2022
DOI: 10.1007/978-1-0716-2233-9_16
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Genome Editing with Cas9 in Lactobacilli

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Cited by 4 publications
(4 citation statements)
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“…The number of people that are being suppressed is smaller. (24) Austin Burt described a sophisticated method using gene driving forces behind genes that only result in death or sterility when both versions are destroyed. When present, these 'genetic load' causes would spread quickly among slightly handicapped heterozygotes and ultimately contribute to a demographic collapse or perhaps extinction as a result of the accumulating burden of regressive genes.…”
Section: Engineered Gene Drivesmentioning
confidence: 99%
See 1 more Smart Citation
“…The number of people that are being suppressed is smaller. (24) Austin Burt described a sophisticated method using gene driving forces behind genes that only result in death or sterility when both versions are destroyed. When present, these 'genetic load' causes would spread quickly among slightly handicapped heterozygotes and ultimately contribute to a demographic collapse or perhaps extinction as a result of the accumulating burden of regressive genes.…”
Section: Engineered Gene Drivesmentioning
confidence: 99%
“…Surprisingly, a single guide RIBONUCLEIC ACID (sgRIBONUCLEIC ACID) of less than 100 base pairings in sequence can instruct CRISPR to cut a particular protospacer in the genome. (24) This instruction RIBONUCLEIC ACID must start with a spacers segment made up of 17-20 base pairs that are equal to the desired gene. Selecting protospacers inside the desired gene, creating one or more guide RIBONUCLEIC ACIDs with compatible separators, and sending CRISPR, those guide RIBONUCLEIC ACIDs, and altered repaired templates devoid of those protospacers into a cell are the steps in the procedure for editing (Figure 3).…”
Section: Genome Editing Using Ribonucleic Acid Guidance Using the Cri...mentioning
confidence: 99%
“…Vento et al utilized two E. coli - Lactobacilli shuttle vectors: one containing SpCas9, tracrRNA, and single spacer CRISPR array; the other containing a dsDNA recombinant engineering template [ 69 ]. L. plantarum was transformed with an E. coli - Lactobacillus shuttle vector carrying a recombineering template (RT) and homologous arm (HA), and L. plantarum was edited using this technique.…”
Section: Development Of Crispr/cas9-based Genome Editing In ...mentioning
confidence: 99%
“…However, dsDNA recombineering assisted by CRISPR/Cas9 was less effective in producing point mutations than ssDNA recombineering. Vento et al used two Escherichia coli-Lactobacilli shuttle vectors to perform genome editing in L. plantarum based on CRISPR/Cas9-mediated dsDNA recombineering (Vento and Beisel 2022). One vector expressed SpCas9, a single spacer CRISPR array, and tracrRNA, and the other vector contained a dsDNA editing template and homologous arm.…”
Section: Crispr/cas9-assisted Dsdna Recombineeringmentioning
confidence: 99%