Biosafety System Lac of Growth

Overview

Figure 1: Biosafety-System Lac of growth.

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Genetic Approach

Rhamnose promoter

Rhamnose

lacI

Naturally the lac operon regulates the catabolism of the disaccharide lactose (4-O-(β-D-Galactopyranosyl)-D-glucopyranose) in E. coli. The operon contains the lactose promoter (plac) and the genes for the catabolism of the Lactose to Glucose and Galactose. Upstream of the lac operator exists the coding sequence for the repressor lacI under the control of a weak promoter (Jacob et al., 1961).
Compared to the catabolism of the sugars L-Rhamnose or L-arabinose Lactose, as a disaccharide has a higher energy content and is therefore used more preferable. This is a reason, why the basal transcription of this promoter is even more higher. The leakiness of the lac promoter is caused by the fact that the lacY need to be expressed for an efficient Lactose uptake, while in the arabinose system the uptake is regulated separate (Görke et al., 2008).
In our Safety-System the lacI (<bbpart>BBa_C0012</bbpart>) is used for the repression of the lactose promoter (plac).

Alanine Racemase

Alanine-Racemase

Terminator

Terminator

Lactose promoter (plac)

Naturally the lac operon regulates the catabolism of the disaccharide lactose (4-O-(β-D-Galactopyranosyl)-D-glucopyranose) in E. coli. The operon consists of a CAP-binding site, the lac promoter, the lac operator and the genes lacZ, lacY and lacA downstream of the promoter. The transcription of the lactose promoter is regulated by the lacI gene, which is found upstream of the operon under the control of a weak promoter. In the absence of lactose the transcription of the genes behind the lactose promoter is blocked caused by the binding of the lacI pressor. While in the presence of Lactose the repressor is released from the operator and the genes can be transcripted. Typically the transcription is enhanced by a high intracellular level of cAMP (Busby, 1999).

Figure 5:Structure of the lactose operon and its regulatory units. In the absence of Lactose the trascription of the genes behind the lactose promoter is blocked. In the presens of Lactose a side reaction of the ß-Galactosidase (gene lacZ) synthesis allolactose, who causes a change in conformation of the lacI. The repressor lacI releases the operator sequnece and the transcription of the lactose operons starts.

The lactose promoter thereby regulates the transcription of the genes lacZ, lacY and lacA. The lacZ gene encodes for the ß-Galactosidase a enzyme, who breaks down the lactose to glucose and galactose. The ß-Galactosidase catalyses additional the degradation from Lactose to Allolactose. By binding on the lacI repressor, it changes his conformation an is not any more able to bind on the operator sequnece and to block the transcription. As only one enzyme is necessary to gain a substrate of the glycolysis is becomes clear, why the degradation of Lactose is more preferable compared to L-arabinose or L-rhamnose.
To realize a preference of lactose, the transcription of the lactose promoter is not repressed as that strong. This is caused by the fact that the lacY gene, coding for the integral membrane protein lactose permease, is necessary for the lactose uptake and has to be transcripted on a low level.
The last gene of the lac operon, lacA, encodes for a Transacetylase, who acetylizes glycosides that can not be metabolized. The acetylated glycosides are transported outside the cell to avoid the accumulation of lactose.
In our Biosafety-System the lac-promoter is used for the regulation of GFP or the Barnase. As the lac promoter shows a high basal transcription, its might not ideal for the regulation of a toxic gene product, but the the Biosafety-System Lac of growth is ideal for comparison with the other Systems to measure the level of basal transcription under repressed and unrepressed conditions. Besides we improved the leakiness of the lactose promoter by adding a second lacI-binding site 12 nt downstream of the excisting bining site. As this distance corresponds to about one whorl of the double helix, this should allow an additional lacI repressor to bind on the other site of the DNA and tighten the repression of the lactose promoter. Unfortunately the improvement of the so called double lac promoter could not be quantified, because lac of time (Lewis, 2005).

Barnase

Barnase

Biosafety-System Lac of growth

Together with the Biosafety-Strain K-12 ∆alr ∆dadX the Biosafety-System Lac of growth takes advantage of this genes by combine them to a powerful device, which allows to control the bacterial cell division. The control of the bacterial growth is thereby active and passive possible. Active by inducing the lactose promoter with IPTG or classically with Lactose and passive by the induction of L-Rhamnose. The passive control makes it possible to control the bacterial cell division in an defined environment, like the MFC by adding continously L-Rhamnose to the media. As shown in the figure below, this leads to an expression of the essential Alanine-Racemase (alr) and the lacI repressor, so that the expression of the RNase Ba is repressed.

Figure x: Biosafety-System Lac of growth in the presens of L-Rhamnose. The essentail Alanine-Racemase (alr) and the repressor lacI are expressed, so that the expression of the RNAse Ba is repressed and the Bacteria grow.

When the bacteria exit the defined environment of the MFC or L-Rhamnose is not added any more to the media, the expression of the Alanine-Racemase (alr) and the lacI repressor decreases, so that the expression of the toxic RNase Ba (Barnase) is not inhibted so strong any more. The cleavage of the intracellular RNA by the Barnase and ideally also the lack of synthesized D-alanine, caused by the repressed Alanine-Racemase inhibits the cell division and makes sure that the bacteria can only grow in the defined area.

Figure x: Biosafety-System Lac of growth outside the defined conditions and a decreased concentration of L-Rhamnose. The expression of the Alanine-Racemase and lacI repressor is reduced and ideally completly shutdown. In contrast the expression of the RNase ba (Barnase is sligthly turned on, leading to cell death by RNA cleavage.

Results

Characterization of the lactose promoter plac

Figure 12: Characterization of the bacterial growth of the plac promoter with GFP (<bbpart>BBa_E0040</bbpart>) in the Biosafety-Strain K-12 ∆alr ∆dadX ∆araC. The bacteria grow faster on M9 minimal media glucose than on M9 minimal media glycerol.

Figure 13: Characterization of the fluorescence of plac promoter with GFP (<bbpart>BBa_E0040</bbpart>) in the Biosafety-Strain K-12 ∆alr ∆dadX ∆araC.

Figure 13: Characterization of the fluorescence of plac promoter with GFP (<bbpart>BBa_E0040</bbpart>) in the Biosafety-Strain K-12 ∆alr ∆dadX ∆araC.

Characterization of the Biosafety-System Lac of growth

Figure 13: Characterization of the fluorescence of plac promoter with GFP (<bbpart>BBa_E0040</bbpart>) in the Biosafety-Strain K-12 ∆alr ∆dadX ∆araC.

Figure 13: Characterization of the fluorescence of plac promoter with GFP (<bbpart>BBa_E0040</bbpart>) in the Biosafety-Strain K-12 ∆alr ∆dadX ∆araC.

Figure 13: Characterization of the fluorescence of plac promoter with GFP (<bbpart>BBa_E0040</bbpart>) in the Biosafety-Strain K-12 ∆alr ∆dadX ∆araC.

Conclusion of the Results

Figure 13: Characterization of the fluorescence of plac promoter with GFP (<bbpart>BBa_E0040</bbpart>) in the Biosafety-Strain K-12 ∆alr ∆dadX ∆araC.

References

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• Voss, Carsten Lindau, Dennis and Flaschel, Erwin (2006) Production of Recombinant RNase Ba and Its Application in Downstream Processing of Plasmid DNA for Pharmaceutical Use [http://onlinelibrary.wiley.com/doi/10.1021/bp050417e/pdf|Biotechnology Progress 22: 737 - 744.].

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