2.4.1.85: cyanohydrin beta-glucosyltransferase
This is an abbreviated version!
For detailed information about cyanohydrin beta-glucosyltransferase, go to the full flat file.
Word Map on EC 2.4.1.85
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2.4.1.85
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sorghum
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cyanogenic
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dhurrin
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bicolor
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glucosylates
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cyp71e1
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three-fold
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bitterness
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stereo-selectively
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r-mandelonitrile
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quantitative-pcr
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diglucoside
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testa
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mill
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amygdalus
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kernels
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batsch
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prunus
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prunasin
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metabolons
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compartmentalised
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non-bitter
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dulcis
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rosaceae
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almond
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erratum
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hypervariable
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regiospecificity
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geraniol
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udp-glucosyltransferase
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agriculture
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biotechnology
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synthesis
- 2.4.1.85
- sorghum
-
cyanogenic
- dhurrin
- bicolor
-
glucosylates
- cyp71e1
-
three-fold
-
bitterness
-
stereo-selectively
-
r-mandelonitrile
-
quantitative-pcr
- diglucoside
- testa
-
mill
- amygdalus
- kernels
- batsch
-
prunus
- prunasin
-
metabolons
-
compartmentalised
-
non-bitter
- dulcis
- rosaceae
- almond
-
erratum
-
hypervariable
-
regiospecificity
- geraniol
- udp-glucosyltransferase
- agriculture
- biotechnology
- synthesis
Reaction
Synonyms
cyanohydrin glucosyltransferase, cyanohydrin glycosyltransferase, glucosyltransferase, uridine diphosphoglucose-p-hydroxymandelonitrile, mandelonitrile glucosyltransferase, sbHMNGT, UDP-glucose-p-hydroxymandelonitrile glucosyltransferase, UDP-glucose:p-hydroxymandelonitrile-O-glucosyltransferase, UDP-glucosyltransferase, UGT85B1, uridine diphosphoglucose-cyanohydrin glucosyltransferase, uridine diphosphoglucose-p-hydroxymandelonitrile glucosyltransferase, uridine diphosphoglucose:aldehyde cyanohydrin beta-glucosyltransferase
ECTree
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Cloned
Cloned on EC 2.4.1.85 - cyanohydrin beta-glucosyltransferase
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cloning of a full-length cDNA encoding enzyme, expression in Escherichia coli JM109, 492-amino acids translation product
gene UGT85B1, DNA and amino acid sequence determination and analysis of wild-type and mutant tcd2 genes. The CYP79A1, CYP71E1 and UGT85B1 genes required for dhurrin synthesis are clustered
recombinant expression in Nicotiana tabacum chloroplasts, coexpression with CYP79A1 and CYP71E1 linked in a tricistronic operon construct with the essential regulatory elements
transgenic Arabidopsis thaliana plants expressing the entire biosynthetic pathway for the tyrosine-derived cyanogenic glucoside dhurrin as accomplished by insertion of CYP79A1, CYP71E2, and UFT85B1 are shown to accumulate 4% dry-weight dhurrin with marginal inadvertent effects on plant morphology, free amino acid pools, transcriptome, and metabolome
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