Efficient cell-free expression with the endogenous E. Coli RNA polymerase and sigma factor 70
© Shin and Noireaux; licensee BioMed Central Ltd. 2010
Received: 9 March 2010
Accepted: 24 June 2010
Published: 24 June 2010
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© Shin and Noireaux; licensee BioMed Central Ltd. 2010
Received: 9 March 2010
Accepted: 24 June 2010
Published: 24 June 2010
Escherichia coli cell-free expression systems use bacteriophage RNA polymerases, such as T7, to synthesize large amounts of recombinant proteins. These systems are used for many applications in biotechnology, such as proteomics. Recently, informational processes have been reconstituted in vitro with cell-free systems. These synthetic approaches, however, have been seriously limited by a lack of transcription modularity. The current available cell-free systems have been optimized to work with bacteriophage RNA polymerases, which put significant restrictions to engineer processes related to biological information. The development of efficient cell-free systems with broader transcription capabilities is required to study complex informational processes in vitro.
In this work, an efficient cell-free expression system that uses the endogenous E. coli RNA polymerase only and sigma factor 70 for transcription was prepared. Approximately 0.75 mg/ml of Firefly luciferase and enhanced green fluorescent protein were produced in batch mode. A plasmid was optimized with different regulatory parts to increase the expression. In addition, a new eGFP was engineered that is more translatable in cell-free systems than the original eGFP. The protein production was characterized with three different adenosine triphosphate (ATP) regeneration systems: creatine phosphate (CP), phosphoenolpyruvate (PEP), and 3-phosphoglyceric acid (3-PGA). The maximum protein production was obtained with 3-PGA. Preparation of the crude extract was streamlined to a simple routine procedure that takes 12 hours including cell culture.
Although it uses the endogenous E. coli transcription machinery, this cell-free system can produce active proteins in quantities comparable to bacteriophage systems. The E. coli transcription provides much more possibilities to engineer informational processes in vitro. Many E. coli promoters/operators specific to sigma factor 70 are available that form a broad library of regulatory parts. In this work, cell-free expression is developed as a toolbox to design and to study synthetic gene circuits in vitro.
Cell-free systems are used to synthesize large amounts of recombinant proteins in a few hours. Cell-free expression, which has many advantages in comparison to cell-based expression, is employed in an increasing number of biotechnology and proteomic applications . Many efforts are made to increase the protein productivity and the functionality of cell-free systems. The energy regeneration is frequently optimized [2–6], new E. coli strains are engineered to stabilize some amino acids or to express proteins with PCR products [7, 8] and preparation of the crude extract is simplified . Current extracts prepared from E. coli cells can deliver between half and one milligram per milliliter of reporter protein after a few hours of incubation in a test tube. To achieve high protein yield, these extracts use bacteriophage RNA polymerases for transcription, such as T7 and T3, with their specific promoters, because they are the most efficient polymerases. Although well established, however, cell-free expression is narrowed to bacteriophage transcription and is not necessarily adapted to all types of applications. Bacteriophage transcription cannot replace endogenous RNA polymerases for the synthesis of particular genes . In cell-free systems, bacteriophage transcription has to be modified to improve expression of specific genes . Reconstitution of cell-free informational processes, and on a broader range the field of in vitro synthetic biology, is limited to bacteriophage RNA polymerases [12–17]. Only a few synthetic bacteriophage promoters regulated by operators have been characterized, such as the T7/lacO system. The reconstitution of informational processes in vitro would greatly benefit from having efficient cell-free systems that offer a greater modularity at the level of transcription. Promoter/operators from E. coli provide much more modularity for transcription . E. coli cell-free extracts working with the endogenous core RNA polymerase and the housekeeping sigma factor 70 were originally prepared to study gene expression mechanisms [19, 20]. However, the endogenous transcription of E. coli extract, which is slower and less efficient than bacteriophage transcription, is not believed to allow efficient in vitro synthesis of proteins. For this reason, bacteriophage transcription has been largely favored at the expense of endogenous transcription systems.
In this work, the preparation of an efficient cell-free expression system that uses the endogenous E. coli RNA polymerase only with sigma factor 70 for transcription is described. Using recent improvements in cell-free preparation and a plasmid with optimized regulatory parts, 0.75 mg/ml (0.6 mg/ml active) of Firefly luciferase (Luc) and 0.75 mg/ml (0.65 mg/ml active) of enhanced green fluorescent protein (eGFP) were produced. The best protein production was obtained with the 3-PGA energy regenerating system. The expression was also characterized with buffers containing either CP or PEP for the energy regeneration. The preparation of the crude extract, which takes only half a day without freezing the cells, was reduced to a routine procedure faster than the preparation of bacteriophage cell-free systems. A new eGFP cDNA was engineered that allow much higher production of the reporter in cell-free system when it is transcribed from an E. coli promoter. The expression and the protein production were characterized with this new enhanced green fluorescent protein and with Luc. This cell-free system can deliver large amounts of proteins without addition of exogenous RNA polymerase.
The crude extract was prepared with E. coli BL21 Rosetta2 cells (Novagen) grown at 37°C in 2xYT medium up to OD600 = 1.5, according to Kigawa et al  and Liu et al . All the following steps were performed either on ice or at 4°C except for the pre-incubation at 37°C. The cells were washed twice and resuspended in S30 buffer A (50 mM Tris, 60 mM potassium glutamate, 14 mM magnesium glutamate, pH 7.7, 2 mM DTT). The cells were broken with a bead-beater (Biospecs Products Inc, mini bead-beater-1) using 0.1 mm glass beads. The extract was clarified by centrifugation at 30000 g for 25 minutes. The clear supernatant was pre-incubated 80 minutes at 37°C followed by a centrifugation at 30000 g for 10 minutes. The clear supernatant was dialyzed against S30 buffer B (5 mM Tris, 60 mM potassium glutamate, 14 mM magnesium glutamate, pH 8.2, 1 mM DTT) for 3 hours with a Slide-A-Lyzer cassette (MWCO 10 kDa, Pierce Biotechnology). The crude extract was stored at -80°C after dialysis. A typical concentration of 27-30 mg/ml of proteins in the crude extract was measured by Bradford assay. The crude extract is stable at least 1 year at -80°C.
The cell-free reactions were composed of 33% crude extract (9-9.5 mg/ml of proteins), the other 66% contained the reaction buffer and the plasmid. The reaction buffers were prepared with slight modifications according to Sitaraman and co-workers for 3-PGA , Kim and Swartz for PEP  and Kim and co-workers for CP . 3-PGA and PEP are natural E. coli substrates, therefore no enzyme was added to the reaction. Creatine phosphate is not a natural substrate for E. coli. Creatine kinase was added according to Kim and co-workers .
50 mM Hepes pH 8, 1.5 mM ATP and GTP each, 0.9 mM CTP and UTP each, 1 mM spermidine, 0.75 mM cAMP, 0.33 mM NAD, 0.26 mM coenzymeA, 30 mM 3-PGA, 0.068 mM folinic acid, 0.2 mg/ml tRNA, 1 mM IPTG.
50 mM Hepes pH 8, 1.5 mM ATP and GTP each, 0.9 mM CTP and UTP each, 1 mM putrescine, 0.75 mM cAMP, 0.33 mM NAD, 0.26 mM coenzymeA, 30 mM PEP, 0.068 mM folinic acid, 0.2 mg/ml tRNA, 1 mM IPTG.
50 mM Hepes pH 8, 1.5 mM ATP and GTP each, 0.9 mM CTP and UTP each, 0.5 mM spermidine, 0.75 mM cAMP, 0.33 mM NAD, 0.26 mM coenzymeA, 67 mM CP, 0.0032 mg/ml creatine kinase, 0.068 mM folinic acid, 0.17 mg/ml tRNA, 1 mM IPTG.
The concentrations of amino acids (0.5-1.5 mM for eGFP and 1.5 mM for Luc, for each amino acid), PEG 8000 (0.5-2%), additional magnesium glutamate (0-10 mM) and additional potassium glutamate (0-120 mM) were adjusted depending on the reporter and the buffer used. The optimum plasmid concentration is discussed in the results and discussion section. The volume of each reaction was 10 μl. The reactions were incubated at 22°C for Luc and 29°C for eGFP with no shaking. The reagents were purchased from Sigma, USB Corporation (GTP, CTP, UTP) and Roche (tRNA, amino acids). The concentrations of magnesium and potassium shown in the graphs are additional to the magnesium and potassium provided by the crude extract. The crude extract brings an additional 4.5 mM of magnesium glutamate and 20 mM of potassium glutamate.
All the plasmids used in this study originate from the plasmid pBEST-Luc (Promega). The list and sequences of the different regulatory parts are reported in the additional file 1 (List on page 1). Luc refers to Firefly luciferase [GenBank: CAA59281.1], eGFP to the enhanced green fluorescent protein [GenBank: CAD97424.1], eGFP-Del6 to the enhanced green fluorescent protein truncated and modified in N-terminal, eGFP-Del6-229 to the enhanced green fluorescent protein truncated and modified in N- and C-terminal, PtacI to the consensus E. coli sigma factor 70 promoter , OR2-OR1-Pr to the lambda repressor Cro promoter [GenBank: J02459.1], UTR1 to the untranslated region containing the T7 g10 leader sequence for highly efficient translation initiation  [GenBank: M35614.1] and T500 to the transcription terminator . The plasmids were prepared according to the standard molecular cloning procedures. Picogreen (Invitrogen) was used to measure plasmid concentrations. The E. coli strain KL740 was purchased from the Coli Genetic Stock Center (Yale) [CGSC#: 4382].
A Wallac Victor III platereader (PerkinElmer) was used to measure eGFP, eGFP-Del6 and eGFP-Del6-229 expression (kinetics and end-point measurements). Pure recombinant eGFP (Clontech) was used for calibration. Luc expression was measured with a custom-built luminometer described previously . Pure Luc and Luc assay kit (Promega) were used for calibration and measurements. Polyacrylamide gel electrophoresis was carried out according to the standard procedures and labeled with SimplyBlue safestain (Invitrogen).
The crude extract was prepared according to Kigawa et al  and Liu et al  with some modifications. The usual buffers S30 A and S30 B used for the preparation of cell-free systems were composed of magnesium glutamate and potassium glutamate instead of the acetate form of the ions . DTT only was used for the washing and the resuspension steps (S30 buffer A) at a concentration of 2 mM instead of the usual combination of 2-mercaptoethanol and DTT. The optimum pH for the S30 buffer A and the S30 buffer B was 7.7 and 8.2 respectively. The cells were broken with a mini bead-beater. This lysis method is more reproducible than the other methods  and this technique is also more affordable. Typically, 4.5 g of cells were resuspended in 4.05 ml of S30 buffer A before adding 23 g of dry beads. The mixture was homogenized before bead beating twice at 4600 rpm for 30 seconds with a pause of 30 seconds in between. The mixture was centrifuged at 30000 g for 25 minutes followed by a pre-incubation of the clear supernatant at 37°C for 80 minutes. The extract was clarified again at 30000 g for 10 minutes before 3 hours of dialysis. The entire preparation, from cell culture to crude extract storage, takes 12 hours and does not present any particular constraints compared to other procedures. The cells do not need to be frozen at any time during the process. The crude extract can be thawed once without any loss of activity. Two liters of cell culture give approximately 6 ml of crude extract with a final protein concentration of 27-30 mg/ml.
eGFP and eGFP variants synthesis as a function of DNA regulatory parts
Plasmid concentration [nM]
Protein production [μM] (mg/ml)
Cell-free expression with E. coli sigma factor 70 promoters can pose significant problems of toxicity due to a potential over-expression of the recombinant protein during plasmid amplification. Although showing some signs of toxicity, the plasmids pBEST-UTR1-Luc and pBEST-UTR1-eGFP-Del6-229 were stable during amplification. A more general solution to this problem was found by switching to the strong Lambda phage promoter Pr flanked by the two operators OR2 and OR1. The E. coli strain KL740, which over-expresses the temperature sensitive Lambda repressor Cl857, was used to efficiently repress and stabilize the plasmids during cell growth at temperatures below 30°C. Potential problems due to increased background expression during plasmid amplification could also be solved by changing the origin of replication. The plasmid pBEST-Luc has a ColE1 origin of replication (few hundreds copies per cell), which can be replaced by a P15A (10-12 copies per cell) or a PSC101 (2-5 copies per cell) origin of replication. Other tightly regulated transcription systems and strains could be also used .
The protein productions measured in this work were comparable to the protein productions obtained with cell-free systems using bacteriophage RNA polymerases. Expression of GFP with a T7 transcription, characterized and quantified in two cell-free systems by Iskakova and co-workers , was comprised between 0.3 and 0.7 mg/ml. A maximum of 0.15 mg/ml of active Luc was measured in two different cell-free systems [12, 14]. Furthermore, the protein production obtained with commercial cell-free systems based on bacteriophage transcription is comprised between 0.5 and 1 mg/ml.
With the CP buffer, the maximum Luc and eGFP-Del6-229 production was only 60% of the amount obtained with 3-PGA. With the PEP buffer, the maximum Luc and eGFP-Del6-229 production was 60% and 100% respectively of the amount obtained with 3-PGA. It is important to note that Luc production was neither greater nor smaller with the different regulatory parts tested with eGFP. The production of Luc with the plasmids pBEST-UTR1-Luc and pBEST-OR2-OR1-Pr-UTR1-Luc-T500 were identical. The plasmid pBEST-OR2-OR1-Pr-UTR1-Luc-T500 was easier to amplify in the E. coli strain KL740.
In this work, an efficient cell-free expression system driven only by the endogenous E. coli RNA polymerase was prepared. Surprisingly, the protein production with this extract is comparable to bacteriophage systems. This new system is as workable as bacteriophage systems and does present any particular constraints. In order to obtain efficient protein production, the reaction conditions and its components were optimized as well as the regulatory parts of the plasmid carrying the recombinant gene. Our work, however, does not exclude further improvements. Other promoters, untranslated regions and terminators could be tested to increase the protein production. We used the three most common ATP regeneration systems, 3-PGA, PEP and CP. Cell-free protein synthesis with this system, however, could also benefit from recent results at the energy regeneration level . In the course of this study, we found that eGFP was not translated efficiently when it was expressed in vitro from an E. coli promoter. The gene encoding the reporter was modified to get highly translatable reporter messenger RNAs. This cell-free system opens new possibilities to synthesize proteins and it broadens the range of potential applications of cell-free systems.
enhanced green fluorescent protein
polyacrylamide gel electrophoresis.
The authors thank Nadezda Monina for technical assistance in the extract preparation, Jonathan Gapp and Catherine Raach for reading and correcting the manuscript. This work was supported by UMN startup funds, BSF Binational Science Foundation grant 2006398, National Science Foundation grant PHY-0750133.
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