Structure and absolute configuration of an unsaturated anteiso fatty acid from Bacillus megaterium.

Simone Hauff, Leif Rilfors, Georg Hottinger, Walter Vetter

文献索引：J. Chromatogr. A. 1217 , 1683-1687, (2010)

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摘要

Gas chromatography in combination with electron ionization mass spectrometry (GC/EI-MS) was used to determine the fatty acids of a membrane lipid from Bacillus megaterium. Special attention was put on the structure and absolute configuration of a monoenoic fatty acid previously described in this sample. GC/EI-MS operated in the selected ion monitoring mode was used to determine twelve fatty acids in the bacterium. Methyl esters were prepared to verify the presence of a 14-methylhexadecenoic acid (a17:1) isomer. The position of the double bond of the a17:1 isomer and four further monoenoic fatty acids was elucidated by means of their picolinyl esters produced by the transesterification of the phospholipid. For the a17:1 isomer, the double bond was located between C-5 and C-6. Silver ion liquid chromatography was used to verify that the double bond was in cis-configuration. The bacterial 14-methylhexadec-5-enoic acid (a17:1Delta5) is chiral due to the stereogenic C-14 carbon. Initial enantioselective measurements were carried out with isomers of a17:1Delta5 which were available in form of racemic and (S)-enantiopure cis- and trans-isomers of a17:1Delta12 previously synthesized. The cis-a17:1Delta12 enantiomers were partly resolved on a chiral stationary phase coated with 50% heptakis(6-O-tert.-butyldimethylsilyl-2,3-di-O-methyl)-beta-cyclodextrin in OV-1701 (beta-TBDM). However, resolution of the enantiomers of the trans-isomer of a17:1Delta12 failed. Only one peak was also observed for the a17:1Delta5 isomer from B. megaterium. Thus, it remained unclear whether the compound a17:1Delta5 was racemic or enantiopure in the sample. To clarify this point, we separated the cis-monoenoic fraction from the saturated fatty acids. Then, the monoenoic fraction was hydrogenated in order to transform a17:1Delta5 into 14-methylhexadecanoic acid (a17:0). This chiral fatty acid was known to be sufficiently enantioseparated on the beta-TBDM column and was found to be (S)-enantiopure in the sample. Hence, these measurements verified that the B. megaterium sample contained enantiopure (S)-a17:1Delta5.2010 Elsevier B.V. All rights reserved.