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Literature summary for 2.7.7.4 extracted from

  • Anjum, N.A.; Gill, R.; Kaushik, M.; Hasanuzzaman, M.; Pereira, E.; Ahmad, I.; Tuteja, N.; Gill, S.S.
    ATP-sulfurylase, sulfur-compounds, and plant stress tolerance (2015), Front. Plant Sci., 6, 210.
    View publication on PubMedView publication on EuropePMC

Activating Compound

Activating Compound Comment Organism Structure
additional information the enzyme in cultured cells responds to sulfate starvation Nicotiana tabacum
additional information the enzyme responds to chilling or cold stress Glycine max
additional information the enzyme responds to increased cadmium level Lepidium sativum
additional information the enzyme responds to increased cadmium level Noccaea caerulescens
additional information the enzyme responds to increased cadmium level Sedum alfredii
additional information the enzyme responds to increased cadmium level, increased salinity, and infection by Phytopthorainfestans and/or Botrytiscinerea Brassica juncea
additional information the enzyme responds to increased glutathione level Lemna gibba
additional information the enzyme responds to increased glutathione level Salvinia minima
additional information the enzyme responds to increased light irradiation Hordeum vulgare
additional information the enzyme responds to increased light irradiation Avena sativa
additional information the enzyme responds to sulfate starvation, and increased salinity, but not to increased light irradiation, H2O2, and glutathione level Brassica napus
additional information the enzyme responds to sulfate starvation, increased cadmium level, increased salinity, and infection by Phytopthorainfestans and/or Botrytiscinerea, but not to increased light irradiation Arabidopsis thaliana
additional information the enzyme responds to sulfate starvation, increased light irradiation, and chilling o cold stress Zea mays

Cloned(Commentary)

Cloned (Comment) Organism
the four ATP-S genes ATPS1,-2,-3, and -4 have N-terminal extensions typ ical of plastid-transit peptides, and are located on different chromosomes Arabidopsis thaliana
the four ATP-S genes ATPS1,-2,-3, and -4 have N-terminal extensions typical of plastid-transit peptides, and are located on different chromosomes Arabidopsis thaliana

Localization

Localization Comment Organism GeneOntology No. Textmining
chloroplast
-
Glycine max 9507
-
chloroplast Arabidopsis thaliana has isozymes with N'-terminal extensions typical of plastid-transit-peptides Arabidopsis thaliana 9507
-
chloroplast Arabidopsis thaliana has isozymes with N-terminal extensions typical of plastid-transit-peptides Arabidopsis thaliana 9507
-
chloroplast isozyme ATPS2 is dually encoded in plastidic and cytosolic forms, where translational initiation at AUGMet1 and AUGMet52 or AUGMet58 produce ATPS2 in plastid and cytosol, respectively Arabidopsis thaliana 9507
-
cytosol isozyme ATPS2 is dually encoded in plastidic and cytosolic forms, where translational initiation at AUGMet1 and AUGMet52 or AUGMet58 produce ATPS2 in plastid and cytosol, respectively Arabidopsis thaliana 5829
-
mitochondrion
-
Glycine max 5739
-
additional information Arabidopsis thaliana has isozymes with N'-terminal extensions typical of plastid-transit-peptides Arabidopsis thaliana
-
-

Metals/Ions

Metals/Ions Comment Organism Structure
Mg2+ required Triticum aestivum
Mg2+ required Hordeum vulgare
Mg2+ required Zea mays
Mg2+ required Nicotiana tabacum
Mg2+ required Avena sativa
Mg2+ required Brassica napus
Mg2+ required Oryza sativa
Mg2+ required Lemna gibba
Mg2+ required Lepidium sativum
Mg2+ required Brassica juncea
Mg2+ required Glycine max
Mg2+ required Noccaea caerulescens
Mg2+ required Camellia sinensis
Mg2+ required Sedum alfredii
Mg2+ required Stanleya pinnata
Mg2+ required Arabidopsis thaliana
Mg2+ required Salvinia minima

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
ATP + sulfate Triticum aestivum
-
diphosphate + adenylyl sulfate
-
?
ATP + sulfate Hordeum vulgare
-
diphosphate + adenylyl sulfate
-
?
ATP + sulfate Zea mays
-
diphosphate + adenylyl sulfate
-
?
ATP + sulfate Nicotiana tabacum
-
diphosphate + adenylyl sulfate
-
?
ATP + sulfate Avena sativa
-
diphosphate + adenylyl sulfate
-
?
ATP + sulfate Brassica napus
-
diphosphate + adenylyl sulfate
-
?
ATP + sulfate Oryza sativa
-
diphosphate + adenylyl sulfate
-
?
ATP + sulfate Lemna gibba
-
diphosphate + adenylyl sulfate
-
?
ATP + sulfate Lepidium sativum
-
diphosphate + adenylyl sulfate
-
?
ATP + sulfate Brassica juncea
-
diphosphate + adenylyl sulfate
-
?
ATP + sulfate Glycine max
-
diphosphate + adenylyl sulfate
-
?
ATP + sulfate Noccaea caerulescens
-
diphosphate + adenylyl sulfate
-
?
ATP + sulfate Camellia sinensis
-
diphosphate + adenylyl sulfate
-
?
ATP + sulfate Sedum alfredii
-
diphosphate + adenylyl sulfate
-
?
ATP + sulfate Stanleya pinnata
-
diphosphate + adenylyl sulfate
-
?
ATP + sulfate Arabidopsis thaliana
-
diphosphate + adenylyl sulfate
-
?
ATP + sulfate Salvinia minima
-
diphosphate + adenylyl sulfate
-
?

Organism

Organism UniProt Comment Textmining
Arabidopsis thaliana O23324 APS3; gene APS3
-
Arabidopsis thaliana Q43870 APS2; gene APS2
-
Arabidopsis thaliana Q9LIK9 APS1; gene APS1
-
Arabidopsis thaliana Q9S7D8 APS4; gene APS4
-
Avena sativa
-
-
-
Brassica juncea
-
-
-
Brassica napus
-
-
-
Camellia sinensis Q1HL01 APS2; isozyme APS2, gene sat
-
Camellia sinensis Q1HL02 APS1; isozyme APS1, gene sat
-
Glycine max I1LWX5 gene Glyma13g06940; gene Glyma13g06940
-
Glycine max I1N6H7 gene Glyma19g05020; gene Glyma19g05020
-
Glycine max I1NGL3 gene Glyma20g28980; gene Glyma20g28980
-
Glycine max Q8SAG1 gene Glyma10g38760; gene Glyma10g38760
-
Hordeum vulgare
-
-
-
Lemna gibba
-
-
-
Lepidium sativum
-
-
-
Nicotiana tabacum
-
-
-
Noccaea caerulescens
-
-
-
Oryza sativa
-
gene sat, two isozymes
-
Salvinia minima
-
-
-
Sedum alfredii
-
-
-
Stanleya pinnata
-
isozymes APS1, APS2, and APS4
-
Triticum aestivum
-
-
-
Zea mays
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
cell culture
-
Nicotiana tabacum
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
ATP + sulfate
-
Triticum aestivum diphosphate + adenylyl sulfate
-
?
ATP + sulfate
-
Hordeum vulgare diphosphate + adenylyl sulfate
-
?
ATP + sulfate
-
Zea mays diphosphate + adenylyl sulfate
-
?
ATP + sulfate
-
Nicotiana tabacum diphosphate + adenylyl sulfate
-
?
ATP + sulfate
-
Avena sativa diphosphate + adenylyl sulfate
-
?
ATP + sulfate
-
Brassica napus diphosphate + adenylyl sulfate
-
?
ATP + sulfate
-
Oryza sativa diphosphate + adenylyl sulfate
-
?
ATP + sulfate
-
Lemna gibba diphosphate + adenylyl sulfate
-
?
ATP + sulfate
-
Lepidium sativum diphosphate + adenylyl sulfate
-
?
ATP + sulfate
-
Brassica juncea diphosphate + adenylyl sulfate
-
?
ATP + sulfate
-
Glycine max diphosphate + adenylyl sulfate
-
?
ATP + sulfate
-
Noccaea caerulescens diphosphate + adenylyl sulfate
-
?
ATP + sulfate
-
Camellia sinensis diphosphate + adenylyl sulfate
-
?
ATP + sulfate
-
Sedum alfredii diphosphate + adenylyl sulfate
-
?
ATP + sulfate
-
Stanleya pinnata diphosphate + adenylyl sulfate
-
?
ATP + sulfate
-
Arabidopsis thaliana diphosphate + adenylyl sulfate
-
?
ATP + sulfate
-
Salvinia minima diphosphate + adenylyl sulfate
-
?

Synonyms

Synonyms Comment Organism
APS1
-
Camellia sinensis
APS2
-
Camellia sinensis
ATP sulfurylase 1
-
Arabidopsis thaliana
ATP sulfurylase 2
-
Arabidopsis thaliana
ATP sulfurylase 3
-
Arabidopsis thaliana
ATP sulfurylase 4
-
Arabidopsis thaliana
ATP-S
-
Triticum aestivum
ATP-S
-
Hordeum vulgare
ATP-S
-
Zea mays
ATP-S
-
Nicotiana tabacum
ATP-S
-
Avena sativa
ATP-S
-
Brassica napus
ATP-S
-
Oryza sativa
ATP-S
-
Lemna gibba
ATP-S
-
Lepidium sativum
ATP-S
-
Brassica juncea
ATP-S
-
Glycine max
ATP-S
-
Noccaea caerulescens
ATP-S
-
Camellia sinensis
ATP-S
-
Sedum alfredii
ATP-S
-
Stanleya pinnata
ATP-S
-
Arabidopsis thaliana
ATP-S
-
Salvinia minima
ATP-sulfurylase
-
Triticum aestivum
ATP-sulfurylase
-
Hordeum vulgare
ATP-sulfurylase
-
Zea mays
ATP-sulfurylase
-
Nicotiana tabacum
ATP-sulfurylase
-
Avena sativa
ATP-sulfurylase
-
Brassica napus
ATP-sulfurylase
-
Oryza sativa
ATP-sulfurylase
-
Lemna gibba
ATP-sulfurylase
-
Lepidium sativum
ATP-sulfurylase
-
Brassica juncea
ATP-sulfurylase
-
Glycine max
ATP-sulfurylase
-
Noccaea caerulescens
ATP-sulfurylase
-
Camellia sinensis
ATP-sulfurylase
-
Sedum alfredii
ATP-sulfurylase
-
Stanleya pinnata
ATP-sulfurylase
-
Arabidopsis thaliana
ATP-sulfurylase
-
Salvinia minima

Cofactor

Cofactor Comment Organism Structure
ATP
-
Triticum aestivum
ATP
-
Hordeum vulgare
ATP
-
Zea mays
ATP
-
Nicotiana tabacum
ATP
-
Avena sativa
ATP
-
Brassica napus
ATP
-
Oryza sativa
ATP
-
Lemna gibba
ATP
-
Lepidium sativum
ATP
-
Brassica juncea
ATP
-
Glycine max
ATP
-
Noccaea caerulescens
ATP
-
Camellia sinensis
ATP
-
Sedum alfredii
ATP
-
Stanleya pinnata
ATP
-
Arabidopsis thaliana
ATP
-
Salvinia minima

Expression

Organism Comment Expression
Camellia sinensis growth on Se enriched soil, suppresses APS1 expression levels in young (or mature) leaves and roots in Camellia sinensis down
Arabidopsis thaliana ATP-S activity/expression can also be controlled/modulated by S-limitation1 (SLIM1), a transcription factor identical to ethylene-insensitive3-like (EIL3) transcription factor in Arabidopsis and the regulator of many S-deficiency responsive genes additional information
Stanleya pinnata under Se-exposure and S-deficiency, Stanleya pinnata hyperaccumulates and tolerates selenium due to its ability to convert SeO24- to non-toxic organic-seleno-compounds by downregulating isozymes APS1, APS2, and APS4. Under S-sufficient and Se-exposure, adoption of different types of regulatory mechanisms and subcellular localization are revealed in Stanleya pinnata, where Se upregulates APS1 and APS4 but is not able to affect APS2 in Stanleya pinnata additional information
Camellia sinensis growth on Se enriched soil, induces APS2 expression levels in young (or mature) leaves and roots in Camellia sinensis up
Nicotiana tabacum the enzyme in cultured cells responds to sulfate starvation up
Glycine max the enzyme responds to chilling or cold stress up
Lepidium sativum the enzyme responds to increased cadmium level up
Noccaea caerulescens the enzyme responds to increased cadmium level up
Sedum alfredii the enzyme responds to increased cadmium level up
Brassica juncea the enzyme responds to increased cadmium level, increased salinity, and infection by Phytopthorainfestans and/or Botrytiscinerea up
Lemna gibba the enzyme responds to increased glutathione level up
Salvinia minima the enzyme responds to increased glutathione level up
Hordeum vulgare the enzyme responds to increased light irradiation up
Avena sativa the enzyme responds to increased light irradiation up
Brassica napus the enzyme responds to sulfate starvation, and increased salinity, but not to increased light irradiation, H2O2, and glutathione level up
Arabidopsis thaliana the enzyme responds to sulfate starvation, increased cadmium level, increased salinity, and infection by Phytopthora infestans and/or Botrytiscinerea, but not to increased light irradiation. S-depletion mediates regulation of ATP-S activity/expression. ATP-S isoforms can be differentially expressed by S-depletion, e.g. isozyme APS3, while isozyme APS2 is insensitive to S-depletion. Arabidopsis thaliana overexpressing or disruption in MYB51-gene shows alterations in ATP-S-transcript levels and activity. Transcription regulation of Arabidopsis thaliana APS genes by external factors, detailed overview up
Arabidopsis thaliana the enzyme responds to sulfate starvation, increased cadmium level, increased salinity, and infection by Phytopthora infestans and/or Botrytiscinerea, but not to increased light irradiation. S-depletion mediates regulation of ATP-S activity/expression. ATP-S isoforms can be differentially expressed by S-depletion, e.g. isozyme APS3, while isozyme APS2 is insentivie to S depletion. Expression of both ATPS1 and ATPS3 isoforms is controlled by all six GSs-related MYBTFs, namely MYB28, MYB29, and MYB76, MYB51, MYB34, and MYB122. Isozymes ATPS1 and ATPS3 are strongly associated with the control of synthesis of aliphatic and indolic GSs, respectively. Arabidopsis thaliana overexpressing or disruption in MYB51-gene shows alterations in ATP-S-transcript levels and activity. Transcription regulation of Arabidopsis thaliana APS genes by external factors, detailed overview up
Arabidopsis thaliana the enzyme responds to sulfate starvation, increased cadmium level, increased salinity, and infection by Phytopthora infestans and/or Botrytiscinerea, but not to increased light irradiation. S-depletion mediates regulation of ATP-S activity/expression. Transcription regulation of Arabidopsis thaliana APS genes by external factors, detailed overview up
Arabidopsis thaliana the enzyme responds to sulfate starvation, increased cadmium level, increased salinity, and infection by Phytopthorainfestans and/or Botrytiscinerea, but not to increased light irradiation. S-depletion-mediates regulation of ATP-S activity/expression. Expression of both ATPS1 and ATPS3 isoforms is controlled by all six GSs-related MYBTFs, namely MYB28, MYB29, and MYB76, MYB51, MYB34, and MYB122. Isozymes ATPS1 and ATPS3 are strongly associated with the control of synthesis of aliphatic and indolic GSs, respectively. Arabidopsis thaliana overexpressing or disruption in MYB51-gene shows alterations in ATP-S-transcript levels and activity. Transcription regulation of Arabidopsis thaliana APS genes by external factors, detailed overview up
Zea mays the enzyme responds to sulfate starvation, increased light irradiation, and chilling o cold stress up

General Information

General Information Comment Organism
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors Triticum aestivum
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors Hordeum vulgare
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors Zea mays
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors Nicotiana tabacum
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors Avena sativa
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors Brassica napus
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors Oryza sativa
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors Lemna gibba
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors Lepidium sativum
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors Brassica juncea
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors Glycine max
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors Noccaea caerulescens
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors Camellia sinensis
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors Sedum alfredii
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors Stanleya pinnata
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors Salvinia minima
metabolism as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors. Transcription regulation of Arabidopsis thaliana APS genes by external factors, detailed overview Arabidopsis thaliana
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Triticum aestivum
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Hordeum vulgare
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Zea mays
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Nicotiana tabacum
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Avena sativa
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Brassica napus
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Oryza sativa
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Lemna gibba
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Lepidium sativum
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Brassica juncea
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Glycine max
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Noccaea caerulescens
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Camellia sinensis
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Sedum alfredii
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Stanleya pinnata
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Arabidopsis thaliana
physiological function S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase Salvinia minima