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IUBMB Comments The enzyme from the rice bean Vigna umbellata (Fabaceae) is highly specific for S -adenosyl-L -methionine. The enzyme also methylates 1L -1,2,4/3,5-cyclohexanepentol, 2,4,6/3,5-pentahydroxycyclohexanone, D ,L -2,3,4,6/5-pentacyclohexanone and 2,2′-anhydro-2-C -hydroxymethyl-myo -inositol, but at lower rates than that of myo -inositol.
The enzyme appears in viruses and cellular organisms
Synonyms imt, pcimt1, myo-inositol o-methyltransferase, inositol methyl transferase, myo-inositol 6-o-methyltransferase, more
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EC 2.1.1.134
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formerly
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inositol 6-O-methyltransferase
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inositol methyl transferase
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methyltransferase, inositol 6-O
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methyltransferase, inositol L-1- (Mesembryanthemum crystallinum clone Imt1 reduced)
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myo-inositol 4-O-methyltransferase
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myo-inositol 6-O-methyltransferase
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myo-inositol O-methyltransferase
S-adenosyl-L-methionine:myo-inositol 6-O-methyltransferase
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IMT
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Imt1
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myo-inositol O-methyltransferase
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myo-inositol O-methyltransferase
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S-adenosyl-L-methionine + myo-inositol = S-adenosyl-L-homocysteine + 1D-4-O-methyl-myo-inositol
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methyl group transfer
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MetaCyc
pinitol biosynthesis I
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S-adenosyl-L-methionine:1D-myo-inositol 4-methyltransferase
The enzyme from the rice bean Vigna umbellata (Fabaceae) is highly specific for S-adenosyl-L-methionine. The enzyme also methylates 1L-1,2,4/3,5-cyclohexanepentol, 2,4,6/3,5-pentahydroxycyclohexanone, D,L-2,3,4,6/5-pentacyclohexanone and 2,2'-anhydro-2-C-hydroxymethyl-myo-inositol, but at lower rates than that of myo-inositol.
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169277-48-9
formerly EC 2.1.1.134
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S-adenosyl-L-methionine + 1L-1,3,4/2,5-cyclohexanepentol
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Substrates: i.e. L-viburnitol Products: -
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S-adenosyl-L-methionine + 2,4,6/3,5-pentahydroxy-cyclohexanone
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Substrates: i.e. myo-inosose-2 Products: -
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S-adenosyl-L-methionine + D,L-2,3,4,6/5-pentahydroxy-cyclohexanone
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Substrates: i.e. myo-inosose-4 Products: -
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S-adenosyl-L-methionine + myo-inositol
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S-adenosyl-L-methionine + myo-inositol
S-adenosyl-L-homocysteine + 1D-4-O-methyl-myo-inositol
S-adenosyl-L-methionine + myo-inositol
S-adenosyl-L-homocysteine + 4-methyl-myo-inositol
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Substrates: - Products: -
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S-adenosyl-L-methionine + myo-inositol
S-adenosyl-L-homocysteine + D-ononitol
S-adenosyl-L-methionine + myo-inositol
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Substrates: the enzyme catalyzes the first step in the biosynthesis of the cyclic sugar alcohol pinitol. The presence of high levels of sugar alcohols correlates with osmotolerance Products: -
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S-adenosyl-L-methionine + myo-inositol
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Substrates: the product 1D-4-O-methyl-myo-inositol is accumulated in response to abiotic stress Products: -
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S-adenosyl-L-methionine + myo-inositol
S-adenosyl-L-homocysteine + 1D-4-O-methyl-myo-inositol
Substrates: during normal growth IMT is repressed, after salinity stress IMT is induced. By inducing expression of IMT and increasing myo-inositol synthesis, metabolic end products accumulate, facilitating sodium sequestration and protecting photosynthesis Products: -
?
S-adenosyl-L-methionine + myo-inositol
S-adenosyl-L-homocysteine + 1D-4-O-methyl-myo-inositol
Substrates: involved in the biosynthesis of pinitol, which is important for osmotic stress response Products: -
?
S-adenosyl-L-methionine + myo-inositol
S-adenosyl-L-homocysteine + 1D-4-O-methyl-myo-inositol
Substrates: - Products: -
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S-adenosyl-L-methionine + myo-inositol
S-adenosyl-L-homocysteine + 1D-4-O-methyl-myo-inositol
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Substrates: - Products: -
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S-adenosyl-L-methionine + myo-inositol
S-adenosyl-L-homocysteine + 1D-4-O-methyl-myo-inositol
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Substrates: accumulation of methylated inositol in plants under salt-stress Products: -
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S-adenosyl-L-methionine + myo-inositol
S-adenosyl-L-homocysteine + 1D-4-O-methyl-myo-inositol
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Substrates: - Products: 1D-4-O-methyl-myo-inositol is accumulated in response to abiotic stresses
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S-adenosyl-L-methionine + myo-inositol
S-adenosyl-L-homocysteine + D-ononitol
Substrates: - Products: -
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S-adenosyl-L-methionine + myo-inositol
S-adenosyl-L-homocysteine + D-ononitol
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Substrates: - Products: D-ononitol is 1-D-4-O-methyl-myo-inositol
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S-adenosyl-L-methionine + myo-inositol
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S-adenosyl-L-methionine + myo-inositol
S-adenosyl-L-homocysteine + 1D-4-O-methyl-myo-inositol
S-adenosyl-L-methionine + myo-inositol
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Substrates: the enzyme catalyzes the first step in the biosynthesis of the cyclic sugar alcohol pinitol. The presence of high levels of sugar alcohols correlates with osmotolerance Products: -
?
S-adenosyl-L-methionine + myo-inositol
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Substrates: the product 1D-4-O-methyl-myo-inositol is accumulated in response to abiotic stress Products: -
?
S-adenosyl-L-methionine + myo-inositol
S-adenosyl-L-homocysteine + 1D-4-O-methyl-myo-inositol
Substrates: during normal growth IMT is repressed, after salinity stress IMT is induced. By inducing expression of IMT and increasing myo-inositol synthesis, metabolic end products accumulate, facilitating sodium sequestration and protecting photosynthesis Products: -
?
S-adenosyl-L-methionine + myo-inositol
S-adenosyl-L-homocysteine + 1D-4-O-methyl-myo-inositol
Substrates: involved in the biosynthesis of pinitol, which is important for osmotic stress response Products: -
?
S-adenosyl-L-methionine + myo-inositol
S-adenosyl-L-homocysteine + 1D-4-O-methyl-myo-inositol
Substrates: - Products: -
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S-adenosyl-L-methionine + myo-inositol
S-adenosyl-L-homocysteine + 1D-4-O-methyl-myo-inositol
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Substrates: - Products: -
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S-adenosyl-L-methionine
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K+
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5 mM, slight stimulation
Na+
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5 mM, slight stimulation
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1L-1,3,4/2,5-cyclohexanepentol
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i.e. L-viburnitol
2,2'-Anhydro-2-C-hydroxymethyl-myo-inositol
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2,4,6/3,5-pentahydroxy-cyclohexanone
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i.e. myo-inosose-2
D,L-2,3,4,6/5-pentahydroxy-cyclohexanone
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i.e. myo-inosose-4
p-chloromercuribenzenesulfonic acid
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0.02 mM
S-adenosyl-L-homocysteine
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most potent inhibitor
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dithiothreitol
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1-20 mM, slight activation
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4.47
1-L-1,3,4/2,5-cyclohexanepentol
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0.67
2,4,6/3,5-pentahydroxy-cyclohexanone
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0.3
D,L-2,3,4,6/5-pentahydroxy-cyclohexanone
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0.063
S-adenosyl-L-methionine
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with myo-inositol as cosubstrate
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additional information
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proteome profile during salt-stress, up-regulation of RNA and protein expression following exposure to salinity, profiling of reaction product by gas chromatography, functional characterization of recombinant protein, regulation of pinitol synthesis pathway under different abiotic stresses, different plant species known to produce pinitol in response to stress listed, accumulation of D-pinitol via inositol is a stress-regulated pathway, presence of D-pinitol synthesizing protein/gene in a wild halophytic rice, absence in domesticated rice, adaptive feature in salt tolerance
additional information
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7 - 8.8
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about 35% of maximal activity at pH 7.0 and pH 8.8
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30 - 55
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30°C: about 40% of maximal activity, 55°C: about 30% of maximal activity
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UniProt
brenda
no activity in Oryza sativa
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Roxb. Tateoka
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SwissProt
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SwissProt
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during normal growth IMT is repressed, after salinity stress IMT is induced
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abiotic stress treatment
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during normal growth IMT is repressed, after salinity stress IMT is induced
brenda
9-days-old
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brenda
Highest Expressing Human Cell Lines
Filter by:
Cell Line Links
Gene Links
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metabolism
exogenous myo-inositol increases salt tolerance and accelerates Crassulacean acid metabolism (CAM) induction in the early juvenile stage of the facultative halophyte Mesembryanthemum crystallinum (ice plant) but not in the late juvenile stage. Ice plants develop salt tolerance during the transition from the juvenile to the adult stage. Myo-inositol is the precursor for the synthesis of compatible solute D-pinitol and promotes Na+ transport in ice plants. Treatment combining high salt and myo-inositol synergistically induces the expression of myo-inositol phosphate synthase (INPS), myo-inositol O-methyltransferase (IMT), and inositol transporters (INTs), which modulate root-to-shoot Na/K ratio and increase leaf D-pinitol content. Sufficient myo-inositol is a prerequisite for high salt tolerance in ice plant
physiological function
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after cold stress, the Imt1 transgenic Arabidopsis plants exhibit stronger growth than the wild type plants
physiological function
tobacco plants transformed with the IMT gene produce up to 2.38 mg of D-ononitol per gram dry weight of leaves. Introduction of IMT, OEPA displaying NAD+-dependent D-ononitol dehydrogenase activity, and OEPB having NADP+-dependent D-pinitol dehydrogenase activity into tobacco plants results in production of D-ononitol and D-pinitol in transformants
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IMT1_MESCR
365
1
40296
Swiss-Prot
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G7JTH4_MEDTR
369
0
41362
TrEMBL
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40000
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x * 40000, SDS-PAGE
40250
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x * 40250, calculation from nucleotide sequence
40300
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2 * or 3 * 40300, SDS-PAGE
additional information
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40 kDa immunoreactive protein under stressed and unstressed conditions in wild rice, an about 60 kDa major band detected by antibodies in domesticated and in wild rice
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x * 41360, calculated from sequence
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x * 40250, calculation from nucleotide sequence
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2 * or 3 * 40300, SDS-PAGE
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5.5
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3 h, at room temperature, about 45% loss of activity compared to maximal stability at pH 7.0-7.6
6.5
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3 h, at room temperature, about 10% loss of activity compared to maximal stability at pH 7.0-7.6
7 - 7.6
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3 h, at room temperature, maximal stability
8
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3 h, at room temperature, about 30% loss of activity compared to maximal stability at pH 7.0-7.6
9
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3 h, at room temperature, about 70% loss of activity compared to maximal stability at pH 7.0-7.6
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45
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30 min, stable up to
50
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30 min, about 40% loss of activity
60
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30 min, complete loss of activity
70
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15 min, sensitive to heat
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activity is lost within a week, when the enzyme is frozen or kept at 4°C without glycerol
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sensitive to proteinase K treatment
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-30°C, 25 mM Tris-HCl, pH 7.6, 2 mM dithiothreitol, 2 mM MgCl2, 0.25 mM ammonium sulfate, 50% glycerol, half-life: 300 d
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gel filtration and SDS-PAGE, recombinant protein
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expressed in Arabidopsis thaliana cultivar Columbia
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expressed in Escherichia coli BL21DE3 PLys(S) strain, pET15b vector
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expression in Escherichia coli
expression in Escherichia coli
expression in Escherichia coli
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Vernon, D.M.; Bohnert, H.J.
A novel methyl transferase induced by osmotic stress in the facultative halophyte Mesembryanthemum crystallinum
EMBO J.
11
2077-2085
1992
Mesembryanthemum crystallinum
brenda
Wanek, W.; Richter, A.
Purification and characterization of myo-inositol 6-O-methyltransferase from Vigna umbellata Ohwi et Ohashi
Planta
197
427-434
1995
Vigna umbellata
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brenda
Nelson, D.E.; Rammesmayer, G.; Bohnert, H.J.
Regulation of cell-specific inositol metabolism and transport in plant salinity tolerance
Plant Cell
10
753-764
1998
Mesembryanthemum crystallinum (P45986)
brenda
Chiera, J.M.; Streeter, J.G.; Finer, J.J.
Ononitol and pinitol production in transgenic soybean containing the inositol methyl transferase gene from Mesembryanthemum crystallinum
Plant Sci.
171
647-654
2006
Mesembryanthemum crystallinum (P45986)
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brenda
Sengupta, S.; Patra, B.; Ray, S.; Majumder, A.L.
Inositol methyl tranferase from a halophytic wild rice, Porteresia coarctata Roxb. (Tateoka): regulation of pinitol synthesis under abiotic stress
Plant Cell Environ.
31
1442-1459
2008
Oryza coarctata, no activity in Oryza sativa
brenda
Zhu, B.; Peng, R.; Xiong, A.; Xu, J.; Fu, X.; Zhao, W.; Jin, X.; Meng, X.; Gao, J.; Cai, R.; Yao, Q.
Transformation with a gene for myo-inositol O-methyltransferase enhances the cold tolerance of Arabidopsis thaliana
Biol. Plant.
56
135-139
2012
Mesembryanthemum crystallinum
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brenda
Pupel, P.; Szablinska-Piernik, J.; Lahuta, L.B.
Two-step D-ononitol epimerization pathway in Medicago truncatula
Plant J.
100
237-250
2019
Medicago truncatula (G7JTH4), Medicago truncatula
brenda
Li, C.H.; Tu, Y.C.; Wen, M.F.; Tien, H.J.; Yen, H.E.
Exogenous myo-inositol increases salt tolerance and accelerates CAM induction in the early juvenile stage of the facultative halophyte Mesembryanthemum crystallinum but not in the late juvenile stage
Funct. Plant Biol.
50
363-377
2023
Mesembryanthemum crystallinum (P45986)
brenda
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