cis,cis-Muconate (ccMA) is a promising platform for use in synthesizing various polymers. A glucose-free ccMA production using Pseudomonas sp. NGC7 from hardwood lignin-derived aromatic compounds was previously reported. In that system, syringyl nucleus compounds were essential for growth. Here, it is shown that NGC7 is available for glucose-free ccMA production even from a mixture of lignin-derived aromatics that does not contain syringyl nucleus compounds. By introducing a gene set for the protocatechuate (PCA)-shunt consisting of PCA 3,4-dioxygenase and PCA decarboxylase into an NGC7-derived strain deficient in PCA 3,4-dioxygenase and ccMA cycloisomerase, it was succeeded in constructing a ccMA-producing strain that grows on a lignin-derived aromatics mixture containing no syringyl nucleus compounds. Finally, it is demonstrated that the engineered strain produced ccMA from sugar cane bagasse alkaline extract in 18.7 mol%. NGC7 is thus shown to be a promising microbial chassis for biochemicals production from lignin-derived aromatics.
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http://dx.doi.org/10.1016/j.biortech.2022.127479 | DOI Listing |
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 PDFInt J Biol Macromol
December 2024
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, China. Electronic address:
Lignin represents a significant source of aromatic hydrocarbons in the natural world. The production of high-value chemicals from lignin has the great potential to effectively address the issue of fossil energy scarcity. In this study, complex sulfides of nickel‑cobalt bimetallic catalysts were prepared via hydrothermal synthesis and subsequently employed in the catalytic hydrogenolysis of CO bonds present in lignin.
View Article and Find Full Text PDFAppl Microbiol Biotechnol
December 2024
Graduate School of Agriculture, Faculty of Agriculture, Meijo University, Nagoya, Aichi, 468-8502, Japan.
Crit Rev Biotechnol
December 2024
Department of Chemical and Biochemical Engineering, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, China.
Muconic acid (MA) is a valuable dicarboxylic acid with three isomers that are extensively utilized in textile and chemical industries. Traditionally, the chemical synthesis of MA consumes nonrenewable petrochemical raw materials and causes significant environmental problems. With the rapid increase in demand for MA, eco-friendly biosynthetic technologies with renewable sources are becoming ideal alternative solutions.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, China. Electronic address:
The efficient hydrogenolysis of CO ether bonds in lignin is the key for producing bio-oil and high-value chemicals. In this work, we synthesized a series of Ni-MOF-derived porous carbon spheres anchored Ni catalysts (Ni/C-x-T) with different metal/ligand molar ratios and calcination temperatures through solvothermal and carbothermal reduction method, and evaluated their catalytic transfer hydrogenolysis (CTH) performance for lignin model compounds using isopropanol as H-donor. The Ni/C-2-400 catalyst exhibited the excellent CTH performance, affording almost 100 % conversion of 2-phenoxy-1-phenylethanol even at a low reaction temperature of 120 °C.
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