Related Experiment Video
Updated: Apr 24, 2026

Essential Components of Borreliella Borrelia burgdorferi In Vitro Transcription Assays
Published on: July 22, 2022
In vitro analysis of carboxyacyl substrate tolerance in the loading and first extension modules of borrelidin
Andrew Hagen1, Sean Poust, Tristan de Rond
1Department of Plant and Microbial Biology, ‡Department of Chemical and Biomolecular Engineering, §Department of Chemistry, ∥QB3 Institute, and ⊥Department of Bioengineering, University of California , Berkeley, California 94270, United States.
Abstract:
The borrelidin polyketide synthase (PKS) begins with a carboxylated substrate and, unlike typical decarboxylative loading PKSs, retains the carboxy group in the final product. The specificity and tolerance of incorporation of carboxyacyl substrate into type I PKSs have not been explored. Here, we show that the first extension module is promiscuous in its ability to extend both carboxyacyl and non-carboxyacyl substrates. However, the loading module has a requirement for substrates containing a carboxy moiety, which are not decarboxylated in situ. Thus, the loading module is the basis for the observed specific incorporation of carboxylated starter units by the borelidin PKS.
More Related Videos
10:37Cultivation Methods of Spirochetes from Borrelia burgdorferi Sensu Lato Complex and Relapsing Fever Borrelia
Published on: November 25, 2022
08:56Synthesis of a Borylated Ibuprofen Derivative Through Suzuki Cross-Coupling and Alkene Boracarboxylation Reactions
Published on: November 30, 2022