Repression of bacterial gene expression by antivitamin B12 binding to a cobalamin riboswitch
Florian J. Widner, Naziyat I. Khan, Evelyne Deery, Martin J. Warren, Michiko E. Taga, Bernhard Kräutler

TL;DR
A synthetic compound that mimics vitamin B12 can block bacterial gene expression and may serve as a new antibiotic.
Contribution
The study reveals a new gene-regulatory activity of an antivitamin B12 analogue in repressing bacterial B12 uptake.
Findings
AdoRhbl mimics AdoCbl in downregulating reporter expression in vitro with high affinity.
AdoRhbl shows strong intracellular activity in E. coli with EC50 values as low as 1.4 nM.
AdoRhbl inhibits B12-dependent enzymes and represses BtuB expression, suggesting antibiotic potential.
Abstract
The E. coli btuB riboswitch is a cobalamin-sensing RNA element that selectively binds coenzyme B12 (adenosylcobalamin, AdoCbl) to downregulate the expression of the outer membrane B12-transporter BtuB. Here, we examined adenosylrhodibalamin (AdoRhbl), the isostructural Rh-analogue of AdoCbl, as a surrogate effector ligand for this riboswitch. Two riboswitch-reporter systems were employed: an engineered E. coli strain with a fluorescent reporter for intracellular AdoCbl-sensing, and a plasmid-based construct for analogous in vitro transcription/translation assays. In the in-vitro system AdoRhbl closely mimicked AdoCbl in down-regulating reporter expression with apparent EC50 values of 2.8 µM and 0.8 µM respectively. In contrast, the engineered E. coli strain revealed much higher effective sensitivities, with EC50 values of 1.4 nM for AdoRhbl and of 6.9 nM for AdoCbl, reflecting strong…
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Taxonomy
TopicsPorphyrin Metabolism and Disorders · Folate and B Vitamins Research · Bacterial Genetics and Biotechnology
