Improved polyhydroxybutyrate production by Saccharomyces cerevisiae through the use of the phosphoketolase pathway1. Issue 8 (26th March 2013)
- Record Type:
- Journal Article
- Title:
- Improved polyhydroxybutyrate production by Saccharomyces cerevisiae through the use of the phosphoketolase pathway1. Issue 8 (26th March 2013)
- Main Title:
- Improved polyhydroxybutyrate production by Saccharomyces cerevisiae through the use of the phosphoketolase pathway1
- Authors:
- Kocharin, Kanokarn
Siewers, Verena
Nielsen, Jens - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The metabolic pathways of the central carbon metabolism in <italic>Saccharomyces cerevisiae</italic> are well studied and consequently <italic>S. cerevisiae</italic> has been widely evaluated as a cell factory for many industrial biological products. In this study, we investigated the effect of engineering the supply of precursor, acetyl‐CoA, and cofactor, NADPH, on the biosynthesis of the bacterial biopolymer polyhydroxybutyrate (PHB), in <italic>S. cerevisiae</italic>. Supply of acetyl‐CoA was engineered by over‐expression of genes from the ethanol degradation pathway or by heterologous expression of the phophoketolase pathway from <italic>Aspergillus nidulans</italic>. Both strategies improved the production of PHB. Integration of <italic>gapN</italic> encoding NADP<sup>+</sup>‐dependent glyceraldehyde‐3‐phosphate dehydrogenase from <italic>Streptococcus mutans</italic> into the genome enabled an increased supply of NADPH resulting in a decrease in glycerol production and increased production of PHB. The strategy that resulted in the highest PHB production after 100 h was with a strain harboring the phosphoketolase pathway to supply acetyl‐CoA without the need of increased NADPH production by <italic>gapN</italic> integration. The results from this study imply that during the exponential growth on glucose, the biosynthesis of PHB in <italic>S. cerevisiae</italic> is likely to be limited by the supply<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The metabolic pathways of the central carbon metabolism in <italic>Saccharomyces cerevisiae</italic> are well studied and consequently <italic>S. cerevisiae</italic> has been widely evaluated as a cell factory for many industrial biological products. In this study, we investigated the effect of engineering the supply of precursor, acetyl‐CoA, and cofactor, NADPH, on the biosynthesis of the bacterial biopolymer polyhydroxybutyrate (PHB), in <italic>S. cerevisiae</italic>. Supply of acetyl‐CoA was engineered by over‐expression of genes from the ethanol degradation pathway or by heterologous expression of the phophoketolase pathway from <italic>Aspergillus nidulans</italic>. Both strategies improved the production of PHB. Integration of <italic>gapN</italic> encoding NADP<sup>+</sup>‐dependent glyceraldehyde‐3‐phosphate dehydrogenase from <italic>Streptococcus mutans</italic> into the genome enabled an increased supply of NADPH resulting in a decrease in glycerol production and increased production of PHB. The strategy that resulted in the highest PHB production after 100 h was with a strain harboring the phosphoketolase pathway to supply acetyl‐CoA without the need of increased NADPH production by <italic>gapN</italic> integration. The results from this study imply that during the exponential growth on glucose, the biosynthesis of PHB in <italic>S. cerevisiae</italic> is likely to be limited by the supply of NADPH whereas supply of acetyl‐CoA as precursor plays a more important role in the improvement of PHB production during growth on ethanol. Biotechnol. Bioeng. 2013; 110: 2216–2224. © 2013 Wiley Periodicals, Inc.</p> </abstract> … (more)
- Is Part Of:
- Biotechnology and bioengineering. Volume 110:Issue 8(2013:Aug.)
- Journal:
- Biotechnology and bioengineering
- Issue:
- Volume 110:Issue 8(2013:Aug.)
- Issue Display:
- Volume 110, Issue 8 (2013)
- Year:
- 2013
- Volume:
- 110
- Issue:
- 8
- Issue Sort Value:
- 2013-0110-0008-0000
- Page Start:
- 2216
- Page End:
- 2224
- Publication Date:
- 2013-03-26
- Subjects:
- Biotechnology -- Periodicals
Bioengineering -- Periodicals
660.6 - Journal URLs:
- http://onlinelibrary.wiley.com/doi/10.1002/bip.v101.5/issuetoc ↗
http://www.interscience.wiley.com ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/bit.24888 ↗
- Languages:
- English
- ISSNs:
- 0006-3592
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2089.850000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3006.xml