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Information on EC 2.4.1.36 - alpha,alpha-trehalose-phosphate synthase (GDP-forming) Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
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The expected taxonomic range for this enzyme is: Eukaryota, Bacteria
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alpha,alpha-trehalose-phosphate synthase (GDP-forming)
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GDP-glucose + glucose 6-phosphate = GDP + alpha,alpha-trehalose 6-phosphate
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hexosyl group transfer
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trehalose biosynthesis III
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GDP-glucose:D-glucose-6-phosphate 1-alpha-D-glucosyltransferase
See also EC 2.4.1.15 [alpha,alpha-trehalose-phosphate synthase (UDP-forming)].
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GDP glucose-glucosephosphate glucosyltransferase
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GDP-glucose-glucose-phosphate glucosyltransferase
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glucosyltransferase, guanosine diphosphoglucose-glucose phosphate
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guanosine diphosphoglucose-glucose phosphate glucosyltransferase
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trehalose phosphate synthase (GDP-forming)
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recombinant enzyme
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UniProt
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ADP-alpha-D-glucose + D-glucose 6-phosphate
ADP + alpha,alpha-trehalose 6-phosphate
CDP-glucose + glucose 6-phosphate
CDP + alpha,alpha-trehalose 6-phosphate
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GDP-alpha-D-glucose + D-glucose 6-phosphate
GDP + alpha,alpha-trehalose 6-phosphate
GDP-glucose + glucose 6-phosphate
GDP + alpha,alpha-trehalose 6-phosphate
TDP-alpha-D-glucose + D-glucose 6-phosphate
TDP + alpha,alpha-trehalose 6-phosphate
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in crude extracts of Propionibacterium freudenreichii, OtsA is specific for ADP-glucose, in contrast to the pure recombinant OtsA, which uses UDP-glucose, GDP-glucose and TDP-glucose, in addition to ADP-glucose. The substrate specificity of OtsA in cell extracts is lost during purification, and the recombinant OtsA becomes specific to ADP-glucose upon incubation with a dialysed cell extract
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TDP-glucose + glucose 6-phosphate
TDP + alpha,alpha-trehalose 6-phosphate
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UDP-alpha-D-glucose + D-glucose 6-phosphate
UDP + alpha,alpha-trehalose 6-phosphate
additional information
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ADP-alpha-D-glucose + D-glucose 6-phosphate
ADP + alpha,alpha-trehalose 6-phosphate
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ADP-alpha-D-glucose + D-glucose 6-phosphate
ADP + alpha,alpha-trehalose 6-phosphate
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in crude extracts of Propionibacterium freudenreichii, OtsA is specific for ADP-glucose, in contrast to the pure recombinant OtsA, which uses UDP-glucose, GDP-glucose and TDP-glucose, in addition to ADP-glucose. The substrate specificity of OtsA in cell extracts is lost during purification, and the recombinant OtsA becomes specific to ADP-glucose upon incubation with a dialysed cell extract
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GDP-alpha-D-glucose + D-glucose 6-phosphate
GDP + alpha,alpha-trehalose 6-phosphate
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in crude extracts of Propionibacterium freudenreichii, OtsA is specific for ADP-glucose, in contrast to the pure recombinant OtsA, which uses UDP-glucose, GDP-glucose and TDP-glucose, in addition to ADP-glucose. The substrate specificity of OtsA in cell extracts is lost during purification, and the recombinant OtsA becomes specific to ADP-glucose upon incubation with a dialysed cell extract
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GDP-alpha-D-glucose + D-glucose 6-phosphate
GDP + alpha,alpha-trehalose 6-phosphate
GDP-glucose is the preferred glycosyl-donor
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GDP-glucose + glucose 6-phosphate
GDP + alpha,alpha-trehalose 6-phosphate
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GDP-glucose + glucose 6-phosphate
GDP + alpha,alpha-trehalose 6-phosphate
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GDP-glucose + glucose 6-phosphate
GDP + alpha,alpha-trehalose 6-phosphate
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responsible for synthesis of trehalose phosphate
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GDP-glucose + glucose 6-phosphate
GDP + alpha,alpha-trehalose 6-phosphate
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GDP-glucose + glucose 6-phosphate
GDP + alpha,alpha-trehalose 6-phosphate
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GDP-glucose + glucose 6-phosphate
GDP + alpha,alpha-trehalose 6-phosphate
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UDP-alpha-D-glucose + D-glucose 6-phosphate
UDP + alpha,alpha-trehalose 6-phosphate
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UDP-alpha-D-glucose + D-glucose 6-phosphate
UDP + alpha,alpha-trehalose 6-phosphate
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in crude extracts of Propionibacterium freudenreichii, OtsA is specific for ADP-glucose, in contrast to the pure recombinant OtsA, which uses UDP-glucose, GDP-glucose and TDP-glucose, in addition to ADP-glucose. The substrate specificity of OtsA in cell extracts is lost during purification, and the recombinant OtsA becomes specific to ADP-glucose upon incubation with a dialysed cell extract
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additional information
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overview on biosynthesis of trehalose
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additional information
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the trehalose-6-phosphate synthase/phosphatase (OtsA-OtsB) pathway plays an important role in the synthesis of trehalose in response to stress
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additional information
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overview on biosynthesis of trehalose
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additional information
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overview on biosynthesis of trehalose
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GDP-glucose + glucose 6-phosphate
GDP + alpha,alpha-trehalose 6-phosphate
additional information
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GDP-glucose + glucose 6-phosphate
GDP + alpha,alpha-trehalose 6-phosphate
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responsible for synthesis of trehalose phosphate
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GDP-glucose + glucose 6-phosphate
GDP + alpha,alpha-trehalose 6-phosphate
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additional information
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overview on biosynthesis of trehalose
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additional information
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the trehalose-6-phosphate synthase/phosphatase (OtsA-OtsB) pathway plays an important role in the synthesis of trehalose in response to stress
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additional information
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overview on biosynthesis of trehalose
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additional information
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overview on biosynthesis of trehalose
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KCl
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upon an increase in the KCl concentration from 0 to 100 mM, the OtsA activity decreases by more than 40%, whereas it is not significantly affected when UDP or GDP-glucose is used as the substrate
NaCl
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an increase in the concentration of NaCl from 0 to 100 mM leads to a decrease in the OtsA activity by more than 35% when ADP-glucose or TDP-glucose is the substrate. When UDP-glucose or GDP-glucose is used as substrate, the OtsA activity is increased by 10-30%
Mg2+
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10 mM, required for maximal activity
Mg2+
stimulation, maximum activity at 2 mM. In absence of Mg2+, 36% of maximum activity
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NaCl
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an increase in the concentration of NaCl from 0 to 100 mM leads to a decrease in the OtsA activity by more than 35% when ADP-glucose or TDP-glucose is the substrate. When UDP-glucose or GDP-glucose is used as substrate, the OtsA activity is increased by 10-30%
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Mn2+
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at 10 mM activity increases 2fold
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0.6
ADP-glucose
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37°C, pH 5.5
2.9 - 7.1
D-glucose 6-phosphate
4 - 7
glucose-6-phosphate
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TDP-glucose
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37°C, pH 5.5
2.9
D-glucose 6-phosphate
37°C
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D-glucose 6-phosphate
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37°C, pH 5.5, cosubstrate: UDP-glucose
4.2
D-glucose 6-phosphate
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37°C, pH 5.5, cosubstrate: ADP-glucose
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D-glucose 6-phosphate
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37°C, pH 5.5, cosubstrate: TDP-glucose
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D-glucose 6-phosphate
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37°C, pH 5.5, cosubstrate: GDP-glucose
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GDP-glucose
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37°C, pH 5.5
0.3
UDP-glucose
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37°C, pH 5.5
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5.3
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activity with ADP-glucose, UDP-glucose and TDP-glucose
5.5
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activitry with GDP-glucose
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5 - 6
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pH 5.0: about 85% of maximal activity, pH 6.0: about 50% of maximal activity
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Streptomyces venezuelae (strain ATCC 10712 / CBS 650.69 / DSM 40230 / JCM 4526 / NBRC 13096 / PD 04745)
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53900
x * 53900, calculated
58000
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4 * 58000, SDS-PAGE, recombinant enzyme
220000
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gel filtration, recombinant enzyme
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tetramer
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4 * 58000, SDS-PAGE, recombinant enzyme
additional information
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overview
additional information
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overview
additional information
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overview
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overview
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expression in Escherichia coli
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G9BXT0_PLEER
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13700
TrEMBL
A0A1J1KTN2_9CYAN
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27688
TrEMBL
A0A1J1JWZ4_9CYAN
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27645
TrEMBL
K7WR81_9NOST
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27606
TrEMBL
K7VW10_9NOST
247
28227
TrEMBL
A0A1J1LCV4_9CYAN
261
29679
TrEMBL
A0A1J1K7V4_9CYAN
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27512
TrEMBL
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Pan, Y.T.; Carroll, J.D.; Elbein, A.D.
Trehalose-phosphate synthase of Mycobacterium tuberculosis. Cloning, expression and properties of the recombinant enzyme
Eur. J. Biochem.
269
6091-6100
2002
Mycobacterium tuberculosis
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Elbein, A.D.
Carbohydrate metabolism in Streptomyces hygroscopicus. I. Enzymatic synthesis of trehalose phosphate from guanosine diphosphate D-glucose-14C
J. Biol. Chem.
242
403-406
1967
Streptomyces hygroscopicus
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Elbein, A.D.; Pan, Y.T.; Pastuszak, I.; Carroll, D.
New insights on trehalose: a multifunctional molecule
Glycobiology
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17-27
2003
insecta, Saccharomyces cerevisiae, Streptomyces sp.
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Cardoso, F.S.; Castro, R.F.; Borges, N.; Santos, H.
Biochemical and genetic characterization of the pathways for trehalose metabolism in Propionibacterium freudenreichii, and their role in stress response
Microbiology
153
270-280
2007
Propionibacterium freudenreichii
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Nobre, A.; Alarico, S.; Fernandes, C.; Empadinhas, N.; da Costa, M.S.
A unique combination of genetic systems for the synthesis of trehalose in Rubrobacter xylanophilus: properties of a rare actinobacterial TreT
J. Bacteriol.
190
7939-7946
2008
Rubrobacter xylanophilus (B8R7Q2)
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