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Doktycz, M. J.

Publications and source records attributed to Doktycz, M. J..

4 recordsLinked to original sources

Data coherence over data volume drives generalisable genome-based prediction of microbial carbon utilisation

Microbial carbon utilisation is a foundational ecological phenotype that remains difficult to predict from genomes despite well-characterised pathways. Machine-learning models generalise poorly across datasets, a failure usually attributed to training-set size and taxonomic bias. To test this, we integrated binary growth phenotypes for 819 strains across 240 carbon sources from four datasets. Balanced accuracy fell from 0.86 within datasets to 0.62 across them, and testing on close relatives recovered only 0.03 of that drop, so mechanistically inconsistent genotype-phenotype relationships drove models to dataset-correlated shortcuts. Restricting training to concordant samples (measured growth matched their annotated pathway) doubled the carbon sources recovering known pathway genes across datasets (6 to 12 of 15), whereas matched random subsets did not. Adding over 8000 literature-curated BacDive genomes to the training set did not improve cross-dataset performance more than the smaller concordant set, suggesting coherence matters more than volume. Because such filtering requires a mechanistic predictor, we tested a mechanism-free alternative combining phylogenetic agreement and experimental labels, which recovered part of the gain but not the recall advantage. Concordance-trained models were bounded specialists, rescuing mechanistic false negatives twice as often as false positives (44\% versus 19\%), mostly metabolic generalists. To locate those bounds, model confidence defined an applicability domain, and prioritising low-confidence genomes for training improved cross-dataset accuracy more than random or diversity-based sampling, especially for the weaker phenotypes. This recasts generalisation in biological machine learning as a problem of label-mechanism agreement and applicability-domain definition, alongside data volume and algorithm choice.

bioinformatics↗

Profiling Expression Strategies for a Type III Polyketide Synthase in a Lysate-Based, Cell-free System

Some of the most metabolically diverse species of bacteria (e.g., Actinobacteria) have higher GC content in their DNA, differ substantially in codon usage, and have distinct protein folding environments compared to tractable expression hosts like Escherichia coli. Consequentially, expressing biosynthetic gene clusters (BGCs) from these bacteria in E. coli frequently results in a myriad of unpredictable issues with protein expression and folding, delaying the biochemical characterization of new natural products. Current strategies to achieve soluble, active expression of these enzymes in tractable hosts, such as BGC refactoring, can be a lengthy trial-and-error process. Cell-free expression (CFE) has emerged as 1) a valuable expression platform for enzymes that are challenging to synthesize in vivo, and as 2) a testbed for rapid prototyping that can improve cellular expression. Here, we use a type III polyketide synthase from Streptomyces griseus, RppA, which catalyzes the formation of the red pigment flaviolin, as a reporter to investigate BGC refactoring techniques. We synergistically tune promoter and codon usage to improve flaviolin production from cell-free expressed RppA. We then assess the utility of cell-free systems for prototyping these refactoring tactics prior to their implementation in cells. Overall, codon harmonization improves natural product synthesis more than traditional codon optimization across cell-free and cellular environments. Refactoring promoters and/or coding sequences via CFE can be a valuable strategy to rapidly screen for catalytically functional production of enzymes from BCGs. By showing the coordinators between CFE versus in vivo expression, this work advances CFE as a tool for natural product research. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=104 SRC="FIGDIR/small/569483v1_ufig1.gif" ALT="Figure 1"> View larger version (21K): org.highwire.dtl.DTLVardef@1aebfceorg.highwire.dtl.DTLVardef@1b289f1org.highwire.dtl.DTLVardef@7e46b4org.highwire.dtl.DTLVardef@53f480_HPS_FORMAT_FIGEXP M_FIG C_FIG

synthetic biology↗

A Lysate Proteome Engineering Strategy for Enhancing Cell-Free Metabolite Production

Cell-free systems present a significant opportunity to harness the metabolic potential of diverse organisms. Removing the cellular context provides the ability to produce biological products without the need to maintain cell viability and enables metabolic engineers to explore novel chemical transformation systems. Crude extracts maintain much of a cells capabilities. However, only limited tools are available for engineering the contents of the extracts used for cell-free systems. Thus, our ability to take full advantage of the potential of crude extracts for cell-free metabolic engineering is limited. Here, we employ Multiplex Automated Genomic Engineering (MAGE) to tag proteins for selective removal from crude extracts so as to specifically direct chemical production. Specific edits to central metabolism are possible without significantly impacting cell growth. Selective removal of pyruvate degrading enzymes are demonstrated that result in engineered crude lysates that are capable of 10 to 20-fold increases of pyruvate production when compared to the non-engineered extract. The described approach melds the tools of systems and synthetic biology to develop cell-free metabolic engineering into a practical platform for both bioprototyping and bioproduction. HighlightsO_LIA novel method of engineering crude cell lysates for enhancing specific metabolic processes is described. C_LIO_LIMultiplex Automated Genomic Engineering (MAGE) can be used to engineer donor strains for improving cell-free metabolite production with minimal impact on cell-growth. C_LIO_LIThe described lysate engineering strategy can specifically direct metabolic flux and create metabolic states not possible in living cells. C_LIO_LIPooling of the central precursor pyruvate was significantly improved through use of this lysate proteome engineering strategy. C_LI

synthetic biology↗

Pore-scale hydrodynamics influence the spatial evolution of bacterial biofilms in a microfluidic porous network

Bacteria occupy heterogeneous environments, attaching and growing within pores in materials, living hosts, and matrices like soil. Systems that permit high-resolution visualization of dynamic bacterial processes within the physical confines of a realistic and tractable porous media environment are rare. Here we use microfluidics to replicate the particle shape and packing density of natural sands in a 2D platform to study the flow-induced spatial evolution of bacterial biofilms underground. We discover that initial bacterial dispersal and particle attachment is a stochastic process driven by bacterial rheotactic transport across pore space velocity gradients. Over time, we find that gravity-driven flow conditions activate different cell-clustering phentoypes in EPS producing and EPS defective bacteria strains, which subsequently changes the overall spatial distribution of cells across the porous media network as colonies grow and alter the fluid dynamics of their microenvironment.

microbiology↗