Part:BBa_K1833000

pT7-eGFP

This part produces GFP in the presence of T7 RNA polymerase. It contains a T7 promoter, a strong RBS, the coding region for GFP, and a double terminator. The GFP is a mutant known as GFPmut3b, and the original citation is as follows:

Cormack, B.P., Valdivia, R.H., and S. Falkow. FACS-optimized mutants of green fluorescent protein (GFP). Gene 173: 33-38 (1996).

(http://www.sciencedirect.com/science/article/pii/0378111995006850)

It has a maximum excitation at 501 nm and maximum emission at 511 nm. For more information, see part BBa_E0040.

Usage and Biology

Figure 1. A typical expression profile of pT7-eGFP in NiCo21(DE3) cells. IPTG induction of the cells lifts the repression of lacUV5 promoter controlling the expression of T7 RNA Polymerase. The eGFP in this part can then be transcribed and translated. The concentrations of IPTG were chosen based on the recommendation that BL21 (DE3) cells and derivatives be induced with IPTG concentrations between 0.5mM and 1mM. As seen from the graph, during the first two hours, 0.2 mM IPTG induces the cells equally as well as does 1mM IPTG. However, after the first two hours, the cells induced with smaller concentrations of IPTG outgrow the other cultures, which ends up yielding more GFP fluorescence. The OD600s of the cultures at 5 hours are shown below in Figure 2.

Sequence and Features

Assembly Compatibility:

• 10
  COMPATIBLE WITH RFC[10]
• 12
  COMPATIBLE WITH RFC[12]
• 21
  COMPATIBLE WITH RFC[21]
• 23
  COMPATIBLE WITH RFC[23]
• 25
  COMPATIBLE WITH RFC[25]
• 1000
  INCOMPATIBLE WITH RFC[1000]

  Illegal BsaI.rc site found at 694