Silver and Magnetic Iron Oxide Nanoparticles-Assisted PCR for the Phytopathogenic Bacteria Ralstonia solanacearum | ||||
| Journal of Plant Protection and Pathology | ||||
| Article 8, Volume 10, Issue 9, September 2019, Page 471-476 PDF (931.83 K) | ||||
| Document Type: Original Article | ||||
| DOI: 10.21608/jppp.2019.63659 | ||||
 View on SCiNiTO | ||||
| Authors | ||||
T. Shoala  1; Rabab M. Abd-El-Aziz2
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| 1Environmental Biotechnology Department, College of Biotechnology, Misr University for Science and Technology, Al-Motamayez District - 6th of October, Egypt | ||||
| 2Plant Bacterial Disease Research Department, Plant Pathology Research Institute, Agricultural Research Center, Giza, Egypt | ||||
| Abstract | ||||
| Nanotechnology became an integrated science in different fields. Integration between nanoscience and molecular diagnosis could enhance the early diagnosis of different pathogens. Enhancement of different molecular techniques by using nanomaterials increases the specificity, sensitivity and application of these techniques in biology. Polymerase chain reaction (PCR) is considered as one of the main basic molecular techniques that could be enhanced by using nanomaterials. Silver (Ag) and magnetic iron oxide (Fe2O3) nanoparticles were chemically synthesized and characterized by using transmission electron microscope (TEM) according to standard protocol. The sizes of Ag and magnetic Fe2O3 nanoparticles were ∼15-20 and ~12-23 nm diameters respectively. DNA template of Ralstonia solanacearum was extracted by using Ag and magnetic Fe2O3 nanoparticles separately and in mixture of both nanomaterials in addition to the control. Extraction of DNA template by using combined nanomaterials increased the DNA yield followed by significant augmentation of the PCR efficacy for small concentration of bacterial DNA template. Inspections of the mechanism of such PCR augmentation suggested an indication of quick transfer of heat in the presence of Ag and magnetic Fe2O3 nanoparticles. Silver and magnetic Fe2O3 nanoparticles-supported PCR could be applicable for reducing the total PCR cycles and enhancing the augmentation of DNA amplicons from a diversity of samples, as well as GC-rich patterns (such as the bacterial genome of R. solanacearum) that are frequently observed to yield disappointing results. | ||||
| Keywords | ||||
| silver; Magnetic; Iron Oxide; Nanoparticles; PCR; Ralstonia solanacearum | ||||
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