1997
DOI: 10.1007/s002489900047
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Hybridization Analysis of Microbial DNA from Fuel Oil–Contaminated and Noncontaminated Soil

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Cited by 55 publications
(49 citation statements)
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“…Enrichment of PAH-degraders is a common phenomenon during the course of PAH biodegradation (Guo et al, 1997;Piskonen et al, 2005). Therefore, in this study, the large enrichment of three TRFLP fragments might also be linked to the enrichment of some PAH-degraders.…”
Section: Discussionmentioning
confidence: 69%
“…Enrichment of PAH-degraders is a common phenomenon during the course of PAH biodegradation (Guo et al, 1997;Piskonen et al, 2005). Therefore, in this study, the large enrichment of three TRFLP fragments might also be linked to the enrichment of some PAH-degraders.…”
Section: Discussionmentioning
confidence: 69%
“…strain DNT; 3, P. putida F1; 4, P. putida HS1; 5, P. putida mt-2. (12,17). PCR with the RMO primers produced an amplicon of approximately 460 bp with P. mendocina KR1 despite two predicted mismatches with each primer.…”
Section: Resultsmentioning
confidence: 99%
“…While in some studies alkB homologs were detected in 10-40% of the bacterial population [97,101,102], other groups did not detect alkB homologs at all [99,100]. AlkB homologs that are closely related to the P. putida GPo1 enzyme appear to be common in gram-negative strains only (probably pseudomonads) [76].…”
Section: Environment/source Methods Conclusion For Alkb Homologs Refmentioning
confidence: 92%
“…Alaskan sediments Colony hybridization with alkB 39% of viable heterotrophs from uncontaminated soil contain alkB gene probe 67% of viable heterotrophs from contaminated soil contain alkB [97] Contaminated soil PCR followed by Southern blot Detection and quantification of alkB (and other genes) in soil: 1-10 with alkB gene probe gene copies per gram of soil can be detected [98 Variety of cold ecosystems PCR, and Southern blots None of the psychrophilic alkane degraders possess genes with alkB gene probe with high homology to P. putida alkB [99] Fuel oil-contaminated site Dot-blots DNA extracted from soil shows no significant hybridization with an alkB-gene probe [100] Shallow aquifer Southern blots 10-20% of the total bacterial community hybridizes with alkB gene probe with an alkB gene probe [101] Various sources PCR with highly degenerate Most alkane-degrading strains contain distantly related alkB homologs (54 bacterial strains) primers for alkB homologs (homology not sufficient for Southern or dot-blots) [50] Shallow aquifer Dot-blots with DNA extracted alkB genotypes start at 11% of total community, and peak at (natural attenuation site) from aquifer samples 52% after injection of synthetic jet fuel in the aquifer [102] Various sources Southern, colony and dot-blots, alkB genes (close homologs) are widespread only in short-chain n-alkane (54 bacterial strains) PCR followed by Southern degrading pseudomonads [76] Rhizosphere vs. bulk soil Multiplex PCR At a contaminated site alkB was 10 times more prevalent in the endophytic community compared to the bulk soil community [103] Propane and butaneDot-blots 8 of 15 strains (including pseudomonads and rhodococci) utilizing bacteria gave a strong signal, and 7 a weak signal with the IMT37 gene [37] Land treatment unit (LTU) PCR, terminal restriction alkB increased in abundance during the first 3 weeks of LTU operation, fragment length polymorphism and comprised > 80% of the total PCR products [104] Arctic and Antarctic soil PCR-hybridization Rhodococcal alkB genes occur in contaminated and pristine soils, and colony hybridization P. putida alkB occurs more frequently in contaminated soils [105] similar genes in other butane degraders (pseudomonads, rhodococci and unidentified bacteria). In a dot-blot experiment, 8 out of 15 propane or butane-degrading bacteria gave a strong signal with the gene-probe, while the remaining 7 gave a weak but detectable signal [37].…”
Section: Environment/source Methods Conclusion For Alkb Homologs Refmentioning
confidence: 99%