TY - JOUR
T1 - Characterization of kinetics and products of the Baeyer-Villiger oxygenase MtmOIV, the key enzyme of the biosynthetic pathway toward the natural product anticancer drug mithramycin from Streptomyces argillaceus
AU - Gibson, Miranda
AU - Nur-E-Alam, Mohammad
AU - Lipata, Fredilyn
AU - Oliveira, Marcos A.
AU - Rohr, Jürgen
PY - 2005/12/21
Y1 - 2005/12/21
N2 - MtmOIV, the key oxygenase of the mithramycin biosynthetic pathway in Streptomyces argillaceus, was proven to act initially as Baeyer-Villiger monooxygenase, but may also catalyze various follow-up reaction steps. The reaction of the overexpressed pure His6-tagged enzyme with its substrate premithramycin B was studied. Various intermediates and products were isolated and physicochemically characterized, several of them being previously unknown compounds. This is the first example in which a bacterial enzyme was unequivocally proven to act as Baeyer-Villigerase with its natural substrate, that is, in its natural context.
AB - MtmOIV, the key oxygenase of the mithramycin biosynthetic pathway in Streptomyces argillaceus, was proven to act initially as Baeyer-Villiger monooxygenase, but may also catalyze various follow-up reaction steps. The reaction of the overexpressed pure His6-tagged enzyme with its substrate premithramycin B was studied. Various intermediates and products were isolated and physicochemically characterized, several of them being previously unknown compounds. This is the first example in which a bacterial enzyme was unequivocally proven to act as Baeyer-Villigerase with its natural substrate, that is, in its natural context.
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U2 - 10.1021/ja055750t
DO - 10.1021/ja055750t
M3 - Article
C2 - 16351075
AN - SCOPUS:29344449110
SN - 0002-7863
VL - 127
SP - 17594
EP - 17595
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 50
ER -