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van der Hooft, J.

Publications and source records attributed to van der Hooft, J..

4 recordsLinked to original sources

The Molecules Gateway: a homogeneous, searchable database of 150k annotated molecules from Actinomycetes

Natural products are a sustainable resource for drug discovery, but their identification in complex mixtures remains a daunting task. We present an automated pipeline that compares, harmonizes and ranks the annotations of LC-HRMS data by different tools. When applied to 7,400 extracts derived from 6,566 strains belonging to 86 actinomycete genera, it yielded 150,000 molecules after processing over 50 million MS features. The web-based Molecules Gateway provides a highly interactive access to experimental and calculated data for these molecules, along with the metadata related to extracts and producer strains. We show how the Molecules Gateway can be used to rapidly identify known hard to find microbial products, unreported analogs of known families and not yet described metabolites. The Molecules Gateway, which complements available repositories of annotated MS data, is experimentally and computationally homogeneous, and thus amenable to global analyses, which show a large and untapped chemical diversity afforded by actinomycetes.

microbiology↗

iPRESTO: automated discovery of biosynthetic sub-clusters linked to specific natural product substructures

Microbial specialised metabolism is full of valuable natural products that are applied clinically, agriculturally, and industrially. The genes that encode their biosynthesis are often physically clustered on the genome in biosynthetic gene clusters (BGCs). Many BGCs consist of multiple groups of co-evolving genes called sub-clusters that are responsible for the biosynthesis of a specific chemical moiety in a natural product. Sub-clusters therefore provide an important link between the structures of a natural product and its BGC, which can be leveraged for predicting natural product structures from sequence, as well as for linking chemical structures and metabolomics-derived mass features to BGCs. While some initial computational methodologies have been devised for sub-cluster detection, current approaches are not scalable, have only been run on small and outdated datasets, or produce an impractically large number of possible sub-clusters to mine through. Here, we constructed a scalable method for unsupervised sub-cluster detection, called iPRESTO, based on topic modelling and statistical analysis of co-occurrence patterns of enzyme-coding protein families. iPRESTO was used to mine sub-clusters across 150,000 prokaryotic BGCs from antiSMASH-DB. After annotating a fraction of the resulting sub-cluster families, we could predict a substructure for 16% of the antiSMASH-DB BGCs. Additionally, our method was able to confirm 83% of the experimentally characterised sub-clusters in MIBiG reference BGCs. Based on iPRESTO-detected sub-clusters, we could correctly identify the BGCs for xenorhabdin and salbostatin biosynthesis (which had not yet been annotated in BGC databases), as well as propose a candidate BGC for akashin biosynthesis. Additionally, we show for a collection of 145 actinobacteria how substructures can aid in linking BGCs to molecules by correlating iPRESTO-detected sub-clusters to MS/MS-derived Mass2Motifs substructure patterns. This work paves the way for deeper functional and structural annotation of microbial BGCs by improved linking of orphan molecules to their cognate gene clusters, thus facilitating accelerated natural product discovery. Author summaryIn this work, we introduce iPRESTO, a tool for scalable unsupervised sub-cluster detection in biosynthetic gene clusters. This detection is important because these biosynthetic hotspots encode many products useful for humanity, such as antibiotics, antitumor agents, or herbicides. Recent technological developments have made identification of biosynthetic loci in genomes straightforward. Yet, methods to connect these inferred biosynthetic genes to the final chemical structures of their cognate metabolites are largely lacking. Being able to reliably predict parts of the final product would constitute a real step forward in natural product genome mining. Therefore, we focussed on constructing a tool to systematically detect and annotate small regions called sub-clusters, which code for the biosynthesis of substructures in the final product, across all genomically inferred biosynthetic diversity. iPRESTO makes it possible to query unknown biosynthetic regions and infer which substructures are present in their metabolic products. This will facilitate more effective prioritization of chemical novelty, as well as linking activities from bioassays and microbiome-associated phenotypes to the metabolites responsible for them.

bioinformatics↗

Implementations of the chemical structural and compositional similarity metric in R and Python

MotivationTandem mass spectrometry (MS/MS) has the potential to substantially improve metabolomics by acquiring spectra of fragmented ions. These fragmentation spectra can be represented as a molecular network, by measuring cosine distances between them, thus identifying signals from the same or similar molecules. Metrics that enable comparison between pairs of samples based on their metabolite profiles are in great need. Taking inspiration from the successful phylogeny-aware beta-diversity measures used in microbiome research, integrating chemical similarity information about the features in addition to their abundances could lead to better insights when comparing metabolite profiles. Chemical Structural and Compositional Similarity (CSCS) is a recently published similarity metric comparing the full set of signals and their chemical similarity between two samples. Efficient, scalable and easily accessible implementations of this algorithm is currently lacking. Here, we present an easily accessible and scalable implementation of CSCS in both python and R, including a version not weighted by intensity information. ResultsWe provide a new implementation of the CSCS algorithm that is over 300 times faster than the published implementation in R, making the algorithm suitable for large-scale metabolomics applications. We also show that adding chemical information enriches existing methods. Furthermore, the R implementation includes functions for exporting molecular networks directly from the mass spectral molecular networking platform GNPS for ease of use for downstream applications. Contactbrejnrod@sund.ku.dk Availabilitygithub.com/askerdb/rCSCS, github.com/askerdb/pyCSCS

bioinformatics↗

Did a plant-herbivore arms race drive chemical diversity in Euphorbia?

The genus Euphorbia is among the most diverse and species-rich plant genera on Earth, exhibiting a near-cosmopolitan distribution and extraordinary chemical diversity, especially across highly toxic macro-and polycyclic diterpenoids. However, very little is known about drivers and evolutionary origins of chemical diversity within Euphorbia. Here, we investigate 43 Euphorbia species to understand how geographic separation over evolutionary time has impacted chemical differentiation. We show that the structurally highly diverse Euphorbia diterpenoids are significantly reduced in species native to the Americas, compared to the Eurasian and African continents, where the genus originated. The localization of these compounds to young stems and roots suggest ecological relevance in herbivory defense and immunomodulatory defense mechanisms match diterpenoid levels, indicating chemoevolutionary adaptation to reduced herbivory pressure.\n\nOne Sentence SummaryGlobal chemo-evolutionary adaptation of Euphorbia affected immunomodulatory defense mechanisms.

evolutionary biology↗