Lactate production yield from engineered yeasts is dependent from the host background, the lactate dehydrogenase source and the lactate export

<p>Abstract</p> <p>Background</p> <p>Metabolic pathway manipulation for improving the properties and the productivity of microorganisms is becoming a well established concept. For the production of important metabolites, but also for a better understanding of the fundam...

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Main Authors: Valli Minoska, Zampella Giuseppe, De Gioia Luca, Sauer Michael, Branduardi Paola, Mattanovich Diethard, Porro Danilo
Format: Article
Language:English
Published: BMC 2006-01-01
Series:Microbial Cell Factories
Online Access:http://www.microbialcellfactories.com/content/5/1/4
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spelling doaj-87a8d55e64214c058e408416e5620d652020-11-24T21:53:02ZengBMCMicrobial Cell Factories1475-28592006-01-0151410.1186/1475-2859-5-4Lactate production yield from engineered yeasts is dependent from the host background, the lactate dehydrogenase source and the lactate exportValli MinoskaZampella GiuseppeDe Gioia LucaSauer MichaelBranduardi PaolaMattanovich DiethardPorro Danilo<p>Abstract</p> <p>Background</p> <p>Metabolic pathway manipulation for improving the properties and the productivity of microorganisms is becoming a well established concept. For the production of important metabolites, but also for a better understanding of the fundamentals of cell biology, detailed studies are required. In this work we analysed the lactate production from metabolic engineered <it>Saccharomyces cerevisiae </it>cells expressing a heterologous lactate dehydrogenase (<it>LDH</it>) gene. The <it>LDH </it>gene expression in a budding yeast cell introduces a novel and alternative pathway for the NAD<sup>+ </sup>regeneration, allowing a direct reduction of the intracellular pyruvate to lactate, leading to a simultaneous accumulation of lactate and ethanol.</p> <p>Results</p> <p>Four different <it>S. cerevisiae </it>strains were transformed with six different wild type and one mutagenised <it>LDH </it>genes, in combination or not with the over-expression of a lactate transporter. The resulting yield values (grams of lactate produced per grams of glucose consumed) varied from as low as 0,0008 to as high as 0.52 g g<sup>-1</sup>. In this respect, and to the best of our knowledge, higher redirections of the glycolysis flux have never been obtained before without any disruption and/or limitation of the competing biochemical pathways.</p> <p>Conclusion</p> <p>In the present work it is shown that the redirection of the pathway towards the lactate production can be strongly modulated by the genetic background of the host cell, by the source of the heterologous Ldh enzyme, by improving its biochemical properties as well as by modulating the export of lactate in the culture media.</p> http://www.microbialcellfactories.com/content/5/1/4
collection DOAJ
language English
format Article
sources DOAJ
author Valli Minoska
Zampella Giuseppe
De Gioia Luca
Sauer Michael
Branduardi Paola
Mattanovich Diethard
Porro Danilo
spellingShingle Valli Minoska
Zampella Giuseppe
De Gioia Luca
Sauer Michael
Branduardi Paola
Mattanovich Diethard
Porro Danilo
Lactate production yield from engineered yeasts is dependent from the host background, the lactate dehydrogenase source and the lactate export
Microbial Cell Factories
author_facet Valli Minoska
Zampella Giuseppe
De Gioia Luca
Sauer Michael
Branduardi Paola
Mattanovich Diethard
Porro Danilo
author_sort Valli Minoska
title Lactate production yield from engineered yeasts is dependent from the host background, the lactate dehydrogenase source and the lactate export
title_short Lactate production yield from engineered yeasts is dependent from the host background, the lactate dehydrogenase source and the lactate export
title_full Lactate production yield from engineered yeasts is dependent from the host background, the lactate dehydrogenase source and the lactate export
title_fullStr Lactate production yield from engineered yeasts is dependent from the host background, the lactate dehydrogenase source and the lactate export
title_full_unstemmed Lactate production yield from engineered yeasts is dependent from the host background, the lactate dehydrogenase source and the lactate export
title_sort lactate production yield from engineered yeasts is dependent from the host background, the lactate dehydrogenase source and the lactate export
publisher BMC
series Microbial Cell Factories
issn 1475-2859
publishDate 2006-01-01
description <p>Abstract</p> <p>Background</p> <p>Metabolic pathway manipulation for improving the properties and the productivity of microorganisms is becoming a well established concept. For the production of important metabolites, but also for a better understanding of the fundamentals of cell biology, detailed studies are required. In this work we analysed the lactate production from metabolic engineered <it>Saccharomyces cerevisiae </it>cells expressing a heterologous lactate dehydrogenase (<it>LDH</it>) gene. The <it>LDH </it>gene expression in a budding yeast cell introduces a novel and alternative pathway for the NAD<sup>+ </sup>regeneration, allowing a direct reduction of the intracellular pyruvate to lactate, leading to a simultaneous accumulation of lactate and ethanol.</p> <p>Results</p> <p>Four different <it>S. cerevisiae </it>strains were transformed with six different wild type and one mutagenised <it>LDH </it>genes, in combination or not with the over-expression of a lactate transporter. The resulting yield values (grams of lactate produced per grams of glucose consumed) varied from as low as 0,0008 to as high as 0.52 g g<sup>-1</sup>. In this respect, and to the best of our knowledge, higher redirections of the glycolysis flux have never been obtained before without any disruption and/or limitation of the competing biochemical pathways.</p> <p>Conclusion</p> <p>In the present work it is shown that the redirection of the pathway towards the lactate production can be strongly modulated by the genetic background of the host cell, by the source of the heterologous Ldh enzyme, by improving its biochemical properties as well as by modulating the export of lactate in the culture media.</p>
url http://www.microbialcellfactories.com/content/5/1/4
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