Biology subjects

Oyedele, A. S.

Publications and source records attributed to Oyedele, A. S..

3 recordsLinked to original sources

bioRxiv2026

Identification of Siderophores with Unexpected Antibacterial Properties from Actinoplanes teichomyceticus

Actinoplanes teichomyceticus is a well-established producer of bioactive secondary metabolites, including the glycopeptide antibiotic teicoplanin. Although its antibiotic biosynthetic capacity has been extensively investigated, its siderophore diversity and any additional biological functions of these iron-chelating metabolites remain comparatively underexplored. We identified a reproducibly bioactive, teicoplanin-independent fraction that inhibited Bacillus spizizenii. Molecular networking applied to this fraction identified hydroxamate ferrioxamine and desferrioxamine-type siderophores as the dominant metabolites, including acylated analogs detected as Al3+- and Fe3+-chelated species. Robust siderophore secretion was confirmed by the CAS assay. Notably, siderophore-enriched fractions exhibited selective antibacterial activity against Gram-positive bacteria, with minimum inhibitory concentrations of approximately 16 {micro}g/mL against B. spizizenii and partial inhibition of Staphylococcus aureus, while no activity was observed against Escherichia coli. Synthetic C7 and C9 acyl-desferrioxamine analogs showed enhanced antibacterial activity upon Al3 chelation, indicating a metal-dependent bioactivity. These findings reveal an unexpected antibacterial role for ferrioxamine-type siderophores produced by A. teichomyceticus, extending their function beyond iron acquisition, possibly through a "Trojan horse" (or "Trojan metal") mechanism.

biochemistry↗

bioRxiv2024

Assessing the ability of ChatGPT to extract natural product bioactivity and biosynthesis data from publications

Natural products are an excellent source of therapeutics and are often discovered through the process of genome mining, where genomes are analyzed by bioinformatic tools to determine if they have the biosynthetic capacity to produce novel or active compounds. Recently, several tools have been reported for predicting natural product bioactivities from the sequence of the biosynthetic gene clusters that produce them. These tools have the potential to accelerate the rate of natural product drug discovery by enabling the prioritization of novel biosynthetic gene clusters that are more likely to produce compounds with therapeutically relevant bioactivities. However, these tools are severely limited by a lack of training data, specifically data pairing biosynthetic gene clusters with activity labels for their products. There are many reports of natural product biosynthetic gene clusters and bioactivities in the literature that are not included in existing databases. Manual curation of these data is time consuming and inefficient. Recent developments in large language models and the chatbot interfaces built on top of them have enabled automatic data extraction from text, including scientific publications. We investigated how accurate ChatGPT is at extracting the necessary data for training models that predict natural product activity from biosynthetic gene clusters. We found that ChatGPT did well at determining if a paper described discovery of a natural product and extracting information about the products bioactivity. ChatGPT did not perform as well at extracting accession numbers for the biosynthetic gene cluster or producers genome although using an altered prompt improved accuracy.

bioinformatics↗

bioRxiv2024

Statistical Coupling Analysis Predicts Correlated Motions in Dihydrofolate Reductase

The role of dynamics in enzymatic function is a highly debated topic. Dihydrofolate reductase (DHFR), due to its universality and the depth with which it has been studied, is a model system in this debate. Myriad previous works have identified networks of residues in positions near to and remote from the active site that are involved in dynamics and others that are important for catalysis. For example, specific mutations on the Met20 loop in E. coli DHFR (N23PP/S148A) are known to disrupt millisecond-timescale motions and reduce catalytic activity. However, how and if networks of dynamically coupled residues influence the evolution of DHFR is still an unanswered question. In this study, we first identify, by statistical coupling analysis and molecular dynamic simulations, a network of coevolving residues, which possess increased correlated motions. We then go on to show that allosteric communication in this network is selectively knocked down in N23PP/S148A mutant E. coli DHFR. Finally, we identify two sites in the human DHFR sector which may accommodate the Met20 loop double proline mutation while preserving dynamics. These findings strongly implicate protein dynamics as a driving force for evolution.

biochemistry↗