Optimization and presentation of a protocol for protoplast isolation, regeneration and gene transfer in potato
ObjectiveThe unique characteristics of plant protoplasts have made them a powerful tool for researchers to study the genetic modification of plant cells. The most important prerequisite for the use of protoplasts is the ability to extract them easily and in large quantities, and to cultivate and reg...
| Main Authors: | , , |
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| Format: | Article |
| Language: | fas |
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Shahid Bahonar University of Kerman
2022-09-01
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| Series: | مجله بیوتکنولوژی کشاورزی |
| Subjects: | |
| Online Access: | https://jab.uk.ac.ir/article_3438_e4d1bc928407bedb25d3adb39dd67e96.pdf |
| Summary: | ObjectiveThe unique characteristics of plant protoplasts have made them a powerful tool for researchers to study the genetic modification of plant cells. The most important prerequisite for the use of protoplasts is the ability to extract them easily and in large quantities, and to cultivate and regenerate them for cell colony formation and plant production. The most common method of extracting protoplasts from plant tissues is the enzymatic method. The concentration and composition of enzymes and isolation and culture steps are key factors in protoplast extraction. This study aimed to investigate the effect of these factors on protoplasts of in vitro potatoes (Solanum tuberosum L.) and to develop an efficient and suitable method for their extraction, transfection, callus formation, and regeneration. Materials and methodsFor protoplast isolation from commercial and common Agria cultivars of potato, different treatments of Cellulase and Macerozyme enzymes concentration, incubation time in an enzyme solution, and isolation steps on leaf tissue, stem, and aerial part of in vitro plantlets were investigated. The effects of different hormone concentrations on the culture and regeneration of protoplasts were studied. After protoplast isolation, the efficiency of transfection by PEG 4000 using pBin61-GFP plasmid was evaluated. ResultsThe best results were obtained from leaf explants and the highest number of protoplasts (2×106 protoplasts per ml) were extracted from leaf mesophilic tissues after 16 hours incubation in an enzyme solution (1% Cellulase and 0.2% Macerozyme). The transfection efficiency of protoplasts by PEG with 40% concentration and duration of 30 minutes was 50%. The MS medium containing 5 mg/L NAA and 0.1 mg/L BAP was selected as the best culture medium for callus induction. In this hormonal treatment, 100% of callus induction from protoplasts was obtained after about one month. The best medium for plant regeneration and shooting from callus was the combination of 2 mg/L Zeatin with 0.1 mg/L GA3 and 0.01 mg/L NAA with 86% efficiency. ConclusionsBased on the results, the described protocol for protoplast extraction and gene transfer in this study provides the necessary steps for genetic engineering, transformation, and gene expression in the potato plant. |
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| ISSN: | 2228-6705 2228-6500 |