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dc.contributor.authorAsande, Lydia K.
dc.contributor.authorOmwoyo, Richard O.
dc.contributor.authorOduor, Richard O.
dc.contributor.authorNyaboga, Evans N.
dc.date.accessioned2024-01-29T13:17:28Z
dc.date.available2024-01-29T13:17:28Z
dc.date.issued2020
dc.identifier.citationAsande, L. K., Omwoyo, R. O., Oduor, R. O., & Nyaboga, E. N. (2020). A simple and fast Agrobacterium-mediated transformation system for passion fruit KPF4 (Passiflora edulis f. edulis× Passiflora edulis f. flavicarpa). Plant Methods, 16, 1-12.en_US
dc.identifier.otherhttps://doi.org/10.1186/s13007-020-00684-4
dc.identifier.urihttps://ir-library.ku.ac.ke/handle/123456789/27321
dc.descriptionArticleen_US
dc.description.abstractAbstract Background: Passion fruit (Passifora edulis Sims) is an important horticultural crop in the tropics and subtropics, where it has great commercial potential due to high demand for fresh edible fruits and processed juice as well as source of raw materials in cosmetic industries. Genetic engineering shows great potential in passion fruit improvement and can compensate for the limitations of conventional breeding. Despite the success achieved in genetic modifcation of few passion fruit varieties, transgenic passion fruit production is still difcult for farmer-preferred cultivars. Therefore, it is important to establish a simple and fast Agrobacterium-mediated cell transformation of commercial hybrid passion fruit KPF4 (Passifora edulis f. edulis×Passifora edulis f. favicarpa). Results: In the present study, we have developed a simple and fast Agrobacterium-mediated transformation system for hybrid passion fruit KPF4 using leaf disc explants. Factors afecting the rate of transient beta (β)-glucuronidase (gusA) expression and consequently transformation efciency were optimized as follows: Agrobacterium cell density with an OD600 of 0.5, 30 min infection time, 3 days of co-cultivation duration and the incorporation of 200 µM acetosyringone into Agrobacterium infection suspension medium. Using the optimized conditions, transgenic plants of KPF4 were produced within 2 months with an average transformation efciency of 0.67%. The β-glucuronidase (GUS) histochemical staining confrmed the expression and integration of an intron-containing gusA gene into transformed leaf discs and transgenic plant lines of KPF4. The presence of gusA gene in the transgenic plants was confrmed by polymerase chain reaction (PCR). The results confrmed that the gusA gene was efciently integrated into the passion fruit genome. Conclusions: The developed transformation protocol is simple and rapid and could be useful for functional genomic studies and transferring agronomically important traits into passion fruit hybrid KPF4. This study developed a method that can be used to transfer traits such as resistance to viral diseases, low fruit quality and short storage life. To the best of our knowledge, this is the frst report on genetic transformation system for commercial passion fruit hybrid KPF4.en_US
dc.description.sponsorshipNational Research Fund of Kenya ten_US
dc.language.isoenen_US
dc.publisherSpringer Natureen_US
dc.subjectPassifora edulis Simsen_US
dc.subjectAgrobacterium-mediated transformationen_US
dc.subjectTransient gusA expression,en_US
dc.subjectTransformation efciencyen_US
dc.titleA simple and fast Agrobacterium-mediated transformation system for passion fruit KPF4 (Passifora edulis f. edulis×Passifora edulis f. favicarpa)en_US
dc.typeArticleen_US


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