Enantiomeric separation of triacylglycerols containing fatty acids with a ring (cyclofatty acids)
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
32317104
DOI
10.1016/j.chroma.2020.461103
PII: S0021-9673(20)30324-1
Knihovny.cz E-resources
- Keywords
- Chaulmoogra oil, Cyclic fatty acids, Enantiomeric separation, Non-aqueous reversed-phase-HPLC, Sterculic seeds, Triacylglycerols,
- MeSH
- Chromatography, Reverse-Phase MeSH
- Cyclopropanes analysis MeSH
- Spectrometry, Mass, Electrospray Ionization MeSH
- Fatty Acids, Monounsaturated analysis MeSH
- Fatty Acids analysis chemistry isolation & purification MeSH
- Plant Oils chemistry MeSH
- Sterculia chemistry MeSH
- Stereoisomerism MeSH
- Triglycerides chemistry MeSH
- Chromatography, High Pressure Liquid MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- chaulmoogra oil MeSH Browser
- Cyclopropanes MeSH
- Fatty Acids, Monounsaturated MeSH
- malvalic acid MeSH Browser
- Fatty Acids MeSH
- Plant Oils MeSH
- sterculic acid MeSH Browser
- Triglycerides MeSH
Triacylglycerols (TAGs) containing cyclofatty acids (cycloFAs) from two oilseeds of Sterculia foetida and Hydnocarpus wightiana were analysed using both reversed-phase (RP18) and chiral phase columns. TAGs were identified using high-resolution electrospray ionization mass spectrometry in the positive ion mode. Fifty-five molecular species of TAGs have been identified in sterculic oil, 27 of which contained at least one cyclopropenyl-FA (e.g., malvalic or sterculic acids). The structures of regioisomers and enantiomers were determined for five major TAGs with cyclopropenyl-FAs. One hundred thirty-six TAGs were identified in chaulmoogra oil, 71 of which contained at least one cyclopentenyl-FA (e.g., gorlic, chaulmoogric, and hydnocarpic acids, etc.). Furthermore, in three molecular species, regioisomers and enantiomers were identified using HPLC on a chiral phase column. Eight molecular species of TAGs were prepared through organic synthesis to facilitate the identification of enantiomers. Retention times of fatty acid-containing triacylglycerols with one ring and one double bond are very similar to triacylglycerols with a dienoic fatty acid, but elution times are shorter. For example, dimalvaloylpalmitate elutes earlier than dilinoleylpalmitate. The order of elution of TAGs on the chiral column differs. In TAGs with 2 degrees of unsaturation (ring and double bond, e.g. PStP-StPP-PPSt), the order of elution is symmetric-asymmetric-asymmetric TAGs. TAGs with 4 degrees of unsaturation (one ring and three double bonds or two rings and two double bonds) present a different pattern. When TAGs contain two rings and two double bonds, the order of elution TAGs is asymmetric-symmetric-asymmetric (StStP-StPSt-PStSt); when TAGs contain a ring and 3 double bonds, the elution order is symmetric-asymmetric-asymmetric TAGs (OStO-StOO-OOSt). In species with a higher degree of unsaturation (e.g., 5), the elution order of the TAGs is asymmetric-asymmetric-symmetric (e.g. CCO-OCC-COC).
The Czech Academy of Sciences Institute of Microbiology Vídeňská 1083 142 20 Prague 4 Czech Republic
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