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Biology subjects

Dekker, L.

Publications and source records attributed to Dekker, L..

5 recordsLinked to original sources

Generative design and construction of functional plasmids with a DNA language model

DNA language models offer a new paradigm for sequence design, yet their ability to generate functional genomic sequences remains underexplored. Plasmids act as a good testbed for evaluating DNA language model generation potential due to their simplicity and ease of construction. Here, we develop an end-to-end pipeline for generative design of Escherichia coli plasmid backbones, from large-scale data curation through fine-tuning, sampling, bioinformatic assessment, and candidate selection. A curated plasmid library was assembled from PlasmidScope and Addgene, and PlasmidGPT, a GPT-2-style DNA model, was fine-tuned on these corpora using circular-aware batching and random crops. Generations (1,000 per model) were produced under two prompting strategies: a minimal ATG seed to expose default tendencies, and a GFP cassette to enforce functional context. From 1000 generated synthetic plasmids, 16 candidates survived strict filtering and these were prioritised for wet-lab validation. Three shortlisted plasmids were synthesised and found to be functional, supporting growth, antibiotic resistance, and GFP expression in E. coli. These represent, to our knowledge, the first full AI-generated plasmids to be synthesised and validated in vivo. This work demonstrates that curated fine-tuning and prompt-aware generation enable DNA language models to progress from raw sequence sampling to experimentally testable plasmid designs. The approach offers a foundation for extending DNA design optimisation beyond E. coli, toward broader applications across engineering biology.

synthetic biology↗

An antimicrobial peptide expression platform for targeting pathogenic bacterial species

Bacteriocins are antimicrobial peptides that are naturally produced by many bacteria. They hold great potential in the fight against antibiotic resistant bacteria, including ESKAPE pathogens. However, they often have low stability in vivo and therefore, may not be effective when administered orally. Engineered live biotherapeutic products (eLBPs) that secrete bacteriocins can be created to deliver bacteriocins directly at the site of infection. Here we develop a modular bacteriocin secretion platform that can be used to express and secrete multiple bacteriocins from non-pathogenic Escherichia coli host strains. As a proof of concept we create Enterocin A and Enterocin B secreting strains that show strong antimicrobial activity against Enterococcus faecalis and Enterococcus faecium, and characterise this activity in both solid culture and liquid co-culture. We then develop a Lokta-Volterra model that can be used to capture the interactions of these competitor strains. We show that simultaneous exposure to EntA and EntB can delay the point of Enterococcus growth. Our system has the potential to be used as an eLBP to secrete additional bacteriocins for the targeted killing of other pathogenic bacteria.

synthetic biology↗

Emergent digital bio-computation through spatial diffusion and engineered bacteria

Building computationally capable biological systems has long been an aim of synthetic biology. The potential utility of biocomputing devices ranges from biosafety and environmental applications to diagnosis and personalised medicine. Here we present work for the design of bacterial computers which use spatial patterning to process information. Our computers are composed of bacterial colonies which, inspired by patterning in embryo development, receive information in the form of diffusible morphogen-like signals. A computation is encoded by the physical locations of the input sources of morphogen and the output receiver colonies. We demonstrate, mathematically and with engineered Escherichia coli, the simple digital logic capability of single bacterial colonies and show how additional colonies are required to build complex functions. Inspired by electronic design automation, an algorithm for designing optimal spatial circuits computing two-level digital functions is presented. This enhances the capability of our system to complex digital functions without increasing the biological complexity. We extend our experimental system to incorporate biosensing colonies as morphogen sources, demonstrating how a diagnostic device might be constructed. Our approach will open up new ways to perform biological computation, with applications in bioengineering, biomaterials and biosensing. Ultimately, these computational bacterial communities will help us explore information processing in natural biological systems.

synthetic biology↗

Komagataeibacter tool kit (KTK): a modular cloning system for multigene constructs and programmed protein secretion from cellulose producing bacteria

Bacteria proficient at producing cellulose are an attractive synthetic biology host for the emerging field of Engineered Living Materials (ELMs). Species from the Komagataeibacter genus produce high yields of pure cellulose materials in a short time with minimal resources, and pioneering work has shown that genetic engineering in these strains is possible and can be used to modify the material and its production. To accelerate synthetic biology progress in these bacteria, we introduce here the Komagataeibacter tool kit (KTK), a standardised modular cloning system based on Golden Gate DNA assembly that allows DNA parts to be combined to build complex multigene constructs expressed in bacteria from plasmids. Working in Komagataeibacter rhaeticus, we describe basic parts for this system, including promoters, fusion tags and reporter proteins, before showcasing how the assembly system enables more complex designs. Specifically, we use KTK cloning to reformat the Escherichia coli curli amyloid fibre system for functional expression in K. rhaeticus, and go on to modify it as a system for programming protein secretion from the cellulose producing bacteria. With this toolkit, we aim to accelerate modular synthetic biology in these bacteria, and enable more rapid progress in the emerging ELMs community.

synthetic biology↗

Transcriptional terminators allow leak-free chromosomal integration of genetic constructs in cyanobacteria

Cyanobacteria are promising candidates for sustainable bioproduction of chemicals from sunlight and carbon dioxide. However, the genetics and metabolism of cyanobacteria are less well understood than model heterotrophic organisms, and the suite of well characterised cyanobacterial genetic tools and parts is less mature and complete. Transcriptional terminators use specific RNA structures to halt transcription and are routinely used in both natural and recombinant contexts to achieve independent control of gene expression and insulate genes and operons from one another. Insulating gene expression can be particularly important when heterologous/synthetic genetic constructs are inserted at genomic locations where transcriptional read-through from chromosomal promoters occurs, resulting in poor control of expression of the introduced genes. To date, few terminators have been described and characterised in cyanobacteria. In this work, nineteen heterologous, synthetic or putative native Rho-independent (intrinsic) terminators were tested in the model freshwater cyanobacterium, Synechocystis sp. PCC 6803, from which eleven strong terminators were identified. A subset of these strong terminators was then used to successfully insulate a chromosomally-integrated rhamnose-inducible rhaBAD expression system from hypothesised read-through from a neighbouring chromosomal promoter, resulting in greatly improved inducible control. The addition of validated strong terminators to the cyanobacterial toolkit will allow improved independent control of introduced genes.

synthetic biology↗