Search bioRxiv⌕ Search

bioRxiv · 10.1101/2025.06.13.659482

Machine Learning-Assisted Pathway Optimization in Large Combinatorial Design Spaces: a p-Coumaric Acid Case Study

Abstract

Combinatorial pathway optimization is an important tool for industrial metabolic engineering to improve titer, yield, or productivity of strains. Machine learning has been increasingly applied on many aspects of the Design-Build-Test-Learn (DBTL) cycle, an engineering framework that aims to navigate through the large landscape of theoretically possible designs using an iterative approach. While machine learning-assisted recommendation strategies have been successfully used to optimize strains, they have so far been limited to relatively small design spaces with few targeted elements. This small design space may limit key strengths of these approaches, such as strong predictive capabilities of supervised machine learning and exploration-exploitation schemes widely used in reinforcement learning and Bayesian optimization. In this work, two DBTL cycles are performed on Saccharomyces cerevisiae for p-coumaric acid production. We first perform a large library transformation on eighteen genes with twenty promoters, which expands the size of the combinatorial design space significantly (approximately 170 million configurations), followed by a smaller model-guided recommendation round. We use a machine learning-assisted recommendation strategy, based on the gradient bandit algorithm, parametrized to balance explo- ration and exploitation. We show that our recommendation strategy has a better performance than strain recommendation strategy using greedy strategies, such as feature importance-based methods. While balancing between exploration and exploitation has been shown to be impor- tant in many applications, we provide the first direct experimental illustration of this effect by recommending strains for scenarios with increasing exploitative-ness. A clear effect of the exploration-exploitation scenario on the p-coumaric acid production distribution of strains is observed, where a balanced scenario shows a higher variation in production over an exploratory or exploitative scenario. Interestingly, using an alternative top-producing parent strain with this balanced exploration-exploitation scheme gives the highest p-coumaric acid production, suggest- ing that model predictions outside of the training data distribution can still be used to perform successful strain recommendation. Overall, these results suggest that using machine learning- assisted strategies with balanced exploration-exploitation can be used to efficiently explore large combinatorial design spaces. The best engineered strain shows an increase in p-coumaric acid production of 137% over the parent strains and a 0.07g/g yield on glucose.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Abeel, T., van Lent, P., Hoek, R. v. d., Schmitz, J., Paz, S. M., Kooi, I., Jonkers, M., Zwartjens, P.. 2025-06-18. Machine Learning-Assisted Pathway Optimization in Large Combinatorial Design Spaces: a p-Coumaric Acid Case Study. https://doi.org/10.1101/2025.06.13.659482

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Single-Component Photo-Crosslinked Lipoic Acid Functionalized Mucin Hydrogels: Dynamic Mucus Mimetics for Antiviral Protection

Native mucus protects epithelial surfaces through viscoelastic networks of disulfide-linked mucins. However, commercially available mucins often fail to reconstitute comparable mechanical and barrier properties, while synthetic and hybrid mucus mimetics require polymeric crosslinkers that may alter mucus-like composition. Inspired by the native architecture, we directly functionalized porcine gastric and bovine submaxillary mucins with -lipoic acid to develop a single-component, photo-crosslinkable hydrogels. Upon UV irradiation (365 nm), the modified mucins rapidly form disulfide-crosslinked networks without added photo-initiator/ polymeric crosslinkers, two orders of magnitude faster as compared with PEG-SH approaches. The resulting mucin-lipoic acid (MUC-LA) hydrogels exhibit mucus-relevant properties, including tunable viscoelasticity, redox responsiveness, self-healing, and size-dependent restrictions on nanoparticle transport. In transwell-based infection models, MUC-LA hydrogels (2-3%) mimicking the healthy airway mucus (G' {approx} 10-20 Pa) suppress epithelial infection by SARS-CoV-2 and influenza A virus. Crosslinked MUC-LA provides greater protection against SARS-CoV-2 than the non-crosslinked, whereas both formulations suppress influenza A infection, suggesting distinct contributions from network formation and mucin-associated interactions. These findings establish a dynamic, mucus-mimetic platform integrating rapid photo-gelation, controllable mechanics, selective transport, and antiviral barrier functionality. MUC-LA hydrogels offer opportunities to investigate mucosal transport and host-pathogen interactions, with potential applications in drug delivery, and as biomaterials.

bioengineering↗

A Fibrous Optofluidic Probe for Endovascular Sensing of Blood Oxygenation and Flow Velocity

Local hemodynamic information including blood oxygenation and flow velocity could guide vascular interventions, yet obtaining these parameters in deep, narrow vessels remains challenging. Here, we report a flexible, submillimeter-scale fibrous optofluidic probe for endovascular sensing of blood oxygenation and flow velocity. The probe integrates a polymer optical fiber for light transmission with a microfluidic tube for dye injection, enabling spectroscopic oximetry and fluorescence dilution-based velocimetry through a single device. Via vascular intervention, we demonstrate local hemodynamic sensing in rabbit arteries and angiography-guided deployment in canine carotid arteries. The probe captures local changes in blood oxygenation and flow velocity during vascular occlusion and reperfusion, revealing hemodynamic disturbances that are not reflected in peripheral monitors. These results illustrate the complementary information provided by local oximetry and velocimetry and establish a compact optofluidic platform for quantitative hemodynamic monitoring during vascular interventions.

bioengineering↗

Broad-spectrum in situ genetic reprogramming of native microbiomes

Complex microbial communities are found throughout terrestrial, aquatic, and animal-associated ecosystems. Genetic modification of discrete microbial taxa within native communities represents a powerful tool to study and augment microbiome functions. Herein, we develop Synthetic Phage Assisted Reprogrammable and Targetable Addition (SPARTA) as a one-step strategy for packaging, delivering, and integrating large synthetic DNA into a broad range of native microbiomes. SPARTA leverages a broad-spectrum synthetic phage particle for in situ genome engineering within complex soil, freshwater, and mammalian fecal microbiomes, reprogramming 59 native species across 16 families. By modulating SPARTA components, we further demonstrated tunability of SPARTA towards targeted microbiome population. Additionally, we built a novel companion tool to quantitatively identify engineered taxa, named 16S crRNA-guided inference of bacterial engineering sequencing or ScRibe-seq. The SPARTA-ScRibe-seq pipeline delivered and validated functional synthetic gene clusters in diverse native microbiomes while preserving the original microbial community structure. Together, this novel genome engineering framework constitutes an end-to-end programmable platform for rational and customizable reprogramming of native microbiomes.

bioengineering↗