Hannah Minges focuses on the investigation of two different FAD-dependent halogenases in order to analyze and improve their applicability for chemoenzymatic approaches in chemistry. Owing to beneficial features, like high selectivity and benign reaction conditions, nature's toolkit for halogenation provides several advantages, whereas conventional chemical strategies require hazardous reagents and suffer from low selectivity. Therefore, enzymatic halogenation arises as promising alternative in the synthesis of valuable chemicals. One project focuses on the generation of a thermostable variant of the tryptophan halogenase Thal by means of directed evolution. The second project deals with the investigation of the marine halogenase Bmp5. This enzyme is of synthetic interest because it preferably introduces bromine into phenol compounds, whereas chlorination cannot take place. Contents

• Halogenating Enzymes
• Identification of a Thermostable Thal Variant by Directed Evolution

• Establishment of the Brominase Bmp5 for Synthetic Application Target GroupsLecturers, students and researchers in biological chemistry and chemistry The AuthorHannah Minges, a Ph.D student at Bielefeld University, works on the optimization of tryptophan halogenases by means of directed evolution.

  Autorentext
  Hannah Minges, a Ph.D student at Bielefeld University, works on the optimization of tryptophan halogenases by means of directed evolution.

  Inhalt

Halogenating Enzymes.- Identification of a Thermostable Thal Variant by Directed Evolution.- Establishment of the Brominase Bmp5 for Synthetic Application.