Reporter

Part:BBa_K1033250:Experience

Designed by: Anders Edlund   Group: iGEM13_Uppsala   (2013-09-13)


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Applications of BBa_K1033250

Utah State used this fluorescent protein in their 2015 for a project engineering Lactococcus lactis to detect and fight against phi31 phage infection. It was not tested in L. lactis but did display function in E. coli when paired with three L. lactis promoters. (see Figures 1 and 2).

Utah_State_2015_MCherry_Fluorescence_Chart_Version_2.jpg

Figure 1. Fluorescence levels from three constructs using synthetic promoters from Jensen and Hammer (1998) in E. coli excited at 530/25 with emissions read at 590/35. cp8 from part BBa_K1820017, cp11 from part BBa_K1820018, and cp44 from part BBa_K1820019

Utah_State_2015_Fluorescence_small.jpg

Figure 2. Fluorescence E.coli bacteria with Lactococcus lactis promoters and sfGFP(Bs) (left) and mCherry(Lr) (right)

Referrence: Jensen, P. R., Hammer, K. (1998). The Sequence of Spacers between the Consensus Sequences Modulates the Strength of Prokaryotic Promoters. Appl Environ Microbiol. 1998 Jan; 64(1): 82–87. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC124675/

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