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Rockx, S.

Publications and source records attributed to Rockx, S..

2 recordsLinked to original sources

SynCom101: A web-based platform for the standardized design of functionally tailored synthetic microbial communities

BackgroundSynthetic microbial communities (SynComs) are essential tools for dissecting the causal mechanisms in host-microbiota interactions. To date, however, SynCom design suffers from a lack of standardization, typically oscillating between arbitrary strain selection and computational pipelines that misalign with experimental design. As microbiome research transitions toward functionally defined community systems with reproducible experimental outcomes, there is a strong need for a user-friendly platform that integrates multi-dimensional genomic and/or biological data into a standardized and tailored SynComs design. ResultsHere, we present SynCom101, a web-based platform that democratizes the design of reproducible, hypothesis-driven SynComs. SynCom101 accommodates diverse input formats including genomic annotations and laboratory-obtained phenotypic traits, allowing users to customize their design criteria with high flexibility. The platform utilizes a parsimony algorithm to ensure computational scalability for large datasets, complemented by an optional correlation-aware mode to account for microbial compatibility and co-occurrence patterns when ecological interactions among strains are available. A core innovation of SynCom101 is its suite of trait-weighting modules, which empowers researchers to strategically guide the selection algorithm toward maximal functional trait coverage, the emulation of natural community architectures, or the enrichment of positively correlated microbial assemblages to enhance community stability. We showcase the functionalities of the platform by in silico design of communities from different datasets, demonstrating its capacity to generate concise, functionally prioritized SynComs aligned with targeted design objectives. ConclusionBy providing a transparent, parameter-documented workflow, SynCom101 ensures that community design is no longer a "black box" but a reproducible scientific record. This platform establishes a necessary standard for in silico community assembly, facilitating the transition from descriptive microbiome studies toward high-throughput, predictive functional screening and cross-study comparability. AvailabilitySynCom101 can be accessed via the web interface (https://syncom101.bioinformatics.nl/). The datasets used for case studies are available on Zenodo (https://doi.org/10.5281/zenodo.18310451). The source code is available at Git (https://git.wur.nl/jiayi.jing/syncom101).

bioinformatics↗

Implementation of a Clostridium luticellarii genome-scale model for upgrading syngas fermentations

Syngas fermentation is a powerful platform for converting waste streams into sustainable carboxylic acid precursors for value-added biochemicals. Steel mills produce significant syngas, yet industrial microbial syngas valorization remains unrealized. The most promising syngas-converting biocat-alysts consist of Clostridia species, such as Clostridium kluyveri, Clostridium autoethanogenum, and Clostridium ljungdahlii. Clostridium luticellarii, a recently discovered species, shares close phylogenetic ties with these organisms. Preliminary metabolic studies suggest its potential for syngas acetogenesis as well as chain elongation. In this study, we create iSJ444, a constraint-based metabolic model of C. luticellarii using iHN637 of a close relative C. ljungdahlii as a starting point. Model predictions support hypothesized methanol and syngas pathways from the metabolic characterization studies; however, the use of propionate could not be accurately predicted. Thermodynamic Flux Analysis (TFA) reveals that C. luticellarii maintains stable energy dissipation across most reactions when exposed to varying pH, with significant increases observed in reactions associated with the Wood-Ljungdahl pathway (WLP), such as the HACD1 reaction, at higher pH (6.5), suggesting an adaptive role in energy management under neutral conditions. Flux sampling simulations exploring metabolic flux distributions show that C. luticellarii might fit into syngas fermenting platforms. In both cases, high hydrogen-to-carbon source ratios result in better production of (iso)butyrate and caproate. We present a minimal genome-scale metabolic model of C. luticellarii as a foundation for further exploration and optimization. Although our predictions of its metabolic behavior await experimental validation, they underscore the potential of C. luticellarii to enhance syngas fermentation platforms. HighlightsO_LIiSJ444 models C. luticellarii metabolism for syngas fermentation and chain elongation. C_LIO_LIThermodynamic flux analysis (TFA) reveals adaptive energy balancing in pathways. C_LIO_LISimulations highlight C. luticellarii as a producer of value-added biochemicals like butyrate, isobutyrate, and caproate C_LIO_LIMetabolic insights from iSJ444 suggest efficient syngas conversion using varied substrates for industrial use. C_LI

systems biology↗