98%
921
2 minutes
20
Levulinic acid is a versatile platform molecule with potential to be used as an intermediate in the synthesis of many value-added products used across different industries, from cosmetics to fuels. Thus far, microbial biosynthetic pathways having levulinic acid as a product or an intermediate are not known, which restrains the development and optimization of a microbe-based process envisaging the sustainable bioproduction of this chemical. One of the doors opened by synthetic biology in the design of microbial systems is the implementation of new-to-nature pathways, that is, the assembly of combinations of enzymes not observed , where the enzymes can use not only their native substrates but also non-native ones, creating synthetic steps that enable the production of novel compounds. Resorting to a combined approach involving complementary computational tools and extensive manual curation, in this work, we provide a thorough prospect of candidate biosynthetic pathways that can be assembled for the production of levulinic acid in or . Out of the hundreds of combinations screened, five pathways were selected as best candidates on the basis of the availability of substrates and of candidate enzymes to catalyze the synthetic steps (that is, those steps that involve conversions not previously described). Genome-scale metabolic modeling was used to assess the performance of these pathways in the two selected hosts and to anticipate possible bottlenecks. Not only does the herein described approach offer a platform for the future implementation of the microbial production of levulinic acid but also it provides an organized research strategy that can be used as a framework for the implementation of other new-to-nature biosynthetic pathways for the production of value-added chemicals, thus fostering the emerging field of synthetic industrial microbiotechnology.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acssynbio.0c00518 | DOI Listing |
Bioresour Technol
September 2025
Department of Polymer Materials and Engineering, College of Materials and Metallurgy, Guizhou University, Guiyang 550025, China; Technology Innovation Center for High-Efficiency Utilization of Bamboo-Based Biomass in Guizhou Province, Guiyang 550025, China. Electronic address:
Worldwide, marine shell waste generated from the seafood industry has emerged as a significant environmental challenge. Indeed, this shell waste represents an abundant source of various valuable products, particularly chitin. However, the extraction and subsequent processing of chitin are hindered by the inherently resistant structure of these chitin-rich feedstocks, coupled with strong hydrogen bonding between chitin chains.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, China; Key Laboratory of New Low-carbon Green Chemical Technology, Education Department of Guangxi Zhuang Autonomous Region, Nanning 530004, China. Electronic address:
The conversion of cellulose to levulinic acid (LA) catalyzed by solid acid is of great significance for high-value utilization of cellulosic biomass, while conventional solid acid catalysts exhibit unsatisfactory activity and stability. Herein, a strategy of supramolecular network-mediated spatial confinement-electronic bridge framework was proposed to construct a biomass carbon-coated AlZr (CA-AZ@BC) solid acid catalyst with Brønsted and Lewis dual-acid sites for high-efficiency conversion of cellulose. Based on a self-assembly sodium lignosulfonate-citric acid-bimetal supramolecular network, the specific spatial confinement effect of the supramolecular framework ensured the dispersibility and stability of active sites in the CA-AZ@BC catalyst.
View Article and Find Full Text PDFMolecules
August 2025
Facultad de Ciencias de la Salud, Universidad San Jorge, Campus Universitario, Autov. A23 km 299, Villanueva de Gállego, 50830 Zaragoza, Spain.
Bioactive compounds (BCs) are naturally occurring molecules found in plants, fungi, and microorganisms that can provide health benefits beyond nutrition. However, in order to administer them, they must be extracted from these organisms. This study reviews the extraction of anti-inflammatory bioactive compounds using deep eutectic systems (DESs).
View Article and Find Full Text PDFRSC Adv
August 2025
Polyoxometalates and Catalysis Laboratory, Department of Chemistry, Faculty of Science, The Maharaja Sayajirao University of Baroda Vadodara- 390020 Gujarat India
In present scenario the synthesis of sustainable biofuel additive using hydrogenation of biomass derived compound with green hydrogen source gained tremendous attention due to the fast-growing attention on the circular economy. So, in this work, we demonstrated the liquid phase hydrogenation of levulinic acid to γ-valerolactone using biomass derived green hydrogen source over a non-noble metal based heterogenous catalyst. Here, a non-noble metal-based catalyst, comprising nickel exchanged 12-tungstophosphoric acid anchored Zeolite HY, was synthesized and thoroughly characterized using various techniques, including EDS, NH-TPD, BET, FTIR, UV-vis-NIR, XPS, and HRTEM.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
Key Laboratory of Multiphase Flow Reaction and Separation Engineering of Shandong Province, State Key Laboratory Base of Eco-chemical Engineering, College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, People's Republic of China. Electronic address: liuyuequst
The high efficiency production of renewable resources has been widely used in fuel and synthetic chemistry. In this work, a series of novel, efficient Pd@mSiO-xCeO bifunctional yolk-shell catalysts have been developed and applied to the preparation of γ-valerolactone by the hydrogenation of levulinic acid. The results showed that CeO can effectively improve the catalytic performance of the catalyst, then achieve 100 % conversion of levulinic acid and 97 % selectivity of γ-valerolactone.
View Article and Find Full Text PDF