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Development of Improved Anaerobic Growth of 'Bacillus Mojavensis' Strain JF-2 for the purpose of Improved Anaerobic Biosurfactant Production for Enhanced Oil Recovery. Topical Report, June 1, 2002-May 31, 2004.


DE2004834171

Publication Date 2004
Personal Author McInerney, M. J.; Folmsbee, M.
Page Count 60
Abstract Our work focuses on the use of microorganisms to recover petroleum hydrocarbons that remain entrapped after current recovery technologies reach their economic limit. Capillary forces between the hydrocarbon and aqueous phases are largely responsible for trapping the hydrocarbons in the pores of the rock and large reductions in the interfacial tension between the hydrocarbon and aqueous phases are needed for hydrocarbon mobilization (1-3, 10, 11). Microorganisms produce a variety of biosurfactants (4), several of which generate the ultra low interfacial tensions needed for hydrocarbon mobilization (4, 5, 8). In particular, the lipopeptide biosurfactant produced by Bacillus mojavensis strain JF-2 reduces the interfacial tension between hydrocarbon and aqueous phases to very low levels (<0.016 mN/m) (8) (9). B. mojavensis JF-2 grows under the environmental conditions found in many oil reservoirs, i. e., anaerobic, NaCl concentrations up to 80 g l(sup -1), and temperatures up to 45 C (6, 7), making it ideally suited for in situ applications. However, anaerobic growth of B. mojavensis JF-2 was inconsistent and difficult to replicate, which limited its use for in situ applications. Our initial studies revealed that enzymatic digests, such as Proteose Peptone, were required for anaerobic growth of Bacillus mojavensis JF-2. Subsequent purification of the growth-enhancing factor in Proteose Peptone resulted in the identification of the growth-enhancing factor as DNA or deoxyribonucleosides. The addition of salmon sperm DNA, herring sperm DNA, E. coli DNA or synthetic DNA (single or double stranded) to Medium E all supported anaerobic growth of JF-2. Further, we found that JF-2 required all four deoxyribonucleosides (deoxyadeonosine, deoxyguanosine, deoxycytidine and thymidine) for growth under strict anaerobic conditions. The requirement for the deoxyribonucleosides did not occur under aerobic growth conditions. DNA was not used as a sole energy source; sucrose was required for anaerobic growth and biosurfactant production in DNA-supplemented Medium E. In addition to DNA or deoxyribonucleosides, nitrate, amino acids and vitamins were all required for anaerobic growth of JF-2. Bacillus mojavensisT (ABO21191).
Keywords
  • Enhanced recovery
  • Microorganisms
  • Petroleum
  • Anaerobic conditions
  • DNA
  • Amino acids
  • Hydrocarbons
  • Peptone
  • Bacillus
  • Saccharose
  • Spermatozoa
  • Strains
  • Thymidine
Source Agency
  • Technical Information Center Oak Ridge Tennessee
Corporate Authors Oklahoma Univ., Norman. Dept. of Botany and Microbiology.; Department of Energy, Washington, DC.
Supplemental Notes Sponsored by Department of Energy, Washington, DC.
Document Type Technical Report
NTIS Issue Number 200516
Development of Improved Anaerobic Growth of 'Bacillus Mojavensis' Strain JF-2 for the purpose of Improved Anaerobic Biosurfactant Production for Enhanced Oil Recovery. Topical Report, June 1, 2002-May 31, 2004.
Development of Improved Anaerobic Growth of 'Bacillus Mojavensis' Strain JF-2 for the purpose of Improved Anaerobic Biosurfactant Production for Enhanced Oil Recovery. Topical Report, June 1, 2002-May 31, 2004.
DE2004834171

  • Enhanced recovery
  • Microorganisms
  • Petroleum
  • Anaerobic conditions
  • DNA
  • Amino acids
  • Hydrocarbons
  • Peptone
  • Bacillus
  • Saccharose
  • Spermatozoa
  • Strains
  • Thymidine
  • Technical Information Center Oak Ridge Tennessee
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