Evidence map›Paper›PMID 8246840›Full record

ReviewMicrobiological reviews1993

Phosphoenolpyruvate:carbohydrate phosphotransferase systems of bacteria.

P W Postma, J W Lengeler, G R Jacobson

Open access · diamondAbstract readReview
In one paragraph

Review in Microbiological reviews, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 613 papers.

0numbers the graph read from it
0cells of the map it votes in
613citing papers in PubMed
65.2field-weighted citation impact, top 1% 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

613 citing papers in PubMed, 1,782 citations in OpenAlex.

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  7. Atypical catabolite repression ofMicrobiology (Reading, England) · 2026
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  12. Journal of bacteriology · 2025
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  17. Structural insight intoActa biochimica et biophysica Sinica · 2025
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553 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

P W PostmaE. C. Slater Institute, University of Amsterdam, The Netherlands.
J W Lengeler
G R Jacobson
University of Amsterdam · NL

Funding

STRUCTURE AND MECHANISM OF THE E COLI MANNITOL PERMEASER01GM028226 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI JACOBSON, GARY R · 1985 to 1997
–
NIGMS NIH HHS GM28226
6 · The paper itself

Abstract

Numerous gram-negative and gram-positive bacteria take up carbohydrates through the phosphoenolpyruvate (PEP):carbohydrate phosphotransferase system (PTS). This system transports and phosphorylates carbohydrates at the expense of PEP and is the subject of this review. The PTS consists of two general proteins, enzyme I and HPr, and a number of carbohydrate-specific enzymes, the enzymes II. PTS proteins are phosphoproteins in which the phospho group is attached to either a histidine residue or, in a number of cases, a cysteine residue. After phosphorylation of enzyme I by PEP, the phospho group is transferred to HPr. The enzymes II are required for the transport of the carbohydrates across the membrane and the transfer of the phospho group from phospho-HPr to the carbohydrates. Biochemical, structural, and molecular genetic studies have shown that the various enzymes II have the same basic structure. Each enzyme II consists of domains for specific functions, e.g., binding of the carbohydrate or phosphorylation. Each enzyme II complex can consist of one to four different polypeptides. The enzymes II can be placed into at least four classes on the basis of sequence similarity. The genetics of the PTS is complex, and the expression of PTS proteins is intricately regulated because of the central roles of these proteins in nutrient acquisition. In addition to classical induction-repression mechanisms involving repressor and activator proteins, other types of regulation, such as antitermination, have been observed in some PTSs. Apart from their role in carbohydrate transport, PTS proteins are involved in chemotaxis toward PTS carbohydrates. Furthermore, the IIAGlc protein, part of the glucose-specific PTS, is a central regulatory protein which in its nonphosphorylated form can bind to and inhibit several non-PTS uptake systems and thus prevent entry of inducers. In its phosphorylated form, P-IIAGlc is involved in the activation of adenylate cyclase and thus in the regulation of gene expression. By sensing the presence of PTS carbohydrates in the medium and adjusting the phosphorylation state of IIAGlc, cells can adapt quickly to changing conditions in the environment. In gram-positive bacteria, it has been demonstrated that HPr can be phosphorylated by ATP on a serine residue and this modification may perform a regulatory function.

Indexed as

Bacterial ProteinsPhosphoenolpyruvate Sugar Phosphotransferase SystemAdenylyl CyclasesAmino Acid SequenceBacteriaBiological TransportCarbohydrate MetabolismChemotaxisCyclic AMPEnergy MetabolismGene Expression Regulation, BacterialGenes, BacterialMolecular Sequence DataOperonPhosphorylationProtein ConformationAdenylyl CyclasesBacterial ProteinsCyclic AMPPhosphoenolpyruvate Sugar Phosphotransferase System

Identifiers

PMID8246840
PMCPMC372926
OpenAlexW2130394726

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.