A Novel Heme-Thiolate Peroxygenase AaeAPO and Its Implications for C-H Activation Chemistry: Springer Theses
Autor Xiaoshi Wangen Limba Engleză Hardback – 26 oct 2015
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Specificații
ISBN-13: 9783319032351
ISBN-10: 3319032356
Pagini: 171
Ilustrații: XXXII, 130 p.
Dimensiuni: 155 x 235 x 17 mm
Greutate: 0.41 kg
Ediția:1st ed. 2016
Editura: Springer International Publishing
Colecția Springer
Seria Springer Theses
Locul publicării:Cham, Switzerland
ISBN-10: 3319032356
Pagini: 171
Ilustrații: XXXII, 130 p.
Dimensiuni: 155 x 235 x 17 mm
Greutate: 0.41 kg
Ediția:1st ed. 2016
Editura: Springer International Publishing
Colecția Springer
Seria Springer Theses
Locul publicării:Cham, Switzerland
Public țintă
ResearchCuprins
From the Contents: Hydrocarbon Oxygenation by Heme-Thiolate Enzymes.- Efficient and Selective Alkane Hydroxylation Reactions Catalyzed by the Fungal Peroxygenase AaeAPO.- Hydrocarbon Hydroxylations Catalyzed by AaeAPO: Evidence of Radical Intermediates and Kinetic Isotope Effects.
Notă biografică
Xiaoshi Wang received her B.Sc. in chemistry from Nanjing University, China in 2007. She obtained her Ph.D. in chemistry from Chemistry Department of Princeton University in August 2013. Her major research project in Prof. John T. Groves group is function and mechanistic investigation on C-H oxygenation reactions catalyzed by heme-thiolate enzymes. Subsequently, she became a post-doc fellow working with Prof. Benjamin Garcia at Perelman School of Medicine, University of Pennsylvania, focusing on studying chromatin protein PTMs during epigenetic processes.
Textul de pe ultima copertă
In this thesis, Xiaoshi Wang investigates the function and mechanism of a newly discovered heme-thiolate peroxygenase, AaeAPO. This enzyme class comes from Agrocybe aegerita and is used in the conversion of inert hydrocarbons to alcohols. Xiaoshi's work focuses on an extracellular P450 enzyme which is not limited in its stability and lack of solubility and therefore is relevant for widespread industrial use. The author demonstrates that the peroxygenase catalyzes a wide range of reactions. In some cases the author even describes very difficult transformations in molecules that are highly inert. Her detailed investigations provide a mechanistic framework for how the peroxygenase catalyzes such a large number of reactions. A major highlight of this thesis is the identification of key short-lived intermediates in the catalytic cycle of the peroxygenase, using rapid kinetic and spectroscopic methods, as well as the elucidation of the thermodynamic properties of these high-energy intermediates. This work adds new insight into an important class of enzymes.
Caracteristici
Nominated as an outstanding Ph.D. thesis by Princeton University, USA Represents significant scientific advance in the field of heme-thiolate enzymes Provides clear and colorful illustrations with original research data Give complete and detailed enzymatic function studies and mechanistic frameworks Includes supplementary material: sn.pub/extras