Gas-phase organic acids are ubiquitous in the atmosphere with mixing ratios of several species, such as formic acid and acetic acid, often as high as several parts per billion by volume (ppbv). Organic acids are produced via photochemical reactions and are also directly emitted from various sources, including combustion, microbial activity, vegetation, soils, and ruminants. We present measurements of gas-phase formic, acetic, propionic, pyruvic, and pentanoic acids from a site near Boise, Idaho, in August 2019 made by iodide-adduct chemical ionization mass spectrometry (CIMS). The site is adjacent to a major interstate highway and beyond the urban/suburban core is surrounded by national forests to the north and northeast and by farmland to the west and south. Maximum mixing ratios of formic, acetic, propionic, and pentanoic acid were typically near 10, 3, 0.4, and 0.2 ppbv, respectively. Observed daytime concentrations of these acids were mostly consistent with other studies, but concentrations were persistently the highest at night between 20:00 to 8:00 (local standard time). Such elevated nighttime concentrations are unlike most other reported organic acid measurements. Although there were times when organic acid concentrations were enhanced by mobile source emissions, the organic acid concentrations appear to be mainly controlled by noncombustion surface primary emissions. Source apportionment by positive matrix factorization (PMF) supports the importance of significant noncombustion, nonphotochemical emissions. Two agricultural surface sources were identified and estimated to contribute to greater than half of total observed concentrations of formic and acetic acid. In contrast to the other measured organic acids, but in agreement with all other reported measurements in the literature, pyruvic acid concentrations peaked during the daytime and were largely controlled by photochemistry.
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http://dx.doi.org/10.1021/acsestair.4c00138 | DOI Listing |
Methods Mol Biol
January 2025
Biomic Auth, Bioanalysis and Omics Laboratory, Center for Interdisciplinary Research and Innovation, Aristotle University, Thessaloniki, Greece.
Metabolomics aims at identification and quantitation of key end point metabolites, basically polar, in order to study changes in biochemical activities in response to pathophysiological stimuli or genetic modifications. Targeted profiling assays enjoying a growing popularity over the last years with LC-MS/MS as a powerful tool for development of such (semi-)quantitative methods for a large number of metabolites. Here we describe a method for absolute quantitation of ca.
View Article and Find Full Text PDFActa Diabetol
January 2025
Department of Obstetrics, Women's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Objective: The objective is to investigate the differences in urinary organic acid (OA) profiles and metabolism between healthy control (HC) pregnant women and those with gestational diabetes mellitus (GDM) during the second trimester and third trimester of pregnancy.
Methods: A total of 66 HC pregnant women and 32 pregnant women with GDM were assessed for 107 hydrophilic metabolites in urine samples collected during the second and third trimester of pregnancy using tandem mass spectrometry. The urine OA profiles for each group were obtained, and metabolomic analysis and discussion were conducted.
J Food Sci
January 2025
Spice and Beverage Research Institute, Chinese Academy of Tropical Agricultural Sciences, Wanning, China.
Fermentation is crucial for inducing desirable flavor and aroma profiles in cocoa products. This research focused on identifying microbial strains isolated from spontaneous cocoa fermentation in Hainan through 16S and Internal Transcribed Spacer (ITS) sequencing. Pectinase activity was screened, and metabolic dynamics of sugars and organic acids were analyzed using high-performance liquid chromatography.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Shanghai Institute of Materia Medica Chinese Academy of Sciences, Chemical Biology Research Center, 201203, Shanghai, CHINA.
Aldolases are powerful C-C bond-forming enzymes for asymmetric organic synthesis because of their supreme stereoselectivity, diverse electrophiles and nucleophiles, and promising scalability. Stereodivergent engineering of aldolases to tune the selectivity for the synthesis of stereoisomers of chiral molecules is highly desirable but has rarely been reported. This study documented the semirational engineering of the decarboxylative aldolase UstD with the focused rational iterative site-specific mutagenesis (FRISM) strategy to perform a C-C bond-forming reaction with dione electrophiles.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Institute of Organic Chemistry, University of Leipzig, 04103 Leipzig, Germany.
The enantioselective synthesis of 1,4-dicarbonyl compounds continues to pose a significant challenge in organic synthesis, and a catalytic process which generates two adjacent stereogenic centers with full stereochemical control is lacking until now. The 1,4-relationship of the functional groups requires an Umpolung strategy as one of the α-carbonyl positions has to be inverted into an electrophilic center to react with a normal enolate. We report herein the highly enantio- and diastereoselective addition of silyl ketene acetals toward electrophilic 1-azaallyl cations to furnish chiral 4-hydrazonoesters, which are masked 1,4-dicarbonyl compounds.
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