Article ID Journal Published Year Pages File Type
1259644 Current Opinion in Chemical Biology 2012 7 Pages PDF
Abstract

The structurally and mechanistically simple type III polyketide synthases (PKSs) catalyze iterative condensations of CoA thioesters to produce a variety of polyketide scaffolds with remarkably diverse structures and biological activities. By exploiting the enzymes, we combined precursor-directed biosynthesis with nitrogen-containing substrates and structure-based enzyme engineering and generated unnatural, novel polyketide–alkaloid scaffolds with promising biological activities. The nucleophilic nitrogen atom and the engineered enzymes thus facilitated the formation of additional CC and CN bonds during the enzymatic transformations. The methodology will contribute to the further production of chemically and structurally divergent, unnatural natural products, as well as the rational design of novel biocatalysts with unprecedented catalytic functions.

Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (177 K)Download as PowerPoint slideHighlights► By exploiting type III polyketide synthases, we generated unnatural novel polyketide–alkaloids. ► We used a combination of the precursor-directed biosynthesis and structure-based mutagenesis. ► The basic nitrogen atom facilitated the formation of additional CC and CN bonds during the enzyme reactions. ► The methodology will contribute to the further production of unnatural natural products. ► The methodology will contribute to the further production of novel biocatalysts.

Related Topics
Physical Sciences and Engineering Chemistry Chemistry (General)
Authors
,