A simple and fastAgrobacterium-mediated transformation system for passion fruit KPF4 (Passiflora edulisf.edulis x Passiflora edulisf.flavicarpa)

被引:21
作者
Asande, Lydia K. [1 ,2 ]
Omwoyo, Richard O. [1 ]
Oduor, Richard O. [3 ]
Nyaboga, Evans N. [2 ]
机构
[1] Kenyatta Univ, Dept Plant Sci, POB 43844-00100, Nairobi 00100, Kenya
[2] Univ Nairobi, Dept Biochem, POB 30197-00100, Nairobi, Kenya
[3] Kenyatta Univ, Dept Biochem & Biotechnol, POB 43844-00100, Nairobi, Kenya
关键词
Passiflora edulisSims; Agrobacterium-mediated transformation; TransientgusA expression; Transformation efficiency; TRITICUM-AESTIVUM L; GENETIC-TRANSFORMATION; AGROBACTERIUM-TUMEFACIENS; HIGH-EFFICIENCY; OPTIMIZATION; REGENERATION; GLUCURONIDASE; RESISTANCE; EXPLANTS; PLANTS;
D O I
10.1186/s13007-020-00684-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background Passion fruit (Passiflora edulisSims) 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 modification of few passion fruit varieties, transgenic passion fruit production is still difficult for farmer-preferred cultivars. Therefore, it is important to establish a simple and fastAgrobacterium-mediated cell transformation of commercial hybrid passion fruit KPF4 (Passiflora edulisf.edulis x Passiflora edulisf.flavicarpa). Results In the present study, we have developed a simple and fastAgrobacterium-mediated transformation system for hybrid passion fruit KPF4 using leaf disc explants. Factors affecting the rate of transient beta (beta)-glucuronidase (gusA) expression and consequently transformation efficiency were optimized as follows:Agrobacteriumcell density with an OD(600)of 0.5, 30 min infection time, 3 days of co-cultivation duration and the incorporation of 200 mu M acetosyringone intoAgrobacteriuminfection suspension medium. Using the optimized conditions, transgenic plants of KPF4 were produced within 2 months with an average transformation efficiency of 0.67%. The beta-glucuronidase (GUS) histochemical staining confirmed the expression and integration of an intron-containinggusA gene into transformed leaf discs and transgenic plant lines of KPF4. The presence ofgusA gene in the transgenic plants was confirmed by polymerase chain reaction (PCR). The results confirmed that thegusA gene was efficiently 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 first report on genetic transformation system for commercial passion fruit hybrid KPF4.
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页数:12
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