Fig. 1 in 3-O-glycosylation of kaempferol restricts the supply of the benzenoid precursor of ubiquinone (Coenzyme Q) in Arabidopsis thaliana

Fig. 1 in 3-O-glycosylation of kaempferol restricts the supply of the benzenoid precursor of ubiquinone (Coenzyme Q) in Arabidopsis thaliana

Fig. 1. Metabolic origins of 4-hydroxybenzoate for ubiquinone biosynthesis in plant cells. Note that chemical modeling of the peroxidative cleavage of kaempferol predicts that peroxidases do not act on kaempferol itself, but on its α-diketone tautomer. The formation of the latter is contingent on th...

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Hauptverfasser: Soubeyrand, Eric, Latimer, Scott, Bernert, Ann C., Keene, Shea A., Johnson, Timothy S., Shin, Doosan, Block, Anna K., Colquhoun, Thomas A., Sch, Anton R., Affner, Kim, Jeongim, Basset, Gilles J.
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Biodiversity
Taxonomy
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creator Soubeyrand, Eric
Latimer, Scott
Bernert, Ann C.
Keene, Shea A.
Johnson, Timothy S.
Shin, Doosan
Block, Anna K.
Colquhoun, Thomas A.
Sch, Anton R.
Affner
Kim, Jeongim
Basset, Gilles J.
description Fig. 1. Metabolic origins of 4-hydroxybenzoate for ubiquinone biosynthesis in plant cells. Note that chemical modeling of the peroxidative cleavage of kaempferol predicts that peroxidases do not act on kaempferol itself, but on its α-diketone tautomer. The formation of the latter is contingent on the presence of a double bond between C-2 and C-3 and a free C-3- OH on the C-ring. Dashed arrows indicate unknown and/or multiple steps. Ara, arabinosyl; Glu, glucosyl; Rha, Rhamnosyl; UGT78D1, flavonol 3-O-rhamnosyltransferase; UGT78D2, flavonol 3-O-glucosyltransferase; UGT78D3, flavonol 3-O- arabinosyltransferase.
doi_str_mv 10.5281/zenodo.8258431
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title Fig. 1 in 3-O-glycosylation of kaempferol restricts the supply of the benzenoid precursor of ubiquinone (Coenzyme Q) in Arabidopsis thaliana
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