<i>Zymobacter palmae</i> Pyruvate Decarboxylase is Less Effective Than That of <i>Zymomonas mobilis</i> for Ethanol Production in Metabolically Engineered <i>Synechocystis</i> sp. PCC6803

To produce bioethanol from model cyanobacteria such as <i>Synechocystis</i>, a two gene cassette consisting of genes encoding pyruvate decarboxylase (PDC) and alcohol dehydrogenase (ADH) are required to transform pyruvate first to acetaldehyde and then to ethanol. However the partition o...

Full description

Bibliographic Details
Main Authors: Lorraine Quinn, Patricia Armshaw, Tewfik Soulimane, Con Sheehan, Michael P. Ryan, J. Tony Pembroke
Format: Article
Language:English
Published: MDPI AG 2019-10-01
Series:Microorganisms
Subjects:
Online Access:https://www.mdpi.com/2076-2607/7/11/494
id doaj-0791ff8e04974c669e6110090ebd4df9
record_format Article
spelling doaj-0791ff8e04974c669e6110090ebd4df92020-11-25T00:39:17ZengMDPI AGMicroorganisms2076-26072019-10-0171149410.3390/microorganisms7110494microorganisms7110494<i>Zymobacter palmae</i> Pyruvate Decarboxylase is Less Effective Than That of <i>Zymomonas mobilis</i> for Ethanol Production in Metabolically Engineered <i>Synechocystis</i> sp. PCC6803Lorraine Quinn0Patricia Armshaw1Tewfik Soulimane2Con Sheehan3Michael P. Ryan4J. Tony Pembroke5Department of Chemical Sciences, School of Natural Sciences and the Bernal Institute, University of Limerick, V94 T9PX Limerick, IrelandDepartment of Chemical Sciences, School of Natural Sciences and the Bernal Institute, University of Limerick, V94 T9PX Limerick, IrelandDepartment of Chemical Sciences, School of Natural Sciences and the Bernal Institute, University of Limerick, V94 T9PX Limerick, IrelandSchool of Engineering, University of Limerick, V94 T9PX Limerick, IrelandDepartment of Chemical Sciences, School of Natural Sciences and the Bernal Institute, University of Limerick, V94 T9PX Limerick, IrelandDepartment of Chemical Sciences, School of Natural Sciences and the Bernal Institute, University of Limerick, V94 T9PX Limerick, IrelandTo produce bioethanol from model cyanobacteria such as <i>Synechocystis</i>, a two gene cassette consisting of genes encoding pyruvate decarboxylase (PDC) and alcohol dehydrogenase (ADH) are required to transform pyruvate first to acetaldehyde and then to ethanol. However the partition of pyruvate to ethanol comes at a cost, a reduction in biomass and pyruvate availability for other metabolic processes. Hence strategies to divert flux to ethanol as a biofuel in <i>Synechocystis</i> are of interest. PDC from <i>Zymobacter palmae</i> (ZpPDC) has been reported to have a lower Km then the <i>Zymomonas mobilis</i> PDC (ZmPDC), which has traditionally been used in metabolic engineering constructs. The <i>Zppdc</i> gene was combined with the native <i>slr1192</i> alcohol dehydrogenase gene (<i>adh</i>A) in an attempt to increase ethanol production in the photoautotrophic cyanobacterium <i>Synechocystis</i> sp. PCC 6803 over constructs created with the traditional Zmpdc. Native (Zppdc) and codon optimized (<i>ZpOpdc</i>) versions of the ZpPDC were cloned into a construct where <i>pdc</i> expression was controlled via the <i>psb</i>A2 light inducible promoter from <i>Synechocystis</i> sp. PCC 6803. These constructs were transformed into wildtype <i>Synechocystis</i> sp. PCC 6803 for expression and ethanol production. Ethanol levels were then compared with identical constructs containing the <i>Zmpdc</i>. While strains with the <i>Zppdc</i> (UL071) and <i>ZpOpdc</i> (UL072) constructs did produce ethanol, levels were lower compared to a control strain (UL070) expressing the pdc from <i>Zymomonas mobilis</i>. All constructs demonstrated lower biomass productivity illustrating that the flux from pyruvate to ethanol has a major effect on biomass and ultimately overall biofuel productivity. Thus the utilization of a PDC with a lower Km from <i>Zymobacter palmae</i> unusually did not result in enhanced ethanol production in <i>Synechocystis</i> sp. PCC 6803.https://www.mdpi.com/2076-2607/7/11/494alcohol dehydrogenase (adh)biofuelscyanobacteriaethanolpyruvate decarboxylase (pdc)renewable energy<i>synechocystis</i> sp. pcc 6803
collection DOAJ
language English
format Article
sources DOAJ
author Lorraine Quinn
Patricia Armshaw
Tewfik Soulimane
Con Sheehan
Michael P. Ryan
J. Tony Pembroke
spellingShingle Lorraine Quinn
Patricia Armshaw
Tewfik Soulimane
Con Sheehan
Michael P. Ryan
J. Tony Pembroke
<i>Zymobacter palmae</i> Pyruvate Decarboxylase is Less Effective Than That of <i>Zymomonas mobilis</i> for Ethanol Production in Metabolically Engineered <i>Synechocystis</i> sp. PCC6803
Microorganisms
alcohol dehydrogenase (adh)
biofuels
cyanobacteria
ethanol
pyruvate decarboxylase (pdc)
renewable energy
<i>synechocystis</i> sp. pcc 6803
author_facet Lorraine Quinn
Patricia Armshaw
Tewfik Soulimane
Con Sheehan
Michael P. Ryan
J. Tony Pembroke
author_sort Lorraine Quinn
title <i>Zymobacter palmae</i> Pyruvate Decarboxylase is Less Effective Than That of <i>Zymomonas mobilis</i> for Ethanol Production in Metabolically Engineered <i>Synechocystis</i> sp. PCC6803
title_short <i>Zymobacter palmae</i> Pyruvate Decarboxylase is Less Effective Than That of <i>Zymomonas mobilis</i> for Ethanol Production in Metabolically Engineered <i>Synechocystis</i> sp. PCC6803
title_full <i>Zymobacter palmae</i> Pyruvate Decarboxylase is Less Effective Than That of <i>Zymomonas mobilis</i> for Ethanol Production in Metabolically Engineered <i>Synechocystis</i> sp. PCC6803
title_fullStr <i>Zymobacter palmae</i> Pyruvate Decarboxylase is Less Effective Than That of <i>Zymomonas mobilis</i> for Ethanol Production in Metabolically Engineered <i>Synechocystis</i> sp. PCC6803
title_full_unstemmed <i>Zymobacter palmae</i> Pyruvate Decarboxylase is Less Effective Than That of <i>Zymomonas mobilis</i> for Ethanol Production in Metabolically Engineered <i>Synechocystis</i> sp. PCC6803
title_sort <i>zymobacter palmae</i> pyruvate decarboxylase is less effective than that of <i>zymomonas mobilis</i> for ethanol production in metabolically engineered <i>synechocystis</i> sp. pcc6803
publisher MDPI AG
series Microorganisms
issn 2076-2607
publishDate 2019-10-01
description To produce bioethanol from model cyanobacteria such as <i>Synechocystis</i>, a two gene cassette consisting of genes encoding pyruvate decarboxylase (PDC) and alcohol dehydrogenase (ADH) are required to transform pyruvate first to acetaldehyde and then to ethanol. However the partition of pyruvate to ethanol comes at a cost, a reduction in biomass and pyruvate availability for other metabolic processes. Hence strategies to divert flux to ethanol as a biofuel in <i>Synechocystis</i> are of interest. PDC from <i>Zymobacter palmae</i> (ZpPDC) has been reported to have a lower Km then the <i>Zymomonas mobilis</i> PDC (ZmPDC), which has traditionally been used in metabolic engineering constructs. The <i>Zppdc</i> gene was combined with the native <i>slr1192</i> alcohol dehydrogenase gene (<i>adh</i>A) in an attempt to increase ethanol production in the photoautotrophic cyanobacterium <i>Synechocystis</i> sp. PCC 6803 over constructs created with the traditional Zmpdc. Native (Zppdc) and codon optimized (<i>ZpOpdc</i>) versions of the ZpPDC were cloned into a construct where <i>pdc</i> expression was controlled via the <i>psb</i>A2 light inducible promoter from <i>Synechocystis</i> sp. PCC 6803. These constructs were transformed into wildtype <i>Synechocystis</i> sp. PCC 6803 for expression and ethanol production. Ethanol levels were then compared with identical constructs containing the <i>Zmpdc</i>. While strains with the <i>Zppdc</i> (UL071) and <i>ZpOpdc</i> (UL072) constructs did produce ethanol, levels were lower compared to a control strain (UL070) expressing the pdc from <i>Zymomonas mobilis</i>. All constructs demonstrated lower biomass productivity illustrating that the flux from pyruvate to ethanol has a major effect on biomass and ultimately overall biofuel productivity. Thus the utilization of a PDC with a lower Km from <i>Zymobacter palmae</i> unusually did not result in enhanced ethanol production in <i>Synechocystis</i> sp. PCC 6803.
topic alcohol dehydrogenase (adh)
biofuels
cyanobacteria
ethanol
pyruvate decarboxylase (pdc)
renewable energy
<i>synechocystis</i> sp. pcc 6803
url https://www.mdpi.com/2076-2607/7/11/494
work_keys_str_mv AT lorrainequinn izymobacterpalmaeipyruvatedecarboxylaseislesseffectivethanthatofizymomonasmobilisiforethanolproductioninmetabolicallyengineeredisynechocystisisppcc6803
AT patriciaarmshaw izymobacterpalmaeipyruvatedecarboxylaseislesseffectivethanthatofizymomonasmobilisiforethanolproductioninmetabolicallyengineeredisynechocystisisppcc6803
AT tewfiksoulimane izymobacterpalmaeipyruvatedecarboxylaseislesseffectivethanthatofizymomonasmobilisiforethanolproductioninmetabolicallyengineeredisynechocystisisppcc6803
AT consheehan izymobacterpalmaeipyruvatedecarboxylaseislesseffectivethanthatofizymomonasmobilisiforethanolproductioninmetabolicallyengineeredisynechocystisisppcc6803
AT michaelpryan izymobacterpalmaeipyruvatedecarboxylaseislesseffectivethanthatofizymomonasmobilisiforethanolproductioninmetabolicallyengineeredisynechocystisisppcc6803
AT jtonypembroke izymobacterpalmaeipyruvatedecarboxylaseislesseffectivethanthatofizymomonasmobilisiforethanolproductioninmetabolicallyengineeredisynechocystisisppcc6803
_version_ 1725294066371919872