Controlled Delivery and Light‐Induced Release of Magic Spot Nucleotides in <i>Escherichia coli</i>

C Christoph Popp (Faculty of Chemistry and Pharmacy Institute of Organic Chemistry &amp; CIBSS Centre For Integrative Biological Signalling Studies Albert‐Ludwigs University Freiburg Freiburg Germany) P Patrick Moser (Faculty of Chemistry and Pharmacy Institute of Organic Chemistry &amp; CIBSS Centre For Integrative Biological Signalling Studies Albert‐Ludwigs University Freiburg Freiburg Germany) A Anselm Schwoerbel (Faculty of Chemistry and Pharmacy Institute of Organic Chemistry &amp; CIBSS Centre For Integrative Biological Signalling Studies Albert‐Ludwigs University Freiburg Freiburg Germany) X Xinwei Liu J Johannes Freitag P Pinku Sarmah (Faculty of Medicine Institute For Biochemistry and Molecular Biology, ZBMZ Albert‐Ludwigs University Freiburg Freiburg Germany) I Isabel Prucker R Robert Zscherp (Department of Chemistry and Molecular Biology Division of Organic and Medicinal Chemistry University of Gothenburg Gothenburg Sweden) X Xuan Wang P Philipp Klahn H Hans‐Georg Koch (Faculty of Medicine Institute For Biochemistry and Molecular Biology, ZBMZ Albert‐Ludwigs University Freiburg Freiburg Germany) G Gert Bange H Henning J. Jessen

Abstract

ABSTRACT The “magic spot” nucleotides (MSNs) ppGpp and pppGpp constitute bacterial alarmones that orchestrate the conserved stringent response, a global regulatory mechanism enabling bacteria to adapt to nutrient deprivation and other environmental stresses. Current strategies to manipulate MSN levels rely mainly on genetic or environmental approaches, which are slow and lack temporal control. Chemical tools such as photocaged MSN analogues could provide such temporal control over MSN levels. However, the high negative charge of MSNs prevents spontaneous passage through the complex bacterial cell envelope. Here, we report the synthesis of photocaged, clickable, and isotope‐labeled MSN analogues and their delivery into Escherichia coli comparing different approaches. A cyclodextrin‐based synthetic nucleotide transporter facilitated uptake. Upon 400 nm irradiation, these probes were photo‐released inside living cells, where we tracked their conversion from pppGpp to ppGpp by capillary electrophoresis mass spectrometry and demonstrated their ability to alter growth in a (p)ppGpp 0 mutant. These probes lay the foundation for spatially and temporally controlled studies of MSN function and of other highly negatively charged metabolites in vivo.

Article Details

Volume / Issue Vol. 65, Issue 15
Published April 06, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (13)

C

Christoph Popp

Faculty of Chemistry and Pharmacy Institute of Organic Chemistry &amp; CIBSS Centre For Integrative Biological Signalling Studies Albert‐Ludwigs University Freiburg Freiburg Germany

P

Patrick Moser

Faculty of Chemistry and Pharmacy Institute of Organic Chemistry &amp; CIBSS Centre For Integrative Biological Signalling Studies Albert‐Ludwigs University Freiburg Freiburg Germany

A

Anselm Schwoerbel

Faculty of Chemistry and Pharmacy Institute of Organic Chemistry &amp; CIBSS Centre For Integrative Biological Signalling Studies Albert‐Ludwigs University Freiburg Freiburg Germany

X

Xinwei Liu

J

Johannes Freitag

P

Pinku Sarmah

Faculty of Medicine Institute For Biochemistry and Molecular Biology, ZBMZ Albert‐Ludwigs University Freiburg Freiburg Germany

I

Isabel Prucker

R

Robert Zscherp

Department of Chemistry and Molecular Biology Division of Organic and Medicinal Chemistry University of Gothenburg Gothenburg Sweden

X

Xuan Wang

P

Philipp Klahn

H

Hans‐Georg Koch

Faculty of Medicine Institute For Biochemistry and Molecular Biology, ZBMZ Albert‐Ludwigs University Freiburg Freiburg Germany

G

Gert Bange

H

Henning J. Jessen