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Quantification of Bacterial Histidine Kinase Autophosphorylation Using a Nitrocellulose Binding Assay
Published on: January 11, 2017
5-Thiohistidine N-Acetyltransferase from Proteiniphilum Saccharofermentans
Cangsong Liao1, David Lim1,2, Gladwin Suryatin Alim1
1Department of Chemistry, University of Basel, Mattenstrasse 22, Basel, 4002, Switzerland.
None:
Ovothiol A is a 5-thiohistidine derivative biosynthesized by a broad range of prokaryotic and eukaryotic organisms. Its redox-active mercaptoimidazole side chain is believed to protect cells from oxidative stress. The three enzymes that produce ovothiol A from histidine, cysteine, and S-adenosyl methionine have been identified and characterized. In contrast, no enzymes are known that produce other 5-thiohistidine derivatives. Here, a small family of acetyl-coenzyme A-dependent transferases is described that produce N-acetyl-5-thiohistidine. The discovery of these enzymes from Proteiniphilum saccharofermentans and related Bacteroidota provides evidence that the 5-thiohistidine class may be structurally and functionally more diverse than previously thought.

