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 |
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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. |
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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 |
Author_xml | – sequence: 1 givenname: Kazunari surname: Sei fullname: Sei, Kazunari email: sei@mail.yamanashi.ac.jp organization: Department of Civil and Environmental Engineering, Faculty of Engineering, University of Yamanashi, 4-3-11 Takeda, Kofu, Yamanashi 400-8511, Japan – sequence: 2 givenname: Yoshiro surname: Sugimoto fullname: Sugimoto, Yoshiro organization: Department of Civil and Environmental Engineering, Faculty of Engineering, University of Yamanashi, 4-3-11 Takeda, Kofu, Yamanashi 400-8511, Japan – sequence: 3 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 – sequence: 4 givenname: Hideaki surname: Maki fullname: Maki, Hideaki organization: National Institute for Environmental Studies, 16-2 Onogawa, Tsukuba, Ibaraki 305-8506, Japan – sequence: 5 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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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 |
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