Comparison of engineered Saccharomyces cerevisiae and engineered Escherichia coli for the production of an optically pure keto alcohol.
(2009) In Applied Microbiology and Biotechnology 84. p.487-497- Abstract
- In this study, the production of enantiomerically pure (1R,4S,6S)-6-hydroxy-bicyclo[2.2.2]octane-2-one ((-)-2) through stereoselective bioreduction was used as a model reaction for the comparison of engineered Saccharomyces cerevisiae and engineered Escherichia coli as biocatalysts. For both microorganisms, over-expression of the gene encoding the NADPH-dependent aldo-keto reductase YPR1 resulted in high purity of the keto alcohol (-)-2 (>99% ee, 97-98% de). E. coli had three times higher initial reduction rate but S. cerevisiae continued the reduction reaction for a longer time period, thus reaching a higher conversion of the substrate (95%). S. cerevisiae was also more robust than E. coli, as demonstrated by higher viability during... (More)
- In this study, the production of enantiomerically pure (1R,4S,6S)-6-hydroxy-bicyclo[2.2.2]octane-2-one ((-)-2) through stereoselective bioreduction was used as a model reaction for the comparison of engineered Saccharomyces cerevisiae and engineered Escherichia coli as biocatalysts. For both microorganisms, over-expression of the gene encoding the NADPH-dependent aldo-keto reductase YPR1 resulted in high purity of the keto alcohol (-)-2 (>99% ee, 97-98% de). E. coli had three times higher initial reduction rate but S. cerevisiae continued the reduction reaction for a longer time period, thus reaching a higher conversion of the substrate (95%). S. cerevisiae was also more robust than E. coli, as demonstrated by higher viability during bioreduction. It was also investigated whether the NADPH regeneration rate was sufficient to supply the over-expressed reductase with NADPH. Five strains of each microorganism with varied carbon flux through the NADPH regenerating pentose phosphate pathway were genetically constructed and compared. S. cerevisiae required an increased NADPH regeneration rate to supply YPR1 with co-enzyme while the native NADPH regeneration rate was sufficient for E. coli. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1392318
- author
- Skorupa Parachin, Nadia LU ; Carlquist, Magnus LU and Gorwa-Grauslund, Marie-Francoise LU
- organization
- publishing date
- 2009
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Applied Microbiology and Biotechnology
- volume
- 84
- pages
- 487 - 497
- publisher
- Springer
- external identifiers
-
- wos:000269180600009
- pmid:19352650
- scopus:69249222975
- pmid:19352650
- ISSN
- 1432-0614
- DOI
- 10.1007/s00253-009-1964-1
- language
- English
- LU publication?
- yes
- id
- e51ff633-8bef-495e-854b-6cccbc7af298 (old id 1392318)
- date added to LUP
- 2016-04-01 14:09:16
- date last changed
- 2022-03-29 19:23:49
@article{e51ff633-8bef-495e-854b-6cccbc7af298,
abstract = {{In this study, the production of enantiomerically pure (1R,4S,6S)-6-hydroxy-bicyclo[2.2.2]octane-2-one ((-)-2) through stereoselective bioreduction was used as a model reaction for the comparison of engineered Saccharomyces cerevisiae and engineered Escherichia coli as biocatalysts. For both microorganisms, over-expression of the gene encoding the NADPH-dependent aldo-keto reductase YPR1 resulted in high purity of the keto alcohol (-)-2 (>99% ee, 97-98% de). E. coli had three times higher initial reduction rate but S. cerevisiae continued the reduction reaction for a longer time period, thus reaching a higher conversion of the substrate (95%). S. cerevisiae was also more robust than E. coli, as demonstrated by higher viability during bioreduction. It was also investigated whether the NADPH regeneration rate was sufficient to supply the over-expressed reductase with NADPH. Five strains of each microorganism with varied carbon flux through the NADPH regenerating pentose phosphate pathway were genetically constructed and compared. S. cerevisiae required an increased NADPH regeneration rate to supply YPR1 with co-enzyme while the native NADPH regeneration rate was sufficient for E. coli.}},
author = {{Skorupa Parachin, Nadia and Carlquist, Magnus and Gorwa-Grauslund, Marie-Francoise}},
issn = {{1432-0614}},
language = {{eng}},
pages = {{487--497}},
publisher = {{Springer}},
series = {{Applied Microbiology and Biotechnology}},
title = {{Comparison of engineered Saccharomyces cerevisiae and engineered Escherichia coli for the production of an optically pure keto alcohol.}},
url = {{http://dx.doi.org/10.1007/s00253-009-1964-1}},
doi = {{10.1007/s00253-009-1964-1}},
volume = {{84}},
year = {{2009}},
}