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Dioxygenation of the Biphenyl Dioxygenation Product

Dioxygenation of the Biphenyl Dioxygenation Product Dioxygenation of the Biphenyl Dioxygenation Product Heike Overwin a , Myriam González b , Valentina Méndez b , Michael Seeger b , Victor Wray c and Bernd Hofer a a Department of Chemical Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany b Laboratorio de Microbiología Molecular y Biotecnología Ambiental, Departamento de Química, Universidad Técnica Federico Santa María, Valparaíso, Chile c Department of Molecular Structural Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany ABSTRACT Two biphenyl dioxygenases (BphAs) were shown to catalyze dioxygenation of biphenyldienediol in the nonoxidized ring to form the respective symmetrical biphenyl-bis-dienediol. This novel metabolite served as a growth substrate for both BphA source strains. Its catabolism through the upper bph pathway of Burkholderia xenovorans LB400 was analyzed. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Applied and Environmental Microbiology American Society For Microbiology

Dioxygenation of the Biphenyl Dioxygenation Product

Applied and Environmental Microbiology , Volume 78 (12): 4529 – Jun 15, 2012

Abstract

Dioxygenation of the Biphenyl Dioxygenation Product Heike Overwin a , Myriam González b , Valentina Méndez b , Michael Seeger b , Victor Wray c and Bernd Hofer a a Department of Chemical Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany b Laboratorio de Microbiología Molecular y Biotecnología Ambiental, Departamento de Química, Universidad Técnica Federico Santa María, Valparaíso, Chile c Department of Molecular Structural Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany ABSTRACT Two biphenyl dioxygenases (BphAs) were shown to catalyze dioxygenation of biphenyldienediol in the nonoxidized ring to form the respective symmetrical biphenyl-bis-dienediol. This novel metabolite served as a growth substrate for both BphA source strains. Its catabolism through the upper bph pathway of Burkholderia xenovorans LB400 was analyzed.

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References (19)

Publisher
American Society For Microbiology
Copyright
Copyright © 2012 by the American society for Microbiology.
ISSN
0099-2240
eISSN
1098-5336
DOI
10.1128/AEM.00492-12
pmid
22504819
Publisher site
See Article on Publisher Site

Abstract

Dioxygenation of the Biphenyl Dioxygenation Product Heike Overwin a , Myriam González b , Valentina Méndez b , Michael Seeger b , Victor Wray c and Bernd Hofer a a Department of Chemical Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany b Laboratorio de Microbiología Molecular y Biotecnología Ambiental, Departamento de Química, Universidad Técnica Federico Santa María, Valparaíso, Chile c Department of Molecular Structural Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany ABSTRACT Two biphenyl dioxygenases (BphAs) were shown to catalyze dioxygenation of biphenyldienediol in the nonoxidized ring to form the respective symmetrical biphenyl-bis-dienediol. This novel metabolite served as a growth substrate for both BphA source strains. Its catabolism through the upper bph pathway of Burkholderia xenovorans LB400 was analyzed.

Journal

Applied and Environmental MicrobiologyAmerican Society For Microbiology

Published: Jun 15, 2012

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