Ayesha Ahmed Chaudhri’s research while affiliated with Goethe University Frankfurt and other places

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Publications (3)


The role and mechanisms of canonical and non-canonical tailoring enzymes in bacterial terpenoid biosynthesis
  • Literature Review
  • Full-text available

February 2025

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36 Reads

Natural Product Reports

Yuya Kakumu

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Ayesha Ahmed Chaudhri

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Eric J N Helfrich

This review explores recent insights into the roles and enzymatic mechanisms of canonical and non-canonical tailoring enzymes in shaping and modifying terpene hydrocarbon scaffolds during bacterial terpene biosynthesis.

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MIBiG 4.0: advancing biosynthetic gene cluster curation through global collaboration

December 2024

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842 Reads

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16 Citations

Nucleic Acids Research

Mitja M. Zdouc

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Kai Blin

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Nico L. L. Louwen

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[...]

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Specialized or secondary metabolites are small molecules of biological origin, often showing potent biological activities with applications in agriculture, engineering and medicine. Usually, the biosynthesis of these natural products is governed by sets of co-regulated and physically clustered genes known as biosynthetic gene clusters (BGCs). To share information about BGCs in a standardized and machine-readable way, the Minimum Information about a Biosynthetic Gene cluster (MIBiG) data standard and repository was initiated in 2015. Since its conception, MIBiG has been regularly updated to expand data coverage and remain up to date with innovations in natural product research. Here, we describe MIBiG version 4.0, an extensive update to the data repository and the underlying data standard. In a massive community annotation effort, 267 contributors performed 8304 edits, creating 557 new entries and modifying 590 existing entries, resulting in a new total of 3059 curated entries in MIBiG. Particular attention was paid to ensuring high data quality, with automated data validation using a newly developed custom submission portal prototype, paired with a novel peer-reviewing model. MIBiG 4.0 also takes steps towards a rolling release model and a broader involvement of the scientific community. MIBiG 4.0 is accessible online at https://mibig.secondarymetabolites.org/.


Functional Redundancy and Dual Function of a Hypothetical Protein in the Biosynthesis of Eunicellane-Type Diterpenoids

November 2024

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19 Reads

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4 Citations

ACS Chemical Biology

Many complex terpenoids, predominantly isolated from plants and fungi, show drug-like physicochemical properties. Recent advances in genome mining revealed actinobacteria as an almost untouched treasure trove of terpene biosynthetic gene clusters (BGCs). In this study, we characterized a terpene BGC with an unusual architecture. The selected BGC includes, among others, genes encoding a terpene cyclase fused to a truncated reductase domain and a cytochrome P450 monooxygenase (P450) that is split over three gene fragments. Functional characterization of the BGC in a heterologous host led to the identification of several new members of the trans-eunicellane family of diterpenoids, the euthailols, that feature unique oxidation patterns. A combination of bioinformatic analyses, structural modeling studies, and heterologous expression revealed a dual function of the pathway-encoded hypothetical protein that acts as an isomerase and an oxygenase. Moreover, in the absence of other tailoring enzymes, a P450 hydroxylates the eunicellane scaffold at a position that is not modified in other eunicellanes. Surprisingly, both the modifications installed by the hypothetical protein and one of the P450s exhibit partial redundancy. Bioactivity assays revealed that some of the euthailols show growth inhibitory properties against Gram-negative ESKAPE pathogens. The characterization of the euthailol BGC in this study provides unprecedented insights into the partial functional redundancy of tailoring enzymes in complex diterpenoid biosynthesis and highlights hypothetical proteins as an important and largely overlooked family of tailoring enzymes involved in the maturation of complex terpenoids.

Citations (1)


... BlastP analysis from MIBiG reveals that Dip20 has close homology to QbsL (43% identity, 63% similarity) in the siderophore quinolobactin pathway. 30 QbsL is a hybrid protein with an AMP-dependent ligase and synthetase domain (N-terminal) and a methylase domain (C-terminal), facilitating the carboxylic acid activation and O-methylation of a hydroxyl group, respectively, on a precursor xanthurenic acid. 31 We propose that the dipyrimicin pathway adopts the minor route in caerulomycin biosynthesis as its primary pathway where Dip9 hydroxylates C3', followed by C4'-OH methylation by Dip20. ...

Reference:

AI-assisted isolation of bioactive Dipyrimicins from Amycolatopsis azurea and identification of its corresponding dip biosynthetic gene cluster
MIBiG 4.0: advancing biosynthetic gene cluster curation through global collaboration

Nucleic Acids Research