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pyridylaminated beta-(1,4)-xylotriose + UDP-D-xylose
pyridylaminated beta-(1,4)-xylotetraose + UDP
-
-
-
-
?
UDP-D-galacturonic acid + (1,4-beta-D-galacturonic acid)n
UDP + (1,4-beta-D-galacturonic acid)n+1
homogalacturonan synthase activity (substrate: galacturonic acid, GalA) decreased in absence of ATCSLD5 (ATCSLD5-1 mutant line)
-
-
?
UDP-D-xylose + ((1,4-beta-D-xylooligosaccharide)n)-anthranilic acid
UDP + ((1,4-beta-D-xylooligosaccharide)n+1)-anthranilic acid
-
0.1 mM UDP-xylose + 0.5 mM anthranilic acid (AA) labelled xylooligosaccharides (Xyl(2) to Xyl(6)) as acceptor, 200 microgram microsomes, 21°C, pH 6.8, in presence of 5 mM MnCl2, 1 mM dithiothreitol, 0.5% Triton X-100
xylooligosaccharides (up to Xyl(12)) purified by HPLC and analysed by MALDI-TOF mass spectrometry
-
?
UDP-D-xylose + (1,4-beta-D-xylan)7
UDP + (1,4-beta-D-xylan)8
-
-
-
-
?
UDP-D-xylose + (1,4-beta-D-xylan)8
UDP + (1,4-beta-D-xylan)9
-
-
-
-
?
UDP-D-xylose + (1,4-beta-D-xylan)9
UDP + (1,4-beta-D-xylan)10
-
-
-
-
?
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
UDP-D-xylose + (1,4-beta-D-xylooligosaccharide)n
UDP + (1,4-beta-D-xylooligosaccharide)n+1
-
0.1 mM radiolabelled UDP-D-xylose + 0.2 microgram/microlitre (1,4-beta-D-xylopyranose)6, 100 microgram microsomes, 21°C, pH 6.8, in presence of 5 mM MnCl2, 1 mM dithiothreitol, 0.5% Triton X-100, reaction dependent on time and protein concentration
reduction in XylT activity in microsomal fraction of stems from irx9 mutant plants compared to wild-type plants in presence of exogenous substrates can be abolished by complementation with wild-type IRX9 gene, product quantification by scintillation counting
-
?
UDP-D-xylose + (1,4-beta-D-xylopyranose)6
UDP + (1,4-beta-D-xylopyranose)7
-
-
-
-
?
UDP-D-xylose + 4-O-methyl-glucuronoxylan
UDP + ?
-
-
-
-
?
UDP-D-xylose + arabinoxylan
UDP + ?
-
-
-
-
?
UDP-D-xylose + beta-1,4-xylotetraose
UDP + ?
UDP-D-xylose + beta-1,4-xylotriose
UDP + ?
UDP-D-xylose + xylotetraose
?
microsomes isolated from transgenic BY2 cells are tested for XylT activity using xylotetraose (Xyl4) as an acceptor and UDP-xylose as a donor. XylT activity can not use the xylose monomer as an acceptor. Xylosyl residues are readily transferred onto xylooligomers ranging from 2 to 6 residues, resulting in the production of xylooligosaccharides with up to 11 xylosyl residues
-
-
?
UDP-D-xylose + [(1->4)-beta-D-xylan]n
UDP + [(1->4)-beta-D-xylan]n+1
additional information
?
-
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
-
-
-
?
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
-
-
-
-
?
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
-
catalyzes synthesis of the xylan main chain during the biogenesis of the plant cell wall
-
-
?
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
-
precipitation of product by 70% ethanol (final concentration) in presence of wheat arabinoxylan, followed by washing and scintillation counting, control for incorporation into (1,4-beta-D-xylan) by digestion with endo-xylanase
-
?
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
beta-(1,4)-xylan synthase activity, biosynthesis of xylan (major component of dicot wood)
-
-
?
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
microsomes isolated from transgenic BY2 cells are tested for XylT activity using xylotetraose (Xyl4) as an acceptor and UDP-xylose as a donor. Up to five xylosyl residues with beta-(1,4)-linkages are able to be incorporated by IRX9/IRX14-expressing microsomes
-
-
?
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
-
-
with high substrate concentration or prolonged incubation, three polysaccharides other than neutral xylan are synthesized, one of these is apparently a glycolipid, and the other two are apparently glucuronoxylans
?
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
-
substrate are e.g. higher xylooligosaccharide or xylans from different sources, chain elongation by formation of beta(1,4)-linkages, xylooligosaccharide substrates can be pyrimidylaminated or derivatized with 2-aminopyridine at their reducing ends and still serve as substrates, substrate can contain single 4-O-methyl-glucuronic acid residues
-
-
?
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
-
-
-
-
?
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
-
formation of hemicellulose of cell wall
-
-
?
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
-
-
-
-
?
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
-
-
-
-
?
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
-
catalyzes synthesis of the xylan main chain during the biogenesis of the plant cell wall
-
-
?
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
-
-
-
-
?
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
-
-
-
?
UDP-D-xylose + (1,4-beta-D-xylan)n
UDP + (1,4-beta-D-xylan)n+1
-
-
-
-
?
UDP-D-xylose + beta-1,4-xylotetraose
UDP + ?
-
-
-
-
?
UDP-D-xylose + beta-1,4-xylotetraose
UDP + ?
-
-
-
-
?
UDP-D-xylose + beta-1,4-xylotetraose
UDP + ?
-
-
-
-
?
UDP-D-xylose + beta-1,4-xylotriose
UDP + ?
-
the reaction leads to extension of the beta-1,4-xylotriose by up to five xylose residues, beta-1,4-xylotetraose, beta-1,4-xylopentose, and beta-1,4-xylohexose
-
-
?
UDP-D-xylose + beta-1,4-xylotriose
UDP + ?
-
the reaction leads to extension of the beta-1,4-xylotriose by up to five xylose residues, beta-1,4-xylotetraose, beta-1,4-xylopentose, and beta-1,4-xylohexose
-
-
?
UDP-D-xylose + beta-1,4-xylotriose
UDP + ?
-
the reaction leads to extension of the beta-1,4-xylotriose by up to five xylose residues, beta-1,4-xylotetraose, beta-1,4-xylopentose, and beta-1,4-xylohexose
-
-
?
UDP-D-xylose + [(1->4)-beta-D-xylan]n
UDP + [(1->4)-beta-D-xylan]n+1
-
-
-
-
?
UDP-D-xylose + [(1->4)-beta-D-xylan]n
UDP + [(1->4)-beta-D-xylan]n+1
-
-
-
-
?
UDP-D-xylose + [(1->4)-beta-D-xylan]n
UDP + [(1->4)-beta-D-xylan]n+1
-
-
-
-
?
UDP-D-xylose + [(1->4)-beta-D-xylan]n
UDP + [(1->4)-beta-D-xylan]n+1
-
-
-
-
?
additional information
?
-
-
xylosyltransferase (XylT) activity, biosynthesis of xylan, a major component of dicot wood
-
-
?
additional information
?
-
-
synthesis of xylooligosaccharides from Xyl(6)-anthranilic acid by XylT activity in microsomal fractions of stems from irx9 mutant plants: after up to 5 h mixture of Xyl(7) to Xyl(9) only, Xyl(7) predominates
-
-
?
additional information
?
-
-
synthesis of xylooligosaccharides from Xyl(6)-anthranilic acid by XylT activity in microsomal fractions of stems from wild-type plants: after 2 h Xyl(7) to Xyl(9) predominate, after 5 h increased proportion of Xyl(10) to Xyl(12)
-
-
?
additional information
?
-
-
Xyl(1)-anthranilic acid is not acceptor for XylT activity in microsomal fractions of stems from wild-type plants
-
-
?
additional information
?
-
-
Xyl(2)-anthranilic acid is a weak acceptor for XylT activity in microsomal fractions of stems from wild-type plants
-
-
?
additional information
?
-
-
Xyl(3)-anthranilic acid to Xyl(6)-anthranilic acid are readily accepted by XylT activity in microsomal fractions of stems from wild-type plants
-
-
?
additional information
?
-
-
Xyl(4)-anthranilic acid is acceptor for synthesis of xylooligosaccharides of sizes from Xyl(5) to Xyl(11) by XylT activity in microsomal fractions of stems from wild-type plants within 2 h, prolonged incubation time (5-8 h) leads to increased proportion of Xyl(9) to Xyl(11) but not to synthesis of longer xylooligosaccharides
-
-
?
additional information
?
-
-
no activity with UDP-glucose, UDP-arabinopyranose, or UDP-arabinofuranose
-
-
?
additional information
?
-
-
substrate specificity
-
-
?
additional information
?
-
-
metabolic flux control and alterations during light reduction
-
-
?
additional information
?
-
-
no activity with UDP-glucose, UDP-arabinopyranose, or UDP-arabinofuranose
-
-
?
additional information
?
-
-
no activity with UDP-glucose, UDP-arabinopyranose, or UDP-arabinofuranose
-
-
?
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IRX9_ARATH
351
1
40059
Swiss-Prot
Secretory Pathway (Reliability: 4)
IRX14_ARATH
525
1
59099
Swiss-Prot
other Location (Reliability: 5)
A0A7C9E0W8_OPUST
525
1
59989
TrEMBL
other Location (Reliability: 1)
A0A0B2SNQ3_GLYSO
1037
8
116493
TrEMBL
other Location (Reliability: 4)
A0A2H9ZTK2_9ASPA
1040
6
115242
TrEMBL
Chloroplast (Reliability: 3)
A0A2P6PTJ0_ROSCH
1136
8
126332
TrEMBL
Chloroplast (Reliability: 3)
A0A0B2RTM1_GLYSO
933
8
105827
TrEMBL
Mitochondrion (Reliability: 5)
A0A2I0B3R8_9ASPA
976
7
109595
TrEMBL
other Location (Reliability: 3)
A0A2G9HD41_9LAMI
1056
8
118955
TrEMBL
Chloroplast (Reliability: 3)
A0A7C9ECP8_OPUST
500
1
57674
TrEMBL
other Location (Reliability: 1)
A0A072V7S9_MEDTR
1023
8
115575
TrEMBL
other Location (Reliability: 5)
G7KCB0_MEDTR
1121
8
125959
TrEMBL
Mitochondrion (Reliability: 5)
A0A2I0AJI9_9ASPA
1163
8
129476
TrEMBL
Mitochondrion (Reliability: 4)
A0A2P6QNZ5_ROSCH
1059
8
118574
TrEMBL
Chloroplast (Reliability: 2)
A0A2G9GCR0_9LAMI
557
5
62578
TrEMBL
other Location (Reliability: 5)
A0A7C9D3C4_OPUST
170
0
19328
TrEMBL
other Location (Reliability: 3)
G7JSR7_MEDTR
1142
8
128300
TrEMBL
Chloroplast (Reliability: 4)
A0A2G9H5V2_9LAMI
1120
8
125824
TrEMBL
Chloroplast (Reliability: 3)
A0A7C9EER1_OPUST
483
1
54789
TrEMBL
Mitochondrion (Reliability: 5)
A0A0B2PAX9_GLYSO
1100
8
123295
TrEMBL
other Location (Reliability: 3)
A0A7C9DVR2_OPUST
127
0
14271
TrEMBL
Secretory Pathway (Reliability: 4)
A0A2P6PAM1_ROSCH
1117
8
125736
TrEMBL
Chloroplast (Reliability: 4)
A0A2G9H9R5_9LAMI
215
2
24576
TrEMBL
Mitochondrion (Reliability: 1)
A0A396IZT0_MEDTR
71
0
7706
TrEMBL
other Location (Reliability: 5)
A0A5B7BVR5_DAVIN
1172
5
131875
TrEMBL
Chloroplast (Reliability: 1)
A0A0B2SP28_GLYSO
147
0
16400
TrEMBL
other Location (Reliability: 2)
A0A0B2RG13_GLYSO
152
0
16776
TrEMBL
other Location (Reliability: 2)
A0A2I0B5B5_9ASPA
1329
7
146863
TrEMBL
Chloroplast (Reliability: 1)
A0A396IV81_MEDTR
201
3
23381
TrEMBL
other Location (Reliability: 2)
A0A7C9EK28_OPUST
422
0
47667
TrEMBL
other Location (Reliability: 4)
A0A0B2QGN1_GLYSO
1151
6
128229
TrEMBL
Chloroplast (Reliability: 1)
A0A072VH75_MEDTR
1105
6
123667
TrEMBL
Chloroplast (Reliability: 4)
A0A0B2RLS7_GLYSO
1084
6
121340
TrEMBL
Chloroplast (Reliability: 3)
A0A396H871_MEDTR
817
4
92773
TrEMBL
other Location (Reliability: 2)
A0A2G9I344_9LAMI
1154
6
129291
TrEMBL
Chloroplast (Reliability: 1)
A0A7C9E1W0_OPUST
126
0
14069
TrEMBL
other Location (Reliability: 3)
A0A2P6SPU8_ROSCH
1157
8
129749
TrEMBL
Chloroplast (Reliability: 5)
A0A2I0A3I7_9ASPA
1160
8
129562
TrEMBL
Chloroplast (Reliability: 5)
A0A2G9I167_9LAMI
848
6
95398
TrEMBL
other Location (Reliability: 5)
A0A2G9GYR8_9LAMI
1056
8
118941
TrEMBL
Chloroplast (Reliability: 3)
A0A2I0ACG0_9ASPA
1135
8
126782
TrEMBL
Chloroplast (Reliability: 5)
A0A2G9GUT9_9LAMI
1148
6
128577
TrEMBL
Chloroplast (Reliability: 5)
G7KSQ6_MEDTR
1171
5
130870
TrEMBL
Chloroplast (Reliability: 1)
A0A2I0ATH5_9ASPA
990
6
109571
TrEMBL
Chloroplast (Reliability: 3)
A0A2G9G0C8_9LAMI
458
5
51433
TrEMBL
Mitochondrion (Reliability: 4)
A0A396IYV2_MEDTR
210
0
23509
TrEMBL
other Location (Reliability: 2)
A0A396H212_MEDTR
159
0
18017
TrEMBL
Mitochondrion (Reliability: 1)
A0A7C9EMF4_OPUST
496
1
56268
TrEMBL
other Location (Reliability: 3)
A0A7C8YPU6_OPUST
342
0
38162
TrEMBL
other Location (Reliability: 2)
G7ICK2_MEDTR
1133
6
127166
TrEMBL
Chloroplast (Reliability: 3)
A0A7C8ZHA3_OPUST
164
0
18924
TrEMBL
other Location (Reliability: 2)
B9HH87_POPTR
510
0
57330
TrEMBL
other Location (Reliability: 2)
B9IJ10_POPTR
357
0
40159
TrEMBL
other Location (Reliability: 4)
CSLD5_ARATH
1181
0
132587
Swiss-Prot
-
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Bailey, R.W.; Hassid, W.Z.
Xylan synthesis from uridine-diphosphate-D-xylose by particulate preparations from immature corncobs
Proc. Natl. Acad. Sci. USA
56
1586-1593
1966
Zea mays
brenda
Suzuki, K.; Ingold, E.; Suguyama, M.; Komamine, A.
Xylan synthase activity in isolated mesophyll cells of Zinnia elegans durind differentiation to treachery elements
Plant Cell Physiol.
32
303-306
1991
Zinnia elegans
-
brenda
Ben-Arie, R.; Ordin, L.; Kindinger, J.I.
Cell-free xylan synthesizing enzyme system from Avena sativa
Plant Cell Physiol.
14
427-434
1973
Avena sativa
-
brenda
Bolwell, G.P.; Northcote, D.H.
Arabinan synthase and xylan synthase activities of Phaseolus vulgaris. Subcellular localization and possible mechanism of action
Biochem. J.
210
497-507
1983
Phaseolus vulgaris
brenda
Odzuck, W.; Kauss, H.
Biosynthesis of pure araban and xylan
Phytochemistry
11
2489-2494
1972
Vigna mungo
-
brenda
Bolwell, G.P.; Northcote, D.H.
Induction by growth factors of polysaccharide synthases in bean cell suspension cultures
Biochem. J.
210
509-515
1983
Phaseolus vulgaris
brenda
Dalessandro, G.; Northcote, D.H.
xylan synthetase activity in differentiated xylem cells of sycamore trees (Acer pseudoplatasnus)
Planta
151
53-60
1981
Acer pseudoplatanus
brenda
Dalessandro, G.; Northcote, D.H.
Increase of xylan synthetase activity during xylem differentiation of the vascular cambium of sycamore and poplar trees
Planta
151
61-67
1981
Acer pseudoplatanus, Populus x canadensis
brenda
Baydoun, E.A.H.; Waldron, K.W.; Brett, C.T.
The interaction of xylosyltransferase and glucuronyltransferase involved in glucuronoxylan synthesis in pea (Pisum sativum) epicotyls
Biochem. J.
257
853-858
1989
Pisum sativum
brenda
Baydoun, E.A.H.; Brett, C.T.
Distribution of xylosyltransferases and glucuronyltransferase within the Golgi apparatus in etiolated pea (Pisum sativum L.) epicotyls
J. Exp. Bot.
48
1209-1214
1997
Pisum sativum
-
brenda
Gregory, A.C.E.; Smith, C.; Kerry, M.E.; Wheatley, E.R.; Bolwell, G.P.
Comparative subcellular immunolocation of polypeptides associated with xylan and callose synthases in French bean (Phaseolus vulgaris) during secondary wall formation
Phytochemistry
59
249-259
2002
Phaseolus vulgaris
brenda
Kerry, M.E.; Gregory, A.C.E.; Bolwell, G.P.
Differential behaviour of four plant polysaccharide synthases in the presence of organic solvents
Phytochemistry
57
1055-1060
2001
Phaseolus vulgaris
brenda
Urahara, T.; Tsuchiya, K.; Kotake, T.; Tohno-oka, T.; Komae, K.; Kawada, N.; Tsumuraya, Y.
A beta-(1->4)-xylosyltransferase involved in the synthesis of arabinoxylans in developing barley endosperms
Physiol. Plant.
122
169-180
2004
Hordeum vulgare
-
brenda
Orfila, C.; S?rensen, S.O.; Harholt, J.; Geshi, N.; Crombie, H.; Truong, H.N.; Reid, J.S.; Knox, J.P.; Scheller, H.V.
QUASIMODO1 is expressed in vascular tissue of Arabidopsis thaliana inflorescence stems, and affects homogalacturonan and xylan biosynthesis
Planta
222
613-622
2005
Arabidopsis thaliana
brenda
Lee, C.; ONeill, M.A.; Tsumuraya, Y.; Darvill, A.G.; Ye, Z.
The irregular xylem9 mutant is deficient in xylan xylosyltransferase activity
Plant Cell Physiol.
48
1624-1634
2007
Arabidopsis thaliana
brenda
Bernal, A.J.; Jensen, J.K.; Harholt, J.; S?rensen, S.; Moller, I.; Blaukopf, C.; Johansen, B.; de Lotto, R.; Pauly, M.; Scheller, H.V.; Willats, W.G.
Disruption of ATCSLD5 results in reduced growth, reduced xylan and homogalacturonan synthase activity and altered xylan occurrence in Arabidopsis
Plant J.
52
791-802
2007
Arabidopsis thaliana (Q9SRW9)
brenda
Lee, C.; Zhong, R.; Ye, Z.H.
Arabidopsis family GT43 members are xylan xylosyltransferases required for the elongation of the xylan backbone
Plant Cell Physiol.
53
135-143
2012
Arabidopsis thaliana (Q8L707), Arabidopsis thaliana (Q9ZQC6), Arabidopsis thaliana
brenda
Lee, C.; Zhong, R.; Ye, Z.
Biochemical characterization of xylan xylosyltransferases involved in wood formation in poplar
Plant Signal. Behav.
7
332-337
2012
Populus trichocarpa (B9HH87), Populus trichocarpa (B9IJ10)
brenda
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