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Expanding ester biosynthesis in Escherichia coli.

Nature chemical biology (2014-03-13)
Gabriel M Rodriguez, Yohei Tashiro, Shota Atsumi
ABSTRACT

To expand the capabilities of whole-cell biocatalysis, we have engineered Escherichia coli to produce various esters. The alcohol O-acyltransferase (ATF) class of enzyme uses acyl-CoA units for ester formation. The release of free CoA upon esterification with an alcohol provides the free energy to facilitate ester formation. The diversity of CoA molecules found in nature in combination with various alcohol biosynthetic pathways allows for the biosynthesis of a multitude of esters. Small to medium volatile esters have extensive applications in the flavor, fragrance, cosmetic, solvent, paint and coating industries. The present work enables the production of these compounds by designing several ester pathways in E. coli. The engineered pathways generated acetate esters of ethyl, propyl, isobutyl, 2-methyl-1-butyl, 3-methyl-1-butyl and 2-phenylethyl alcohols. In particular, we achieved high-level production of isobutyl acetate from glucose (17.2 g l(-1)). This strategy was expanded to realize pathways for tetradecyl acetate and several isobutyrate esters.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
2-Methyl-1-propanol, suitable for HPLC, 99.5%
Supelco
2-Methyl-1-propanol, analytical standard
Sigma-Aldrich
Isobutyl alcohol, natural, ≥99%, FCC, FG
Sigma-Aldrich
Isobutyl alcohol, ≥99%, FCC, FG