Engineering Hexuronic Acid Catabolism
| AUTHOR | Dantas Hugo |
| PUBLISHER | LAP Lambert Academic Publishing (08/06/2014) |
| PRODUCT TYPE | Paperback (Paperback) |
Description
Metabolic engineering targets for the production of high-value compounds. Citrus peel is produced 15,000,000 t per year worldwide causing environmental problems. Its main constituent is D-galacturonic acid and can be converted to useful chemicals using genetically engineered strains. Engineered Aspergillus niger were used in solid and submerged state fermentation to convert orange peel to L-galactonate in a consolidate process. The gaaB coding for L-galactonate dehydrogenase was deleted ( gaaB) and ii) the gaaB was deleted and the gaaA coding for D-galacturonate reductase was overexpressed ( gaaB-gaaA). gaaB was able to convert up to 87 % of D-galacturonic acid to L-galactonate. Also, in this work, the eukaryotic D-Glucuronic acid pathway was studied. A decarboxylase that converts 3-keto-L-gulonate to L-xylulose remains poorly characterized and the gene is not known. A coupled enzyme assay was used to detect its activity. In the assay, ammonium sulfate precipitates from bovine liver extract were coupled with engineered L-gulonate-3-dehydrogenase and L-xylulose reductase. A 3-keto-L-gulonate decarboxylase activity could not be detected."
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Product Format
Product Details
ISBN-13:
9783659580345
ISBN-10:
3659580341
Binding:
Paperback or Softback (Trade Paperback (Us))
Content Language:
English
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Page Count:
68
Carton Quantity:
104
Product Dimensions:
6.00 x 0.16 x 9.00 inches
Weight:
0.25 pound(s)
Feature Codes:
Illustrated
Country of Origin:
US
Subject Information
BISAC Categories
Science | Life Sciences - Microbiology
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publisher marketing
Metabolic engineering targets for the production of high-value compounds. Citrus peel is produced 15,000,000 t per year worldwide causing environmental problems. Its main constituent is D-galacturonic acid and can be converted to useful chemicals using genetically engineered strains. Engineered Aspergillus niger were used in solid and submerged state fermentation to convert orange peel to L-galactonate in a consolidate process. The gaaB coding for L-galactonate dehydrogenase was deleted ( gaaB) and ii) the gaaB was deleted and the gaaA coding for D-galacturonate reductase was overexpressed ( gaaB-gaaA). gaaB was able to convert up to 87 % of D-galacturonic acid to L-galactonate. Also, in this work, the eukaryotic D-Glucuronic acid pathway was studied. A decarboxylase that converts 3-keto-L-gulonate to L-xylulose remains poorly characterized and the gene is not known. A coupled enzyme assay was used to detect its activity. In the assay, ammonium sulfate precipitates from bovine liver extract were coupled with engineered L-gulonate-3-dehydrogenase and L-xylulose reductase. A 3-keto-L-gulonate decarboxylase activity could not be detected."
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