Phospho-beta-glucosidase from Fusobacterium mortiferum: Purification, cloning, and inactivation by 6-phosphoglucono-delta-lactone

Thompson, J; Robrish, SA; Bouma, CL; Freedberg, DI; Folk, JE

HERO ID

4940986

Reference Type

Journal Article

Year

1997

HERO ID 4940986
In Press No
Year 1997
Title Phospho-beta-glucosidase from Fusobacterium mortiferum: Purification, cloning, and inactivation by 6-phosphoglucono-delta-lactone
Authors Thompson, J; Robrish, SA; Bouma, CL; Freedberg, DI; Folk, JE
Journal Journal of Bacteriology
Volume 179
Issue 5
Page Numbers 1636-1645
Abstract 6-Phosphoryl-beta-D-glucopyranosyl:6-phosphoglucohydrolase (P-beta-glucosidase, EC 3.2.1.86) has been purified from Fusobacterium mortiferum. Assays for enzyme activity and results from Western immunoblots showed that P-beta-glucosidase (M(r), 53,000; pI, 4.5) was induced by growth of F. mortiferum on beta-glucosides. The novel chromogenic and fluorogenic substrates, p-nitrophenyl-beta-D-glucopyranoside-6-phosphate (pNP beta Glc6P) and 4-methylumbelliferyl-beta-D-glucopyranoside-6-phosphate (4MU beta Glc6P), respectively, were used for the assay of P-beta-glucosidase activity. The enzyme hydrolyzed several P-beta-glucosides, including the isomeric disaccharide phosphates cellobiose-6-phosphate, gentiobiose-6-phosphate, sophorose-6-phosphate, and laminaribiose-6-phosphate, to yield glucose-6-phosphate and appropriate aglycons. The kinetic parameters for each substrate are reported. P-beta-glucosidase from F. mortiferum was inactivated by 6-phosphoglucono-delta-lactone (P-glucono-delta-lactone) derived via oxidation of glucose 6-phosphate. The pbgA gene that encodes P-beta-glucosidase from F. mortiferum has been cloned and sequenced. The first 42 residues deduced from the nucleotide sequence matched those determined for the N terminus by automated Edman degradation of the purified enzyme. From the predicted sequence of 466 amino acids, two catalytically important glutamyl residues have been identified, Comparative alignment of the amino acid sequences of P-beta-glucosidase from Escherichia coli and F. mortiferum indicates potential binding sites for the inhibitory P-glucono-delta-lactone to the enzyme from F. mortiferum.
Doi 10.1128/jb.179.5.1636-1645.1997
Wosid WOS:A1997WP41500028
Is Certified Translation No
Dupe Override 4940986
Is Public Yes