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<p> <b>FIGURE 1:</b> 12% SDS-PAGE gel showing strong expression of a protein of approximately 163 kDa in the sample that was induced with 1% arabinose for three hours at 37°C. Consistent with Cas9 expression. No corresponding band found in the uninduced control. </p> | <p> <b>FIGURE 1:</b> 12% SDS-PAGE gel showing strong expression of a protein of approximately 163 kDa in the sample that was induced with 1% arabinose for three hours at 37°C. Consistent with Cas9 expression. No corresponding band found in the uninduced control. </p> | ||
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| + | =='''T4 Phage infection by British Columbia 2013 '''== | ||
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<img src="https://static.igem.org/mediawiki/2013/9/98/Growth_Curves.jpg"></img> | <img src="https://static.igem.org/mediawiki/2013/9/98/Growth_Curves.jpg"></img> | ||
Revision as of 03:15, 28 September 2013
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Applications of BBa_K1129006
CRISPRs (Clustered Regularly Interspaced Short Palindromic Repeats) are loci found in some bacterial and archaeal genomes that, together with associated Cas (CRISPR-associated) genes function as an adaptive immune system in prokaryotes. While the details of immunity-conferring “spacer” sequence acquisition are still being worked out, it is known that exogenous DNA is processed by Cas proteins into short (~30 base) sequences that are adjacent to the Protospacer Adjacent Motif (PAM) site. These short pieces of DNA are then incorporated into the host genome between repeat sequences to form the spacer elements. The repeat-spacer-repeat array is constitutively expressed (pre-CRISPR RNAs, pre-crRNAs) and processed by Cas proteins to form small RNAs (crRNAs). The small RNAs are then loaded into Cas proteins and guide them to initiate the sequence-specific cleavage of the target sequence (or the protospacer)
SDS-PAGE Protein Expression of Cas9 by British Columbia iGEM 2013
The Cas9 construct was transformed into E. cloni® 10G, plated on LB agar plates made with chloramphenicol (33ug/mL), and grown overnight at 37°C.
A single colony was picked and grown overnight in LB (with chloramphenicol) at 30C and shaking (1000 rpm). Growth was very slow for the Cas9 culture and OD was only ~0.6 in the morning. Several aliquots of 175 uL were taken and placed in separate wells of a 96-well plate. They were induced with varying concentrations of arabinose (0, 0.5%, 1%, and 2%) for three hours at 37°C and 1000 rpm.
OD was measured and it was determined that there was a tradeoff between induction concentration and growth. The highest induction concentration that also had relatively good growth was 1% arabinose (OD=1.17 vs 0.98 for 2% induction and 1.67 for non-induced). This culture and the non-induced control was collected, centrifuged, resuspended in SDS-PAGE loading buffer, and boiled for 10 minutes. They were loaded in a 12% gel and run at 150V for 1 hour and 10 minutes.
The gels were stained with InstantBlue overnight and destained with water for several hours.
There is a large, dark band in the Cas9 lane at the approximate size of Cas9 (163 kDa) that is not present in the uninduced control (Figure 1). This would be consistent with the successful expression of the Cas9 protein.
FIGURE 1: 12% SDS-PAGE gel showing strong expression of a protein of approximately 163 kDa in the sample that was induced with 1% arabinose for three hours at 37°C. Consistent with Cas9 expression. No corresponding band found in the uninduced control.
T4 Phage infection by British Columbia 2013
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