Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
ADP-alpha-D-glucose + phosphate
alpha-D-glucose 1-phosphate + ADP
alpha-D-galactose 1-phosphate + GDP
GDP-alpha-D-galactose + phosphate
Substrates: -
Products: -
r
alpha-D-glucose 1-phosphate + GDP
GDP-alpha-D-glucose + phosphate
alpha-D-mannose 1-phosphate + GDP
GDP-alpha-D-mannose + phosphate
alpha-L-galactose 1-phosphate + GDP
GDP-alpha-L-galactose + phosphate
alpha-L-gulose 1-phosphate + GDP
GDP-beta-L-gulose + phosphate
Substrates: -
Products: -
r
GDP-alpha-D-galactose + phosphate
alpha-D-galactose 1-phosphate + GDP
Substrates: -
Products: -
r
GDP-alpha-D-galactose + phosphate
GDP + alpha-D-galactose 1-phosphate
Substrates: -
Products: -
r
GDP-alpha-D-glucose + alpha-D-mannose 1-phosphate
alpha-D-glucose 1-phosphate + GDP-alpha-D-mannose
GDP-alpha-D-glucose + phosphate
alpha-D-glucose 1-phosphate + GDP
GDP-alpha-D-mannose + phosphate
alpha-D-mannose 1-phosphate + GDP
GDP-beta-L-galactose + alpha-D-mannose 1-phosphate
beta-L-galactose 1-phosphate + GDP-alpha-D-mannose
GDP-beta-L-galactose + phosphate
GDP + beta-L-galactose 1-phosphate
GDP-beta-L-gulose + phosphate
alpha-L-gulose 1-phosphate + GDP
Substrates: -
Products: -
r
UDP-alpha-D-galactose + phosphate
alpha-D-galactose 1-phosphate + UDP
UDP-alpha-D-glucose + phosphate
alpha-D-glucose 1-phosphate + UDP
additional information
?
-
ADP-alpha-D-glucose + phosphate

alpha-D-glucose 1-phosphate + ADP
Substrates: 0.4% of the activity with GDP-L-galactose
Products: -
r
ADP-alpha-D-glucose + phosphate
alpha-D-glucose 1-phosphate + ADP
Substrates: 0.1% of the activity with GDP-L-galactose
Products: -
r
alpha-D-glucose 1-phosphate + GDP

GDP-alpha-D-glucose + phosphate
Substrates: -
Products: -
r
alpha-D-glucose 1-phosphate + GDP
GDP-alpha-D-glucose + phosphate
Substrates: -
Products: -
r
alpha-D-mannose 1-phosphate + GDP

GDP-alpha-D-mannose + phosphate
Substrates: -
Products: -
r
alpha-D-mannose 1-phosphate + GDP
GDP-alpha-D-mannose + phosphate
Substrates: -
Products: -
r
alpha-L-galactose 1-phosphate + GDP

GDP-alpha-L-galactose + phosphate
Substrates: -
Products: -
r
alpha-L-galactose 1-phosphate + GDP
GDP-alpha-L-galactose + phosphate
Substrates: -
Products: -
r
alpha-L-galactose 1-phosphate + GDP
GDP-alpha-L-galactose + phosphate
Substrates: -
Products: -
r
GDP-alpha-D-glucose + alpha-D-mannose 1-phosphate

alpha-D-glucose 1-phosphate + GDP-alpha-D-mannose
Substrates: -
Products: -
?
GDP-alpha-D-glucose + alpha-D-mannose 1-phosphate
alpha-D-glucose 1-phosphate + GDP-alpha-D-mannose
Substrates: -
Products: -
?
GDP-alpha-D-glucose + phosphate

alpha-D-glucose 1-phosphate + GDP
Substrates: -
Products: -
r
GDP-alpha-D-glucose + phosphate
alpha-D-glucose 1-phosphate + GDP
Substrates: -
Products: -
r
GDP-alpha-D-mannose + phosphate

alpha-D-mannose 1-phosphate + GDP
Substrates: -
Products: -
r
GDP-alpha-D-mannose + phosphate
alpha-D-mannose 1-phosphate + GDP
Substrates: -
Products: -
r
GDP-alpha-D-mannose + phosphate
alpha-D-mannose 1-phosphate + GDP
Substrates: 3.7% of the activity with GDP-L-galactose
Products: -
r
GDP-alpha-D-mannose + phosphate
alpha-D-mannose 1-phosphate + GDP
Substrates: 0.1% of the activity with GDP-L-galactose
Products: -
r
GDP-beta-L-galactose + alpha-D-mannose 1-phosphate

beta-L-galactose 1-phosphate + GDP-alpha-D-mannose
Substrates: -
Products: -
?
GDP-beta-L-galactose + alpha-D-mannose 1-phosphate
beta-L-galactose 1-phosphate + GDP-alpha-D-mannose
Substrates: -
Products: -
?
GDP-beta-L-galactose + alpha-D-mannose 1-phosphate
beta-L-galactose 1-phosphate + GDP-alpha-D-mannose
Substrates: -
Products: -
?
GDP-beta-L-galactose + alpha-D-mannose 1-phosphate
beta-L-galactose 1-phosphate + GDP-alpha-D-mannose
Substrates: -
Products: -
?
GDP-beta-L-galactose + phosphate

GDP + beta-L-galactose 1-phosphate
Substrates: enzyme guanylylates a conserved active site His residue with GDP-L-galactose, forming L-galactose 1-phosphate for vitamin C synthesis, and regeneration of the enzyme with phosphate to form GDP
Products: -
r
GDP-beta-L-galactose + phosphate
GDP + beta-L-galactose 1-phosphate
Substrates: preferred substrate
Products: -
r
GDP-beta-L-galactose + phosphate
GDP + beta-L-galactose 1-phosphate
Substrates: reaction proceeds through a covalent guanylated histidine residue within the histidine triad motif
Products: -
r
GDP-beta-L-galactose + phosphate
GDP + beta-L-galactose 1-phosphate
Substrates: -
Products: -
r
UDP-alpha-D-galactose + phosphate

alpha-D-galactose 1-phosphate + UDP
Substrates: 0.2% of the activity with GDP-L-galactose
Products: -
r
UDP-alpha-D-galactose + phosphate
alpha-D-galactose 1-phosphate + UDP
Substrates: 0.1% of the activity with GDP-L-galactose
Products: -
r
UDP-alpha-D-glucose + phosphate

alpha-D-glucose 1-phosphate + UDP
Substrates: 2.1% of the activity with GDP-L-galactose
Products: -
r
UDP-alpha-D-glucose + phosphate
alpha-D-glucose 1-phosphate + UDP
Substrates: 0.3% of the activity with GDP-L-galactose
Products: -
r
additional information

?
-
Substrates: no substrates: UDP-alpha-D-glucose, UDP-alpha-D-galactose, or ADP-alpha-D-glucose
Products: -
?
additional information
?
-
-
Substrates: no substrates: UDP-alpha-D-glucose, UDP-alpha-D-galactose, or ADP-alpha-D-glucose
Products: -
?
additional information
?
-
Substrates: poor reactivity of hexose 1-phosphates as acceptors
Products: -
?
additional information
?
-
Substrates: poor reactivity of hexose 1-phosphates as acceptors
Products: -
?
additional information
?
-
-
Substrates: poor reactivity of hexose 1-phosphates as acceptors
Products: -
?
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
GDP-alpha-D-glucose + alpha-D-mannose 1-phosphate
alpha-D-glucose 1-phosphate + GDP-alpha-D-mannose
GDP-beta-L-galactose + alpha-D-mannose 1-phosphate
beta-L-galactose 1-phosphate + GDP-alpha-D-mannose
GDP-beta-L-galactose + phosphate
GDP + beta-L-galactose 1-phosphate
Substrates: enzyme guanylylates a conserved active site His residue with GDP-L-galactose, forming L-galactose 1-phosphate for vitamin C synthesis, and regeneration of the enzyme with phosphate to form GDP
Products: -
r
GDP-alpha-D-glucose + alpha-D-mannose 1-phosphate

alpha-D-glucose 1-phosphate + GDP-alpha-D-mannose
Substrates: -
Products: -
?
GDP-alpha-D-glucose + alpha-D-mannose 1-phosphate
alpha-D-glucose 1-phosphate + GDP-alpha-D-mannose
Substrates: -
Products: -
?
GDP-beta-L-galactose + alpha-D-mannose 1-phosphate

beta-L-galactose 1-phosphate + GDP-alpha-D-mannose
Substrates: -
Products: -
?
GDP-beta-L-galactose + alpha-D-mannose 1-phosphate
beta-L-galactose 1-phosphate + GDP-alpha-D-mannose
Substrates: -
Products: -
?
GDP-beta-L-galactose + alpha-D-mannose 1-phosphate
beta-L-galactose 1-phosphate + GDP-alpha-D-mannose
Substrates: -
Products: -
?
GDP-beta-L-galactose + alpha-D-mannose 1-phosphate
beta-L-galactose 1-phosphate + GDP-alpha-D-mannose
Substrates: -
Products: -
?
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
malfunction

-
antisense transgenic tomato plants with about 50% decrease in ascorbate (AsA) content are obtained in order to investigate the role of GGP against chilling stress. The suppression of SlGGP could decrease ascorbate levels and enhance plant sensitivity to chilling stress-induced oxidative stresses
malfunction
deficiency of GDP-L-galactose phosphorylase reduces tomato fruit yield, the whole fruit biomass accumulation is reduced in mutant lines. The SlGGP1 mutants display decreased concentrations of ascorbate in roots, leaves, flowers, and fruit. The initiation of anthesis is delayed in ggp1 plants but the number of flowers is similar to wild type. The number of fruits is reduced in ggp1 mutants with an increased individual weight. Ethylene production is higher in the mutant lines than wild-type fruit at the breaker and red stages. Effects of source-sink manipulation on fruit yield characteristics, overview
malfunction
the VTC2 amiRNA lines grow more slowly, have lower chlorophyll content, and are more susceptible to stress than the control strains. Ascorbate concentrations in VTC2 amiRNA lines are reduced to 10% of wild-type level. In the VTC2 amiRNA lines, the mRNA abundances of APX1 and DHAR1, the main chloroplastic forms, are about 40% lower than in the EV2 control
malfunction
ascorbate concentrations are negligible in both null segregant (NS) and 35S-OsGGP brown rice (BR, unpolished grain), but significantly increased in 35S-OsGGP germinated brown rice (GBR) relative to NS. Foliar ascorbate concentrations are significantly increased in 35S-OsGGP plants in the vegetative growth phase relative to NS, but significantly reduced at the reproductive growth phase and are associated with reduced OsGGP transcript levels. The 35S-OsGGP plants do not display altered salt tolerance at the vegetative growth phase despite having elevated ascorbate concentrations
malfunction
-
the VTC2 amiRNA lines grow more slowly, have lower chlorophyll content, and are more susceptible to stress than the control strains. Ascorbate concentrations in VTC2 amiRNA lines are reduced to 10% of wild-type level. In the VTC2 amiRNA lines, the mRNA abundances of APX1 and DHAR1, the main chloroplastic forms, are about 40% lower than in the EV2 control
-
metabolism

GDP-L-galactose phosphorylase (GGP) catalyzes the first step committed to ascorbic acid synthesis. The ascorbate biosynthetic pathway critically participates in tomato development and fruit production
metabolism
Chlamydomonas VTC2 lacks negative feedback regulation by ascorbate in the physiological concentration range. Ascorbate biosynthesis is also highly regulated in Chlamydomonas albeit via mechanisms distinct from those described in land plants. Dependence of Asc biosynthesis on the photosynthetic electron transport chain
metabolism
GDP-L-galactose phosphorylase is the rate-limiting enzyme of the L-galactose pathway
metabolism
-
Chlamydomonas VTC2 lacks negative feedback regulation by ascorbate in the physiological concentration range. Ascorbate biosynthesis is also highly regulated in Chlamydomonas albeit via mechanisms distinct from those described in land plants. Dependence of Asc biosynthesis on the photosynthetic electron transport chain
-
physiological function

upregulating the expression of VTC in cultivar Baihe-35-1 results in a gradual increase in the ascorbic acid concentration of leaves inoculated with Erysiphe necator
physiological function
transgenic tobbacco plants expressing GGP and subjected to chilling stress accumulate less H2O2, demonstrate lower levels of ion leakage and malondialdehyde, and acquire higher net photosynthetic rate, higher maximum photochemical efficiency of PSII, and higher D1 protein content compared with the wild-type plants. The transgenic plants subjected to chilling stress also show higher GDP-L-galactose phosphorylase activity, increased ascorbate content as well as ascorbate peroxidase and oxidizable P700 activities than wild-type plants
physiological function
GGP has a critical role in modulating ascorbate concentrations in kiwifruit species under abiotic stresses
physiological function
-
GGP has a critical role in modulating ascorbate concentrations in kiwifruit species under abiotic stresses
physiological function
GDP-L-galactose phosphorylase is required for ascorbic acid synthesis. Participation of GDP-L-galactose phosphorylase and ascorbate in tomato fruit production and quality
physiological function
GDP-L-galactose phosphorylase plays a pivotal role in ascorbate biosynthesis. In contrast to plants, there is no circadian regulation of ascorbate biosynthesis, photosynthesis is not required per se for ascorbate biosynthesis, and Chlamydomonas VTC2 lacks negative feedback regulation by ascorbate in the physiological concentration range
physiological function
-
upregulating the expression of VTC in cultivar Baihe-35-1 results in a gradual increase in the ascorbic acid concentration of leaves inoculated with Erysiphe necator
-
physiological function
-
GDP-L-galactose phosphorylase plays a pivotal role in ascorbate biosynthesis. In contrast to plants, there is no circadian regulation of ascorbate biosynthesis, photosynthesis is not required per se for ascorbate biosynthesis, and Chlamydomonas VTC2 lacks negative feedback regulation by ascorbate in the physiological concentration range
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
G224D
less than 0.1% of wild-type activity
H238N
less than 0.1% of wild-type activity
S290F
less than 0.1% of wild-type activity
additional information

construction of isoforms Vtc2/Vtc5 double mutants. Double mutants show growth arrest immediately upon germination and the cotyledons subsequently bleach. Normal growth is restored by supplementation with ascorbate or L-galactose. vtc2-1 leaves contain more mannose 6-phosphate than wild-type
additional information
construction of isoforms Vtc2/Vtc5 double mutants. Double mutants show growth arrest immediately upon germination and the cotyledons subsequently bleach. Normal growth is restored by supplementation with ascorbate or L-galactose. vtc2-1 leaves contain more mannose 6-phosphate than wild-type
additional information
-
construction of isoforms Vtc2/Vtc5 double mutants. Double mutants show growth arrest immediately upon germination and the cotyledons subsequently bleach. Normal growth is restored by supplementation with ascorbate or L-galactose. vtc2-1 leaves contain more mannose 6-phosphate than wild-type
additional information
construction of isoforms Vtc2/Vtc5 double mutants. Double mutants show growth arrest immediately upon germination and the cotyledons subsequently bleach. Normal growth is restored by supplementation with ascorbate or L-galactose
additional information
construction of isoforms Vtc2/Vtc5 double mutants. Double mutants show growth arrest immediately upon germination and the cotyledons subsequently bleach. Normal growth is restored by supplementation with ascorbate or L-galactose
additional information
-
construction of isoforms Vtc2/Vtc5 double mutants. Double mutants show growth arrest immediately upon germination and the cotyledons subsequently bleach. Normal growth is restored by supplementation with ascorbate or L-galactose
additional information
Chlamydomonas reinhardtii strain cw15-325 is used as recipient strain for transformation with VTC2 amiRNA. The VTC2 gene encoding GDP-L-galactose phosphorylase is targeted using artificial microRNAs. Upon H2O2 stress, alanine and proline accumulated, whereas the amount of cystine strongly decreases in the VTC2 amiRNA lines. The amounts of aspartic acid, lysine and ornithine are lower in the VTC2 amiRNA lines under control conditions, but these differences are much smaller following H2O2 stress. Changes in the tricarboxylic acid cycle intermediates are also apparent. Following H2O2 treatment, the amount of pyruvic acid and citric acid decreases, but the amounts of malic acid and succinic acid increases in all the lines. Furthermore, the amount of mannose and glycerol-3-phosphate decreases in the VTC2 amiRNA lines. Phenotype analysis, overview
additional information
-
Chlamydomonas reinhardtii strain cw15-325 is used as recipient strain for transformation with VTC2 amiRNA. The VTC2 gene encoding GDP-L-galactose phosphorylase is targeted using artificial microRNAs. Upon H2O2 stress, alanine and proline accumulated, whereas the amount of cystine strongly decreases in the VTC2 amiRNA lines. The amounts of aspartic acid, lysine and ornithine are lower in the VTC2 amiRNA lines under control conditions, but these differences are much smaller following H2O2 stress. Changes in the tricarboxylic acid cycle intermediates are also apparent. Following H2O2 treatment, the amount of pyruvic acid and citric acid decreases, but the amounts of malic acid and succinic acid increases in all the lines. Furthermore, the amount of mannose and glycerol-3-phosphate decreases in the VTC2 amiRNA lines. Phenotype analysis, overview
additional information
-
Chlamydomonas reinhardtii strain cw15-325 is used as recipient strain for transformation with VTC2 amiRNA. The VTC2 gene encoding GDP-L-galactose phosphorylase is targeted using artificial microRNAs. Upon H2O2 stress, alanine and proline accumulated, whereas the amount of cystine strongly decreases in the VTC2 amiRNA lines. The amounts of aspartic acid, lysine and ornithine are lower in the VTC2 amiRNA lines under control conditions, but these differences are much smaller following H2O2 stress. Changes in the tricarboxylic acid cycle intermediates are also apparent. Following H2O2 treatment, the amount of pyruvic acid and citric acid decreases, but the amounts of malic acid and succinic acid increases in all the lines. Furthermore, the amount of mannose and glycerol-3-phosphate decreases in the VTC2 amiRNA lines. Phenotype analysis, overview
-
additional information
construction of hemizygous and homozygous OsGGP overexpressing plants using the constitutive dual CaMV 35S promoter and Agrobacterium-mediated transformation leading to 5-9fold increased ascorbate concentrations in homozygous plants compared to low amounts in heterozygous and wild-type plants. Phenotype analysis, overview. Ascorbate concentrations are positively correlated with ferritin cn Caco-2 cells exposed to in vitro digests of NS and 35S-OsGGP BR and GBR samples
additional information
analysis of the phenotype of two SlGGP1-deficient EMS Micro-Tom mutants. Fruits of the ggp1 plants produce more ethylene and show higher firmness and soluble solids content than the wild-type after the breaker stage. Leaf CO2 uptake decreases about 50% in both ggp1 mutants at saturating light conditions; however, O2 production in an enriched CO2 atmosphere is only 19% higher in wild-type leaves. Leaf conductance that is largely reduced in both mutants may be the main limitation for photosynthesis. Ethylene production is higher in the mutant lines than wild-type fruit at the breaker and red stages
additional information
-
analysis of the phenotype of two SlGGP1-deficient EMS Micro-Tom mutants. Fruits of the ggp1 plants produce more ethylene and show higher firmness and soluble solids content than the wild-type after the breaker stage. Leaf CO2 uptake decreases about 50% in both ggp1 mutants at saturating light conditions; however, O2 production in an enriched CO2 atmosphere is only 19% higher in wild-type leaves. Leaf conductance that is largely reduced in both mutants may be the main limitation for photosynthesis. Ethylene production is higher in the mutant lines than wild-type fruit at the breaker and red stages
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
expression is induced by Erysiphe necator and defense signaling molecules, including salicylic acid, methyl jasmonate, and ethephon
expression of the VTC2 gene is rapidly induced by H2O2 and 1O2 resulting in a manifold increase in ascorbate content. The Chlamydomonas reinhardtii cell wall-deficient strain cw15-325 carrying a mutation in the argininosuccinate lyase (ARG7) with the VTC2-specific amiRNA vectors. In the case of the CDS-targeting amiRNA (VTC2-A) construct, 96 arginine-prototrophic colonies are tested by PCR and 89 of them are found to carry the whole amiRNA cassette. For the VTC2 3'-UTR-targeting amiRNA (VTC2-B) construct, 45 of the 96 tested arginine-prototrophic colonies carry the whole amiRNA cassette. Their Asc content shows a strong reduction (at least 80% reduction in 70% of the strains). In the VTC2 amiRNA lines, the mRNA abundances of APX1 and DHAR1, the main chloroplastic forms, are about 40% lower than in the EV2 control. The mutant lines also respond to high-light treatment
in leaves treated by continuous darkness or light, abscisic acid or methyljasmonate, heat, or a hypoxic environment, there is some correlation between the relative levels of GGP mRNA and ascorbate concentrations. In transformed tobacco plants, activity of the GGP promoter is induced by all of these treatments
expression is induced by Erysiphe necator and defense signaling molecules, including salicylic acid, methyl jasmonate, and ethephon

expression is induced by Erysiphe necator and defense signaling molecules, including salicylic acid, methyl jasmonate, and ethephon
-
-
expression of the VTC2 gene is rapidly induced by H2O2 and 1O2 resulting in a manifold increase in ascorbate content. The Chlamydomonas reinhardtii cell wall-deficient strain cw15-325 carrying a mutation in the argininosuccinate lyase (ARG7) with the VTC2-specific amiRNA vectors. In the case of the CDS-targeting amiRNA (VTC2-A) construct, 96 arginine-prototrophic colonies are tested by PCR and 89 of them are found to carry the whole amiRNA cassette. For the VTC2 3'-UTR-targeting amiRNA (VTC2-B) construct, 45 of the 96 tested arginine-prototrophic colonies carry the whole amiRNA cassette. Their Asc content shows a strong reduction (at least 80% reduction in 70% of the strains). In the VTC2 amiRNA lines, the mRNA abundances of APX1 and DHAR1, the main chloroplastic forms, are about 40% lower than in the EV2 control. The mutant lines also respond to high-light treatment

expression of the VTC2 gene is rapidly induced by H2O2 and 1O2 resulting in a manifold increase in ascorbate content. The Chlamydomonas reinhardtii cell wall-deficient strain cw15-325 carrying a mutation in the argininosuccinate lyase (ARG7) with the VTC2-specific amiRNA vectors. In the case of the CDS-targeting amiRNA (VTC2-A) construct, 96 arginine-prototrophic colonies are tested by PCR and 89 of them are found to carry the whole amiRNA cassette. For the VTC2 3'-UTR-targeting amiRNA (VTC2-B) construct, 45 of the 96 tested arginine-prototrophic colonies carry the whole amiRNA cassette. Their Asc content shows a strong reduction (at least 80% reduction in 70% of the strains). In the VTC2 amiRNA lines, the mRNA abundances of APX1 and DHAR1, the main chloroplastic forms, are about 40% lower than in the EV2 control. The mutant lines also respond to high-light treatment
-
-
in leaves treated by continuous darkness or light, abscisic acid or methyljasmonate, heat, or a hypoxic environment, there is some correlation between the relative levels of GGP mRNA and ascorbate concentrations. In transformed tobacco plants, activity of the GGP promoter is induced by all of these treatments

in leaves treated by continuous darkness or light, abscisic acid or methyljasmonate, heat, or a hypoxic environment, there is some correlation between the relative levels of GGP mRNA and ascorbate concentrations. In transformed tobacco plants, activity of the GGP promoter is induced by all of these treatments
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Dowdle, J.; Ishikawa, T.; Gatzek, S.; Rolinski, S.; Smirnoff, N.
Two genes in Arabidopsis thaliana encoding GDP-l-galactose phosphorylase are required for ascorbate biosynthesis and seedling viability
Plant J.
52
673689
2007
Arabidopsis thaliana (Q8RWE8), Arabidopsis thaliana (Q9FLP9), Arabidopsis thaliana
brenda
Linster, C.L.; Gomez, T.A.; Christensen, K.C.; Adler, L.N.; Young, B.D.; Brenner, C.; Clarke, S.G.
Arabidopsis VTC2 encodes a GDP-L-galactose phosphorylase, the last unknown enzyme in the Smirnoff-Wheeler pathway to ascorbic acid in plants
J. Biol. Chem.
282
18879-18885
2007
Arabidopsis thaliana (Q8RWE8), Arabidopsis thaliana
brenda
Linster, C.L.; Adler, L.N.; Webb, K.; Christensen, K.C.; Brenner, C.; Clarke, S.G.
A second GDP-L-galactose phosphorylase in Arabidopsis en route to vitamin C. Covalent intermediate and substrate requirements for the conserved reaction
J. Biol. Chem.
283
18483-18492
2008
Arabidopsis thaliana (Q8RWE8), Arabidopsis thaliana (Q9FLP9), Arabidopsis thaliana
brenda
Mueller-Moule, P.
An expression analysis of the ascorbate biosynthesis enzyme VTC2
Plant Mol. Biol.
68
31-41
2008
Arabidopsis thaliana
brenda
Wang, L.Y.; Li, D.; Deng, Y.S.; Lv, W.; Meng, Q.W.
Antisense-mediated depletion of tomato GDP-L-galactose phosphorylase increases susceptibility to chilling stress
J. Plant Physiol.
170
303-314
2013
Solanum lycopersicum
brenda
Hou, H.M.; Li, H.E.; Gao, M.; Wang, H.; Jiao, C.; Wang, X.P.
Expression of a GDP-L-galactose phosphorylase-like gene in a Chinese wild Vitis species induces responses to Erysiphe necator and defense signaling molecules
Genet. Mol. Res.
12
3830-3844
2013
Vitis pseudoreticulata (G3LW45), Vitis pseudoreticulata Baihe-35-l (G3LW45)
brenda
Wang, L.; Meng, X.; Yang, D.; Ma, N.; Wang, G.; Meng, Q.
Overexpression of tomato GDP-L-galactose phosphorylase gene in tobacco improves tolerance to chilling stress
Plant Cell Rep.
33
1441-1451
2014
Solanum lycopersicum (H9D2D6), Solanum lycopersicum
brenda
Li, J.; Liang, D.; Li, M.; Ma, F.
Light and abiotic stresses regulate the expression of GDP-L-galactose phosphorylase and levels of ascorbic acid in two kiwifruit genotypes via light-responsive and stress-inducible cis-elements in their promoters
Planta
238
535-547
2013
Actinidia deliciosa (D3JYW8), Actinidia deliciosa, Actinidia eriantha
brenda
Broad, R.; Bonneau, J.; Beasley, J.; Roden, S.; Sadowski, P.; Jewell, N.; Brien, C.; Berger, B.; Tako, E.; Glahn, R.; Hellens, R.; Johnson, A.
Effect of rice GDP-L-galactose phosphorylase constitutive overexpression on ascorbate concentration, stress tolerance, and iron bioavailability in rice
Front. Plant Sci.
11
595439
2020
Oryza sativa Japonica Group (Q2QWM9)
brenda
Vidal-Meireles, A.; Neupert, J.; Zsigmond, L.; Rosado-Souza, L.; Kovacs, L.; Nagy, V.; Galambos, A.; Fernie, A.R.; Bock, R.; Toth, S.Z.
Regulation of ascorbate biosynthesis in green algae has evolved to enable rapid stress-induced response via the VTC2 gene encoding GDP-L-galactose phosphorylase
New Phytol.
214
668-681
2017
Chlamydomonas reinhardtii (A0A2K3D0V9), Chlamydomonas reinhardtii, Chlamydomonas reinhardtii cw15-325 (A0A2K3D0V9)
brenda
Alegre, M.L.; Steelheart, C.; Baldet, P.; Rothan, C.; Just, D.; Okabe, Y.; Ezura, H.; Smirnoff, N.; Gergoff Grozeff, G.E.; Bartoli, C.G.
Deficiency of GDP-L-galactose phosphorylase, an enzyme required for ascorbic acid synthesis, reduces tomato fruit yield
Planta
251
54
2020
Solanum lycopersicum (H9D2D6), Solanum lycopersicum
brenda