Title of article :
3-O-α-d-Glucopyranosyl-l-rhamnose phosphorylase from Clostridium phytofermentans
Author/Authors :
Takanori Nihira، نويسنده , , Hiroyuki Nakai، نويسنده , , Motomitsu Kitaoka، نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 2012
Pages :
4
From page :
94
To page :
97
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.
Keywords :
Clostridium phytofermentans , 3-O-?-d-Glucopyranosyl-l-rhamnose phosphorylase , Glycoside hydrolase family 65 , Reversible phosphorolysis
Journal title :
Carbohydrate Research
Serial Year :
2012
Journal title :
Carbohydrate Research
Record number :
967487
Link To Document :
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