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A novel aldose-aldose oxidoreductase for co-production of D-xylonate and xylitol from D-xylose with Saccharomyces cerevisiae.

Wiebe MG, Nygård Y, Oja M, Andberg M, Ruohonen L, Koivula A, Penttilä M, Toivari M - Appl. Microbiol. Biotechnol. (2015)

Bottom Line: Deletion of the gene encoding the major aldose reductase, Gre3p, did not affect xylitol production in the strain expressing Cc aaor, but decreased xylitol production in the strain expressing Zm gfor.In addition, expression of Cc aaor together with the D-xylonolactone lactonase encoding the gene xylC from C. crescentus slightly increased the final concentration and initial volumetric production rate of both D-xylonate and D-xylitol.These results suggest that C. crescentus AAOR is a novel type of oxidoreductase able to convert the single aldose substrate D-xylose to both its oxidized and reduced product.

View Article: PubMed Central - PubMed

Affiliation: VTT, Technical Research Centre of Finland Ltd., P.O. Box 1000, FI-02044 VTT, Espoo, Finland.

ABSTRACT
An open reading frame CC1225 from the Caulobacter crescentus CB15 genome sequence belongs to the Gfo/Idh/MocA protein family and has 47 % amino acid sequence identity with the glucose-fructose oxidoreductase from Zymomonas mobilis (Zm GFOR). We expressed the ORF CC1225 in the yeast Saccharomyces cerevisiae and used a yeast strain expressing the gene coding for Zm GFOR as a reference. Cell extracts of strains overexpressing CC1225 (renamed as Cc aaor) showed some Zm GFOR type of activity, producing D-gluconate and D-sorbitol when a mixture of D-glucose and D-fructose was used as substrate. However, the activity in Cc aaor expressing strain was >100-fold lower compared to strains expressing Zm gfor. Interestingly, C. crescentus AAOR was clearly more efficient than the Zm GFOR in converting in vitro a single sugar substrate D-xylose (10 mM) to xylitol without an added cofactor, whereas this type of activity was very low with Zm GFOR. Furthermore, when cultured in the presence of D-xylose, the S. cerevisiae strain expressing Cc aaor produced nearly equal concentrations of D-xylonate and xylitol (12.5 g D-xylonate l(-1) and 11.5 g D-xylitol l(-1) from 26 g D-xylose l(-1)), whereas the control strain and strain expressing Zm gfor produced only D-xylitol (5 g l(-1)). Deletion of the gene encoding the major aldose reductase, Gre3p, did not affect xylitol production in the strain expressing Cc aaor, but decreased xylitol production in the strain expressing Zm gfor. In addition, expression of Cc aaor together with the D-xylonolactone lactonase encoding the gene xylC from C. crescentus slightly increased the final concentration and initial volumetric production rate of both D-xylonate and D-xylitol. These results suggest that C. crescentus AAOR is a novel type of oxidoreductase able to convert the single aldose substrate D-xylose to both its oxidized and reduced product.

No MeSH data available.


Related in: MedlinePlus

Production of D-xylonate and xylitol in flask cultures of S. cerevisiae strains expressing aaor of C. crescentus or gfor of Z. mobilis. Medium containing D-glucose and D-xylose was buffered with CaCO3
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Fig2: Production of D-xylonate and xylitol in flask cultures of S. cerevisiae strains expressing aaor of C. crescentus or gfor of Z. mobilis. Medium containing D-glucose and D-xylose was buffered with CaCO3

Mentions: S. cerevisiae strains expressing Cc aaor or Zm gfor were grown in flasks in SC-ura medium containing 10 g D-glucose l−1, 20 g D-xylose l−1 and 10 g CaCO3 l−1. The strain expressing Cc aaor produced 12.5 g D-xylonate l−1 and 11.5 g xylitol l−1, whereas the strain expressing Zm gfor and the control strain both produced 5 g xylitol l−1 but no D-xylonate (< 1 g l−1) (Fig. 2).Fig. 2


A novel aldose-aldose oxidoreductase for co-production of D-xylonate and xylitol from D-xylose with Saccharomyces cerevisiae.

Wiebe MG, Nygård Y, Oja M, Andberg M, Ruohonen L, Koivula A, Penttilä M, Toivari M - Appl. Microbiol. Biotechnol. (2015)

Production of D-xylonate and xylitol in flask cultures of S. cerevisiae strains expressing aaor of C. crescentus or gfor of Z. mobilis. Medium containing D-glucose and D-xylose was buffered with CaCO3
© Copyright Policy - OpenAccess
Related In: Results  -  Collection

Show All Figures
getmorefigures.php?uid=PMC4628093&req=5

Fig2: Production of D-xylonate and xylitol in flask cultures of S. cerevisiae strains expressing aaor of C. crescentus or gfor of Z. mobilis. Medium containing D-glucose and D-xylose was buffered with CaCO3
Mentions: S. cerevisiae strains expressing Cc aaor or Zm gfor were grown in flasks in SC-ura medium containing 10 g D-glucose l−1, 20 g D-xylose l−1 and 10 g CaCO3 l−1. The strain expressing Cc aaor produced 12.5 g D-xylonate l−1 and 11.5 g xylitol l−1, whereas the strain expressing Zm gfor and the control strain both produced 5 g xylitol l−1 but no D-xylonate (< 1 g l−1) (Fig. 2).Fig. 2

Bottom Line: Deletion of the gene encoding the major aldose reductase, Gre3p, did not affect xylitol production in the strain expressing Cc aaor, but decreased xylitol production in the strain expressing Zm gfor.In addition, expression of Cc aaor together with the D-xylonolactone lactonase encoding the gene xylC from C. crescentus slightly increased the final concentration and initial volumetric production rate of both D-xylonate and D-xylitol.These results suggest that C. crescentus AAOR is a novel type of oxidoreductase able to convert the single aldose substrate D-xylose to both its oxidized and reduced product.

View Article: PubMed Central - PubMed

Affiliation: VTT, Technical Research Centre of Finland Ltd., P.O. Box 1000, FI-02044 VTT, Espoo, Finland.

ABSTRACT
An open reading frame CC1225 from the Caulobacter crescentus CB15 genome sequence belongs to the Gfo/Idh/MocA protein family and has 47 % amino acid sequence identity with the glucose-fructose oxidoreductase from Zymomonas mobilis (Zm GFOR). We expressed the ORF CC1225 in the yeast Saccharomyces cerevisiae and used a yeast strain expressing the gene coding for Zm GFOR as a reference. Cell extracts of strains overexpressing CC1225 (renamed as Cc aaor) showed some Zm GFOR type of activity, producing D-gluconate and D-sorbitol when a mixture of D-glucose and D-fructose was used as substrate. However, the activity in Cc aaor expressing strain was >100-fold lower compared to strains expressing Zm gfor. Interestingly, C. crescentus AAOR was clearly more efficient than the Zm GFOR in converting in vitro a single sugar substrate D-xylose (10 mM) to xylitol without an added cofactor, whereas this type of activity was very low with Zm GFOR. Furthermore, when cultured in the presence of D-xylose, the S. cerevisiae strain expressing Cc aaor produced nearly equal concentrations of D-xylonate and xylitol (12.5 g D-xylonate l(-1) and 11.5 g D-xylitol l(-1) from 26 g D-xylose l(-1)), whereas the control strain and strain expressing Zm gfor produced only D-xylitol (5 g l(-1)). Deletion of the gene encoding the major aldose reductase, Gre3p, did not affect xylitol production in the strain expressing Cc aaor, but decreased xylitol production in the strain expressing Zm gfor. In addition, expression of Cc aaor together with the D-xylonolactone lactonase encoding the gene xylC from C. crescentus slightly increased the final concentration and initial volumetric production rate of both D-xylonate and D-xylitol. These results suggest that C. crescentus AAOR is a novel type of oxidoreductase able to convert the single aldose substrate D-xylose to both its oxidized and reduced product.

No MeSH data available.


Related in: MedlinePlus