Publications by authors named "Thomasset B"

The circadian clock plays a critical role in regulating plant physiology and metabolism. However, the way in which the clock impacts the regulation of lipid biosynthesis in seeds is partially understood. In the present study, we characterized the seed fatty acid (FA) and glycerolipid (GL) compositions of pseudo-response regulator mutants.

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Lipoic acid (LA, 6,8-dithiooctanoic acid) is a sulfur containing coenzyme essential for the activity of several key enzymes involved in oxidative and single carbon metabolism in most bacteria and eukaryotes. LA is synthetized by the concerted activity of the octanoyltransferase (LIP2, EC 2.3.

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Flax ( L.) seed oil, which accumulates in the embryo, and mucilage, which is synthesized in the seed coat, are of great economic importance for food, pharmaceutical as well as chemical industries. Theories on the link between oil and mucilage production in seeds consist in the spatio-temporal competition of both compounds for photosynthates during the very early stages of seed development.

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Article Synopsis
  • A novel water-soluble polysaccharide called AGP1 was isolated from Anethum graveolens seeds and characterized through various chemical and instrumental analysis techniques.
  • AGP1 consists mainly of glucose, galactose, mannose, and arabinose, with good thermal stability up to 275 °C and notable in vitro antioxidant properties.
  • In turkey sausages, AGP1 at 0.3% (w/w) acted as an effective preservative, reducing lipid peroxidation and improving pH and bacterial stability during cold storage, highlighting its potential for use in the food and nutraceutical industries.
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Past research has sought to improve the production of cyclopropane fatty acids by the oleaginous yeast Yarrowia lipolytica by heterologously expressing the E. coli fatty acid synthase gene and improving cultivation processes. Cyclopropane fatty acids display properties that hold promise for biofuel applications.

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Lipoyl synthases are key enzymes in lipoic acid biosynthesis, a co-factor of several enzyme complexes involved in central metabolism. Plant pyruvate dehydrogenase complex (PDH), located in mitochondria and plastids, catalyses the first step of fatty acid biosynthesis in these organelles. Among their different components, the E2 subunit requires the lipoic acid prosthetic group to be active.

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Flax ( L.) oil is an important source of α-linolenic (C18:3 ω-3). This polyunsaturated fatty acid is well known for its nutritional role in human and animal diets.

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Article Synopsis
  • - The GC-Orbitrap, launched in 2015, improved sensitivity and resolution for mass spectrometry but showed ion ratio changes in mass spectra when using the standard 70 eV electron ionization method.
  • - This study explored how different acquisition and sample parameters affected these ion modifications in fatty acid methyl esters (FAMEs), revealing that relative ion intensities depended on factors like mass range, C-TRAP offset values, and sample concentration, which varied by molecule.
  • - The findings indicated that these changes in ion ratios were influenced by metastable ions in the C-TRAP, suggesting that the 70 eV electron ionization mass spectra from the GC-Orbitrap are significantly molecule-dependent.
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Article Synopsis
  • Plant de novo fatty acid synthesis occurs in plastids, starting with the production of acetyl-CoA from pyruvate via the pyruvate dehydrogenase complex (PDH), requiring the cofactor lipoic acid.
  • The enzymes involved in lipoic acid biosynthesis are octanoyltransferase (LIP2) and lipoyl synthase (LIP1), with specific mutants affecting lipid and fatty acid profiles in seeds and seedlings.
  • Analysis using gas chromatography and mass spectrometry showed that octanoyltransferase mutants exhibited altered fatty acid compositions, with a more significant impact in the LIP2p2 isoform mutant, indicating its role in regulating fatty acid synthesis in seeds.
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The effect of Pimpinella saxifraga essential oil (PSEO) addition (1-3%) in sodium alginate coating on the bacterial and oxidative stability of cheese was studied during refrigerated storage. The GC-HRMS analysis of PSEO showed that anethole, pseudoisoeugenol and p-anisaldehyde were the main components. The PSEO exhibited strong in vitro DPPH radical scavenging activity (IC = 6.

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In the context of the growing demand for α-linolenic acid due to its high nutritional value as a polyunsaturated fatty acid, we have investigated the contribution of 2-lysophosphatidic acid acyltransferase (LPAAT) enzymes from flax (Linum usitatissimum) in the accumulation of α-linolenic acid into the oil fraction of flax seed. We have isolated the cDNAs encoding three class A microsomal LPAAT2 isoforms from developing flax seeds. The three isoforms, denominated LPAAT2A, LPAAT2A2 and LPAAT2B, are able to complement the LPAAT deficient JC201 E.

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Cyclopropane fatty acids, which can be simply converted to methylated fatty acids, are good unusual fatty acid candidates for long-term resistance to oxidization and low-temperature fluidity useful for oleochemistry and biofuels. Cyclopropane fatty acids are present in low amounts in plants or bacteria. In order to develop a process for large-scale biolipid production, we expressed 10 cyclopropane fatty acid synthases from various organisms in the oleaginous yeast Yarrowia lipolytica, a model yeast for lipid metabolism and naturally capable of producing large amounts of lipids.

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Background: The mucilage is a model to study the polysaccharide biosynthesis since it is produced in large amounts and composed of complex polymers. In addition, it is of great economic interest for its technical and nutritional value. A fast method for phenotyping the released mucilage and the seed morphometric parameters will be useful for fundamental, food, pharmaceutical and breeding researches.

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Fatty acid methyl esters (FAMEs), which are commonly used to characterize lipids, have several limitations to conclude on many structures. 3-Pyridylcarbinol esters (3-PCE) are used to characterize fatty acid structures [1], in particular, to identify ring and double bond positions on the carbon chain. Chromatographic separation of these esters is complex due to their polarity and high boiling points.

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Article Synopsis
  • C labeling analysis of amino acids is crucial for understanding carbon flow in plant cells due to their diverse biosynthesis pathways and locations.
  • A new method using capillary electrophoresis-high resolution mass spectrometry (CE-HRMS) is compared to traditional GC-MS, offering improved accuracy without the need for derivatization.
  • Findings from this study reveal that valine, leucine, and alanine are not derived from the same pyruvate pool during the reserve accumulation phase in flax seeds.
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Xerophyta humilis is a poikilochlorophyllous monocot resurrection plant used as a model to study vegetative desiccation tolerance. Dehydration imposes tension and ultimate loss of integrity of membranes in desiccation sensitive species. We investigated the predominant molecular species of glycerolipids present in root and leaf tissues, using multiple reaction monitoring mass spectrometry, and then analysed changes therein during dehydration and subsequent rehydration of whole plants.

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Article Synopsis
  • This article discusses research related to the paper "13C labeling analysis of sugars by high resolution-mass spectrometry for Metabolic Flux Analysis" by Acket et al. (2017).
  • It compares the expected values of free sugars' mass isotopomer composition using previous low-resolution methods (GC-MS) with a new high-resolution mass spectrometry (LC-HRMS) approach.
  • For detailed discussions and deeper data insights, readers are directed to refer to Acket et al. (2017).
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Conjugated linoleic acids (CLAs) have been found to have beneficial effects on human health when used as dietary supplements. However, their availability is limited because pure, chemistry-based production is expensive, and biology-based fermentation methods can only create small quantities. In an effort to enhance microbial production of CLAs, four genetically modified strains of the oleaginous yeast Yarrowia lipolytica were generated.

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Metabolic flux analysis is particularly complex in plant cells because of highly compartmented metabolism. Analysis of free sugars is interesting because it provides data to define fluxes around hexose, pentose, and triose phosphate pools in different compartment. In this work, we present a method to analyze the isotopomer distribution of free sugars labeled with carbon 13 using a liquid chromatography-high resolution mass spectrometry, without derivatized procedure, adapted for Metabolic flux analysis.

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We describe an approach to extract (13)C-labeled sugars (glucose, fructose, maltose, sucrose, myo-inositol as well as glucose from starch) from plant tissues and to analyze their isotopomer distribution by gas chromatography-mass spectrometry (GC-MS). Sugars are derivatized with N,O-bis(trimethylsilyl) trifluoroacetamide (BSTFA) into their Si(CH3)3 derivatives. Electronic and chemical ionizations are used to obtain suitable fragments for metabolic flux analysis (MFA).

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Background: Flax (Linum usitatissimum L.) is an economically important fiber and oil crop that has been grown for thousands of years. The genome has been recently sequenced and transcriptomics are providing information on candidate genes potentially related to agronomically-important traits.

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The tricarboxylic acid (TCA) cycle is involved in the complete oxidation of organic acids to carbon dioxide in aerobic cells. It not only uses the acetyl-CoA derived from glycolysis but also uses breakdown products of proteins, fatty acids, and nucleic acids. Therefore, the TCA cycle involves numerous carbon fluxes through central metabolism to produce reductant power and transfer the generated electrons to the aerobic electron transport system where energy is formed by oxidative phosphorylation.

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Article Synopsis
  • - The study compared two types of flax target probes (25-mers and 60-mers) using consistent lab techniques to evaluate their performance in measuring gene expression.
  • - Results showed that both probe types produced reliable data, but the 60-mers had higher hybridization efficiency and sensitivity, allowing for the detection of more genes.
  • - The conclusion emphasized that while both array types are effective, the 60-mers provide a better and more comprehensive understanding of candidate genes related to various biological functions.
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Metabolic flux analysis, using 13C labeled substrates, has become a powerful methodology for quantifying intracellular fluxes. Most often, analysis is restricted to nuclear magnetic resonance or mass spectrometry measurement of 13C label incorporation into protein amino acids. However, amino acid isotopomer distribution insufficiently covers the entire network of central metabolism, especially in plant cells with highly compartmented metabolism, and analysis of other metabolites is required.

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