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Team:Cambridge/Bioluminescence/G28
From 2010.igem.org
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James Slock from King's College, PA kindly provided us with plasmids carrying the genes responsible for bioluminescence in ''V. fischeri''. Using Long-Range PCR, we extracted these genes and assembled them into a new operon. As described in the [https://2010.igem.org/Team:Cambridge/Bioluminescence/Background Background section], the lux operon in ''V. fischeri'' is under tight quorum sensing control. In the absence of LuxR protein and AHL the Lux genes are virtually inactive. | James Slock from King's College, PA kindly provided us with plasmids carrying the genes responsible for bioluminescence in ''V. fischeri''. Using Long-Range PCR, we extracted these genes and assembled them into a new operon. As described in the [https://2010.igem.org/Team:Cambridge/Bioluminescence/Background Background section], the lux operon in ''V. fischeri'' is under tight quorum sensing control. In the absence of LuxR protein and AHL the Lux genes are virtually inactive. | ||
| - | + | In order to relieve this control, we used [https://2010.igem.org/Team:Cambridge/Gibson/Introduction Gibson Assembly] to produce an operon consisting of Lux C, D, A, B, E (in this order, reflecting ''V. fischeri'') under the arabinose-induced promoter pBAD ([http://partsregistry.org/Part:BBa_I0500 BBa_i0500]). We called this construct G28. It caused bright and reproducible light output in the transformed E.coli Top10 cells. This new BioBrick ([http://partsregistry.org/Part:BBa_K325909 BBa_K325909]) can be used as an arabinose->light device and is a very useful part if the aim is to get a high bacterial light output. Many of the images in our [https://2010.igem.org/Team:Cambridge/Photos Photo Gallery] were created using Top10 cell transformed with this part. | |
=h-ns mutants= | =h-ns mutants= | ||
Revision as of 11:43, 26 October 2010
James Slock from King's College, PA kindly provided us with plasmids carrying the genes responsible for bioluminescence in V. fischeri. Using Long-Range PCR, we extracted these genes and assembled them into a new operon. As described in the Background section, the lux operon in V. fischeri is under tight quorum sensing control. In the absence of LuxR protein and AHL the Lux genes are virtually inactive.
In order to relieve this control, we used Gibson Assembly to produce an operon consisting of Lux C, D, A, B, E (in this order, reflecting V. fischeri) under the arabinose-induced promoter pBAD ([http://partsregistry.org/Part:BBa_I0500 BBa_i0500]). We called this construct G28. It caused bright and reproducible light output in the transformed E.coli Top10 cells. This new BioBrick ([http://partsregistry.org/Part:BBa_K325909 BBa_K325909]) can be used as an arabinose->light device and is a very useful part if the aim is to get a high bacterial light output. Many of the images in our Photo Gallery were created using Top10 cell transformed with this part.
h-ns mutants
To test the theory that H-NS proteins repress the Lux genes by interacting with their coding regions, we transformed two E.coli mutant strains with this construct and measured their light output. The strains we used were GM230 hns-205::Tn10, which has a C-terminal deletion in the H-NS gene and BW25113 Δhns::kan, a strain from a knockout library. In the literature, h-ns mutant strains have been described as producing much brighter luminescence than wild type strains. While we could not reproduce a higher peak brightness, it was apparent that the knockout strain maintained its light output for much longer than wild type, which showed a steep reduction in brightness upon entering stationary phase. This phenomenon (Abrupt Decline in Luciferase Activity - or ADLA) has been described by [http://www.springerlink.com/content/w73k840k27866462/fulltext.pdf Koga et al. 2004]. However, this paper suggests that the effect of H-NS on luminescence is not due to expression of the lux genes, but occurs indirectly via the cell's redox pool, in particular the availability of FMNH2.
