Separation of Hydroxylated Metabolites of Fatty Acids (C10-C18) on a μPorasil Silica Column Using an Isocratic HPLC System

1986 ◽  
Vol 9 (8) ◽  
pp. 1711-1725 ◽  
Author(s):  
M. J. Clarke ◽  
R. L. Hawke ◽  
R. M. Welch
Proteins ◽  
1987 ◽  
pp. 383-394
Author(s):  
J. E. Shively ◽  
D. Hawke ◽  
R. M. Kutny ◽  
B. Krieger ◽  
J. L. Glajch

2004 ◽  
Vol 10 (3) ◽  
pp. 157-161 ◽  
Author(s):  
S. K. Lo ◽  
B. S. Baharin ◽  
C. P. Tan ◽  
O. M. Lai

High-purity diacylglycerol (DAG) oil was enzymatically obtained from palm oil deodoriser distillate (PODD). Free fatty acids from PODD were esterified with glycerol (2.5:1 fatty acid to glycerol molar ratio) in the presence of 10% (w/w of oil) Rhizomucor mieheilipase (Lipozyme RM IM) and 30% (w/w of oil) molecular sieves and incubated for 6h at 65 °C in a 50 mL bioreactor. After esterification, the products were deacidified by alkaline extraction and the DAG oil was further purified by silica column chromatography. After purification, up to 85.2% (w/w) of DAG was obtained. DAG profile, fatty acid composition, iodine value, slip melting point and thermal profiles were determined.


2021 ◽  
Vol 12 ◽  
Author(s):  
Kai-Di Ni ◽  
Jun-Yan Liu

The cytochrome P450 (CYP) ω-hydroxylases are a subfamily of CYP enzymes. While CYPs are the main metabolic enzymes that mediate the oxidation reactions of many endogenous and exogenous compounds in the human body, CYP ω-hydroxylases mediate the metabolism of multiple fatty acids and their metabolites via the addition of a hydroxyl group to the ω- or (ω-1)-C atom of the substrates. The substrates of CYP ω-hydroxylases include but not limited to arachidonic acid, docosahexaenoic acid, eicosapentaenoic acid, epoxyeicosatrienoic acids, leukotrienes, and prostaglandins. The CYP ω-hydroxylases-mediated metabolites, such as 20-hyroxyleicosatrienoic acid (20-HETE), 19-HETE, 20-hydroxyl leukotriene B4 (20-OH-LTB4), and many ω-hydroxylated prostaglandins, have pleiotropic effects in inflammation and many inflammation-associated diseases. Here we reviewed the classification, tissue distribution of CYP ω-hydroxylases and the role of their hydroxylated metabolites in inflammation-associated diseases. We described up-regulation of CYP ω-hydroxylases may be a pathogenic mechanism of many inflammation-associated diseases and thus CYP ω-hydroxylases may be a therapeutic target for these diseases. CYP ω-hydroxylases-mediated eicosanods play important roles in inflammation as pro-inflammatory or anti-inflammatory mediators, participating in the process stimulated by cytokines and/or the process stimulating the production of multiple cytokines. However, most previous studies focused on 20-HETE,and further studies are needed for the function and mechanisms of other CYP ω-hydroxylases-mediated eicosanoids. We believe that our studies of CYP ω-hydroxylases and their associated eicosanoids will advance the translational and clinal use of CYP ω-hydroxylases inhibitors and activators in many diseases.


2013 ◽  
Vol 80 (1) ◽  
pp. 360-365 ◽  
Author(s):  
Sandra M. Heinzelmann ◽  
Nicole J. Bale ◽  
Ellen C. Hopmans ◽  
Jaap S. Sinninghe Damsté ◽  
Stefan Schouten ◽  
...  

ABSTRACTPhospholipid-derived fatty acids (PLFAs) are commonly used to characterize microbial communitiesin situand the phylogenetic positions of newly isolated microorganisms. PLFAs are obtained through separation of phospholipids from glycolipids and neutral lipids using silica column chromatography. We evaluated the performance of this separation method for the first time using direct detection of intact polar lipids (IPLs) with high-performance liquid chromatography–mass spectrometry (HPLC-MS). We show that under either standard or modified conditions, the phospholipid fraction contains not only phospholipids but also other lipid classes such as glycolipids, betaine lipids, and sulfoquinovosyldiacylglycerols. Thus, commonly reported PLFA compositions likely are not derived purely from phospholipids and perhaps may not be representative of fatty acids present in living microbes.


Lipids ◽  
1994 ◽  
Vol 29 (8) ◽  
pp. 547-553 ◽  
Author(s):  
Herng-Hsiang Lo ◽  
Gwendolyn A. Bartek ◽  
Susan M. Fischer

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