EC Explorer

2.4.1.243

6^G-fructosyltransferase

[1-β-D-fructofuranosyl-(2→1)-]_m+1-α-D-glucopyranoside + [1-β-D-fructofuranosyl-(2→1)-]_n-α-D-glucopyranoside = [1-β-D-fructofuranosyl-(2→1)-]_m-α-D-glucopyranoside + [1-β-D-fructofuranosyl-(2→1)-]_n-β-D-fructofuranosyl-(2→6)-α-D-glucopyranoside (m > 0; n ≥ 0)

fructan:fructan 6^G-fructosyltransferase, 1^F(1-β-D-fructofuranosyl)m sucrose:1F(1-β-D-fructofuranosyl)nsucrose 6^G-fructosyltransferase, 6^G-FFT, 6^G-FT, 6^G-fructotransferase

1^F-oligo[β-D-fructofuranosyl-(2→1)-]sucrose 6^G-β-D-fructotransferase

79633-28-6

Inulins are polysaccharides consisting of linear or branched D-fructofuranosyl chains attached to the fructosyl residue of sucrose by a β(2→1) linkage. This enzyme catalyses the transfer of the terminal (2→1)-linked -D-fructosyl group of an inulin chain onto O-6 position of the glucose residue of another inulin molecule [1]. For example, if 1-kestose [1F-(β-D-fructofuranosyl)sucrose] is both the donor and recipient in the reaction shown above, i.e., if m = 1 and n = 1, then the products will be sucrose and 6^G-di-β-D-fructofuranosylsucrose. In this notation, the superscripts F and G are used to specify whether the fructose or glucose residue of the sucrose carries the substituent. Alternatively, this may be indicated by the presence and/or absence of primes (see http://www.chem.qmul.ac.uk/iupac/2carb/36.html#362). Sucrose cannot be a donor substrate in the reaction (i.e. m cannot be zero) and inulin cannot act as an acceptor. Side reactions catalysed are transfer of a β-D-fructosyl group between compounds of the structure 1^F-(1-β-D-fructofuranosyl)m-6^G-(1-β-D-fructofuranosyl)n sucrose, where m ≥ 0 and n = 1 for the donor, and m ≥ 0 and n ≥ 0 for the acceptor.

created 2006