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0.044 - 0.2
UDP-alpha-D-glucose
0.017
ADP
-
isoform SUS1, at pH 7.0 and 37°C
4.37
D-fructose
-
isoform SUS1, with UDP-alpha-D-glucose as cosubstrate, at pH 9.5 and 25°C
4.97
D-fructose
-
isoform SUS4, with UDP-alpha-D-glucose as cosubstrate, at pH 9.5 and 25°C
12.4
D-fructose
-
isoform SUS6, with UDP-alpha-D-glucose as cosubstrate, at pH 9.5 and 25°C
42
D-fructose
-
isoform SUS3, with UDP-alpha-D-glucose as cosubstrate, at pH 9.5 and 25°C
31.58
sucrose
-
isoform SUS1, with UDP as cosubstrate, at pH 6.0 and 25°C
48
sucrose
cosubstrate UDP, pH 7.0, 37°C
53
sucrose
cosubstrate UDP, pH 7.0, 37°C
53
sucrose
-
isoform SUS1, with UDP as cosubstrate, at pH 7.0 and 37°C
145
sucrose
cosubstrate ADP, pH 7.0, 37°C
185
sucrose
cosubstrate ADP, pH 7.0, 37°C
185
sucrose
-
isoform SUS1, with ADP as cosubstrate, at pH 7.0 and 37°C
0.085
UDP
-
isoform SUS1, at pH 6.0 and 25°C
0.39
UDP
-
isoform SUS1, at pH 7.0 and 37°C
0.044
UDP-alpha-D-glucose
-
isoform SUS1, at pH 9.5 and 25°C
0.056
UDP-alpha-D-glucose
-
isoform SUS6, at pH 9.5 and 25°C
0.069
UDP-alpha-D-glucose
-
isoform SUS4, at pH 9.5 and 25°C
0.2
UDP-alpha-D-glucose
-
isoform SUS3, at pH 9.5 and 25°C
0.05
UDP-glucose
-
pH 7.6, temperature not specified in the publication
25
UDP-glucose
-
pH 7.6, temperature not specified in the publication
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isozyme SUS4
brenda
-
brenda
-
brenda
-
at 3 d and 10 d after flowering, SUS protein localized to the silique wall, seed coat, funiculus, and endosperm. By 13 d after flowering, SUS protein is detected in the embryo and aleurone layer, but is absent from the seed coat and funiculus
brenda
isozyme SUS6
brenda
-
at 3 d and 10 d after flowering, SUS protein localized to the silique wall, seed coat, funiculus, and endosperm. By 13 d after flowering, SUS protein is detected in the embryo and aleurone layer, but is absent from the seed coat and funiculus
brenda
-
brenda
-
brenda
-
at 3 d and 10 d after flowering, SUS protein localized to the silique wall, seed coat, funiculus, and endosperm. By 13 d after flowering, SUS protein is detected in the embryo and aleurone layer, but is absent from the seed coat and funiculus. Within the silique wall, SUS localizes specifically to the companion cells, indicating that SUS activity may be required to provide energy for phloem transport activities in the silique wall
brenda
-
brenda
-
brenda
isozyme expresssion patterns during development differ from each other
brenda
-
brenda
-
brenda
-
brenda
isoform SuSy1 is expressed exclusively in phloem companion cells
brenda
isoform SuSy4 is expressed exclusively in phloem companion cells
brenda
-
brenda
-
at 3 d and 10 d after flowering, SUS protein localized to the silique wall, seed coat, funiculus, and endosperm. By 13 d after flowering, SUS protein is detected in the embryo and aleurone layer, but is absent from the seed coat and funiculus
brenda
-
brenda
-
at 3 d and 10 d after flowering, SUS protein localized to the silique wall, seed coat, funiculus, and endosperm. By 13 d after flowering, SUS protein is detected in the embryo and aleurone layer, but is absent from the seed coat and funiculus
brenda
-
-
brenda
-
brenda
isozyme expresssion patterns during development differ from each other
brenda
-
brenda
isozyme SUS1
brenda
-
brenda
isozye SUS5
brenda
-
brenda
-
at 3 d and 10 d after flowering, SUS protein localized to the silique wall, seed coat, funiculus, and endosperm. By 13 day after flowering, SUS protein is detected in the embryo and aleurone layer, but is absent from the seed coat and funiculus. Co-localization of SUS protein and starch grains in the seed coat at 3 and 10 day after flowering indicates that SUS may be involved in temporary starch deposition during the early stages of seed development
brenda
-
brenda
-
brenda
-
brenda
-
-
brenda
isozyme SUS5
brenda
additional information
nematode-induced syncytium in roots, isozymes expression analysis, overview
brenda
additional information
nematode-induced syncytium in roots, isozymes expression analysis, overview
brenda
additional information
nematode-induced syncytium in roots, isozymes expression analysis, overview
brenda
additional information
nematode-induced syncytium in roots, isozymes expression analysis, overview
brenda
additional information
nematode-induced syncytium in roots, isozymes expression analysis, overview
brenda
additional information
nematode-induced syncytium in roots, isozymes expression analysis, overview
brenda
additional information
-
nematode-induced syncytium in roots, isozymes expression analysis, overview
brenda
additional information
nematode-induced syncytium in roots, isozymes expression analysis, overview
brenda
additional information
nematode-induced syncytium in roots, isozymes expression analysis, overview
brenda
additional information
nematode-induced syncytium in roots, isozymes expression analysis, overview
brenda
additional information
nematode-induced syncytium in roots, isozymes expression analysis, overview
brenda
additional information
nematode-induced syncytium in roots, isozymes expression analysis, overview
brenda
additional information
nematode-induced syncytium in roots, isozymes expression analysis, overview
brenda
additional information
-
nematode-induced syncytium in roots, isozymes expression analysis, overview
brenda
additional information
-
not detected in developing xylem tissue of elongating stem
brenda
additional information
not detected in developing xylem tissue of elongating stem
brenda
additional information
not detected in developing xylem tissue of elongating stem
brenda
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metabolism
the enzyme is involved in the metabolic regulation of the sucrose metabolism, overview
malfunction
mutants defective in sucrose synthase display a conditional phenotype in terms of low-oxygen tolerance, lower tolerance of the sus1/sus4 mutant for hypoxia compared to wild-type
malfunction
systemically affected sugar levels and enzyme activities in the shoots of the enzyme mutants, suggesting changes in the source-sink relationship. In sink tissues, sucrose is cleaved to make glucose and fructose available for energy-gaining reactions, macromolecule and amino acid biosynthesis. Heterodera schachtii root infection affects systemic sucrose processing
physiological function
role for sucrose synthase as part of the acclimation mechanism to anoxia in dicotyledons. Contribution of sucrose synthases to the fermentative metabolism linked to the ability to survive low-oxygen conditions. Isozyme SUS4 is not required for the sucrose-ethanol transition in seedlings under low-oxygen conditions. Sucrose synthase contributes to ethanol production under anoxia
physiological function
role of the sucrose-cleaving enzymes sucrose synthases in the development of endoparasitic nematodes, the cyst forming Heterodera schachtii and the root-knot forming Meloidogyne javanica. The parasites influence the regulation of enzyme transcription, general role of sucrose-degrading enzymes during plant-nematode interactions, overview. Sucrose synthases play particular roles in nematode-induced feeding sites
malfunction
mutants defective in sucrose synthase display a conditional phenotype in terms of low-oxygen tolerance
malfunction
mutants defective in sucrose synthase display a conditional phenotype in terms of low-oxygen tolerance, lower tolerance of the sus1/sus4 mutant for hypoxia compared to wild-type
malfunction
systemically affected sugar levels and enzyme activities in the shoots of the enzyme mutants, suggesting changes in the source-sink relationship. In sink tissues, sucrose is cleaved to make glucose and fructose available for energy-gaining reactions, macromolecule and amino acid biosynthesis. Heterodera schachtii root infection affects systemic sucrose processing
metabolism
sucrose synthase is involved in UDP-glucose formation, the principal nucleoside diphosphate in the sucrose cleavage reaction and in trehalose biosynthesis
metabolism
the enzyme is involved in the metabolic regulation of the sucrose metabolism, overview
physiological function
the enzyme is involved in various physiological processes including seed growth and resistance to biotic and abiotic stresses
physiological function
-
enzymic activities in organs of a mutant lacking the activities of isoforms sus1, sus2, sus3, sus4 is about 80-90% of those found in wild-type
physiological function
isoform Sus2 knockout mutant shows 30-50% less sucrose synthase activity than wild-type and therefore accumulates 40% more sucrose and 50% less fructose at 15 days after flowering. Mutation does not affect the hexose phosphate pool, but leads to 30-70% less starch in embryo and seed coat. Lipid content is are 55% higher at 9-15 days after flowering. Final seed size and composition are unaltered due to an earlier cessation of growth, thus giving rise to an apparent silent phenotype of mature mutant seeds
physiological function
isoform Sus3 knockout mutant shows 30-50% less sucrose synthase activity than wild-type and therefore accumulates 40% more sucrose and 50% less fructose at 15 days after flowering. Mutation does not affect the hexose phosphate pool, but leads to 30-70% less starch in embryo and seed coat. Lipid content is are 55% higher at 9-15 days after flowering. Final seed size and composition are unaltered due to an earlier cessation of growth, thus giving rise to an apparent silent phenotype of mature mutant seeds
physiological function
mutant lacking isoforms sus1/sus2/sus3/sus4 displays wild-type SUS5 and SUS6 expression levels in leaf, whereas leaves of the sus5/sus6 mutant display wild-type SUS1-4 expression levels. Sucrose synthase activity in leaves and stems of the sus1/sus2/sus3/sus4 and sus5/sus6 plants is about 85% of that of wild-type leaves, which can support normal cellulose and starch biosynthesis
physiological function
role for sucrose synthase as part of the acclimation mechanism to anoxia in dicotyledons. Contribution of sucrose synthases to the fermentative metabolism linked to the ability to survive low-oxygen conditions. Isozyme SUS1 is not required for the sucrose-ethanol transition in seedlings under low-oxygen conditions. Sucrose synthase contributes to ethanol production under anoxia
physiological function
role for sucrose synthase as part of the acclimation mechanism to anoxia in dicotyledons. Contribution of sucrose synthases to the fermentative metabolism linked to the ability to survive low-oxygen conditions. Sucrose synthase contributes to ethanol production under anoxia
physiological function
role of the sucrose-cleaving enzymes sucrose synthases in the development of endoparasitic nematodes, the cyst forming Heterodera schachtii and the root-knot forming Meloidogyne javanica. The parasites influence the regulation of enzyme transcription, general role of sucrose-degrading enzymes during plant-nematode interactions, overview. Sucrose synthases play particular roles in nematode-induced feeding sites
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additional information
generation and analysis of isozyme mutant lines
additional information
generation and analysis of isozyme mutant lines
additional information
generation and analysis of isozyme mutant lines
additional information
generation and analysis of isozyme mutant lines
additional information
generation and analysis of isozyme mutant lines
additional information
generation and analysis of isozyme mutant lines
additional information
-
generation and analysis of isozyme mutant lines
additional information
generation of a sus4 mutant and a sus1/sus4 double mutant. Gene sus4 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
generation of a sus4 mutant and a sus1/sus4 double mutant. Gene sus4 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
generation of a sus4 mutant and a sus1/sus4 double mutant. Gene sus4 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
generation of a sus4 mutant and a sus1/sus4 double mutant. Gene sus4 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
generation of a sus4 mutant and a sus1/sus4 double mutant. Gene sus4 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
generation of a sus4 mutant and a sus1/sus4 double mutant. Gene sus4 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
manipulation of sugar levels in transgenic plants by overexpressing sucrose synthase
additional information
manipulation of sugar levels in transgenic plants by overexpressing sucrose synthase
additional information
manipulation of sugar levels in transgenic plants by overexpressing sucrose synthase
additional information
manipulation of sugar levels in transgenic plants by overexpressing sucrose synthase
additional information
manipulation of sugar levels in transgenic plants by overexpressing sucrose synthase
additional information
manipulation of sugar levels in transgenic plants by overexpressing sucrose synthase
additional information
gene SUS2 does not display an altered pattern of expression as a consequence of the lack of SUS1
additional information
gene SUS2 does not display an altered pattern of expression as a consequence of the lack of SUS1
additional information
gene SUS2 does not display an altered pattern of expression as a consequence of the lack of SUS1
additional information
gene SUS2 does not display an altered pattern of expression as a consequence of the lack of SUS1
additional information
gene SUS2 does not display an altered pattern of expression as a consequence of the lack of SUS1
additional information
gene SUS2 does not display an altered pattern of expression as a consequence of the lack of SUS1
additional information
gene SUS3 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene SUS3 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene SUS3 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene SUS3 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene SUS3 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene SUS3 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene sus5 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene sus5 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene sus5 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene sus5 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene sus5 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene sus5 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene sus6 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene sus6 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene sus6 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene sus6 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene sus6 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
gene sus6 does not display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
generation and analysis of isozyme mutant lines
additional information
generation and analysis of isozyme mutant lines
additional information
generation and analysis of isozyme mutant lines
additional information
generation and analysis of isozyme mutant lines
additional information
generation and analysis of isozyme mutant lines
additional information
generation and analysis of isozyme mutant lines
additional information
-
generation and analysis of isozyme mutant lines
additional information
generation of a sus1 mutant and a sus1/sus4 double mutant. None of the other five genes display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
generation of a sus1 mutant and a sus1/sus4 double mutant. None of the other five genes display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
generation of a sus1 mutant and a sus1/sus4 double mutant. None of the other five genes display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
generation of a sus1 mutant and a sus1/sus4 double mutant. None of the other five genes display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
generation of a sus1 mutant and a sus1/sus4 double mutant. None of the other five genes display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
generation of a sus1 mutant and a sus1/sus4 double mutant. None of the other five genes display an altered pattern of expression as a consequence of the lack of SUS1. Impact of SUS mutations on ethanol production and ATP/ADP ratio under low-oxygen conditions, overview
additional information
manipulation of sugar levels in transgenic plants by overexpressing sucrose synthase
additional information
manipulation of sugar levels in transgenic plants by overexpressing sucrose synthase
additional information
manipulation of sugar levels in transgenic plants by overexpressing sucrose synthase
additional information
manipulation of sugar levels in transgenic plants by overexpressing sucrose synthase
additional information
manipulation of sugar levels in transgenic plants by overexpressing sucrose synthase
additional information
manipulation of sugar levels in transgenic plants by overexpressing sucrose synthase
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Fallahi, H.; Scofield, G.N.; Badger, M.R.; Chow, W.S.; Furbank, R.T.; Ruan, Y.L.
Localization of sucrose synthase in developing seed and siliques of Arabidopsis thaliana reveals diverse roles for SUS during development
J. Exp. Bot.
59
3283-3295
2008
Arabidopsis thaliana
brenda
Siddique, S.; Endres, S.; Atkins, J.M.; Szakasits, D.; Wieczorek, K.; Hofmann, J.; Blaukopf, C.; Urwin, P.E.; Tenhaken, R.; Grundler, F.M.; Kreil, D.P.; Bohlmann, H.
Myo-inositol oxygenase genes are involved in the development of syncytia induced by Heterodera schachtii in Arabidopsis roots
New Phytol.
184
457-472
2009
Arabidopsis thaliana (F4K5W8), Arabidopsis thaliana (P49040), Arabidopsis thaliana (Q00917), Arabidopsis thaliana (Q9FX32), Arabidopsis thaliana (Q9LXL5), Arabidopsis thaliana (Q9M111)
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
Zheng, Y.; Anderson, S.; Zhang, Y.; Garavito, R.M.
The structure of sucrose synthase-1 from Arabidopsis thaliana and its functional implications
J. Biol. Chem.
286
36108-36118
2011
Arabidopsis thaliana (P49040), Arabidopsis thaliana
brenda
Almagro, G.; Baroja-Fernandez, E.; Munoz, F.J.; Bahaji, A.; Etxeberria, E.; Li, J.; Montero, M.; Hidalgo, M.; Sesma, M.T.; Pozueta-Romero, J.
No evidence for the occurrence of substrate inhibition of Arabidopsis thaliana sucrose synthase-1 (AtSUS1) by fructose and UDP-glucose
Plant Signal. Behav.
7
799-802
2012
Arabidopsis thaliana
brenda
Angeles-Nunez, J.G.; Tiessen, A.
Arabidopsis sucrose synthase 2 and 3 modulate metabolic homeostasis and direct carbon towards starch synthesis in developing seeds
Planta
232
701-718
2010
Arabidopsis thaliana (Q00917), Arabidopsis thaliana (Q9M111)
brenda
Baroja-Fernandez, E.; Munoz, F.J.; Li, J.; Bahaji, A.; Almagro, G.; Montero, M.; Etxeberria, E.; Hidalgo, M.; Sesma, M.T.; Pozueta-Romero, J.
Sucrose synthase activity in the sus1/sus2/sus3/sus4 Arabidopsis mutant is sufficient to support normal cellulose and starch production
Proc. Natl. Acad. Sci. USA
109
321-326
2012
Arabidopsis thaliana (P49040), Arabidopsis thaliana (Q9M111)
brenda
Nguyen, Q.; Luan, S.; Wi, S.; Bae, H.; Lee, D.; Bae, H.
Pronounced phenotypic changes in transgenic tobacco plants overexpressing sucrose synthase may reveal a novel sugar signaling pathway
Front. Plant Sci.
6
1216
2016
Arabidopsis thaliana (F4K5W8), Arabidopsis thaliana (P49040), Arabidopsis thaliana (Q00917), Arabidopsis thaliana (Q9FX32), Arabidopsis thaliana (Q9LXL5), Arabidopsis thaliana (Q9M111)
brenda
Cabello, S.; Lorenz, C.; Crespo, S.; Cabrera, J.; Ludwig, R.; Escobar, C.; Hofmann, J.
Altered sucrose synthase and invertase expression affects the local and systemic sugar metabolism of nematode-infected Arabidopsis thaliana plants
J. Exp. Bot.
65
201-212
2014
Arabidopsis thaliana (F4K5W8), Arabidopsis thaliana (P49040), Arabidopsis thaliana (Q00917), Arabidopsis thaliana (Q9FX32), Arabidopsis thaliana (Q9LXL5), Arabidopsis thaliana (Q9M111), Arabidopsis thaliana
brenda
Santaniello, A.; Loreti, E.; Gonzali, S.; Novi, G.; Perata, P.
A reassessment of the role of sucrose synthase in the hypoxic sucrose-ethanol transition in Arabidopsis
Plant Cell Environ.
37
2294-2302
2014
Arabidopsis thaliana (F4K5W8), Arabidopsis thaliana (P49040), Arabidopsis thaliana (Q00917), Arabidopsis thaliana (Q9FX32), Arabidopsis thaliana (Q9LXL5), Arabidopsis thaliana (Q9M111), Arabidopsis thaliana Col-0 (F4K5W8), Arabidopsis thaliana Col-0 (P49040), Arabidopsis thaliana Col-0 (Q00917), Arabidopsis thaliana Col-0 (Q9FX32), Arabidopsis thaliana Col-0 (Q9LXL5), Arabidopsis thaliana Col-0 (Q9M111)
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
Yao, D.; Gonzales-Vigil, E.; Mansfield, S.D.
Arabidopsis sucrose synthase localization indicates a primary role in sucrose translocation in phloem
J. Exp. Bot.
71
1858-1869
2020
Arabidopsis thaliana, Arabidopsis thaliana (P49040), Arabidopsis thaliana (Q00917)
brenda