4.3 Article

Isolation and characterization of a novel sphingomonad capable of growth with chrysene as sole carbon and energy source

期刊

FEMS MICROBIOLOGY LETTERS
卷 241, 期 2, 页码 143-150

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ELSEVIER SCIENCE BV
DOI: 10.1016/j.femsle.2004.10.012

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polycyclic aromatic hydrocarbons; chrysene; sphingomonas; biofilm; biphasic culture medium; non-aqueous-phase liquid; [C-14]chrysene mineralization

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A bacterial strain able to grow in pure culture with chrysene as sole added carbon and energy source was isolated from PAH-contaminated soil after successive enrichment cultures in a biphasic growth medium. Initially, growth occurred in the form of a biofilm at the interface between the aqueous and non-aqueous liquid phases. However, after a certain time, a transition occurred in the enrichment cultures, with growth occurring in suspension and a concomitant increase in the rate of chrysene degradation. The strain responsible for chrysene degradation in these cultures, named Sphingomonas sp. CHY-1, was identified by 16S rDNA sequencing as a novel sphingomonad, the closest relative in the databases being Sphingomonas xenophaga BN6(T) (96% sequence identity). Both these strains clustered with members of the genera Sphingobium and Rhizomonas, but could not be categorically assigned to either genus. Sphingomonas sp. CHY-1 was characterized in terms of its growth on chrysene and other PAH, and the kinetics of chrysene degradation and C-14-chrysene mineralization were measured. At an initial chrysene concentration of 0.5 g1(-1) silicone oil, and an organic/aqueous phase ratio of 1:4, chrysene was 50% degraded after 5 days incubation and 97.5% degraded after 35 days. The protein content of cultures reached a maximum value of 11.5 mugml(-1) aqueous phase, corresponding to 92 mgg(-1) chrysene. C-14-labelled chrysene was 50% mineralized after 6-8 weeks incubation, 10.7% of the radioactivity was incorporated into cell biomass and 8.4% was found in the aqueous culture supernatant. Sphingomonas sp. CHY-1 also grew on naphthalene, phenanthrene and anthracene, and naphthalene was the preferred substrate, with a doubling time of 6.9 h. (C) 2004 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.

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