Engineering redox homeostasis to develop efficient alcohol-producing microbial cell factories

Abstract The biosynthetic pathways of most alcohols are linked to intracellular redox homeostasis, which is crucial for life. This crucial balance is primarily controlled by the generation of reducing equivalents, as well as the (reduction)-oxidation metabolic cycle and the thiol redox homeostasis s...
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Autor*in:	Zhao, Chunhua [verfasserIn] Zhao, Qiuwei Li, Yin Zhang, Yanping

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2017

Schlagwörter:	Redox homeostasis Metabolic engineering Alcohol Cofactor engineering Glutathione Reducing equivalent

Anmerkung:	© The Author(s) 2017

Übergeordnetes Werk:	Enthalten in: Microbial cell factories - London : Biomed Central, 2002, 16(2017), 1 vom: 24. Juni
Übergeordnetes Werk:	volume:16 ; year:2017 ; number:1 ; day:24 ; month:06

Links:	Volltext

DOI / URN:	10.1186/s12934-017-0728-3

Katalog-ID:	SPR028571606

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520			\|a Abstract The biosynthetic pathways of most alcohols are linked to intracellular redox homeostasis, which is crucial for life. This crucial balance is primarily controlled by the generation of reducing equivalents, as well as the (reduction)-oxidation metabolic cycle and the thiol redox homeostasis system. As a main oxidation pathway of reducing equivalents, the biosynthesis of most alcohols includes redox reactions, which are dependent on cofactors such as NADH or NADPH. Thus, when engineering alcohol-producing strains, the availability of cofactors and redox homeostasis must be considered. In this review, recent advances on the engineering of cellular redox homeostasis systems to accelerate alcohol biosynthesis are summarized. Recent approaches include improving cofactor availability, manipulating the affinity of redox enzymes to specific cofactors, as well as globally controlling redox reactions, indicating the power of these approaches, and opening a path towards improving the production of a number of different industrially-relevant alcohols in the near future.
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allfields	10.1186/s12934-017-0728-3 doi (DE-627)SPR028571606 (SPR)s12934-017-0728-3-e DE-627 ger DE-627 rakwb eng Zhao, Chunhua verfasserin aut Engineering redox homeostasis to develop efficient alcohol-producing microbial cell factories 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2017 Abstract The biosynthetic pathways of most alcohols are linked to intracellular redox homeostasis, which is crucial for life. This crucial balance is primarily controlled by the generation of reducing equivalents, as well as the (reduction)-oxidation metabolic cycle and the thiol redox homeostasis system. As a main oxidation pathway of reducing equivalents, the biosynthesis of most alcohols includes redox reactions, which are dependent on cofactors such as NADH or NADPH. Thus, when engineering alcohol-producing strains, the availability of cofactors and redox homeostasis must be considered. In this review, recent advances on the engineering of cellular redox homeostasis systems to accelerate alcohol biosynthesis are summarized. Recent approaches include improving cofactor availability, manipulating the affinity of redox enzymes to specific cofactors, as well as globally controlling redox reactions, indicating the power of these approaches, and opening a path towards improving the production of a number of different industrially-relevant alcohols in the near future. Redox homeostasis (dpeaa)DE-He213 Metabolic engineering (dpeaa)DE-He213 Alcohol (dpeaa)DE-He213 Cofactor engineering (dpeaa)DE-He213 Glutathione (dpeaa)DE-He213 Reducing equivalent (dpeaa)DE-He213 Zhao, Qiuwei aut Li, Yin aut Zhang, Yanping aut Enthalten in Microbial cell factories London : Biomed Central, 2002 16(2017), 1 vom: 24. Juni (DE-627)355987651 (DE-600)2091377-1 1475-2859 nnns volume:16 year:2017 number:1 day:24 month:06 https://dx.doi.org/10.1186/s12934-017-0728-3 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 16 2017 1 24 06
spelling	10.1186/s12934-017-0728-3 doi (DE-627)SPR028571606 (SPR)s12934-017-0728-3-e DE-627 ger DE-627 rakwb eng Zhao, Chunhua verfasserin aut Engineering redox homeostasis to develop efficient alcohol-producing microbial cell factories 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2017 Abstract The biosynthetic pathways of most alcohols are linked to intracellular redox homeostasis, which is crucial for life. This crucial balance is primarily controlled by the generation of reducing equivalents, as well as the (reduction)-oxidation metabolic cycle and the thiol redox homeostasis system. As a main oxidation pathway of reducing equivalents, the biosynthesis of most alcohols includes redox reactions, which are dependent on cofactors such as NADH or NADPH. Thus, when engineering alcohol-producing strains, the availability of cofactors and redox homeostasis must be considered. In this review, recent advances on the engineering of cellular redox homeostasis systems to accelerate alcohol biosynthesis are summarized. Recent approaches include improving cofactor availability, manipulating the affinity of redox enzymes to specific cofactors, as well as globally controlling redox reactions, indicating the power of these approaches, and opening a path towards improving the production of a number of different industrially-relevant alcohols in the near future. Redox homeostasis (dpeaa)DE-He213 Metabolic engineering (dpeaa)DE-He213 Alcohol (dpeaa)DE-He213 Cofactor engineering (dpeaa)DE-He213 Glutathione (dpeaa)DE-He213 Reducing equivalent (dpeaa)DE-He213 Zhao, Qiuwei aut Li, Yin aut Zhang, Yanping aut Enthalten in Microbial cell factories London : Biomed Central, 2002 16(2017), 1 vom: 24. Juni (DE-627)355987651 (DE-600)2091377-1 1475-2859 nnns volume:16 year:2017 number:1 day:24 month:06 https://dx.doi.org/10.1186/s12934-017-0728-3 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 16 2017 1 24 06
allfields_unstemmed	10.1186/s12934-017-0728-3 doi (DE-627)SPR028571606 (SPR)s12934-017-0728-3-e DE-627 ger DE-627 rakwb eng Zhao, Chunhua verfasserin aut Engineering redox homeostasis to develop efficient alcohol-producing microbial cell factories 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2017 Abstract The biosynthetic pathways of most alcohols are linked to intracellular redox homeostasis, which is crucial for life. This crucial balance is primarily controlled by the generation of reducing equivalents, as well as the (reduction)-oxidation metabolic cycle and the thiol redox homeostasis system. As a main oxidation pathway of reducing equivalents, the biosynthesis of most alcohols includes redox reactions, which are dependent on cofactors such as NADH or NADPH. Thus, when engineering alcohol-producing strains, the availability of cofactors and redox homeostasis must be considered. In this review, recent advances on the engineering of cellular redox homeostasis systems to accelerate alcohol biosynthesis are summarized. Recent approaches include improving cofactor availability, manipulating the affinity of redox enzymes to specific cofactors, as well as globally controlling redox reactions, indicating the power of these approaches, and opening a path towards improving the production of a number of different industrially-relevant alcohols in the near future. Redox homeostasis (dpeaa)DE-He213 Metabolic engineering (dpeaa)DE-He213 Alcohol (dpeaa)DE-He213 Cofactor engineering (dpeaa)DE-He213 Glutathione (dpeaa)DE-He213 Reducing equivalent (dpeaa)DE-He213 Zhao, Qiuwei aut Li, Yin aut Zhang, Yanping aut Enthalten in Microbial cell factories London : Biomed Central, 2002 16(2017), 1 vom: 24. Juni (DE-627)355987651 (DE-600)2091377-1 1475-2859 nnns volume:16 year:2017 number:1 day:24 month:06 https://dx.doi.org/10.1186/s12934-017-0728-3 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 16 2017 1 24 06
allfieldsGer	10.1186/s12934-017-0728-3 doi (DE-627)SPR028571606 (SPR)s12934-017-0728-3-e DE-627 ger DE-627 rakwb eng Zhao, Chunhua verfasserin aut Engineering redox homeostasis to develop efficient alcohol-producing microbial cell factories 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2017 Abstract The biosynthetic pathways of most alcohols are linked to intracellular redox homeostasis, which is crucial for life. This crucial balance is primarily controlled by the generation of reducing equivalents, as well as the (reduction)-oxidation metabolic cycle and the thiol redox homeostasis system. As a main oxidation pathway of reducing equivalents, the biosynthesis of most alcohols includes redox reactions, which are dependent on cofactors such as NADH or NADPH. Thus, when engineering alcohol-producing strains, the availability of cofactors and redox homeostasis must be considered. In this review, recent advances on the engineering of cellular redox homeostasis systems to accelerate alcohol biosynthesis are summarized. Recent approaches include improving cofactor availability, manipulating the affinity of redox enzymes to specific cofactors, as well as globally controlling redox reactions, indicating the power of these approaches, and opening a path towards improving the production of a number of different industrially-relevant alcohols in the near future. Redox homeostasis (dpeaa)DE-He213 Metabolic engineering (dpeaa)DE-He213 Alcohol (dpeaa)DE-He213 Cofactor engineering (dpeaa)DE-He213 Glutathione (dpeaa)DE-He213 Reducing equivalent (dpeaa)DE-He213 Zhao, Qiuwei aut Li, Yin aut Zhang, Yanping aut Enthalten in Microbial cell factories London : Biomed Central, 2002 16(2017), 1 vom: 24. Juni (DE-627)355987651 (DE-600)2091377-1 1475-2859 nnns volume:16 year:2017 number:1 day:24 month:06 https://dx.doi.org/10.1186/s12934-017-0728-3 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 16 2017 1 24 06
allfieldsSound	10.1186/s12934-017-0728-3 doi (DE-627)SPR028571606 (SPR)s12934-017-0728-3-e DE-627 ger DE-627 rakwb eng Zhao, Chunhua verfasserin aut Engineering redox homeostasis to develop efficient alcohol-producing microbial cell factories 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2017 Abstract The biosynthetic pathways of most alcohols are linked to intracellular redox homeostasis, which is crucial for life. This crucial balance is primarily controlled by the generation of reducing equivalents, as well as the (reduction)-oxidation metabolic cycle and the thiol redox homeostasis system. As a main oxidation pathway of reducing equivalents, the biosynthesis of most alcohols includes redox reactions, which are dependent on cofactors such as NADH or NADPH. Thus, when engineering alcohol-producing strains, the availability of cofactors and redox homeostasis must be considered. In this review, recent advances on the engineering of cellular redox homeostasis systems to accelerate alcohol biosynthesis are summarized. Recent approaches include improving cofactor availability, manipulating the affinity of redox enzymes to specific cofactors, as well as globally controlling redox reactions, indicating the power of these approaches, and opening a path towards improving the production of a number of different industrially-relevant alcohols in the near future. Redox homeostasis (dpeaa)DE-He213 Metabolic engineering (dpeaa)DE-He213 Alcohol (dpeaa)DE-He213 Cofactor engineering (dpeaa)DE-He213 Glutathione (dpeaa)DE-He213 Reducing equivalent (dpeaa)DE-He213 Zhao, Qiuwei aut Li, Yin aut Zhang, Yanping aut Enthalten in Microbial cell factories London : Biomed Central, 2002 16(2017), 1 vom: 24. Juni (DE-627)355987651 (DE-600)2091377-1 1475-2859 nnns volume:16 year:2017 number:1 day:24 month:06 https://dx.doi.org/10.1186/s12934-017-0728-3 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 16 2017 1 24 06
language	English
source	Enthalten in Microbial cell factories 16(2017), 1 vom: 24. Juni volume:16 year:2017 number:1 day:24 month:06
sourceStr	Enthalten in Microbial cell factories 16(2017), 1 vom: 24. Juni volume:16 year:2017 number:1 day:24 month:06
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Redox homeostasis Metabolic engineering Alcohol Cofactor engineering Glutathione Reducing equivalent
isfreeaccess_bool	true
container_title	Microbial cell factories
authorswithroles_txt_mv	Zhao, Chunhua @@aut@@ Zhao, Qiuwei @@aut@@ Li, Yin @@aut@@ Zhang, Yanping @@aut@@
publishDateDaySort_date	2017-06-24T00:00:00Z
hierarchy_top_id	355987651
id	SPR028571606
language_de	englisch
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author	Zhao, Chunhua
spellingShingle	Zhao, Chunhua misc Redox homeostasis misc Metabolic engineering misc Alcohol misc Cofactor engineering misc Glutathione misc Reducing equivalent Engineering redox homeostasis to develop efficient alcohol-producing microbial cell factories
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topic_title	Engineering redox homeostasis to develop efficient alcohol-producing microbial cell factories Redox homeostasis (dpeaa)DE-He213 Metabolic engineering (dpeaa)DE-He213 Alcohol (dpeaa)DE-He213 Cofactor engineering (dpeaa)DE-He213 Glutathione (dpeaa)DE-He213 Reducing equivalent (dpeaa)DE-He213
topic	misc Redox homeostasis misc Metabolic engineering misc Alcohol misc Cofactor engineering misc Glutathione misc Reducing equivalent
topic_unstemmed	misc Redox homeostasis misc Metabolic engineering misc Alcohol misc Cofactor engineering misc Glutathione misc Reducing equivalent
topic_browse	misc Redox homeostasis misc Metabolic engineering misc Alcohol misc Cofactor engineering misc Glutathione misc Reducing equivalent
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title	Engineering redox homeostasis to develop efficient alcohol-producing microbial cell factories
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title_full	Engineering redox homeostasis to develop efficient alcohol-producing microbial cell factories
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title_sort	engineering redox homeostasis to develop efficient alcohol-producing microbial cell factories
title_auth	Engineering redox homeostasis to develop efficient alcohol-producing microbial cell factories
abstract	Abstract The biosynthetic pathways of most alcohols are linked to intracellular redox homeostasis, which is crucial for life. This crucial balance is primarily controlled by the generation of reducing equivalents, as well as the (reduction)-oxidation metabolic cycle and the thiol redox homeostasis system. As a main oxidation pathway of reducing equivalents, the biosynthesis of most alcohols includes redox reactions, which are dependent on cofactors such as NADH or NADPH. Thus, when engineering alcohol-producing strains, the availability of cofactors and redox homeostasis must be considered. In this review, recent advances on the engineering of cellular redox homeostasis systems to accelerate alcohol biosynthesis are summarized. Recent approaches include improving cofactor availability, manipulating the affinity of redox enzymes to specific cofactors, as well as globally controlling redox reactions, indicating the power of these approaches, and opening a path towards improving the production of a number of different industrially-relevant alcohols in the near future. © The Author(s) 2017
abstractGer	Abstract The biosynthetic pathways of most alcohols are linked to intracellular redox homeostasis, which is crucial for life. This crucial balance is primarily controlled by the generation of reducing equivalents, as well as the (reduction)-oxidation metabolic cycle and the thiol redox homeostasis system. As a main oxidation pathway of reducing equivalents, the biosynthesis of most alcohols includes redox reactions, which are dependent on cofactors such as NADH or NADPH. Thus, when engineering alcohol-producing strains, the availability of cofactors and redox homeostasis must be considered. In this review, recent advances on the engineering of cellular redox homeostasis systems to accelerate alcohol biosynthesis are summarized. Recent approaches include improving cofactor availability, manipulating the affinity of redox enzymes to specific cofactors, as well as globally controlling redox reactions, indicating the power of these approaches, and opening a path towards improving the production of a number of different industrially-relevant alcohols in the near future. © The Author(s) 2017
abstract_unstemmed	Abstract The biosynthetic pathways of most alcohols are linked to intracellular redox homeostasis, which is crucial for life. This crucial balance is primarily controlled by the generation of reducing equivalents, as well as the (reduction)-oxidation metabolic cycle and the thiol redox homeostasis system. As a main oxidation pathway of reducing equivalents, the biosynthesis of most alcohols includes redox reactions, which are dependent on cofactors such as NADH or NADPH. Thus, when engineering alcohol-producing strains, the availability of cofactors and redox homeostasis must be considered. In this review, recent advances on the engineering of cellular redox homeostasis systems to accelerate alcohol biosynthesis are summarized. Recent approaches include improving cofactor availability, manipulating the affinity of redox enzymes to specific cofactors, as well as globally controlling redox reactions, indicating the power of these approaches, and opening a path towards improving the production of a number of different industrially-relevant alcohols in the near future. © The Author(s) 2017
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title_short	Engineering redox homeostasis to develop efficient alcohol-producing microbial cell factories
url	https://dx.doi.org/10.1186/s12934-017-0728-3
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author2	Zhao, Qiuwei Li, Yin Zhang, Yanping
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up_date	2024-07-03T20:18:08.530Z
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Engineering redox homeostasis to develop efficient alcohol-producing microbial cell factories

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