Related Experiment Video
Updated: Jun 16, 2025

Extraction of Lignin with High β-O-4 Content by Mild Ethanol Extraction and Its Effect on the Depolymerization Yield
Published on: January 7, 2019
Strategies for lignocellulosic hydroxycinnamic acid release and biotransformation into high-value coniferyl alcohol
Robson Tramontina1, Fabio Marcio Squina2
1Departamento de Biologia Funcional e Molecular (BFM), Universidade Estadual de Campinas (UNICAMP), Campinas, SãoPaulo, Brazil; Laboratório de Ciências Moleculares, Universidade de Sorocaba (UNISO), Sorocaba, SãoPaulo, Brazil.
Abstract:
The increasing need for sustainable strategies to valorize lignocellulosic biomass has driven significant advancements in enzymatic and biocatalytic methodologies. This chapter presents an integrated, scalable approach for the release and biotransformation of hydroxycinnamic acids (HCADs), such as ferulic acid (FA) and p-coumaric acid (pCA), into high-value coniferyl alcohol (COL). Utilizing XynZ, a chimeric enzyme with feruloyl esterase and xylanase activities, this method enables efficient hemicellulose degradation and HCAD release. Whole-cell biocatalysis, employing recombinant Escherichia coli co-expressing carboxylic acid reductase (CAR) and aldo-keto reductase (AKR), facilitates the direct biotransformation of HCADs into COL in a streamlined process. A fed-batch strategy further enhanced COL production, achieving up to 1.6 g/L titers. Including alkaline hydrolysis protocols demonstrates a robust alternative for HCAD recovery, offering higher yields than enzymatic methods. This work bridges key gaps in lignocellulosic biomass valorization, providing a state-of-the-art, sustainable, and industrially relevant platform for converting agro-industrial residues into high-value phenolic compounds. The methodologies outlined align with green chemistry principles and address critical challenges, advancing the development of economically viable biorefineries.
More Related Videos
Related Concept Videos
Alcohols from Carbonyl Compounds: Reduction
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
Oxidation of Alcohols
The process of oxidation in a chemical reaction is observed in any of the three forms:
Acid-Catalyzed Dehydration of Alcohols to Alkenes
Preparation of Diols and Pinacol Rearrangement
The reaction begins with transferring a proton from the acid catalyst to one of the hydroxyl groups, producing an oxonium ion.
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview

