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Three-pathway combination for glutathione biosynthesis in Saccharomyces cerevisiae

BACKGROUND: Glutathione (GSH), a pivotal non-protein thiol, can be biosynthesized through three pathways in different organisms: (1) two consecutive enzymatic reactions catalyzed by γ-glutamylcysteine synthetase (Gsh1 or GshA) and glutathione synthetase (Gsh2 or GshB); (2) a bifunctional γ-glutamylc...

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Autores principales: Tang, Liang, Wang, Weiwei, Zhou, Wenlong, Cheng, Kai, Yang, Yan, Liu, Minzhi, Cheng, Kedi, Wang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4574134/
https://www.ncbi.nlm.nih.gov/pubmed/26377681
http://dx.doi.org/10.1186/s12934-015-0327-0
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author Tang, Liang
Wang, Weiwei
Zhou, Wenlong
Cheng, Kai
Yang, Yan
Liu, Minzhi
Cheng, Kedi
Wang, Wei
author_facet Tang, Liang
Wang, Weiwei
Zhou, Wenlong
Cheng, Kai
Yang, Yan
Liu, Minzhi
Cheng, Kedi
Wang, Wei
author_sort Tang, Liang
collection PubMed
description BACKGROUND: Glutathione (GSH), a pivotal non-protein thiol, can be biosynthesized through three pathways in different organisms: (1) two consecutive enzymatic reactions catalyzed by γ-glutamylcysteine synthetase (Gsh1 or GshA) and glutathione synthetase (Gsh2 or GshB); (2) a bifunctional γ-glutamylcysteine synthetase/glutathione synthetase (GshF); (3) an alternative condensation of γ-glutamyl phosphate synthesized by γ-glutamyl kinase (Pro1 or ProB) with cysteine to form γ-glutamylcysteine which was further conjugated to glycine by glutathione synthetase. The Gsh1 and Gsh2 of conventional GSH biosynthetic pathway or the bifunctional GshF reported previously have been independently modulated for GSH production. This study developed a novel three-pathway combination method to improve GSH production in Saccharomyces cerevisiae. RESULTS: A bifunctional enzyme GshF of Actinobacillus pleuropneumoniae was functionally expressed in S. cerevisiae and Pro1 in proline biosynthetic pathway was exploited for improving GSH yield. Moreover, two fusion proteins Gsh2-Gsh1 and Pro1-GshB were constructed to increase the two-step coupling efficiency of GSH synthesis by mimicking the native domain fusion of GshF. The engineered strain W303-1b/FGP with three biosynthetic pathways presented the highest GSH concentration (216.50 mg/L) and GSH production of W303-1b/FGP was further improved by 61.37 % when amino acid precursors (5 mM glutamic acid, 5 mM cysteine and 5 mM glycine) were fed in shake flask cultures. In batch culture process, the recombinant strain W303-1b/FGP also kept high efficiency in GSH production and reached an intracellular GSH content of 2.27 % after 24-h fermentation. CONCLUSIONS: The engineered strains harbouring three GSH pathways displayed higher GSH producing capacity than those with individually modulated pathways. Three-pathway combinatorial biosynthesis of GSH promises more effective industrial production of GSH using S. cerevisiae. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-015-0327-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-45741342015-09-19 Three-pathway combination for glutathione biosynthesis in Saccharomyces cerevisiae Tang, Liang Wang, Weiwei Zhou, Wenlong Cheng, Kai Yang, Yan Liu, Minzhi Cheng, Kedi Wang, Wei Microb Cell Fact Research BACKGROUND: Glutathione (GSH), a pivotal non-protein thiol, can be biosynthesized through three pathways in different organisms: (1) two consecutive enzymatic reactions catalyzed by γ-glutamylcysteine synthetase (Gsh1 or GshA) and glutathione synthetase (Gsh2 or GshB); (2) a bifunctional γ-glutamylcysteine synthetase/glutathione synthetase (GshF); (3) an alternative condensation of γ-glutamyl phosphate synthesized by γ-glutamyl kinase (Pro1 or ProB) with cysteine to form γ-glutamylcysteine which was further conjugated to glycine by glutathione synthetase. The Gsh1 and Gsh2 of conventional GSH biosynthetic pathway or the bifunctional GshF reported previously have been independently modulated for GSH production. This study developed a novel three-pathway combination method to improve GSH production in Saccharomyces cerevisiae. RESULTS: A bifunctional enzyme GshF of Actinobacillus pleuropneumoniae was functionally expressed in S. cerevisiae and Pro1 in proline biosynthetic pathway was exploited for improving GSH yield. Moreover, two fusion proteins Gsh2-Gsh1 and Pro1-GshB were constructed to increase the two-step coupling efficiency of GSH synthesis by mimicking the native domain fusion of GshF. The engineered strain W303-1b/FGP with three biosynthetic pathways presented the highest GSH concentration (216.50 mg/L) and GSH production of W303-1b/FGP was further improved by 61.37 % when amino acid precursors (5 mM glutamic acid, 5 mM cysteine and 5 mM glycine) were fed in shake flask cultures. In batch culture process, the recombinant strain W303-1b/FGP also kept high efficiency in GSH production and reached an intracellular GSH content of 2.27 % after 24-h fermentation. CONCLUSIONS: The engineered strains harbouring three GSH pathways displayed higher GSH producing capacity than those with individually modulated pathways. Three-pathway combinatorial biosynthesis of GSH promises more effective industrial production of GSH using S. cerevisiae. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-015-0327-0) contains supplementary material, which is available to authorized users. BioMed Central 2015-09-16 /pmc/articles/PMC4574134/ /pubmed/26377681 http://dx.doi.org/10.1186/s12934-015-0327-0 Text en © Tang et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Tang, Liang
Wang, Weiwei
Zhou, Wenlong
Cheng, Kai
Yang, Yan
Liu, Minzhi
Cheng, Kedi
Wang, Wei
Three-pathway combination for glutathione biosynthesis in Saccharomyces cerevisiae
title Three-pathway combination for glutathione biosynthesis in Saccharomyces cerevisiae
title_full Three-pathway combination for glutathione biosynthesis in Saccharomyces cerevisiae
title_fullStr Three-pathway combination for glutathione biosynthesis in Saccharomyces cerevisiae
title_full_unstemmed Three-pathway combination for glutathione biosynthesis in Saccharomyces cerevisiae
title_short Three-pathway combination for glutathione biosynthesis in Saccharomyces cerevisiae
title_sort three-pathway combination for glutathione biosynthesis in saccharomyces cerevisiae
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4574134/
https://www.ncbi.nlm.nih.gov/pubmed/26377681
http://dx.doi.org/10.1186/s12934-015-0327-0
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