Biosafety System Lac of Growth

Overview

250px 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.
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.
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.

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.

Barnase

Barnase

System L in the MFC: In this case the mikroorganism is in the MFC with sufficient L-rhamnose. It comes to an expression of lacI which blocks the lac-promoter by binding and alr which switches L-alanine to D-alanine. Because of the fact that lacI blocks the lac-promoter the RNase Ba can't expressed.

System L outside of the MFC: In this case the mikroorganism could get out of the MFC by damage or incorrect handling. Outside of the MFC there isn't enough L-rhamnose. So... E.coli dies.

Results

References

Agnes Ullmann (2001): Escherichia coli Lactose Operon. In: Encyclopedia of Life Sciences

Stumpp et al.: Ein neues, L-Rhamnose-induzierbares Expressionssystem für Escherichia coli, In: Biospektrum 6. Jahrgang S. 33

Carsten Voss, Dennis Lindau, and Erwin Flaschel, Production of Recombinant RNase Ba and Its Application in Downstream Processing of Plasmid DNA for Pharmaceutical Use, Biotechnology Progress, 22, 2006 p. 737-44.

Danuta E. Mossakowska, Kerstin Nyberg, and Alan R. Fersht, Kinetic Characterization of the Recombinant Ribonuclease from Bacillus amyloliquefaciens (Barnase) and Investigation of Key Residues in Catalysis by Site-Directed Mutagenesis, Biochemistry, 28, 1989, p. 3843 – 3850.

C. J. Paddon, N. Vasantha, and R. W. Hartley, Translation and Processing of Bacillus amyloliquefaciens Extracellular Rnase, Journal of Bacteriology, 171, 1989, p. 1185 – 1187.

• Autoren (Jahr) Titel [Link|Paper Ausgabe: Seiten].