Tissue Culture Optimization and Construction of a Suitable Vector for Engineering Very Long-Chain Fatty Acids in Camelina sativa L.
نویسندگان
1 Agricultural Biotechnology Department, Faculty of Agriculture, Azarbaijan Shahid Madani University, Tabriz, Iran
2 Agricultural Biotechnology Department, Faculty of Agriculture, Azarbaijan Shahid Madani University, Tabriz, Iran
3 Department of Plant, Cell and Molecular Biology, Faculty of Natural Science, University of Tabriz, Tabriz, Iran
4 Department of Horticultural Sciences, University of Tabriz, Tabriz, Iran
doi
10.22126/atic.2026.11724.1193چکیده
Oil quality from oilseeds is determined by the fatty acid (FA) content. Fatty Acid Elongase 1 (FAE1) is an essential FA gene that has been genetically modified to change the constitution of fatty acids in oilseed plants. In this study, recombinant vector construction for genome editing of the CsFAE1B, CsFAE1A, and CsFAE1C genes using CRISPR/Cas9 was used to improve the quality of Camelina Sativa oil (which contains about 50% oil and 4% erucic acid). Additionally, camelina tissue culture optimization for recombinant vector transfer was performed concurrently. Finally, gRNA was designed to target three copies of the CsFAE1 genes, and after transfer to the pFGC-pcoCas9 vector, the recombinant vector was confirmed by PCR and enzymatic digestion. The tissue culture optimization results indicated that hormone ratios of 0.5 mg L-1 NAA and 3 mg L-1 BAP for cotyledon and hypocotyl in the Gamborg medium induced embryogenic calluses three weeks after cultivation. Additionally, hormone ratios of 0.5 NAA, 2 BAP, and 1 (mg L-1) Kin led to direct regeneration in cotyledon explants. In future studies, tissue culture optimization and recombinant vector construction for genome editing of FAEs genes could improve oil quality with the genetic transformation of camelina.
