Application | Comment | Organism |
---|---|---|
molecular biology | BADH application as a marker for chloroplast engineering without using antibiotic can avoid transferring antibiotic genes from the plant and thus assists to allay public concern regarding genetic modifications | Solanum lycopersicum |
molecular biology | BADH application as a marker for chloroplast engineering without using antibiotic can avoid transferring antibiotic genes from the plant and thus assists to allay public concern regarding genetic modifications | Zea mays |
molecular biology | BADH application as a marker for chloroplast engineering without using antibiotic can avoid transferring antibiotic genes from the plant and thus assists to allay public concern regarding genetic modifications | Triticum aestivum |
molecular biology | BADH application as a marker for chloroplast engineering without using antibiotic can avoid transferring antibiotic genes from the plant and thus assists to allay public concern regarding genetic modifications | Spinacia oleracea |
molecular biology | BADH application as a marker for chloroplast engineering without using antibiotic can avoid transferring antibiotic genes from the plant and thus assists to allay public concern regarding genetic modifications | Arabidopsis thaliana |
molecular biology | BADH application as a marker for chloroplast engineering without using antibiotic can avoid transferring antibiotic genes from the plant and thus assists to allay public concern regarding genetic modifications | Oryza sativa Japonica Group |
molecular biology | BADH application as a marker for chloroplast engineering without using antibiotic can avoid transferring antibiotic genes from the plant and thus assists to allay public concern regarding genetic modifications | Glycine max |
molecular biology | BADH application as a marker for chloroplast engineering without using antibiotic can avoid transferring antibiotic genes from the plant and thus assists to allay public concern regarding genetic modifications | Hordeum vulgare subsp. vulgare |
molecular biology | BADH application as a marker for chloroplast engineering without using antibiotic can avoid transferring antibiotic genes from the plant and thus assists to allay public concern regarding genetic modifications | Pandanus amaryllifolius |
molecular biology | BADH application as a marker for chloroplast engineering without using antibiotic can avoid transferring antibiotic genes from the plant and thus assists to allay public concern regarding genetic modifications | Ammopiptanthus nanus |
molecular biology | BADH application as a marker for chloroplast engineering without using antibiotic can avoid transferring antibiotic genes from the plant and thus assists to allay public concern regarding genetic modifications | Madhuca longifolia var. latifolia |
molecular biology | BADH application as a marker for chloroplast engineering without using antibiotic can avoid transferring antibiotic genes from the plant and thus assists to allay public concern regarding genetic modifications | Vallaris sp. |
additional information | BADH isolated from spinach is successfully utilised for selection of chloroplast transformation of tobacco in order to prevent the risk of transferring antibiotic resistance genes to gut microbes or the environment | Spinacia oleracea |
Cloned (Comment) | Organism |
---|---|
gene BADH, BADH2 encodes on chromosome 8, sequence comparisons | Oryza sativa Japonica Group |
gene BADH, sequence comparisons | Zea mays |
gene BADH, sequence comparisons | Triticum aestivum |
gene BADH, sequence comparisons | Spinacia oleracea |
gene BADH, sequence comparisons | Oryza sativa Japonica Group |
gene BADH, sequence comparisons | Glycine max |
gene BADH, sequence comparisons | Hordeum vulgare subsp. vulgare |
gene BADH, sequence comparisons, heterologous expression of a BADH gene from Ammopiptanthus nanus in Escherichia coli validates its role in abiotic tolerance | Ammopiptanthus nanus |
gene BADH1, sequence comparisons | Arabidopsis thaliana |
Protein Variants | Comment | Organism |
---|---|---|
additional information | several truncated or recombinant transcripts of BADH1 and BADH2 emerging from an unusual post-transcriptional process have been found in rice resulting in the insertion of exogenous gene sequences and different deletions leading to the elimination of the start codon, the loss of a functional domain and the introduction of a premature termination codon. Non-aromatic rice cultivars comprise a functional BADH2 gene, while aromatic rice cultivars contain a badh2 gene producing a non-functional enzyme because of a premature stop codon. Such a truncated BADH2 enzyme can lead to the accumulation of 2AP, the main fragrant compound | Oryza sativa Japonica Group |
additional information | several truncated or recombinant transcripts of BADH1 and BADH2 emerging from an unusual post-transcriptional process have been found in rice resulting in the insertion of exogenous gene sequences and different deletions leading to the elimination of the start codon, the loss of a functional domain and the introduction of a premature termination codon. Such a truncated BADH2 enzyme can lead to the accumulation of 2AP, the main fragrant compound | Zea mays |
additional information | several truncated or recombinant transcripts of BADH1 and BADH2 emerging from an unusual post-transcriptional process have been found in rice resulting in the insertion of exogenous gene sequences and different deletions leading to the elimination of the start codon, the loss of a functional domain and the introduction of a premature termination codon. Such a truncated BADH2 enzyme can lead to the accumulation of 2AP, the main fragrant compound | Triticum aestivum |
additional information | several truncated or recombinant transcripts of BADH1 and BADH2 emerging from an unusual post-transcriptional process have been found in rice resulting in the insertion of exogenous gene sequences and different deletions leading to the elimination of the start codon, the loss of a functional domain and the introduction of a premature termination codon. Such a truncated BADH2 enzyme can lead to the accumulation of 2AP, the main fragrant compound | Hordeum vulgare subsp. vulgare |
Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|
chloroplast | - |
Spinacia oleracea | 9507 | - |
chloroplast | - |
Arabidopsis thaliana | 9507 | - |
cytosol | - |
Oryza sativa Japonica Group | 5829 | - |
mitochondrion | - |
Arabidopsis thaliana | 5739 | - |
peroxisome | - |
Oryza sativa Japonica Group | 5777 | - |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
betaine aldehyde + NAD+ + H2O | Solanum lycopersicum | - |
betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | Zea mays | - |
betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | Triticum aestivum | - |
betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | Spinacia oleracea | - |
betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | Arabidopsis thaliana | - |
betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | Oryza sativa Japonica Group | - |
betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | Glycine max | - |
betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | Hordeum vulgare subsp. vulgare | - |
betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | Pandanus amaryllifolius | - |
betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | Ammopiptanthus nanus | - |
betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | Madhuca longifolia var. latifolia | - |
betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | Vallaris sp. | - |
betaine + NADH + 2 H+ | - |
? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Ammopiptanthus nanus | - |
- |
- |
Arabidopsis thaliana | Q9S795 | - |
- |
Arabidopsis thaliana | Q9STS1 | - |
- |
Glycine max | B0M1A6 | - |
- |
Hordeum vulgare subsp. vulgare | A4UUF3 | - |
- |
Madhuca longifolia var. latifolia | - |
Bassia latifolia | - |
Oryza sativa Japonica Group | O24174 | several BADH gene paralogues, cv. Cadoux | - |
Oryza sativa Japonica Group | Q84LK3 | several BADH gene paralogues, cv. Cadoux | - |
Pandanus amaryllifolius | A0A2Z2GYT8 | - |
- |
Solanum lycopersicum | - |
- |
- |
Spinacia oleracea | P17202 | - |
- |
Triticum aestivum | Q8LGQ9 | - |
- |
Vallaris sp. | - |
i.e. Vallaris glabra | - |
Zea mays | Q53CF4 | - |
- |
Posttranslational Modification | Comment | Organism |
---|---|---|
additional information | several truncated or recombinant transcripts of BADH1 and BADH2 emerging from an unusual post-transcriptional process have been found in barley | Hordeum vulgare subsp. vulgare |
additional information | several truncated or recombinant transcripts of BADH1 and BADH2 emerging from an unusual post-transcriptional process have been found in maize | Zea mays |
additional information | several truncated or recombinant transcripts of BADH1 and BADH2 emerging from an unusual post-transcriptional process have been found in rice | Oryza sativa Japonica Group |
additional information | several truncated or recombinant transcripts of BADH1 and BADH2 emerging from an unusual post-transcriptional process have been found in wheat | Triticum aestivum |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
flower | - |
Madhuca longifolia var. latifolia | - |
leaf | - |
Spinacia oleracea | - |
leaf | - |
Oryza sativa Japonica Group | - |
leaf | - |
Madhuca longifolia var. latifolia | - |
seed | - |
Oryza sativa Japonica Group | - |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
betaine aldehyde + NAD+ + H2O | - |
Solanum lycopersicum | betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | - |
Zea mays | betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | - |
Triticum aestivum | betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | - |
Spinacia oleracea | betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | - |
Arabidopsis thaliana | betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | - |
Oryza sativa Japonica Group | betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | - |
Glycine max | betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | - |
Hordeum vulgare subsp. vulgare | betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | - |
Pandanus amaryllifolius | betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | - |
Ammopiptanthus nanus | betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | - |
Madhuca longifolia var. latifolia | betaine + NADH + 2 H+ | - |
? | |
betaine aldehyde + NAD+ + H2O | - |
Vallaris sp. | betaine + NADH + 2 H+ | - |
? | |
additional information | rice BADH1 and BADH2 show greater affinity (Km) and higher catalytic efficiency (kcat/ Km) towards amino aldehydes, such as gamma-aminobutyraldehyde (GABald) and gamma-guanidinobutyraldehyde (GGBald), in comparison with betaine aldehyde, cf. EC 1.2.1.19. BADH2 catalysis generates glycine betaine, whereas BADH1 is not able to catalyse glycine betaine formation | Oryza sativa Japonica Group | ? | - |
- |
|
additional information | rice BADH1 and BADH2 show greater affinity (Km) and higher catalytic efficiency (kcat/ Km) towards amino aldehydes, such as gamma-aminobutyraldehyde (GABald) and gamma-guanidinobutyraldehyde (GGBald), in comparison with betaine aldehyde. BADH2 catalysis generates glycine betaine, whereas BADH1 is not able to catalyse glycine betaine formation | Oryza sativa Japonica Group | ? | - |
- |
Synonyms | Comment | Organism |
---|---|---|
ALDH10A8 | - |
Arabidopsis thaliana |
ALDH10A9 | - |
Arabidopsis thaliana |
BADH | - |
Solanum lycopersicum |
BADH | - |
Zea mays |
BADH | - |
Triticum aestivum |
BADH | - |
Spinacia oleracea |
BADH | - |
Arabidopsis thaliana |
BADH | - |
Oryza sativa Japonica Group |
BADH | - |
Glycine max |
BADH | - |
Hordeum vulgare subsp. vulgare |
BADH | - |
Pandanus amaryllifolius |
BADH | - |
Ammopiptanthus nanus |
BADH | - |
Madhuca longifolia var. latifolia |
BADH | - |
Vallaris sp. |
BADH1 | - |
Solanum lycopersicum |
BADH1 | - |
Spinacia oleracea |
BADH1 | - |
Arabidopsis thaliana |
BADH1 | - |
Oryza sativa Japonica Group |
BADH1 | - |
Glycine max |
BADH1 | - |
Hordeum vulgare subsp. vulgare |
BADH1 | - |
Vallaris sp. |
BADH2 | - |
Arabidopsis thaliana |
BADH2 | - |
Oryza sativa Japonica Group |
BADH2 | - |
Pandanus amaryllifolius |
betaine aldehyde dehydrogenase | - |
Solanum lycopersicum |
betaine aldehyde dehydrogenase | - |
Zea mays |
betaine aldehyde dehydrogenase | - |
Triticum aestivum |
betaine aldehyde dehydrogenase | - |
Spinacia oleracea |
betaine aldehyde dehydrogenase | - |
Arabidopsis thaliana |
betaine aldehyde dehydrogenase | - |
Oryza sativa Japonica Group |
betaine aldehyde dehydrogenase | - |
Glycine max |
betaine aldehyde dehydrogenase | - |
Hordeum vulgare subsp. vulgare |
betaine aldehyde dehydrogenase | - |
Pandanus amaryllifolius |
betaine aldehyde dehydrogenase | - |
Ammopiptanthus nanus |
betaine aldehyde dehydrogenase | - |
Madhuca longifolia var. latifolia |
betaine aldehyde dehydrogenase | - |
Vallaris sp. |
Cofactor | Comment | Organism | Structure |
---|---|---|---|
NAD+ | - |
Solanum lycopersicum | |
NAD+ | - |
Zea mays | |
NAD+ | - |
Triticum aestivum | |
NAD+ | - |
Spinacia oleracea | |
NAD+ | - |
Arabidopsis thaliana | |
NAD+ | - |
Oryza sativa Japonica Group | |
NAD+ | - |
Glycine max | |
NAD+ | - |
Hordeum vulgare subsp. vulgare | |
NAD+ | - |
Pandanus amaryllifolius | |
NAD+ | - |
Ammopiptanthus nanus | |
NAD+ | - |
Madhuca longifolia var. latifolia | |
NAD+ | - |
Vallaris sp. |
General Information | Comment | Organism |
---|---|---|
malfunction | some truncated transcripts of BADH are present in several crops. Such truncated transcripts may cause the accumulation of 2AP (2-acetyl-1-pyrroline), which is a key aroma compound. There is a possibility that inhibition of BADH function produces 2AP-based fragrance in main crops because of the existence of BADH isozymes | Zea mays |
malfunction | some truncated transcripts of BADH are present in several crops. Such truncated transcripts may cause the accumulation of 2AP (2-acetyl-1-pyrroline), which is a key aroma compound. There is a possibility that inhibition of BADH function produces 2AP-based fragrance in main crops because of the existence of BADH isozymes | Triticum aestivum |
malfunction | some truncated transcripts of BADH are present in several crops. Such truncated transcripts may cause the accumulation of 2AP (2-acetyl-1-pyrroline), which is a key aroma compound. There is a possibility that inhibition of BADH function produces 2AP-based fragrance in main crops because of the existence of BADH isozymes | Glycine max |
malfunction | some truncated transcripts of BADH are present in several crops. Such truncated transcripts may cause the accumulation of 2AP (2-acetyl-1-pyrroline), which is a key aroma compound. There is a possibility that inhibition of BADH function produces 2AP-based fragrance in main crops because of the existence of BADH isozymes | Hordeum vulgare subsp. vulgare |
malfunction | some truncated transcripts of BADH are present in several crops. Such truncated transcripts may cause the accumulation of 2AP (2-acetyl-1-pyrroline), which is a key aroma compound. There is a possibility that inhibition of BADH function produces 2AP-based fragrance in main crops because of the existence of BADH isozymes. But the BADH transcripts from plant species such as Arabidopsis (Arabidopsis thaliana), spinach (Spinacia oleracea) and tomato (Solanum lycopersicum), correctly process the mRNA | Solanum lycopersicum |
malfunction | some truncated transcripts of BADH are present in several crops. Such truncated transcripts may cause the accumulation of 2AP (2-acetyl-1-pyrroline), which is a key aroma compound. There is a possibility that inhibition of BADH function produces 2AP-based fragrance in main crops because of the existence of BADH isozymes. But the BADH transcripts from plant species such as Arabidopsis (Arabidopsis thaliana), spinach (Spinacia oleracea) and tomato (Solanum lycopersicum), correctly process the mRNA | Spinacia oleracea |
malfunction | some truncated transcripts of BADH are present in several crops. Such truncated transcripts may cause the accumulation of 2AP (2-acetyl-1-pyrroline), which is a key aroma compound. There is a possibility that inhibition of BADH function produces 2AP-based fragrance in main crops because of the existence of BADH isozymes. But the BADH transcripts from plant species such as Arabidopsis (Arabidopsis thaliana), spinach (Spinacia oleracea) and tomato (Solanum lycopersicum), correctly process the mRNA | Arabidopsis thaliana |
malfunction | some truncated transcripts of BADH are present in several crops. Such truncated transcripts may cause the accumulation of 2AP (2-acetyl-1-pyrroline), which is a key aroma compound. There is a possibility that inhibition of BADH function produces 2AP-based fragrance in main crops because of the existence of BADH isozymes. Even though 2AP formation in Bassia latifolia occurs only in flowers (fleshy corolla), in fragrant rice and plants such as Pandanus amaryllifolius and Vallaris glabra, it exists in all aerial parts | Oryza sativa Japonica Group |
malfunction | some truncated transcripts of BADH are present in several crops. Such truncated transcripts may cause the accumulation of 2AP (2-acetyl-1-pyrroline), which is a key aroma compound. There is a possibility that inhibition of BADH function produces 2AP-based fragrance in main crops because of the existence of BADH isozymes. Even though 2AP formation in Bassia latifolia occurs only in flowers (fleshy corolla), in fragrant rice and plants such as Pandanus amaryllifolius and Vallaris glabra, it exists in all aerial parts | Pandanus amaryllifolius |
malfunction | some truncated transcripts of BADH are present in several crops. Such truncated transcripts may cause the accumulation of 2AP (2-acetyl-1-pyrroline), which is a key aroma compound. There is a possibility that inhibition of BADH function produces 2AP-based fragrance in main crops because of the existence of BADH isozymes. Even though 2AP formation in Bassia latifolia occurs only in flowers (fleshy corolla), in fragrant rice and plants such as Pandanus amaryllifolius and Vallaris glabra, it exists in all aerial parts | Madhuca longifolia var. latifolia |
malfunction | some truncated transcripts of BADH are present in several crops. Such truncated transcripts may cause the accumulation of 2AP (2-acetyl-1-pyrroline), which is a key aroma compound. There is a possibility that inhibition of BADH function produces 2AP-based fragrance in main crops because of the existence of BADH isozymes. Even though 2AP formation in Bassia latifolia occurs only in flowers (fleshy corolla), in fragrant rice and plants such as Pandanus amaryllifolius and Vallaris glabra, it exists in all aerial parts | Vallaris sp. |
physiological function | betaine aldehyde dehydrogenase (BADH) leads to production of glycine betaine through the oxidation of betaine aldehyde. BADH is considered a key regulator for glycine betaine formation. Critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses. The BADH gene plays a multifunctional role in plants, detailed overview. It is an important factor in fragrance production, abiotic stresses and antibiotic-free selection of transgenic plants. By providing glycine betaine as a chemical interface, there is a critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses, e.g. drought stress, soil salinity stress, submergence stress, and temperature stress | Solanum lycopersicum |
physiological function | betaine aldehyde dehydrogenase (BADH) leads to production of glycine betaine through the oxidation of betaine aldehyde. BADH is considered a key regulator for glycine betaine formation. Critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses. The BADH gene plays a multifunctional role in plants, detailed overview. It is an important factor in fragrance production, abiotic stresses and antibiotic-free selection of transgenic plants. By providing glycine betaine as a chemical interface, there is a critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses, e.g. drought stress, soil salinity stress, submergence stress, and temperature stress | Zea mays |
physiological function | betaine aldehyde dehydrogenase (BADH) leads to production of glycine betaine through the oxidation of betaine aldehyde. BADH is considered a key regulator for glycine betaine formation. Critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses. The BADH gene plays a multifunctional role in plants, detailed overview. It is an important factor in fragrance production, abiotic stresses and antibiotic-free selection of transgenic plants. By providing glycine betaine as a chemical interface, there is a critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses, e.g. drought stress, soil salinity stress, submergence stress, and temperature stress | Triticum aestivum |
physiological function | betaine aldehyde dehydrogenase (BADH) leads to production of glycine betaine through the oxidation of betaine aldehyde. BADH is considered a key regulator for glycine betaine formation. Critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses. The BADH gene plays a multifunctional role in plants, detailed overview. It is an important factor in fragrance production, abiotic stresses and antibiotic-free selection of transgenic plants. By providing glycine betaine as a chemical interface, there is a critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses, e.g. drought stress, soil salinity stress, submergence stress, and temperature stress | Spinacia oleracea |
physiological function | betaine aldehyde dehydrogenase (BADH) leads to production of glycine betaine through the oxidation of betaine aldehyde. BADH is considered a key regulator for glycine betaine formation. Critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses. The BADH gene plays a multifunctional role in plants, detailed overview. It is an important factor in fragrance production, abiotic stresses and antibiotic-free selection of transgenic plants. By providing glycine betaine as a chemical interface, there is a critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses, e.g. drought stress, soil salinity stress, submergence stress, and temperature stress | Arabidopsis thaliana |
physiological function | betaine aldehyde dehydrogenase (BADH) leads to production of glycine betaine through the oxidation of betaine aldehyde. BADH is considered a key regulator for glycine betaine formation. Critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses. The BADH gene plays a multifunctional role in plants, detailed overview. It is an important factor in fragrance production, abiotic stresses and antibiotic-free selection of transgenic plants. By providing glycine betaine as a chemical interface, there is a critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses, e.g. drought stress, soil salinity stress, submergence stress, and temperature stress | Oryza sativa Japonica Group |
physiological function | betaine aldehyde dehydrogenase (BADH) leads to production of glycine betaine through the oxidation of betaine aldehyde. BADH is considered a key regulator for glycine betaine formation. Critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses. The BADH gene plays a multifunctional role in plants, detailed overview. It is an important factor in fragrance production, abiotic stresses and antibiotic-free selection of transgenic plants. By providing glycine betaine as a chemical interface, there is a critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses, e.g. drought stress, soil salinity stress, submergence stress, and temperature stress | Glycine max |
physiological function | betaine aldehyde dehydrogenase (BADH) leads to production of glycine betaine through the oxidation of betaine aldehyde. BADH is considered a key regulator for glycine betaine formation. Critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses. The BADH gene plays a multifunctional role in plants, detailed overview. It is an important factor in fragrance production, abiotic stresses and antibiotic-free selection of transgenic plants. By providing glycine betaine as a chemical interface, there is a critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses, e.g. drought stress, soil salinity stress, submergence stress, and temperature stress | Hordeum vulgare subsp. vulgare |
physiological function | betaine aldehyde dehydrogenase (BADH) leads to production of glycine betaine through the oxidation of betaine aldehyde. BADH is considered a key regulator for glycine betaine formation. Critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses. The BADH gene plays a multifunctional role in plants, detailed overview. It is an important factor in fragrance production, abiotic stresses and antibiotic-free selection of transgenic plants. By providing glycine betaine as a chemical interface, there is a critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses, e.g. drought stress, soil salinity stress, submergence stress, and temperature stress | Pandanus amaryllifolius |
physiological function | betaine aldehyde dehydrogenase (BADH) leads to production of glycine betaine through the oxidation of betaine aldehyde. BADH is considered a key regulator for glycine betaine formation. Critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses. The BADH gene plays a multifunctional role in plants, detailed overview. It is an important factor in fragrance production, abiotic stresses and antibiotic-free selection of transgenic plants. By providing glycine betaine as a chemical interface, there is a critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses, e.g. drought stress, soil salinity stress, submergence stress, and temperature stress | Ammopiptanthus nanus |
physiological function | betaine aldehyde dehydrogenase (BADH) leads to production of glycine betaine through the oxidation of betaine aldehyde. BADH is considered a key regulator for glycine betaine formation. Critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses. The BADH gene plays a multifunctional role in plants, detailed overview. It is an important factor in fragrance production, abiotic stresses and antibiotic-free selection of transgenic plants. By providing glycine betaine as a chemical interface, there is a critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses, e.g. drought stress, soil salinity stress, submergence stress, and temperature stress | Madhuca longifolia var. latifolia |
physiological function | betaine aldehyde dehydrogenase (BADH) leads to production of glycine betaine through the oxidation of betaine aldehyde. BADH is considered a key regulator for glycine betaine formation. Critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses. The BADH gene plays a multifunctional role in plants, detailed overview. It is an important factor in fragrance production, abiotic stresses and antibiotic-free selection of transgenic plants. By providing glycine betaine as a chemical interface, there is a critical role of BADH in enhancing the tolerance in an extensive range of plants subjected to different destructive abiotic stresses, e.g. drought stress, soil salinity stress, submergence stress, and temperature stress | Vallaris sp. |