Difference between revisions of "Team:TU Dresden/Demonstrate"
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<h2>Achievements</h2> | <h2>Achievements</h2> | ||
<p>We engineered a sender strain (SeSt) with an additional inducible copy of <i>comX</i> and a <i>comX</i>-deficient receiver strain (ReSt) containing the ComX-dependent promoter P<sub><i>srfA</i></sub> fused to the <i>lux</i> operon (Figure 1). Therefore, we could easily detect communication between the co-cultured SeSt and ReSt via ComX by measuring the luminescence output of the ReSt. After proofing this concept using ThinCert™ cell culture inserts (Figure 2) we applied it to Peptidosomes (Figure 3). Consequently we could show communication between encapsulated bacteria and bacteria in the surroundings and made substantial progress in the evaluation of Peptidosomes as a tool for co-cultivation and studies of microbial interactions.</p> | <p>We engineered a sender strain (SeSt) with an additional inducible copy of <i>comX</i> and a <i>comX</i>-deficient receiver strain (ReSt) containing the ComX-dependent promoter P<sub><i>srfA</i></sub> fused to the <i>lux</i> operon (Figure 1). Therefore, we could easily detect communication between the co-cultured SeSt and ReSt via ComX by measuring the luminescence output of the ReSt. After proofing this concept using ThinCert™ cell culture inserts (Figure 2) we applied it to Peptidosomes (Figure 3). Consequently we could show communication between encapsulated bacteria and bacteria in the surroundings and made substantial progress in the evaluation of Peptidosomes as a tool for co-cultivation and studies of microbial interactions.</p> | ||
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<figcaption><b>Figure 1: Growth of the ReSt (A) and ComX-dependent promoter activity of P<sub><i><b>srfA</b></i></sub> (B) in transformation medium (MNGE).</b> In wild type (WT) the promoter is tenfold increased compared to the <i>comX</i>-deficient strain during transition phase.</figcaption> | <figcaption><b>Figure 1: Growth of the ReSt (A) and ComX-dependent promoter activity of P<sub><i><b>srfA</b></i></sub> (B) in transformation medium (MNGE).</b> In wild type (WT) the promoter is tenfold increased compared to the <i>comX</i>-deficient strain during transition phase.</figcaption> | ||
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<figure class="makeresponsive floatleft" style="width:28.362%;"> | <figure class="makeresponsive floatleft" style="width:28.362%;"> | ||
<img src="https://static.igem.org/mediawiki/2017/7/7b/T--TU_Dresden--P_Communication_Demonstration_Figure_3.png" alt="Figure 2: Co-culture of sender strain (SeSt) and receiver strain (ReSt) using ThinCert™ cell culture inserts." class="makeresponsive zoom"/> | <img src="https://static.igem.org/mediawiki/2017/7/7b/T--TU_Dresden--P_Communication_Demonstration_Figure_3.png" alt="Figure 2: Co-culture of sender strain (SeSt) and receiver strain (ReSt) using ThinCert™ cell culture inserts." class="makeresponsive zoom"/> | ||
<figcaption><b>Figure 2: Co-culture of sender strain (SeSt) and receiver strain (ReSt) using ThinCert™ cell culture inserts.</b> The increasing luminescence of the ReSt (inside of the well) co-cultured with the SeSt (found in the insert) induced with xylose (SeSt + ReSt) was documented by a chemoluminescence imaging system. Cultures containing only SeSt or ReSt served as negative controls. The latter exhibites a weak increase of luminescence because of the promoter’s basal activity (t5).</figcaption> | <figcaption><b>Figure 2: Co-culture of sender strain (SeSt) and receiver strain (ReSt) using ThinCert™ cell culture inserts.</b> The increasing luminescence of the ReSt (inside of the well) co-cultured with the SeSt (found in the insert) induced with xylose (SeSt + ReSt) was documented by a chemoluminescence imaging system. Cultures containing only SeSt or ReSt served as negative controls. The latter exhibites a weak increase of luminescence because of the promoter’s basal activity (t5).</figcaption> | ||
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<figure class="makeresponsive floatleft" style="width: 51.0752%;"> | <figure class="makeresponsive floatleft" style="width: 51.0752%;"> | ||
<img src="https://static.igem.org/mediawiki/2017/1/1e/T--TU_Dresden--P_Communication_Demonstration_Figure_4.png" alt="Figure 3: Co-culture of sender strain (SeSt) and receiver strain (ReSt) using Peptidosomes." class="makeresponsive zoom"> | <img src="https://static.igem.org/mediawiki/2017/1/1e/T--TU_Dresden--P_Communication_Demonstration_Figure_4.png" alt="Figure 3: Co-culture of sender strain (SeSt) and receiver strain (ReSt) using Peptidosomes." class="makeresponsive zoom"> | ||
<figcaption><b>Figure 3: Co-culture of sender strain (SeSt) and receiver strain (ReSt) using Peptidosomes.</b> <b>A</b>, <b>B</b> and <b>C</b> illustrate the experimental set-up whereas <b>D</b>, <b>E</b> and <b>F</b> display the results of the well scan. There is only an increase of luminescence (≥ 40 RLU, pink), restricted to the Peptidosomes, if the encapsulated ReSt is cultivated within the SeSt <b>(A, D)</b>. Cultures containing either SeSt <b>(B, E)</b> or encapsulated ReSt <b>(C, F)</b> served as negative controls.</figcaption> | <figcaption><b>Figure 3: Co-culture of sender strain (SeSt) and receiver strain (ReSt) using Peptidosomes.</b> <b>A</b>, <b>B</b> and <b>C</b> illustrate the experimental set-up whereas <b>D</b>, <b>E</b> and <b>F</b> display the results of the well scan. There is only an increase of luminescence (≥ 40 RLU, pink), restricted to the Peptidosomes, if the encapsulated ReSt is cultivated within the SeSt <b>(A, D)</b>. Cultures containing either SeSt <b>(B, E)</b> or encapsulated ReSt <b>(C, F)</b> served as negative controls.</figcaption> | ||
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Revision as of 10:04, 1 November 2017
Peptidosomes
Short description
Peptidosomes are the new fundamental approach for generating and applying encapsulated bacteria. We are creating cages containing a liquid environment inside. The mesh-like structure of the cage allows the selective exchange of compounds via diffusion. Therefore, we are able to benefit from the entrapped cells’ abilities, while still ensuring that they are not released into their surroundings. Peptidosomes can be further enhanced by incorporating magnetic or biological beads – which are also functionalized with proteins – into their peptide-based fibrillary shell.
Achievements
Stability and Diffusion
We proved that we are able to produce stable Peptidosomes with the sizes of 1 µL to 20 µL. Furthermore we showed that a diffusion between the inside of the Peptidosomes and the environment is possible. This was crucial because it’s necessary to make fresh nutrients available for the organism, and/or to allow the release of secreted molecules of interest out of the peptidosome while keeping the bacteria inside.
Encapsulation of bacteria
As demonstrated with different Methods we are able to encapsulate bacteria inside the Peptidosome and detect them. In figure 3 a well scan of a Peptidosome filled with bacteria is shown. You can reconstruct the detection methods with protocol XXX. In addition we proved that the bacteria can grow inside the Peptidosome.
Surface decoration
We proved that it is possible to trap dynabeads inside the shell and attach molecules to them.
Beta-Lactam Biosensor
Short description
Worldwide, multidrug-resistant bacteria are on the rise and provoke the intensive search for novel effective compounds. To simplify the search for new antibiotics and to track the antibiotic pollution in water samples, whole-cell biosensors constitute a helpful investigative tool. In this part of EncaBcillus, we developed a functional and independent heterologous Beta-lactam biosensor in Bacillus subtilis. These specialised cells are capable of sensing a compound of the beta-lactam family and will respond by the production of an easily measurable luminescence signal. We analysed the detection range and sensitivity of the biosensor in response to six different Beta-lactam antibiotics from various subclasses. The evaluated biosensor was then encapsulated into Peptidosomes to proof the concept of our project EncaBcillus. The encapsulation of engineered bacteria allows a simplified handling and increased biosafety, potentially raising the chances for their application in e.g. sewage treatment plants.
Achievements
In this part of the EncaBcillus project, we successfully created and evaluated a novel completely heterologous biosensor for Beta-lactam antibiotics in Bacillus subtilis. This biosensor is able to detect the following Beta-Lactam antibiotics: ampicillin, carbenicillin, cefperazone, cefalexin. cefoxitin and penicillin G in liquid and on solid MH-Medium as illustrated in Figure 1 and 2. Besides the detection range, we analyzed the sensitivity of the biosensor for these specific compounds in several dose-response experiments shown in Figure 3. Furthermore, we demonstrated the applicability of the biosensor when encapsulated into Peptidosomes. As depicted in Figure 4, the biosensor was able to sense the beta-lactam diffusing through the membrane of the Peptidosome. Hereby, we proved the possibility of encapsulating functional engineered bacteria into Peptidosomes and therefore the concept behind our project EncaBcillus.
Signal Peptide Toolbox
Short description
In bacteria, protein secretion is mainly orchestrated by the Sec Pathway via Signal Peptides (SP), which are located at the N-terminus of secreted proteins. The secretion efficiency is not determined by the sequence of the SP alone, but instead is the combined result of an SP with its specific target protein. This necessitates establishing efficient screening procedures to evaluate all possible SP/target protein combinations. We developed such an approach for our Signal Peptide Toolbox, which contains 74 Sec-dependent SPs. It combines combinatorial construction with highly reproducible, quantitative measurements. By applying this procedure, we demonstrate the secretion of three different proteins and succeeded in identifying the most potent SP-protein combination for each of them. This thoroughly evaluated measurement tool, in combination with our SP toolbox (fully available via the partsregistry) enables an organism-independent, straightforward approach to identifying the best combination of SP with any protein of interest.
Achievements
We evaluated and proved the applicability of a powerful toolbox to quickly screen via a high throughput procedure for improved secretion of proteins in bacteria - the Signal Peptide Toolbox. It combines combinatorial construction with highly reproducible, quantitative measurements to maximize secretion levels.
We applied the Signal Peptide Toolbox to three different proteins. Via demonstrating the secretion of sfGFP, amyE and mCherry, and identifying the most potent SP-protein combinations for each of them (Figure 1, 2, 3), we proved the applicability of this powerful toolbox.
Evaluation Vector
Short description
Peptidosomes in combination with Bacillus subtilis offer a perfect platform for enhanced protein overproduction by the means of efficient protein secretion provided through B. subtilis and the easy purification due to the physical separation of bacteria and the end-product in the supernatant facilitated by the Peptidosomes. Naturally, B. subtilis is a strong secretion host and in order to take full advantage of this great potential it is necessary to evaluate all possible combinations of the B. subtilis’ secretion signal peptides and the proteins of interest. Therefore, we developed the Evaluation Vector (EV) which is a powerful genetic tool containing a multiple cloning site (MCS) specifically designed to easily exchange translational fusions composed of the desired protein and a secretion signal peptide.
Achievements
We build a unique multiple cloning site which allows for easy insertion of both, a promoter and two basic or composite parts - the Evaluation Vector. The distinct features of the Evaluation Vector provide an easy cloning and screening workflow (Figure 1).
Additionally, the insertion of reporters to identify positive replacements by insert integration allow for a quick cloning and screening procedure in Escherichia coli. All three different stages of the insertion of expression units can be identified via a three-color scheme easily (Figure 2).
Furthermore, we proved the applicability and functionality of the Evaluation Vector as we evaluated it in the course of the Signal Peptide Toolbox.
Secretion
Short description
In combing Bacillus subtilis powerful secretion capacity with Peptidosomes as a new platform for functional co-cultivation we aim to produce multi protein complexes. Various strains - each secreting distinct proteins of interest - can be cultivated in one reaction hub while being physically separated. In this part of EncaBcillus we study extracelluar protein interaction mediated by the SpyTag/SpyCatcher system. This set-up bears the potential for an effective production of customizable biomaterials or enzyme complexes.
Achievements
We were able to engineer B. subtilis to secret large quantities of mCherry constructs, c-terminally fused with a mini. SpyCatcher or SpyTag (Tags). In Figure 1 we assayed the fluorescence in the supernatant, that surpasses the wilde type by far. The typical red color of mCherry is even visible in the supernatant under day light conditions (Figure 2).
We demonstrated the functionality of our SpyTag/SpyCatcher system via SDS-PAGE (Figure 3). Upon 4 h of incubating the supernatants containing mCherry with either SpyTag or mini. SpyCatcher, we were able to detect the conjugated fusion protein. Thus, we provide evidence for the applicability of co-culturing approaches using Peptidosomes, to produce self conjugation protein complexes.
Communication
Short description
By using Peptidosomes we introduce a new powerful platform for co-culturing. This technique physically separates bacterial populations without limiting their ability to communicate with each other via signalling molecules. This part of EncaBcillus is focused on proving the concept of communication between encapsulated bacteria by making use of the native regulatory system for competence development in Bacillus subtilis which is based on quorum sensing mediated by the ComX pheromone.
Achievements
We engineered a sender strain (SeSt) with an additional inducible copy of comX and a comX-deficient receiver strain (ReSt) containing the ComX-dependent promoter PsrfA fused to the lux operon (Figure 1). Therefore, we could easily detect communication between the co-cultured SeSt and ReSt via ComX by measuring the luminescence output of the ReSt. After proofing this concept using ThinCert™ cell culture inserts (Figure 2) we applied it to Peptidosomes (Figure 3). Consequently we could show communication between encapsulated bacteria and bacteria in the surroundings and made substantial progress in the evaluation of Peptidosomes as a tool for co-cultivation and studies of microbial interactions.
