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Gargantilla Becerra, A.

Publications and source records attributed to Gargantilla Becerra, A..

2 recordsLinked to original sources

ML4SD: Leveraging Machine Learning and High-Throughput Search Algorithms for an Iterative Growth-Coupled Design Innovation

Optimizing microbial biomanufacturing is required if renewable and waste carbon are to replace petrochemical routes at competitive titers, rates, and yields. Growth-coupled (GC) production supports that goal by linking target synthesis to biomass formation, so product formation is required for growth. Constructing knockout strains yielding GC production from a list of candidate genes is labor and time demanding. This results in few in vivo tested designs, which hampers standard machine-learning methods to learn GC patterns for specific bioprocesses. We therefore developed ML4SD, an active-learning Design-Build-Test-Learn (DBTL) cycle that trains ensembles on genome-scale metabolic model (GEM) scores of knockout designs, sampling the next designs from predicted model performance and error. That cycle generalizes only if the initial library is large and diverse, including suboptimal and non-viable designs; libraries restricted to minimal designs or Pareto-optimal knockouts were found to generate models overfitting. To meet those specific demands a novel strain design algorithm, gcSwarms, was developed and tested for a diverse set of bioprocesses within Pseudomonas putida iJN1462. ML4SD was tested with an in silico case study converting lignin-derived 4-hydroxybenzoate to 6-caprolactam, the nylon-6 monomer. ML4SD results showed improvements of up to 164% on carbon yield, recovering a shared SHAP motif that redirects TCA flux through acetyl-CoA. Importantly it reaches that result using 2.5- to 7.1-fold fewer designs than a gcSwarms-only search, demonstrating the data efficiency of this method.

bioinformatics↗

EMBER: A Genome-Scale Approach for a Systematic Characterization of Bacterial Metabolic Heterogeneity through the Growth-Adaptation Trade-Off

Microorganisms maintain resilience in fluctuating environments by operating close to a multi-optimality state, balancing growth rate and adaptability. This trade-off dictates bacterial resilience and often complicates metabolic engineering efforts. Addressing it requires identifying specific pathways responsible for diverting metabolic resources away from desired production goals. For this purpose, we introduce EMBER (Exploration of Metabolic trade-offs Based on the mapping of Expression patterns to Reactions), a novel Genome-scale Metabolic Model (GEM) contextualization approach. EMBER integrates transcriptomic data and flux analysis to computationally distinguish between growth-associated reactions (BARs) and adaptive, non-biomass reactions (NBRs). We applied this framework to analyze the metabolic architectures of three diverse and biotechnologically relevant organisms--P. putida, E. coli, and Synechocystis--across various environmental conditions. We revealed marked variability in adaptive resource allocation, with the heterotrophs dedicating substantially more active genes to NBRs (up to 31%) than the photoautotroph Synechocystis (17.5%). Functional analysis showed that BARs consistently supported core metabolism, while NBRs encoded context-specific adaptive functions aligned with the organisms native environment. Analysis of NBR gene expression variability further suggested that P. putida relies predominantly on Bet-Hedging strategies, whereas E. coli employs more regulated Responsive Switching mechanisms. Overall, EMBER offers a powerful systems biology tool to quantify and functionally interpret metabolic heterogeneity. This systematic identification of NBRs will facilitate precise metabolic engineering efforts via reducing unnecessary fitness costs or harnessing the population heterogeneity for deploying complex biotechnological tasks.

bioinformatics↗