Team:Imperial/EColi

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                                     <li>We have proven system portability by transferring the cellulose production machinery from <em>Gluconacetobacter xylinus</em> into <em>Escherichia coli</em> and demonstrating its functionality in the latter.</li>
                                     <li>We have proven system portability by transferring the cellulose production machinery from <em>Gluconacetobacter xylinus</em> into <em>Escherichia coli</em> and demonstrating its functionality in the latter.</li>
                                     <li>Assembled a fully synthetic, functional, cellulose-producing system in <em>Escherichia coli</em> without engineering signal peptides, indicating that these and the signal peptides of <em>G. xylinus</em> must be of high similarity.</li>
                                     <li>Assembled a fully synthetic, functional, cellulose-producing system in <em>Escherichia coli</em> without engineering signal peptides, indicating that these and the signal peptides of <em>G. xylinus</em> must be of high similarity.</li>
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                                     <li>We were able to successfully maintain the native stoichiometry and ratios of expression of the native host to ensure proper protein folding, complex assembly and correct levels of activity of each of the parts in the process of making cellulose.</li>
+
                                     <li>We were able to successfully set up working stoichiometry and ratios of expression of the operon genes in <em>E. coli</em> that can be fine tuned. This ensures proper protein folding, complex assembly and correct levels of activity of each of the parts in the process of making cellulose.</li>
                                     <li>In summary, we have majorly contributed to the Synthetic Biology community by encouraging the implementation of non-native, complex functions and systems into new hosts and by encouraging the production and uses of bacterial cellulose by a broader range of hosts to widen the applications of such useful biomaterial.</li>
                                     <li>In summary, we have majorly contributed to the Synthetic Biology community by encouraging the implementation of non-native, complex functions and systems into new hosts and by encouraging the production and uses of bacterial cellulose by a broader range of hosts to widen the applications of such useful biomaterial.</li>

Revision as of 22:39, 17 October 2014

Imperial iGEM 2014

E. coli

Overview

Escherichia coli is a very unfussy strain. It is able to grow under a diverse range of conditions, it is very well understood, easy to engineer and there are numerous parts, control circuits, biological manufacturing platforms and various other complex constructs proven functional in this host. For these and other reasons, it is widely used in the Synthetic Biology community as a cloning host and for various other purposes.

However, some Escherichia coli strains only produce cellulose at a specific set of phenotypical conditions (its secretion is generally linked to biofilm formation and stress situations). In order to encourage the use of bacterial cellulose as a functional, modular biomaterial that can become easy, cheap and quick to produce, it is necessary for its corresponding production machinery to be implemented in organisms that are easier and quicker to grow in manufacturing plants and bioreactors.

Here, we confirm that the cellulose production machinery can be transferred into other organisms. We have proven portability of the Acs cellulose operon in Escherichia coli using Congo Red binding assays.

Key Achievements

  • We have contributed significantly to the Registry of Standard Parts by providing the necessary components for the assembly of a 10kB operon for cellulose production in a wide range of organisms.
  • We have proven system portability by transferring the cellulose production machinery from Gluconacetobacter xylinus into Escherichia coli and demonstrating its functionality in the latter.
  • Assembled a fully synthetic, functional, cellulose-producing system in Escherichia coli without engineering signal peptides, indicating that these and the signal peptides of G. xylinus must be of high similarity.
  • We were able to successfully set up working stoichiometry and ratios of expression of the operon genes in E. coli that can be fine tuned. This ensures proper protein folding, complex assembly and correct levels of activity of each of the parts in the process of making cellulose.
  • In summary, we have majorly contributed to the Synthetic Biology community by encouraging the implementation of non-native, complex functions and systems into new hosts and by encouraging the production and uses of bacterial cellulose by a broader range of hosts to widen the applications of such useful biomaterial.

Figure 1
Figure 2

Introduction

TEXT HERE

Aims

Figure 3

By aiming to transfer the cellulose production operon from its native organism Gluconacetobacter xylinus into the lab-friendly strain E. coli, we aimed to emphasize the importance of increasing cellulose production per unit time to achieve a reduction in pellicle growth timeframe and production costs. We also aim to optimize growth conditions by potentially allowing shaking incubation, and to ease genetic engineering and cloning procedures due to the wider availability of functional, already characterized Biobricks to work with cellulose (by having the two highest expressed elements in a high copy plasmid (pSB1C3) and the lowest expressed elements in a low copy plasmids (pSB3k3), and by having two different inducible promoters that allow for an even finer tuning of expression).

Engineering

The cellulose production operon in Gluconacetobacter xylinus is a 10kb genomic region, consisting of four main elements:

  • acsAB, known as cellulose synthase, is made up of two domains: acsA being the catalytic domain, and acsB being the cyclic-di-GMP-binding domain. This modular enzyme requires the second messenger cyclic-di-GMP in order to carry out efficient catalysis.
  • acsC codes for an oligomeric element that gets embedded in the extracellular membrane and allows transport of the growing polymer across the cell membrane into the extracellular environment.
  • acsD is believed to be a non-essential element, although it is a key player in the control of cellulose crystallinity and required for maximal cellulose productivity.

The native operon is highly regulated at transcriptional, translational and post-translational levels. Cellulose production responds to a wide set of internal signals and environmental cues. The native ribosomal binding sites (RBS) are predicted to be weak by translation rate calculators (The Salis Lab RBS calculator and Postech UTR designer ). This is perhaps to reduce noise in gene expression (strong promoter, weak RBS is less noisy that weak promoter strong RBS). The promoter region has not yet been characterized in Gluconacetobacter xylinus, however.

The first step of our computational design engineering was to identify the coding sequences and extract them from NCBI. We removed some native regulation by codon-optimizing the sequences for expression in E.coli and replaced the native RBS’s with the strong B0034 sequence. The 6 base pairs either side of the B0034 RBS were edited with the Salis Lab RBS calculator design function to tune RBS strength output to better preserve the natural stoichiometry.

Finally, in order to allow for even more customizable fine-tuning of the system, the operon was divided and cloned into two separate expression vectors: the AcsAB element was cloned under the control of the inducible pBAD promoter contained within pSB1C3, a high copy plasmid that would contribute to higher expression of Cellulose Synthase. Alternatively, AcsC and AcsD, believed to be expressed at lower levels in G.xylinus, was put under the control of the pLAC promoter and was transferred into a low copy plasmid, pSB3K3 so as to maintain lower levels of expression. This approach provided the following advantages:

  • Reducing the size of the final expression vector avoids complications during assembly and vector take-up, and it also prevents a large construct from becoming a burden for cell growth and vector propagation.
  • By expressing the cellulose production machinery from two separate expression vectors, the following levels of control become available to us: the first being the changes in vector copy number, which directly affects gene expression levels throughout induction, and the second being the ability to activate the system using two different inducers. These key features of our system allow for a larger scope for fine-tuning and optimization of cellulose production levels.
Figure 4: pSB-pBAD-AB and pLAC-CD
Figure 5: acsABCD fragments

With this approach, we allow for our system to be implemented in new range of hosts because a larger set of growth conditions, inducer concentrations and growth phases can be tested in order to achieve the required stoichiometry for the system to become functional.

In order to ease synthesis, the operon sequence was split into 4 fragments of similar sizes. We took advantage of the presence of two restriction sites: An NcoI present within the AcsAB sequence, and a PvuII site contained within AcsC. Furthermore, the BioBrick prefix and suffix were included and any additional sites removed elsewhere.

By standard cloning, these fragments could easily be put together to yield the following constructs:

Figure 6: acsAB and acsCD constructs

Gene Designer served as a very useful tool for assembling constructs and predicting cloning outcomes before proceeding with the experimental procedure. Find above the plasmid maps of our resulting constructs, and refer to Materials and Methods for a deeper insight into the assembly process.

Materials and Methods

Cell Strains and Media Components

Escherichia coli strain DH10B were made chemically competent following a standard protocol and were used to clone the pSB-AraC-pBAD and pSB-LacI-pLAC elements. Additionally, High Efficiency chemically competent DH10B Escherichia coli were purchased from New England Biolabs for assembly of the Acs cellulose-producing operon, which was codon-optimized for expression in E.coli and synthesized by GeneArt. Both strains were grown overnight in liquid cultures (supplemented with specific antibiotics), or on semi-solid LB-Agar plates, provided with the specific antibiotic, as listed on the table below.

Luria Broth Miller (LB) and LB Agar were purchased from VWR, prepared using standard protocols and used throughout the experimental procedure. During characterization, Acs-containing strains were supplemented with 1% D-glucose, 0.1% Arabinose and 0.5mM IPTG.

Plasmid name Vector backbone Antibiotic concentration (ug/ml)
pSB-AraC-pBAD pSB1C3 Chloramphenicol 50
pSB-LacI-pLAC pSB3K3 Kanamycin 25
pSB-AcsAB pSB1C3 Chloramphenicol 50
pSB-AcsCD pSB1C3 Chloramphenicol 50
pSB-AraC-pBAD-AcsAB pSB1C3 Chloramphenicol 50
pSB-LacI-pLAC-CD pSB3K3 Kanamycin 25
List of antibiotics used, in relation to their respective constructs

Chemicals

Congo Red was purchased from Sigma Aldrich (Steiheim, Germany) and diluted in 1x PBS to a concentration of 350 uM. The final Congo Red concentration used during system characterization steps was 20 uM. This was also used, also at a concentration of 20 uM, to make LB Agar Congo Red Assay plates.

Construct Assembly

Cloning of pSB-AraC-pBAD

The AraC and pBAD elements were obtained by PCR, using the Biobricks BBa_K325108, BBa_K325218 and BBa_K325219 as DNA templates, all of which follow the standard structure showed on the image below (left hand side, add legend, add figure number). The primers used during this procedure were as follows:

  • Forward: TACTAGTAGCGGCCGCTGCAG
  • Reverse: GCTAGCCCAAAAAAACGGGTATGGAG
Figure 7 - Plasmid maps describing both the original (left) and engineered (right) AraC-pBAD-containing parts, including all relevant elements. These were designed and cloned in silico on GeneDesigner.

The amplified elements were DpnI-treated following a standard procedure (New England Biolabs), and were subsequently submitted to a purification step (Qiaquick PCR clean up, Qiagen) prior to self-ligation. Three different template concentrations were tested during ligation (specifically 3 ng, 7.5 ng and 15 ng), and were incubated at room temperature for 1h+. The ligation mix was then transformed into chemically competent DH10B Escherichia coli using a standard chemical transformation protocol and plated out on Chloramphenicol-specific LB plates.

Cloning of pSB-LacI-pLAC

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Assembly of AcsAB and AcsCD

Figure 8:

The AcsABCD operon was designed in silico as described in the previous section. It was ordered for synthesis at GenArt in the form of four separate elements of similar sizes, named AcsA, AcsB, AcsC and AcsD, respectively. After synthesis, the constructs were directly transformed into DH10B E.coli using a standard chemical transformation protocol and plated overnight supplied with 50 ug/ml Kanamycin. 5ml LB were inoculated with a freshly growing colony and grown overnight at 37 C, under shaking conditions. Glycerol stocks were produced prior to proceeding with the assembly process.

In order to meet the Registry standards, we aimed to clone these elements into pSB1C3. To do so, we proceeded as described on the diagram. Two separate rounds of digestion were carried out using EcoRI, NcoI, PvuII and PstI to, and the resulting fragments (AcsA, AcsB, AcsC and AcsD and linearized pSB1C3) were submitted to a three-part ligation after dephosphorylation of the vector backbone (rAPid desphosphorylation, Roche). An equimolar ratio amongst all three parts was established during the ligation procedure, which in turn proceeded at 4 degrees overnight. The NEB High Efficiency Transformation protocol was used on NEB 10B cells (New England Biolabs) to propagate the resulting plasmid. Transformed cells were plated and incubated overnight at 37 C. 5 ml LB supplied with 50 ug/ml Chloramphenicol were inoculated with a selection of colonies for further analysis (refer to Results for additional information).

Assembly of pSB-AraC-pBAD-AcsAB

AcsAB was cloned into pSB-AraC-pBAD by Biobrick cloning (figure???). The destination vector was linearized using SpeI and PstI (New England Biolabs), and AcsAB (previously digested with XbaI and PstI, and gel extracted using the Minelute Gel Extraction Kit, by Qiagen) was ligated at a 1:1 ratio throughout an overnight ligation at room temperature. The resulting part was transformed into chemically competent DH10B Escherichia coli and plated on LB Agar+Chloramphenicol plates, grown overnight at 37 C. 5 ml LB falcons supplied with 50 ug/ml Chloramphenicol were inoculated with a selection of freshly grown colonies for further restriction analysis (refer to Results for additional information)

Assembly of pSB-LacI-pLAC-CD

Similarly to 3.4, AcsCD was cloned by BioBrick cloning into the pSB3K3 low copy expression vector containing the LacI-pLAC regulatory elements. Vector and insert were ligated at a 1:1 ratio overnight at room temperature. After transformation and plating on LB Agar+Kanamycin (25 ug/ml), colonies were screened by Greentaq colony PCR, and were further confirmed during the Congo Red Assay.

Making pBAD-AcsAB-containing electrocompetent cells

DH10B E.coli alreaday containing the pBAD-inducible AcsAB element were made electrocompetent in order to be able to proceed with a second round of transformation to insert pLAC-AcsCD. A standard protocol was used during this procedure, and this can be found in the Protocols section.

Electroporation of pSB-pLAC-CD into pSB-pBAD-AB DH10B cells

5ul of miniprepped pSB-pLAC-CD (diluted in ddH2O) were added into 50ul electrocompetent DH10B cells already containing the pBAD-inducible AcsAB element. Electroporation was carried out in in 10mm electrocuvettes at 1.8 kV, 200 Ohm resistance and 25 mF capacitance. 500ul SOC medium was added to the electroporated samples and these were recovered at 37C

Results

Constructs

pSB-AraC-pBAD Assembly

The pSB-AraC-pBAD construct was assembled as described in Materials and Methods. As a preliminary verification step, a restriction analysis was carried out using XbaI and PstI, and results were visualized on a 1% Agarose Gel. A 2-band pattern was obtained, indicating the presence of a ~2kb DNA fragment potentially corresponding to the pSB1C3 vector backbone, and a ~1kb fragment corresponding to the AraC and pBAD elements being cloned. Final confirmation of successful cloning was obtained by gene sequencing of the part in question, using the BioBrick Verification Primers, shown below: (refer to the “Sequencing” section to find a compilation of all confirmed parts)

  • Verification Primer Forward: T GCC ACC TGA CGT CTA AGA A
  • Verification Primer Reverse: ATT ACC GCC TTT GAG TGA GC
Figure x: pSB-AraC-pBAD

pSB-AcsAB and pSB-AcsCD Assembly

Figure x: pSB-AcsAB
Figure x: pSB-AcsCD

pSB-AraC-pBAD-AcsAB Assembly

Figure x: pSB-AraC-pBAD-AcsAB and pSB-LacI-AcsAB

Characterising Cellulose Production

Preliminary Characterization: Congo Red Assay

Data Analysis

Future Work

References