Back to Search
Start Over
3-O-α-d-Glucopyranosyl-l-rhamnose phosphorylase from Clostridium phytofermentans
- Source :
- Carbohydrate Research. 350:94-97
- Publication Year :
- 2012
- Publisher :
- Elsevier BV, 2012.
-
Abstract
- We found an unreported activity of phosphorylase catalyzed by a protein (Cphy1019) belonging to glycoside hydrolase family 65 (GH65) from Clostridium phytofermentans. The recombinant Cphy1019 produced in Escherichia coli did not phosphorolyze α-linked glucobioses, such as trehalose (α1-α1), kojibiose (α1-2), nigerose (α1-3), and maltose (α1-4), which are typical substrates for GH65 enzymes. In reverse phosphorolysis, Cphy1019 utilized only l-rhamnose as the acceptor among various sugars examined with β-d-glucose 1-phosphate as the donor. The reaction product was determined to be 3-O-α-d-glucopyranosyl-l-rhamnose, indicating strict α1-3 regioselectivity. We propose 3-O-α-d-glucopyranosyl-l-rhamnose: phosphate β-d-glucosyltransferase as the systematic name and 3-O-α-d-glucopyranosyl-l-rhamnose phosphorylase as the short name for this novel GH65 phosphorylase.
- Subjects :
- Kojibiose
Phosphorylases
Rhamnose
Nigerose
Disaccharides
Biochemistry
Substrate Specificity
Analytical Chemistry
chemistry.chemical_compound
Glycogen phosphorylase
Glycoside hydrolase
Phosphorolysis
Clostridium
biology
Organic Chemistry
Temperature
Stereoisomerism
General Medicine
Maltose
Hydrogen-Ion Concentration
Clostridium phytofermentans
biology.organism_classification
Kinetics
chemistry
Glucosyltransferases
Subjects
Details
- ISSN :
- 00086215
- Volume :
- 350
- Database :
- OpenAIRE
- Journal :
- Carbohydrate Research
- Accession number :
- edsair.doi.dedup.....6efae024ae29716ac54228627ccc70b6
- Full Text :
- https://doi.org/10.1016/j.carres.2011.12.019