An effective method for Agrobacterium tumefaciens-mediated transformation of Jatropha curcas L. using cotyledon explants

References

• Ha J, Shim S, Lee T, et al. Genome sequence of Jatropha curcas L., a non-edible biodiesel plant, provides a resource to improve seed-related traits. Plant Biotechnol J. 2019;17(2):517–530.
   PubMed Web of Science ®Google Scholar
• Menezes RG, Rao NG, Karanth SS, et al. Jatropha curcas poisoning. Indian J Pediatr. 2005;72(1):75–76.
   Google Scholar
• Adebowale KO, Adedire CO. Chemical composition and insecticidal properties of the underutilized Jatropha curcas seed oil. Afr J Biotechnol. 2006;5(10):901–906.
   Google Scholar
• Ghosh A, Chaudhary DR, Reddy MP, et al. Prospects for Jatropha methyl ester (biodiesel) in India. Int J Environ Stud. 2007;64(6):659–674.
   Google Scholar
• Wu PZ, Zhou CP, Cheng SF, et al. Integrated genome sequence and linkage map of physic nut (Jatropha curcas L.), a biodiesel plant. Plant J. 2015;81(5):810–821.
   PubMed Web of Science ®Google Scholar
• Novatiano C, Pancoro A, Marwani E. Agrobacterium tumefaciens-mediated transformation of Jatropha curcas L. with a polyhydroxyalkanoate gene (phaC). Indones J Biotechnol. 2018;22(2):61–67.
   Google Scholar
• Fufa H, Tesema M, Daksa J. In vitro regeneration protocol through direct organogenesis for Jatropha curcas L. (Euphorbiaceae) accessions in Ethiopia. Afr J Biotechnol. 2019;18(31):991–1003.
   Google Scholar
• El-Sayed M, Aly UI, Mohamed MS, et al. In vitro regeneration and molecular characterization of Jatropha curcas plant. B Nat Res Centre. 2020;44(1):1–12.
   Google Scholar
• Liu Y, Yu L, Zhan Q, et al. High concentration short duration treatment of benzyladenine stimulates adventitious bud regeneration from hypocotyl explants in soybean. Adv Mater Res. 2013;647(1):331–335.
   Google Scholar
• Liu Y, Tong X, Hui WK, et al. Efficient culture protocol for plant regeneration from petiole explants of physiologically mature trees of Jatropha curcas L. Biotechnol Biotec Eq. 2015;29(3):479–488.
   Web of Science ®Google Scholar
• Liu Y, Yin XG, Lu JN, et al. An efficient protocol for inducing regeneration in physic nut (Jatropha curcas L.). Bangl J Bot. 2016;45(4):87–93.
   Web of Science ®Google Scholar
• Li MR, Li HQ, Jiang HW, et al. Establishment of an Agrobacteriuim-mediated cotyledon disc transformation method for Jatropha curcas. Plant Cell Tiss Org. 2008;92(2):173–181.
   Web of Science ®Google Scholar
• Pan JL, Fu QT, Xu ZF. Agrobacterium tumefaciens-mediated transformation of biofuel plant Jatropha curcas using kanamycin selection. Afr J Biotechnol. 2010;9(39):6477–6481.
   Google Scholar
• Misra P, Toppo DD, Mishra MK, et al. Agrobacterium tumefaciens-mediated transformation protocol of Jatropha curcas L. using leaf and hypocotyl segments. J Plant Biochem Biotechnol. 2012;21(1):128–133.
   Web of Science ®Google Scholar
• Qu J, Mao HZ, Chen W, et al. Development of marker-free transgenic Jatropha plants with increased levels of seed oleic acid. Biotechnol Biofuels. 2012;5(1):1–11.
   PubMedGoogle Scholar
• Fu Q, Li C, Tang M, et al. An efficient protocol for Agrobacterium-mediated transformation of the biofuel plant Jatropha curcas, by optimizing kanamycin concentration and duration of delayed selection. Plant Biotechnol Rep. 2015;9(6):405–416.
   PubMed Web of Science ®Google Scholar
• Murashige T, Skoog F. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant. 1962;15(3):473–479.
   Web of Science ®Google Scholar
• Khemkladngoen N, Cartagena J, Shibagaki N, et al. Adventitious shoot regeneration from juvenile cotyledons of a biodiesel producing plant Jatropha curcas L. J Biosci Bioeng. 2011;111(1):67–70.
   PubMed Web of Science ®Google Scholar
• Kumar N, Reddy MP. Thidiazuron (TDZ) induced plant regeneration from cotyledonary petiole explants of elite genotypes of Jatropha curcas: a candidate biodiesel plant. Ind Crop Prod. 2012;39(1):62–68.
   Google Scholar
• Jefferson RA. Assaying chimeric genes in plants: the GUS gene fusion system. Plant Mol Biol Rep. 1987;5(4):387–405.
   Google Scholar
• Hofgen R, Willmitzer L. Storage of competent cells for Agrobacterium transformation. Nucleic Acids Res. 1988;16(20):9877.
   PubMed Web of Science ®Google Scholar
• Khemkladngoen N, Cartagena JA, Fukui K. Physical wounding-assisted Agrobacterium-mediated transformation of juvenile cotyledons of a biodiesel-producing plant, Jatropha curcas L. Plant Biotechnol Rep. 2011;5(3):235–243.
   Web of Science ®Google Scholar
• Li YH, Yang YQ, Liu Y, et al. Overexpression of OsAGO1b induces adaxially rolled leaves by affecting leaf abaxial sclerenchymatous cell development in rice. Rice. 2019;12(1):1–22.
   PubMed Web of Science ®Google Scholar
• Rohela GK, Jogam P, Bylla P, et al. Indirect regeneration and assessment of genetic fidelity of acclimated plantlets by SCoT, ISSR, and RAPD markers in Rauwolfia tetraphylla L.: an endangered medicinal plant. BioMed Res Int. 2019;2019(1):1–14.
   Google Scholar
• Savitikadi P, Jogam P, Rohela GK, et al. Direct regeneration and genetic fidelity analysis of regenerated plants of Andrographis echioides (L.) - An important medicinal plant. Ind Crop Prod. 2020;155(1):112766.
   Google Scholar
• Wei Q, Lu WD, Liao Y, et al. Plant regeneration from epicotyl explant of Jatropha curcas. J Plant Physiol Mol Biol. 2004;30(4):475–478.
   PubMedGoogle Scholar
• Jaganath B, Subramanyam K, Mayavan S, et al. An efficient in planta transformation of Jatropha curcas (L.) and multiplication of transformed plants through in vivo grafting. Protoplasma. 2014;251(3):591–601.
   PubMed Web of Science ®Google Scholar
• Macan GPF, Cardoso JC. In vitro grafting of Psidium guajava in Psidium cattleianum for the management of the Meloidogyne enterolobii. Int J Fruit Sci. 2019;20(2):106–116.
   Google Scholar
• Pahnekolayi MD, Tehranifar A, Samiei L, et al. Optimizing culture medium ingredients and micrografting devices can promote in vitro micrografting of cut roses on different rootstocks. Plant Cell Tiss Org. 2019;137(5):265–274.
   Google Scholar
• Jin SX, Liang SG, Zhang XL, et al. An efficient grafting system for transgenic plant recovery in cotton (Gossypium hirsutum L.). Plant Cell Tiss Org. 2006;85(2):181–185.
   Web of Science ®Google Scholar
• Borchetia S, Das SC, Handique PJ, et al. High multiplication frequency and genetic stability for commercialization of the three varieties of micropropagated tea plants (Camellia spp.). Sci Hortic. 2009;120(4):544–550.
   Web of Science ®Google Scholar
• Kumar N, Anand KG, Reddy MP. In vitro regeneration from petiole explants of non-toxic Jatropha curcas. Ind Crop Prod. 2011;33(1):146–151.
   Web of Science ®Google Scholar
• Hlozáková TK, Polóniová Z, Moravíková J. Feasibility of hygromycin as a selection agent in Agrobacterium-mediated transformation of oilseed rape (Brassica napus L.). J Microbiol Biotechnol Food. 2018;3(2):80–83.
   Google Scholar
• Yang X, Yu X, Zhou Z, et al. A high-efficiency Agrobacterium tumefaciens mediated transformation system using cotyledonary node as explants in soybean (Glycine max L.). Acta Physiol Plant. 2016;38(3):1–10.
   Web of Science ®Google Scholar
• De Vetten N, Wolters AA, Raemakers K, et al. A transformation method for obtaining marker-free plants of a cross-pollinating and vegetatively propagated crop. Nat Biotechnol. 2003;21(4):439–442.
   PubMed Web of Science ®Google Scholar
• Woo HJ, Qin Y, Park SY, et al. Development of selectable marker-free transgenic rice plants with enhanced seed tocopherol content through FLP/FRT-mediated spontaneous auto-excision. PLoS One. 2015;10(7):e0132667.
   PubMed Web of Science ®Google Scholar
• Guo WC, Wang ZA, Luo XL, et al. Development of selectable marker-free transgenic potato plants expressing cry3A against the Colorado potato beetle (Leptinotarsa decemlineata Say). Pest Manag Sci. 2016;72(3):497–504.
   PubMed Web of Science ®Google Scholar
• Costa LD, Piazza S, Campa M, et al. Efficient heat-shock removal of the selectable marker gene in genetically modified grapevine. Plant Cell Tiss Org. 2016;124(1):471–481.
   Google Scholar