Nonlinear Biosynthetic Assembly of Alpiniamide by a Hybrid cis/trans-AT PKS-NRPS

被引:13
|
作者
Sigrist, Renata [1 ]
Luhavaya, Hanna [2 ]
McKinnie, Shaun M. K. [2 ]
da Silva, Amanda Ferreira [1 ]
Jurberg, Igor D. [1 ]
Moore, Bradley S. [2 ,3 ]
de Oliveira, Luciana Gonzaga [1 ]
机构
[1] Univ Campinas UNICAMP, Inst Chem, Dept Organ Chem, BR-13083970 Campinas, SP, Brazil
[2] Univ Calif San Diego, Scripps Inst Oceanog, Ctr Marine Biotechnol & Biomed, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
基金
巴西圣保罗研究基金会; 加拿大自然科学与工程研究理事会;
关键词
NATURAL-PRODUCT DISCOVERY; I POLYKETIDE SYNTHASE; GENE-CLUSTER; HETEROLOGOUS EXPRESSION; DIRECT CLONING; ACID; ACYLTRANSFERASE; BACTERIAL; THIOLACTOMYCIN; ORGANIZATION;
D O I
10.1021/acschembio.0c00081
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alpiniamide A is a linear polyketide produced by Stieptomyces endophytic bacteria. Despite its relatively simple chemical structure suggestive of a linear assembly line biosynthetic construction involving a hybrid polyketide synthase-nonribosomal peptide synthetase enzymatic protein machine, we report an unexpected nonlinear synthesis of this bacterial natural product. Using a combination of genomics, heterologous expression, mutagenesis, isotope-labeling, and chain terminator experiments, we propose that alpiniamide A is assembled in two halves and then ligated into the mature molecule. We show that each polyketide half is constructed using orthogonal biosynthetic strategies, employing either cis- or trans-acyl transferase mechanisms, thus prompting an alternative proposal for the operation of this PKS-NRPS.
引用
收藏
页码:1067 / 1077
页数:11
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