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1.
Biodegradation ; 23(1): 15-24, 2012 Feb.
Article in English | MEDLINE | ID: mdl-21611744

ABSTRACT

Petroleum hydrocarbon is an important energy resource, but it is difficult to exploit due to the presence of dominated heavy constituents such as asphaltenes. In this study, viscosity reduction of Jodhpur heavy oil (2,637 cP at 50°C) has been carried out by the biodegradation of asphalt using a bacterial strain TERIG02. TERIG02 was isolated from sea buried oil pipeline known as Mumbai Uran trunk line (MUT) located on western coast of India and identified as Garciaella petrolearia by 16S rRNA full gene sequencing. TERIG02 showed 42% viscosity reduction when asphalt along with molasses was used as a sole carbon source compared to only asphalt (37%). The viscosity reduction by asphaltene degradation has been structurally characterized by Fourier transform infrared spectroscopy (FTIR). This strain also shows an additional preference to degrade toxic asphalt and aromatics compounds first unlike the other known strains. All these characteristics makes TERIG02 a potential candidate for enhanced oil recovery and a solution to degrading toxic aromatic compounds.


Subject(s)
Eubacterium/metabolism , Hydrocarbons/metabolism , Petroleum , Water Microbiology , Water Pollutants, Chemical/metabolism , Biodegradation, Environmental , Eubacterium/genetics , Phylogeny , RNA, Bacterial/genetics , RNA, Ribosomal, 16S/genetics , Seawater/microbiology , Spectroscopy, Fourier Transform Infrared , Viscosity
2.
Biodegradation ; 21(1): 59-69, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19590967

ABSTRACT

A newly discovered enteric bacterium Leclercia adecarboxylata PS4040, isolated from oily sludge contaminated soil sample was reported for degradation of polycyclic aromatic hydrocarbons (Appl Environ Microbiol 70:3163-3166, 2004a). This strain could degrade 61.5% of pyrene within 20 days when used as sole source of carbon and energy. The time course degradation experiment detected several intermediate products and the metabolites were identified by gas chromatography mass spectrometry analysis. Metabolite I was the detected on the 5th day and was identified as 1-hydroxypyrene and was detected till 10th day. Metabolite II which was detected on 10th day was identified as 1,2-phenanthrenedicarboxylic acid. Metabolite III and Metabolite IV were identified as 2-carboxy benzaldehyde and ortho-phthalic acid, respectively and were detected in the culture broth on 10th and 15th day. 1,2-benzene diol (catechol) was the fifth metabolite detected in the culture extracts on the 15th day and was subsequently reduced on day 20. Identification of Metabolite I as 1-hydroxypyrene was further investigated as this intermediate was not previously reported as a ring oxidation product for degradation of pyrene by bacterial strains. Purification by preparative high performance liquid chromatography and nuclear magnetic resonance spectroscopy, confirmed the identification of Metabolite I as 1-hydroxypyrene. L. adecarboxylata PS4040 could also use 1-hydroxypyrene as a sole source of carbon and energy. Thus a probable pathway for degradation of pyrene by enteric bacterium is proposed in this study, with 1-hydroxypyrene as initial ring oxidation product.


Subject(s)
Enterobacteriaceae/metabolism , Pyrenes/metabolism , Biodegradation, Environmental , Enterobacteriaceae/chemistry , Enterobacteriaceae/isolation & purification , Pyrenes/chemistry , Sewage/microbiology
3.
Can J Microbiol ; 50(6): 405-14, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15284886

ABSTRACT

A total of 96 crude oil-degrading bacterial strains were isolated from 5 geographically diverse sites in India that were contaminated with different types of petroleum hydrocarbons. The strains were identified by sequencing the genes that encode for 16S rRNA. Out of the 96 isolates, 25 strains were identified as Acinetobacter baumannii and selected for the study. All of the selected strains could degrade the total petroleum hydrocarbon fractions of crude oil. These 25 strains were biochemically profiled and grouped into 8 phenovars on the basis of multivariate analysis of their substrate utilization profiles. PCR-based DNA fingerprinting was performed using intergenic repetitive DNA sequences, which divided the selected 25 strains into 7 specific genomic clusters. tRNA intergenic spacer length polymorphism was performed to determine the intra-species relatedness among these 25 strains. It delineated the strains into 8 genomic groups. The present study detected specific variants among the A. baumannii strains with differential degradation capacities for different fractions of crude oil. This could play a significant role in in situ bioremediation. The study also revealed the impact of environmental factors that cause intra-species diversity within the selected strains of A. baumannii.


Subject(s)
Acinetobacter baumannii , Genetic Variation , Petroleum/metabolism , RNA, Transfer/analysis , Soil Pollutants/metabolism , Acinetobacter baumannii/classification , Acinetobacter baumannii/genetics , Acinetobacter baumannii/isolation & purification , Acinetobacter baumannii/metabolism , Biodegradation, Environmental , DNA, Intergenic/analysis , Phylogeny , RNA, Transfer/genetics
4.
Appl Environ Microbiol ; 70(5): 3163-6, 2004 May.
Article in English | MEDLINE | ID: mdl-15128584

ABSTRACT

A bacterial strain, PS4040, capable of degrading polycyclic aromatic hydrocarbons for use as the sole carbon source was isolated from oily-sludge-contaminated soil. The 16S rRNA gene showed 98.8% homology to that of Leclercia adecarboxylata. Comparative molecular typing with the clinical strain of L. adecarboxylata revealed that there were few comigrating and few distinct amplimers among them.


Subject(s)
Enterobacteriaceae/classification , Enterobacteriaceae/isolation & purification , Polycyclic Aromatic Hydrocarbons/metabolism , Pyrenes/metabolism , Soil Microbiology , Bacterial Typing Techniques , Biodegradation, Environmental , DNA, Ribosomal/analysis , Enterobacteriaceae/genetics , Enterobacteriaceae/growth & development , Humans , Molecular Sequence Data , Petroleum , Phenotype , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Soil Pollutants
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