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Model-guided gene circuit design for engineering genetically stable cell populations in diverse applications

Maintaining engineered cell populations genetic stability is a key challenge in synthetic biology. Synthetic genetic constructs compete with a host cells native genes for expression resources, burdening the cell and impairing its growth. This creates a selective pressure favouring mutations which alleviate this growth defect by removing synthetic gene expression. Non-functional mutants thus spread in cell populations, eventually making them lose engineered functions. Past work has attempted to limit mutation spread by coupling synthetic gene expression to survival. However, these approaches are highly context-dependent and must be tailor-made for each particular synthetic gene circuit to be retained. In contrast, we develop and analyse a biomolecular controller which depresses mutant cell growth independently of the mutated synthetic genes identity. Modelling shows how our design can be deployed alongside various synthetic circuits without any re-engineering of its genetic components, outperforming extant gene-specific mutation spread mitigation strategies. Our controllers performance is evaluated using a novel simulation approach which leverages resource-aware cell modelling to directly link a circuits design parameters to its population-level behaviour. Our designs adaptability promises to mitigate mutation spread in an expanded range of applications, whilst our analyses provide a blueprint for using resource-aware cell models in circuit design.

synthetic biology↗

Mechanical interaction enables a collective mode of protocell proliferation

The proliferation of primitive life-forms (known as protocells) without sophisticated cell-division molecular machineries has been an intriguing question in evolutionary biology, synthetic biology, and living matter physics. While various modes of protocell proliferation at the individual level have been proposed, the growth dynamics of protocell colonies (i.e., protocolonies) received less attention. Here we chose to study this question in protocolonies consisting of densely packed protocells derived from wall-deficient L-form bacteria. We discovered that protocolonies proliferated robustly under spatial confinement, while isolated protocells failed to divide and eventually experienced membrane rupture due to imbalance of surface and volume growth. Combining results from quantitative imaging and computational modeling, we attributed this unexpected finding to mechanical shearing between densely packed protocells driven by their growth activities; such mechanical shearing enhances cell deformation, thereby enabling cell division and sustaining population growth in a protocolony. Our study reveals a unique role of self-generated mechanical stresses in the lifestyle of primitive life-forms. The findings may help to understand and control the collective growth dynamics of synthetic protocells or active droplets.

biophysics↗

Integrating Gene Synthesis and Microfluidic Protein Analysis for Rapid Protein Engineering

The capability to rapidly design proteins with novel functions will have a significant impact on medicine, biotechnology, and synthetic biology. Synthetic genes are becoming a commodity, but integrated approaches have yet to be developed that take full advantage of gene synthesis. We developed a solid-phase gene synthesis method based on asymmetric primer extension (APE) and coupled this process directly to high-throughput, on-chip protein expression, purification, and characterization (mechanically induced trapping of molecular interactions, MITOMI). By completely circumventing molecular cloning and cell-based steps, APE-MITOMI reduces the time between protein design and quantitative characterization to 3-4 days. With APE-MITOMI we synthesized and characterized over 440 zinc-finger (ZF) transcription factors (TF), showing that although ZF TFs can be readily engineered to recognize a particular DNA sequence, engineering the precise binding energy landscape remains challenging. We also found that it is possible to engineer ZF - DNA affinity precisely and independently of sequence specificity and that in silico modeling can explain some of the observed affinity differences. APE-MITOMI is a generic approach that should facilitate fundamental studies in protein biophysics, and protein design/engineering.

Bioengineering↗

Finding analytic stationary solutions to the chemical master equation by gluing state spaces at one or two states recursively

Noise is often indispensable to key cellular activities, such as gene expression, necessitating the use of stochastic models to capture its dynamics. The chemical master equation (CME) is a commonly used stochastic model that describes how the probability distribution of a chemically reacting system varies with time. Knowing analytic solutions to the CME can have benefits, such as expediting simulations of multiscale biochemical reaction networks and aiding the design of distributional responses. However, analytic solutions are rarely known. A recent method of computing analytic stationary solutions relies on gluing simple state spaces together recursively at one or two states. We explore the capabilities of this method and introduce algorithms to derive analytic stationary solutions to the CME. We first formally characterise state spaces that can be constructed by performing single-state gluing of paths, cycles or both sequentially. We then study stochastic biochemical reaction networks that consist of reversible, elementary reactions with two-dimensional state spaces. We also discuss extending the method to infinite state spaces and designing stationary distributions that satisfy user-specified constraints. Finally, we illustrate the aforementioned ideas using examples that include two interconnected transcriptional components and chemical reactions with two-dimensional state spaces.\n\nSubject AreasSystems biology, synthetic biology, biomathematics, bioengineering

systems biology↗

DynaRNA: Dynamic RNA Conformation Ensemble Generation with Diffusion Model

RNA plays a wide variety of roles in biological processes. In addition to serving as the coding messenger RNA (mRNA), the vast majority of RNAs function as non-coding RNAs (ncRNAs), where their dynamic structural ensemble is critical for mediating diverse biological functions. However, traditional experimental techniques and molecular dynamics (MD) simulations face significant challenges in characterizing the conformational dynamics of RNA, due to inherent methodological limitations and high computing power cost. We herein presented DynaRNA, a diffusion-based generative model for RNA conformation ensemble. DynaRNA employs denoising diffusion probabilistic model (DDPM) with equivariant graph neural network (EGNN) to directly model RNA 3D coordinates, enabling rapid exploration of RNA conformational space. DynaRNA enables end-to-end generation of RNA conformation ensemble reproducing experimental geometries without the need for Multiple Sequence Alignments (MSA) information. Our results demonstrate that DynaRNA effectively and accurately generate tetranucleotides ensemble with lower intercalation rate than molecular dynamics simulations. Besides, DynaRNA has the ability to capture rare excited states of HIV TAR(trans-activation response) element, and recapitulate de novo folding of tetraloops. DynaRNA serve as a versatile and efficient platform for modeling RNA structural dynamics, with broad implications potential in RNA structural biology, synthetic biology, and therapeutic development.

bioinformatics↗

PromoterAtlas: decoding regulatory sequences across Gammaproteobacteria using a transformer model

Recent advances in deep learning, particularly transformer architectures, have improved computational approaches for biological sequence analysis. Despite these advances, computational models for bacterial promoter prediction have remained limited by small datasets, species-specific training, and binary classification approaches rather than comprehensive annotation frameworks. We present PromoterAtlas, a 1.8M parameter transformer model trained on 9M regulatory sequences from 3,371 gammaproteobacterial species. The model demonstrates recognition of various regulatory elements across different species, including ribosomal binding sites, various types of bacterial promoters, transcription factor binding sites, and terminators. Using this model, we developed a whole-genome promoter annotation tool for Gammaproteobacteria, with various levels of validation that support the predictions of promoters associated with different sigma ({sigma}) factors. Furthermore, we show that the model embeddings encode cross-species evolutionary relationships, clustering promoters by {sigma} factor identity rather than species-specific sequence features. Finally, we show that model embeddings encode regulatory sequence information that enables effective prediction of transcription and translation levels. PromoterAtlas can contribute to our understanding of and ability to engineer bacterial regulatory sequences with potential applications in bacterial biology, synthetic biology, and comparative genomics.

bioinformatics↗

LOBSTERS: a modular vector series with a diverse set of Cas nucleases and plasmid selection markers for multiplex genome editing in Saccharomyces cerevisiae

The budding yeast Saccharomyces cerevisiae is a central model organism in genetics and synthetic biology, yet efficient multiplex genome editing remains difficult because many toolkits are restricted by limited plasmid selection markers and reduced efficiency when targeting multiple loci. In our previous work, we introduced a CRISPR-based system incorporating three nucleases with distinct PAM specificities but it was available only with the URA3 marker. Here we present LOBSTERS, an expanded modular vector series that retains the PAM-diverse nucleases (SpCas9, SaCas9, and enAsCas12a) while extending marker options to seven. This design enables the simultaneous use of multiple plasmids in one transformation, supporting scalable and flexible genome editing. Proof-of-concept experiments demonstrated efficient ADE2 and ADE3 deletions with colorimetric readouts, coordinated tagging of essential proteins (Cdc3 and Cse4) without compromising function, and recapitulation of three quantitative trait variants (RME1, TAO3, and MKT1) underlying sporulation efficiency. Together these results establish LOBSTERS as a robust and versatile platform for multiplex genome editing in S. cerevisiae. By enabling coordinated modification of essential proteins, genetic interactions, and quantitative trait variants, LOBSTERS provides a broadly applicable resource for functional cell biology and synthetic biology in yeast. Significance StatementO_LILOBSTERS integrates three PAM-diverse nucleases with seven plasmid selection markers, overcoming the single-marker limitation of previous yeast genome editing toolkits. C_LIO_LIThe system enables efficient simultaneous editing at multiple loci, demonstrated by functional tagging of essential proteins and recapitulation of quantitative trait variants. C_LIO_LIBy broadening the editable space and lowering barriers to complex genotype construction, LOBSTERS provides a widely applicable resource for yeast cell biology and synthetic biology. C_LI

molecular biology↗

SBOL-OWL: An ontological approach for formal and semantic representation of synthetic genetic circuits

Standard representation of data is key for the reproducibility of designs in synthetic biology. The Synthetic Biology Open Language (SBOL) has already emerged as a data standard to represent genetic circuit designs, and it is based on capturing data using graphs. The language provides the syntax using a free text document which is accessible to humans only. Here, we provide SBOL-OWL, an ontology for a machine understandable definition of SBOL. This ontology acts as a semantic layer for genetic circuit designs. As a result, computational tools can understand the meaning of design entities in addition to parsing structured SBOL data. SBOL-OWL not only describes how genetic circuits can be constructed computationally, it also facilitates the use of several existing Semantic Web tooling for synthetic biology. Here, we demonstrate some of these features, for example, to validate designs and check for inconsistencies. Through the use of SBOL-OWL, queries are simplified and become more intuitive. Moreover, existing reasoners can be used to infer information about genetic circuit designs that cant be directly retrieved using existing querying mechanisms. This ontological representation of the SBOL standard provides a new perspective to the verification, representation and querying of information about synthetic genetic circuits and is important to incorporate complex design information via the integration of biological ontologies.

synthetic biology↗

Dual-function logic gates based on CRISPRi

Developing logic gate circuits that are programmable and reliable for specific functions is a central goal in synthetic biology. Traditional synthetic circuits often rely on protein regulators, which face scalability and resource burden limitations. To overcome these challenges, we introduce a novel approach utilizing dual-function and multi-level logic gates based on the CRISPRi system with dCas9 and sgRNA. This method, implemented in an in vitro transcription system, enables the rapid design and validation of complex logic gates. Our dual-function and multi-level design strategies achieve robust functionality in NOR, NAND, AND, and OR gates, allowing different logic outputs by altering only the inputs while reusing all other modules. This showcases significant advancements in efficiency and scalability for synthetic circuit construction. This work reduces development time and simplifies circuit design, paving the way for more efficient synthetic biology applications.

synthetic biology↗

Biological and synthetic surfactant exposure increase anti-microbial gene occurrence in a freshwater mixed microbial biofilm environment

Aquatic habitats are particularly susceptible to chemical pollution from domestic, agricultural, and industrial sources. Antimicrobials are commonly used in medical and industrial environments to reduce harmful bacteria and biofilms. This has led to the rapid increase in the prevalence of antimicrobial resistant (AMR) genes. Alternate remedies to fight pathogenic bacteria and biofilms are in development including synthetic and biological surfactants such as sodium dodecyl sulphate (SDS) and rhamnolipids respectively. In the aquatic environment these surfactants are present as pollutants with potential to affect biofilm formation and AMR gene occurrence; however, there is limited research showing the actual environmental impact of such exposure. We tested the effects of rhamnolipid and SDS on natural aquatic biofilms in a freshwater stream in Northern Ireland. We grew biofilms on contaminant exposure substrata deployed within the stream over four weeks, and then carried out shotgun sequencing to determine microbial community composition, through 16s rRNA analyses (64,678 classifiable reads identified), and AMR gene occurrence (81 instances of AMR genes over 9 AMR gene classes) through a metagenomic analysis. There were no significant changes in community composition within all systems; however, biofilm exposed to rhamnolipid had a greater number of unique taxa as compared to our SDS treatments and controls. AMR gene prevalence was higher in surfactant-treated biofilms, with biofilm exposed to rhamnolipids having the highest presence of AMR genes and classes compared to the control or SDS treatments, in which genes encoding for rifampin resistance were detected. Our results suggest that the presence of rhamnolipid, and to a lesser extent SDS, encourages an increase in the prevalence of AMR genes in biofilms produced in mixed use water bodies.

microbiology↗

Enzyme promiscuous profiles for protein sequence and reaction annotation

1.1Novel sequencing techniques and biochemical pathway prediction resources provide a wealth of data on novel proteins and computationally predicted enzymatic reactions. Accurate matching of protein sequences to enzymatic activities is crucial for advancing synthetic biology and metabolic engineering efforts. Here we present BridgIT+, a computational workflow that accounts for enzyme promiscuity and accurately predicts protein-reaction and reaction-protein associations. BridgIT+ builds upon the promiscuity-based method for annotating orphan and novel reactions with enzymatic activities, BridgIT, and utilizes position-specific scoring matrices (PSSM). The framework uses sequence alignment and enzyme promiscuity predictions to analyze protein sequences, identify sequence patterns, and create promiscuous protein sequence profiles for each reaction. These profiles allow us to predict the protein sequences most likely involved in the reaction. We showcase BridgIT+ by annotating (i) computationally predicted reactions with proteins and (ii) unannotated proteins of E. coli proteome with enzymatic functions. We demonstrated the performance of BridgIT+ on several biochemical assays and compared it to three current state-of-the-art methods for matching proteins and reactions. We anticipate that the proposed conceptual framework will enhance our understanding of gene-protein-reaction relations and advance biological sequence and reaction annotation in biology and synthetic biology studies.

bioinformatics↗

Co-transcriptional production of programmable RNA condensates and synthetic organelles

Condensation of RNA and proteins is central to cellular functions, and the ability to program it would be valuable in synthetic biology and synthetic cell science. Here we introduce a modular platform for engineering synthetic RNA condensates from tailor-made, branched RNA nanostructures that fold and assemble co-transcriptionally. Up to three orthogonal condensates can form simultaneously and selectively accumulate guest molecules. The RNA condensates can be expressed within synthetic cells to produce membrane-less organelles with controlled number, size, morphology and composition, and that display the ability to selectively capture proteins. The in situ expression of programmable RNA condensates could underpin spatial organisation of functionalities in both biological and synthetic cells.

synthetic biology↗

Identification of novel broad host-range promoter sequences functional in diverse Pseudomonadota by a promoter-trap approach

Finding novel promoter sequences is a cornerstone of synthetic biology. To contribute to the expanding catalog of biological parts, we employed a promoter-trap approach to identify novel sequences within an Antarctic microbial community that act as broad host-range promoters functional in diverse Pseudomonadota. Using Pseudomonas putida KT2440 as host, we generated a library comprising approximately 2,000 clones resulting in the identification of thirteen functional promoter sequences, thereby expanding the genetic toolkit available for this chassis. Some of the discovered promoter sequences prove to be broad host-range as they drove gene expression not only in P. putida KT2440 but also in Escherichia coli DH5, Cupriavidus taiwanensis R1T, Paraburkholderia phymatum STM 815T, Ensifer meliloti 1021, and an indigenous Antarctic bacterium, Pseudomonas sp. UYIF39. Our findings enrich the existing catalog of biological parts, offering a repertoire of broad host-range promoter sequences that exhibit functionality across diverse members of the phylum Pseudomonadota, proving Antarctic microbial community as a valuable resource for prospecting new biological parts for synthetic biology.

synthetic biology↗

Exploiting the Nonlinear Structure of the Antithetic Integral Controller to Enhance Dynamic Performance

The design of biomolecular feedback controllers has been identified as an important goal across a broad range of biological applications spanning synthetic biology, cell therapy, metabolic engineering, etc. This originates from the need to regulate various cellular processes in a robust and timely fashion. Recently, antithetic integral controllers found their way into synthetic biology due to the Robust Perfect Adaptation (RPA) property they endow -- the biological analogue of robust steady-state tracking. The antithetic integral motif hinges on a sequestration reaction between two molecules that annihilates their function. Here, we demonstrate that the complex resulting from the nonlinear sequestration reaction can be leveraged as an inhibitor to enhance the dynamic performance while maintaining the RPA property. We establish that this additional inhibition by the sequestration complex gives rise to a filtered Proportional-Integral (PI) controller thus offering more flexibility in shaping the dynamic response and reducing cell-to-cell variability. Furthermore, we explore the effect of various biological inhibitory mechanisms on the overall performance. The various analyses in the paper are carried out using analytical tools and are supported by numerical simulations. Finally, an experimental validation is performed using the cyberloop -- a hybrid platform where the controller is implemented in silico to control a genetic circuit in vivo.

synthetic biology↗

GreA and GreB enhance Escherichia coli RNA polymerase transcription rate in a reconstituted transcription-translation system

Cell-free environments are becoming viable alternatives for implementing biological networks in synthetic biology. The reconstituted cell-free expression system (PURE) allows characterization of genetic networks under defined conditions but its applicability to native bacterial promoters and endogenous genetic networks is limited due to the poor transcription rate of Escherichia coli RNA polymerase in this minimal system. We found that addition of transcription elongation factors GreA and GreB to the PURE system increased transcription rates of E. coli RNA polymerase from sigma factor 70 promoters up to 6-fold and enhanced the performance of a genetic network. Furthermore, we reconstituted activation of natural E. coli promoters controlling flagella biosynthesis by the transcriptional activator FlhDC and sigma factor 28. Addition of GreA/GreB to the PURE system allows efficient expression from natural and synthetic E. coli promoters and characterization of their regulation in minimal and defined reaction conditions making the PURE system more broadly applicable to study genetic networks and bottom-up synthetic biology.\n\n\n\nO_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=81 SRC=\"FIGDIR/small/024604_ufig1.gif\" ALT=\"Figure 1\">\nView larger version (13K):\norg.highwire.dtl.DTLVardef@53902org.highwire.dtl.DTLVardef@e1ba85org.highwire.dtl.DTLVardef@19c961eorg.highwire.dtl.DTLVardef@143928d_HPS_FORMAT_FIGEXP M_FIG Graphical abstract\n\nC_FIG

Synthetic Biology↗

In Silico Design of Self-Optimizing Integrated Metabolic and Gene Regulatory Networks

Biological organisms acclimatize to varying environmental conditions via active self-regulation of internal gene regulatory networks, metabolic networks, and protein signaling networks. While much work has been done to elucidate the topologies of individual networks in isolation, understanding of inter-network regulatory mechanisms remains limited. This shortcoming is of particular relevance to synthetic biology. Synthetic biological circuits tend to lose their engineered functionality over generational time, primarily due to the deleterious stress that they exert on their host organisms. To reduce this stress (and thus minimize loss of functionality) synthetic circuits must be sensitive to the health of the host organism. Development of integrated regulatory systems is therefore essential to robust synthetic biological systems. The aim of this study was to develop integrated gene-regulatory and metabolic networks which self-optimize in response to varying environmental conditions. We performed in silico evolution to develop such networks using a two-step approach: (1) We optimized metabolic networks given a constrained amount of available enzyme. Here, we found that a proportional relationship between flux control coefficients and enzyme mass holds in all linear sub-networks of branched networks, except those sub-networks which contain allosteric regulators. Network optimization was performed by iteratively redistributing enzyme until flux through the network was maximized. Optimization was performed for a range of boundary metabolite conditions to develop a profile of optimal enzyme distributions as a function of environmental conditions. (2) We generated and evolved randomized gene regulatory networks to modulate the enzymes of a target metabolic pathway. The objective of the gene regulatory networks was to produce the optimal distribution of metabolic network enzymes given specific boundary metabolite conditions of the target network. Competitive evolutionary algorithms were applied to optimize the specific structures and kinetic parameters of the gene regulatory networks. With this method, we demonstrate the possibility of algorithmic development of integrated adaptive gene and metabolic regulatory networks which dynamically self-optimize in response to changing environmental conditions.

Bioengineering↗

ATP Regeneration from Pyruvate in the PURE System

The Protein synthesis Using Recombinant Elements ( PURE) system is a minimal biochemical system capable of carrying out cell-free protein synthesis using defined enzymatic components. This study extends PURE by integrating an ATP regeneration system based on pyruvate oxidase, acetate kinase, and catalase. The new pathway generates acetyl phosphate from pyruvate, phosphate, and oxygen, which is used to rephosphorylate ATP in situ. Successful ATP regeneration requires a high initial concentration of[~] 10 mM phosphate buffer, which surprisingly does not affect the protein synthesis activity of PURE. The pathway can function independently or in combination with the existing creatine-based system in PURE; the combined system produces up to 233 {micro}g/ml of mCherry, an enhancement of 78% compared to using the creatine system alone. The results are reproducible across multiple batches of homemade PURE, and importantly also generalise to commercial systems such as PURExpress(R) from New England Biolabs. These results demonstrate a rational bottom-up approach to engineering PURE, paving the way for applications in cell-free synthetic biology and synthetic cell construction.

synthetic biology↗

A semi-synthetic strategy for derivatization of the violacein natural product scaffold

Natural products and their analogues are often challenging to synthesise due to their complex scaffolds and embedded functional groups. Solely relying on engineering the biosynthesis of natural products may lead to limited compound diversity. Integrating synthetic biology with synthetic chemistry allows rapid access to much more diverse portfolios of xenobiotic compounds which may accelerate the discovery of new therapeutics. As a proof-of-concept, by supplementing an Escherichia coli strain expressing the violacein biosynthesis pathway with 5-bromo-tryptophan in vitro or tryptophan 7-halogenase RebH in vivo, 6 halogenated analogues of violacein or deoxyviolacein were generated, demonstrating promiscuity of the violacein biosynthesis pathway. Furthermore, 20 new derivatives were generated from 5-brominated violacein analogues via Suzuki-Miyaura cross-coupling reaction directly using the crude extract without prior purification. Herein, we demonstrate a flexible and rapid approach to access diverse chemical space that can be applied to a wide range of natural product scaffolds.

synthetic biology↗