@article { ISI:000269655600014,
	title = {Mechanistic Analysis of the Blood Group Antigen-Cleaving endo-beta-Galactosidase from Clostridium perfringens},
	journal = {BIOCHEMISTRY},
	volume = {48},
	number = {35},
	year = {2009},
	month = {SEP 8},
	pages = {8396-8404},
	abstract = {The A and B antigens are of vital importance in blood transfusion and organ transplantation. The specificity of EABase, ail endo-beta-galactosidase from C. perfringens, toward the cleavage of A and B trisaccharides from glycoconjugates is unique and holds significant potential for use in modifying blood group antigens on cell surfaces, The mechanism of this enzyme and others in its family (GH98) and the identities of its catalytic residues have not previously been experimentally determined. Direct H-1 NMR analysis of the hydrolysis of a synthetic substrate, DNP-beta-A-trisaccharide, by EABase revealed that EABase is an inverting endo-beta-galactosidase. Both activated and nonactivated substrates were used to kinetically characterize EABase and its mutants (E354A, D429A, D453A, E467A, and E506A) at pH 6.0, 37 degrees C. Hydrolysis of DNP-beta-A-trisaccharide by EABase follows normal Michaelis-Menten kinetics with an apparent K-M of 64 +/- 3 mu M and a k(cat) of 105 +/- 5 min(-1). Mutation of two putative active site residues, D453 and E506, to alanine resulted in complete loss of activity, strongly suggesting that one or both of these residues functions as the base catalyst. The kinetic data also strongly suggest that E354 is the acid catalyst since the activity of the E354A mutant with nonactivated natural substrates is 1100-fold lower than that of the wild type enzyme, while its activity is only 10-fold lower when assayed with an activated aryl glycoside substrate DNP-beta-A-trisaccharide). Further Support is obtained through comparison of pH profiles for the wild type and E354A mutants: mutation of the acid catalyst eliminates the basic limb from the bell-shaped pH-dependence of k(cat)/K-M seen for the wild type enzyme.},
	issn = {0006-2960},
	doi = {10.1021/bi900991h},
	author = {Shaikh, Fathima Aidha and Randriantsoa, Mialy and Withers, Stephen G.}
}
