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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.
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页码:2702 / 2709
页数:8
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