Hostname: page-component-8448b6f56d-jr42d Total loading time: 0 Render date: 2024-04-16T22:02:42.141Z Has data issue: false hasContentIssue false

Fatty Acid Composition of Lipids from Sulphuroxidizing and Methylotrophic Bacteria from Thyasirid and Lucinid Bivalves

Published online by Cambridge University Press:  11 May 2009

J. Gregor Fullarton
Affiliation:
NERC Unit of Aquatic Biochemistry, Department of Biological and Molecular Sciences, University of Stirling, Stirling, FK9 4LA
P. Wood
Affiliation:
Division of Life Sciences, King's College London, Campden Hill Road, London, W8 7AH
John R. Sargent
Affiliation:
NERC Unit of Aquatic Biochemistry, Department of Biological and Molecular Sciences, University of Stirling, Stirling, FK9 4LA

Extract

Lipids of sulphur-oxidizing bacteria isolated from Thyasim flexuosa had large amounts of 18:l(n-7) together with lesser amounts of both 16:l(n-7) and 16:0 as their major fatty acids. Smaller amounts of the cyclopropyl fatty acids, cyclic δ9,10 C16 and especially cyclic δll,12 C18 were also present. A similar pattern was found for methylotrophic bacteria isolated from Thyasira, Myrtea and Lucinoma, except that 16:l(n-7) and 16:0 were both present in larger amounts than 18:l(n-7) and small amounts of cyclic δ9,10 C16 and lesser amounts of cyclic All,12 C18 were present in all cases. The fatty acids 18:l(n-7), 16:l(n-7), 16:0, cyclic δ9,10 C16, and cyclic δll,12 C18 were all present in varying amounts in several free-living, non-marine, sulphur-oxidizing bacteria analysed, and in one bacterium both cyclic δ9,10 C18 and cyclic δll,12 C20 were abundant. Branched-chain fatty acids and polyunsaturated fatty acids were not detected in any of the sulphur-oxidizing or methylotrophic bacteria analysed. The lipids of the sulphur-oxidizing and methylotrophic bacteria consisted largely of phosphatidylethanolamine, phosphatidylglycerol and cardiolipin. The results are discussed in terms of fatty acids as indicators of nutritional relationships in bacterial-invertebrate symbioses.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 1995

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Ben-Mlih, F., Marty, J.-C. & Fiala-Médioni, A., 1992. Fatty acid composition in deep hydrothermal vent symbiotic bivalves. Journal of Lipid Research, 33, 17971806.Google Scholar
Cary, S.C., Fisher, C.R. & Felbeck, H., 1988. Mussel growth supported by methane as sole carbon and energy source. Science. New York, 240, 7880.Google Scholar
Cavanaugh, C.M., 1983. Symbiotic chemoautotrophic bacteria in marine invertebrates from sulphide-rich habitats. Nature, London, 302, 5861.CrossRefGoogle Scholar
Cavanaugh, C.M., Gardiner, S.L., Jones, M.L., Jannasch, H.W. & Waterbury, J.B., 1981. Prokaryotic cells in the hydrothermal vent tube worm Riftia pachyptila Jones: possible chemoautotrophic symbionts. Science, New York, 213, 340342.Google Scholar
Cavanaugh, C.M., Levering, P.R., Maki, J.S., Mitchell, R. & Lidstrom, M.E., 1987. Symbiosis of methylotrophic bacteria and deep-sea mussels. Nature, London, 325, 346348.Google Scholar
Childress, J.J., Fisher, C.R., Brooks, J.M., Kennicutt, M.C Ii, Bidigare, R. & Anderson, A.E., 1986. A methanotrophic marine molluscan (Bivalvia, Mytilidae) symbiosis: mussels fueled by gas. Science, New York, 233, 13061308.Google Scholar
Christie, W.W., Brechany, E.Y. & Stefanov, K., 1988. Silver ion high-performance chromatography and gas chromatography – mass spectroscopy in the analysis of complex fatty acid mixtures. Chemistry and Physics of Lipids, 46, 127135.Google Scholar
Conway, N. & Capuzzo, J.McD., 1990. The use of biochemical indicators in the study of trophic interactions in animal-bacterial symbioses:Solemya velum, a case study. In Trophic relationships in the marine environment. Proceedings of the 24th European Marine Biology Symposium (ed. M., Barnes and R.N., Gibson), pp. 553564. Aberdeen University Press.Google Scholar
Conway, N. & Capuzzo, J.McD., 1991. Incorporation and utilization of bacterial lipids in the Solemya velum symbiosis. Marine Biology, 108, 277291.Google Scholar
Dando, P.R., Southward, A.J., Southward, E.C., Terwilliger, N.B. & Terwilliger, R.C., 1985. Sulphur-oxidising bacteria and haemoglobin in gills of the bivalve mollusc Myrtea spinifera. Marine Ecology Progress Series, 23, 8598.Google Scholar
Distel, D.L. & Wood, A.P., 1992. Characterisation of the gill symbiont of Thyasira flexuosa (Thyasiridae: Bivalvia) by use of polymerase chain reaction and 16S rRNA sequence analysis. Journal of Bacteriology, 174, 63176320.Google Scholar
Eccleston, M. & Kelly, D.P., 1978. Oxidation kinetics and chemostat growth kinetics of Thiobacillus ferrooxidans on tetrathionate and thiosulphate. Journal of Bacteriology, 134, 718727.Google Scholar
Felbeck, H., 1983. Sulfide oxidation and carbon fixation by the gutless clam Solemya reidi: an animal-bacteria symbiosis. Journal of Comparative Physiology, 152, 311.CrossRefGoogle Scholar
Felbeck, H., Childress, J.J. & Somero, G.N., 1981. Calvin-Benson cycle and sulphide oxidation enzymes in animals from sulphide-rich habitats. Nature, London, 293, 291293.Google Scholar
Fisher, C.R. & Childress, J.J., 1984. Substrate oxidation by trophosome tissue from Riftia pachyptila Jones (phylum Pogonophora). Marine Biology Letters, 5, 171183.Google Scholar
Folch, J., Lees, M. & Sloane-Stanley, G.H., 1957. A simple method for the isolation and purification of total lipids from animal tissues. Journal of Biological Chemistry, 226, 497509.CrossRefGoogle ScholarPubMed
Fry, B., Gest, H. & Hayes, J.M., 1983. Sulphur isotopic compositions of deep-sea hydrothermal vent animals. Nature, London, 306, 5152.Google Scholar
Fullarton, J.G., Dando, P.R., Sargent, J.R., Southward, A.J. & Southward, E.C., 1995. Fatty acids of marine invertebrates containing symbiotic bacteria: hydrothermal vent Ridgeia piscesae and inshore bivalves. Journal of the Marine Biological Association of the United Kingdom, 75, 455468.Google Scholar
Harwood, J.L. & Russell, N.J., 1984. Lipids in plants and microbes. London: George Allen & Unwin.Google Scholar
Jannasch, H.W. & Mottl, M.J., 1985. Geomicrobiology of deep-sea hydrothermal vents. Science, New York, 229, 717725.Google Scholar
Jannasch, H.W. & Taylor, C.D., 1984. Deep-sea microbiology. Annual Review of Microbiology, 38, 487514.CrossRefGoogle ScholarPubMed
Karl, D.M., Wirsen, C.O. & Jannasch, H.W., 1980, Deep-sea primary production at the Galapagos hydrothermal vents. Science, New York, 207, 13451347.Google Scholar
Katayama-Fujimura, Y., Tsuzaki, N. & Kuraishi, H., 1982. Ubiquinone, fatty acid and DNA base composition determination as a guide to the taxonomy of the genus Thiobacillus. Journal of General Microbiology, 128, 15991611.Google Scholar
Mason, J., Kelly, D.P. & Wood, A.P., 1987. Chemolithotrophic and autotrophic growth of Thermothrix thiopara and some thiobacilli on thiosulphate and polythionites and a reassessment of the growth yields of Thx. thiopara in chemostat culture. Journal of General Microbiology, 133, 12491256.Google Scholar
Olsen, R.E. & Henderson, R.J., 1989. The rapid analysis of neutral and polar marine lipids using double-development HPTLC and scanning densitometry. Journal of Experimental Marine Biology and Ecology, 129, 189197.Google Scholar
Parkes, R.J., 1987. Analysis of microbial communities within sediments using biomarkers. In Ecology of microbial communities (ed. M., Fletcher et al.), pp. 147177. Cambridge University Press.Google Scholar
Powell, M.A. & Somero, G.N., 1986. Hydrogen sulfide oxidation is coupled to oxidative phosphorylation in mitochondria of Solemya reidi. Science, New York, 233, 563566.Google Scholar
Sargent, J.R., Bell, J.G., Bell, M.V., Henderson, R.J. & Tocher, D.R., 1993. The metabolism of phospholipids and polyunsaturated fatty acids in fish. In Aquaculture: fundamental and applied aspects (ed. B., Lahlou and P., Vitiello), pp. 103124. Washington, DC: American Geophysical Union. [Coastal and Estuarine Studies no. 43.]Google Scholar
Sargent, J.R., Henderson, R.J. & Tocher, D.R., 1989. The lipids. In Fish nutrition, 2nd ed. (ed. J.R., Halver), pp. 154219. Academic Press.Google Scholar
Sargent, J.R., Parkes, R.J., Mueller-Harvey, I. & Henderson, R.J., 1987. Lipid biomarkers in marine ecology. In Microbes in the sea (ed. M.A., Sleigh), pp. 119138. Chichester: Ellis Horwood.Google Scholar
Schmaljohann, R. & Flügel, H.J., 1987. Methane-oxidizing bacteria in Pogonophora. Sarsia, 72, 9199.Google Scholar
Southward, A.J., Southward, E.C., Dando, P.R., Barrett, R.L. & Ling, R., 1986. Chemoautotrophic function of bacterial symbionts in small Pogonophora. Journal of the Marine Biological Association of the United Kingdom, 66, 415437.Google Scholar
Southward, A.J., Southward, E.C., Dando, P.R., Rau, G.H., Felbeck, H. & Flügel, H., 1981. Bacterial symbionts and low13C/12C ratios in tissues of Pogonophora indicate unusual nutrition and metabolism. Nature, London, 293, 616620.Google Scholar
Southward, E.C., 1982. Bacterial symbionts in Pogonophora. Journal of the Marine Biological Association of the United Kingdom, 62, 889906.Google Scholar
Southward, E.C., 1987. Contribution of symbiotic chemoautotrophs to the nutrition of benthic invertebrates. In Microbes in the sea (ed. M.A., Sleigh), pp. 83118. Chichester: Ellis Horwood.Google Scholar
Spiro, B., Greenwood, P.B., Southward, A.J. & Dando, P.R., 1986. 13C/12C ratios in marine invertebrates from reducing sediments: confirmation of nutritional importance of chemoautotrophic endosymbiotic bacteria. Marine Ecology Progress Series, 28, 233240.CrossRefGoogle Scholar
Wood, A.P. & Kelly, D.P., 1988. Isolation and physiological characterisation of Thiobacillus aquaesulis sp. nov., a novel facultatively autotrophic moderate thermophile. Archives of Micro-biology, 149, 339343.Google Scholar
Wood, A.P. & Kelly, D.P., 1989a. Methylotrophic and autotrophic bacteria isolated from lucinid and thyasirid bivalves containing symbiotic bacteria in their gills. Journal of the Marine Biological Association of the United Kingdom, 69, 165179.Google Scholar
Wood, A.P. & Kelly, D.P., 1989b. Isolation and physiological characterisation of Thiobacillus thyasiris sp. nov., a novel marine facultative autotroph and the putative symbiont of Thyasira flexuosa. Archives of Microbiology, 152, 160166.Google Scholar
Wood, A.P. & Kelly, D.P., 1993. Reclassification of Thiobacillus thyasiris as Thiomicrospira thyasirae comb, nov., an organism exhibiting pleomorphism in response to environmental conditions. Archives of Microbiology, 159, 4547.Google Scholar
Zhukova, N.V., Kharlamenko, V.I., Svetashev, V.I. & Rodionov, I. A., 1992. Fatty acids as markers of bacterial symbionts of marine bivalve molluscs. Journal of Experimental Marine Biology and Ecology, 162, 253263.CrossRefGoogle Scholar