Crisper Technology in The Bacteria

Ahmed, Noor Maath; Dheeb, Batol Imran

doi:10.21608/eajbsg.2022.234958

Crisper Technology in The Bacteria

Document Type : Original Article

Authors

¹ Biology Department, College of Science, Tikrit University,

² Department of Pathological Analyses, College of Applied science, University of Samarra

10.21608/eajbsg.2022.234958

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