Autodisplay of active sorbitol dehydrogenase (SDH) yields a whole cell biocatalyst for the synthesis of rare sugars
J Jose, S von Schwichow - Chembiochem, 2004 - Wiley Online Library
J Jose, S von Schwichow
Chembiochem, 2004•Wiley Online LibraryWhole cell biocatalysts are attractive technological tools for the regio‐and enantioselective
synthesis of products, especially from substrates with several identical reactive groups. In
the present study, a whole cell biocatalyst for the synthesis of rare sugars from polyalcohols
was constructed. For this purpose, sorbitol dehydrogenase (SDH) from Rhodobacter
sphaeroides, a member of the short‐chain dehydrogenase/reductase (SDR) family, was
expressed on the surface of Escherichia coli using Autodisplay. Autodisplay is an efficient …
synthesis of products, especially from substrates with several identical reactive groups. In
the present study, a whole cell biocatalyst for the synthesis of rare sugars from polyalcohols
was constructed. For this purpose, sorbitol dehydrogenase (SDH) from Rhodobacter
sphaeroides, a member of the short‐chain dehydrogenase/reductase (SDR) family, was
expressed on the surface of Escherichia coli using Autodisplay. Autodisplay is an efficient …
Abstract
Whole cell biocatalysts are attractive technological tools for the regio‐ and enantioselective synthesis of products, especially from substrates with several identical reactive groups. In the present study, a whole cell biocatalyst for the synthesis of rare sugars from polyalcohols was constructed. For this purpose, sorbitol dehydrogenase (SDH) from Rhodobacter sphaeroides, a member of the short‐chain dehydrogenase/reductase (SDR) family, was expressed on the surface of Escherichia coli using Autodisplay. Autodisplay is an efficient surface display system for Gram‐negative bacteria and is based on the autotransporter secretion pathway. Transport of SDH to the outer membrane was monitored by SDS‐PAGE and Western blotting of different cell fractions. The surface exposure of the enzyme could be verified by immunofluorescence microscopy and fluorescence activated cell sorting (FACS). The activity of whole cells displaying SDH at the surface was determined in an optical test. Specific activities were found to be 12 mU per 3.3×108 cells for the conversion of D‐glucitol (sorbitol) to D‐fructose, 7 mU for the conversion D‐galactitol to D‐tagatose, and 17 mU for the conversion of L‐arabitol to L‐ribulose. The whole cell biocatalyst obtained by surface display of SDH could also produce D‐glucitol from D‐fructose (29 mU per 3.3×108 cells).
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