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. 1987 Apr 15;243(2):481–485. doi: 10.1042/bj2430481

Determination of arrangement of isoprene units in pig liver dolichol by 13C-n.m.r. spectroscopy.

Y Tanaka, H Sato, A Kageyu, T Tomita
PMCID: PMC1147880  PMID: 3632632

Abstract

The arrangement of isoprene units in pig liver dolichol-18, -19 and -20 was determined by 1H- and 13C-n.m.r. spectroscopies. The alignment of trans and cis isoprene units was found to be in the order: dimethylallyl unit, two trans units, a sequence of 14-16 cis units, and a saturated isoprene unit terminated with a hydroxyl group, which verified the presumed chemical structure of dolichol. The absence of geometric isomers was confirmed. A slight amount of impurity was detected in each reversed-phase h.p.l.c. fraction of dolichol obtained by a conventional method. Detailed assignments of the 13C-n.m.r. spectrum were given for these dolichols by using model compounds and INEPT (insensitive nuclei enhanced by polarization transfer) measurement. The chemical structure of synthetic dolichol-19, which was prepared by the addition of a saturated isoprene unit to the polyprenol-18 isolated from Ginkgo biloba, was confirmed to be identical with that of pig liver dolichol-19.

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Selected References

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  1. Adair W. L., Jr, Robertson S. Absolute configuration of dolichol. Biochem J. 1980 Sep 1;189(3):441–445. doi: 10.1042/bj1890441. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BURGOS J., HEMMING F. W., PENNOCK J. F., MORTON R. A. DOLICHOL: A NATURALLY-OCCURRING C100 ISOPRENOID ALCOHOL. Biochem J. 1963 Sep;88:470–482. [PMC free article] [PubMed] [Google Scholar]
  3. Butterworth P. H., Hemming F. W. Intracellular distribution of the free and esterified forms of dolichol in pig liver. Arch Biochem Biophys. 1968 Nov;128(2):503–508. doi: 10.1016/0003-9861(68)90057-x. [DOI] [PubMed] [Google Scholar]
  4. Feeney J., Hemming F. W. Nuclear magnetic resonance spectrometry of naturally occurring polyprenols. Anal Biochem. 1967 Jul;20(1):1–15. doi: 10.1016/0003-2697(67)90258-8. [DOI] [PubMed] [Google Scholar]
  5. Gough D. P., Hemming F. W. The characterization and stereochemistry of biosynthesis of dolichols in rat liver. Biochem J. 1970 Jun;118(1):163–166. doi: 10.1042/bj1180163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Grange D. K., Adair W. L., Jr Studies on the biosynthesis of dolichyl phosphate: evidence for the in vitro formation of 2,3-dehydrodolichyl phosphate. Biochem Biophys Res Commun. 1977 Dec 7;79(3):734–740. doi: 10.1016/0006-291x(77)91173-1. [DOI] [PubMed] [Google Scholar]
  7. Ibata K., Mizuno M., Takigawa T., Tanaka Y. Long-chain betulaprenol-type polyprenols from the leaves of Ginkgo biloba. Biochem J. 1983 Aug 1;213(2):305–311. doi: 10.1042/bj2130305. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Martin H. G., Thorne K. J. Synthesis of radioactive dolichol from (4S-3H)mevalonate in the regenerating rat liver. Biochem J. 1974 Feb;138(2):277–280. doi: 10.1042/bj1380277. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Mańkowski T., Jankowski W., Chojnacki T., Franke P. C55-Dolichol: occurrence in pig liver and preparation by hydrogenation of plant undecaprenol. Biochemistry. 1976 May 18;15(10):2125–2130. doi: 10.1021/bi00655a015. [DOI] [PubMed] [Google Scholar]
  10. Pullarkat R. K., Reha H. Accumulation of dolichols in brains of elderly. J Biol Chem. 1982 Jun 10;257(11):5991–5993. [PubMed] [Google Scholar]
  11. Tanaka Y., Takagi M. Structural characterization of ficaprenol-11 by 13C nuclear magnetic resonance. Biochem J. 1979 Oct 1;183(1):163–165. doi: 10.1042/bj1830163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Wong T. K., Decker G. L., Lennarz W. J. Localization of dolichol in the lysosomal fraction of rat liver. J Biol Chem. 1982 Jun 10;257(11):6614–6618. [PubMed] [Google Scholar]

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