Difference between revisions of "Team:TU Dresden/Demonstrate"
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<h1 class="box-heading">Peptidosomes</h1> | <h1 class="box-heading">Peptidosomes</h1> | ||
| − | <h2>Short | + | <h2>Short Description</h2> |
<p>Peptidosomes are the new fundamental approach for generating and applying encapsulated bacteria. | <p>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. | 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. | ||
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| − | + | <a class="read-more" href="https://2017.igem.org/Team:TU_Dresden/Project/Peptidosomes"></a> | |
</div> | </div> | ||
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<div class="contentbox"> | <div class="contentbox"> | ||
<h1 class="box-heading">Beta-Lactam Biosensor</h1> | <h1 class="box-heading">Beta-Lactam Biosensor</h1> | ||
| − | <h2>Short | + | <h2>Short Description</h2> |
<p>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 <i>Bacillus subtilis</i>. 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.</p> | <p>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 <i>Bacillus subtilis</i>. 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.</p> | ||
<hr> | <hr> | ||
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</div> | </div> | ||
</div> | </div> | ||
| + | <a class="read-more" href="https://2017.igem.org/Team:TU_Dresden/Project/Biosensor"></a> | ||
</div> | </div> | ||
<div class="contentbox"> | <div class="contentbox"> | ||
<h1 class="box-heading">Signal Peptide Toolbox</h1> | <h1 class="box-heading">Signal Peptide Toolbox</h1> | ||
| − | <h2>Short | + | <h2>Short Description</h2> |
<p>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 Parts Registry) enables an organism-independent, straightforward approach to identifying the best combination of SP with any protein of interest.</p> | <p>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 Parts Registry) enables an organism-independent, straightforward approach to identifying the best combination of SP with any protein of interest.</p> | ||
<hr> | <hr> | ||
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</figure> | </figure> | ||
</figure> | </figure> | ||
| + | <a class="read-more" href="https://2017.igem.org/Team:TU_Dresden/Measurement"></a> | ||
</div> | </div> | ||
<div class="contentbox"> | <div class="contentbox"> | ||
<h1 class="box-heading"> Evaluation Vector</h1> | <h1 class="box-heading"> Evaluation Vector</h1> | ||
| − | <h2>Short | + | <h2>Short Description</h2> |
<p>Peptidosomes in combination with <i>Bacillus subtilis</i> offer a perfect platform for enhanced protein overproduction by the means of efficient protein secretion provided through <i>B. subtilis</i> and the easy purification due to the physical separation of bacteria and the end-product in the supernatant facilitated by the Peptidosomes. Naturally, <i>B. subtilis</i> 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 <i>B. subtilis’</i> 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.</p> | <p>Peptidosomes in combination with <i>Bacillus subtilis</i> offer a perfect platform for enhanced protein overproduction by the means of efficient protein secretion provided through <i>B. subtilis</i> and the easy purification due to the physical separation of bacteria and the end-product in the supernatant facilitated by the Peptidosomes. Naturally, <i>B. subtilis</i> 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 <i>B. subtilis’</i> 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.</p> | ||
<hr> | <hr> | ||
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<p>Furthermore, we proved the applicability and functionality of the Evaluation Vector as we evaluated it in the course of the Signal Peptide Toolbox.</p> | <p>Furthermore, we proved the applicability and functionality of the Evaluation Vector as we evaluated it in the course of the Signal Peptide Toolbox.</p> | ||
</figure> | </figure> | ||
| + | <a class="read-more" href="https://2017.igem.org/Team:TU_Dresden/Composite_Part"></a> | ||
</div> | </div> | ||
<div class="contentbox"> | <div class="contentbox"> | ||
<h1 class="box-heading">Secretion</h1> | <h1 class="box-heading">Secretion</h1> | ||
| − | <h2>Short | + | <h2>Short Description</h2> |
| − | <p>In combining <i>Bacillus subtilis</i> 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 | + | <p>In combining <i>Bacillus subtilis'</i> 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 setup bears the potential for an effective production of customizable biomaterials or enzyme complexes.</p> |
<hr> | <hr> | ||
<h2>Achievements</h2> | <h2>Achievements</h2> | ||
| − | <p> We were able to engineer <i> B. subtilis </i> to secret large quantities of mCherry constructs, | + | <p> We were able to engineer <i> B. subtilis </i> to secret large quantities of mCherry constructs, C-terminally fused with a mini. SpyCatcher or SpyTag (Tags). In Figure 12 we assayed the fluorescence of the supernatant containing mCherry SpyCatcher/SpyTag constructs, which surpasses the wild type by far. The typical red color of mCherry is even visible in the supernatant under day light conditions (Figure 13).</p> |
| − | <p>We demonstrated the functionality of our SpyTag/SpyCatcher system via SDS-PAGE (Figure 14). Upon 4 | + | <p>We demonstrated the functionality of our SpyTag/SpyCatcher system via SDS-PAGE (Figure 14). Upon 4 hr 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.<p> |
<figure> | <figure> | ||
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<figure class="makeresponsive floatleft" style="width: 33.50%;"> | <figure class="makeresponsive floatleft" style="width: 33.50%;"> | ||
<img class="zoom" src="https://static.igem.org/mediawiki/2017/b/bb/T--TU_Dresden--secretion--results7.png" alt="Figure 14: SDS gel with crude and purified supernatants."> | <img class="zoom" src="https://static.igem.org/mediawiki/2017/b/bb/T--TU_Dresden--secretion--results7.png" alt="Figure 14: SDS gel with crude and purified supernatants."> | ||
| − | <figcaption><b>Figure 14: SDS gel with crude and purified supernatants.</b> Expression of the multi copy mCherry constructs was induced with 1% Xylose and the supernatants were harvested after 16 h of incubation. The his-tagged proteins were purified with Ni-NTA agarose beads. Lane 1 was loaded with 3 μl of NEB´s “Color Prestained Protein Standard Broad Range” ladder. Crude (c) and purified (p) supernatant of wild-type (WT) are shown as a control in lane 2 and 3. Lane 4 and 5 contain the supernatant of <i>B. subtilis</i> producing mCherry-mini. SpyCatcher fusion protein (36,6 kDa). Lane 4 and 5 contain the supernatant of <i>B. subtilis</i> producing mCherry-SpyTag fusion protein (31,9 kDa). The crude supernatants of the two mCherry producing strains were combined, incubated for 4 | + | <figcaption><b>Figure 14: SDS gel with crude and purified supernatants.</b> Expression of the multi copy mCherry constructs was induced with 1% Xylose and the supernatants were harvested after 16 h of incubation. The his-tagged proteins were purified with Ni-NTA agarose beads. Lane 1 was loaded with 3 μl of NEB´s “Color Prestained Protein Standard Broad Range” ladder. Crude (c) and purified (p) supernatant of wild-type (WT) are shown as a control in lane 2 and 3. Lane 4 and 5 contain the supernatant of <i>B. subtilis</i> producing mCherry-mini. SpyCatcher fusion protein (36,6 kDa). Lane 4 and 5 contain the supernatant of <i>B. subtilis</i> producing mCherry-SpyTag fusion protein (31,9 kDa). The crude supernatants of the two mCherry producing strains were combined, incubated for 4 hr, purified and loaded onto lane 8 and 9. The fusion product of the mCherry constructs is visable in the crude and purified supernatant. |
</figcaption></figure> | </figcaption></figure> | ||
</figure> | </figure> | ||
| − | + | <a class="read-more" href="https://2017.igem.org/Team:TU_Dresden/Project/Secretion"></a> | |
</div> | </div> | ||
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<h1 class="box-heading"> Communication</h1> | <h1 class="box-heading"> Communication</h1> | ||
| − | <h2>Short | + | <h2>Short Description</h2> |
| − | <p>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 | + | <p>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 signaling 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 <i>Bacillus subtilis</i> which is based on quorum sensing mediated by the ComX pheromone.</p> |
<hr> | <hr> | ||
| Line 184: | Line 187: | ||
| − | + | <a class="read-more" href="https://2017.igem.org/Team:TU_Dresden/Project/Communication"></a> | |
</div> | </div> | ||
</main> | </main> | ||
Latest revision as of 13:51, 13 December 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
We proved that we are able to produce stable Peptidosomes with the sizes of 1 µL to 20 µL (Figure 1). Furthermore we showed that diffusion between the inside of the Peptidosomes and the environment is possible (Figure 2). This was crucial because it is necessary to make fresh nutrients available for the organism and to allow the release of secreted molecules of interest out of the peptidosome while keeping the bacteria inside.
As demonstrated with different methods, we are able to encapsulate bacteria inside the Peptidosome and detect them, i.e. with the plate reader well-scan technique (Figure 3). In addition we proved that the bacteria can also grow inside the Peptidosome.
By trapping Dynabeads inside the shell and attaching molecules to them we managed to decorate the surface (Figure 4).
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. Besides the detection range, we analyzed the sensitivity of the biosensor for these specific compounds in several dose-response experiments shown in Figure 5. Furthermore, we demonstrated the applicability of the biosensor when encapsulated into Peptidosomes. As depicted in Figure 6, 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.
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 Parts Registry) 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 7, 8, 9), 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 built 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 10).
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 11).
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 combining 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 setup 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 12 we assayed the fluorescence of the supernatant containing mCherry SpyCatcher/SpyTag constructs, which surpasses the wild type by far. The typical red color of mCherry is even visible in the supernatant under day light conditions (Figure 13).
We demonstrated the functionality of our SpyTag/SpyCatcher system via SDS-PAGE (Figure 14). Upon 4 hr 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 signaling 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 15). 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 16) we applied it to Peptidosomes (Figure 17). 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.
