Use of site-directed mutagenesis to identify the galactosyltransferase binding sites for UDP-galactose.
Biochem Biophys Res Commun
; 206(1): 362-9, 1995 Jan 05.
Article
in En
| MEDLINE
| ID: mdl-7818542
ABSTRACT
Site-directed mutagenesis was utilized to identify binding sites for UDP-galactose in galactosyltransferase (EC 2.4.1.22). Mutant cDNAs were generated by a procedure based on PCR, and the mutated enzymes were expressed in E.coli cells. The mutant enzymes were purified by Ni-NTA Sephadex, and the degree of purification was judged by SDS-PAGE. Purified mutant GTs, F305L, P306V, N307S, N308S, showed dramatic decreases in activities in comparison with the activity of the wild-type GT. Enzyme kinetic analysis revealed that the Km values of F305L, P306V, N307S and N308S for UDP-galactose were, respectively, 9-, 11-, 50- and 20-fold higher than the Km of wild-type GT, but the Km values for manganese were not significantly different from that of the wild-type GT. The quartet mutant F305L/P306V/N307S/N308S showed no activity. From the results of this study it is concluded that amino acids, Phe-305, Pro-306, Asn-307 and Asn-308, in GT are most probably involved in GT catalysis or are located close to the UDP-galactose binding region but are not involved in the binding of manganese.
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Uridine Diphosphate Galactose
/
Lactose Synthase
Language:
En
Journal:
Biochem Biophys Res Commun
Year:
1995
Document type:
Article