Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1979 Oct;38(4):742–746. doi: 10.1128/aem.38.4.742-746.1979

Microbial growth on hydrocarbons: terminal branching inhibits biodegradation.

T L Schaeffer, S G Cantwell, J L Brown, D S Watt, R R Fall
PMCID: PMC243570  PMID: 539824

Abstract

A variety of octane-utilizing bacteria and fungi were screened for growth on some terminally branched dimethyloctane derivatives to explore the effects of iso- and anteiso-termini on the biodegradability of such hydrocarbons. Of 27 microbial strains tested, only 9 were found to use any of the branched hydrocarbons tested as a sole carbon source, and then only those hydrocarbons containing at least one iso-terminus were susceptible to degradation. Anteiso-or isopropenyl termini prevented biodegradation. None of the hydrocarbonoclastic yeasts tested was able to utilize branched-hydrocarbon growth sustrates. In the case of pseudomonads containing the OCT plasmid, whole-cell oxidation of n-octane was poorly induced by terminally branched dimethyloctanes. In the presence of a gratuitous inducer of the octane-oxidizing enzymes, the iso-branched 2,7-dimethyloctane was slowly oxidized by whole cells, whereas the anteiso-branched 3,6-dimethyloctane was not oxidized at all. This microbial sampling dramatically illustrated the deleterious effect of alkyl branching, especially anteiso-terminal branching, on the biodegradation of hydrocarbons.

Full text

PDF
742

Selected References

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

  1. Bartha R. The microbiology of aquatic oil spills. Adv Appl Microbiol. 1977;22:225–266. doi: 10.1016/s0065-2164(08)70164-3. [DOI] [PubMed] [Google Scholar]
  2. Benson S., Fennewald M., Shapiro J., Huettner C. Fractionation of inducible alkane hydroxylase activity in Pseudomonas putida and characterization of hydroxylase-negative plasmid mutations. J Bacteriol. 1977 Nov;132(2):614–621. doi: 10.1128/jb.132.2.614-621.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Benson S., Shapiro J. Induction of alkane hydroxylase proteins by unoxidized alkane in Pseudomonas putida. J Bacteriol. 1975 Aug;123(2):759–760. doi: 10.1128/jb.123.2.759-760.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Benson S., Shapiro J. Plasmid-determined alcohol dehydrogenase activity in alkane-utilizing strains of Pseudomonas putida. J Bacteriol. 1976 May;126(2):794–798. doi: 10.1128/jb.126.2.794-798.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Billiar R. B., Knappenberger M., Little B. Xanthine oxidase for calibration of the oxygen electrode apparatus. Anal Biochem. 1970 Jul;36(1):101–104. doi: 10.1016/0003-2697(70)90336-2. [DOI] [PubMed] [Google Scholar]
  6. Cantwell S. G., Lau E. P., Watt D. S., Fall R. R. Biodegradation of acyclic isoprenoids by Pseudomonas species. J Bacteriol. 1978 Aug;135(2):324–333. doi: 10.1128/jb.135.2.324-333.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Chakrabarty A. M. Plasmids in Pseudomonas. Annu Rev Genet. 1976;10:7–30. doi: 10.1146/annurev.ge.10.120176.000255. [DOI] [PubMed] [Google Scholar]
  8. Cofone L., Jr, Walker J. D., Cooney J. J. Utilization of hydrocarbons by Cladosporium resinae. J Gen Microbiol. 1973 May;76(1):243–246. doi: 10.1099/00221287-76-1-243. [DOI] [PubMed] [Google Scholar]
  9. Davey J. F., Gibson D. T. Bacterial metabolism of para- and meta-xylene: oxidation of a methyl substituent. J Bacteriol. 1974 Sep;119(3):923–929. doi: 10.1128/jb.119.3.923-929.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Fall R. R., Brown J. L., Schaeffer T. L. Enzyme recruitment allows the biodegradation of recalcitrant branched hydrocarbons by Pseudomonas citronellolis. Appl Environ Microbiol. 1979 Oct;38(4):715–722. doi: 10.1128/aem.38.4.715-722.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Grund A., Shapiro J., Fennewald M., Bacha P., Leahy J., Markbreiter K., Nieder M., Toepfer M. Regulation of alkane oxidation in Pseudomonas putida. J Bacteriol. 1975 Aug;123(2):546–556. doi: 10.1128/jb.123.2.546-556.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Klug M. J., Markovetz A. J. Utilization of aliphatic hydrocarbons by micro-organisms. Adv Microb Physiol. 1971;5:1–43. doi: 10.1016/s0065-2911(08)60404-x. [DOI] [PubMed] [Google Scholar]
  13. Lough A. K. The chemistry and biochemistry of phytanic, pristanic and related acids. Prog Chem Fats Other Lipids. 1973;14(1):1–48. doi: 10.1016/0079-6832(75)90001-4. [DOI] [PubMed] [Google Scholar]
  14. Markovetz A. J., Jr, Cazin J., Allen J. E. Assimilation of alkanes and alkenes by fungi. Appl Microbiol. 1968 Mar;16(3):487–489. doi: 10.1128/am.16.3.487-489.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. McKenna E. J., Coon M. J. Enzymatic omega-oxidation. IV. Purification and properties of the omega-hydroxylase of Pseudomonas oleovorans. J Biol Chem. 1970 Aug 10;245(15):3882–3889. [PubMed] [Google Scholar]
  16. McKenna E. J., Kallio R. E. The biology of hydrocarbons. Annu Rev Microbiol. 1965;19:183–208. doi: 10.1146/annurev.mi.19.100165.001151. [DOI] [PubMed] [Google Scholar]
  17. Meyer S. A., Anderson K., Brown R. E., Smith M. T., Yarrow D., Mitchell G., Ahearn D. G. Physiological and DNA characterization of Candida maltosa, a hydrocarbon-utilizing yeast. Arch Microbiol. 1975 Aug 28;104(3):225–231. doi: 10.1007/BF00447328. [DOI] [PubMed] [Google Scholar]
  18. Nieder M., Shapiro J. Physiological function of the Pseudomonas putida PpG6 (Pseudomonas oleovorans) alkane hydroxylase: monoterminal oxidation of alkanes and fatty acids. J Bacteriol. 1975 Apr;122(1):93–98. doi: 10.1128/jb.122.1.93-98.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Palleroni N. J., Doudoroff M., Stanier R. Y., Solánes R. E., Mandel M. Taxonomy of the aerobic pseudomonads: the properties of the Pseudomonas stutzeri group. J Gen Microbiol. 1970 Feb;60(2):215–231. doi: 10.1099/00221287-60-2-215. [DOI] [PubMed] [Google Scholar]
  20. Pirnik M. P., Atlas R. M., Bartha R. Hydrocarbon metabolism by Brevibacterium erythrogenes: normal and branched alkanes. J Bacteriol. 1974 Sep;119(3):868–878. doi: 10.1128/jb.119.3.868-878.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Pirnik M. P. Microbial oxidation of methyl branched alkanes. CRC Crit Rev Microbiol. 1977 Sep;5(4):413–422. doi: 10.3109/10408417709102812. [DOI] [PubMed] [Google Scholar]
  22. Scott C. C., Makula S. R., Finnerty W. R. Isolation and characterization of membranes from a hydrocarbon-oxidizing Acinetobacter sp. J Bacteriol. 1976 Jul;127(1):469–480. doi: 10.1128/jb.127.1.469-480.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. van Eyk J., Bartels T. J. Paraffin oxidation in Pseudomonas aeruginosa. I. Induction of paraffin oxidation. J Bacteriol. 1968 Sep;96(3):706–712. doi: 10.1128/jb.96.3.706-712.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. van der Linden A. C., Thijsse G. J. The mechanisms of microbial oxidations of petroleum hydrocarbons. Adv Enzymol Relat Areas Mol Biol. 1965;27:469–546. doi: 10.1002/9780470122723.ch10. [DOI] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES