Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1995 Sep;177(18):5327–5333. doi: 10.1128/jb.177.18.5327-5333.1995

Unique cholesteryl glucosides in Helicobacter pylori: composition and structural analysis.

Y Hirai 1, M Haque 1, T Yoshida 1, K Yokota 1, T Yasuda 1, K Oguma 1
PMCID: PMC177327  PMID: 7665522

Abstract

A chloroform-methanol-extracted lipid of Helicobacter pylori was studied. Three kinds of glycolipids, accounting for about 25% (wt/wt) of the total lipid, were detected and identified to be cholesteryl glucosides. The structures of two of them were determined to be cholesteryl-alpha-D-glucopyranoside and cholesteryl-6-O-tetrade-canoyl-alpha-D-glucopyranoside, and the plausible structure of the third one was identified as cholesteryl-6-O-phosphatidyl-alpha-D-glucopyranoside. Cholesteryl glucosides are very rare in animals and bacteria. Furthermore, those in H. pylori had an alpha-glycosidic linkage, which is rather unusual for natural glycosides, and a phosphate-linked cholesteryl glycoside like the cholesteryl-6-O-phosphatidyl-alpha-D-glucopyranoside has not been reported previously. As the cholesterol glucosides were detected in strains obtained from diverse geographical locations, the presence of cholesteryl glucosides in H. pylori is a very unique and a characteristic feature of the species. These findings add a new facet to the physiology and biochemistry, especially the cholesterol and glucose metabolism, of H. pylori. Furthermore, the cholesteryl glucosides of H. pylori showed hemolytic activities.

Full Text

The Full Text of this article is available as a PDF (351.7 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Allain C. C., Poon L. S., Chan C. S., Richmond W., Fu P. C. Enzymatic determination of total serum cholesterol. Clin Chem. 1974 Apr;20(4):470–475. [PubMed] [Google Scholar]
  2. BEISS U. ZUR PAPIERCHROMATOGRAPHISCHEN AUFTRENNUNG VON PFLANZENLIPIDEN. J Chromatogr. 1964 Jan;13:104–110. doi: 10.1016/s0021-9673(01)95079-4. [DOI] [PubMed] [Google Scholar]
  3. Cover T. L., Blaser M. J. Helicobacter pylori and gastroduodenal disease. Annu Rev Med. 1992;43:135–145. doi: 10.1146/annurev.me.43.020192.001031. [DOI] [PubMed] [Google Scholar]
  4. DITTMER J. C., LESTER R. L. A SIMPLE, SPECIFIC SPRAY FOR THE DETECTION OF PHOSPHOLIPIDS ON THIN-LAYER CHROMATOGRAMS. J Lipid Res. 1964 Jan;5:126–127. [PubMed] [Google Scholar]
  5. De Rosa M., Gambacorta A., Gliozzi A. Structure, biosynthesis, and physicochemical properties of archaebacterial lipids. Microbiol Rev. 1986 Mar;50(1):70–80. doi: 10.1128/mr.50.1.70-80.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. FOLCH J., LEES M., SLOANE STANLEY G. H. A simple method for the isolation and purification of total lipides from animal tissues. J Biol Chem. 1957 May;226(1):497–509. [PubMed] [Google Scholar]
  7. FRANCOIS C., MARSHALL R. D., NEUBERGER A. Carbohydrates in protein. 4. The determination of mannose in hen's-egg albumin by radioisotope dilution. Biochem J. 1962 May;83:335–341. doi: 10.1042/bj0830335. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Geis G., Leying H., Suerbaum S., Opferkuch W. Unusual fatty acid substitution in lipids and lipopolysaccharides of Helicobacter pylori. J Clin Microbiol. 1990 May;28(5):930–932. doi: 10.1128/jcm.28.5.930-932.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Goodwin C. S., McCulloch R. K., Armstrong J. A., Wee S. H. Unusual cellular fatty acids and distinctive ultrastructure in a new spiral bacterium (Campylobacter pyloridis) from the human gastric mucosa. J Med Microbiol. 1985 Apr;19(2):257–267. doi: 10.1099/00222615-19-2-257. [DOI] [PubMed] [Google Scholar]
  10. Hayami M., Okabe A., Sasai K., Hayashi H., Kanemasa Y. Presence and synthesis of cholesterol in stable staphylococcal L-forms. J Bacteriol. 1979 Dec;140(3):859–863. doi: 10.1128/jb.140.3.859-863.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Hessey S. J., Spencer J., Wyatt J. I., Sobala G., Rathbone B. J., Axon A. T., Dixon M. F. Bacterial adhesion and disease activity in Helicobacter associated chronic gastritis. Gut. 1990 Feb;31(2):134–138. doi: 10.1136/gut.31.2.134. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hu L. T., Mobley H. L. Purification and N-terminal analysis of urease from Helicobacter pylori. Infect Immun. 1990 Apr;58(4):992–998. doi: 10.1128/iai.58.4.992-998.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hussell T., Isaacson P. G., Crabtree J. E., Spencer J. The response of cells from low-grade B-cell gastric lymphomas of mucosa-associated lymphoid tissue to Helicobacter pylori. Lancet. 1993 Sep 4;342(8871):571–574. doi: 10.1016/0140-6736(93)91408-e. [DOI] [PubMed] [Google Scholar]
  14. KATES M., ALLISON A. C., JAMES A. T. Phosphatides of human blood cells and their role in spherocytosis. Biochim Biophys Acta. 1961 Apr 15;48:571–582. doi: 10.1016/0006-3002(61)90055-5. [DOI] [PubMed] [Google Scholar]
  15. Kanemasa Y., Yoshioka T., Hayashi H. Alteration of the phospholipid composition of Staphylococcus aureus cultured in medium containing NaCl. Biochim Biophys Acta. 1972 Nov 30;280(3):444–450. [PubMed] [Google Scholar]
  16. Kastelic-Suhadolc T. Cholesteryl glucoside in Candida bogoriensis. Biochim Biophys Acta. 1980 Nov 7;620(2):322–325. doi: 10.1016/0005-2760(80)90213-1. [DOI] [PubMed] [Google Scholar]
  17. Lambert M. A., Patton C. M., Barrett T. J., Moss C. W. Differentiation of Campylobacter and Campylobacter-like organisms by cellular fatty acid composition. J Clin Microbiol. 1987 Apr;25(4):706–713. doi: 10.1128/jcm.25.4.706-713.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Livermore B. P., Bey R. F., Johnson R. C. Lipid metabolism of Borrelia hermsi. Infect Immun. 1978 Apr;20(1):215–220. doi: 10.1128/iai.20.1.215-220.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Mayberry W. R., Smith P. F. Structures and properties of acyl diglucosylcholesterol and galactofuranosyl diacylglycerol from Acholeplasma axanthum. Biochim Biophys Acta. 1983 Aug 1;752(3):434–443. doi: 10.1016/0005-2760(83)90273-4. [DOI] [PubMed] [Google Scholar]
  20. Mendz G. L., Hazell S. L., Burns B. P. Glucose utilization and lactate production by Helicobacter pylori. J Gen Microbiol. 1993 Dec;139(12):3023–3028. doi: 10.1099/00221287-139-12-3023. [DOI] [PubMed] [Google Scholar]
  21. Mobley H. L., Cortesia M. J., Rosenthal L. E., Jones B. D. Characterization of urease from Campylobacter pylori. J Clin Microbiol. 1988 May;26(5):831–836. doi: 10.1128/jcm.26.5.831-836.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Nagamachi E., Shibuya S., Hirai Y., Matsushita O., Tomochika K., Kanemasa Y. Adaptational changes of fatty acid composition and the physical state of membrane lipids following the change of growth temperature in Yersinia enterocolitica. Microbiol Immunol. 1991;35(12):1085–1093. doi: 10.1111/j.1348-0421.1991.tb01630.x. [DOI] [PubMed] [Google Scholar]
  23. Okabe H., Uji Y., Nagashima K., Noma A. Enzymic determination of free fatty acids in serum. Clin Chem. 1980 Oct;26(11):1540–1543. [PubMed] [Google Scholar]
  24. Olivieri R., Bugnoli M., Armellini D., Bianciardi S., Rappuoli R., Bayeli P. F., Abate L., Esposito E., de Gregorio L., Aziz J. Growth of Helicobacter pylori in media containing cyclodextrins. J Clin Microbiol. 1993 Jan;31(1):160–162. doi: 10.1128/jcm.31.1.160-162.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Patel K. R., Smith P. F., Mayberry W. R. Comparison of lipids from Spiroplasma citri and corn stunt spiroplasma. J Bacteriol. 1978 Nov;136(2):829–831. doi: 10.1128/jb.136.2.829-831.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. RENKONEN O. Determination of glycerol in phosphatides. Biochim Biophys Acta. 1962 Jan 29;56:367–369. doi: 10.1016/0006-3002(62)90580-2. [DOI] [PubMed] [Google Scholar]
  27. ROTHBLAT G. H., SMITH P. F. Nonsaponifiable lipids of representative pleuropneumonia-like organisms. J Bacteriol. 1961 Oct;82:479–491. doi: 10.1128/jb.82.4.479-491.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Segal R., Shud F., Milo-Goldzweig I. Hemolytic properties of synthetic glycosides. J Pharm Sci. 1978 Nov;67(11):1589–1592. doi: 10.1002/jps.2600671123. [DOI] [PubMed] [Google Scholar]
  29. Smith P. F. Biosynthesis of cholesteryl glucoside by Mycoplasma gallinarum. J Bacteriol. 1971 Dec;108(3):986–991. doi: 10.1128/jb.108.3.986-991.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Stedman R. L. The chemical composition of tobacco and tobacco smoke. Chem Rev. 1968 Apr;68(2):153–207. doi: 10.1021/cr60252a002. [DOI] [PubMed] [Google Scholar]
  31. Unidentified curved bacilli on gastric epithelium in active chronic gastritis. Lancet. 1983 Jun 4;1(8336):1273–1275. [PubMed] [Google Scholar]
  32. Unidentified curved bacilli on gastric epithelium in active chronic gastritis. Lancet. 1983 Jun 4;1(8336):1273–1275. [PubMed] [Google Scholar]
  33. Wotherspoon A. C., Doglioni C., Diss T. C., Pan L., Moschini A., de Boni M., Isaacson P. G. Regression of primary low-grade B-cell gastric lymphoma of mucosa-associated lymphoid tissue type after eradication of Helicobacter pylori. Lancet. 1993 Sep 4;342(8871):575–577. doi: 10.1016/0140-6736(93)91409-f. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES