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이성국

Lee, Sung Kuk
Synthetic Biology & Metabolic Engineering Lab.
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Substrate utilization patterns during BTEX biodegradation by an o-xylene-degrading bacterium Ralstonia sp PHS1

Author(s)
Lee, Sung KukLee, SB
Issued Date
2002-12
URI
https://scholarworks.unist.ac.kr/handle/201301/6777
Fulltext
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0037003635
Citation
JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, v.12, no.6, pp.909 - 915
Abstract
The biodegradation of BTEX components (benzene, toluene, ethylbenzene, o-xylene, m-xylene, and p-xylene) individually and in mixtures was investigated using the o-xylene-degrading thermo-tolerant bacterium Ralstonia sp. strain PHS1, which utilizes benzene, toluene, ethylbenzene, or o-xylene as its sole carbon source. The results showed that as a single substrate for growth, benzene was superior to both toluene and ethylbenzene. While growth inhibition was severe at higher o-xylene concentrations, no inhibition was observed (up to 100 mg 1-1) with ethylbenzene. In mixtures of BTEX compounds, the PHS1 culture was shown to degrade all six BTEX components and the degradation rates were in the order of benzene, toluene, o-xylene, ethylbenzene, and m- and p-xylene. m-Xylene and p-xylene were found to be co-metabolized by this microorganism in the presence of the growth-supporting BTEX compounds. In binary mixtures containing the growth substrates (benzene, toluene, ethylbenzene, and o-xylene), PHS1 degraded each BTEX compound faster when it was alone than when it was a component of a BTEX mixture, although the degree of inhibition varied according to the substrates in the mixtures. p-Xylene was shown to be the most potent inhibitor of BTEX biodegradation in binary mixtures. On the other hand, the degradation rates of the non-growth substrates (m-xylene and p-xylene) were significantly enhanced by the addition of growth substrates. The substrate utilization patterns between PHS1 and other microorganisms were also examined.
Publisher
KOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY
ISSN
1017-7825

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