Difference between revisions of "Part:BBa K2457004"

Revision as of 21:29, 1 November 2017 (view source) Giomaklouf (Talk | contribs) (→‎Characterization) ← Older edit		Revision as of 21:29, 1 November 2017 (view source) Giomaklouf (Talk | contribs) (→‎Characterization) Newer edit →
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	BBa_K2457000 was used by Amazonas_Brazil team in CROUT experiments and CRIN experiments.		BBa_K2457000 was used by Amazonas_Brazil team in CROUT experiments and CRIN experiments.
−	<p>CRIN (CRISPeasy-in method): Designed for knock-in strategy for bacterial genome editing based on CRISPR/Cas9</p>	+	CRIN (CRISPeasy-in method): Designed for knock-in strategy for bacterial genome editing based on CRISPR/Cas9</p>
	<p>RESULTADOS DE CRIN AQUI JU</p>		<p>RESULTADOS DE CRIN AQUI JU</p>

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Revision as of 21:29, 1 November 2017

Donor DNA for HDR into LacZ

BBa_K2457004 was engineered to be a building block of the standard BioBrick toolbox for bacterial genome: the ([http://2017.igem.org/Team:Amazonas_Brazil pCRISPeasy]). This BioBrick is the key part of the CRISPeasy-in (CRIN) framework, developed in 2017 by the Amazonas_Brazil team to make easier and accessible the genome editing based on CRISPR/Cas9. In this construction stays the gene of the template DNA that will be inserted in the edited genome. It's the first Registry vector for a Donor DNA.

Figure 1: BBa K2457004 circuit

Usage and Biology

Composed by the JK26 promoter, the coding sequence of the Green Fluorescent Protein (GFP) and the ilvBN terminator. It has 1810bp and was designed to contain two homologous arms with 300bp from the Operon Lac in the bacterial genome. Between the homologous arms, lies the GFP gene, flanked by NheI sites, allowing an RFC10 versatile one-step compatibility, the insertion of any other gene in GFP site. It has this structure especially for homology recognition by RecA enzyme which will break through the BioBrick to restore the cleaved sequence in the genome, having the aimed gene integrated.

Design

Characterization

BBa_K2457000 was used by Amazonas_Brazil team in CROUT experiments and CRIN experiments.

CRIN (CRISPeasy-in method): Designed for knock-in strategy for bacterial genome editing based on CRISPR/Cas9

RESULTADOS DE CRIN AQUI JU

Sequencing

Figure 2:Sequencing electropherogram from BBa_K2457004

Figure 3:Alignment of the designed sequence and our final construction from BBa_K2457004.

Sequence and Features</p>