Crisper Technology in The Bacteria | ||||
| Egyptian Academic Journal of Biological Sciences, G. Microbiology | ||||
| Article 13, Volume 14, Issue 1, June 2022, Page 155-162 PDF (594.82 K) | ||||
| Document Type: Original Article | ||||
| DOI: 10.21608/eajbsg.2022.234958 | ||||
 View on SCiNiTO | ||||
| Authors | ||||
| Noor Maath Ahmed1; Batol Imran Dheeb2 | ||||
| 1Biology Department, College of Science, Tikrit University, | ||||
| 2Department of Pathological Analyses, College of Applied science, University of Samarra | ||||
| Abstract | ||||
| In minuscule life forms, CRISPR-Cas9 structures work as an adaptable enemy of bacterial bacteriophage reactions. After ailment, Cas1 and Cas2 work as spacers inside the bacterial CRISPR locus, meddling with the union of short famous genome progressions (Phase 1). During re-receptiveness, the CRISPR locus, along with tracrRNA, is passed on as pre-crRNA (Phase 2). The pre-crRNA is changed over to gRNAs, which join the Cas9 ribonucleoprotein and lead it to explicit regions in the assaulting bacteriophage genome, bringing about Cas9-interceded cleavage. From "CRISPR-Cas9 Adaptive Immune System of Streptococcus pyogenes Against Bacteriophages," "CRISPR-Cas9 Adaptive Immune System of Streptococcus pyogenes Against Bacteriophages" was republished | ||||
| Keywords | ||||
| Crisper Technology; Bacteria; patients; DNA ligase; unfamiliar DNA opposition; variation; impedance; genome composing; development | ||||
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