Cometabolism recognizes that microorganisms can transform non-growth-supporting substrates. The term "cometabolism" was first introduced over 30 years ago and has been redefined, criticized, and used widely ever since. In this review we have examined the aerobic cometabolism of chlorinated solvents, with a particular emphasis on the cometabolism of trichloroethylene. Monooxygenases or dioxygenases with relaxed substrate ranges initiate these transformations. The physiological role of the oxygenases is to initiate the metabolism of growth-supporting substrates (e.g., methane, propane, butane, toluene, ethylene, and ammonia). Diverse enzymes catalyze these oxidative reactions with chlorinated solvents. Synthesis of most of these enzymes is induced by the presence of the growth-supporting substrate and is largely regulated at the level of gene transcription. The genes that code for a given oxygenase are usually clustered together in a single operon and often share homology with counterparts that code for the subunits of related oxygenases in other bacteria. During cometabolism the growth-supporting and non-growth-supporting substrates can both bind to the oxygenase. Transformation of chlorinated solvents by these enzymes presents the cell with a new set of compounds. Some of these compounds are toxic to the cells, others are stable products that are expelled from the cell, and in a few cases the cells utilize the products. The combined effects of cometabolism can have a profound influence on a cell.
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http://dx.doi.org/10.1023/a:1012089908518 | DOI Listing |
J Am Chem Soc
January 2025
State Key Laboratory of Medicinal Chemical Biology, Frontiers Science Centre for New Organic Matter, Tianjin Key Laboratory of Biosensing and Molecular Recognition, Research Centre for Analytical Sciences, College of Chemistry, School of Medicine and Frontiers Science Center for Cell Responses, Nankai University, Tianjin 300071, P. R. China.
Carbon monoxide (CO) gas therapy, as an emerging therapeutic strategy, is promising in tumor treatment. However, the development of a red or near-infrared light-driven efficient CO release strategy is still challenging due to the limited physicochemical characteristics of the photoactivated carbon monoxide-releasing molecules (photoCORMs). Here, we discovered a novel photorelease CO mechanism that involved dual pathways of CO release via photosensitization.
View Article and Find Full Text PDFRSC Adv
January 2025
Programa de Pós-Graduação em Ciência e Engenharia de Materiais, Universidade Federal Rural do Semi-Árido (UFERSA) CEP 59625-900 Mossoró RN Brazil
Chalcones demonstrate significant absorption in the near ultraviolet-visible spectrum, making them valuable for applications such as solar cells, light-emitting diodes, and nonlinear optics. This study investigates four dibenzalacetone derivatives (DBAd), DBA, DBC, DEP, and DMA, examining the impact of electron-donating and electron-withdrawing groups and conjugation elongation on their electronic structure in solvents of varying polarities. Using the Polarizable Continuum Model (PCM) and time-dependent density functional theory (TD-DFT), we characterized the excited states of these compounds.
View Article and Find Full Text PDFPhytochem Anal
January 2025
Department of Pharmacognosy, Institute of Pharmaceutical Sciences, University of Graz, Graz, Austria.
Environ Sci Technol
January 2025
Department of Civil and Environmental Engineering, Clarkson University, Potsdam, New York 13699, United States.
The nonthermal destruction of aqueous film-forming foam (AFFF) stockpiles, one of the major culprits responsible for water and soil contamination by per- and polyfluoroalkyl substances (PFAS), is extremely challenging because of the coexistence of mixed recalcitrant PFAS and complicated organic matrices at extremely high concentrations. To date, the complete defluorination of undiluted AFFF at ambient conditions has not been demonstrated. This study reports a novel piezoelectric ball milling approach for treating AFFF with a total organic fluorine concentration of 9080 mg/L and total organic carbon of 234 g/L.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
State Key Laboratory for Physical Chemistry of Solid Surfaces, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), Department of Chemistry, Xiamen University, Xiamen, 361005, China.
A pyrrole-fused analogue of warped nanographene, designated as deca-nitrogen doped 'WNG' (azaWNG), was synthesized through the annular fusion of decapyrroylcorannulene. The resulting azaWNG exhibited extremely limited solubility in common organic solvents and was characterized solely by mass spectrometry. Theoretical calculations revealed that azaWNG has a sunflower-like molecular structure with electron-deficient corannulene as the core and electron-rich pyrrole as the petals, demonstrating a significantly narrower energy gap compared to all-carbon WNG.
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