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Understanding biocatalyst inhibition by carboxylic acids

Carboxylic acids are an attractive biorenewable chemical in terms of their flexibility and usage as precursors for a variety of industrial chemicals. It has been demonstrated that such carboxylic acids can be fermentatively produced using engineered microbes, such as Escherichia coli and Saccharomyc...

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Autores principales: Jarboe, Laura R., Royce, Liam A., Liu, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3760142/
https://www.ncbi.nlm.nih.gov/pubmed/24027566
http://dx.doi.org/10.3389/fmicb.2013.00272
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author Jarboe, Laura R.
Royce, Liam A.
Liu, Ping
author_facet Jarboe, Laura R.
Royce, Liam A.
Liu, Ping
author_sort Jarboe, Laura R.
collection PubMed
description Carboxylic acids are an attractive biorenewable chemical in terms of their flexibility and usage as precursors for a variety of industrial chemicals. It has been demonstrated that such carboxylic acids can be fermentatively produced using engineered microbes, such as Escherichia coli and Saccharomyces cerevisiae. However, like many other attractive biorenewable fuels and chemicals, carboxylic acids become inhibitory to these microbes at concentrations below the desired yield and titer. In fact, their potency as microbial inhibitors is highlighted by the fact that many of these carboxylic acids are routinely used as food preservatives. This review highlights the current knowledge regarding the impact that saturated, straight-chain carboxylic acids, such as hexanoic, octanoic, decanoic, and lauric acids can have on E. coli and S. cerevisiae, with the goal of identifying metabolic engineering strategies to increase robustness. Key effects of these carboxylic acids include damage to the cell membrane and a decrease of the microbial internal pH. Certain changes in cell membrane properties, such as composition, fluidity, integrity, and hydrophobicity, and intracellular pH are often associated with increased tolerance. The availability of appropriate exporters, such as Pdr12, can also increase tolerance. The effect on metabolic processes, such as maintaining appropriate respiratory function, regulation of Lrp activity and inhibition of production of key metabolites such as methionine, are also considered. Understanding the mechanisms of biocatalyst inhibition by these desirable products can aid in the engineering of robust strains with improved industrial performance.
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spelling pubmed-37601422013-09-11 Understanding biocatalyst inhibition by carboxylic acids Jarboe, Laura R. Royce, Liam A. Liu, Ping Front Microbiol Microbiology Carboxylic acids are an attractive biorenewable chemical in terms of their flexibility and usage as precursors for a variety of industrial chemicals. It has been demonstrated that such carboxylic acids can be fermentatively produced using engineered microbes, such as Escherichia coli and Saccharomyces cerevisiae. However, like many other attractive biorenewable fuels and chemicals, carboxylic acids become inhibitory to these microbes at concentrations below the desired yield and titer. In fact, their potency as microbial inhibitors is highlighted by the fact that many of these carboxylic acids are routinely used as food preservatives. This review highlights the current knowledge regarding the impact that saturated, straight-chain carboxylic acids, such as hexanoic, octanoic, decanoic, and lauric acids can have on E. coli and S. cerevisiae, with the goal of identifying metabolic engineering strategies to increase robustness. Key effects of these carboxylic acids include damage to the cell membrane and a decrease of the microbial internal pH. Certain changes in cell membrane properties, such as composition, fluidity, integrity, and hydrophobicity, and intracellular pH are often associated with increased tolerance. The availability of appropriate exporters, such as Pdr12, can also increase tolerance. The effect on metabolic processes, such as maintaining appropriate respiratory function, regulation of Lrp activity and inhibition of production of key metabolites such as methionine, are also considered. Understanding the mechanisms of biocatalyst inhibition by these desirable products can aid in the engineering of robust strains with improved industrial performance. Frontiers Media S.A. 2013-09-03 /pmc/articles/PMC3760142/ /pubmed/24027566 http://dx.doi.org/10.3389/fmicb.2013.00272 Text en Copyright © Jarboe, Royce and Liu. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Jarboe, Laura R.
Royce, Liam A.
Liu, Ping
Understanding biocatalyst inhibition by carboxylic acids
title Understanding biocatalyst inhibition by carboxylic acids
title_full Understanding biocatalyst inhibition by carboxylic acids
title_fullStr Understanding biocatalyst inhibition by carboxylic acids
title_full_unstemmed Understanding biocatalyst inhibition by carboxylic acids
title_short Understanding biocatalyst inhibition by carboxylic acids
title_sort understanding biocatalyst inhibition by carboxylic acids
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3760142/
https://www.ncbi.nlm.nih.gov/pubmed/24027566
http://dx.doi.org/10.3389/fmicb.2013.00272
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