Xenorhabdin I
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| Category | Antibiotics |
| Catalog number | BBF-00967 |
| CAS | 92680-94-9 |
| Molecular Weight | 270.37 |
| Molecular Formula | C11H14N2O2S2 |
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Description
Xenorhabdin is a dithiopyrrolidone antibiotic isolated from Xenorhabdus bovienii. It has antimicrobial and insecticidal activity.
Specification
| IUPAC Name | N-(5-oxo-4H-dithiolo[4,3-b]pyrrol-6-yl)hexanamide |
| Canonical SMILES | CCCCCC(=O)NC1=C2C(=CSS2)NC1=O |
| InChI | InChI=1S/C11H14N2O2S2/c1-2-3-4-5-8(14)13-9-10-7(6-16-17-10)12-11(9)15/h6H,2-5H2,1H3,(H,12,15)(H,13,14) |
| InChI Key | YBDAGRFUBLIKGW-UHFFFAOYSA-N |
Properties
| Antibiotic Activity Spectrum | bacteria; parasites |
| Boiling Point | 521.2±50.0 °C at 760 mmHg |
| Melting Point | 192-193°C |
| Density | 1.4±0.1 g/cm3 |
Reference Reading
1. Structure and biosynthesis of xenoamicins from entomopathogenic Xenorhabdus
Qiuqin Zhou, Florian Grundmann, Marcel Kaiser, Matthias Schiell, Sophie Gaudriault, Andreas Batzer, Michael Kurz, Helge B Bode Chemistry. 2013 Dec 2;19(49):16772-9. doi: 10.1002/chem.201302481. Epub 2013 Nov 7.
During the search for novel natural products from entomopathogenic Xenorhabdus doucetiae DSM17909 and X. mauleonii DSM17908 novel peptides named xenoamicins were identified in addition to the already known antibiotics xenocoumacin and xenorhabdin. Xenoamicins are acylated tridecadepsipeptides consisting of mainly hydrophobic amino acids. The main derivative xenoamicin A (1) was isolated from X. mauleonii DSM17908, and its structure elucidated by detailed 1D and 2D NMR experiments. Detailed MS experiments, also in combination with labeling experiments, confirmed the determined structure and allowed structure elucidation of additional derivatives. Moreover, the xenoamicin biosynthesis gene cluster was identified and analyzed in X. doucetiae DSM17909, and its participation in xenoamicin biosynthesis was confirmed by mutagenesis. Advanced Marfey's analysis of 1 showed that the absolute configuration of the amino acids is in agreement with the predicted stereochemistry deduced from the nonribosomal peptide synthetase XabABCD. Biological testing revealed activity of 1 against Plasmodium falciparum and other neglected tropical diseases but no antibacterial activity.
2. iPRESTO: Automated discovery of biosynthetic sub-clusters linked to specific natural product substructures
Joris J R Louwen, Satria A Kautsar, Sven van der Burg, Marnix H Medema, Justin J J van der Hooft PLoS Comput Biol. 2023 Feb 9;19(2):e1010462. doi: 10.1371/journal.pcbi.1010462. eCollection 2023 Feb.
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.
3. Biosynthesis and function of simple amides in Xenorhabdus doucetiae
Edna Bode, Yue He, Tien Duy Vo, Roland Schultz, Marcel Kaiser, Helge B Bode Environ Microbiol. 2017 Nov;19(11):4564-4575. doi: 10.1111/1462-2920.13919. Epub 2017 Oct 13.
Xenorhabdus doucetiae, the bacterial symbiont of the entomopathogenic nematode Steinernema diaprepesi produces several different fatty acid amides. Their biosynthesis has been studied using a combination of analysis of gene deletions and promoter exchanges in X. doucetiae and heterologous expression of candidate genes in E. coli. While a decarboxylase is required for the formation of all observed phenylethylamides and tryptamides, the acyltransferase XrdE encoded in the xenorhabdin biosynthesis gene cluster is responsible for the formation of short chain acyl amides. Additionally, new, long-chain and cytotoxic acyl amides were identified in X. doucetiae infected insects and when X. doucetiae was grown in Galleria Instant Broth (GIB). When the bioactivity of selected amides was tested, a quorum sensing modulating activity was observed for the short chain acyl amides against the two different quorum sensing systems from Chromobacterium and Janthinobacterium.
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Bio Calculators
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