» Articles » PMID: 32233071

Green Conversion of 5-hydroxymethylfurfural to Furan-2,5-dicarboxylic Acid by Heterogeneous Expression of 5-hydroxymethylfurfural Oxidase in Pseudomonas Putida S12

Overview
Date 2020 Apr 2
PMID 32233071
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Transforming petrochemical processes into bioprocesses has become an important goal of sustainable development. The chemical synthesis of 2,5-furandicarboxylic acid (FDCA) from 5-hydroxymethylfurfural (HMF) is expensive and environmentally unfavourable. The study aims to investigate a whole-cell biocatalyst for efficient biotransformation of HMF to FDCA. For the first time, a genetically engineered Pseudomonas putida S12 strain expressing 5-hydroxymethylfurfural oxidase (HMFO) was developed for the biocatalytic conversion of HMF to FDCA. This whole-cell biocatalyst produced 35.7 mM FDCA from 50 mM HMF in 24 h without notable inhibition. However, when the initial HMF concentration was elevated to 100 mM, remarkable inhibition on FDCA production was observed, resulting in a reduction of FDCA yield to 42%. We solve this substrate inhibition difficulty by increasing the inoculum density. Subsequently, we used a fed-batch strategy by maintaining low HMF concentration in the culture to maximize the final FDCA titre. Using this approach, 545 mM of FDCA was accumulatively produced after 72 hs, which is the highest production rate per unit mass of cells to the best of our knowledge.

Citing Articles

Development of genetic tools for heterologous protein expression in a pentose-utilizing environmental isolate of Pseudomonas putida.

Gauttam R, Eng T, Zhao Z, Rana Q, Simmons B, Yoshikuni Y Microb Biotechnol. 2023; 16(3):645-661.

PMID: 36691869 PMC: 9948227. DOI: 10.1111/1751-7915.14205.


Enzymatic Cascade for the Synthesis of 2,5-Furandicarboxylic Acid in Biphasic and Microaqueous Conditions: 'Media-Agnostic' Biocatalysts for Biorefineries.

Milic M, Bystrom E, Dominguez de Maria P, Kara S ChemSusChem. 2022; 15(9):e202102704.

PMID: 35438241 PMC: 9322558. DOI: 10.1002/cssc.202102704.


Widespread distribution of genes in Proteobacteria reveals key enzymes for 5-hydroxymethylfurfural conversion.

Donoso R, Gonzalez-Toro F, Perez-Pantoja D Comput Struct Biotechnol J. 2021; 19:2160-2169.

PMID: 33995910 PMC: 8091172. DOI: 10.1016/j.csbj.2021.04.017.


Biocatalysis: Enzymatic Synthesis for Industrial Applications.

Wu S, Snajdrova R, Moore J, Baldenius K, Bornscheuer U Angew Chem Int Ed Engl. 2020; 60(1):88-119.

PMID: 32558088 PMC: 7818486. DOI: 10.1002/anie.202006648.


Green conversion of 5-hydroxymethylfurfural to furan-2,5-dicarboxylic acid by heterogeneous expression of 5-hydroxymethylfurfural oxidase in Pseudomonas putida S12.

Hsu C, Kuo Y, Liu Y, Tsai S Microb Biotechnol. 2020; 13(4):1094-1102.

PMID: 32233071 PMC: 7264871. DOI: 10.1111/1751-7915.13564.

References
1.
Delidovich I, Hausoul P, Deng L, Pfutzenreuter R, Rose M, Palkovits R . Alternative Monomers Based on Lignocellulose and Their Use for Polymer Production. Chem Rev. 2015; 116(3):1540-99. DOI: 10.1021/acs.chemrev.5b00354. View

2.
Tao F, Shen Y, Fan Z, Tang H, Xu P . Genome sequence of Pseudomonas putida S12, a potential platform strain for industrial production of valuable chemicals. J Bacteriol. 2012; 194(21):5985-6. PMC: 3486094. DOI: 10.1128/JB.01482-12. View

3.
Yang C, Huang C . Biotransformation of 5-hydroxy-methylfurfural into 2,5-furan-dicarboxylic acid by bacterial isolate using thermal acid algal hydrolysate. Bioresour Technol. 2016; 214:311-318. DOI: 10.1016/j.biortech.2016.04.122. View

4.
Khoo K, Lee S, Ooi C, Fu X, Miao X, Ling T . Recent advances in biorefinery of astaxanthin from Haematococcus pluvialis. Bioresour Technol. 2019; 288:121606. DOI: 10.1016/j.biortech.2019.121606. View

5.
Ramos J, Sol Cuenca M, Molina-Santiago C, Segura A, Duque E, Gomez-Garcia M . Mechanisms of solvent resistance mediated by interplay of cellular factors in Pseudomonas putida. FEMS Microbiol Rev. 2015; 39(4):555-66. DOI: 10.1093/femsre/fuv006. View