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1 ucan oligosaccharides was not accompanied by transglycosylation.
2 ssible pyrimidine nucleosides and subsequent transglycosylation.
3 ing to residual activities of hydrolysis and transglycosylation.
4 dioactive oligosaccharide-to-oligosaccharide transglycosylation.
5 ctive in general than the Endo-S mutants for transglycosylation.
6 c acceptor toward some endoglycosynthases in transglycosylation.
7 y but are able to take glycan oxazolines for transglycosylation.
8 o enzymatic activities, transpeptidation and transglycosylation.
9 t favored nonfucosylated GlcNAc acceptor for transglycosylation.
10 implying the presence of enzymes that favour transglycosylation.
11  the enzymatic synthesis of disaccharides by transglycosylation.
12 N322Q was much more efficient than N322A for transglycosylation.
13 osidase despite its lower activity caused by transglycosylation.
14 to act as critical catalytic residues in the transglycosylation.
15 ers using a tandem endoglycosidase-catalyzed transglycosylation.
16 duct as well as to its enhanced activity for transglycosylation.
17 e the high-mannose-type glycan oxazoline for transglycosylation.
18 structure in the resulting glycoprotein upon transglycosylation.
19  synthesis in S. aureus by interference with transglycosylation.
20 ting molecular grafting during integrational transglycosylation.
21 ylation whereas they inhibited restructuring transglycosylation.
22  the lac operon, is the preferred product of transglycosylation.
23 alytic mechanism, substrate specificity, and transglycosylation acceptor specificity of guinea pig li
24                    Additionally, it also has transglycosylation activities on lactose, lactulose, mal
25 e resulting mutants for their hydrolysis and transglycosylation activities.
26                    These mutants possess the transglycosylation activity but lack the hydrolytic acti
27 ites -2, -3 and +2 and showed an increase in transglycosylation activity compared with the wild type.
28 that lacks hydrolytic activity but possesses transglycosylation activity for glycoengineering.
29                 These data indicate that the transglycosylation activity of CBG derives from the form
30  report here our study on the hydrolytic and transglycosylation activity of recombinant Endo-D and it
31 g the 2-position could have an impact on the transglycosylation activity of several GHs.
32                                          The transglycosylation activity of the endo-beta-N-acetylglu
33 lycoproteins was described that explores the transglycosylation activity of the endo-beta-N-acetylglu
34    This finding, coupled with the remarkable transglycosylation activity of the EndoS glycosynthase m
35  different properties, some possessed potent transglycosylation activity with diminished hydrolysis a
36  glycosynthases that demonstrated remarkable transglycosylation activity with only marginal or no pro
37                        Endo-D also possesses transglycosylation activity with sugar oxazoline as the
38 nt variants that are unable to dimerize lack transglycosylation activity, but are still able to induc
39 ci holds that peptidoglycan synthesis (i.e., transglycosylation and cross-linking) is restricted spat
40 ntrolling the balance between hydrolysis and transglycosylation and driving the elongation of beta(1-
41 at residues implicated in the enhancement of transglycosylation and synthetic capacity are proximal t
42  catalytic steps involving glycosylation and transglycosylation, and four noncatalytic steps involvin
43  a broad substrate specificity of Endo-A for transglycosylation, and the chemoenzymatic method descri
44 ndoglycosidase-catalyzed deglycosylation and transglycosylation approach is emerging as a promising p
45 e-transfer steps preceding glycosylation and transglycosylation are the main reason for the remarkabl
46 ylation, using the endoglycosidase-catalyzed transglycosylation as the key reaction.
47                                 The RNA-TAG (transglycosylation at guanosine) is carried out by a bac
48 ptibility of these enzymes to inhibition and transglycosylation at high glucose or cellobiose concent
49  and vancomycin are comparable inhibitors of transglycosylation, but that oritavancin is a more poten
50          To elucidate the molecular basis of transglycosylation by MalQ, we have determined three cry
51 uated as substrates for the Endo-A-catalyzed transglycosylation by use of ribonuclease B as a model s
52 ue that both integrational and restructuring transglycosylation can contribute to both wall-assembly
53 specificities, active site organization, and transglycosylation capacity.
54 terminus, was able to serve as acceptors for transglycosylation catalyzed by Endo-A and EndoM-N175A.
55 tadynamics simulations, that it is tuned for transglycosylation (DeltaG() = 12 kcal/mol).
56                                 It catalyzes transglycosylation/disproportionation reactions in which
57 everal mutants showed significantly enhanced transglycosylation efficiency over the wild type enzyme.
58 sn or alpha1,6-fucosyl-GlcNAc-polypeptide in transglycosylation, enabling a highly convergent synthes
59 of TDP-desosamine was also demonstrated in a transglycosylation experiment.
60                            The importance of transglycosylation for cell wall assembly is thus firmly
61 apshots" of substrate binding and hydrolysis/transglycosylation giving the first insights into the me
62  of knowledge about the molecular details of transglycosylation hampers the rational design of TGs.
63                  We measured remarkably high transglycosylation:hydrolysis ratios under optimized con
64 sm of action of oritavancin is inhibition of transglycosylation (important in peptidoglycan synthesis
65 t control the balance between hydrolysis and transglycosylation in these enzymes are not understood.
66 irst experimental evidence for restructuring transglycosylation in vivo.
67 ntennary glycan oxazolines as substrates for transglycosylation, in contrast to previously reported e
68  complex N-glycan oxazoline as substrate for transglycosylation, indicating their strict substrate sp
69 s at least 3 known mechanisms: inhibition of transglycosylation, inhibition of transpeptidation, and
70 rence in vivo of two types of interpolymeric transglycosylation: "integrational" (in which a newly se
71                             Its capacity for transglycosylation is a factor in this activation.
72 of peptidoglycan synthesis via inhibition of transglycosylation is common to all glycopeptides (vanco
73 emarkable in predominantly catalysing hetero-transglycosylation: its preferred donor substrates (cell
74                                    This slow transglycosylation may provide a mechanism in vivo for f
75 carbose-derived decasaccharide by a two-step transglycosylation mechanism.
76 to-oligosaccharides except maltose for which transglycosylation nonetheless dominated across a range
77             This confirms that restructuring transglycosylation occurred between pairs of previously
78 1-->4) > (1-->2) > (1-->6)] with significant transglycosylation occurring in the early stages of the
79                                   With time, transglycosylation occurs, generating (GlcNAc)8 from the
80                                              Transglycosylation of galactomannan from the membrane to
81 the present study, a novel in situ enzymatic transglycosylation of stevioside has been developed by p
82                 The results confirm that the transglycosylation of stevioside led to an enrichment in
83 rmined the minimal sequence requirements for transglycosylation of unmodified DNA by E. coli TGT.
84 are enzymes that catalyze the hydrolysis and transglycosylation of xyloglucan polymers in plant cell
85 r three proteins are capable of carrying out transglycosylation of xyloglucans.
86 (a) polysaccharide-to-[(3) H]oligosaccharide transglycosylation or (b) non-radioactive oligosaccharid
87 cells, either via direct re-incorporation by transglycosylation or via internalization and metabolic
88 duct assisted" molecular mechanism favouring transglycosylation over hydrolysis.
89 were tested in rutinosylation of tyrosol via transglycosylation process from rutin.
90                 Kinetic study shows that the transglycosylation reaction follows a sequential mechani
91                       The enzyme catalyzes a transglycosylation reaction in which guanine is eliminat
92 EC 2.4.2.29) catalyzes a posttranscriptional transglycosylation reaction involved in the incorporatio
93 -981 and Asn-1029 significantly affected the transglycosylation reaction, indicating their essential
94                   The alpha1,2FT catalyzes a transglycosylation reaction, resulting in syntheses of t
95 ase for the 4-OH of GlcNAc to facilitate the transglycosylation reaction.
96 , forming new polymers through non-enzymatic transglycosylation reactions (TGRs).
97 rmediate and that the specificity of CBG for transglycosylation reactions is different from its speci
98 Kinetic studies revealed that correction for transglycosylation reactions is necessary to derive corr
99  provided evidence that transpeptidation and transglycosylation reactions occur in pathogenic Chlamyd
100 density increase suggests that restructuring transglycosylation reactions occurred between the now wa
101 g peptidoglycan via the transpeptidation and transglycosylation reactions of cell wall synthesis, gen
102              CBG also catalyzes a variety of transglycosylation reactions, which have been been shown
103 yuridine via acid catalyzed anomerization or transglycosylation reactions.
104 sugar chains through glycosynthase-catalyzed transglycosylation reactions.
105  binding through hydrolysis, condensation or transglycosylation reactions.
106 ly (11 and 16 kcal/mol for glycosylation and transglycosylation, respectively) and alters the conform
107 ctly with bacterial proteins involved in the transglycosylation step of cell wall biosynthesis.
108                                          The transglycosylation step of cell wall synthesis is a prim
109 ed a set of small molecules that inhibit the transglycosylation step of peptidoglycan synthesis to di
110 Consequently, daptomycin did not inhibit the transglycosylation step of PG biosynthesis.
111               We describe the improvement of transglycosylation (TG) by chitinase D from Serratia pro
112 sidues and a novel endoglycosidase-catalyzed transglycosylation that simultaneously added two N-glyca
113                        During the process of transglycosylation, the quencher-appended polyprenol is
114 N-glycans to Fc-GlcNAc antibody for in vitro transglycosylation to generate homogeneous antibodies wi
115 hydrolysis was also accompanied by extensive transglycosylation to give transitory accumulations of h
116 isotope internal standard was synthesized by transglycosylation using a recombinant alpha-amylase.
117 still able to catalyze N-glycan synthesis by transglycosylation using activated oxazoline donors.
118 nthesized as a novel prebiotic candidate via transglycosylation using recombinant amylomaltase (AMase
119 IgG1-Fc through an endoglycosidase-catalyzed transglycosylation, using sugar oxazolines as the donor
120              It was found that the enzymatic transglycosylation was efficient with native GlcNAc-cont
121 ion to our molecular model for Dfg5-mediated transglycosylation, we provide a rationale for how GPI-C
122                                    To detect transglycosylation, we shifted heavy rose cells into lig
123  some of the glycosyl linkages formed during transglycosylation were (1-->6)-beta.
124 rates for XETs) did not affect integrational transglycosylation whereas they inhibited restructuring
125 ar oxazoline as the donor substrate, but the transglycosylation yield is low due to enzymatic hydroly

 
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