Heterologous Expression of Epoxomicin in Escherichia coli

Epoxomicin is an epoxyketone proteasome inhibitor with synthetic derivatives approved or under investigation for treatment of multiple myeloma. To leverage the advantages of Escherichia coli as a rapidly growing and readily engineered host for the production of epoxomicin and analogues, we expressed codon-optimized versions of the epoxomicin biosynthetic genes, epxD, epxE, and epxF. Epoxomicin was detected, but the major product was a ketone resulting from α,β-keto acid precursor decarboxylation. Epoxomicin yield was improved by altering the copy numbers of each gene and creating a fusion of epxE and epxF. Our optimized system offers promise for efficient engineering and biosynthesis of improved epoxomicin analogues.

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Publication Details

Journal
Figshare
Published
2025-01-01
DOI
https://doi.org/10.25455/wgtn.29947673
Citations
1
Primary Topic
Geochemistry and Geologic Mapping
Type
article
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article

Heterologous Expression of Epoxomicin in Escherichia coli

1 citations
Figshare
Geochemistry and Geologic Mapping
article

Heterologous Expression of Epoxomicin in Escherichia coli

article en
1 citations

Abstract

Epoxomicin is an epoxyketone proteasome inhibitor with synthetic derivatives approved or under investigation for treatment of multiple myeloma. To leverage the advantages of Escherichia coli as a rapidly growing and readily engineered host for the production of epoxomicin and analogues, we expressed codon-optimized versions of the epoxomicin biosynthetic genes, epxD, epxE, and epxF. Epoxomicin was detected, but the major product was a ketone resulting from α,β-keto acid precursor decarboxylation. Epoxomicin yield was improved by altering the copy numbers of each gene and creating a fusion of epxE and epxF. Our optimized system offers promise for efficient engineering and biosynthesis of improved epoxomicin analogues.

Figshare
Victoria University of Wellington (NZ)
Openalex Percentile: Top 69%
Geochemistry and Geologic Mapping
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