Fatty Acids
They can be saturated or unsaturated, and have a wide range of chain lengths.
Fatty acids are essential nutrients, serving as energy sources and structural components of cell membranes.
Imbalances in fatty acid profiles have been linked to numerous health conditions, including cardiovascular disease, diabetes, and inflammation.
Optimization of fatty acid research is key to advancing our understanding and therapeutic applications in this dynamic field of study.
Most cited protocols related to «Fatty Acids»
To develop the food list for the short-FFQ, we selected and combined items and supporting questions from the original long-FFQ. We selected the three major foods and beverages that contributed to inter-individual variation for each of 40 nutrients according to a cumulative R2 for the 40 nutrients,16 based on the multiple regression coefficient with total intake of a specific nutrient as the dependent variable and its intake from each food as the explanatory variable. Inter-individual variation was calculated by gender among 45 869 men and 52 989 women who responded to the JPHC Study 10-year follow-up survey. Consequently, cumulative R2 for the nutrients ranged from 0.4 to 1.0. For potential inter-individual variation in intake of specific food groups, some foods, such as coffee, were added. Ultimately, 66 food and beverage items were selected for the short-FFQ. In this validation study, information on alcoholic beverages was substituted with those from the long-FFQ (united with overall information of lifestyle), because these questions were not included in the short-FFQ. This was because information on alcoholic beverage intake was structured in pages for lifestyle other than diet, such as smoking status and physical activity, and the reproducibility of alcoholic beverage intake was relatively high even if questionnaires were administered at a 1-year interval.17 (link),18 (link)Intakes of energy, 53 nutrients, and 29 food groups were calculated using the Standard Tables of Food Composition in Japan 2010,19 Standard Tables of Food Composition in Japan Fifth Revised and Enlarged Edition 2005 For Fatty Acids,20 and a specifically developed food composition table for isoflavones in Japanese foods.21 (link)
Healthy plant food groups included whole grains, fruits, vegetables, nuts, legumes, vegetable oils, and tea/coffee, whereas less healthy plant food groups included fruit juices, sugar-sweetened beverages, refined grains, potatoes, and sweets/desserts. Animal food groups included animal fats, dairy, eggs, fish/seafood, meat (poultry and red meat), and miscellaneous animal-based foods.
Settings specific for each tested program were as follows.
LipidXplorer: 'MS threshold' was set to 100 and 'MS/MS threshold' to 5 counts per peak area; 'Resolution gradient' was set to 1; other common spectra import settings were as in Additional file
LipidQA (spectra were imported as *.raw files): 'MS error' and the 'MS/MS error' were both set to 0.3 Da; 'Finnigan Filter', on; 'Quantification', off; 'Mode selection', Neg. Mode; 'If MS2 spectra were centroided', checked. Only species with a score above 0.5 were accepted. The current version of LipidQA is available at [51 ].
Lipid Search version 2.0 beta: 'SearchType' was set to 'MS2,MS3'; 'ExpType' to 'Infusion'; 'Precursor tol' to '0.3 Da'; 'Product peak tol' to 0.3 Da; 'Intensity threshold' to 0.01; 'Threshold type' to Relative; 'M-score Threshold' to 10.0. The current version of LipidSearch is available at [52 ].
LipidProfiler v.1.0.97: the software was used for creating a reference list of lipids in the E. coli extract and utilized a separate dataset acquired on a QSTAR Pulsar i mass spectrometer by the MPIS method. Intensity threshold was set to 0.2%; all lipid species reported as 'confirmed results' in at least four independent acquisitions.
Most recents protocols related to «Fatty Acids»
Example 5
The content of free fatty acids in the oils and products was determined by neutralization titrimetry. The free fatty acids, about 0.2 g of the sample, were titrated with 0.04 mol·L−1 NaOH solution in a Mettler model DG20 automatic titrator up to a pH of 11.0 and the acidity of the sample was determined from Equation 3.
Alternatively, for samples with a larger volume, the free fatty acids, from about 0.5 to 1 g of the sample, were titrated with 0.25 mol·L−1 NaOH solution using phenolphthalein as indicator and the acidity of the sample was determined from Equation 3.
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- V=volume of sodium hydroxide used in titration of the sample (mL);
- M=molarity of the NaOH solution (mol·L−1);
- AG=molecular weight of the fatty acid present in highest concentration in the oil* (g);
- m=sample weight (g).
- *Soya oil=linoleic acid (280 g); castor oil=ricinoleic acid (298 g).
Example 8
65% coconut oil, 20% rice bran oil, 10% palm oil, 5% castor oil.
100% KOH, 25% KCl, 25% NaCl (salts based on oils weight)
A hard bar 3.5 kg/cm2 a week after unmolding. 1.5:1 water to soap dilution easily dispersed to a very thick pearlescent liquid soap. Good lather and skin feel.
Example 10
The linear peptide was prepared by solid phase method as per the analogous process given for Example 2, Part A starting with Fmoc protected Isoleucine was first coupled with Wang resin and then sequentially other amino acids were coupled. The grafting of activated fatty acid chain, Moiety C-OSu over the linear peptide by following analogous process of Example 2, Part B afforded the Compound 15.
Example 6
Strain 5 was subjected to another round of mutagenesis with increasing concentrations and exposure time to 4-NQO (37 μM for 30 minutes at 28° C.). This population of cells was subsequently subdivided and grown in standard lipid production medium supplemented with a range of cerulenin concentrations (7-50 μM). Cells from all concentrations were pooled and fractionated over a 60% Percoll/0.15 M NaCl density gradient. Oil laden cells recovered from a density zone of 1.02 g/mL were plated and assessed for glucose consumption and fatty acid profile. One of these clones was subsequently stabilized and given the strain designation “Strain 6”.
Example 10
The linear peptide was prepared by solid phase method as per the analogous process given for Example 2, Part A starting with Fmoc protected Isoleucine was first coupled with Wang resin and then sequentially other amino acids were coupled. The grafting of activated fatty acid chain, Moiety C-OSu over the linear peptide by following analogous process of Example 2, Part B afforded the Compound 15.
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More about "Fatty Acids"
These versatile molecules can be classified as saturated or unsaturated, and exhibit a wide range of chain lengths.
Fatty acids are essential nutrients, functioning as energy sources and structural components of cell membranes.
Imbalances in fatty acid profiles have been linked to numerous health conditions, including cardiovascular disease, diabetes, and inflammation.
Optimization of fatty acid research is key to advancing our understanding and therapeutic applications in this dynamic field of study.
Bovine serum albumin (BSA) and fatty acid-free BSA are commonly used in fatty acid research to provide a carrier for these hydrophobic molecules.
The Supelco 37 Component FAME Mix is a reference standard that contains a variety of fatty acid methyl esters, allowing for the identification and quantification of fatty acids in samples.
Palmitic acid and oleic acid are two of the most abundant and well-studied fatty acids, playing crucial roles in energy metabolism and cell signaling.
The GC-2010 and GC-2010 Plus gas chromatography systems are powerful analytical tools used to separate, identify, and quantify fatty acids in complex samples.
Methanol and fetal bovine serum (FBS) are also important components in fatty acid research, as they are used in the extraction and analysis of these lipid molecules.
By leveraging the insights gained from these related topics, researchers can optimize their fatty acid studies and uncover new discoveries that will drive progress in this dynamic field.