Evidence map›Paper›PMID 27601356›Full record

ArticleJournal of bacteriology2016

Identification of a Novel N-Acetylmuramic Acid Transporter in Tannerella forsythia.

Angela Ruscitto, Isabel Hottmann, Graham P Stafford, Christina Schäffer, Christoph Mayer, Ashu Sharma

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bacteriology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Microbiology spectrum · 2026
    Article
  3. Obtaining Muramic Acid fromLife (Basel, Switzerland) · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Persistence ofCurrent oral health reports · 2020
    Article
  13. Article
  14. Article
  15. Review
  16. Frontiers in microbiology · 2018
    Article
  17. Review
  18. Article
  19. Article
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

6 authors at 4 institutions in 4 countries.

Angela RuscittoDepartment of Oral Biology, University at Buffalo, Buffalo, New York, USA.
Isabel HottmannInterfaculty Institute of Microbiology and Infection Medicine Tübingen, IMIT, Department of Microbiology & Biotechnology, University of Tübingen, Tübingen, Germany.
Graham P StaffordOral and Maxillofacial Pathology, University of Sheffield, Sheffield, United Kingdom.
Christina SchäfferDepartment for NanoBiotechnology, NanoGlycobiology Unit, Universität für Bodenkultur Wien, Vienna, Austria.
Christoph MayerInterfaculty Institute of Microbiology and Infection Medicine Tübingen, IMIT, Department of Microbiology & Biotechnology, University of Tübingen, Tübingen, Germany christoph.mayer@uni-tuebingen.de sharmaa@buffalo.edu.
Ashu SharmaDepartment of Oral Biology, University at Buffalo, Buffalo, New York, USA christoph.mayer@uni-tuebingen.de sharmaa@buffalo.edu.
University at Buffalo, State University of New York · USUniversity of Tübingen · DEBOKU University · ATUniversity of Sheffield · GB

Funding

T. forsythia TLR2 ligands and surface glycans coordinate periodontal inflammationR01DE014749 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI SHARMA, ASHU · 2003 to 2018
$4.9M
Advanced Training in Oral BiologyT32DE023526 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI Stefan Hans-Klaus Ruhl · 2013 to 2026
$3.7M
Novel Mechanisms of Peptidoglycan Synthesis in Tannerella forsythiaR21DE022870 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI SHARMA, ASHU · 2014 to 2015
$438k
Austrian Science Fund FWF P 24317NIDCR NIH HHS R01 DE014749NIDCR NIH HHS R21 DE022870NIDCR NIH HHS T32 DE023526
6 · The paper itself

Abstract

Tannerella forsythia is a Gram-negative periodontal pathogen lacking the ability to undergo de novo synthesis of amino sugars N-acetylmuramic acid (MurNAc) and N-acetylglucosamine (GlcNAc) that form the disaccharide repeating unit of the peptidoglycan backbone. T. forsythia relies on the uptake of these sugars from the environment, which is so far unexplored. Here, we identified a novel transporter system of T. forsythia involved in the uptake of MurNAc across the inner membrane and characterized a homolog of the Escherichia coli MurQ etherase involved in the conversion of MurNAc-6-phosphate (MurNAc-6-P) to GlcNAc-6-P. The genes encoding these components were identified on a three-gene cluster spanning Tanf_08375 to Tanf_08385 located downstream from a putative peptidoglycan recycling locus. We show that the three genes, Tanf_08375, Tanf_08380, and Tanf_08385, encoding a MurNAc transporter, a putative sugar kinase, and a MurQ etherase, respectively, are transcriptionally linked. Complementation of the Tanf_08375 and Tanf_08380 genes together in trans, but not individually, rescued the inability of an E. coli mutant deficient in the phosphotransferase (PTS) system-dependent MurNAc transporter MurP as well as that of a double mutant deficient in MurP and components of the PTS system to grow on MurNAc. In addition, complementation with this two-gene construct in E. coli caused depletion of MurNAc in the medium, further confirming this observation. Our results show that the products of Tanf_08375 and Tanf_08380 constitute a novel non-PTS MurNAc transporter system that seems to be widespread among bacteria of the Bacteroidetes phylum. To the best of our knowledge, this is the first identification of a PTS-independent MurNAc transporter in bacteria. IMPORTANCE: In this study, we report the identification of a novel transporter for peptidoglycan amino sugar N-acetylmuramic acid (MurNAc) in the periodontal pathogen T. forsythia It has been known since the late 1980s that T. forsythia is a MurNAc auxotroph relying on environmental sources for this essential sugar. Most sugar transporters, and the MurNAc transporter MurP in particular, require a PTS phosphorelay to drive the uptake and concurrent phosphorylation of the sugar through the inner membrane in Gram-negative bacteria. Our study uncovered a novel type of PTS-independent MurNAc transporter, and although so far, it seems to be unique to T. forsythia, it may be present in a range of bacteria both of the oral cavity and gut, especially of the phylum Bacteroidetes.

Indexed as

Bacterial ProteinsEscherichia coliGlycoside HydrolasesMembrane Transport ProteinsMuramic AcidsPeptidoglycanTannerella forsythiaBacterial ProteinsGlycoside HydrolasesMembrane Transport ProteinsMuramic AcidsN-acetylmuramic acidPeptidoglycan

Identifiers

PMID27601356
PMCPMC5075041
OpenAlexW2510712700

What OpenQuestion holds

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Registered trials

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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.