Growth, natural relationships, cellular fatty acids and metabolic adaptation of sulfate-reducing bacteria that utilize long-chain alkanes under anoxic conditions

Arch Microbiol. 1998 Oct;170(5):361-9. doi: 10.1007/s002030050654.

Abstract

Natural relationships, improvement of anaerobic growth on hydrocarbons, and properties that may provide clues to an understanding of oxygen-independent alkane metabolism were studied with two mesophilic sulfate-reducing bacteria, strains Hxd3 and Pnd3. Strain Hxd3 had been formerly isolated from an oil tank; strain Pnd3 was isolated from marine sediment. Strains Hxd3 and Pnd3 grew under strictly anoxic conditions on n-alkanes in the range of C12-C20 and C14-C17, respectively, reducing sulfate to sulfide. Both strains shared 90% 16 S rRNA sequence similarity and clustered with classified species of completely oxidizing, sulfate-reducing bacteria within the delta-subclass of Proteobacteria. Anaerobic growth on alkanes was stimulated by alpha-cyclodextrin, which served as a non-degradable carrier for the hydrophobic substrate. Cells of strain Hxd3 grown on hydrocarbons and alpha-cyclodextrin were used to study the composition of cellular fatty acids and in vivo activities. When strain Hxd3 was grown on hexadecane (C16H34), cellular fatty acids with C-odd chains were dominant. Vice versa, cultures grown on heptadecane (C17H36) contained mainly fatty acids with C-even chains. In contrast, during growth on 1-alkenes or fatty acids, a C-even substrate yielded C-even fatty acids, and a C-odd substrate yielded C-odd fatty acids. These results suggest that anaerobic degradation of alkanes by strain Hxd3 does not occur via a desaturation to the corresponding 1-alkenes, a hypothetical reaction formerly discussed in the literature. Rather an alteration of the carbon chain by a C-odd carbon unit is likely to occur during activation; one hypothetical reaction is a terminal addition of a C1 unit. In contrast, fatty acid analyses of strain Pnd3 after growth on alkanes did not indicate an alteration of the carbon chain by a C-odd carbon unit, suggesting that the initial reaction differed from that in strain Hxd3. When hexadecane-grown cells of strain Hxd3 were resuspended in medium with 1-hexadecene, an adaptation period of 2 days was observed. Also this result is not in favor of an anaerobic alkane degradation via the corresponding 1-alkene.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological
  • Alkanes / metabolism
  • Alkenes / metabolism
  • Bacteria, Anaerobic / chemistry
  • Bacteria, Anaerobic / classification
  • Bacteria, Anaerobic / isolation & purification
  • Bacteria, Anaerobic / physiology*
  • Base Sequence
  • Chromatography, Gas
  • Cyclodextrins / metabolism
  • Fatty Acids / analysis
  • Geologic Sediments / microbiology
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • Sulfates / metabolism
  • Sulfides / analysis
  • Sulfur-Reducing Bacteria / chemistry
  • Sulfur-Reducing Bacteria / classification
  • Sulfur-Reducing Bacteria / isolation & purification
  • Sulfur-Reducing Bacteria / physiology*
  • Time Factors
  • Water Microbiology

Substances

  • Alkanes
  • Alkenes
  • Cyclodextrins
  • Fatty Acids
  • Sulfates
  • Sulfides
  • n-hexadecane
  • heptadecane

Associated data

  • GENBANK/Y17501
  • GENBANK/Y17698