Monitoring of alkane-degrading bacteria in a sea-water microcosm during crude oil degradation by polymerase chain reaction based on alkane-catabolic genes

Summary Behaviour of microbial populations responsible for degrading n‐alkanes, a major component of crude oil, was monitored during crude oil degradation in a sea‐water microcosm by both traditional colony culturing and molecular techniques. A DNA extraction method applicable to crude oil‐amended s...

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Published in:Environmental microbiology Vol. 5; no. 6; pp. 517 - 522
Main Authors: Sei, Kazunari, Sugimoto, Yoshiro, Mori, Kazuhiro, Maki, Hideaki, Kohno, Tetsuro
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Science Ltd 01-06-2003
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Abstract Summary Behaviour of microbial populations responsible for degrading n‐alkanes, a major component of crude oil, was monitored during crude oil degradation in a sea‐water microcosm by both traditional colony culturing and molecular techniques. A DNA extraction method applicable to crude oil‐amended sea‐water samples was developed to obtain DNA applicable to most probable number (MPN) polymerase chain reaction (PCR). The population of alkane‐degrading bacteria responsible for degradation of n‐alkanes in a crude oil‐amended microcosm altered, so that shorter alkanes were degraded first by alkane‐degrading bacteria possessing alkane hydroxylase genes from group I (Kohno et al., 2002, Microb Environ 17: 114–121) and longer ones afterwards by those possessing alkane hydroxylase genes from group II. Thus, the degradation mechanism of the n‐alkanes can be clarified during crude oil degradation. Application of the method of detecting different types of alkane‐catabolic genes, as shown in the present study, enabled bacterial groups preferring alkanes of either shorter or longer chain lengths to be enumerated selectively.
AbstractList Summary Behaviour of microbial populations responsible for degrading n‐alkanes, a major component of crude oil, was monitored during crude oil degradation in a sea‐water microcosm by both traditional colony culturing and molecular techniques. A DNA extraction method applicable to crude oil‐amended sea‐water samples was developed to obtain DNA applicable to most probable number (MPN) polymerase chain reaction (PCR). The population of alkane‐degrading bacteria responsible for degradation of n‐alkanes in a crude oil‐amended microcosm altered, so that shorter alkanes were degraded first by alkane‐degrading bacteria possessing alkane hydroxylase genes from group I (Kohno et al., 2002, Microb Environ 17: 114–121) and longer ones afterwards by those possessing alkane hydroxylase genes from group II. Thus, the degradation mechanism of the n‐alkanes can be clarified during crude oil degradation. Application of the method of detecting different types of alkane‐catabolic genes, as shown in the present study, enabled bacterial groups preferring alkanes of either shorter or longer chain lengths to be enumerated selectively.
Behaviour of microbial populations responsible for degrading n-alkanes, a major component of crude oil, was monitored during crude oil degradation in a sea-water microcosm by both traditional colony culturing and molecular techniques. A DNA extraction method applicable to crude oil-amended sea-water samples was developed to obtain DNA applicable to most probable number (MPN) polymerase chain reaction (PCR). The population of alkane-degrading bacteria responsible for degradation of n-alkanes in a crude oil-amended microcosm altered, so that shorter alkanes were degraded first by alkane-degrading bacteria possessing alkane hydroxylase genes from group I (Kohno et al., 2002, Microb Environ 17: 114-121) and longer ones afterwards by those possessing alkane hydroxylase genes from group II. Thus, the degradation mechanism of the n-alkanes can be clarified during crude oil degradation. Application of the method of detecting different types of alkane-catabolic genes, as shown in the present study, enabled bacterial groups preferring alkanes of either shorter or longer chain lengths to be enumerated selectively.
Behaviour of microbial populations responsible for degrading n ‐alkanes, a major component of crude oil, was monitored during crude oil degradation in a sea‐water microcosm by both traditional colony culturing and molecular techniques. A DNA extraction method applicable to crude oil‐amended sea‐water samples was developed to obtain DNA applicable to most probable number (MPN) polymerase chain reaction (PCR). The population of alkane‐degrading bacteria responsible for degradation of n ‐alkanes in a crude oil‐amended microcosm altered, so that shorter alkanes were degraded first by alkane‐degrading bacteria possessing alkane hydroxylase genes from group I (Kohno et al ., 2002, Microb Environ 17: 114–121) and longer ones afterwards by those possessing alkane hydroxylase genes from group II. Thus, the degradation mechanism of the n ‐alkanes can be clarified during crude oil degradation. Application of the method of detecting different types of alkane‐catabolic genes, as shown in the present study, enabled bacterial groups preferring alkanes of either shorter or longer chain lengths to be enumerated selectively.
Author Kohno, Tetsuro
Sei, Kazunari
Maki, Hideaki
Mori, Kazuhiro
Sugimoto, Yoshiro
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  givenname: Yoshiro
  surname: Sugimoto
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  organization: Department of Civil and Environmental Engineering, Faculty of Engineering, University of Yamanashi, 4-3-11 Takeda, Kofu, Yamanashi 400-8511, Japan
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  givenname: Kazuhiro
  surname: Mori
  fullname: Mori, Kazuhiro
  organization: Department of Civil and Environmental Engineering, Faculty of Engineering, University of Yamanashi, 4-3-11 Takeda, Kofu, Yamanashi 400-8511, Japan
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  givenname: Hideaki
  surname: Maki
  fullname: Maki, Hideaki
  organization: National Institute for Environmental Studies, 16-2 Onogawa, Tsukuba, Ibaraki 305-8506, Japan
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  givenname: Tetsuro
  surname: Kohno
  fullname: Kohno, Tetsuro
  organization: Department of Civil and Environmental Engineering, Faculty of Engineering, University of Yamanashi, 4-3-11 Takeda, Kofu, Yamanashi 400-8511, Japan
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Snippet Summary Behaviour of microbial populations responsible for degrading n‐alkanes, a major component of crude oil, was monitored during crude oil degradation in a...
Behaviour of microbial populations responsible for degrading n-alkanes, a major component of crude oil, was monitored during crude oil degradation in a...
Behaviour of microbial populations responsible for degrading n ‐alkanes, a major component of crude oil, was monitored during crude oil degradation in a...
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SubjectTerms Alkanes - metabolism
Bacteria - genetics
Bacteria - metabolism
Biodegradation, Environmental
Cytochrome P-450 CYP4A - genetics
Cytochrome P-450 CYP4A - metabolism
DNA, Bacterial - analysis
DNA, Ribosomal - analysis
Petroleum - metabolism
Polymerase Chain Reaction
Seawater
Water Microbiology
Title Monitoring of alkane-degrading bacteria in a sea-water microcosm during crude oil degradation by polymerase chain reaction based on alkane-catabolic genes
URI https://api.istex.fr/ark:/67375/WNG-KG8KDD06-1/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1046%2Fj.1462-2920.2003.00447.x
https://www.ncbi.nlm.nih.gov/pubmed/12755719
https://search.proquest.com/docview/18882887
Volume 5
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