Rapid, Affordable, and Uncomplicated Production of Bacterial Cell-free Lysate

Summary

This protocol describes a rapid and simple method to produce bacterial lysate for cell-free gene expression, using an engineered strain of Escherichia coli and requiring only standard laboratory equipment.

Abstract

Cell-free gene expression offers the power of biology without the complications of a living organism. Although many such gene expression systems exist, most are quite expensive to buy and/or require special equipment and finely honed expertise to produce effectively. This protocol describes a method to produce bacterial cell-free lysate that supports high levels of gene expression, using only standard laboratory equipment and requiring minimal processing. The method uses an Escherichia coli strain producing an endolysin that does not affect growth, but which efficiently lyses a harvested cell pellet following a simple freeze-thaw cycle. The only further processing required is a brief incubation followed by centrifugation to clear the autolysate of cellular debris. Dynamic gene circuits can be achieved through heterologous expression of the ClpX protease in the cells before harvesting. An E. coli strain lacking the lacZ gene can be used for high-sensitivity, cell-free biosensing applications using a colorimetric or fluorescent readout. The entire protocol requires as few as 8-9 hours, with only 1-2 hours of hands-on labor from inoculation to completion. By reducing the cost and time to obtain cell-free lysate, this method should increase the affordability of cell-free gene expression for various applications.

Introduction

Gene expression in cell-free lysates has several advantages over using live cells^1,2,3,4. Lysates can be easily modified biochemically and used in conditions that could be detrimental to or impossible to achieve in live cells. Gene expression circuits do not have to contend or compete with host biological processes, and testing new genetic circuits is as simple as adding DNA. For these reasons, cell-free gene expression has found various applications, from biosensors^5,6 to rapidly prototyping synthetic gene circuits^7,8 to developing artificial cells⁹. Most cell-free gene expression utilizes cellular lysates that have been highly processed, generally requiring long and complex protocols, specialized equipment, and/or sensitive steps that can lead to significant variation between users and batches^10,11.

This paper describes a simple, efficient method for producing cell-free lysate that requires minimal processing and expertise (Figure 1A)¹². The method relies on E. coli cells that are engineered to lyse following a simple freeze-thaw cycle. The cells express an endolysin from phage lambda that degrades the cell wall. As the cells are growing, this endolysin remains in the cytoplasm, sequestered from the cell wall. However, a simple freeze-thaw cycle disrupts the cytoplasmic membrane, releasing the endolysin into the periplasm, where it degrades the cell wall, resulting in rapid cell lysis. The protocol can be completed with only a few hours of hands-on work and requires only a freezer, a centrifuge capable of 30,000 × g (for optimal results; lower speeds can be used with more care not to disturb the pellet), a vortex mixer, and a simple buffer solution. Functional lysate can even be produced by freeze-drying the cells and rehydrating them in situ. However, this method produces lysates with lower activity, presumably due to the remaining cell debris.

The lysates are highly active for cell-free gene expression, and they can be enhanced in various ways depending on the end use. The rate of protein synthesis can be further increased by concentrating the lysate using standard spin concentrators. Linear DNA can be protected from degradation by adding purified GamS protein. Protein degradation, necessary for more complex circuit dynamics such as oscillation, can be achieved by co-expressing a ClpX hexamer in the autolysate-producing strain¹³. Finally, LacZ-based visual readouts are enabled by using an autolysate strain lacking lacZ. Overall, this method produces highly active cell-free lysate that is suitable for a wide range of applications.

Protocol

1. Prepare media and buffers.

1. Prepare 2xYTPG medium.
   1. Mix 62 g 2xYT powder, 5.99 g potassium phosphate monobasic, 13.93 g potassium phosphate dibasic, and deionized water to 2 L.
   2. Autoclave on liquid cycle with an exposure time of 30 min¹⁴.
   3. To 400 mL of 2xYTP media from 1.1.2, add 7.2 g D-glucose (dextrose) and mix until dissolved.
   4. Filter-sterilize through a 0.2 µm filter.
2. Prepare S30A buffer.
   1. Mix Tris-HCl (pH 7.7, 50 mM final concentration), potassium glutamate (60 mM final), and magnesium glutamate (14 mM final).
   2. Adjust the pH to 7.7 using 10 M KOH.
3. Prepare Solution 1 (see Table 1).
   1. Resuspend 4-(2-hydroxyethyl)-1- piperazineethanesulfonic acid (HEPES) in 2 mL of water.
   2. Adjust the pH to 8.0 using KOH.
   3. Add all other components from Table 1.
   4. Adjust the pH to 7.6 using 10 M KOH. Filter-sterilize.
4. Prepare 2.5x premix solution (see Table 2).
   1. Mix all the components in Table 2.
   2. Adjust the pH to 7.5 using KOH.
   3. Aliquot and freeze at -80 °C.
      ​NOTE: A 20 µL reaction uses 8.9 µL of premix.

2. Prepare cells.

1. Streak the autolysate cells onto LB agar plates containing 50 µg/mL ampicillin using an inoculating loop and grow at 37 °C (see Note 1).
2. Pick a single colony into a starter culture of LB/ampicillin medium using a pipet tip and grow at 37 °C overnight.
3. Inoculate 400 mL of 2xYTPG medium containing 50 µg/mL ampicillin with 400 µL of starter culture, and grow at 37 °C in a 1 L Erlenmeyer flask, shaking at 300 rpm.
4. Periodically measure the culture's optical density at 600 nm (OD₆₀₀) using a spectrophotometer to read an optical cuvette with a 1 cm path length. When the OD₆₀₀ exceeds 1, begin diluting the culture 5-fold before measurements to ensure that the measurements remain within the linear range of a typical laboratory spectrophotometer. Continue growing the cells until the 5-fold diluted culture reaches OD₆₀₀ of 0.3 (corresponding to a culture OD₆₀₀ of 1.5).

3. Prepare the lysate.

1. Prepare S30A buffer supplemented with 2 mM dithiothreitol (DTT). Mix 3 mL of S30A buffer with 6 µL of DTT stock solution at 1 M. Place on ice for use in step 3.7.
2. Harvest the cells by centrifuging at 1800 × g for 15 min at room temperature.
3. Discard the supernatant by pouring it off and using a pipet to remove any remaining liquid.
4. Resuspend the pellet in 45 mL of cold (4-10 °C) S30A buffer using a vortex mixer.
5. Weigh an empty 50 mL centrifuge tube, transfer the cells into it, and repeat steps 3.2-3.3 to wash the cells.
6. Weigh the pellet, subtracting the weight of an empty 50 mL tube. Make sure to carefully aspirate any remaining supernatant to ensure an accurate measurement of pellet weight.
   NOTE: A typical yield is ~1.3 g of cell pellet from 400 mL of production culture.
7. Add 2 volumes of cold S30A buffer supplemented with 2 mM dithiothreitol, i.e., 2 mL of buffer for every 1 g of cell pellet, and resuspend the cells by vigorously vortex mixing.
8. Freeze the cells. Place the 50 mL tube containing the cells in a -20 °C or -80 °C freezer until the pellet is thoroughly frozen.
   NOTE: The freezing step is a good stopping point for the day.
9. Thaw the cells in a room temperature water bath.
10. Vortex vigorously for 2-3 min.
11. Incubate at 37 °C for 45 min with shaking at 300 rpm.
12. Clear the sample of heavy cellular debris by centrifuging in transparent centrifuge tubes at 30,000 × g for 45 min at 4 °C.
    NOTE: If a centrifuge capable of 30,000 x g is not available, centrifuge for 45 min at 21,000 × g, and use additional caution in step 3.13, as the pellet will be less compact.
13. Carefully transfer the supernatant to a new tube with a pipet, avoiding disturbing the pellet as much as possible. If the transferred supernatant is contaminated with material from the pellet, repeat the previous step.
14. Transfer the supernatant to 1.5 mL centrifuge tubes and centrifuge once more at 21,000 × g (or the maximum speed of a tabletop centrifuge) for 5 min.
15. Aliquot the cleared autolysate into the desired volumes, carefully avoiding any remaining pellet, and freeze at -80 °C or use immediately.
    ​NOTE: A single 20 µL reaction uses 8 µL of autolysate.

4. Cell-free gene expression

NOTE: The autolysate is now ready for any desired end-use. The following is an example standard protocol for cell-free gene expression.

1. For a 20 µL reaction, mix on ice 8 µL of autolysate and 8.9 µL of premix. See NOTE at the end of the protocol section regarding the optimization of magnesium glutamate and PEG 8000 concentrations.
2. Add DNA (e.g., pBEST-OR2-OR1-Pr-UTR1-deGFP-T500 to a final concentration of 8 nM), any other reagents, and water to 20 µL.
3. Place the reaction in a 384-well microplate and measure the fluorescence time course and/or endpoints using a plate reader. For green fluorescent protein (GFP), use an excitation wavelength of 485 nm and an emission wavelength of 520 nm.

5. Protocol modifications

NOTE: The following modifications of the protocol enable it to serve other applications.

1. Cell-free gene expression using linear DNA templates
   1. Perform the steps in section 4, supplementing the reaction with 2.2 µM purified GamS protein (expressed and purified as described¹²) before the addition of the linear DNA.
2. Cell-free gene expression incorporating protein degradation
   1. In step 2.1, use autolysate cells containing the plasmid pACYC-FLAG-dN6-His (see the Table of Materials). In all growth media, additionally include 34 µg/mL chloramphenicol.
   2. In step 2.3, include 40 µM isopropyl β-D-1-thiogalactopyranoside (IPTG) in the growth medium to induce expression from the plasmid.
   3. Repeat steps 3.2-3.4 (washing) two additional times (for a total of three washes) to ensure the complete removal of chloramphenicol, which is a translation inhibitor. For the first two washes (step 3.4), substitute S30A buffer with phosphate-buffered saline (pH 7.4).
   4. In step 4.2, supplement with an additional 3 mM ATP (added from a stock solution of 100 mM ATP in water, pH 7.2) and 4.5 mM magnesium glutamate (using a 1 M stock solution in water) (final concentrations) to compensate for high ATP use by ClpXP, as well as chelation of magnesium by the additional ATP.
3. Cell-free gene expression using LacZ-based readouts (including colorimetric)
   1. In step 2.1, use autolysate cells that do not natively express LacZ (see the Table of Materials).
4. Alternatively, prepare the lysate directly from freeze-dried cells.
   1. Perform all steps from 1.1 to 3.7.
   2. Mix 8 µL of cell suspension with 8.9 µL of premix.
   3. Add plasmid DNA (if desired), other custom reagents, and water to reach a final volume of 20 µL.
   4. Transfer the reaction to a 384-well microplate and freeze-dry it.
      NOTE: Freeze-dried samples can be stored for up to a week and possibly longer.
   5. To begin the reaction, rehydrate it with 18 µL of deionized water supplemented with any desired DNA or other reagents.
   6. Follow the fluorescence dynamics in a plate reader.

NOTE 1: Autolysate cells are designed to lyse upon a freeze-thaw cycle, so it is particularly important to use cryoprotectant when making frozen stocks. We froze stocks in 24% wt/vol glycerol and stored them at -80 °C.

NOTE 2: Magnesium ions and PEG 8000 are critical for lysate performance. The base 2.5x premix, based on previously published data, contains 6 mM magnesium glutamate and 4.8% wt/vol PEG 8000, which become 2.4 mM and 1.9%, respectively, in the final reaction. The autolysate prepared with the protocol here typically performs best with an additional 5 mM Mg-glutamate and 1.5% PEG 8000 in the final reaction. However, this can be optimized in the range of an additional 0-10 mM Mg glutamate and an additional 0-3% PEG 8000 (compared to the base premix). To prepare the premix with the recommended additional 5 mM Mg-glutamate and 1.5% PEG 8000 (final concentrations), mix 380 µL of premix with 4.75 µL of magnesium glutamate at 1 M and 36.1 µL of PEG 8000 at 40% weight/volume.

Results

Representative results can be observed by using autolysate to express GFP from a constitutively expressing plasmid, here pBEST-OR2-OR1-Pr-UTR1-deGFP-T500, and recording a time course of GFP fluorescence in a plate reader (Figure 1B). A dilution series of plasmid DNA found strong expression even at 1 nM DNA. Compared to a commercially available lysate, the autolysate can produce a greater total yield and achieved a greater maximum production rate, calculated as the time derivative of the GFP ...

Discussion

The protocol described here yields highly active bacterial lysate for cell-free gene expression. The key is to use cells carrying the plasmid pAD-LyseR, which expresses the lambda phage endolysin cytosolically. These cells are potentiated to lyse themselves upon permeabilization of the inner membrane, allowing the endolysin access to the cell wall, which the method achieves through a simple freeze-thaw cycle. Because the cells effectively lyse themselves, the product is referred to as autolysate. After the cells have lys...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
2xYT media	EMD Millipore	4.85008	or equivalent
3-PGA	Sigma Aldrich	P8877	or equivalent
Amicon Ultra-15 centrifugal filter unit, 3 kDa cutoff	Millipore Sigma	UFC900308	optional, can be used to concentrate lysate, select concentrator capacity appropriate for the volume to be concentrated
ampicillin	Sigma Aldrich	A0166-5G	or carbenicillin, a more stable variant
ATP	Sigma Aldrich	A8937	or equivalent
cAMP	Sigma Aldrich	A9501	or equivalent
CoA	Sigma Aldrich	C4282	or equivalent
CTP	United States Biosciences	14121	or equivalent
D-glucose (dextrose)	Fisher Scientific	AAA1749603	or equivalent
dithiothreitol (DTT)	Sigma Aldrich	D0632-1G	or equivalent
E. coli BL21-Gold (DE3) carrying pAD-LyseR	Addgene	99244
E. coli BL21-Gold (DE3) ΔlacZ carrying pAD-LyseR	Addgene	99245
Folinic acid	Sigma Aldrich	F7878	or equivalent
GTP	United States Biosciences	16800	or equivalent
HEPES	Sigma Aldrich	H3375-25G	or equivalent
LB media	Fisher Scientific	DF0446075	or equivalent
magnesium glutamate	Sigma Aldrich	49605-250G	or equivalent
NAD	Sigma Aldrich	N6522	or equivalent
potassium glutamate	Sigma Aldrich	G1501-100G	or equivalent
potassium hydroxide (KOH)	Sigma Aldrich	221473-25G	for adjusting pH
potassium phosphate dibasic	Fisher Scientific	BP363-500	or equivalent
potassium phosphate monobasic	Fisher Scientific	BP362-500	or equivalent
Spermidine	Sigma Aldrich	85558	or equivalent
Tris-HCl	Fisher Scientific	9310500GM	or equivalent
tRNA mix	Roche	10109541001	or equivalent
UTP	United States Biosciences	23160	or equivalent