Efficient biochemical production of acetoin from carbon dioxide using Cupriavidus necator H16

Abstract Background Cupriavidus necator is the best-studied knallgas (also termed hydrogen oxidizing) bacterium and provides a model organism for studying the production of the storage polymer polyhydroxybutyrate (PHB). Genetically engineered strains could be applied for the autotrophic production o...

Full description

Bibliographic Details
Main Authors: Carina Windhorst, Johannes Gescher
Format: Article
Language:English
Published: BMC 2019-06-01
Series:Biotechnology for Biofuels
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13068-019-1512-x
id doaj-93f6bbddb1864ffc81a32a74b59e40e3
record_format Article
spelling doaj-93f6bbddb1864ffc81a32a74b59e40e32020-11-25T03:04:13ZengBMCBiotechnology for Biofuels1754-68342019-06-0112111110.1186/s13068-019-1512-xEfficient biochemical production of acetoin from carbon dioxide using Cupriavidus necator H16Carina Windhorst0Johannes Gescher1Department of Applied Biology, Institute for Applied Biosciences, Karlsruhe Institute of TechnologyDepartment of Applied Biology, Institute for Applied Biosciences, Karlsruhe Institute of TechnologyAbstract Background Cupriavidus necator is the best-studied knallgas (also termed hydrogen oxidizing) bacterium and provides a model organism for studying the production of the storage polymer polyhydroxybutyrate (PHB). Genetically engineered strains could be applied for the autotrophic production of valuable chemicals. Nevertheless, the efficiency of the catalyzed processes is generally believed to be lower than with acetogenic bacteria. Experimental data on the potential efficiency of autotrophic production with C. necator are sparse. Hence, this study aimed at developing a strain for the production of the bulk chemical acetoin from carbon dioxide and to analyze the carbon and electron yield in detail. Results We developed a constitutive promoter system based on the natural PHB promoter of this organism. Codon-optimized versions of the acetolactate dehydrogenase (alsS) and acetolactate decarboxylase (alsD) from Bacillus subtilis were cloned under control of the PHB promoter in order to produce acetoin from pyruvate. The production process’s efficiency could be significantly increased by deleting the PHB synthase phaC2. Further deletion of the other PHB synthase encoded in the genome (phaC1) led to a strain that produced acetoin with > 100% carbon efficiency. This increase in efficiency is most probably due to a minor amount of cell lysis. Using a variation in hydrogen and oxygen gas mixtures, we observed that the optimal oxygen concentration for the process was between 15 and 20%. Conclusion To the best of our knowledge, this study describes for the first time a highly efficient process for the chemolithoautotrophic production of the platform chemical acetoin.http://link.springer.com/article/10.1186/s13068-019-1512-xCupriavidus necator H16Ralstonia eutropha H16AcetoinAutotrophPlatform chemicalPolyhydroxybutyrate
collection DOAJ
language English
format Article
sources DOAJ
author Carina Windhorst
Johannes Gescher
spellingShingle Carina Windhorst
Johannes Gescher
Efficient biochemical production of acetoin from carbon dioxide using Cupriavidus necator H16
Biotechnology for Biofuels
Cupriavidus necator H16
Ralstonia eutropha H16
Acetoin
Autotroph
Platform chemical
Polyhydroxybutyrate
author_facet Carina Windhorst
Johannes Gescher
author_sort Carina Windhorst
title Efficient biochemical production of acetoin from carbon dioxide using Cupriavidus necator H16
title_short Efficient biochemical production of acetoin from carbon dioxide using Cupriavidus necator H16
title_full Efficient biochemical production of acetoin from carbon dioxide using Cupriavidus necator H16
title_fullStr Efficient biochemical production of acetoin from carbon dioxide using Cupriavidus necator H16
title_full_unstemmed Efficient biochemical production of acetoin from carbon dioxide using Cupriavidus necator H16
title_sort efficient biochemical production of acetoin from carbon dioxide using cupriavidus necator h16
publisher BMC
series Biotechnology for Biofuels
issn 1754-6834
publishDate 2019-06-01
description Abstract Background Cupriavidus necator is the best-studied knallgas (also termed hydrogen oxidizing) bacterium and provides a model organism for studying the production of the storage polymer polyhydroxybutyrate (PHB). Genetically engineered strains could be applied for the autotrophic production of valuable chemicals. Nevertheless, the efficiency of the catalyzed processes is generally believed to be lower than with acetogenic bacteria. Experimental data on the potential efficiency of autotrophic production with C. necator are sparse. Hence, this study aimed at developing a strain for the production of the bulk chemical acetoin from carbon dioxide and to analyze the carbon and electron yield in detail. Results We developed a constitutive promoter system based on the natural PHB promoter of this organism. Codon-optimized versions of the acetolactate dehydrogenase (alsS) and acetolactate decarboxylase (alsD) from Bacillus subtilis were cloned under control of the PHB promoter in order to produce acetoin from pyruvate. The production process’s efficiency could be significantly increased by deleting the PHB synthase phaC2. Further deletion of the other PHB synthase encoded in the genome (phaC1) led to a strain that produced acetoin with > 100% carbon efficiency. This increase in efficiency is most probably due to a minor amount of cell lysis. Using a variation in hydrogen and oxygen gas mixtures, we observed that the optimal oxygen concentration for the process was between 15 and 20%. Conclusion To the best of our knowledge, this study describes for the first time a highly efficient process for the chemolithoautotrophic production of the platform chemical acetoin.
topic Cupriavidus necator H16
Ralstonia eutropha H16
Acetoin
Autotroph
Platform chemical
Polyhydroxybutyrate
url http://link.springer.com/article/10.1186/s13068-019-1512-x
work_keys_str_mv AT carinawindhorst efficientbiochemicalproductionofacetoinfromcarbondioxideusingcupriavidusnecatorh16
AT johannesgescher efficientbiochemicalproductionofacetoinfromcarbondioxideusingcupriavidusnecatorh16
_version_ 1724682263074963456