Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Fucosyltransferase, fucosylation

Table 4. Substrate specificity of deoxygenated acceptors for a-(l->3/4)fucosyltransferase fucosylation... Table 4. Substrate specificity of deoxygenated acceptors for a-(l->3/4)fucosyltransferase fucosylation...
To overcome the synthetic and inhibition problems, an integrated recycling system is applied. GTP and Fuc-l-P are transformed by GDP-fucosyl-pyro-phosphorylase to pyrophosphate and the activated donor (GDP-Fuc) [71]. This in turn in the presence of al-3/4-fucosyltransferase fucosylates the acceptor Gal)3l-4GlcNAc at the GlcNAc-3-position or the acceptor Gal)3l-3GlcNAc at the GlcNAc-4-position. The released GDP is phosphorylated to GTP with pyruvate kinase employing the activated phosphate donor phosphenol pyruvate, which in... [Pg.34]

This class of enzymes includes galactoside 3(4)-L-fucosyl-transferase, [EC 2.4.1.65] glycoprotein 6-a-L-fucosyl-transferase [EC 2.4.1.68], galactoside 2-ce-L-fucosyltran-sferase [EC 2.4.1.69], and galactoside 3-fucosyltransferase [EC 2.4.1.152]. [Pg.303]

Galactoside 2-L-fucosyltransferase [EC 2.4.1.69], also known as blood group H a-2-fucosyltransferase, catalyzes the reaction of GDP-L-fucose with /8-D-galacto-syl-R to produce GDP and a-L-fucosyl-l,2-/3-D-galac-tosyl-R. Lactose can also act as the acceptor substrate. [Pg.306]

Fucosyltransferase in pea microsomal preparations also fucosylated exogenously-added xyloglucan acceptors in addition to endogenous primers... [Pg.23]

Several fucosyltransferases have been isolated and used for in vitro synthesis. The Lewis A al,4-fucosyltransferase transfers unnatural fucose derivatives in from their GDP esters [23]. The enzyme al,3-fiicosyltransferase has been used to L-fucosylate the 3-position of the GlcNAc of A-acetyllactosamine and of sialyl a2,3-N-acetyllactosamine [24]. Several acceptor substrates with modifications in the GlcNAc residue could also be... [Pg.490]

M. coturnix ceramide. Intriguingly, fucosylated glycolipids obtained from E. multilocularis were found to possess only short-chain fatty acids with 16 and 18 carbon atoms (mainly 0 6 0 and C18h 0), which might indicate that the (a1-3)-fucosyltransferase involved in the biosynthesis of such compounds requires an acceptor substrate with shorter fatty acids, whereas ((51 -6)-galactosyltransferase from this source obviously accepts all kinds of galacto-sylceramide precursors (Persat et al., 1992). [Pg.417]

Vanzin, G. F., Madson, M., Carpita, N. C., Raikhel, N. V, Keegstra, K., and Reiter, W. D., The mur2 mutant of Arabidopsis thaliana lacks fucosylated xyloglucan because of a lesion in fucosyltransferase AtFUTl. Proc Natl AcadSci USA 2002, 99 (5), 3340-5. [Pg.1534]

Fig. 8. Enzymatic fucosylation with integrated cofactor regeneration (Enzymes vi cf. Fig. 2, xi GDP-fucose-pyrophosphorylase, xii al-3/4-fucosyltransferase) [72]... [Pg.35]

Here again, it is as probes that carba-oligosaccharides find their best applications. Compounds 7 and 8 were both submitted to the action of a-(l-3/4)-fucosyltransferase in the presence of GDP-fucose. Only 7 was accepted and fucosylated to give the Lewis analog 9 showing that this enzyme has a different mode of action regarding the synthesis of Lewis s (Scheme 8.3) [16]. [Pg.369]

G. Formation of the fucosyl a 1,3-linkage using txl,3-fucosyltransferase without regeneration of GDP-Fuc 499... [Pg.580]


See other pages where Fucosyltransferase, fucosylation is mentioned: [Pg.376]    [Pg.376]    [Pg.23]    [Pg.282]    [Pg.319]    [Pg.320]    [Pg.320]    [Pg.322]    [Pg.491]    [Pg.202]    [Pg.109]    [Pg.310]    [Pg.412]    [Pg.640]    [Pg.646]    [Pg.34]    [Pg.169]    [Pg.583]    [Pg.1781]    [Pg.2258]    [Pg.2275]    [Pg.2276]    [Pg.2277]    [Pg.2277]    [Pg.2281]    [Pg.2283]    [Pg.2283]    [Pg.232]    [Pg.269]    [Pg.317]    [Pg.96]    [Pg.128]    [Pg.129]    [Pg.135]    [Pg.147]   


SEARCH



Fucosyl

Fucosylation

Fucosylations

Fucosyltransferase

Fucosyltransferase/fucosyl transferase

© 2024 chempedia.info