Identification and characterization of BAHD hydroxycinnamoyltransferases in the fern Neoblechnum brasiliense
Maximilian Ufland, Maike Petersen

TL;DR
This study identifies and characterizes nine BAHD acyltransferases in the fern Neoblechnum brasiliense, revealing their roles in transferring hydroxycinnamoyl units onto various substrates.
Contribution
The paper reports the first detailed characterization of BAHD hydroxycinnamoyltransferases in the fern Neoblechnum brasiliense.
Findings
Nine BAHD acyltransferases were identified and heterologously expressed in N. brasiliense.
NbHCT1 and 2 showed high catalytic efficiency with shikimic acid as the acceptor substrate.
Phylogenetic analysis grouped several enzymes into clade V, known for shikimate and quinate hydroxycinnamoyltransferases.
Abstract
Neoblechnum brasiliense, a leptosporangiate fern of the family Blechnaceae, is known to have a rich phenolic metabolism. Rosmarinic acid and blechnic acid B have been detected beside chlorogenic acid. As BAHD acyltransferases often are responsible for the formation of this kind of esters, for example, rosmarinic acid synthases or 4‐coumaroyl‐CoA:shikimic or quinic acid hydroxycinnamoyltransferases, nine coding sequences for BAHD acyltransferases were amplified from N. brasiliense and heterologously expressed. All enzymes proved to be active with p‐coumaroyl‐CoA as acyl donor as well as other hydroxycinnamoyl‐CoA derivatives. Four enzymes (NbHCT4, 6, 7, 9) accepted various alcohols and amines but only to a very low extent. High catalytic efficiency was observed for NbHCT1 and 2 that preferred shikimic acid as acceptor substrate, while NbHCT3 was most active with quinic acid and is part…
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Taxonomy
TopicsPlant Gene Expression Analysis · Plant biochemistry and biosynthesis · Microbial Natural Products and Biosynthesis
