Expanding the genetic toolbox for prokaryotic synthetic biology is a promising strategy for enhancing the dynamic range of gene expression and enabling new engineered applications for research and biomedicine. Here, we reverse the current trend of moving genetic parts from prokaryotes to eukaryotes and demonstrate that the activating eukaryotic transcription factor QF and its corresponding DNA-binding sequence can be moved to E. coli to introduce transcriptional activation, in addition to tight off states. We further demonstrate that the QF transcription factor can be used in genetic devices that respond to low input levels with robust and sustained output signals. Collectively, we show that eukaryotic gene regulator elements are functional in prokaryotes and establish a versatile and broadly applicable approach for constructing genetic circuits with complex functions. These genetic tools hold the potential to improve biotechnology applications for medical science and research.
The field of synthetic biology has revolutionized how cells can be reprogrammed through the assembly of genetic parts, or modules, into more complex genetic circuits. This approach is broadly applicable to many organisms and provides a means to control cell behavior in new and predictable ways1,2,3,4,5,6,7,8,9,10,11,12,13. To accomplish this, genetic parts are often taken from diverse organisms and used to establish orthogonal, independent functions within cells14,15. Orthogonal control elements of genetic circuits do not exist naturally in the host organism and as a result are unlikely to interfere with, or be compromised by, host signaling events. Genetic parts are traditionally moved from prokaryotic organisms to more complex eukaryotic cells to provide orthogonal gene control in higher organisms16,17,18,19,20,21; however, genetic parts from eukaryotes are rarely, if ever, moved from eukaryotes to prokaryotes.
Transcription factors are DNA-binding proteins that repress or activate transcription by binding to a specific DNA sequence within the genome, and they have been widely used to build genetic circuits that regulate gene expression. In prokaryotes, repressor proteins are predominately used to control gene expression because prokaryotic genes are on by default22. Most prokaryotes have a single RNA polymerase (RNAP) that recognizes all of the promoters and transcribes all the RNA in the organism unless repressor proteins block RNAP from binding to the promoter sequence. Inducible transcription in bacteria is most commonly achieved by de-repression, or the removal of repressor proteins, to enable the binding of RNAP and the transcription of downstream gene(s)23.
The bacteriophage T7 promoter and corresponding T7 RNA polymerase (T7RNAP) are widely used in bacteria for high recombinant protein production24. Since the endogenous RNAP does not bind to the T7 promoter, the system provides orthogonal control of gene expression in prokaryotes. Because T7RNAP is highly selective for the T7 promoter, transcription of downstream genes is also selective25. This system can be made inducible by controlling the transcription of T7RNAP using bacterial systems such as AraC26, LacI27, and TetR14 and placing their respective DNA-binding sites upstream of an endogenous promoter that drives the expression of T7RNAP. The repressor proteins of these systems bind to their respective DNA-binding sites to prevent the transcription of T7RNAP. In the presence of their small molecule inducer, arabinose, isopropyl β-D-1-thiogalactopyranoside (IPTG), and anhydrotetracycline (aTc), respectively, the repressor proteins become dislodged from their binding sites, enabling endogenous RNAP to bind and transcribe T7RNAP. To date, the inducible T7 promoter is the most widely used orthogonal system in prokaryotes for high levels of recombinant protein production28.
We propose an alternative approach to orthogonal regulation of gene expression in prokaryotes that investigates circuits regulated by transcriptional activators rather than baseline repression. To accomplish this, we reversed the conventional approach of moving gene regulatory parts from prokaryotes to eukaryotes by moving the activating eukaryotic transcription factor QF and its corresponding DNA-binding site, QUAS, from the filamentous fungus Neurospora crassa to bacteria. When glucose levels are low, the fungus utilizes the regulatory genes from its quinic acid (QA) gene cluster (qa) to use quinic acid as a carbon source29,30. The qa gene cluster includes a gene encoding the transcription factor QF. QUAS is found upstream of the qa gene cluster and other QF regulated genes. QF is a transcriptional activator that promotes the transcription of downstream genes when it binds to QUAS. The qa gene cluster also encodes the negative regulator QS that prevents QF from binding to the transcriptional machinery at its activation domain preventing the transcription of downstream genes. Transcriptional repression can be reversed with the addition of quinic acid (Supplementary Fig. 1). The interactions of QF, QUAS, and QS are collectively referred to as the Q system. A second generation of the QF transcription factor (QF2) that has the middle region of the protein removed to decrease toxicity in other organisms was used in this study31.
Various components of the Q system have been successfully applied to regulate gene expression in Drosophila31,32,33, cultured mammalian cells34,35, zebrafish36, and Caenorhabditis elegans (C. elegans)37. To test whether qa clusters of genes function in prokaryotes, we moved the gene encoding the QF transcription factor and its QUAS binding site to expression plasmids specific for bacteria. We found that the QUAS binding domain introduced robust transcriptional activation in the presence of QF when placed downstream of the T7 promoter. In contrast, when the QUAS binding domain was placed upstream of the T7 promoter, tight transcriptional repression in the absence of QF was observed. Moreover, we demonstrate the versatility of this genetic tool in bacteria by showing its compatibility with the TetR system, and show that it has a broad dynamic range of regulated gene expression. Using the eukaryotic Q system, we present alternative strategies for controlling gene expression in bacteria that expand the genetic toolbox in prokaryotic synthetic biology and enhances the production capabilities of mRNA and proteins for biotechnology applications.
The position of QUAS relative to the T7 promoter enables switch-like gene expression
To investigate whether QF could mediate orthogonal gene control in prokaryotes, the 16 base pair QUAS DNA sequence was placed directly upstream of a T7 promoter (QUAS-0-T7) driving the expression of GFP (Supplementary Table 2). The construct was tested in the BL21(D3) strain of E. coli. This bacterial strain transcribes T7RNAP upon induction with IPTG. Unless otherwise stated, all experiments presented are in the presence of 0.5 mM IPTG to induce the transcription of T7RNAP. We placed a degradation tag on the C-terminal end of GFP to limit its half-life and enable more accurate reporting of gene expression dynamics in our circuits38,39,40. In the absence of QUAS, the T7 promoter actively transcribes GFP following T7RNAP transcription with IPTG induction (Fig. 1a, top construct). However, inserting a single QUAS binding site directly upstream of the T7 promoter prevents GFP expression despite the presence of IPTG and induction of T7RNAP (Fig. 1a, middle construct; b top construct), with GFP fluorescence equivalent to the background fluorescence level of untransformed cells (Supplementary Fig. 2). When QF is introduced in a separate plasmid, the QUAS-0-T7 system is activated and expression of GFP can be detected within the first hour. Three hours after IPTG induction, GFP fluorescence surpassed the level from the T7 promoter control (Fig. 1a). Thus, when T7RNAP is present upon IPTG induction, the eukaryotic transcription factor QF can activate gene expression in bacteria beyond baseline levels. The QUAS-0-T7 circuit has switch-like behavior with a tight off state and robust activation of GFP expression that was dependent on the expression of QF.
Since cis-regulatory elements in eukaryotes can function upstream and downstream of promoters, we evaluated the impact on gene expression of placing QUAS downstream of the T7 promoter (T7-0-QUAS) (Fig. 1b). Repositioning QUAS resulted in GFP expression similar to that of the T7 control (Fig. 1b) with both circuits reaching their peak GFP expression in the absence of QF 2 h after IPTG induction of T7RNAP. For both circuits, expression quickly diminished 3 h after of T7RNAP induction and reached baseline expression by 4 h. In contrast, GFP expression from the T7-0-QUAS system in the presence of QF was greater starting at hour two when compared to the T7-0-QUAS without QF and the T7 control (Fig. 1b). Together these experiments demonstrated that QUAS can function on either side of the transcriptional start site in bacteria. Moreover, placing QUAS downstream of the T7 promoter enabled higher and more sustained GFP expression in the presence of QF than when QUAS was placed upstream of the T7 promoter; though, baseline expression was not blocked and resembled the T7 control (Fig. 1a, b).
Upstream placement of QUAS tightly represses gene expression
Placement of QUAS upstream of the T7 promoter prevented GFP expression despite the presence of T7RNAP after the addition of IPTG (Fig. 1a, b ). To further evaluate the extent of T7 promoter silencing, GFP was replaced with ccdB (Fig. 1c), a highly toxic protein in the CcdB/CcdA toxin/antitoxin system that causes severe DNA damage and cell death41,42,43,44,45. We demonstrated that E. coli cells containing QUAS-0-T7-ccdB constructs continue to grow over a 4-h time period without growth inhibition or cell death, presumably due to the tight off state that QUAS provides (Fig. 1c and Supplementary Fig. 3). In contrast, QF activated expression of ccdB from QUAS-0-T7, causing 99% cell death within 2 h of induction of T7RNAP (Fig. 1c). We conclude that placing QUAS upstream of the T7 promoter establishes a tightly regulated switch that can maintain tight off states and rapidly activates in the presence of QF.
QUAS spacing upstream of the T7 promoter impacts gene expression
For other upstream activation sequences, the position of the sequence relative to the promoter influences the efficacy of transcription initiation46. To determine whether the location of QUAS upstream of the T7 promoter influences GFP gene expression, QUAS was placed at various positions upstream of the T7 promoter (Fig. 2). Because one half-turn of the DNA double-helix is ~5 base pairs, the placement of QUAS was shifted in intervals of 5 base pairs, enabling the bound QF orientation to be rotated one half-turn. QUAS was placed 5, 10, or 15 base pairs upstream of the T7 promoter (Fig. 2 and Supplemental Table 2). These differ from QUAS-0-T7 where the QUAS and T7 sequences were adjacent. We investigated the modifications’ impact on the duration of gene expression by observing GFP fluorescence over a 10-h time period (Fig. 2). All three QUAS-spacing plasmids produced switch-like expression with tight off states in the absence of QF, and activation of gene expression in the presence of QF. Of the positions tested, the QUAS placed 10 base pairs upstream of the T7 promoter (QUAS-10-T7) produced the highest expression of GFP in the presence of QF (Fig. 2b). In addition, QUAS-10-T7 with QF maintained a robust level of expression for a longer period of time when compared to all other upstream locations (Fig. 2a, c).
QUAS downstream of the T7 promoter enables amplification of gene expression
Since the relative position of QUAS upstream of T7 influenced expression, we also investigated the impact of positioning QUAS at different downstream locations relative to the T7 promoter. Similar to the upstream placements, QUAS was placed at 5, 10, and 15 base pairs downstream of the T7 promoter (Fig. 3). In all cases, we kept the distance between the end of the QUAS and the ribosome binding site (RBS) the same in addition to the distance between the RBS and start codon of the downstream gene (Supplementary Table 2). The relative position of the QUAS insertion impacted the intensity and duration of GFP expression. This position-dependent effect was accentuated with the addition of QF, which resulted in the highest and most sustained levels of expression from T7-15-QUAS. Expression from the T7-15-QUAS + QF construct lasted 6 h longer than the T7-15-QUAS and T7 controls (Fig. 3). While our flow cytometry results indicate that the bacteria maintain fairly homogeneous populations throughout this time course, after 6 h of IPTG induction of T7RNAP we could detect heterogeneity in the T7-0-QUAS and T7-0-QUAS + QF populations of bacteria with the emergence of a sub-population with reduced GFP fluorescence (Supplementary Fig. 4). This is likely due to the cells entering the stationary phase, where they stop producing GFP (Supplementary Fig. 6). Due to the degradation tag on GFP, we observe rapid degradation of fluorescence once it enters this growth phase (Supplementary Fig. 4). Despite this, the majority of the bacteria-containing T7-0-QUAS and T7-0-QUAS + QF maintained GFP expression over the course of the 10-h experiment compared to the controls. Overall, the bacteria with T7-0-QUAS and T7-0-QUAS + QF had higher levels of GFP expression per cell than T7-GFP control cells (Supplementary Fig. 4).
Design of activator-repressor based genetic circuits
To generate high-performance of programmable bacteria with enhanced regulated production of mRNA and protein, we coupled QF and its QUAS DNA-binding site with the TetR system to create a collection of genetic devices that mediated specific responses to aTc. Unlike other regulatory systems, the unique position-dependent characteristics of QUAS in bacteria makes this a highly versatile and modular component for custom-made genetic devices. The response characteristics of these circuits were evaluated relative to the traditional TetR system using a graded series of aTc concentrations over a 10-h culture period (Supplementary Fig. 5). For the analysis of our devices, each circuit was compared to the maximum expression of GFP attained through the activation by the traditional TetR system, which is represented by a dashed line (Fig. 4). We sought to design genetic devices that were off in the uninduced state, therefore each design of these devices contains a QUAS sequence positioned upstream of the T7 promoter to take advantage of the tight off state created by this configuration.
Placing QUAS 5 base pairs upstream of the T7 promoter driving the expression of GFP produces a biosensor similar to the traditional TetR system (Fig. 4a and Supplementary Fig. 5). In this design, the TetR repressor proteins bind to the tetO sites located in two places: downstream of the T7 promoter driving the expression of QF and downstream of the T7 promoter driving the expression of GFP, repressing the transcription of both QF and GFP (Fig. 4a, top circuit). The addition of aTc produces a conformational change in the TetR proteins, causing them to no longer bind to the TetO sites. T7RNAP is then permitted to bind to the promoter to transcribe QF and GFP (Fig. 4a, bottom circuit). This circuit design enables higher GFP expression compared to the traditional TetR system (Fig. 4a, dotted line and Supplementary Fig. 5). Similar to the traditional TetR system, lower concentrations of aTc (≤100 ng/mL) could be distinguished within the first 4 h; however, beyond 4 h these lower concentrations were indistinguishable, and only the higher concentrations of aTc (≥300 ng/mL) gave a robust fluorescence response over the 10 hours compared to the traditional TetR system.
Since placing the QUAS sequence 10 base pairs upstream of the T7 promoter gave the highest protein production in the presence of QF (Fig. 2b), we studied whether this configuration would significantly increase the sensitivity to aTc (Fig. 4b). To control the activation of QF, this circuit was designed to produce QF in the presence of aTc by placing a TetO site upstream of the QF gene and the expression of GFP was regulated by the activation of QF binding to the QUAS binding site. In the absence of aTc, the TetR proteins repress the transcription of QF preventing it from activating the expression of GFP (Fig. 4b, top circuit). In the presence of aTc, the TetR proteins no longer bind to the TetO site, enabling T7RNAP to bind to the T7 promoters and transcribe QF for the activation of GFP transcription (Fig. 4b, bottom circuit). When aTc was added to the system, an increase in background expression was observed (0 ng/ml aTc) (Fig. 4b), however, the GFP output was significantly higher in the presence of aTc compared to the traditional TetR system (Fig. 4b, dotted line and Supplementary Fig. 5).
Biological signal filters describe genetic devices that can be activated only by an input signal confined to a certain range and activation is blocked with inputs outside of that range. High-pass genetic filter devices are only activated with high input signal. We next sought to construct a high-pass filter device by coupling the benefit of the tight off observed with QUAS upstream of the T7 promoter and the higher expression level observed when QF was constitutively expressed. To decrease the background expression in the absence of aTc, we designed this circuit to produce more TetR proteins by removing the T7 terminator sequence between the QF and the tetR genes (Fig. 4c). The T7 terminator encodes a DNA sequence that causes T7RNAP to terminate transcription and is placed after each gene to prevent T7RNAP read-through47. Removing the T7 terminator after QF enhances the transcription of tetR because the T7 promoter upstream of QF continues to transcribe through the T7 promoter that drives the expression of the Tet repressor gene and ultimately produces more TetR proteins. These TetR proteins repress the transcription of tetR and GFP. This circuit design results in the repression of GFP expression to background levels. The addition of aTc removes the transcriptional repression and results in robust expression of GFP that resembles a high-pass filter sensor where only high concentrations of aTc activate gene expression (Fig. 4c). Notably, this high-pass filter has high expression levels in the first 3 h after inducing with aTc, almost eight times higher than that seen with the traditional TetR system (Fig. 4c, dotted line and Supplementary Fig. 5).
To explore an approach for the mass-production of mRNA and protein, we designed a circuit that constitutively expressed QF with QUAS located directly upstream a T7 promoter and GFP (Fig. 4d). A TetO site was added directly downstream of the T7 promoter driving GFP expression to make the expression of GFP inducible (Fig. 4d). In the absence of aTc, the TetR proteins bind to the TetO site, preventing T7RNAP from binding and transcribing GFP (Fig. 4d, top circuit). The addition of aTc de-represses the transcription of GFP (Fig. 4d, bottom circuit). In this design, the QF transcription factor appears to over-power the Tet repressor proteins and activates high GFP expression regardless of whether aTc is in the culture in the first few hours. By hour 5, aTc enables greater expression of GFP compared to the traditional TetR system (Fig. 4d, dotted line and Supplementary Fig. 5) for up to 9 h after induction. This circuit design is capable of producing at least thirty times higher gene expression compared to the traditional TetR system.
Developing unique genetic circuits and repurposing genetic regulatory elements to reprogram cellular function has led to new opportunities for clinical applications48,49 and has the potential to influence the therapeutic response to public health crises. Here, we demonstrate the utility of an unconventional approach in which eukaryotic genetic elements are used to regulate gene expression in bacteria. Moreover, we demonstrate that this approach is highly versatile and can be engineered to provide tight regulatory control or amplified gene expression based upon the position of the eukaryotic QUAS relative to the T7 bacteriophage promoter. Furthermore, due to its eukaryotic origins, this system is orthogonal to existing regulatory tools in bacteria and therefore can be used to generate more sophisticated genetic circuits for therapeutic and research efforts than currently available.
The eukaryotic fungus Neurospora crassa uses a genetic circuit to direct the catabolism of quinic acid as a carbon source in certain metabolic states. This cluster of genes is known as the Q system and utilizes genes from the qa gene cluster. In brief, the gene cluster is on when QF binds to QUAS and activates downstream gene expression, and it is off when the negative regulator QS associates with QF and prevents its binding to activate transcription. The natural circuit switches between states via quinic acid. Quinic acid prevents QS from binding to QF, freeing the QF activation domain and re-activating gene expression. While we found that QUAS and the QF transcription factor are functional in prokaryotes, we have not seen any effect of adding QS to the system, suggesting that this arm of the Q system is not functional in this context. One possibility is that the QS function requires post-translational modifications that do not occur in bacteria. More importantly, we have found that QUAS has distinct regulatory functions in the absence of these other components of the Q system when placed upstream of the T7 promoter in bacteria. In this location, it inhibits transcription and does so with sufficient efficacy to enable cell survival when controlling the expression of toxic genes.
While the functional consequence of placing QUAS directly upstream of the T7 promoter is clear, the molecular mechanisms by which it prevents transcription in bacteria have not been identified. We hypothesize that native bacterial repressor proteins may bind to QUAS and block T7RNAP from binding the adjacent T7 promoter. This possibility is consistent with the repressive nature of gene regulation in bacteria. This unknown repressor protein could be displaced by QF due to its higher binding affinity for QUAS, enabling T7RNAP to bind to the T7 promoter and initiate gene expression. Alternatively, QUAS may introduce conformational changes to the local DNA structure that makes the adjacent T7 promoter inaccessible to T7RNAP, and that this inhibition is released when the QUAS is bound by QF. Mechanistically this could be analogous to heterochromatin in eukaryotes, with QF functioning like a pioneer transcription factor that stabilizes the DNA structure in a configuration compatible with RNA polymerase binding and transcription initiation.
The impact of placing QUAS downstream of the T7 promoter highlights the dual function of this cis-regulatory element when utilized in bacteria. In this position QUAS does not have a repressive function but enables significant QF-dependent amplification of gene expression. Levels of GFP expression in the presence of QF showed amplification from the T7 promoter and were much greater than that of T7 alone, exceeding levels of gene expression not seen from any other bacterial expression system. One hypothesis for why the highest gene expression level is observed when QUAS is placed fifteen base pairs downstream of the promoter is that this position gives more space for the QF transcription factor and the T7RNAP to both bind and enable more robust expression of the downstream gene.
Altogether, it is important to note that QUAS, while typically described as an upstream activator, facilitates both the activation and repression of gene expression in bacteria. Moreover, we demonstrate that it can function both upstream and downstream of a promoter sequence. Based upon these observations we would suggest that it is more appropriate to refer to the QUAS sequence as a QF binding site rather than QUAS which more aptly describes transcriptional activation from an upstream cis-regulatory element.
Mechanistically, it is noteworthy that QF can function as a transcriptional activator in a bacterial system because bacteria rarely utilize activators for transcriptional regulation since they typically use repression and de-repression systems for regulating gene expression. Bacterial synthetic biologists have long sought a transcriptional activator to increase gene expression levels. To date, all bacterial systems, with a few exceptions, are repressive in nature. Of these exceptions, the LuxR system is an activator that turns on gene expression at pLuxI promoters when the molecule 3-oxy-hexanoyl-L-homoserine lactone, or autoinducer AI is present50. In addition, efforts have been made to achieve activation at bacterial promoters that requires the use of catalytically inactive Cas9 and guide RNAs51. Some success has been achieved with increasing expression of T7 promoters in bacteria, but this requires protein engineering23. The Q system, on the other hand, requires a single activating protein (QF) and binding domain (QUAS), which is not limited by requiring unique inducers that function to activate gene expression at T7 promoters. The influence that eukaryotic regulatory elements may have on endogenous bacterial gene expression have not been directly tested by our experimental approach; however, they seem unlikely to be significant since activators have not evolved in this context. From a synthetic biology perspective, the efficacy of QF and QUAS in bacteria has significant utility as an independent regulatory system. For example, the large range of control with respect to the orthogonal T7 promoter offers unique advantages in genetic circuit design. Other systems, such as the TetR and LacI systems, function within a narrow range downstream of the T7 promoter, with the upstream positions viable only in unique applications52,53,54. The freedom of placing QUAS relatively far from the promoter allows the placement of additional modules, thereby enabling the design of complex genetic circuits.
We demonstrate the unique programmability of the Q system in bacteria by creating genetic devices that are capable of sensing low input levels and responding with strong output signals. This has the potential to be useful in sensor and diagnostic applications. For example, synthetic biology-based diagnostics have demonstrated that programmable RNA sensors can be engineered to function in a low cost, paper-based, cell-free platform55,56,57,58,59,60,61. These diagnostics are stable at room temperature, and have the potential to meet the needs in low-resource settings. A challenge to many diagnostics is the detection and amplification of small amounts of sample to give a robust readout. Here, we demonstrate that our genetic devices are capable of maintaining a tight off state and detecting small amounts of sample to produce a readout that is significantly higher than standard devices. Coupling our system to cell-free platforms may help improve the rapid detection of a pathogen, contaminant, or antigen that needs to be detected to inform a proper response. In addition, with the emergence of mRNA-based vaccines as a therapeutic intervention, it is possible that these genetic tools can be used to produce high levels of mRNA and protein for biotechnology applications.
QUAS T7 promoter construction
A single 16-mer QUAS (GGGTAATCGCTTATCC) was oriented upstream or downstream of the T7 promoter sequence. A degradation tag was PCR amplified onto the C-terminal end of the GFP gene and cloned into the QUAS-0-T7 or T7-0-QUAS vectors by restriction enzyme cloning (Supplementary Table 1). The degradation tag sequence (DAS + 4) was chosen to leverage bacterial ssrA degradation machinery to allow for the rapid degradation of GFP and CcdB53. To maintain transcription in the T7-0-QUAS expression system, the two base pairs immediately downstream of the promoter were conserved (GG), and QUAS was inserted after these two base pairs (T7-0-QUAS) (Supplementary Table 2). Downstream spacing is notated by counting the number of base pairs between the conserved nucleotides (GG) at the 5′ end of T7 and the start of the QUAS. Upstream spacing plasmids (QUAS-5-T7, QUAS-10-T7, and QUAS-15-T7) and downstream spacing plasmids (T7-5-QUAS, T7-10-QUAS, and T7-15-QUAS) were cloned using gBlocks (IDT) (Supplementary Table 2). For the downstream designs, care was taken to keep the spacing of the end of QUAS and the ribosome binding site (RBS) the same, in addition to the spacing between the RBS and the start codon (Supplementary Table 2). The gBlocks were digested and ligated into backbones containing the high copy ColEI replication of origin, ampicillin resistance, and expression backbone containing GFP with a degradation tag. The QF expression plasmid was constructed by PCR amplifying the QF2 sequence from pAC-7-QFBDAD (Addgene plasmid #46096)31 (Supplementary Table 1) and inserting it downstream of a T7lacO promoter in a vector backbone with kanamycin resistance and a high copy p15A origin of replication using restriction enzyme cloning. The QUAS-0-T7-ccdB plasmid was constructed by PCR amplifying ccdB with the degradation tag (Supplementary Table 1) and using restriction enzyme cloning to insert the amplicon into the QUAS-0-T7 vector in place of GFP. All plasmid transformations to build the constructs used DH5α chemically competent cells (ThermoFisher). The plasmids constructed in this study (Supplementary Table 3) have been deposited in Addgene.
GFP expression experiments
GFP expression experiments were conducted with chemically competent BL21(DE3) E. coli (ThermoFisher) engineered to express T7RNAP when induced with isopropyl β-D-1-thiogalactopyranoside (IPTG). Expression experiments without QF were conducted by transforming the GFP expression plasmid alone (e.g., single transformation) into the BL21(DE3) cells. Expression experiments with QF were conducted by co-transforming the GFP expression plasmid and the QF expression plasmid into BL21(DE3). For each experiment, three colonies of transformed BL21(DE3) were picked and grown overnight in LB (Fisher Scientific) with antibiotic selection (100 μg/mL carbenicillin and/or 50 μg/mL kanamycin) at 37 °C and shaken at 280 RPM. The overnight culture was diluted 1:50 in LB with antibiotic selection, grown at 37 °C, and shaken at 280 RPM. This dilution started at about 0.03 OD and took ~1–2 h of growth (lag phase) before the cultures reached an OD of 0.2 (the beginning of log phase). This log phase OD was determined by obtaining growth curves for all experiential conditions (Supplementary Fig. 6). Cultures were induced with 0.5 mM IPTG at an OD600 (Synergy HTX Reader, Biotek) of ~0.2. Induction served as the time zero point for all experiments. This plate reader corrects the pathlength for each plate used and 300 μl of bacterial culture was consistently taken for all OD measurements.
Samples were diluted 1:400 in PBS and analyzed on a CytoFLEX S cytometer (Beckman Coulter) using a 488 nm laser and a 525/50 filter for Figs. 2, 3, 4 and Supplemental Fig. 5. All other figures were constructed using data obtained from a DXP flow cytometer (Cytek) using a 488 nm laser and a 530/30 filter. Measurements were taken at time points 1–10 h post induction with IPTG. Populations of 10,000 cells were used to calculate GFP fluorescence. Flow cytometery data were collected using CytExpert (version 188.8.131.52 Beckman Coulter) and flow data were analyzed using Flowing Software (Cell Imaging Core, Turkey Centre for Biotech) or FlowJo and MATLAB (The MathWorks, Inc.). Bacterial cells were identified and gated by plotting the side scatter (SSC) vs. forward scatter (FSC) on a log scale (Supplementary Fig. 7). GFP fluorescence data in Figs. 1, 2, 3, and Supplemental Fig. 2 were normalized by dividing the mean fluorescence of each sample by that of the T7 control 1 h after induction.
CcdB expression experiments
QUAS-0-T7 expression experiments without QF were conducted by transforming the expression plasmid alone (without QF) into BL21(DE3) cells. Experiments with QUAS-0-T7 and QF were conducted by co-transforming the expression plasmid with the QF expression plasmid into BL21(DE3) cells. Three colonies of transformed BL21(DE3) were picked and grown overnight in LB (Fisher Scientific) with antibiotic selection at 37 °C and shaken at 280 RPM. The overnight culture was diluted 1:50 in LB with selection antibiotics and grown at 37 °C with shaking at 280 RPM. Cultures were induced with 10 μM IPTG at an OD600 (Synergy HTX Reader, Biotek) of ~0.2. IPTG induction of T7RNAP was used as the time point zero for all experiments. For each hour (0–4) post induction, samples were serially diluted 1:10 in PBS and plated on LB agar plates with antibiotic selection. These plates were incubated at 37 °C overnight, and colonies were counted the next day to calculate colony forming units (CFUs).
Q and TetR system
Genetic circuits containing both TetR and Q system genetic parts were synthesized as gene fragments (IDT) (Supplementary Fig. 2) and inserted into plasmid backbones. A plasmid containing both T7 TetO QF and T7 LacO TetR was PCR amplifying from the T7 LacO TetR region and inserting it into the T7 TetO QF plasmid (Supplementary Fig. 1). Constructs containing GFP were placed in backbones with the high copy ColE1 origin of replication and ampicillin resistance. Circuits expressing QF and/or TetR contain the high copy p15A origin of replication and kanamycin resistance. GFP expression was measured using a flow cytometer as described in the GFP expression experiments; however, cultures were induced at OD600 ~ 0.1. Anhydrotetracycline (cat. no. AAJ66688MA, Alfa Aesar) was dissolved in ethanol according to manufacturer’s directions and stored at −20 °C. Fresh dilutions were prepared for each experiment using water to achieve the reported concentrations. GFP expression was measured using a flow cytometer, as described in the GFP expression experiments.
Bacterial colonies in biological triplicates were grown overnight in 1.5 mL of LB with antibiotics. The following morning, OD600 was measured, and the overnight cultures were diluted 1:50 in fresh LB and antibiotics. Two milliliters of diluted culture were added to 15 mL, round-bottom tubes (Falcon), one tube for every measurement. Starting at the time of dilution, OD600 measurements were taken every 30 min using the same procedure described in GFP expression experiments (Supplementary Fig. 6). A new 2-mL, culture sample was used for each measurement to maintain the same air-to-media ratio for all measurements.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
All data collected to evaluate the conclusions in this work are presented in the paper and/or in the Supplementary Materials. All plasmids generated in this study have been deposited in Addgene (Supplementary Table 3). Reagents or additional data are available from the corresponding author upon request. Source data are provided with this paper.
All MATLAB code used to analyze the data can be found in the Supplementary Software file.
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We thank Chelsea Gibbs for technical assistance with some of the cloning steps and other members of the lab for stimulating conversations about this work. This work was supported by the University of Utah startup funds. The authors gratefully acknowledge the funding sources from the National Science Foundation CAREER Program (CBET-1554017), the Office of Naval Research Young Investigator Program (N00014-16-1-3012), the National Institute of Health Trailblazer Award (1R21EB025413-01), and the National Institutes of Health Director New Innovator Award (1DP2CA250006-01). This work was also supported by the University of Utah Flow Cytometry Facility funded by the National Cancer Institute (5P30CA042014-24), and by the National Center for Research of the National Institutes of Health (1S10RR026802-01).
The authors declare no competing interests.
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MacDonald, I.C., Seamons, T.R., Emmons, J.C. et al. Enhanced regulation of prokaryotic gene expression by a eukaryotic transcriptional activator. Nat Commun 12, 4109 (2021). https://doi.org/10.1038/s41467-021-24434-9
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