Cell-free protein synthesis energized by slowly-metabolized maltodextrin
© Wang and Zhang; licensee BioMed Central Ltd. 2009
Received: 21 February 2009
Accepted: 28 June 2009
Published: 28 June 2009
Cell-free protein synthesis (CFPS) is a rapid and high throughput technology for obtaining proteins from their genes. The primary energy source ATP is regenerated from the secondary energy source through substrate phosphorylation in CFPS.
Distinct from common secondary energy sources (e.g., phosphoenolpyruvate – PEP, glucose-6-phosphate), maltodextrin was used for energizing CFPS through substrate phosphorylation and the glycolytic pathway because (i) maltodextrin can be slowly catabolized by maltodextrin phosphorylase for continuous ATP regeneration, (ii) maltodextrin phosphorylation can recycle one phosphate per reaction for glucose-1-phosphate generation, and (iii) the maltodextrin chain-shortening reaction can produce one ATP per glucose equivalent more than glucose can. Three model proteins, esterase 2 from Alicyclobacillus acidocaldarius, green fluorescent protein, and xylose reductase from Neurospora crassa were synthesized for demonstration.
Slowly-metabolized maltodextrin as a low-cost secondary energy compound for CFPS produced higher levels of proteins than PEP, glucose, and glucose-6-phospahte. The enhancement of protein synthesis was largely attributed to better-controlled phosphate levels (recycling of inorganic phosphate) and a more homeostatic reaction environment.
Cell-free protein synthesis (CFPS) is widely used for the production of in vivo cytotoxic, regulatory, or unstable proteins that are difficult to express in living cells [1–3] and for the incorporation of unnatural amino acids into protein polypeptides [4–6]. Also, CFPS can be applied for high-throughput screening of target proteins [7, 8], functional tool for proteomics [7, 9], and the development of point-of-care medicines [10, 11]. Also, CFPS is the fastest method to produce a desired protein within one day [9, 12].
Protein synthesis is an energy-intensive process. The primary energy source ATP is regenerated from the secondary energy source through substrate phosphorylation in CFPS . Common secondary energy compounds such as creatine phosphate, phosphoenolpyruvate (PEP), acetate phosphate, glucose-6-phosphate (G6P), 3-phosphoglycerate, and fructose-1,6-biphosphate, contain high-energy phosphate bonds for regenerating ATP. Consequently, ATP regeneration accompanied with the consumption of phosphate-containing substrate leads to an increase in inorganic phosphate. High concentrations of inorganic phosphate severely impair protein biosynthesis, likely due to precipitation of free magnesium ions [14, 15]. Magnesium ions are essentially important for nucleoside triphosphate synthesis, protein translation, and translation termination [16, 17].
In addition to the effects of phosphate and the costs of a secondary energy source, stable pH is vital for high protein yields [18, 21]. It is well known that well-controlled continuous CFPS systems have high protein yields [3, 22]. But continuous CFPS systems with complicated configurations are hard to scale up for high-throughput applications and are not efficient for utilizing costly reagents . It would be appealing to use slowly-metabolized secondary energy sources in batch reactions, which likely mimic the well-controlled continuous reactions.
In this study, to avoid phosphate accumulation and to maintain a relatively homeostatic reaction environment for CFPS, we designed a novel ATP regeneration system starting from low-cost maltodextrin and ending with acetate and lactate, by using a combination of maltodextrin phosphorylase, phosphoglucomutase, glycolysis, and the PNAOx system.
A new ATP regeneration pathway
Synthesis of esterase
Changes in pH were measured during the protein synthesis process (Fig. 3B). At the beginning, the initial pHs for the four reactions were around pH 7.4–7.6. The pH from the reactions energized by maltodextrin, PEP, glucose and G6P decreased slowly to 6.9, 6.6, 6.5 and 6.2 after one hour, respectively, and then levelled off. The reaction energized by maltodextrin exhibited the least pH fluctuation, from 7.6 to 6.9.
Concentrations of ATP in the reaction mixtures were measured during the process of protein synthesis (Fig. 3C). In the case of maltodextrin, the ATP level decreased slowly; its levels remained above 0.15 mM for the first two hours. In the case of PEP, the ATP level was highest at the beginning, quickly decreased from 2.67 mM to 0.58 mM, and then levelled off. PEP was an easily metabolized substrate, resulting in higher levels of ATP as compared to other slowly-metabolized substrates of maltodextrin, G6P, and glucose. The measured ATP concentration was the combinatorial result of continuous in situ ATP regeneration and ATP consumption for protein synthesis and nonproductive hydrolysis. Recently, it was found that CFPS had a low ATP binding constant (i.e., KmATP = 27 uM) , suggesting that ATP levels in CFPS (Fig. 3C) were saturated, i.e., the protein synthesis rates did not depend on the ATP levels [19, 21].
Synthesis of CBM-GFP and xylose reductase
CFPS energized by maltodextrin presented relatively high levels of EST2, CBM-GFP and xylose reductase as compared with three other secondary energy sources – glucose, G6P, and PEP. Maltodextrin provided relatively homeostatic conditions, such as no phosphate accumulation and less fluctuation in pH (Fig. 3A &3B). Slowly metabolized maltodextrin in batch CFPS was somewhat like continuous CFPS with regard to well-controlled reaction conditions.
The major advantages of using slowly-metabolized maltodextrin are to avoid inorganic phosphate accumulation to inhibitory levels and to maintain a relatively homeostatic environment (e.g., phosphate, pH, and ATP) for protein synthesis. Proper levels of inorganic phosphate are also required for effective synthesis of nucleoside triphosphate (NTP) from nucleoside diphosphate (NDP) for high level protein synthesis [18, 19]. Using phosphate-free maltodextrin does not release net phosphate. In contrast, it can decrease free phosphate levels by substrate phosphorylation and keep phosphate levels nearly constant. In addition, maltodextrin is not a substrate of E. coli endogenous phosphatases. Therefore, the challenge associated with non-productive hydrolysis of phosphate-containing compounds [19, 28] has been partially addressed by using maltodextrin.
The importance of pH control in CFPS has long been recognized [18, 21]. More stable pH in the case of maltodextrin was largely attributed to no phosphate accumulation and less formation of organic acids (e.g., lactate and acetate) due to the generation of more ATP per substrate consumed (Additional file 1). The latter speculation has been validated by product assays, in which 40, 18 and 18 mM lactate were produced from glucose, maltodextrin and PEP, respectively, after a 1 hour reaction. Swartz and his coworkers also reported that a strong pH-capacity buffer (Bis-Tris, pH 6.5) increased protein synthesis levels .
EST2 was used as a major model protein for CFPS in this study. Due to its high-sensitivity and thermal stability, it had been applied not only for CFPS [4, 23, 24] but also for detecting nucleic acid hybridization [29, 30]. Since EST2 has a specific activity of 1100 U/mg based on p-nitrophenylbutyrate at 25°C , its levels can be measured as low as 72 pM, superior to 14C radioactivity-labelled amino acids. We also used the Roche High-Yield in vitro protein synthesis system as a control to express EST2 protein at a level of 0.21 mg per mL. The previous EST2 levels by CFPS were 0.15–0.20 mg per mL [24, 29]. The expression level (0.28 mg of EST2 per mL) energized by maltodextrin was the highest so far.
A number of secondary energy substrates were compared based on their ATP yields and phosphate release (Additional file 1). Acetyl-phosphate, creatine-phosphate, 3-phosphoglycerate (3-PGA), and PEP generated one ATP and released one inorganic phosphate [13, 32–34]. ATP regeneration potential through the PANOx system was approximately one ATP per two pyruvate with an acetate/lactate = ~1:1. In principle, one molecule of glucose, G6P and fructose-1, 6-biphosphate can regenerate three, four and five molecules of ATP and release zero, one and two phosphate, respectively. One glucose equivalent of maltodextrin can produce four molecules of ATP, while it does not release phosphate (Eq. 5). Maltodextrin is better than glucose because generation of G1P mediated by glucan phosphorylases from polysaccharides does not consume ATP so that one molecule of ATP is saved from glucose phosphorylation catalyzed by ATP-dependent hexokinase [35–37]. It is well known that ATP consumption of CFPS is not coupled to ATP regeneration [18, 20], which is different from in vivo protein synthesis [38, 39]. But slowly-metabolized maltodextrin can enhance the protein synthesis yield and decrease energy dissipation because they can avoid an initial high concentration of the secondary energy compound, most of which was hydrolyzed by E. coli endogenous phosphatases. For example, approximately 70% of 30 mM PEP was hydrolyzed within the first 30 min by endogenous phosphatase in the E. coli cell extract .
In addition to the high product levels associated with more homeostatic conditions, maltodextrin is a low-cost substrate. The secondary energy compound cost accounts for a significant fraction of total CFPS cost [18, 40]. For example, PEP costs $1.20 per mL of reaction mixture (30 mM PEP), while glucose and maltodextrin cost only $0.0002 and $0.001 per mL of reaction mixture, respectively, based on Sigma-Aldrich prices. Although a small amount of maltodextrin phosphorylase (0.009 U per reaction) and phosphoglucomutase (0.06 U per reaction) added some extra costs for the entire systems, two over-expressed recombinant enzymes in E. coli were produced and used in this study [41, 42]. It is anticipated that costs of supplementary enzymes will be decreased to very low levels. The use of maltodextrin in CFPS can not only dramatically decrease the cost of secondary energy but also increase synthesized protein levels.
The use of maltodextrin as a secondary energy source for cell-free protein synthesis was shown to synthesize proteins with several advantages: relatively high protein synthesis, no phosphate accumulation, little change in pH, and low cost. The slowly generated G1P from maltodextrin followed by glycolysis provided relatively homeostatic CFPS environments.
A total tRNA mixture from E. coli MRE600 and the in vitro protein synthesis system (RTS 100 E. coli High-yield Kit) were obtained from Roche Diagnostics (Indianapolis, IN, USA). The 20 amino-acid mixture was purchased from Spectra Stable Isotopes (Columbia, MD, USA). The recombinant α-glucan phosphorylase and phosphoglucomutase from Clostridium thermocellum were prepared as described elsewhere [41, 42]. The plasmid pIVEX2.3d-est2 encoding the esterase 2 (est2) from Alicyclobacillus acidocaldarius was described elsewhere . The plasmid pET26b-XR encoding xylose reductase from Neurospora crassa was described elsewhere . The plasmid pCG encoding cellulose-binding module and green fluorescent protein (CBM-GFP) was described previously . Pfx50 DNA polymerase and Ni-NTA agarose were purchased from Invitrogen Co. (Carlsbad, CA, USA). E. coli Bl21(DE3) was purchased from Novagen (Gibbstown, NJ, USA). The rest of the reagents were purchased from Sigma-Aldrich (St. Louis, MO, USA).
Construction of the expression plasmids
The plasmids of pIVEX2.3d-xr for xylose reductase and pIVEX2.3d-cg for CBM-GFP were constructed based on the plasmid pIVEX2.3d-est2. The DNA fragment of xylose reductase gene was amplified by the primers Xr-F (5'-GACTGACTCATATGGTTCCTGCTATCAAGCTCAAC-3') and Xr-R (5'-GACTGACTTGATCATCAGTGGTGGTGGTGGTGG-3') on the DNA template of pET26b-XR (bolded nucleotide sequences are NdeI and BclI sites). The plasmid pIVEX2.3d-xr was constructed after NdeI- and BclI-digestion of PCR product and ligation with the NdeI- and BamHI-digested plasmid pIVEX2.3d-est2. The plasmid pIVEX2.3d-cg for CBM-GFP was constructed by ligation of the NdeI- and BamHI-digested CBM-GFP DNA fragment from the plasmid pCG and ligation with the NdeI- and BamHI-digested pIVEX2.3d-est2. The plasmids were validated by DNA sequencing.
Preparation of the E. coliS12 extract
The E. coli S12 extracts were prepared from E. coli BL21(DE3) according to the Kim protocol . The strain was grown in 4 litres of 2xYT medium in a 6.6-L NBS BioFlo 310 Bioreactor (Edison, NJ). The cultivation conditions were 37°C, 200 rpm, and 1.0 vvm. When the absorbance (A600) reached 0.6, a final concentration of 1 mM IPTG was added, and then agitation and airflow rates were increased to 300 rpm and 2.0 vvm respectively. The cells were harvested in the middle exponential phase (A600 = ~4.0). After centrifugation, the cell pellets were washed by an ice-cooled 10 mM Tris-acetate buffer (pH 8.2) with 60 mM potassium glutamate, 14 mM magnesium acetate, 1 mM DTT, and 0.05% beta-mercaptoethnaol three times and then were stored in -80°C. The cell extract was prepared by French Press at a pressure of 20,000 psi. After centrifugation at 12,000 relative centrifugal force (RCF) for 10 min, the supernatant was briefly incubated at 37°C in 10 mM Tris-acetate buffer (pH 8.2) with 60 mM potassium glutamate, 14 mM magnesium acetate, 1 mM DTT for 10 min and then was stored at -80°C for future cell-free protein synthesis. The S12 extracts had 33 mg of cellular protein per mL.
Cell-free protein biosynthesis
The CFPS mixture (30 μL, final volume) consisted of 57 mM of Hepes-KOH (pH 8.2), 1.2 mM of ATP, 0.85 mM of CTP, GTP and UTP (each), 0.6 mM cAMP, 2 mM of DTT, 0.17 mg per mL of E. coli MRE600 total tRNA mixture, 90 mM of potassium glutamate, 80 mM of ammonium acetate, 12 mM of magnesium acetate, 34 μg per mL of l-5-formyl-5,6,7,8-tetrahydrofolic acid, 1.5 mM each of 20 amino acids, 2% (w/v) of PEG 8000, 10 U per mL of pyruvate kinase, 5 nM template DNA, 0.33 mM NAD, 0.26 mM CoA, and 27% (v/v) of the S12 extract. The secondary energy compound (30 mM) was either PEP, glucose, G6P, or maltodextrin. CFPS was conducted at 37°C. When maltodextrin was used as a secondary energy source, the reaction solution was supplemented with 0.009 U of the recombinant C. thermocellum α-glucan phosphorylase and 0.06 U of phosphoglucomutase to generate glucose-1-phosphate (G1P) from maltodextrin for energizing CFPS.
Esterase activity staining on polyacrylamide gel
The protein esterase 2 in the CFPS solution was separated by SDS-polyacrylamide gel in a 100 mM Tris-HCl (pH 7.5). After electrophoresis and EST2 renaturation by removing SDS, the gel was mixed with the substrate (β-naphthylacetate) and the product (β-naphthol) was linked with Fast Blue BB for the formation of an insoluble color complex, indicating the presence and amount of EST2 [24, 46]. Subsequently, the other proteins in the gels were strained by the Coomassie blue dye .
Molar concentration of EST2 (mol/L) was determined by the ratio of the spectrophotometric assay of esterase activity to its molar-specific activity according to [EST2] = (A405/min-0.016)/6.10 × 108, where A405/min is absorbance of a 1-cm path length at 405 nm per minute for a EST2 concentration ranging from 0.02 to 1 nM . Two μL of the reaction mixture were withdrawn and diluted 100-fold in an assay buffer (30 mM Tris-HCl, pH 7.5, 200 mM NaCl and 0.05% Triton X-100). Either 2 μL of the diluted EST2 solution or a further 10-fold diluted EST2 solution was mixed to a final 250 μL of the assay buffer containing 0.2 mM p-nitrophenylbutyrate. The synthesized CBM-GFP protein was quantified in a 50 mM Hepes solution (pH 7.0) using a BioTek multi-detection microplate reader with a reference of purified CBM-GFP expressed by E. coli [44, 48]. The synthesized XR protein was determined by Ni-NTA adsorption and desorption followed by the Bio-Rad Bradford assay.
Concentration of inorganic phosphate in the reaction mixture was determined by using a mild-pH phosphate assay as described elsewhere . Concentration of ATP was measured by the Promega ATP assay kit (Madison, WI) based on the known concentration of ATP standards, as described elsewhere  with modifications. A 2 μL reaction mixture was diluted by 100-fold in the EST2 activity assay buffer, and then 50 μL diluted solution was added into 450 μL of water that had been boiled to denature ATP hydrolysis enzymes, i.e. ATPase and phosphatases . The diluted solution stood on ice until the ATP assay. The pH of the CFPS solution was measured by using an Orion 9810BN micro-pH probe (Beverly, MA) at 37°C. Concentration of lactate was measured with a Beckman-Coulter HPLC (Fullerton, CA) equipped with the Bio-Rad HPX-87 column as described elsewhere .
This work was supported to YHPZ from the Air Force Office of Scientific Research (FA9550-08-1-0145), the DOE BioEnergy Science Center (BESC), and the DuPont Young Professor Award. We thank Professor Mathias Sprinzl of the University of Bayreuth for providing the EST2 expression plasmid and Professor Huiming Zhao of UIUC for xylose reductase plasmid pET26b-XR.
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