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Biodegradation and transformation of 44- and 24-dihalodiphenyl ethers by Sphingomonas sp. strain SS33.

机译:鞘氨醇单胞菌(Sphingomonas sp。)对44-和24-二卤代二苯基醚的生物降解和转化。菌株SS33。

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摘要

The bacterium Sphingomonas sp. strain SS33, obtained from parent diphenyl ether-mineralizing strain SS3 (S. Schmidt, R.-M. Wittich, D. Erdmann, H. Wilkes, W. Francke, and P. Fortnagel, Appl. Environ. Microbiol. 58:2744-2750, 1992) after several weeks of adaptation on 4,4'-difluorodiphenyl ether as the new target compound, also utilized 4,4'-dichlorodiphenyl ether for growth. Intermediary halocatechols were also mineralized via the ortho pathway by type I enzymes. 4,4'-Dibromodiphenyl ether was not used as a carbon source although transformation by resting cells yielded mononuclear haloaromatic compounds, such as 4-bromophenol and 4-bromocatechol. The same was true for the conversion of 2,4-dichlorodiphenyl ether, which yielded the respective (halo-) phenols and (halo-) catechols.
机译:细菌鞘氨醇单胞菌菌株SS33,得自母体二苯醚矿化菌株SS3(S.Schmidt,R.-M.Wittich,D.Erdmann,H.Wilkes,W.Franke和P.Fortnagel,Appl.Environ.Microbiol.58:2744 -2750,1992)在适应了4,4'-二氟二苯醚作为新的目标化合物几周后,也利用4,4'-二氯二苯醚进行生长。中间卤代邻苯二酚也通过I型酶通过邻位途径矿化。尽管通过静息细胞的转化产生了单核卤代芳族化合物,例如4-溴苯酚和4-溴邻苯二酚,但没有将4,4'-二溴二苯醚用作碳源。 2,4-二氯二苯醚的转化也是如此,这产生了各自的(卤代)酚和(卤代)儿茶酚。

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