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EC Tree
IUBMB Comments Although UDP is generally considered to be the preferred nucleoside diphosphate for sucrose synthase, numerous studies have shown that ADP serves as an effective acceptor molecule to produce ADP-glucose [3-9]. Sucrose synthase has a dual role in producing both UDP-glucose (necessary for cell wall and glycoprotein biosynthesis) and ADP-glucose (necessary for starch biosynthesis) .
The taxonomic range for the selected organisms is: Glycine max The expected taxonomic range for this enzyme is: Bacteria, Eukaryota, Archaea
Synonyms
sucrose synthase, sucrose synthetase, susy1, mtsucs1, rsus3, sucrose synthase 1, psnsusy2, susy2, sucrose synthase 2, sucrose synthase 3,
more
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glucosyltransferase, uridine diphosphoglucose-fructose
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sucrose synthetase
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sucrose-UDP glucosyltransferase
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sucrose-uridine diphosphate glucosyltransferase
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UDP-glucose-fructose glucosyltransferase
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UDP-glucose:D-fructose 2-alpha-D-glucosyltransferase
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uridine diphosphoglucose-fructose glucosyltransferase
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hexosyl group transfer
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NDP-glucose:D-fructose 2-alpha-D-glucosyltransferase
Although UDP is generally considered to be the preferred nucleoside diphosphate for sucrose synthase, numerous studies have shown that ADP serves as an effective acceptor molecule to produce ADP-glucose [3-9]. Sucrose synthase has a dual role in producing both UDP-glucose (necessary for cell wall and glycoprotein biosynthesis) and ADP-glucose (necessary for starch biosynthesis) [10].
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ADP + sucrose
ADP-alpha-D-glucose + D-fructose
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r
ADP-alpha-D-glucose + D-fructose
ADP + sucrose
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r
CDP + sucrose
CDP-alpha-D-glucose + D-fructose
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r
CDP-alpha-D-glucose + D-fructose
CDP + sucrose
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r
dTDP + sucrose
dTDP-alpha-D-glucose + D-fructose
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r
dTDP-alpha-D-glucose + D-fructose
dTDP + sucrose
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r
dUDP + sucrose
dUDP-alpha-D-glucose + D-fructose
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r
dUDP-alpha-D-glucose + D-fructose
dUDP + sucrose
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r
GDP + sucrose
GDP-alpha-D-glucose + D-fructose
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r
GDP-alpha-D-glucose + D-fructose
GDP + sucrose
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r
NDP + sucrose
NDP-alpha-D-glucose + D-fructose
the reaction is catalyzed at low pH values
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r
NDP-alpha-D-glucose + D-fructose
NDP + sucrose
UDP + sucrose
UDP-alpha-D-glucose + D-fructose
UDP + sucrose
UDP-glucose + D-fructose
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?
UDP-alpha-D-glucose + D-fructose
UDP + sucrose
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r
UDP-glucose + D-fructose
UDP + sucrose
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UDPglucose + D-fructose
UDP + sucrose
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r
ADP-glucose + D-fructose
ADP + sucrose
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r
CDP-glucose + D-fructose
CDP + sucrose
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r
GDP-glucose + D-fructose
GDP + sucrose
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r
UDP + sucrose
UDP-glucose + D-fructose
UDPglucose + D-fructose
UDP + sucrose
NDP-alpha-D-glucose + D-fructose
NDP + sucrose
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r
NDP-alpha-D-glucose + D-fructose
NDP + sucrose
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r
NDP-alpha-D-glucose + D-fructose
NDP + sucrose
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r
NDP-alpha-D-glucose + D-fructose
NDP + sucrose
the reaction is catalyzed at high pH values
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r
UDP + sucrose
UDP-alpha-D-glucose + D-fructose
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r
UDP + sucrose
UDP-alpha-D-glucose + D-fructose
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r
UDP + sucrose
UDP-alpha-D-glucose + D-fructose
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r
UDP + sucrose
UDP-glucose + D-fructose
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?
UDP + sucrose
UDP-glucose + D-fructose
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also substrate: ADP
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UDP + sucrose
UDP-glucose + D-fructose
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substrate: CDP
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UDP + sucrose
UDP-glucose + D-fructose
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ADP is less effective
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UDPglucose + D-fructose
UDP + sucrose
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r
UDPglucose + D-fructose
UDP + sucrose
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r
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NDP + sucrose
NDP-alpha-D-glucose + D-fructose
the reaction is catalyzed at low pH values
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r
NDP-alpha-D-glucose + D-fructose
NDP + sucrose
UDP-glucose + D-fructose
UDP + sucrose
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?
NDP-alpha-D-glucose + D-fructose
NDP + sucrose
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r
NDP-alpha-D-glucose + D-fructose
NDP + sucrose
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r
NDP-alpha-D-glucose + D-fructose
NDP + sucrose
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r
NDP-alpha-D-glucose + D-fructose
NDP + sucrose
the reaction is catalyzed at high pH values
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r
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additional information
Ser11 is primary phosphorylation site, phosphorylation does not affect kinetics but partitioning between membrane and cytosol
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additional information
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Ser11 is primary phosphorylation site, phosphorylation does not affect kinetics but partitioning between membrane and cytosol
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Mg2+
13 mM used in assay conditions
additional information
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no activation by K+, Na+, NH4+, Cl-, Br-, F-, NO3-, phosphate, sulfate, borate, acetate, citrate
Ca2+
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activation of sucrose synthesis
Ca2+
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slight activation of sucrose cleavage at 10 mM
Mg2+
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activation
Mg2+
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slight activation of sucrose cleavage
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quercetin
the enzyme is tolerant to quercetin up to a concentration of 1.5 mM
additional information
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not inhibitory: DTT, GSH, 2-mercaptoethanol, EDTA
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additional information
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not inhibitory: fructose 6-phosphate, glucose 1-phosphate, glucose 6-phosphate, fructose 1,6-diphosphate
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additional information
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not inhibitory: galactose, mannose, maltose, raffinose, 3-phosphoglycerate, phosphoenolpyruvate, ethanol, succinate, 2-oxoglutarate, glutamine, NAD+, diphosphate
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allantoin
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activation, sucrose synthesis
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0.13
ADP
at pH 7.5 and 30°C
1.6
ADP-alpha-D-glucose
at pH 7.5 and 30°C
3.7
D-fructose
with UDP-alpha-D-glucose as cosubstrate, at pH 7.5 and 30°C
31.3
sucrose
with UDP as cosubstrate, at pH 7.5 and 30°C
0.005
UDP
at pH 7.5 and 30°C
0.012
UDP-alpha-D-glucose
at pH 7.5 and 30°C
0.012 - 0.033
UDPglucose
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0.98 - 1.66
fructose
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cosubstrate CDP
0.98 - 1.66
fructose
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cosubstrate ADPglucose
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2.07
ADP
at pH 7.5 and 30°C
2.9
ADP-alpha-D-glucose
at pH 7.5 and 30°C
21.5
D-fructose
with UDP-alpha-D-glucose as cosubstrate, at pH 7.5 and 30°C
20
sucrose
with UDP as cosubstrate, at pH 7.5 and 30°C
20
UDP
at pH 7.5 and 30°C
21.5
UDP-alpha-D-glucose
at pH 7.5 and 30°C
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5 - 8.2
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about 90% of maximal activity at pH 5.0 and about half-maximal activity at pH 8.2, sucrose cleavage
7.5 - 10
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about half-maximal activity at pH 7.5 and about 90% of maximal activity at pH 10.0, sucrose synthesis
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UniProt
brenda
recombinant enzyme
UniProt
brenda
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nodulaid inoculum: Rhizobium japonicum CB 1809
brenda
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Bradyrhizobium japonicum strains
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brenda
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SUS_SOYBN
805
0
92244
Swiss-Prot
other Location (Reliability: 5 )
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90000
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4 * 90000, SDS-PAGE
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tetramer
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4 * 90000, SDS-PAGE
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S11A
phosphorylation still occurs, but weakly
S11C
phosphorylation still occurs, but weakly
S11D
phosphorylation still occurs, but weakly
additional information
N-terminal truncation, phosphorylations still occurs, but weakly
additional information
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N-terminal truncation, phosphorylations still occurs, but weakly
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2-mercaptoethanol stabilizes
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4°C, 20 mM potassium phosphate buffer, pH 7.0, 5 mM 2-mercaptoethanol, 4 weeks stable
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Ni-NTA column chromatography
Strep tag affinity chromatography
Strep-Tactin column chromatography
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DNA and amino acid sequence determination and analysis, phylogenetic analysis
expressed in Escherichia coli BL21(DE3) cells
expressed in Escherichia coli BL21-Gold (DE3) cells
expression in Escherichia coli
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synthesis
a biocatalytic cascade of polyphosphate kinase and sucrose synthase is developed for synthesis of nucleotide-activated derivatives of glucose
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Morell, M.; Copeland, L.
Sucrose synthase of soybean nodules
Plant Physiol.
78
149-154
1985
Glycine max
brenda
Thummler, F.; Verma, D.P.S.
Nodulin-100 of soybean is the subunit of sucrose synthase regulated by the availability of free heme in nodules
J. Biol. Chem.
262
14730-14736
1987
Glycine max
brenda
Zhang, X.Q.; Lund, A.A.; Sarath, G.; Cerny, R.L.; Roberts, D.M.; Chollet, R.
Soybean nodule sucrose synthase (nodulin-100): further analysis of its phosphorylation using recombinant and authentic root-nodule enzymes
Arch. Biochem. Biophys.
371
70-82
1999
Glycine max (P13708), Glycine max
brenda
Abid, G.; Silue, S.; Muhovski, Y.; Jacquemin, J.M.; Toussaint, A.; Baudoin, J.P.
Role of myo-inositol phosphate synthase and sucrose synthase genes in plant seed development
Gene
439
1-10
2009
Arabidopsis thaliana (F4K5W8), Arabidopsis thaliana (P49040), Arabidopsis thaliana (Q00917), Citrus unshiu (Q9SLY2), Citrus x paradisi, Coffea arabica (Q0E7D4), Daucus carota (O49845), Eucalyptus grandis (Q00P15), Eucalyptus grandis (Q00P16), Glycine max (P13708), Glycine max, Gossypium hirsutum (Q9XGB7), Gossypium hirsutum, Oryza sativa (P31924), Pisum sativum (O24301), Pisum sativum (O81610), Pisum sativum (Q9AVR8), Pisum sativum (Q9T0M9), Solanum lycopersicum (P49037), Solanum tuberosum (Q84T18), Vicia faba (P31926), Zea mays
brenda
Pei, J.; Sun, Q.; Gu, N.; Zhao, L.; Fang, X.; Tang, F.; Cao, F.
Production of isoorientin and isovitexin from luteolin and apigenin using coupled catalysis of glycosyltransferase and sucrose synthase
Appl. Biochem. Biotechnol.
190
601-615
2020
Glycine max (P13708), Glycine max
brenda
Schmoelzer, K.; Gutmann, A.; Diricks, M.; Desmet, T.; Nidetzky, B.
Sucrose synthase A unique glycosyltransferase for biocatalytic glycosylation process development
Biotechnol. Adv.
34
88-111
2016
Anabaena sp., Arabidopsis thaliana, Beta vulgaris, Vicia faba, Helianthus tuberosus, Hordeum vulgare, Ipomoea batatas, Manihot esculenta, Nitrosomonas europaea, Oryza sativa, Vigna radiata, Pisum sativum, Prunus persica, Pyrus pyrifolia, Saccharum sp., Solanum tuberosum, Zea mays, Thermosynechococcus vestitus, Acidithiobacillus caldus, Solanum chmielewskii, Glycine max (P13708)
brenda
Gutmann, A.; Lepak, A.; Diricks, M.; Desmet, T.; Nidetzky, B.
Glycosyltransferase cascades for natural product glycosylation Use of plant instead of bacterial sucrose synthases improves the UDP-glucose recycling from sucrose and UDP
Biotechnol. J.
12
1600557
2017
Acidithiobacillus caldus (A0A059ZV61), Acidithiobacillus caldus, Glycine max (P13708), Glycine max, Acidithiobacillus caldus ATCC 51756 (A0A059ZV61)
brenda
Pei, J.; Chen, A.; Zhao, L.; Cao, F.; Li, X.; Xiao, W.
Synergistic catalysis of glycosyltransferase and sucrose synthase to produce isoquercitrin through glycosylation of quercetin
Chem. Nat. Compd.
55
453-457
2019
Glycine max (P13708)
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brenda
Kulmer, S.; Gutmann, A.; Lemmerer, M.; Nidetzky, B.
Biocatalytic cascade of polyphosphate kinase and sucrose synthase for synthesis of nucleotide-activated derivatives of glucose
Adv. Synth. Catal.
359
292-301
2017
Acidithiobacillus caldus (A0A059ZV61), Glycine max (P13708), Acidithiobacillus caldus ATCC 51756 (A0A059ZV61)
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brenda