Evidence map›Paper›PMID 27780866›Full record

ArticleThe Journal of biological chemistry2016

Identification of Two Phosphate Starvation-induced Wall Teichoic Acid Hydrolases Provides First Insights into the Degradative Pathway of a Key Bacterial Cell Wall Component.

Cullen L Myers, Franco K K Li, Byoung-Mo Koo, Omar M El-Halfawy, Shawn French, Carol A Gross, Natalie C J Strynadka, Eric D Brown

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.8field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 44 citations in OpenAlex.

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  9. Cryo-EM analysis ofScience advances · 2024
    Article
  10. Comparative chemical genomics inProceedings of the National Academy of Sciences of the United States of America · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Cullen L MyersFrom the Department of Biochemistry and Biomedical Sciences and.
Franco K K Lithe Department of Biochemistry and Center for Blood Research, University of British Columbia, Vancouver, British Columbia V6T 1Z3, Canada.
Byoung-Mo Koothe Department of Microbiology and Immunology, University of California at San Francisco, San Francisco, California 94158.
Omar M El-HalfawyFrom the Department of Biochemistry and Biomedical Sciences and.
Shawn FrenchFrom the Department of Biochemistry and Biomedical Sciences and.
Carol A Grossthe Department of Microbiology and Immunology, University of California at San Francisco, San Francisco, California 94158.
Natalie C J Strynadkathe Department of Biochemistry and Center for Blood Research, University of British Columbia, Vancouver, British Columbia V6T 1Z3, Canada.
Eric D BrownFrom the Department of Biochemistry and Biomedical Sciences and ebrown@mcmaster.ca.
McMaster University · CAUniversity of British Columbia · CAUniversity of California, San Francisco · US

Funding

Cellular homeostasis pathways in bacteriaR35GM118061 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GROSS, CAROL ANNE · 2016 to 2025
$9.0M
Gene Function and Pathway Analysis Using Systems Level Approaches in ProkaryotesR01GM102790 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GROSS, CAROL ANNE · 2012 to 2015
$1.8M
NIGMS NIH HHS R01 GM102790NIGMS NIH HHS R35 GM118061
6 · The paper itself

Abstract

The cell wall of most Gram-positive bacteria contains equal amounts of peptidoglycan and the phosphate-rich glycopolymer wall teichoic acid (WTA). During phosphate-limited growth of the Gram-positive model organism Bacillus subtilis 168, WTA is lost from the cell wall in a response mediated by the PhoPR two-component system, which regulates genes involved in phosphate conservation and acquisition. It has been thought that WTA provides a phosphate source to sustain growth during starvation conditions; however, WTA degradative pathways have not been described for this or any condition of bacterial growth. Here, we uncover roles for the Bacillus subtilis PhoP regulon genes glpQ and phoD as encoding secreted phosphodiesterases that function in WTA metabolism during phosphate starvation. Unlike the parent 168 strain, ΔglpQ or ΔphoD mutants retained WTA and ceased growth upon phosphate limitation. Characterization of GlpQ and PhoD enzymatic activities, in addition to X-ray crystal structures of GlpQ, revealed distinct mechanisms of WTA depolymerization for the two enzymes; GlpQ catalyzes exolytic cleavage of individual monomer units, and PhoD catalyzes endo-hydrolysis at nonspecific sites throughout the polymer. The combination of these activities appears requisite for the utilization of WTA as a phosphate reserve. Phenotypic characterization of the ΔglpQ and ΔphoD mutants revealed altered cell morphologies and effects on autolytic activity and antibiotic susceptibilities that, unexpectedly, also occurred in phosphate-replete conditions. Our findings offer novel insight into the B. subtilis phosphate starvation response and implicate WTA hydrolase activity as a determinant of functional properties of the Gram-positive cell envelope.

Indexed as

Bacterial ProteinsPhosphoric Diester HydrolasesBacillus subtilisCell WallCrystallography, X-RayHydrolysisMutationRegulonBacterial ProteinsglpQ protein, BacteriaPhoP protein, BacteriaPhosphoric Diester HydrolasesteichoicaseBacillusenzyme kineticsenzyme mechanismglpQgram-positive bacteriahydrolasephoDphosphate starvationwall teichoic acid

Identifiers

PMID27780866
PMCPMC5207077
OpenAlexW2532347595

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.