Difference between revisions of "Team:TU Dresden/Project/Peptidosomes"

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<p>Hier muss noch eine Einleitung stehen, die dem Background angepasst ist!</p>
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<p><b>Hier muss noch eine Einleitung stehen, die dem Background angepasst ist!</b></p>
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    <figure class="makeresponsive floatleft" style="width: 50%;">
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      <img src="https://static.igem.org/mediawiki/2017/0/0c/T--TU_Dresden--pHchange.png"
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          alt="The color change of the peptidosomes with pH indicator during production"
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      <figcaption><b>Figure 1: The color change of the peptidosomes with pH indicator during production</b> A) Peptidosomes before exposure to CO2, red colored are peptidosomes with pH indicator, transparent ones without, B) Peptidosomes after the exposure, only the peptidosomes with pH indicator have a discoloration (yellow).</figcaption>
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      <img src="https://static.igem.org/mediawiki/2017/3/31/T--TU_Dresden--peptidosomesizes.png"
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          alt="Different sizes of Peptidosomes"
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      <figcaption><b>Figure 2: Different sizes of Peptidosomes</b> </figcaption>
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<p>For making the pH-drop visible and colour the peptidosomes we used the pH- indicator cresol red, which acquires a red or violet tone with pH of 7 and higher (initially the Fmoc-FF solution has a pH of 10.5), and turns yellow at pH 6 and below. The pH indicator was added to the Fmoc-FF solution and produced the peptidosomes as describes in (LINK TO DESIGN).</p>
 
<p>For making the pH-drop visible and colour the peptidosomes we used the pH- indicator cresol red, which acquires a red or violet tone with pH of 7 and higher (initially the Fmoc-FF solution has a pH of 10.5), and turns yellow at pH 6 and below. The pH indicator was added to the Fmoc-FF solution and produced the peptidosomes as describes in (LINK TO DESIGN).</p>
 
<p>We created Peptidosomes with a range of 1 to 20 µL successfully. For discovering the optimal exposure time to CO2 we varied it between 30 sec and 20 min. We found out, that the ones with an exposure time of 10 min were the most stable ones, showing stability after several days, even under 37°C incubation with shaking. </p>
 
<p>We created Peptidosomes with a range of 1 to 20 µL successfully. For discovering the optimal exposure time to CO2 we varied it between 30 sec and 20 min. We found out, that the ones with an exposure time of 10 min were the most stable ones, showing stability after several days, even under 37°C incubation with shaking. </p>
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<p>With a really straight forward experiment, including the help of the pH-indicator we were able to prove that a diffusion between the inside of the peptidosome and the surrounding environment is possible. We transferred Peptidosomes to water or LB-Media and measured the time it took for the colour to disappear, or in other words, the time it takes for the coloured solution inside the cage to diffuse out of it. </p>
 
<p>With a really straight forward experiment, including the help of the pH-indicator we were able to prove that a diffusion between the inside of the peptidosome and the surrounding environment is possible. We transferred Peptidosomes to water or LB-Media and measured the time it took for the colour to disappear, or in other words, the time it takes for the coloured solution inside the cage to diffuse out of it. </p>
 
<p>Proving that diffusion between the inside of the peptidosome and the environment is possible, we wanted to know next if diffusion between two peptidosomes which are in direct contact is possible. For this experiment only one of the two connected peptidosomes contained coloured solution. Over the lapse of around 1.5 hours, it was possible to observe how the colour was disseminating to the non-coloured peptidosome until it reached an equilibrium (Figure X), proving that there is diffusion, or intercommunication, between the two peptidosomes. </p>
 
<p>Proving that diffusion between the inside of the peptidosome and the environment is possible, we wanted to know next if diffusion between two peptidosomes which are in direct contact is possible. For this experiment only one of the two connected peptidosomes contained coloured solution. Over the lapse of around 1.5 hours, it was possible to observe how the colour was disseminating to the non-coloured peptidosome until it reached an equilibrium (Figure X), proving that there is diffusion, or intercommunication, between the two peptidosomes. </p>
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<p>Additionally, to the previous described method, we used a microinjection-technique to inject a coloured solution to the inside of the peptidosome (figure XXX). To close the hole that was probably opened on the membrane by the introducing the glass capillary, the peptidosome was exposed again for 5 min to CO2. Afterwards it was transferred to water. As shown in figure XXX D) the peptidosome was stable. </p>
 
<p>Additionally, to the previous described method, we used a microinjection-technique to inject a coloured solution to the inside of the peptidosome (figure XXX). To close the hole that was probably opened on the membrane by the introducing the glass capillary, the peptidosome was exposed again for 5 min to CO2. Afterwards it was transferred to water. As shown in figure XXX D) the peptidosome was stable. </p>
 
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<p>Treatment 1 was a negative control, since the strain of B. subtilis (wildtype) cannot develop in absence of nitrogen, so no growth at all was expected. Treatment 2 was the positive control: with the nitrogen supplement, B. subtilis should be able to grow. These expectations corresponded with reality: colonies grew in treatment 2 but none in treatment 1. Treatments 3 and 4 did not result in colony growth either, meaning that the Fmoc-FF cannot be used as a source of nitrogen for the bacteria. </p>
 
<p>Treatment 1 was a negative control, since the strain of B. subtilis (wildtype) cannot develop in absence of nitrogen, so no growth at all was expected. Treatment 2 was the positive control: with the nitrogen supplement, B. subtilis should be able to grow. These expectations corresponded with reality: colonies grew in treatment 2 but none in treatment 1. Treatments 3 and 4 did not result in colony growth either, meaning that the Fmoc-FF cannot be used as a source of nitrogen for the bacteria. </p>
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<p>The experiment to test the tolerance was performed as follows: B. subtilis culture was divided in four treatments, varying the pH of the culture in each one; 7 (normal growth condition as a control), 8, 9, and 10. NaOH was used to induce the different changes in the pH for each treatment, and was added after one hour of cultivation. The experiment was carried out in a plate reader to follow the change of the optical density (OD 600) which correlates with bacterial growth. </p>
 
<p>The experiment to test the tolerance was performed as follows: B. subtilis culture was divided in four treatments, varying the pH of the culture in each one; 7 (normal growth condition as a control), 8, 9, and 10. NaOH was used to induce the different changes in the pH for each treatment, and was added after one hour of cultivation. The experiment was carried out in a plate reader to follow the change of the optical density (OD 600) which correlates with bacterial growth. </p>
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<p>The graph shows the growth of the organisms under each condition. It can be observed that from pH 7 to 9, no significant change in the growth is observed. However, under pH 10, the organism stops its growth. To check if the bacteria was still viable after the high pH treatment, it was transferred to growth plates with neutral pH. There, it was observed that B. subtilis was able to recover and growth normally, meaning that the organism can survive the process of encapsulation. </p>
 
<p>The graph shows the growth of the organisms under each condition. It can be observed that from pH 7 to 9, no significant change in the growth is observed. However, under pH 10, the organism stops its growth. To check if the bacteria was still viable after the high pH treatment, it was transferred to growth plates with neutral pH. There, it was observed that B. subtilis was able to recover and growth normally, meaning that the organism can survive the process of encapsulation. </p>
  
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We performed a plate reader assay using the well-scan-mode. In this mode, the whole well is scanned to detect the exact position of a signal, either fluorescence or luminescence. Its absence is displayed in a map with a green colour, while the position of the fluorescence/luminescence source appears as red. </p>
 
We performed a plate reader assay using the well-scan-mode. In this mode, the whole well is scanned to detect the exact position of a signal, either fluorescence or luminescence. Its absence is displayed in a map with a green colour, while the position of the fluorescence/luminescence source appears as red. </p>
 
<p>The well scan maps appear completely green where fluorescence/luminescence is absent, i.e. water and empty peptidosome. Wells containing a sample of the day culture and lyophilized eGFP solved in water show a red colour in the whole map. However, a localized red spot over a green background is observed where the source of fluorescence/luminescence is contained: the cells trapped inside the peptidosomes. This shows that when the peptidosome with cells inside is transferred to water, bacteria cannot diffuse away, but its kept contained within the structure, resulting in a localized red signal. </p>
 
<p>The well scan maps appear completely green where fluorescence/luminescence is absent, i.e. water and empty peptidosome. Wells containing a sample of the day culture and lyophilized eGFP solved in water show a red colour in the whole map. However, a localized red spot over a green background is observed where the source of fluorescence/luminescence is contained: the cells trapped inside the peptidosomes. This shows that when the peptidosome with cells inside is transferred to water, bacteria cannot diffuse away, but its kept contained within the structure, resulting in a localized red signal. </p>
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<h4> Fluorescence microscopy</h4>
 
<h4> Fluorescence microscopy</h4>
 
<p>The encapsulation of B. subtitilis expressing sfGFP in a constitutive way was also demonstrated by the fluorescence microscopy. In this experiment, the bacteria were encapsulated as described. As seen in Figure X, the peptidosome emitted green light what proved the existence of sfGFP-expressing bacteria. </p>
 
<p>The encapsulation of B. subtitilis expressing sfGFP in a constitutive way was also demonstrated by the fluorescence microscopy. In this experiment, the bacteria were encapsulated as described. As seen in Figure X, the peptidosome emitted green light what proved the existence of sfGFP-expressing bacteria. </p>
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<p>By introducing the treatments, the number of colonies was reduced from several hundreds to an average of .7 for the washing steps and 1.7 for the low pH treatment. After analysing the results, we concluded that the washing steps are important to reduce the number of cells released in the supernatant, whereas the treatment with acid broth does not add a significant effect on this. In that way, by introducing the washing steps and also reducing the concentration of cells in the peptidosomes, the amount of bacteria present on the outer surface of the membrane was importantly diminished, fact that was corroborated by performing a second cryo-SEM and showed below. </p>
 
<p>By introducing the treatments, the number of colonies was reduced from several hundreds to an average of .7 for the washing steps and 1.7 for the low pH treatment. After analysing the results, we concluded that the washing steps are important to reduce the number of cells released in the supernatant, whereas the treatment with acid broth does not add a significant effect on this. In that way, by introducing the washing steps and also reducing the concentration of cells in the peptidosomes, the amount of bacteria present on the outer surface of the membrane was importantly diminished, fact that was corroborated by performing a second cryo-SEM and showed below. </p>
 +
 
<p>In the second measurement the number of detectable bacteria that lie or are integrated on the membrane is significantly lower. Only a few individual fibers are visible and the surface is wrinkled. (figure XX A), B)) </p>
 
<p>In the second measurement the number of detectable bacteria that lie or are integrated on the membrane is significantly lower. Only a few individual fibers are visible and the surface is wrinkled. (figure XX A), B)) </p>
 
<p>Only on the peptidosome with the low pH treatment, a cell that was not integrated in the membrane was observed (D). </p>
 
<p>Only on the peptidosome with the low pH treatment, a cell that was not integrated in the membrane was observed (D). </p>
 
<p>The results of the growth experiment with the additional treatments were confirmed microscopically. There was no significant improvement in the peptidosomes treated with acid LB medium compared to the sole integration of wash steps. Only a single cell, which could relieve from the peptidosome, was detected. This confirms the reduced number of colonies in the supernatant of the growth experiment when carrying out the additional treatment methods. </p>
 
<p>The results of the growth experiment with the additional treatments were confirmed microscopically. There was no significant improvement in the peptidosomes treated with acid LB medium compared to the sole integration of wash steps. Only a single cell, which could relieve from the peptidosome, was detected. This confirms the reduced number of colonies in the supernatant of the growth experiment when carrying out the additional treatment methods. </p>
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<p>The one loosely attached cell might be a problem for some applications where the surrounding medium is expected to be free of bacteria, therefore, the manufacturing technique of peptidosomes should be adapted accordingly. An adequate method for this could be introducing the cells by microinjection, since there is not a chance that bacteria can be attached to the outer part of the membrane. </p>
 
<p>The one loosely attached cell might be a problem for some applications where the surrounding medium is expected to be free of bacteria, therefore, the manufacturing technique of peptidosomes should be adapted accordingly. An adequate method for this could be introducing the cells by microinjection, since there is not a chance that bacteria can be attached to the outer part of the membrane. </p>
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<p>Nevertheless, the surface of DynaBeads can be decorated with His-Tag protein. For the “proof of principle” experiments His-Tag GFP were selected due to its availability and easy imaging procedure. First, the Invitrogen Protocol was optimized for our goals and tested for DynaBeads decoration with histidine-tagged GFP (Picture 1). </p>
 
<p>Nevertheless, the surface of DynaBeads can be decorated with His-Tag protein. For the “proof of principle” experiments His-Tag GFP were selected due to its availability and easy imaging procedure. First, the Invitrogen Protocol was optimized for our goals and tested for DynaBeads decoration with histidine-tagged GFP (Picture 1). </p>
 
<p>To prove the surface of the Dynabeads enveloped to the Peptidosome membrane availability for the decoration the labeling procedure was applied after the Peptidosome formation in both Binding/Wash Buffer and LB media (Picture 2). </p>
 
<p>To prove the surface of the Dynabeads enveloped to the Peptidosome membrane availability for the decoration the labeling procedure was applied after the Peptidosome formation in both Binding/Wash Buffer and LB media (Picture 2). </p>
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<p>In conclusion, here we proved the possibility of Peptidosome surface decoration with histidine-tagged molecules that can be used for various applications where enzymatic activity of the surface of Peptidosome or Peptidosome immobilization is required. Surface decoration protocol is compatible with almost any goals due to its flexibility, as the  
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<p>In conclusion, here we proved the possibility of Peptidosome surface decoration with histidine-tagged molecules that can be used for various applications where enzymatic activity of the surface of Peptidosome or Peptidosome immobilization is required. Surface decoration protocol is compatible with almost any goals due to its flexibility, as the decoration procedure can be performed before and after Peptidosome formation in the specific Binding/Washing buffer or just in the LB media. </p>
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decoration procedure can be performed before and after Peptidosome formation in the specific Binding/Washing buffer or just in the LB media. </p>
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Revision as of 19:29, 30 October 2017

It´s a trap!

Abstract

Peptidosomes are the new fundamental approach for generating and applying encapsulated bacteria. By the creation of spherical compartments containing a liquid environment inside, bacteria are still able to grow and fulfil a given task. The mesh-like structure of the sphere allows the selective exchange of compounds via diffusion, but holds the bacteria trapped inside. 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 themselves can be functionalized with proteins – into their peptide-based fibrillary shell.

Background

Bacteria are omnipresent in biotechnology and applied projects. They can be used as hosts to produce nearly any biological compound of interest such as: drugs, vaccines, enzymes, antibiotics or even fuels and solvents. Their fast life cycle and comparable low requirements of living conditions highlight their industrial relevance. Over the last decades, the main focus to increase yields laid on extensive metabolic engineering and optimizing growth conditions.

Yet, there are more aspect which need to be considered when producing a compound of interest. First, where is the product of interest found: inside of the producing strain or will it be secreted to the surrounding media? Second, what is necessary to separate the valuable end-product from the bacteria? And maybe most important, how to assure a safe use of genetically engineered production strains?
If you would like to know more on encapsulated bacteria in Peptdisomes and boosting the production of a compound of interest check out our: Signal Peptide Toolbox and Peptide Secretion sections.

To address these major biological and technical questions, the TU Dresden iGEM team presents EncaBcillus. Using Bacillus subtilis as model organism we introduce a new fundamental approach for cultivation of bacteria: the Peptidsomes. These Peptidosmes are buildup of self-assembled Fmoc dipeptide phenylalanines (Fmoc-FF) and are able to form spherical cages. The cages hold back the bacteria from the surrounding but are freely diffusible for smaller molecules. We show, that B. subtilis is able to grow, while encapsulated inside of the Pepdiosomes and demonstrate the applicability of two (fluorescence and luminescence) reports for the use with Pepdiosomes.

While evaluating this new method of bacterial immobilization, we established two applications using Peptidsomes:

Design

Fmoc-FF

For their many and very interesting properties, nanostructures are gaining great attention in the area of material sciences. Nanostructures are assemblies or clusters ordered within nanoscopic dimensions. Sometimes the building blocks of the nanostructures (with organic or inorganic sources) can assemble themselves, obeying several non-covalent forces that dictate their organization in supramolecular structures. These interactions can be for example hydrogen bonds, van der waals forces, aromatic interactions, among others [1]. We set our focus on the self-assembling building block Fmoc-FF (9-fluorenylmethoxycarbonyl diphenylalanine).

Fig 1 Chemical structure of Fmoc-FF
Fig 1 Chemical structure of Fmoc-FF

In 2003, while studying the mechanisms that direct the self-assembly of amyloid fibrils by short aromatic peptides, It was observed that the dipeptide diphenylalanine (FF), the core recognition motif of the Alzheimer’s β-amyloid polypeptide, was self-assembling into nanotubular structures in aqueous solution [2]. With the help of X-ray diffraction techniques, it was observed that self-assembly occurred due to the tight stacking of the phenyl rings in the dipeptide [3] Later, while studying the interactions in the process, the chemical group 9-fluorenylmethoxycarbonyl (Fmoc) was added at the N terminal of the dipeptide. The Fmoc cap was introducing an additional aromatic group, facilitating the self-assembly into typical amyloid-like fibrils [4].

Later an interesting property was discovered: it is possible to trigger the self-assembly of the dipeptide in solution. at a pH higher than 8, the dipeptide stayed in solution, but when slowly adding concentrated hydrochloric acid to reach pH levels below 8, a clear gel was formed [5].

At alkaline pH, the molecules are negatively charged and therefore repealing each other. If the pH drops, protonation of the molecules occurs, neutralizing the negative charge and permitting the self-assembly of the dipeptide into the aforementioned fibers [6]. In 2012 the formation of the mesh was induced by exposing a solution of Fmoc-FF with gaseous CO2 [7]. The gas reacts with the water and disassociates into bicarbonate ions and protons, which acidifies the solution and triggers the self-assembly of the dipeptide.

Peptidosome creation

Using the mentioned method of Braun and Cardoso (2012) we build our Peptidosomes. The challenge was to build a closed round cage formed by an Fmoc-FF membrane surrounding a liquid core. For this we use an ultra-hydrophobic surface. When deposited on an ultra-hydrophobic surface, a droplet of water will minimize the contact with this surface. This will result in a droplet with a contact angle higher than 160°. In other words, the droplet will remain stable almost as a perfect sphere [8].

To prepare a Peptidosome, a droplet of Fmoc-FF solution is placed on the mentioned membrane, keeping its spherical shape due to the ultrahydrophobicity. Afterwards the droplet is exposed directly with CO2. The ultrahydrophobic PTFE membrane allows CO2 to reach the entire surface of the droplet, even the small contact surface on the permeable membrane.

Exposing with CO2 causes a pH change in the droplet. Carbonic acid is formed when the gas comes into contact with water. The carbonic acid subsequently dissociates into bicarbonate ions and hydrogen ions.

The reaction of carbon dioxide and water leads to the formation of carbonic acid, which dissociates into bicarbonate ions and hydrogen ions. All reactions are reversible.

Cresol red was added as pH indicator to follow the drop of the pH during the experiment. A red / violet coloration can be seen in the basic pH. With acidification to a pH below 7.0, the solution turns yellow.

The Fmoc-FF solution has a pH of 10.5. Exposing with CO2 reduces the pH value. The carboxy group of the Fmoc-FF is protonated, neutralizing the negative charge and triggering the self-assembling of the dipeptide molecules. Since the CO2 only comes into contact with the surface of the droplet, a fibrillar network is formed only there, while the inside of the droplet retains its liquid state.

Schematic representation of the change of the Fmoc-FF molecule during peptidosome production
Figure 2: Schematic representation of the change of the Fmoc-FF molecule during peptidosome production The molecule is present in its ionized form before the exposure to CO2. During the exposure, the membrane of neutralized self-assembled Fmoc-FFs forms around the drop. The core of the drop remains in the liquid, unassembled form.

Bacteria encapsulated in Peptidosomes

We wanted to characterize and prove the function of our Peptidosome with the use of Bacillus subtilis. This was a totally new approach since Fmoc-FF was never brought in contact with bacteria.

To encapsulate the bacteria we took samples of overnight cultures and day cultures prepared in LB media.

As soon as the day cultures had reached an OD600 between 0.2 and 0.6, the required amount of culture for the experiment was centrifuged for 5 min at 16,000 g. The supernatant was then discarded and the pellet resuspended in Fmoc-FF solution. Droplets of 15 μL of this solution were deposited on an ultrahydrophobic membrane and exposed with CO2.

For the growth experiments (LINK) Peptidosomes with an OD600 of 0.02 were created.

We performed multiple assays to prove the encapsulating and growth inside the Peptidsosome.

  • Plate reader well scan
  • Stereo fluorescence microscopie

Results

1. Characterization of Peptidosomes

Hier muss noch eine Einleitung stehen, die dem Background angepasst ist!

The color change of the peptidosomes with pH indicator during production
Figure 1: The color change of the peptidosomes with pH indicator during production A) Peptidosomes before exposure to CO2, red colored are peptidosomes with pH indicator, transparent ones without, B) Peptidosomes after the exposure, only the peptidosomes with pH indicator have a discoloration (yellow).
Different sizes of Peptidosomes
Figure 2: Different sizes of Peptidosomes

For making the pH-drop visible and colour the peptidosomes we used the pH- indicator cresol red, which acquires a red or violet tone with pH of 7 and higher (initially the Fmoc-FF solution has a pH of 10.5), and turns yellow at pH 6 and below. The pH indicator was added to the Fmoc-FF solution and produced the peptidosomes as describes in (LINK TO DESIGN).

We created Peptidosomes with a range of 1 to 20 µL successfully. For discovering the optimal exposure time to CO2 we varied it between 30 sec and 20 min. We found out, that the ones with an exposure time of 10 min were the most stable ones, showing stability after several days, even under 37°C incubation with shaking.

The final aim of the project is the encapsulation and cultivation of bacteria inside the peptidosomes. For this, it is crucial that while the Fmoc-FF network should not let the organisms escape, it should allow the interchange and communication with the surrounding environment, for example, to make available fresh nutrients for the organism, and/or to allow the release of secreted molecules of interest out of the peptidosome while keeping the bacteria inside.

With a really straight forward experiment, including the help of the pH-indicator we were able to prove that a diffusion between the inside of the peptidosome and the surrounding environment is possible. We transferred Peptidosomes to water or LB-Media and measured the time it took for the colour to disappear, or in other words, the time it takes for the coloured solution inside the cage to diffuse out of it.

Proving that diffusion between the inside of the peptidosome and the environment is possible, we wanted to know next if diffusion between two peptidosomes which are in direct contact is possible. For this experiment only one of the two connected peptidosomes contained coloured solution. Over the lapse of around 1.5 hours, it was possible to observe how the colour was disseminating to the non-coloured peptidosome until it reached an equilibrium (Figure X), proving that there is diffusion, or intercommunication, between the two peptidosomes.

Additionally, to the previous described method, we used a microinjection-technique to inject a coloured solution to the inside of the peptidosome (figure XXX). To close the hole that was probably opened on the membrane by the introducing the glass capillary, the peptidosome was exposed again for 5 min to CO2. Afterwards it was transferred to water. As shown in figure XXX D) the peptidosome was stable.

2. Encapsulation of Bacillus subtilis in Peptidosomes

Before the encapsulation of B. subtilis inside the peptidosomes, it was necessary to perform experiments to study possible interactions between the organism and the dipeptide, for example, whether the bacteria can use Fmoc-FF as a nitrogen source, or if the organism can survive the process of encapsulation, since the bacterial pellet is resuspended in the alkaline Fmoc-FF solution.

Can Fmoc-FF use B. subtilis. as a nitrogen source?

Special culture plates were created using Jensen’s medium. This type of medium has all the basic nutrients that bacteria needs for its development, with exception of nitrogen.

Four treatments were tested:

  • 1) Nitrogen free Jensen’s medium
  • 2) Jensen’s medium supplemented with nitrogen (adding Fe [III] ammonium citrate and Potassium glutamate)
  • 3) Jensen’s medium mixed with Fmoc-FF
  • 4) Jensen’s medium with Fmoc-FF added over the dried plates

Treatment 1 was a negative control, since the strain of B. subtilis (wildtype) cannot develop in absence of nitrogen, so no growth at all was expected. Treatment 2 was the positive control: with the nitrogen supplement, B. subtilis should be able to grow. These expectations corresponded with reality: colonies grew in treatment 2 but none in treatment 1. Treatments 3 and 4 did not result in colony growth either, meaning that the Fmoc-FF cannot be used as a source of nitrogen for the bacteria.

Tolerance of B. subtilis against alkaline pH

The experiment to test the tolerance was performed as follows: B. subtilis culture was divided in four treatments, varying the pH of the culture in each one; 7 (normal growth condition as a control), 8, 9, and 10. NaOH was used to induce the different changes in the pH for each treatment, and was added after one hour of cultivation. The experiment was carried out in a plate reader to follow the change of the optical density (OD 600) which correlates with bacterial growth.

The graph shows the growth of the organisms under each condition. It can be observed that from pH 7 to 9, no significant change in the growth is observed. However, under pH 10, the organism stops its growth. To check if the bacteria was still viable after the high pH treatment, it was transferred to growth plates with neutral pH. There, it was observed that B. subtilis was able to recover and growth normally, meaning that the organism can survive the process of encapsulation.

Bacillus subtilis in Peptidosomes

Once it was proven that B. subtilis can survive the designed encapsulation process, and that the organism cannot use the building block Fmoc-FF as a nitrogen source, experiments to entrap the bacteria started.

For this we resuspended an appropriate amount of bacteria in the Fmoc-FF solution. Afterwards droplets of this were deposited on the ultrahydrophobic membrane and exposed to CO2 for 10 minutes and afterwards transferred to water or LB media.

Well Scan experiment

For the first experiments of encapsulation, we used the B. subtilis strains TMB4131 W168 lacA::erm Pveg_sfGFP and TMB3090 W168 sacA::cat Pveg_luxABCDE. The first strain has the characteristic of expressing sfGFP in a constitutive way, which was useful to prove the presence of bacteria in the peptidosomes by detecting the fluorescence expressed by the cells. TMB3090 expresses luciferase in a constitutive way, which makes a detection of a luminescence signal possible. We performed a plate reader assay using the well-scan-mode. In this mode, the whole well is scanned to detect the exact position of a signal, either fluorescence or luminescence. Its absence is displayed in a map with a green colour, while the position of the fluorescence/luminescence source appears as red.

The well scan maps appear completely green where fluorescence/luminescence is absent, i.e. water and empty peptidosome. Wells containing a sample of the day culture and lyophilized eGFP solved in water show a red colour in the whole map. However, a localized red spot over a green background is observed where the source of fluorescence/luminescence is contained: the cells trapped inside the peptidosomes. This shows that when the peptidosome with cells inside is transferred to water, bacteria cannot diffuse away, but its kept contained within the structure, resulting in a localized red signal.

Fluorescence microscopy

The encapsulation of B. subtitilis expressing sfGFP in a constitutive way was also demonstrated by the fluorescence microscopy. In this experiment, the bacteria were encapsulated as described. As seen in Figure X, the peptidosome emitted green light what proved the existence of sfGFP-expressing bacteria.

The Growth of B.subtilis in Peptidosomes

The method we used to check the growth and reproduction of bacteria inside the peptidosome was performed by generating peptidosomes loaded with a known amount of bacteria. Some peptidosomes were plated on LB agar right after being generated, while other peptidosomes were incubated in LB broth at 37°C for 3.5 and 7 hours and afterwards plated and incubated overnight. An increase in the number of colonies formed by the incubated peptidosomes means that bacteria can grow inside the structure. The result is shown in the next table.

As observed on the results, the number of colonies in the plates are increasing after 3.5 h of incubation, until finally after 7 hours it is not possible to count the amount of colonies anymore, meaning that the cells can reproduce inside the cages, therefore, peptidosomes are indeed suitable for the establishment of bacterial cultures.

When performing that experiment, we discovered bacterial growth in the supernatant where the peptidosomes were incubated. To figure out the reason for this, cryo-Scanning Electron Microscopy (cryo-SEM) was used to image bacteria-loaded peptidosomes. The results are showed below.

As observed in the images, some cells are completely or only partially integrated into the membrane, composed by a mesh of fibers. This cells found on the outer surface of the membrane, if released, can be responsible for the bacterial growth on the supernatant. Therefore we designed a second growth experiment, in which also the whole supernatant of each peptidosome was plated with the purpose of observing the amount of bacteria released there.

Two extra treatments were tested, the first one consisted in adding “washing” steps, meaning that the peptidosomes were transferred twice to fresh media before their incubation. We hypothesized that the bacteria on the outer membrane would be released and left behind after the transfers. The second treatment that we tested consisted in pre-incubating the peptidosome in LB broth adjusted to have an acid pH, this with the finality of closing the membrane to entrap even more the cells, triggering the self-assembly of the unreacted Fmoc-FF solution still present in the peptidosome.

By introducing the treatments, the number of colonies was reduced from several hundreds to an average of .7 for the washing steps and 1.7 for the low pH treatment. After analysing the results, we concluded that the washing steps are important to reduce the number of cells released in the supernatant, whereas the treatment with acid broth does not add a significant effect on this. In that way, by introducing the washing steps and also reducing the concentration of cells in the peptidosomes, the amount of bacteria present on the outer surface of the membrane was importantly diminished, fact that was corroborated by performing a second cryo-SEM and showed below.

In the second measurement the number of detectable bacteria that lie or are integrated on the membrane is significantly lower. Only a few individual fibers are visible and the surface is wrinkled. (figure XX A), B))

Only on the peptidosome with the low pH treatment, a cell that was not integrated in the membrane was observed (D).

The results of the growth experiment with the additional treatments were confirmed microscopically. There was no significant improvement in the peptidosomes treated with acid LB medium compared to the sole integration of wash steps. Only a single cell, which could relieve from the peptidosome, was detected. This confirms the reduced number of colonies in the supernatant of the growth experiment when carrying out the additional treatment methods.

The one loosely attached cell might be a problem for some applications where the surrounding medium is expected to be free of bacteria, therefore, the manufacturing technique of peptidosomes should be adapted accordingly. An adequate method for this could be introducing the cells by microinjection, since there is not a chance that bacteria can be attached to the outer part of the membrane.

3. Surface decoration

The properties of self-assembled FmocFF membrane allow tiny objects, such as Dynabeads, to be enveloped in the wall of the Peptidosome. Dynabeads envelopment enables the control of the Peptidosome movements in the magnetic field, that in combination with other features like producing strain encapsulation and small molecules or proteins diffusion, provides a powerful delivery tool, which can be used in various applications (Video- magnetosome).

Nevertheless, the surface of DynaBeads can be decorated with His-Tag protein. For the “proof of principle” experiments His-Tag GFP were selected due to its availability and easy imaging procedure. First, the Invitrogen Protocol was optimized for our goals and tested for DynaBeads decoration with histidine-tagged GFP (Picture 1).

To prove the surface of the Dynabeads enveloped to the Peptidosome membrane availability for the decoration the labeling procedure was applied after the Peptidosome formation in both Binding/Wash Buffer and LB media (Picture 2).

In conclusion, here we proved the possibility of Peptidosome surface decoration with histidine-tagged molecules that can be used for various applications where enzymatic activity of the surface of Peptidosome or Peptidosome immobilization is required. Surface decoration protocol is compatible with almost any goals due to its flexibility, as the decoration procedure can be performed before and after Peptidosome formation in the specific Binding/Washing buffer or just in the LB media.