.C.; Pasqual, M.; Doria, J. Acclimatization of Musa spp. seedlings using endophytic Bacillus spp. and Buttiauxella agrestis strains. Microbiol. Res. 2021, 248, 126750. [CrossRef] · DOI
- Hoang, N.N.; Kitaya, Y.; Shibuya, T.; Endo, R. Effects of supporting materials in in vitro acclimatization stage on ex vitro growth of wasabi plants. Sci. Hortic. 2020, 261, 109042. [CrossRef] · DOI
- Acquaah, G. Clonal propagation and in vitro culture. In Principles of Plant Genetics and Breeding, 2nd ed.; Acquaah, G., Ed.; John Wiley & Sons, Ltd.: Hoboken, NJ, USA, 2012; pp. 146-170.
- Jevremović, S.; Subotić, A.; Miljković, D.; Trifunović, M.; Petrić, M.; Cingel, A. Clonal fidelity of chrysanthemum cultivars after long term micropropagation by stem segment culture. VII International symposium on in vitro culture and horticultural breeding. Acta Hortic. 2012, 961, 211-216. [CrossRef] · DOI
- Chin, C.K.; Lee, Z.H.; Mubbarakh, S.A.; Antony, J.J.J.; Chew, B.L.; Subramaniam, S. Effects of plant growth regulators and activated charcoal on somaclonal variations of protocorm-like bodies (PLBs) of Dendrobium Sabin Blue orchid. Biocatal. Agric. Biotechnol. 2019, 22, 101426. [CrossRef] · DOI
- Bradaï, F.; Sánchez-Romero, C.; Martín, C. Somaclonal variation in olive (Olea europaea L.) plants regenerated via somatic embryogenesis: Influence of genotype and culture age on genetic stability. Sci. Hortic. 2019, 251, 260-266. [CrossRef] · DOI · Paper page
- Dhurve, L.; Kumar, A.; Bhaskar, J.; Sobhana, A.; Francies, R.M.; Mathew, D. Wide variability among the 'Mauritius' somaclones demonstrates somaclonal variation as a promising improvement strategy in pineapple (Ananas comosus L.). Plant Cell Tissue Organ Cult. 2021, 145, 701-705. [CrossRef] · DOI
- Noormohammadi, Z.; Habibollahi, H.; Farahani, F.; Sheidai, M. Molecular analysis of somaclonal variation in Linum usitatissimum and L. album. Plant Gene 2020, 24, 100261. [CrossRef] · DOI
- Solano, M.C.P.; Ruız, J.S.; Arnao, M.R.; Castro, O.C.; Tovar, M.E.G.; Bello, J.J.B. Evaluation of in vitro shoot multiplication and ISSR marker based assessment of somaclonal variants at different subcultures of vanilla (Vanilla planifolia Jacks). Physiol. Mol. Biol. Plants 2019, 25, 561-567. [CrossRef] [PubMed] · DOI
- Sreelekshmi, R.; Siril, E.A. Effective reversal of hyperhydricity leading to efficient micropropagation of Dianthus chinensis L. 3 Biotech 2021, 11, 95. [CrossRef] · DOI
- Gao, H.; Xia, X.; An, L.; Xin, X.; Liang, Y. Reversion of hyperhydricity in pink (Dianthus chinensis L.) plantlets by AgNO 3 and its associated mechanism during in vitro culture. Plant Sci. 2017, 254, 1-11. [CrossRef] · DOI
- Park, S.W.; Jeon, J.H.; Kim, H.S.; Park, Y.M.; Aswath, C.; Joung, H. Effect of sealed and vented gaseous microenvironments on the hyperhydricity of potato shoots in vitro. Sci. Hortic. 2004, 99, 199-205. [CrossRef] · DOI
- Gómez, C.; Ríos, D.; Sánchez-Olate, M. Effect of successive subculture on adventitious caulogenesis of Eucalyptus globulus. Bosque 2007, 28, 13-17. (In Spanish) [CrossRef] 100. Bayraktar, M.; Hayta-Smedley, S.; Unal, S.; Varol, N.; Gurel, A. Micropropagation and prevention of hyperhydricity in olive (Olea europaea L.) cultivar 'Gemlik'. S. Afr. J. Bot. 2020, 128, 264-273. [CrossRef] 101. · DOI
- Zárate-Salazar, J.R.; de Souza, L.M.; de Morais, M.B.; Neto, L.P.; Willadino, L.; Gouveia-Neto, A.; Ulisses, C. Light-emitting diodes and gas exchange facilitation minimize hyperhydricity in Lippia grata: Physiological, biochemical and morpho anatomical aspects. S. Afr. J. Bot. 2020, 135, 164-171. [CrossRef] 102. Sreelekshmi, R.; Siril, E.A.; Muthukrishnan, S. Role of Biogenic Silver Nanoparticles on Hyperhydricity Reversion in Dianthus chinensis L. an In Vitro Model Culture. J. Plant Growth Regul. 2021, 41, 23-39. [CrossRef] 103. Liu, M.; Jiang, F.; Kong, X.; Tian, J.; Wu, Z.; Wu, Z. Effects of multiple factors on hyperhydricity of Allium sativum L. Sci. Hortic. 2017, 217, 285-296. [CrossRef] 104. Franck, T.; Kevers, C.; Gaspar, T.; Dommes, J.; Deby, C.; Greimers, R.; Serteyn, D.; Deby-Dupont, G. Hyperhydricity of Prunus avium shoots cultured on gelrite: A controlled stress response. Plant Physiol. Biochem. 2004, 42, 519-527. [CrossRef] 105. Al-Mayahi, A.M.W.; Ali, A.H. Effects of different types of gelling agents on in vitro organogenesis and some physicochemical properties of date palm buds, Showathy cv. Folia Oecol. 2021, 48, 110-117. [CrossRef] 106. Quiala, E.; Jiménez-Tello, M.V.; Barbón, R.; Chávez, M.; de Feria, M.; La, O.M.; Pérez, M. Influence of 6-Benzyladenine and gelling agent on the reduction of hyperhydricity in Tectona grandis L. Rev. Colomb. Biotecnol. 2014, 16, 129. [CrossRef] 107. Ivanova, M.; van Staden, J. Influence of gelling agent and cytokinins on the control of hyperhydricity in Aloe polyphylla. Plant Cell Tissue Organ Cult. 2011, 104, 13-21. [CrossRef] 108. Sreelekshmi, R.; Siril, E.A. Influence of polyamines on hyperhydricity reversion and its associated mechanism during microprop- agation of China pink (Dianthus chinensis L.). Physiol. Mol. Biol. Plants 2020, 26, 2035-2045. [CrossRef] [PubMed] 109. · DOI
- Pence, V.C.; Finke, L.R.; Niedz, R.P. Evaluating a DOE screen to reduce hyperhydricity in the threatened plant, Cycladenia humilis var. jonesii. In Vitro Cell. Dev. Biol. Plant 2020, 56, 215-229. [CrossRef] 110. Gao, H.; Xu, D.; Zhang, H.; Cheng, X.; Yang, Q. Effects of culture medium composition and PEG on hyperhydricity in Dendrobium officinale. In Vitro Cell. Dev. Biol. Plant 2020, 56, 143-149. [CrossRef] 111. Surakshitha, N.C.; Soorianathasundaram, K.; Ganga, M.; Raveendran, M. Alleviating shoot tip necrosis during in vitro propagation of grape cv. Red Globe. Sci. Hortic. 2019, 248, 118-125. [CrossRef] 112. Kabylbekova, B.; Kovalchuk, I.; Mukhitdinova, Z.; Turdiyev, T.; Kairova, G.; Madiyeva, G.; Reed, B.M. Reduced major minerals and increased minor nutrients improve micropropagation in three apple cultivars. In Vitro Cell. Dev. Biol. Plant 2020, 56, 335-349. [CrossRef] 113. Al-Aizari, A.A.; Al-Obeed, R.S.; Mohamed, M.A.H. Improving micropropagation of some grape cultivars via boron, calcium and phosphate. Electron. J. Biotechnol. 2020, 48, 95-100. [CrossRef] 114. Nezami-Alanagh, E.; Garoosi, G.A.; Landín, M.; Gallego, P.P. Computer-based tools provide new insight into the key factors that cause physiological disorders of pistachio rootstocks cultured in vitro. Sci. Rep. 2019, 9, 9740. [CrossRef] [PubMed] 115. · DOI
- Cheong, E.J.; Na, M.; Jeong, U. The effect of endophytic bacteria on in vitro shoot growth of Prunus yedoensis and its identification and elimination. In Vitro Cell. Dev. Biol. Plant 2020, 56, 200-206. [CrossRef] 116. Thakur, M.; Sharma, V.; Luharch, R. Propagation of plum (Prunus salicina L.) cultivar Frontier in vitro through control of shoot tip necrosis (STN) and validation of genetic integrity using ISSR markers. Plant Physiol. Rep. 2021, 26, 238-246. [CrossRef] 117. Martin, K.P.; Zhang, C.L.; Slater, A.; Madassery, J. Control of shoot necrosis and plant death during micro-propagation of banana and plantains (Musa spp.). Plant Cell Tissue Organ Cult. 2007, 88, 51-59. [CrossRef] 118. Naaz, A.; Shahzad, A.; Anis, M. Effect of adenine sulphate interaction on growth and development of shoot regeneration and inhibition of shoot tip necrosis under in vitro condition in adult Syzygium cumini L.-A multipurpose tree. Appl. Biochem. Biotechnol. 2014, 173, 90-102. [CrossRef] 119. Park, J.S.; Naing, A.H.; Kim, C.K. Effects of ethylene on shoot initiation, leaf yellowing, and shoot tip necrosis in roses. Plant Cell Tissue Organ Cult. 2016, 127, 425-431. [CrossRef] 120. · DOI
- Kumari, M.; Clarke, H.J.; Small, I.; Siddique, K.H.M. Albinism in Plants: A Major Bottleneck in Wide Hybridization, Androgenesis and Doubled Haploid Culture. CRC Crit. Rev. Plant Sci. 2009, 28, 393-409. [CrossRef] 121. Isah, T. Changes in the biochemical parameters of albino, hyperhydric and normal green leaves of Caladium bicolor cv. "Bleeding hearts" in vitro long-term cultures. J. Photochem. Photobiol. B Biol. 2019, 191, 88-98. [CrossRef] [PubMed] 122. · DOI
- Sara, H.C.; René, G.H.; Rosa, U.C.; Angela, K.G.; Clelia, D.P. Agave angustifolia albino plantlets lose stomatal physiology function by changing the development of the stomatal complex due to a molecular disruption. Mol. Genet Genom. 2020, 295, 787-805. [CrossRef] [PubMed] 123. Zhao, P.K.; Wang, K.; Zhang, W.; Liu, H.Y.; Du, L.P.; Hu, H.R.; Ye, X.G. Comprehensive analysis of differently expressed genes and proteins in albino and green plantlets from a wheat anther culture. Biol. Plant. 2017, 61, 255-265. [CrossRef] 124. Harada, T.; Sato, T.; Asaka, D.; Matsukawa, I. Large-scale deletions of rice plastid DNA in anther culture. Theor. Appl. Genet. 1991, 81, 157-161. [CrossRef] [PubMed] 125. Yaronskaya, E.; Ziemann, V.; Walter, G.; Averina, N.; Borner, T.; Grimm, B. Metabolic control of the tetrapyrrole biosynthetic pathway for porphyrin distribution in the barley mutant albostrians. Plant J. 2003, 35, 512-522. [CrossRef] 126. Schmitz-Linneweber, C.; Williams-Carrier, R.E.; Williams-Voelker, P.M.; Kroeger, T.S.; Vichas, A.; Barkan, A. A pentatricopeptide repeat protein facilitates the trans-splicing of the maize chloroplast rps12 pre-mRNA. Plant Cell 2006, 18, 2650-2663. [CrossRef] 127. · DOI
- Day, A.; Ellis, T.H.N. Deleted forms of plastid DNA in albino plants from cereal anther culture. Curr. Genet. 1985, 9, 671-678. [CrossRef] 128. Dunford, R.; Walden, R. Plastid genome structure and plastid related transcript levels in albino barley plants derived from anther culture. Curr. Genet. 1991, 20, 339-347. [CrossRef] 129. Migneault, A.; Sandhu, H.; Per McCord, P.; Zhao, D.; Erickson, J. Albinism in Sugarcane: Significance, Research Gaps, and Potential Future Research Developments. Sugar Tech. 2019, 21, 536-541. [CrossRef] 130. Canonge, J.; Roby, C.; Hamon, C.; Potin, P.; Pfannschmidt, T.; Philippot, M. Occurrence of albinism during wheat androgenesis is correlated with repression of the key genes required for proper chloroplast biogenesis. Planta 2021, 254, 123. [CrossRef] [PubMed] 131. · DOI
- Jacquard, C.; Nolin, F.; Hecart, C.; Rashal, D.G.I.; Dhondt-Cordelier, S.; Rajbir, S.; Devaux, S.P.; Mazeyrat-Gourbeyre, F.; Clement, C. Microspore embryogenesis and programmed cell death in barley: Effects of copper on albinism in recalcitrant cultivars. Plant Cell Rep. 2009, 28, 1329-1339. [CrossRef] 132. · DOI
- Ćalić, D.; Bohanec, B.; Devrnja, N.; Milojević, J.; Tubić, L. Impact of abscisic acid in overcoming the problem of albinism in horse chestnut androgenic embryos. Trees 2013, 27, 755-762. [CrossRef] 133. Gailis, A.; Samsone, I.; Šēnhofa, S.; Girgžde, E.; Kāpostin , š, R.; Jansons, A. Silver birch (Betula pendula Roth.) culture initiation in vitro and genotype determined differences in micropropagation. New Forests 2021, 52, 791-806. [CrossRef] 134. Bonga, J.M.; Klimaszewska, K.K.; von Aderkas, P. Recalcitrance in clonal propagation, in particular of conifers. Plant Cell Tissue Organ Cult. 2010, 100, 241-254. [CrossRef] 135. Bonga, J.M. Can explant choice help resolve recalcitrance problems in in vitro propagation, a problem still acute especially for adult conifers? Trees 2017, 31, 781-789. [CrossRef] 136. Teixeira da Silva, J.A. The role of thin cell layers in regeneration and transformation in orchids. Plant Cell Tissue Organ Cult. 2013, 113, 149-161. [CrossRef] 137. Teixeira da Silva, J.A.; Dobranszki, J. Plant thin cell layers: A 40-year celebration. J. Plant Growth Regul. 2013, 32, 922-943. [CrossRef] 138. Parthibhan, S.; Rao, M.V.; Teixeira da Silva, J.A.; Kumar, T.S. Somatic embryogenesis from stem thin cell layers of Dendrobium aqueum. Biol. Plant. 2018, 62, 439-450. [CrossRef] 139. · DOI
- Bairwa, V.K.; Kachhwaha, S.; Kothari, S.L. Phloroglucinol Mediated Shoot Bud Elongation in Capsicum annuum L. Natl. Acad. Sci. Lett. 2012, 35, 331-335. [CrossRef] 140. Chen, Y.; Lin, S.; Duguid, S.; Dribnenki, P.; Kenaschuk, E. Effect of sucrose concentration on elongation of shoots from flax anther culture. Plant Cell Tissue Organ Cult. 2003, 72, 181-183. [CrossRef] 141. · DOI
- Dewir, Y.H.; Nurmansyah; Naidoo, Y.; Teixeira da Silva, J.A. Thidiazuron-induced abnormalities in plant tissue cultures. Plant Cell Rep. 2018, 37, 1451-1470. [CrossRef] [PubMed] 142. Ha, N.T.M.H.; Do, C.M.; Hoang, T.T.; Ngo, N.D.; Bui, L.V.; Nhut, D.T. The effect of cobalt and silver nanoparticles on overcoming leaf abscission and enhanced growth of rose (Rosa hybrida L. 'Baby Love') plantlets cultured in vitro. Plant Cell Tissue Organ Cult. 2020, 141, 393-405. [CrossRef] 143. Mahmoud, L.M.; Grosser, J.W.; Dutt, M. Silver compounds regulate leaf drop and improve in vitro regeneration from mature tissues of Australian finger lime (Citrus australasica). Plant Cell Tissue Organ Cult. 2020, 141, 455-464. [CrossRef] 144. Jin, J.; Essemine, J.; Duan, J.; Xie, Q.; Zhu, J.; Cai, W. Regeneration of active endogenous IAA in rice calli following acclimation to 2, 4 D free medium. Plant Growth Regul. 2021, 93, 203-220. [CrossRef] 145. Pischke, M.S.; Huttlin, E.L.; Hegeman, A.D.; Sussman, M.R. A Transcriptome-Based Characterization of Habituation in Plant Tissue Culture. Plant Physiol. 2006, 140, 1255-1278. [CrossRef] 146. Meins, F., Jr. Habituation: Heritable variation in the requirement of cultured plant cells for hormones. Annu. Rev. Genet 1989, 23, 395-408. [CrossRef] [PubMed] 147. Gautheret, G. Hétéro-auxine et cultures de tissues végétaux. Bull. Soc. Chim. Biol. 1942, 24, 13-47. 148. Jin, J.; Essemine, J.; Duan, J.; Zhu, J.; Cai, W. Rice calli may decelerate its metabolism to adapt hormone free medium. Plant Cell Tissue Organ Cult. 2021, 145, 223-238. [CrossRef] 149. Wikandari, R.; Manikharda; Baldermann, S.; Ningrum, A.; Taherzadeh, M.J. Application of cell culture technology and genetic engineering for production of future foods and crop improvement to strengthen food security. Bioengineered 2021, 12, 11305-11330. [CrossRef] 150. Sudheer, W.N.; Thiruvengadam, M.; Nagella, P. A comprehensive review on tissue culture studies and secondary metabolite production in Bacopa monnieri L. Pennell: A nootropic plant. Crit. Rev. Biotechnol. 2022, 12, 1-15. [CrossRef] [PubMed] 151. Srivastava, D.K.; Thakur, A.K.; Kumar, P. Agricultural Biotechnology: Latest Research and Trends; Springer: Singapore, 2021; pp. 1-36. [CrossRef] 152. Gupta, S.; Chaturvedi, P. Commercial Scale Tissue Culture for Horticulture and Plantation Crops; Springer: Singapore, 2022; pp. 1-21. [CrossRef] 153. Nhut, D.T.; Tung, H.T.; Yeung, E.C.-T. Plant Tissue Culture: New Techniques and Application in Horticultural Species of Tropical Region; Springer: Singapore, 2022; pp. 1-24. [CrossRef] 154. Moyo, M.; Bairu, M.W.; Amoo, S.O.; Van Staden, V. Plant biotechnology in South Africa: Micropropagation research endeavours, prospects and challenges. S. Afr. J. Bot. 2011, 77, 996-1011. [CrossRef] 155. Nithya, V.; Kamalam, M. Standardization of a protocol for micropropagation of Eupatorium glandulosum L. an important medicinal plant. Plant Cell Tissue Organ Cult. 2021, 146, 339-344. [CrossRef] 156. Rafiq, S.; Rather, Z.A.; Bhat, R.A.; Nazki, I.T.; AL-Harbi, M.S.; Banday, N.; Farooq, I.; Samra, B.N.; Khan, M.H.; Ahmed, A.F.; et al. Standardization of in vitro micropropagation procedure of Oriental Lilium Hybrid Cv. 'Ravenna'. Saudi J. Biol. Sci. 2021, 28, 7581-7587. [CrossRef] [PubMed] 157. Bhat, M.S.; Rather, Z.A.; Nazki, I.T.; Banday, N.; Wani, T.; Rafiq, S.; Farooq, I.; Noureldeen, A.; Darwish, H. Standardization of in vitro micropropagation of Winter Jasmine (Jasminum nudiflorum) using nodal explants. Saudi J. Biol. Sci. 2022, 29, 3425-3431. [CrossRef] [PubMed] · DOI
- Authors
- Abdalla, N., El-Ramady, H., Seliem, M. K., El-Mahrouk, M. E., Taha, N., Bayoumi, Y., Shalaby, T. A., & Dobránszki, J.
- Affiliations
- University of Debrecen (HU)
- Kafrelsheikh University (EG)
- Ornamental and Floriculture Department, Horticulture Research Institute, Antoniadis, Alexandria 21599, Egypt
- Agricultural Research Center (EG)
- Corresponding author
- Abdalla, Neama
- El-Ramady, Hassan
- ORCID
- Venue
- Horticulturae
- Publisher
- MDPI AG
- Published
- 2022-07-25
- Volume
- 8
- Issue
- 8
- Pages
- 677
- ISSN
- 2311-7524 (ISSN-L)
- OpenAlex
- W4287835779
- Cited by
- 177
- References
- 148
- Citations by year
- 2026: 40 · 2025: 72 · 2024: 34 · 2023: 27 · 2022: 4
- FWCI
- 11.18
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Horticulturae (publishedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Research, Development and Innovation Fund of Hungary (TKP2021-EGA-20, TKP2021-EGA, AK-00184-003/2021)
- Hungarian Tempus Public Foundation (TPF), Bilateral State Scholarships (TKP2021-EGA-20, TKP2021-EGA, AK-00184-003/2021)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant tissue culture and regeneration
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Flowering Plant Growth and Cultivation
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Growth and nutrition in plants
- Keywords
- micropropagation, tissue culture, contamination, browning, in vitro rooting, somaclonal variation, hyperhydricity, shoot tip necrosis, recalcitrance
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