Measurement of crude-cell-extract glycerol dehydratase activity in recombinant Escherichia coli using coupled-enzyme reactions.

Citation data:

Journal of industrial microbiology & biotechnology, ISSN: 1476-5535, Vol: 44, Issue: 3, Page: 477-488

Publication Year:
2017
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Repository URL:
http://scholarworks.unist.ac.kr/handle/201301/22217
PMID:
28093656
DOI:
10.1007/s10295-017-1902-7
Author(s):
Sankaranarayanan, Mugesh; Seol, Eunhee; Kim, Yeonhee; Chauhan, Ashish Singh; Park, Sunghoon
Publisher(s):
Springer Nature; SPRINGER HEIDELBERG
Tags:
Biochemistry, Genetics and Molecular Biology; Immunology and Microbiology; Glycerol dehydratase (GDHt); Enzyme activity Coupled enzyme; α-ketoglutaric semialdehyde dehydrogenase; Yeast-alcohol dehydrogenase; Real-time monitoring; Crude-cell extract
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article description
Glycerol dehydratase (GDHt), which converts glycerol to 3-hydroxypropionaldehyde, is essential to the production of 1,3-propanediol (1,3-PDO) or 3-hydroxypropionic acid (3-HP). A reliable GDHt activity assay in crude-cell extract was developed. In the assay, GDHt converted 1,2-propanediol (1,2-PDO) to propionaldehyde, which was further converted to 1-propionic acid by aldehyde dehydrogenase (KGSADH) or to 1-propanol by yeast-alcohol dehydrogenase (yADH), while the NADH concentration change was monitored spectrophotometrically. Cells should be disintegrated by Bead Beater/French Press, not by chemical methods (BugBuster/B-PER™), because the reagents significantly inactivated GDHt and coupling enzymes. Furthermore, in the assay mixture, a much higher activity of KGSADH (>200-fold) or yADH (>400-fold) than that of GDHt should have been maintained. Under optimal conditions, both KGSADH and yADH showed practically the same activity. The coupled-enzyme assay method established here should prove to be applicable to recombinant strains developed for the production of 3-HP and/or 1,3-PDO from glycerol.