Team:Bielefeld-Germany/Biosafety/Biosafety System S
From 2013.igem.org
Biosafety System AraCtive
Overview
The Biosafety-System araCtive <bbpart>BBa_K1172909</bbpart> is an improvement of the Biobrick <bbpart>BBa_K914014</bbpart> by changing the first promoter into the rhamnose promoter PRha, integration of the alanine racemase <bbpart>BBa_K1172901</bbpart> and usage of the repressor AraC to regulate the transcription of the Barnase behind the PBAD promoter. Because of the tight repression of this promoter, this system has the lowest basal transcription of the Barnase and is therefore the most active and attractive one.
Genetic Approach
Rhamnose promoter PRha
The promoter PRha (<bbpart>BBa_K914003</bbpart>) naturally regulates the catabolism of the hexose L-rhamnose. The advantage of the operon for further usage is its solely positive regulation. The regulon consists of the promoter PRhaT, which regulates the expression of the protein RhaT for the uptake of L-rhamnose and the two operons rhaSR and rhaBAD.
The operon rhaSR regulates the genes rhaS and rhaR, whose translated proteins are responsible for the positive activation of the L-rhamnose catabolism, while the operon rhaBAD regulates the genes for the direct catabolism of L-rhamnose.
When L-rhamnose is present, it acts as an inducer by binding to the regulatory protein RhaR. RhaR regulates his own expression and the expression of the regulatory gene rhaS by inhibiting or, in the presence of L-rhamnose, activating the operon RhaSR. Normally the expression level is modest, but it can be enhanced by a higher level of intracellular cAMP, which increases in the absence of glucose. So, in the presence of L-rhamnose and a high concentration of intracellular cAMP, the activator protein RhaR is expressed on higher level, resulting in an activation of the promoter PRhaT for an efficient L-rhamnose uptake and an activation of the operon rhaBAD. The L-rhamnose is than broken down into dihydroxyacetone phosphate and lactate aldehyde by the enzymes of the operon rhaBAD (Wickstrum et al., 2005).
A brief schematic summary of the regulation is shown in Figure 2.
Dihydroxyacetone phosphate can be metabolized in the glycolysis pathway, while lactate aldehyde is oxidated to lactate under aerobic conditions and reduced to L-1,2,-propandiol under anaerobic conditions.
This degradation of L-rhamnose can be separated in three steps. In the first step the L-rhamnose is turned into L-rhamnulose by an isomerase (gene rhaA). The catabolism continues by the a kinase (gene rhaB), which phosphorylates the L-rhamnulose to L-rhamnulose-1-phosphate. This is finally hydrolyzed by Aldolase (gene rhaD) to dihydroxyacetone phosphate and lactate aldehyde (Baldoma et al., 1988).
Four our Safety-System the rhamnose promoter PRha is used to control the expression of the repressor AraC and the essential alanine racemase, because this promoter has an even lower basal transcription then the arabinose promoter PBAD. This is needed to tightly repress the expression of the alanine racemase (alr) and therefore take advantage of the double-kill switch. Although the rhamnose promoter PRha is characterized by a very low basal transcription it can not be used for the control of the toxic RNase Ba (Barnase), which ist needed for the alanine racemase (alr), the other part of the double-kill switch. In conclusion this promoter is the best choice for the first part of the Biosafety-System, as it is tightly repressed in the absence of L-Rhamnose, but activated in its presence.
Repressor AraC
The araC gene is naturally found in E. coli and is coding for the 32 kDa AraC protein, which regulates the expression of the genes required for the uptake and catabolism of the pentose L-arabinose. The genes for the catabolism of arabinose are under the control of the arabinose promoter PBAD, which is both positively and negatively regulated by the repressor AraC. Naturally in the presence of L-arabinose the expression of those genes is activated, while it is repressed in its absence. Besides the AraC protein regulates its own transcription under the control of the so called PC promoter. Compared to the PBAD promoter the PC promoter as well as the araC gene are therefore transcribted in opposite direction (Schleif, 2010).
Naturally in the absence of L-arabinose the AraC protein is found in its repressor conformation, binding to the O2-region and I1-region. Binding two AraC proteins to this domains is leading to a protein-protein-interaction of AraC forming a dimer. This AraC is responsible for the tight repression of the PC and the PBAD promoter by forming a DNA-loop to inhibit the initiation of the RNA-polymerase (see Figure 4 above).
When L-arabinose is present in the media the operon changes to the active form. Following this conditions the araC protein functions as activator by binding to the I1- and I2-region of the operator region. This causes transcription of the genes behind the PBAD and the PC promoter. Depending on the intracellular level of cAMP the transcription of both the genes behind the promoters PBAD and PC can even be enhanced. In the absence of glucose the cell reaches a high level of cAMP as a signal molecule. CAMP binds as the typically CRP-cAMP complex binds in front of the AraC activator and increases the binding affinity of the RNA-polymerase, so that the genes behind the PBAD promoter are expressed on higher levels. Beside the transcription affinity of the PBAD promoter the AraC protein also regulates the genes araE and the operon consisting the genes araFGH, which are necessary for an efficient uptake of L-arabinose (Cass, 1988).
The auto-regulation of the araC gene itself works both in the presence and absence of L-arabinose. In presence of L-arabinose the DNA-loop which prevents also the transcription of the PBAD promoter also inhibits the transcription of araC. When L-arabinose is present and the AraC concentration is high enough, its auto-regulates its own transcription by dimerization between the araO1- and the araO2-region. This leads to an other DNA-loop, inhibiting solely the transcription of the genes behind the PC promoter (Hamilton, 1988).
For our Biosafety-System we decided to use the arabinose PBAD promoter, because this promoter is really tight regulated by AraC, and shows no basal transcription in the complete absence of AraC. Additional this promoter is repressed by glucose and basal transcription is activated in the presence of cAMP.
Alanine racemase Alr
The alanine racemase Alr (EC 5.1.1.1) from the gram-negative enteric bacteria Escherichia coli is a racemase, which catalyses the reversible conversion of L-alanine into the enantiomer D-alanine. For this reaction the cofactor pyridoxal-5'-phosphate (PLP) is typically needed. The constitutive expressed alanine racemase (alr) is naturally responsible for the accumulation of D-alanine, which is an essential component of the bacterial cell wall, because it is used for the crosslinkage of peptidoglykan (Walsh, 1989).
The usage of D-alanine instead of a typically L-amino acids prevents cleavage by peptidases. However a lack of D-alanine causes to a bacteriolytic characteristics. In the absence of D‑alanine dividing cells will lyse rapidly. This perception is used for our Biosafety-Strain, a D-alanine auxotrophic mutant (K-12 ∆alr ∆dadX). The Biosafety-Strain grows only with a plasmid containing the alanine racemase (<bbpart>BBa_K1172901</bbpart>) with a complementation of the D-alanine auxotrophy. Consequently the alanine racemase is essential for bacterial cell division. This approach guarantees a high plasmid stability, which is extremely important when the plasmid contains a toxic gene like the Barnase. In addition this construction provides the possibility for the implementation of a double kill-switch system. Because if the expression of the alanine racemase is repressed and there is no D-alanine-Supplementation in the media, cells will not grow.
Terminator
Terminators are essential for the end of an operon. In procaryots two types of terminators exist. The rho-depending and the rho-independing terminator. Rho-independing terminators are characterized by their stem-loop forming sequence. In general the terminator-region can be divided into four regions. Starting with a GC-rich region, which performs the stem and is followed by the loop-region. The third region is made up from the opposite part of the stem, so that this region concerns also a high GC-content. The terminator region closes with a poly uracil region, which destabilizes the binding of the RNA-polymerase. The stem-loop of the terminator causes a distinction of the DNA and the translated RNA. Consequently the binding of the RNA-polymerase is cancelled and the transcription ends after the stem-loop (Carafa et al., 1990).
For our Bioafety-System araCtive the terminator is necessary to avoid that the expression of the genes under control of the Rhamnose promoter PRha, like the Repressor AraC and the Alanine-Racemase (alr) results in the transcription of the genes behind the Arabinose promoter PBAD, which contains the toxic Barnase <bbpart>BBa_K1172904</bbpart> and would lead to cell death.
Arabinose promoter PBAD
The arabinose promoter PBAD controls the expression of the genes, which are necessary for the catabolism of the pentose arabinose. The expression is regulated by the activator and repressor AraC. The genes of this operon convert the pentose to xylose, which can be catalyzed into fructose-1,6-diphosphate and subsequently becomes so part of the glycolysis. The conversion of L-arabinose is realized in three steps. First the isomerase (gene A) catalyses the reaction from L-arabinose into the isomer L-ribulose. In the second step the Ribulose-kinase (gene B) phosphorylates the L-ribulose to L-ribulose-monophosphat. For this reaction ATP is needed. At least the L-ribulose-monophosphate is converted to D-Xylose-5-phosphat by the L-ribulose-5-phosphate-epimerase (gene D, Schleif, 2010).
For our Safety-System we used the arabinose promoter PBAD for the regulation of the toxic gene product Barnase. As this promoter has very low basal transcription and as the expression of the genes behind this promoter is strict depending on the presence of AraC for activating the transcription, it is possible to use the arabinose promoter PBAD to control the expression of a toxic gene product without causing cell death.
RNase Ba (Barnase)
The Barnase (EC 3.1.27) is a 12 kDa extracellular microbial ribonuclease, which is naturally found in the gram-positive soil bacteria Bacillus amyloliquefaciens and consists of a single chain of 110 amino acids. The Barnase (RNase Ba) catalyses the cleavage of single stranded RNA, whereat the hydrolysis of the dinucleotides has the highest affinity to the structure GpN. In the first step of the RNA-degradation a cyclic intermediate is formed by transesterification and afterwards this intermediate is hydrolysed yielding in a 3'-nucleotide (Mossakowska et al., 1989).
In Bacillus amyloliquefaciens the activity ot the Barnase (RNase Ba) is inhibited intracellular by the Inhibitor called barstar. Barstar consists of only 89 amino acids and binds with a high affinity to the toxic Barnase. This prevents the cleavage of the intracellular RNA in the host organism (Paddon et al., 1989). Therefore the Barnase naturally acts only outside the cell and is translocated under natural conditions. For the Biosafety-System araCtive we modified this aspect by cloning only the sequence responsible for the cleavage of the RNA, but not the signal sequence of the native Barnase, which is essential for the extracellular transport.
As shown in the graphic below, the transcription of the DNA, which encodes the Barnase produces a 474 nt RNA. The translation of the RNA starts about 25 nucleotides downstream from the transcription start and can be divided into two parts. The first part (colored in orange) is translated into a signal peptide at the amino-terminus of the Barnase coding RNA. This part is responsible for the extracellular translocation of the RNase Ba, while the peptide sequence for the active Barnase starts 142 nucleotides downstream from the transcription start (colored in red).
For the Biosafety-System araCtive we only used the coding sequence (<bbpart>BBa_K1172904</bbpart>) of the Barnase to prevent the extracellular translocation of the toxic gene product. Translation of the barnase gene leads to a rapid cell death if the expression of the Barnase isn't repressed by the repressor AraC of our Biosafety-System.
Biosafety-System araCtive
Combining the gene described above with the Biosafety-Strain K-12 ∆alr ∆dadX results in a powerful device, allowing us to control the bacterial cell division. The control of the bacterial growth is possible either active or passive. Active by inducing the PBAD promoter with L-arabinose and passive by the induction of L-rhamnose. The passive control makes it possible to control the bacterial cell division in a defined closed environment, like the MFC, by continously adding L-rhamnose to the medium. As shown in the figure below, this leads to an expression of the essential Alanine-Racemase (alr) and the araC repressor, so that the expression of the RNase Ba is repressed.
In the event that bacteria exit the defined environment of the MFC or L-rhamnose is not added to the medium any more, both the expression of the alanine Racemase (Alr) and the AraC repressor decrease, so that the expression of the toxic RNase Ba (Barnase) is not inhibited as strongly as before. The cleavage of the intracellular RNA by the Barnase and the lack of synthesized D-alanine, caused by the repressed alanine racemase inhibit the cell division and makes sure that the bacteria can only grow in the defined area.
Results
Characterization of the arabinose promoter pBAD
First of all the arabinose promoter PBAD was characterized to get a first impression of its basal transcription rate. Therefore the bacterial growth was investigated under the pressure of the unrepressed PBAD promoter on different carbon source using M9 minimal medium with either glucose or glycerol. The transcription rate was identified by fluorescence measurement of GFP <bbpart>BBa_E0040</bbpart> from behind the PBAD promoter using the BioBrick <bbpart>BBa_I13541</bbpart>.
As shown in Figure 12 below, the bacteria adapted better on glucose then on glycerol. This is caused by the fact, that glucose is the more powerful energy source of this two, because it posses more carbon atoms in comparison to glycerol. For the investigation of the basal transcription the fluorescence measurement, shown in Figure 13, is more interesting.
It can be seen that both the wild type E. coli K-12 and the Biosafety-Strain E. coli K-12 ∆alr ∆dadX ∆araC show about the same fluorescence on glucose (blue and black curve) but differ on glycerin. This can be explained by the fact that glucose itself represses the arabinose promoter PBAD, while glycerol does not. In the presence of glucose the intracellular concentration of cAMP is low to repress the inefficient catabolism of arabinose, so that the glucose is catabolized first by the bacteria resulting in an optimal growth. In the absence of glucose intracellular cAMP increases, which enhances the transcription of the most operons for alternative catabolic pathways. This causes, that the expression of GFP under the control of the PBAD promoter decreases on glycerol. Another different can be seen between the wild type (orange curve) and the Biosafety-Strain K-12 ∆alr ∆dadX ∆araC (red curve).
The Biosafety-Strain shows lower expression then the wild type, but has about the same growth rate, according to Figure 12. The reason for this characteristic is caused by the deleted AraC protein in the Biosafety-Strain. Because the AraC protein functions not only as are repressor but also as an activator the transcription rate decreases in the Biosafety-Strain.
The effect that glucose represses the transcription of the PBAD promoter becomes more clear by analysis of the specific production rate, as shown in Figure 14. The specific production rate was thereby calculated via equation (1) :
With the specific production rate of GFP it can be demonstrated that the building of GFP differs extremely between the cultivation on glucose and glycerol. The specific production rate is constantly very low, when using glucose as carbon source, but shows a constant higher level in the cultivation with glycerol.
Because the specific production rate was calculated between every single measurement point, the curve in Figure 14 is not smoothed and so the fluctuations have to be ignored, as they do not stand for are real fluctuations in the transcription or expression of GFP. They are caused by the growth curve and the fluorescence curve. And as neither of this curves are ideal, the fluctuations are caused. Nevertheless this graph shows clearly the difference between the two carbon sources.
Characterization of the Biosafety-System araCtive
The Biosafety-System araCtive was characterized on M9 minimal medium using glycerol as carbon source. As for the characterization of the pure arabinose promoter PBAD above, the bacterial growth and the fluorescence of GFP <bbpart>BBa_E0040</bbpart> was measured. Therefore the wild type and the Biosafety-Strain E. coli K-12 ∆alr ∆dadX containing the Biosafety-Plasmid <bbpart>BBa_K1172909</bbpart> were cultivated once with the induction of 1% L-Rhamnose and once only on glycerol.
As shown in Figure 15, it is obviously that the bacteria, who were induced with 1 % L-rhamnose (blue and black curve) grow significant slower than on pure glycerol (orange and red curve). This is attributed to the high metabolic pressure of the induced bacteria. The expression of the repressor AraC and the alanine racemase (Alr) simultaneously causes a high outlay of the cells, so that they grow slower then the uninduced cells, who expresses only GFP. Additional the arabinose promoter PBAD is tightly regulated, so that the expression even with a small amount of the repressor AraC is not that high and therefore not as stressful.
Comparing the bacterial growth with the fluorescence in Figure 16, it can be seen that the fluorescence seems to follow the same trend than the bacterial growth. The uninduced cells shows approximately an exponential rise of fluorescence, while in comparision the fluorescence of the induced bacteria increases only slowly.
From the Figure 16 above it can not be clearly seen if the expression of the repressor AraC does effect the transcription of GFP or not. The slower growth of the bacteria is a first indication that the repressor AraC and the alanine racemase (Alr) are highly expressed, but the growth of the bacteria shows nearly the same trend as the fluorescence. So it could be possible that the repressor does not effect the expression level of GFP under the control of the arabinose promoter PBAD. This becomes more clear by the calculation of the specific production rate of GFP by equation (1) . As shown in Figure 18 below the specific production rate differs clearly between the uninduced Biosafety-System and the Biosafety-System induced by 1% L-rhamnose. The production of GFP in the presence of L-rhamnose (red curve) is always lower than in its absence (orange curve), so that the expression of GFP is repressed in the presence of L-rhamnose.
Because the specific production rate of GFP was calculated between every single measurement point, the curve in Figure 18 is not smoothed and so the fluctuations have to be ignored, as they do not stand for are real fluctuations in the transcription or expression of GFP. They are caused by the growth curve and the fluorescence curve. And as neither of this measured curves are ideal, the fluctuations are the result. Nevertheless it can be demonstrated, that the production of GFP is reduced significantly in the presence of L-rhamnose and AraC respectively. So the Biosafety-System araCtive works.
Conclusion of the Results
As the expression level of GFP is increased in the absence of L-Rhamnose and decreased in its presence, the Biosafety-System araCtive works as aspected. In figure 18 the specific production rates after 7,5 hours are compared. It can be seen that the expression level of the pBAD promoter decreases in the uninduced Safety-Strain compared to the uninduced second part of the Biosafety-System and that the induction with L-Rhamnose leads to a tight repression of the transcription and therefore the expression of GFP.
References
- Baldoma L and Aguilar J (1988) Metabolism of L-Fucose and L-Rhamnose in Escherichia coli: Aerobic-Anaerobic Regulation of L-Lactaldehyde Dissimilation [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC210658/pdf/jbacter00179-0434.pdf|Journal of Bacteriology 170: 416 - 421.].
- Carafa, Yves d'Aubenton Brody, Edward and Claude (1990) Thermest Prediction of Rho-independent Escherichia coli Transcription Terminators - A Statistical Analysis of their RNA Stem-Loop Structures [http://ac.els-cdn.com/S0022283699800059/1-s2.0-S0022283699800059-main.pdf?_tid=ede07e2a-2a92-11e3-b889-00000aab0f6c&acdnat=1380629809_2d1a59e395fc69c8608ab8b5aea842f7|Journal of molecular biology 216: 835 - 858].
- Cass, Laura G. and Wilcoy, Gary (1988) Novel Activation of araC Expression and a DNA Site Required for araC Autoregulation in Escherichia coli B/r [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC211425/pdf/jbacter00187-0394.pdf|Journal of Bacteriology 170: 4174 - 4180].
- Hamilton, Eileen P. and Lee, Nancy (1988) Three binding sites for AraC protein are required for autoregulation of araC in Escherichia coli [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC279856/pdf/pnas00258-0029.pdf|Proc Natl Acad Sci U S A 85: 1749 - 53].
- Mossakowska, Danuta E. Nyberg, Kerstin and Fersht, Alan R. (1989) Kinetic Characterization of the Recombinant Ribonuclease from Bacillus amyloliquefaciens (Barnase) and Investigation of Key Residues in Catalysis by Site-Directed Mutagenesis [http://pubs.acs.org/doi/pdf/10.1021/bi00435a033|Biochemistry 28: 3843 - 3850.].
- Paddon, C. J. Vasantha, N. and Hartley, R. W. (1989) Translation and Processing of Bacillus amyloliquefaciens Extracellular Rnase [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC209718/pdf/jbacter00168-0575.pdf|Journal of Bacteriology 171: 1185 - 1187.].
- Schleif, Robert (2010) AraC protein, regulation of the L-arabinose operon in Escherichia coli, and the light switch mechanism of AraC action [http://gene.bio.jhu.edu/Ourspdf/127.pdf|FEMS microbial reviews 34: 779 - 796.].
- 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.].
- Walsh, Christopher (1989) Enzymes in the D-alanine branch of bacterial cell wall peptidoglycan assembly. [http://www.jbc.org/content/264/5/2393.long|Journal of biological chemistry 264: 2393 - 2396.]
- Wickstrum, J.R., Santangelo, T.J., and Egan, S.M. (2005) Cyclic AMP receptor protein and RhaR synergistically activate transcription from the L-rhamnose-responsive rhaSR promoter in Escherichia coli. [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1251584/?report=reader|Journal of Bacteriology 187: 6708 – 6719.].