Project

• Overview
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  • Post-Jamboree
• Human Practices
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  • Design
  • Killswitch
  • Regulation
  • Kill Genes
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• FRED
  • Toxin Sensing
  • Electroreporting
  • Modelling
  • Device Prototype
• OSCAR
  • Decarboxylation
  • Decatecholization
  • Flux Analysis
  • Bioreactor
  • Upgrading
  • Desulfurization
  • Denitrogenation
• Synergy
• References
• Attributions

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Background

When designing our actual kill genes, we needed to consider again the challenges of our environment. Many of the restriction enzymes found in the registry such as BamHI and Bgl2 are active only at temperatures around 37 C. Although our bioreactor may be at this temperature, the surrounding environment likely would not be. As the surrounding environment would be where our kill genes should be active, we needed to pick enzymes that would work at much lower temperatures. We also wanted enzymes that would cut very frequently in the E. Coli genome.

We ended up choosing genes for two novel kill enzyme: S7 micrococcal nuclease and CviAII. Both of these enzyme are active at very low temperatures (near 0 C). Through sequence analysis of the E. coli genome, we also determined that they cut extremely frequently in the genome, much more so than Bgl2 or BamHI even combined (figure 1).

S7 micrococcal nuclease

S7 nuclease is native to Staphylococcus aureus. S. aureus uses this enzyme to destroy extracellular DNA when it infects humans. S7 has both endo and exonuclease activity. This enzyme has a preference for -AT rich regions as opposed to -GC rich regions. However, this enzyme digests the DNA into <200 bp fragments. Ideally this enzyme will be present both intracellularly and extracellularly. We synthesized this enzyme from IDT. However this came with a mutation which altered a lysine residue to an isoleucine thereby making the enzyme dysfunctional.

CviAII restriction enzyme

CviAII is a restriction endonuclease that was sourced from the Chlorella virus PBCV-1 (Zhang et al., 1992). Our team selected this enzyme for three reasons. Firstly, this enzyme recognizes small, four-base pair restriction sites as opposed to other restriction enzymes such as the six-base cutter BamHI from the 2007 Berkely team (BBa_I716462). Henceforth, the CviAII restriction site is 16 times more prevalent in the E. coli genome and causes finer degradation of genetic material. Secondly, CviAII is able to cut Dam and Dcm methylated sites in the E. coli genome, and this decreased selectivity increases prevalence of cut sites.Finally, the temperature optimum for CviAII functionality is 23 degrees Celsius (Zhang et al., 1992). This optimum is closer to temperature conditions in the tailings ponds, and thus, CviAII will exhibit better enzyme activity as opposed to other enzymes in the registry with higher operating temperatures.

Nuclease assay: our nucleases versus those in the 2011 registry (BglII and BamHI):

In order to compare the S7 and CviAII to other nucleases in the 2011 registry, we used combinations of commercial enzymes from New England Biolabs against E. coli genomic preps. Please view the nuclease assay protocol. As shown in Figure one, S7 activity is extremely rapid and shows degradation at the zero time point. Following 45 minutes of incubation time, S7 and CviAII have chewed up the E. coli genome into small fragments whereas BamHI and BglII treated fragments are significantly larger. After 90 minutes, S7 and CviAII have sheared the genome into pieces <200 bp in size whereas there is no difference in the lanes with BglII and BamHI are similar to the 45 minutes time point.

Figure 1: This assay compares the enzymes present in the regitry i.e, BglII and BamHI to the enzymes added by us, S7 and CviAII. This shows that S7 and CviAII degrade the DNA much quicker than BglII and BamHI combined.