2010
DOI: 10.1016/j.phytochem.2010.08.003
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Phenolamides: Bridging polyamines to the phenolic metabolism

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Cited by 247 publications
(249 citation statements)
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“…While BAHD proteins are responsible for the acylation of aliphatic and arylmonoamine acceptors, GNAT enzymes are active on arylamines (Bassard et al, 2010). Although they are from two distinct protein families that show low sequence identity, the BAHD N-acyltransferases, Os-THTs and Os-TBTs, identified in our study demonstrate that proteins from both families can act on aryldiamines (Tables 2 and 3; Jang et al, 2004;Kang et al, 2006).…”
Section: Discussionmentioning
confidence: 67%
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“…While BAHD proteins are responsible for the acylation of aliphatic and arylmonoamine acceptors, GNAT enzymes are active on arylamines (Bassard et al, 2010). Although they are from two distinct protein families that show low sequence identity, the BAHD N-acyltransferases, Os-THTs and Os-TBTs, identified in our study demonstrate that proteins from both families can act on aryldiamines (Tables 2 and 3; Jang et al, 2004;Kang et al, 2006).…”
Section: Discussionmentioning
confidence: 67%
“…Since the selectivity on hydroxycinnamoyl-CoA is present in BAHD enzymes of all plant species (D'Auria, 2006;Bassard et al, 2010), from moss to legumes, we assume that Os-THTs were derived from one ancient BAHD protein that preserved its selectivity for acyl donors and evolved new catalytic capabilities in selecting tryptamine/serotonin as acyl acceptors. Protein BLAST searches in Phytozome and NCBI databases did not find orthologs among the 29 core Eudicotyledons and three Gymnosperms (even at 40% identity) but did detect them in Amborella trichopoda and Nelumbo nucifera and in one primitive Eudicotyledon, Aquiclegia coerrulea ( Figure 10B).…”
Section: Discussionmentioning
confidence: 99%
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