How inverting β-1,4-galactosyltransferase-1 can quench a high charge of the by-product UDP3− in catalysis: a QM/MM study of enzymatic reaction with native and UDP-5′ thio galactose substrates

• Published in: Organic & biomolecular chemistry Vol. 18; no. 38; pp. 7585 - 7596
• Main Author: Kóňa, J
• Format: Journal Article
• Language: English
• Published: Cambridge Royal Society of Chemistry 14.10.2020
• Subjects: Byproducts; Catalysis; Energy; Enzymes; Galactose; Molecular modelling; Molecular orbitals; Substrates
• ISSN: 1477-0520; 1477-0539; 1477-0539
• DOI: 10.1039/d0ob01490g

The catalysis of inverting glycosyltransferases consists of several biophysical and biochemical processes during which the transfer of a sugar residue from the purine phosphate donor substrate to an acceptor substrate occurs with stereo-inversion of the anomeric C1 center at a product. During catalysis a highly charged phosphate by-product (UDP3−) is formed and a mechanism of how the enzyme stabilizes it back to the UDP2− form is not known. Using methods of molecular modeling (hybrid DFT-QM/MM calculations) we proposed and validated a catalytic mechanism of bovine inverting β-1,4-galactosyltransferase-1 (β4Gal-T1) with native (UDP-galactose) and thio donor substrates (UDP-5′ thio galactose). We focused on three aspects of the mechanism not yet investigated: (i) the formation of an oxocarbenium ion intermediate, which was only found for the retaining glycosyltransferases for the time being; (ii) the mechanism of stabilization of a highly charged phosphate by-product (UDP3−) back to its standard in vivo form (UDP2−); (iii) explanation for why in experimental measurements the rate of catalysis with the thio donor substrate is only 8% of the rate of that with the natural substrate. To understand the differences in the interaction patterns between the complexes enzyme : UDP-Gal and enzyme : UDP-5S-Gal, fragmented molecular orbital (FMO) decomposition energy analysis was carried out at the DFT level.