User:Etienne Robillard/Notebook/Chemtrails911 notebook/Agent Ecoli:PhosphohistidineTransferaseComponent
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| - | == Agent Ecoli:Phosphohistidine Transferase | + | == Agent Ecoli:Phosphohistidine Transferase Component == |
=== OmpR and LuxR === | === OmpR and LuxR === | ||
| - | + | * Orthogonal phosphorus-degrading enzymes are key in (auto)catalytic regulation of lacZ-bound phosphate-histidine residues - see N-methyl nucleosidase (3.2.2.35) and this [http://2012.igem.org/Team:TU_Munich/Project/Caffeine page] for references. | |
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== See also == | == See also == | ||
Current revision
Contents |
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 (3.2.2.35) and this page for references.
See also
- 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 2.7.13.3
- 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)
