CO2-Induced Transcriptional Reorganization: Molecular Basis of Capnophillic Lactic Fermentation in Thermotoga neapolitana

Capnophilic lactic fermentation (CLF) is a novel anaplerotic pathway able to convert sugars to lactic acid (LA) and hydrogen using CO2 as carbon enhancer in the hyperthermophilic bacterium Thermotoga neapolitana. In order to give further insights into CLF metabolic networks, we investigated the tran...

Full description

Bibliographic Details
Main Authors: Giuliana d’Ippolito, Simone Landi, Nunzia Esercizio, Mariamichella Lanzilli, Marco Vastano, Laura Dipasquale, Nirakar Pradhan, Angelo Fontana
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-02-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fmicb.2020.00171/full
id doaj-777d114107804d929b49eab9b0c3ff36
record_format Article
spelling doaj-777d114107804d929b49eab9b0c3ff362020-11-25T02:04:52ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2020-02-011110.3389/fmicb.2020.00171488770CO2-Induced Transcriptional Reorganization: Molecular Basis of Capnophillic Lactic Fermentation in Thermotoga neapolitanaGiuliana d’IppolitoSimone LandiNunzia EsercizioMariamichella LanzilliMarco VastanoLaura DipasqualeNirakar PradhanAngelo FontanaCapnophilic lactic fermentation (CLF) is a novel anaplerotic pathway able to convert sugars to lactic acid (LA) and hydrogen using CO2 as carbon enhancer in the hyperthermophilic bacterium Thermotoga neapolitana. In order to give further insights into CLF metabolic networks, we investigated the transcriptional modification induced by CO2 using a RNA-seq approach. Transcriptomic analysis revealed 1601 differentially expressed genes (DEGs) in an enriched CO2 atmosphere over a total of 1938 genes of the T. neapolitana genome. Transcription of PFOR and LDH genes belonging to the CLF pathway was up-regulated by CO2 together with 6-phosphogluconolactonase (6PGL) and 6-phosphogluconate dehydratase (EDD) of the Entner–Doudoroff (ED) pathway. The transcriptomic study also revealed up-regulation of genes coding for the flavin-based enzymes NADH-dependent reduced ferredoxin:NADP oxidoreductase (NFN) and NAD-ferredoxin oxidoreductase (RNF) that control supply of reduced ferredoxin and NADH and allow energy conservation-based sodium translocation through the cell membrane. These results support the hypothesis that CO2 induces rearrangement of the central carbon metabolism together with activation of mechanisms that increase availability of the reducing equivalents that are necessary to sustain CLF. In this view, this study reports a first rationale of the molecular basis of CLF in T. neapolitana and provides a list of target genes for the biotechnological implementation of this process.https://www.frontiersin.org/article/10.3389/fmicb.2020.00171/fulllactic acidpyruvateglycolysishydrogenasethermophilicRNA-seq
collection DOAJ
language English
format Article
sources DOAJ
author Giuliana d’Ippolito
Simone Landi
Nunzia Esercizio
Mariamichella Lanzilli
Marco Vastano
Laura Dipasquale
Nirakar Pradhan
Angelo Fontana
spellingShingle Giuliana d’Ippolito
Simone Landi
Nunzia Esercizio
Mariamichella Lanzilli
Marco Vastano
Laura Dipasquale
Nirakar Pradhan
Angelo Fontana
CO2-Induced Transcriptional Reorganization: Molecular Basis of Capnophillic Lactic Fermentation in Thermotoga neapolitana
Frontiers in Microbiology
lactic acid
pyruvate
glycolysis
hydrogenase
thermophilic
RNA-seq
author_facet Giuliana d’Ippolito
Simone Landi
Nunzia Esercizio
Mariamichella Lanzilli
Marco Vastano
Laura Dipasquale
Nirakar Pradhan
Angelo Fontana
author_sort Giuliana d’Ippolito
title CO2-Induced Transcriptional Reorganization: Molecular Basis of Capnophillic Lactic Fermentation in Thermotoga neapolitana
title_short CO2-Induced Transcriptional Reorganization: Molecular Basis of Capnophillic Lactic Fermentation in Thermotoga neapolitana
title_full CO2-Induced Transcriptional Reorganization: Molecular Basis of Capnophillic Lactic Fermentation in Thermotoga neapolitana
title_fullStr CO2-Induced Transcriptional Reorganization: Molecular Basis of Capnophillic Lactic Fermentation in Thermotoga neapolitana
title_full_unstemmed CO2-Induced Transcriptional Reorganization: Molecular Basis of Capnophillic Lactic Fermentation in Thermotoga neapolitana
title_sort co2-induced transcriptional reorganization: molecular basis of capnophillic lactic fermentation in thermotoga neapolitana
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2020-02-01
description Capnophilic lactic fermentation (CLF) is a novel anaplerotic pathway able to convert sugars to lactic acid (LA) and hydrogen using CO2 as carbon enhancer in the hyperthermophilic bacterium Thermotoga neapolitana. In order to give further insights into CLF metabolic networks, we investigated the transcriptional modification induced by CO2 using a RNA-seq approach. Transcriptomic analysis revealed 1601 differentially expressed genes (DEGs) in an enriched CO2 atmosphere over a total of 1938 genes of the T. neapolitana genome. Transcription of PFOR and LDH genes belonging to the CLF pathway was up-regulated by CO2 together with 6-phosphogluconolactonase (6PGL) and 6-phosphogluconate dehydratase (EDD) of the Entner–Doudoroff (ED) pathway. The transcriptomic study also revealed up-regulation of genes coding for the flavin-based enzymes NADH-dependent reduced ferredoxin:NADP oxidoreductase (NFN) and NAD-ferredoxin oxidoreductase (RNF) that control supply of reduced ferredoxin and NADH and allow energy conservation-based sodium translocation through the cell membrane. These results support the hypothesis that CO2 induces rearrangement of the central carbon metabolism together with activation of mechanisms that increase availability of the reducing equivalents that are necessary to sustain CLF. In this view, this study reports a first rationale of the molecular basis of CLF in T. neapolitana and provides a list of target genes for the biotechnological implementation of this process.
topic lactic acid
pyruvate
glycolysis
hydrogenase
thermophilic
RNA-seq
url https://www.frontiersin.org/article/10.3389/fmicb.2020.00171/full
work_keys_str_mv AT giulianadippolito co2inducedtranscriptionalreorganizationmolecularbasisofcapnophilliclacticfermentationinthermotoganeapolitana
AT simonelandi co2inducedtranscriptionalreorganizationmolecularbasisofcapnophilliclacticfermentationinthermotoganeapolitana
AT nunziaesercizio co2inducedtranscriptionalreorganizationmolecularbasisofcapnophilliclacticfermentationinthermotoganeapolitana
AT mariamichellalanzilli co2inducedtranscriptionalreorganizationmolecularbasisofcapnophilliclacticfermentationinthermotoganeapolitana
AT marcovastano co2inducedtranscriptionalreorganizationmolecularbasisofcapnophilliclacticfermentationinthermotoganeapolitana
AT lauradipasquale co2inducedtranscriptionalreorganizationmolecularbasisofcapnophilliclacticfermentationinthermotoganeapolitana
AT nirakarpradhan co2inducedtranscriptionalreorganizationmolecularbasisofcapnophilliclacticfermentationinthermotoganeapolitana
AT angelofontana co2inducedtranscriptionalreorganizationmolecularbasisofcapnophilliclacticfermentationinthermotoganeapolitana
_version_ 1724940554886709248