Heterologous Expression of Epoxomicin in Escherichia coli

被引:1
|
作者
Messenger, Sarah R. [1 ,2 ]
Ackerley, David F. [1 ,2 ]
Calcott, Mark J. [1 ,2 ]
机构
[1] Victoria Univ Wellington, Sch Biol Sci, Wellington 6012, New Zealand
[2] Victoria Univ Wellington, Maurice Wilkins Ctr Mol Biodiscovery, Wellington 6012, New Zealand
来源
ACS SYNTHETIC BIOLOGY | 2024年 / 13卷 / 09期
关键词
epoxomicin; heterologous expression; naturalproducts; nonribosomal peptides; NRPS engineering; biosynthesis; PROTEASOME INHIBITOR; CODON USAGE; EPOXYKETONE; BIOSYNTHESIS; DESIGN; AGENT;
D O I
10.1021/acssynbio.4c00430
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 alpha,beta-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.
引用
收藏
页码:2702 / 2709
页数:8
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