User:Etienne Robillard/Notebook/Agent Ecoli:PhosphohistidineTransferaseComponent
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Revision as of 12:16, 30 July 2013 by Etienne Robillard (User:Etienne Robillard/Notebook/Chemtrails911 notebook/Agent Ecoli:PhosphohistidineTransferaseComponent moved to User:Etienne Robillard/Notebook/Agent Ecoli:PhosphohistidineTransferaseComponent)
Agent Ecoli:Phosphohistidine Transferase Component
OmpR and LuxR
- Orthogonal phosphorus-degrading enzymes are key in (auto)catalytic regulation of lacZ-bound phosphate-histidine residues - see N-methyl nucleosidase (18.104.22.168) and this page for references.
- E. coli restriction-modification system
- Standard E. coli Strain for BioBricks - and this paper
- Start up genome engineering [with the M13 phage genome] - [a picture is HERE]
- Beta-galactosidase assay - EC 22.214.171.124
- sequence for M13k07 reengineered plasmid : Note : If pMR101 is a gene vector derived from pACYC177 then clearly the resulting plasmid cloning vector will be a synthetic construct derived from a M13 like bacteriophage, thus the use of restriction enzymes for acquiring inter-species genes (OmpR/EnvZ) is likely a positive indicator of a scheme to induce horizontal gene regulation using bacterial conjugation like sex in elephants and the E. coli K-12 MG1655 strain.
- The Matrix (1999)