Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1971 Apr;106(1):25–30. doi: 10.1128/jb.106.1.25-30.1971

Effect of Temperature on the Fatty Acid Composition of Thermus aquaticus

Paul H Ray 1,2, David C White 1,2, Thomas D Brock 1,2
PMCID: PMC248639  PMID: 5551637

Abstract

Thermus aquaticus contains four major fatty acids, iso-C15 (28%), iso-C16 (9%), normal-C16 (13%), and iso-C17 (48%), when grown at 70 C, as determined by gas chromatography and mass spectrometry. Small amounts of iso-C12, normal-C12:1, iso-C13, normal-C14, iso-C14, and normal-C15:1 were also detected. A change in growth temperature (50 to 75 C at 5-C intervals) affects a shift in the proportions of some of the fatty acids. The proportions of the monoenoic and branched-C17 fatty acids decreased and the proportions of the higher-melting iso-C16 and normal-C16 fatty acids increased. Cells grown at 75 C contained 70% more total fatty acids than cells grown at 50 C. The largest increases, in absolute amounts, were in the content of iso-C16 and normal-C16 fatty acids, with only a 1.6-fold increase in the major iso-C15 and iso-C17 fatty acids. There was a 2.5-fold decrease in normal-C15:1 and at least a 24-fold decrease in anteiso-C17, which is present at 50 and 55 C but not at higher temperatures. There was no difference in proportion or amount of fatty acids between exponential and stationary-phase cells grown at 70 C. When cells were grown on glutamate instead of yeast-extract and tryptone at 70 C, the total fatty acid content remained constant, but there was an increase in the proportions of iso-C16 and normal-C16 fatty acids concomitant with a decrease in the proportions of the iso-C15 and iso-C17 fatty acids.

Full text

PDF
25

Selected References

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

  1. BARTLETT G. R. Phosphorus assay in column chromatography. J Biol Chem. 1959 Mar;234(3):466–468. [PubMed] [Google Scholar]
  2. BLIGH E. G., DYER W. J. A rapid method of total lipid extraction and purification. Can J Biochem Physiol. 1959 Aug;37(8):911–917. doi: 10.1139/o59-099. [DOI] [PubMed] [Google Scholar]
  3. Brock T. D., Edwards M. R. Fine structure of Thermus aquaticus, an extreme thermophile. J Bacteriol. 1970 Oct;104(1):509–517. doi: 10.1128/jb.104.1.509-517.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Brock T. D., Freeze H. Thermus aquaticus gen. n. and sp. n., a nonsporulating extreme thermophile. J Bacteriol. 1969 Apr;98(1):289–297. doi: 10.1128/jb.98.1.289-297.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Brock T. D. Life at high temperatures. Evolutionary, ecological, and biochemical significance of organisms living in hot springs is discussed. Science. 1967 Nov;158(3804):1012–1019. doi: 10.1126/science.158.3804.1012. [DOI] [PubMed] [Google Scholar]
  6. Card G. L., Georgi C. E., Militzer W. E. Phospholipids from Bacillus stearothermophilus. J Bacteriol. 1969 Jan;97(1):186–192. doi: 10.1128/jb.97.1.186-192.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cho K. Y., Salton M. R. Fatty acid composition of bacterial membrane and wall lipids. Biochim Biophys Acta. 1966 Feb 1;116(1):73–79. doi: 10.1016/0005-2760(66)90093-2. [DOI] [PubMed] [Google Scholar]
  8. Daron H. H. Fatty acid composition of lipid extracts of a thermophilic Bacillus species. J Bacteriol. 1970 Jan;101(1):145–151. doi: 10.1128/jb.101.1.145-151.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Heinen W., Klein H. P., Volkmann C. M. Fatty acid composition of Thermus aquaticus at different growth temperatures. Arch Mikrobiol. 1970;72(2):199–202. doi: 10.1007/BF00409525. [DOI] [PubMed] [Google Scholar]
  10. KANESHIRO T., MARR A. G. cis-9,10-Methylene hexadecanoic acid from the phospholipids of Escherichia coli. J Biol Chem. 1961 Oct;236:2615–2619. [PubMed] [Google Scholar]
  11. Marr A. G., Ingraham J. L. EFFECT OF TEMPERATURE ON THE COMPOSITION OF FATTY ACIDS IN ESCHERICHIA COLI. J Bacteriol. 1962 Dec;84(6):1260–1267. doi: 10.1128/jb.84.6.1260-1267.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. RADIN N. S., BROWN J. R., LAVIN F. B. The preparative isolation of cerebrosides. J Biol Chem. 1956 Apr;219(2):977–983. [PubMed] [Google Scholar]
  13. RAPPORT M. M., ALONZO N. Photometric determination of fatty acid ester groups in phospholipides. J Biol Chem. 1955 Nov;217(1):193–198. [PubMed] [Google Scholar]
  14. Shen P. Y., Coles E., Foote J. L., Stenesh J. Fatty acid distribution in mesophilic and thermophilic strains of the genus Bacillus. J Bacteriol. 1970 Aug;103(2):479–481. doi: 10.1128/jb.103.2.479-481.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. White D. C., Cox R. H. Indentification and localization of the fatty acids in Haemophilus parainfluenzae. J Bacteriol. 1967 Mar;93(3):1079–1088. doi: 10.1128/jb.93.3.1079-1088.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. White D. C., Frerman F. E. Extraction, characterization, and cellular localization of the lipids of Staphylococcus aureus. J Bacteriol. 1967 Dec;94(6):1854–1867. doi: 10.1128/jb.94.6.1854-1867.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. White D. C., Tucker A. N., Sweeley C. C. Characterization of the iso-branched sphinganines from the ceramide phospholipids of Bacteroides melaninogenicus. Biochim Biophys Acta. 1969 Dec 17;187(4):527–532. doi: 10.1016/0005-2760(69)90050-2. [DOI] [PubMed] [Google Scholar]

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

RESOURCES