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1 lactose by constitutively expressing alpha-L-fucosidase.
2 iles of N-glycans enzymatically treated with fucosidase.
3 es carrying a BODIPY fluorophore for alpha-l-fucosidase.
4 ctosidase, alpha-L-arabinosidase and alpha-L-fucosidase.
5 c) or by pretreatment of cells with alpha1-2 fucosidase.
6 d molecules, fucose metabolism and two alpha-fucosidases.
7 cattering in contrast to reported multimeric fucosidases.
8 mbrane-bound beta-glucosidases and two alpha-fucosidases.
9 ansferase 4 (FUT4) and downregulated alpha-L-fucosidase 1 (FUCA1) gene expression, while sialofucosyl
10 can degradation via the glycosidase, alpha-l-fucosidase 1 (FUCA1), which removes fucose from glycans.
11 found that the vaccine is first processed by fucosidase 1 in the early endosome of dendritic cells to
12 ion of HMO-bound fucose and the abundance of fucosidase (a bacterial gene that digests fucose moietie
13  To improve upon previous assays for alpha-l-fucosidase, a fluorescence based immunoassay was produce
14       AXY8 was identified to encode an alpha-fucosidase acting on XyG that was previously designated
15 rans-beta-galactosidase (but not trans-alpha-fucosidase) activities that graft sugar residues from on
16 ctosidase (BGAL) variants with enhanced beta-fucosidase activity (tenfold increase in k(cat)/K(M) in
17 me to visualize and locate lysosomal alpha-l-fucosidase activity in human cells.
18                                      Alpha-L-fucosidase (ALF) is an exoglycosidase that is involved i
19 ase that also shows beta-galactosidase, beta-fucosidase, alpha-arabinofuranosidase, and alpha-arabino
20 ltaL YA constitutively co-expressing alpha-L-fucosidase and a red fluorescence protein (RFP) exhibite
21  potential fine specificities of an alpha1-2-fucosidase and an alpha2-3,6,8-neuraminidase.
22 two species by virtue of production of alpha-fucosidase and glyoxylic acid positivity.
23 lity of [(14)C]fucosylated AGPs to alpha(1,2)fucosidase, and not to alpha(1,3/4)fucosidase, indicated
24         However, unlike in Arabidopsis, both fucosidases are likely cytosolic.
25 d be explained if cytosolic xyloglucan alpha-fucosidases are the ancestral state in angiosperms, with
26        Lactobacillus casei produces an alpha-fucosidase, called AlfC, with specificity towards alpha(
27                                        Alpha-fucosidases comprise a large enzyme family that recogniz
28 e calibration curves for quantifying alpha-l-fucosidase concentrations in both PBS and human blood se
29                 Cell-attached sialidases and fucosidases displayed mucin-binding and their inhibition
30 agenomic data, we predict that extracellular fucosidases encoded by co-existing members such as Rumin
31 sylation of glycoproteins using alpha(1-3,4)-fucosidase, endo-beta-galactosidase, and PNGase F disrup
32 glycoside hydrolase family 29 (GH29) alpha-L-fucosidase from plant pathogenic fungus Fusarium gramine
33              The DNA sequence of the evolved fucosidase gene showed 13 base changes, resulting in six
34                                          The fucosidase had significantly lower action where sialic a
35                                  The evolved fucosidase has a 10- to 20-fold increased kcat/Km for th
36                         Detection of alpha-l-fucosidase has been shown to have relevance in diagnosin
37                 Although the use of specific fucosidases has been successfully employed for assigning
38 osidase SpGH92, we anticipate that the alpha-fucosidases identified here will be important factors in
39 y8 gave unique insights into the role of the fucosidase in XyG metabolism in vivo.
40 s host glycans and the likely roles of alpha-fucosidases in this.
41 due E274 of the Lactobacillus casei alpha1,6-fucosidase, including E274A, E274S, and E274G, acted as
42 alpha(1,2)fucosidase, and not to alpha(1,3/4)fucosidase, indicated that an alpha(1,2) linkage is form
43 in the development of fucosyltransferase and fucosidase inhibitors.
44  catalytic base and shares similarity with L-fucosidases/L-galactosidases of family GH95.
45        In addition, Bifidobacterium alpha1,2-fucosidase may promote Bifidobacterium adhesion to the m
46                                 Furthermore, fucosidase-mediated defucosylation of xyloglucan, but no
47 tructural analyses revealed an unprecedented fucosidase modular arrangement and explained the sialyl
48  an enzymatic transfucosylation with a novel fucosidase mutant, which was shown to be able to use mod
49 osaccharides but were unable to complement a fucosidase mutant.
50 trate specificity revealed that the alpha1,6-fucosidase mutants could introduce an alpha1,6-fucose mo
51                  Late-stage treatment with a fucosidase or sialidase to remove blocking fucosides or
52 r CHO and COS), pBK-RSV-tyrosinase, and pCP4-fucosidase plasmids, respectively, by electroporation in
53  alpha-xylosidase, beta-galactosidase, alpha-fucosidase, soluble beta-glucosidase and GPI-anchored be
54 e showed a 66-fold increase in p-nitrophenyl fucosidase specific activity.
55 noassay was produced implementing an alpha-l-fucosidase specific antibody (FUCA2).
56            The immobilization of the alpha-l-fucosidase-specific antibody onto a quartz slide was inv
57  when systemic cells were treated with alpha-fucosidase, suggesting that the GlcNAc beta 1-4GlcNAc mo
58 screening enabled the identification of beta-fucosidases that are significantly more active (180-fold
59 cteroides thetaiotaomicron produces multiple fucosidases that cleave fucose from host glycans, result
60 0 amino acids were constructed as artificial fucosidases that exhibit selective carbohydrate cleavage
61                      Fucosyltransferases and fucosidases, the main enzymes involved in the incorporat
62 mon feature shared by several bacterial GH29 fucosidases to various extents.
63 L-fucose, which we confirmed by showing that fucosidase-treated cells, largely, failed to activate co
64                                              Fucosidase treatment of T84 cells resulted in significan
65 D-galactosidase, beta-D-galactosidase, alpha-fucosidase, trypsin-like activity, and chymotrypsin was
66 of a glycoside hydrolase family GH29 alpha-L-fucosidase unveiling a Michaelis (ES) complex in a (1)C(
67                            An efficient beta-fucosidase was evolved by DNA shuffling from the Escheri
68  and an immunoassay for detection of alpha-l-fucosidase was produced.
69  most closely resembles inverting GH95 alpha-fucosidase, which displays the highest specificity with