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Team:Edinburgh/Bacterial/Blue light producer
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Revision as of 15:58, 26 October 2010
Overview: The blue light producer
The construction of a blue light producer requires the combination of bacterial luciferase LuxAB with an extra protein called lumazine (LumP). According to O'Kane and Lee (1985), this will shift the wavelength of the bacterial luciferase towards the blue spectrum (from 495 nm to 478 nm), giving us a light which can hopefully activate our blue light sensor. Last year's Edinburgh team already made both of these parts individually, so all we had to do was fuse them together and add a constitutive promoter before determining whether the wavelength of the light output had been altered.
Figure 1: Emission spectra of LuxAB (in solid black line). The LuxAB depicted is that from Vibrio campbellii, but sources confirm that other bacterial luciferases produce similar spectral graphs.
Image: Suadee et al. (2008)
Strategy
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Problems
The LuxAB which last year's team made and stored is failing to transform correctly. Colonies that ought to be growing white are growing blue (LuxAB should have replaced the lacZ' in the vector, EdinbrickI). A similar thing is happening with LumP and RFP, where cells are still growing red, despite the fact that the RFP ought to have been removed when LumP was inserted last year.
We have come across several PCR products not yet inserted into vectors with which we are hoping to start this part of the project (i.e. the bit which should already have been done by last year according to their lab notes) again.
We eventually resolved these problems by using the alternative PCR products which were perfectly capable of being cloned into pSB1C3.
BioBricks
Both lumP and luxAB have already been submitted as BioBricks in pSB1A3 by last year's Edinburgh team, but we are re-submitting slightly modified versions in pSB1C3.
We are also submitting a luxAB-lumP fusion construct in pSB1C3 with a constitutive promoter which can be used for blue light production. We have confirmation of working luxAB with the promoter in question.
BBa_K322139: bacterial luciferase luxAB, updated version of BBa_K216008.
BBa_K322312: luxCDE (required for luxAB expression), updated version of BBa_K216017.
BBa_K322007: lumP (shifts luxAB to blue), updated version of BBa_K216007.
BBa_K322140: luxAB under lac promoter.
BBa_K322141: luxAB and luxCDE under lac promoter.
BBa_K322149: luxAB and lumP composite part.
BBa_K322150: luxAB and lumP under lac promoter.
Characterisation
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References
O'Kane, D. J. & Lee, J. (1985). Chemical characterization of lumazine protein from Photobacterium leiognathi: comparison with lumazine protein from Photobacterium phosphoreum. Biochemistry 24, 1467-1475.
Suadee, C., Nijvipakul, S., et al. (2008). LuxG Is a Functioning Flavin Reductase for Bacterial Luminescence. J. Bacteriol. 190(5): 1531-1538
Edinburgh 2009 team wiki, https://2009.igem.org/Team:Edinburgh.
