Difference between revisions of "Part:BBa K3409009"

Revision as of 08:00, 26 October 2020

Expression of receptor binding protein (gp37) on the outer membrane of Escherichia coli

Contains the elements necessary to recognize and bind an Escherichia coli bacteria.The major component is the gene product (gp) 37 which codes for the T4 bacteriophage recpetor binding protein (RBP) conferring the ability to recongize another target bacteria (E.coli in this case). Gp37 will be directed to the outer membrane of our model organism, E. coli K12. This will be achieved thanks to the co-expressed Lpp-OmpA gene. The Lpp-OmpA is an existing part designed by the NCTU-Formosa team in 2015 (Part: BBa_K1694002). It consists of a N-terminal acids of the lipoprotein (Lpp) sequence followed by amino acids of outer membrane protein A (OmpA). By fusing gp37 to the C-ter end of Lpp-OmpA, it can be displayed on the outer membrane of E. coli. This BioBrick also contains a cleavage site, the TEV cleavage site, which is a unique cleavage site of the cysteine protease from the Tobacco Etch Virus (TEV). This cleavage site is followed by a His-tag in case of a purification step which can be performed with Ni2+ chromatography columns.

Two chaperones proteins (gp38 and chaperone protein 57A) are present as well for the physical appearance of the gp37.

Characterization

Revelation of the presence of gp37 via immunofluorescence labelling

The aim was to detect the receptor binding protein gp37 expressed and directed to the membrane thanks to the co-expressed Lpp-OmpA genes. This is achieved using fused His-tag placed after the OmpA and before the gp37. Thus, the His-tag was targeted with a primary monoclonal anti-his antibody conjugated to a fluorescence marker, fluorescein isothiocyanate (FITC), which has excitation and emission spectrum peak wavelengths of approximately 495 nm/519 nm, detectable with a fluorescence spectrophotometer.

Bibliography

Sequence and Features