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A Cobalamin Activity-Based Probe Enables Microbial Cell Growth and Finds New Cobalamin-Protein Interactions across Domains
Understanding the factors that regulate microbe function and microbial community assembly, function, and fitness is a grand challenge. A critical factor and an important enzyme cofactor and regulator of gene expression is cobalamin (vitamin B ). Our knowledge of the roles of vitamin B is limited, be...
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Published in: | Applied and environmental microbiology 2018-09, Vol.84 (18) |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Understanding the factors that regulate microbe function and microbial community assembly, function, and fitness is a grand challenge. A critical factor and an important enzyme cofactor and regulator of gene expression is cobalamin (vitamin B
). Our knowledge of the roles of vitamin B
is limited, because technologies that enable
characterization of microbial metabolism and gene regulation with minimal impact on cell physiology are needed. To meet this need, we show that a synthetic probe mimic of B
supports the growth of B
-auxotrophic bacteria and archaea. We demonstrate that a B
activity-based probe (B
-ABP) is actively transported into
cells and converted to adenosyl-B
-ABP akin to native B
Identification of the proteins that bind the B
-ABP
in
, a
sp. and
, demonstrate the specificity for known and novel B
protein targets. The B
-ABP also regulates the B
dependent RNA riboswitch
and the transcription factor EutR. Our results demonstrate a new approach to gain knowledge about the role of B
in microbe functions. Our approach provides a powerful nondisruptive tool to analyze B
interactions in living cells and can be used to discover the role of B
in diverse microbial systems.
We demonstrate that a cobalamin chemical probe can be used to investigate
roles of vitamin B
in microbial growth and regulation by supporting the growth of B
auxotrophic bacteria and archaea, enabling biological activity with three different cell macromolecules (RNA, DNA, and proteins), and facilitating functional proteomics to characterize B
-protein interactions. The B
-ABP is both transcriptionally and translationally able to regulate gene expression analogous to natural vitamin B
The application of the B
-ABP at biologically relevant concentrations facilitates a unique way to measure B
microbial dynamics and identify new B
protein targets in bacteria and archaea. We demonstrate that the B
-ABP can be used to identify
protein interactions across diverse microbes, from
to microbes isolated from naturally occurring phototrophic biofilms to the salt-tolerant archaea
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ISSN: | 0099-2240 1098-5336 |
DOI: | 10.1128/AEM.00955-18 |