Microbial synthesis of a branched-chain ester platform from organic waste carboxylates

Processing of lignocellulosic biomass or organic wastes produces a plethora of chemicals such as short, linear carboxylic acids, known as carboxylates, derived from anaerobic digestion. While these carboxylates have low values and are inhibitory to microbes during fermentation, they can be biologica...

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Published inMetabolic engineering communications Vol. 3; no. C; pp. 245 - 251
Main Authors Layton, Donovan S., Trinh, Cong T.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.12.2016
Elsevier
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Online AccessGet full text
ISSN2214-0301
2214-0301
DOI10.1016/j.meteno.2016.08.001

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Summary:Processing of lignocellulosic biomass or organic wastes produces a plethora of chemicals such as short, linear carboxylic acids, known as carboxylates, derived from anaerobic digestion. While these carboxylates have low values and are inhibitory to microbes during fermentation, they can be biologically upgraded to high-value products. In this study, we expanded our general framework for biological upgrading of carboxylates to branched-chain esters by using three highly active alcohol acyltransferases (AATs) for alcohol and acyl CoA condensation and modulating the alcohol moiety from ethanol to isobutanol in the modular chassis cell. With this framework, we demonstrated the production of an ester library comprised of 16 out of all 18 potential esters, including acetate, propionate, butanoate, pentanoate, and hexanoate esters, from the 5 linear, saturated C2-C6 carboxylic acids. Among these esters, 5 new branched-chain esters, including isobutyl acetate, isobutyl propionate, isobutyl butyrate, isobutyl pentanoate, and isobutyl hexanoate were synthesized in vivo. During 24h in situ fermentation and extraction, one of the engineered strains, EcDL208 harnessing the SAAT of Fragaria ananassa produced ~63mg/L of a mixture of butyl and isobutyl butyrates from glucose and butyrate co-fermentation and ~127mg/L of a mixture of isobutyl and pentyl pentanoates from glucose and pentanoate co-fermentation, with high specificity. These butyrate and pentanoate esters are potential drop-in liquid fuels. This study provides better understanding of functional roles of AATs for microbial biosynthesis of branched-chain esters and expands the potential use of these esters as drop-in biofuels beyond their conventional flavor, fragrance, and solvent applications. •Expand the general framework for microbial biosynthesis of branched-chain ester platforms.•Biologically upgrade 5 carboxylates to 16 out of a total of 18 potential esters.•Characterize in vivo three alcohol acyltransferases for branched-chain ester biosynthesis.•Discuss targeted esters as potential fuels beyond flavor, fragrant, and solvent applications.
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USDOE Office of Science (SC), Biological and Environmental Research (BER). Biological Systems Science Division
AC05-00OR22725
ISSN:2214-0301
2214-0301
DOI:10.1016/j.meteno.2016.08.001