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    <subfield code="2">doi</subfield>
    <subfield code="a">10.1128/JB.00286-06</subfield>
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    <subfield code="2">sideral</subfield>
    <subfield code="a">90564</subfield>
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    <subfield code="a">ART-2006-90564</subfield>
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    <subfield code="a">eng</subfield>
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    <subfield code="a">Funhoff, E. G.</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">CYP153A6, a Soluble P450 Oxygenase Catalyzing Terminal-Alkane Hydroxylation</subfield>
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    <subfield code="c">2006</subfield>
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    <subfield code="a">The first and key step in alkane metabolism is the terminal hydroxylation of alkanes to 1-alkanols, a reaction catalyzed by a family of integral-membrane diiron enzymes related to Pseudomonas putida GPo1 AlkB, by a diverse group of methane, propane, and butane monooxygenases and by some membrane-bound cytochrome P450s. Recently, a family of cytoplasmic P450 enzymes was identified in prokaryotes that allow their host to grow on aliphatic alkanes. One member of this family, CYP153A6 from Mycobacterium sp. HXN-1500, hydroxylates medium-chain-length alkanes (C6 to C11) to 1-alkanols with a maximal turnover number of 70 min−1 and has a regiospecificity of ≥95% for the terminal carbon atom position. Spectroscopic binding studies showed that C6-to-C11 aliphatic alkanes bind in the active site with Kd values varying from ∼20 nM to 3.7 μM. Longer alkanes bind more strongly than shorter alkanes, while the introduction of sterically hindering groups reduces the affinity. This suggests that the substrate-binding pocket is shaped such that linear alkanes are preferred. Electron paramagnetic resonance spectroscopy in the presence of the substrate showed the formation of an enzyme-substrate complex, which confirmed the binding of substrates observed in optical titrations. To rationalize the experimental observations on a molecular scale, homology modeling of CYP153A6 and docking of substrates were used to provide the first insight into structural features required for terminal alkane hydroxylation.</subfield>
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    <subfield code="a">All rights reserved</subfield>
    <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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    <subfield code="a">3.993</subfield>
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    <subfield code="a">MICROBIOLOGY</subfield>
    <subfield code="b">16 / 88 = 0.182</subfield>
    <subfield code="c">2006</subfield>
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    <subfield code="a">Bauer, U.</subfield>
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    <subfield code="a">Garcia Rubio, Ines</subfield>
    <subfield code="0">(orcid)0000-0002-1827-1250</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Witholt, B.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">van Beilen, J. B.</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">188, 14 (2006), 5220-5227</subfield>
    <subfield code="p">J. bacteriol.</subfield>
    <subfield code="t">JOURNAL OF BACTERIOLOGY</subfield>
    <subfield code="x">0021-9193</subfield>
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