Computational design of carboxylase for the synthesis of 4-hydroxyisophthalic acid from p-hydroxybenzoic acid by fixing CO.

J Environ Manage

College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, 100029, China; National Energy R&D Center for Biorefinery, Beijing University of Chemical Technology, Beijing, 100029, China. Electronic address:

Published: August 2024


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Carbon dioxide (CO) emissions constitute the primary contribution to global climate change. Synthetic CO fixation represents an exceptionally appealing and sustainable method for carbon neutralization. Unlike the limitations of chemical catalysis, biological CO fixation displays high selectivity and the ability to operate under mild conditions. The superfamily of amidohydrolases has demonstrated the ability to synthesize a range of aromatic monocarboxylic acids. However, there is a scarcity of reported carboxylases capable of synthesizing aromatic dicarboxylic acids. Among these, 4-hydroxyisophthalic acid holds significant potential for applications across various fields, yet no enzyme has been reported for its synthesis. In this study, we developed for the first time that exhibits starting activity in fixing CO to synthesize 4-hydroxyisophthalic acid. Furthermore, we have devised a computational strategy that effectively enhances the catalytic activity of this enzyme. A focused library comprising only 13 variants was generated. Experimental validation confirmed a threefold improvement in the carboxylation activity of the optimal variant (L47M). The computational enzyme design strategy proposed in this paper demonstrates broad applicability in developing carboxylases for synthesizing other aromatic dicarboxylic acids. This lays the groundwork for leveraging biocatalysis in industrial synthesis for CO fixation.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jenvman.2024.121703DOI Listing

Publication Analysis

Top Keywords

4-hydroxyisophthalic acid
12
synthesizing aromatic
8
aromatic dicarboxylic
8
dicarboxylic acids
8
computational design
4
design carboxylase
4
carboxylase synthesis
4
synthesis 4-hydroxyisophthalic
4
acid
4
acid p-hydroxybenzoic
4

Similar Publications

Mechanism, Kinetics and Modelling of Phenol Carboxylation Reactions with CO.

Int J Mol Sci

December 2024

Department of Catalysis and Chemical Reaction Engineering, National Institute of Chemistry, Hajdrihova 19, 1000 Ljubljana, Slovenia.

Combining carboxylation reactions using carbon dioxide (CO) as a reactant with phenol results in creation of new C-C bonds, and represents one of the most promising routes in sustainable utilization of ubiquitous and readily available resources for production of highly valuable products. This study provides a detailed and well-structured investigation of the effect of various reaction conditions (reactant loading, reaction duration, temperature, CO pressure) on the carboxylation of phenol. Sodium phenoxide carboxylation showed well-resolved trends with variation of temperature and time, and resulted in production of salicylic acid (SA) in the range of 11.

View Article and Find Full Text PDF

Computational design of carboxylase for the synthesis of 4-hydroxyisophthalic acid from p-hydroxybenzoic acid by fixing CO.

J Environ Manage

August 2024

College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, 100029, China; National Energy R&D Center for Biorefinery, Beijing University of Chemical Technology, Beijing, 100029, China. Electronic address:

Carbon dioxide (CO) emissions constitute the primary contribution to global climate change. Synthetic CO fixation represents an exceptionally appealing and sustainable method for carbon neutralization. Unlike the limitations of chemical catalysis, biological CO fixation displays high selectivity and the ability to operate under mild conditions.

View Article and Find Full Text PDF

Potentiation of paraquat toxicity by inhibition of the antioxidant defenses and protective effect of the natural antioxidant, 4-hydroxyisopthalic acid in Drosophila melanogaster.

Comp Biochem Physiol C Toxicol Pharmacol

September 2022

Neurobiology laboratory, Department of Zoology, University of Mysore, Manasagangotri, Mysuru 570006, Karnataka, India. Electronic address:

Exposure to pesticides such as paraquat (PQ) is known to induce oxidative stress-mediated damage, which is implicated in neurodegenerative diseases. The antioxidant enzymes are part of the endogenous defense mechanisms capable of protecting against oxidative damage, and down-regulation of these enzymes results in elevated oxidative stress. In this study, we have evaluated the protective action of 4-hydroxyisophthalic acid (DHA-I), a novel bioactive molecule from the roots of D.

View Article and Find Full Text PDF

Purpose: 4-Hydroxyisophthalic acid (4-HIA) is a bioactive compound present in the roots of , which has attracted considerable attention in attenuating oxidative stress-related neurodegenerative diseases. However, its efficacy is limited because of its low solubility and bioavailability. Therefore, the present study aimed to encapsulate 4-HIA using biocompatible copolymer polylactide-co-glycolide (PLGA) and evaluate its antioxidant and neuroprotective potential.

View Article and Find Full Text PDF

Screening and characterization of a novel reversible 4-hydroxyisophthalic acid decarboxylase from Cystobasidium slooffiae HTK3.

Biosci Biotechnol Biochem

June 2021

Department of Applied Chemistry, Faculty of Science and Engineering, Waseda University, Shinjuku-ku, Tokyo, Japan.

Owing to carboxylation activity, reversible decarboxylases can use CO2 as a C1-building block to produce useful carboxylic acids. Although many reversible decarboxylases can synthesize aromatic monocarboxylic acids, only a few reversible decarboxylases have been reported to date that catalyze the synthesis of aromatic dicarboxylic acids. In the present study, a reversible 4-hydroxyisophthalic acid decarboxylase was identified in Cystobasidium slooffiae HTK3.

View Article and Find Full Text PDF