Programmable site-specific nucleases, such because the clustered often interspaced brief palindromic repeat (CRISPR)/ CRISPR-associated protein 9 (Cas9) ribonucleoproteins (RNPs), have allowed creation of priceless knockout mutations and focused gene modifications in Chlamydomonas (Chlamydomonas reinhardtii). Nonetheless, in walled strains, current strategies for modifying genes missing a selectable phenotype contain co-transfection of RNPs and exogenous double-stranded DNA (dsDNA) encoding […]
