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Zehetner, L.

Publications and source records attributed to Zehetner, L..

5 recordsLinked to original sources

Beyond benchmark accuracy: machine-learning turnover-number predictors require system-level validation

Enzyme turnover numbers (kcat) are essential for kinetic models and enzyme-constrained genome-scale metabolic models (ecGEMs), but measured values are sparse and therefore increasingly estimated using machine learning (ML). Although these predictors are commonly evaluated by global regression metrics, their practical utility depends on how errors propagate through downstream models. We benchmarked six current kcat predictors on a curated BRENDA-derived dataset and five of them on EnzyExtract. To assess the influence of training-set proximity, we compared each benchmark dataset with the available training data for each predictor. We then used the predicted kcat values to parameterize ecGEMs of Saccharomyces cerevisiae and evaluated growth predictions across 19 conditions. We find that benchmark accuracy is moderate even on the BRENDA-derived dataset and drops sharply on EnzyExtract, where all predictors achieve R2 values of 0.20 or lower. This decline is accompanied by substantially lower overlap between the benchmark and training datasets, with exact sequence matches ranging from 24% to 78% for BRENDA, compared with 9% to 26% for EnzyExtract. However, that overlap alone does not explain differences in generalization across predictors. Moreover, downstream performance is also not explained by benchmark ranking. Across 19 conditions, none of the tool-specific ecGEMs consistently reproduces the experimentally observed variation in growth. In glucose minimal medium, the weakest benchmark performer yields the most accurate growth prediction in the downstream ecGEMs, whereas higher-ranked predictors produce larger deviations in growth. We trace this mismatch to localized errors at high-leverage positions in yeast's metabolic network, where underpredicted mitochondrial ADP/ATP carrier turnover numbers restrict adenine nucleotide exchange and impose an apparent limitation on cytosolic ATP supply. Relaxing this constraint shifts predicted growth toward the experimental reference. Thus, ML-derived kcat values can affect not only quantitative growth predictions but also the phenotype a mechanistic model appears to identify. These results argue for application-driven validation of biological parameter predictors in the downstream systems they are intended to support.

bioinformatics↗

Dark matter of an orchid: metagenome of the microbiome associated with the rhizosphere of Dactylorhiza traunsteineri

Plant microbiota forms complex co-associations with its host, promoting health in natural environments. Root-associated bacteria (RAB) colonize root compartments and can modulate plant functions by producing bioactive compounds as part of their secondary metabolism. We present an in-depth analysis of the rhizosphere-associated microbiome of the endangered marsh orchid Dactylorhiza traunsteineri. Using deep sequencing of 16S rRNA genes, we identified Proteobacteria, Actinobacteria, Myxococcota, Bacteroidota, and Acidobacteria as predominant phyla associated with the rhizosphere of D. traunsteineri. Using deep shotgun metagenomics and de novo assembly, we extracted high-quality metagenome-assembled genomes (MAGs), revealing significant metabolic and biosynthetic potentials of the D. traunsteineris RABs. Our study offers a comprehensive investigation into the microbial community of the D. traunsteineri rhizosphere, highlighting a potential novel source of critical bioactive substances. Our study offers novel insights and a robust platform for future investigations into D. traunsteineris rhizosphere, crucial for understanding plant-microbe interactions and aiding conservation efforts for endangered orchids.

microbiology↗

A community-consensus reconstruction of Chinese Hamster metabolism enables structural systems biology analyses to decipher metabolic rewiring in lactate-free CHO cells

Genome-scale metabolic models (GEMs) are indispensable for studying and engineering cellular metabolism. Here, we present iCHO3K, a community-consensus, manually-curated reconstruction of the Chinese Hamster metabolic network. In addition to accounting for 11004 reactions associated with 3597 genes, iCHO3K includes 3489 protein structures and structural descriptors for >70% of its 7377 metabolites, enabling deeper exploration of the link between molecular structure and cellular metabolism. We used iCHO3K to contextualize transcriptomics and metabolomics data from a CHO cell line in which lactate secretion is abolished. We found the reduced glycolytic flux and enhanced TCA cycle flux were accompanied by an elevated NADH and PEP levels in these cells, consistent with experimental measurements. Leveraging iCHO3Ks structural annotations, we identified candidate binding interactions of NADH and PEP with glycolytic enzymes showing model-predicted differential flux, suggesting novel allosteric regulation associated with the observed decrease in glucose uptake and glycolysis. Overall, iCHO3K offers a valuable framework for systematic integration of omics data, improved flux predictions, and structure-guided insights, thus advancing CHO cell engineering and enhancing biomanufacturing efficiency.

systems biology↗

Improving HEK293-based AAV-production using GSMMs, and a multi-omics approach

HEK293 cells are a versatile cell line extensively used in the production of recombinant proteins and viral vectors, notably Adeno-associated virus (AAV) [12]. Despite their high transfection efficiency and adaptability to various culture conditions, challenges remain in achieving sufficient yields of active viral particles. This study presents a comprehensive multi-omics analysis of two HEK293 strains under good manufacturing practice conditions, focusing on the metabolic and cellular responses during AAV production. The investigation included lipidomic, exometabolomic, and transcriptomic profiling across different conditions and time points. Genome-scale metabolic models (GSMMs) were reconstructed for these strains to elucidate metabolic shifts and identify potential bottlenecks in AAV production. Notably, the study revealed significant differences between a High-producing (HP) and a Low-producing (LP) HEK293 strains, highlighting pseudohypoxia in the LP strain. Key findings include the identification of hypoxia-inducible factor 1-alpha (HIF1alpha) as a critical regulator in the LP strain, linking pseudohypoxia to poor AAV productivity. Inhibition of HIF1alpha resulted in immediate cessation of cell growth and a 2-fold increase in viral capsid production, albeit with a decreased number of viral genomes, impacting the full-to-empty particle ratio. This suggests that while HIF1alpha inhibition enhances capsid assembly, it simultaneously hampers nucleotide synthesis via the pentose phosphate pathway (PPP), necessary for genome packaging.

bioengineering↗

Differential logistic PCA for large-scale comparison of GSMMs and pathway analysis

Genome-scale metabolic models (GSMMs) offer a holistic view of biochemical reaction networks, enabling in-depth analyses of metabolism across species and tissues in multiple conditions. However, comparing GSMMs against each other poses challenges as current dimensionality reduction algorithms or clustering methods lack mechanistic interpretability, and often rely on subjective assumptions. Here, we propose a new approach utilizing logisitic principal component analysis (LPCA) that efficiently clusters GSMMs while singling out mechanistic differences in terms of reactions and pathways that drive the categorization. We applied LPCA to multiple diverse datasets, including GSMMs of 222 Escherichia-strains, 343 budding yeasts (Saccharomycotina), 80 human tissues, and 2943 Firmicutes strains. Our findings demonstrate LPCAs effectiveness in preserving microbial phylogenetic relationships and discerning human tissue-specific metabolic profiles, exhibiting comparable performance to traditional methods like t-distributed stochastic neighborhood embedding (t-SNE) and Jaccard coefficients. Moreover, the subsystems and associated reactions identified by LPCA align with existing knowledge, underscoring its reliability in dissecting GSMMs and uncovering the underlying drivers of separation. Authors summaryGenome-scale metabolic models (GSMMs) are comprehensive representations of all the biochemical reactions that occur within an organism, enabling insights into cellular processes. Our study introduces logisitic principal component analysis (LPCA) to explore and compare these biochemical networks across different species and tissues only based on the presence or absence of reactions, summarized in a binary matrix. LPCA analyzes these binary matrices of specific biochemical reactions, identifying significant differences and similarities. We applied LPCA to a range of datasets, including bacterial strains, fungi, and human tissues. Our findings demonstrate LPCAs effectiveness in distinguishing microbial phylogenetic relationships and discerning tissue-specific profiles in humans. LPCA also offers precise information on the biochemical drivers of these differences, contributing to a deeper understanding of metabolic subsystems. This research showcases LPCA as a valuable method for examining the complex interplay of reactions within GSMMs, offering insights that could support further scientific investigation into metabolic processes.

systems biology↗