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Benzylic and Aryl Hydroxylations of m-Xylene by the o-Xylene Dioxygenase from Rhodococcus sp. Strain DK17

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Title
Benzylic and Aryl Hydroxylations of m-Xylene by the o-Xylene Dioxygenase from Rhodococcus sp. Strain DK17
Other Titles
Rhodococcus sp. strain DK17 유래 o-xylene dioxygenase 에 의해 촉매되는 m-xylene의 benzylic & aryl 산소화반응
Authors
Yoo, Miyoun
Kim, Eungbin
Zylstra, Gerben J.
Kang, Beom Sik
Kim, Dockyu
Keywords
Benzylic hydroxylation; Rhodococcus; meta Effect; o-Xylene dioxygenase
Issue Date
2009
Citation
Yoo, Miyoun, et al. 2009. Benzylic and Aryl Hydroxylations of m-Xylene by the o-Xylene Dioxygenase from Rhodococcus sp. Strain DK17. American Society for Microbiology. American Society for Microbiology. 2009.05.18~.
Abstract
The o-xylene dioxygenase (XDO) from Rhodococcus sp. strain DK17 possesses the ability to perform distinct regioselective hydroxylations with the size and position of the substituent group determining the number and position of the dihydroxylation on the aromatic ring. Escherichia coli cells harboring a recombinant plasmid with the DK17 XDO genes were cotransformed with the pKJE7 chaperon plasmid for higher expression and stable maintenance of XDO, and then used for bioconversion of m‑
xylene . Gas chromatography-mass spectrometry analysis of the oxidation products detected 3-methylbenzylalcohol and 2,4-dimethylphenol as a major and a minor metabolite in a ratio of 8:2, respectively. A molecular modeling study suggests that the DK17 XDO holds xylene isomers at a kink region between α6 and α7 helices of the active site in a position, so that one side of the aromatic ring is blocked by helix α6. Although the substrate-binding pocket of XDO is modeled to be spacious when a xylene isomer binds as a substrate, m-xylene is unlikely to locate at the active site with a methyl group facing the kink region because such a configuration would not fit within the substrate-binding pocket. m-Xylene molecule can flip horizontally to expose the meta-position methyl group to the catalytic motif. In this configuration, 3‑
methylbenzylalcohol could be formed as a product presumably due to the meta effect, which states that the meta methyl group of m-xylene would not allow binding and catalysis of aryl hydroxylation of XDO. Alternatively, m-xylene molecule can rotate counterclockwise from the previously mentioned position, which would allow the catalytic motif to hydroxylate at C-4 yielding 2,4-dimethylphenol as a product. To our best knowledge, 2,4-dimethylphenol have not been seen before in the oxidation of m-xylene. The present work demonstrates that the DK17 o-xylene dioxygenase has an ability to oxidize m-xylene through both benzylic and aryl hydrxylations although the
URI
http://repository.kopri.re.kr/handle/201206/7930
Conference Name
American Society for Microbiology
Conference Place
American Society for Microbiology
Conference Date
2009.05.18~
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