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We have submitted two new parts to the registry and further characterised an existing part.
pT7- E. coli optimised - KillerRed (EOKR)
KillerRed is a red fluorescent protein that generates reactive oxygen species after illumination with light between the wavelengths of 540-580nm[1].
We further characterised this kill switch by illuminating induced cultures 24 hours after induction with IPTG as well as uninduced cultures. After 6 hours in the light box CFU’s were counted to determine if the kill switch was successful. This was also reproduced on cultures grown in a ministat for 120 and 168 hours to test how long the kill switch remains functional. The full protocol can be found here and the results can be found here.
The mechanism by which KillerRed kills cells isn’t fully understood yet
Here we are submitting KillerRed as a composite part under a T7 promoter (code), an Elowitz ribosome binding site (BBa_B0034) and a double terminator (BBa_B0015).
The sequence for KillerRed protein coding region can be found here (BBa_K1141002)
BBa_K1914003
pT7- E. coli optimised - KillerOrange (EOKO)
KillerOrange is a mutant of the fluorescent protein KillerRed (BBa_K1141002, BBa_K1491015) activated by blue and green light. It carries a tryptophan-based chromophore that is novel for photosensitizers [2].
KillerOrange has an excitation maximum of 512 nm and emission maximum at 555 nm and its absorbance spectrum has two peaks, at 455 and 514 nm.
It is believed that was confers KillerOrange's ability to generate reactive oxygen species depends on a water-filler channel reaching the chromophore area from the end cap of the β-barrel [3].
The mechanism by which KillerOrange kills cells isn’t fully understood yet[3].
We characterised this part in the same way as KillerRed (protocol), and the results of which can be found here
Here we are submitting KillerOrange as a composite part under a T7 promoter (code), an Elowitz ribosome binding site (BBa_B0034) and a double terminator (BBa_B0015).
The sequence for KillerOrange protein coding region can be found here (BBa_K1914000)
BBa_K1914001
LysozymeC
Lysozyme C from chicken egg white, attacks the cell wall in bacteria by hydrolysing the β-1,4 linkages between N-acetylmuramic acid and N-acetylglucosamine of peptidoglycan [4].
We are submitting this Lysozyme C as a composite part under a T7 promoter, an Elowitz ribosome binding site (biobrick code) and a double terminator (BBa_B0015). We have codon optimised the protein coding region, added a FLAG tag and signal peptide directing Lysozyme to the periplasm. The sequence for just Lysozyme C can be found here (biobrick code).
Characterisation of this part involved using the Enzcheck assay kit which detects lysozyme activity as a measure of fluorescence as well as using the same protocol we used to characterise KillerRed (protocol)and the results of which can be found here
Here we are submitting lysozymeC as a composite part under a T7 promoter (code), an Elowitz ribosome binding site (BBa_B0034) and a double terminator (BBa_B0015).
The sequence for LysozymeC protein coding region can be found here (BBa_K1914004)
BBa_K1914005
