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Hopanoids are among the most widespread biomarkers of bacteria that are used as indicators for past and present bacterial activity. Our understanding of the production, function, and distribution of hopanoids in bacteria has improved greatly, partly due to genetic, culture-independent studies. Culture-based studies are important to determine hopanoid function and the environmental conditions under which these compounds are produced. This study compares the lipid inventory of Rhodopseudomonas palustris strain TIE-1 under anoxic photoautotrophic conditions using either H2 or Fe(II) as electron donor. The high amount to which adenosylhopane is produced irrespective of the used electron donor suggests a specific function of this compound rather than its exclusive role as an intermediate in bacteriohopanepolyol biosynthesis. C-2 methylated hopanoids and tetrahymanol account for as much as 59% of the respective C-2 methylated/non-methylated homologs during growth with Fe(II) as electron donor, as compared with 24% C-2 methylation for growth with H2 . This observation reveals that C-2 methylated hopanoids have a specific function and are preferentially synthesized in response to elevated Fe(II) concentrations. The presence of C-2 methylated pentacyclic triterpenoids has commonly been used as a biosignature for the interpretation of paleoenvironments. These new findings suggest that increased C-2 methylation may indicate anoxic ferrous conditions, in addition to other environmental stressors that have been previously reported.
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http://dx.doi.org/10.1111/gbi.12033 | DOI Listing |
RSC Adv
September 2025
Process and Environmental Engineering Laboratory (LIPE), Faculty of Chemistry, University of Science and Technology of Oran Mohamed Boudiaf P. O. Box 1503, El Mnaouer 31000 Oran Algeria.
In this contribution, Molecular Electron Density Theory (MEDT) is employed to investigate the (3 + 2) cycloaddition reaction between ()--methyl--(2-furyl)-nitrone 1 and but-2-ynedioic acid 2. DFT calculations at the M06-2X-D3/6-311+G(d,p) level of theory under solvent-free conditions at room temperature show that this reaction proceeds CA3-Z diastereoselectivity, with the formation of the CA3-Z cycloadduct being both thermodynamically and kinetically more favoured than the CA4-Z one. Reactivity parameters obtained from CDFT calculations reveal that compound 1 predominantly behaves as a nucleophile with moderate electrophilic features, in contrast to compound 2, which demonstrates strong electrophilicity and limited nucleophilic ability.
View Article and Find Full Text PDFInorg Chem
August 2025
Hubei Institute of Aerospace Chemotechnology, Xiangyang 441003, China.
Acetylene (CH), as a crucial chemical feedstock, and its purification from multicomponent light hydrocarbon mixtures is industrially challenging. Herein, we used the 3-methyl-4-(4-1,2,4-triazol-4-yl) benzoic acid (HL) ligand and CoSO·7HO to assemble a novel metal-organic framework (MOF), [Co(L)(OH)(SO) (HO)]·DMA·4HO (), with porous channels decorated with accessible active sites including an open metal center, an uncoordinated carboxylate group, functional methyl groups, and sulfate anions. The adsorption capacities are 64.
View Article and Find Full Text PDFACS Earth Space Chem
August 2025
Centre de Recherche sur les Ions, les Matériaux et la Photonique Normandie University, ENSICAEN, UNICAEN, CEA, CNRS, CIMAP, Caen 14000, France.
Studying the physicochemical properties of ice in astronomical environments is crucial to understanding the chemical processes involved in cosmic events such as comet and planet formation. The physical characteristics and chemical evolution on the surfaces of cosmic objects such as comets or interstellar grains offer key insights into these processes. This study focuses on α-pinene, a carbon- and hydrogen-rich molecule, which serves as a model for investigating radical-driven synthesis of more complex molecules under space-like conditions.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
School of Physical Science and Technology, Shanghai Key Laboratory of High-Resolution Electron Microscopy, State Key Laboratory of Advanced Medical Materials and Devices, ShanghaiTech University, Shanghai, 201210, China.
A series of sulfate-pillared metal azolate frameworks (MAFs) were synthesized via a multivariate (MTV) strategy to systematically tune framework flexibility and gas separation performance. The monotonic sulfate-pillared MAF, Zn(daTz)SO (where daTz = 3,5-diamino-1,2,4-triazolate), exhibits pronounced structural dynamics upon adaptive guest inclusions, driven by triazolate linker rotation and reversible Zn─O bonds rearrangement, enabling dynamic pore modulation for efficient CO, CH, and CH uptakes. Incorporation of an asymmetric, non-amino linker effectively suppresses framework flexibility by reducing intraframework hydrogen bonding, resulting in a locked structure with enhanced selectivity for CO over light hydrocarbons.
View Article and Find Full Text PDFMolecules
July 2025
Chemical Sciences Department, The Radical Reactions Research Center, Ariel University, Ariel 4070000, Israel.
The DFT method was used to evaluate the adsorption of methyl radicals and the evolution of ethane on the M(111) (M = Co, Ni, Pd, Pt) surfaces, eight metal atoms, in aqueous medium. A maximum of five and four radicals can be adsorbed on Co(111) and Ni(111), respectively, and six on Pd(111) and Pt(111) (top site). The ethane evolution occurs via the Langmuir-Hinshelwood (LH) or Eley-Rideal (ER) mechanisms.
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