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Fig. 3 | Biotechnology for Biofuels and Bioproducts

Fig. 3

From: Challenges and advances in biotechnological approaches for the synthesis of canolol and other vinylphenols from biobased p-hydroxycinnamic acids: a review

Fig. 3

Model of the catalytic mechanism of the L. plantarum PAD for decarboxylation of pCA [84]. The corresponding amino acids identified in B. subtilis PAD are indicated in red color [85]. The carboxyl moiety of pCA is linked to residues Tyr18 and Tyr20 in this enzyme. Deprotonation of the hydroxyl group of pCA by residue Glu71 (first step) leads to the formation of a semi-quinone intermediate whose decarboxylation generates 4-vinylphenol (second step)

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