Evaluation of genetic diversity among Pseudomonas citronellolis strains isolated from oily sludge-contaminated sites.

Appl Environ Microbiol

Centre of Bioresources and Biotechnology, TERI School of Advanced Studies, Habitat Place, Lodhi Road, New Delhi 110003, India.

Published: March 2003

AI Article Synopsis

  • Researchers studied 150 bacterial strains capable of degrading total petroleum hydrocarbons (TPH) in soil contaminated with oily sludge from oil refineries, focusing on their diversity.
  • The predominant species found was Pseudomonas citronellolis, and 29 strains were selected for further analysis, revealing significant genetic diversity based on geoclimatic factors, sludge type, and contamination age.
  • Molecular typing techniques, including Rep-PCR and PCR-based ribotyping, successfully distinguished 12 genotypic groups and 7 genomic patterns among the P. citronellolis strains, demonstrating their potential for high-resolution genetic analysis.

Article Abstract

The diversity among a set of bacterial strains that have the capacity to degrade total petroleum hydrocarbons (TPH) in soil contaminated with oily sludge (hazardous hydrocarbon waste from oil refineries) was determined. TPH is composed of alkane, aromatics, nitrogen-, sulfur-, and oxygen-containing compound, and asphaltene fractions of crude oil. The 150 bacterial isolates which could degrade TPH were isolated from soil samples obtained from diverse geoclimatic regions of India. All the isolates were biochemically characterized and identified with a Biolog microbial identification system and by 16S rDNA sequencing. Pseudomonas citronellolis predominated among the 150 isolates obtained from six different geographically diverse samplings. Of the isolates, 29 strains of P. citronellolis were selected for evaluating their genetic diversity. This was performed by molecular typing with repetitive sequence (Rep)-based PCR with primer sets ERIC (enterobacterial repetitive intergenic consensus), REP (repetitive extragenic palindromes), and BOXAIR and PCR-based ribotyping. Strain-specific and unique genotypic fingerprints were distinguished by these molecular typing strategies. The 29 strains of P. citronellolis were separated into 12 distinguishable genotypic groups by Rep-PCR and into seven genomic patterns by PCR-based ribotyping. The genetic diversity of the strains was related to the different geoclimatic isolation sites, type of oily sludge, and age of contamination of the sites. These results indicate that a combination of Rep-PCR fingerprinting and PCR-based ribotyping can be used as a high-resolution genomic fingerprinting method for elucidating intraspecies diversity among strains of P. citronellolis.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC150093PMC
http://dx.doi.org/10.1128/AEM.69.3.1435-1441.2003DOI Listing

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