David Rudner

Professor

Harvard Medical School

United States

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David Rudner is a Professor at Harvard Medical School in the United States. His research focuses on bacterial cell wall synthesis, lipid synthesis, and spore germination, as evidenced by his recent publications. Notable topics include the modulation of cellular turgor in response to cell wall defects, enzymatic roles in lipid carrier replenishment, and mechanisms of signaling during spore germination in Bacillus subtilis.

Articles (19)

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2025

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2020

Collaborators (7)

Xindan Wang

Assistant Professor

Indiana State University

UNITED STATES

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Andrew Kruse

Assistant Professor

Harvard Medical School

UNITED STATES

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Christopher D. A. Rodrigues

University of Warwick

UNITED KINGDOM

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Angelika Gründling

Professor of Molecular Microbiology

Imperial College London

UNITED KINGDOM

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Dena Lyras

MONASH UNIVERSITY

AUSTRALIA

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Richard Baker

Assistant Professor

University of North Carolina at Chapel Hill

UNITED STATES

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Assaf Alon

Assistant Professor

Yale University School of Medicine

UNITED STATES

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David Rudner

Research Interests

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About

Articles (19)

PgpP is a broadly conserved phosphatase required for phosphatidylglycerol lipid synthesis

Cyclic-di-AMP modulates cellular turgor in response to defects in bacterial cell wall synthesis

Two new enzymes that liberate undecaprenyl-phosphate to replenish the carrier lipid pool during envelope stress

FacZ is a GpsB-interacting protein that prevents aberrant division-site placement in Staphylococcus aureus

Bacillus subtilis uses the SigM signaling pathway to prioritize the use of its lipid carrier for cell wall synthesis

SwrA-mediated Multimerization of DegU and an Upstream Activation Sequence Enhance Flagellar Gene Expression in Bacillus subtilis

SpoVAF and FigP assemble into oligomeric ion channels that enhance spore germination

Identification and characterization of the Bacillus subtilis spore germination protein GerY

Bacterial spore germination receptors are nutrient-gated ion channels

Two broadly conserved families of polyprenyl-phosphate transporters

MacP bypass variants of Streptococcus pneumoniae PBP2a suggest a conserved mechanism for the activation of bifunctional cell wall synthases

Intrinsically disordered protein regions are required for cell wall homeostasis inBacillus subtilis

WhyD tailors surface polymers to prevent premature bacteriolysis and direct cell elongation in Streptococcus pneumoniae

The SpoVA membrane complex is required for dipicolinic acid import during sporulation and export during germination

Genetic Evidence for Signal Transduction within the Bacillus subtilis GerA Germinant Receptor

The WalR-WalK Signaling Pathway Modulates the Activities of both CwlO and LytE through Control of the Peptidoglycan Deacetylase PdaC in Bacillus subtilis

Dormant spores sense amino acids through the B subunits of their germination receptors

XerD unloads bacterial SMC complexes at the replication terminus

A dynamic, ring-forming MucB / RseB-like protein influences spore shape in Bacillus subtilis

Collaborators (7)

Xindan Wang

Andrew Kruse

Christopher D. A. Rodrigues

Angelika Gründling

Dena Lyras

Richard Baker

Assaf Alon

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