Evidence map›Paper›PMID 40469723›Full record

ArticleFrontiers in microbiology2025

Establishment of an efficient one-step enzymatic synthesis of cyclic-2,3-diphosphoglycerate.

Christina Stracke, Benjamin H Meyer, Simone A De Rose, Erica Elisa Ferrandi, Ilya V Kublanov, Michail N Isupov, Nicholas J Harmer, Daniela Monti, Jennifer Littlechild, Felix Müller and 3 more

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Christina StrackeMolecular Enzyme Technology and Biochemistry, Environmental Microbiology and Biotechnology, Centre for Water and Environmental Research (CWE), University of Duisburg-Essen, Essen, Germany.
Benjamin H MeyerMolecular Enzyme Technology and Biochemistry, Environmental Microbiology and Biotechnology, Centre for Water and Environmental Research (CWE), University of Duisburg-Essen, Essen, Germany.
Simone A De RoseHenry Wellcome Building for Biocatalysis, Biosciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, United Kingdom.
Erica Elisa FerrandiIstituto di Scienze e Tecnologie Chimiche "G. Natta" (SCITEC), Consiglio Nazionale delle Ricerche, Milan, Italy.
Ilya V KublanovWinogradsky Institute of Microbiology, Federal Research Center of Biotechnology, Russian Academy of Sciences, Moscow, Russia.
Michail N IsupovHenry Wellcome Building for Biocatalysis, Biosciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, United Kingdom.
Nicholas J HarmerLiving Systems Institute, Faculty of Health and Life Sciences, University of Exeter, Exeter, United Kingdom.
Daniela MontiIstituto di Scienze e Tecnologie Chimiche "G. Natta" (SCITEC), Consiglio Nazionale delle Ricerche, Milan, Italy.
Jennifer LittlechildHenry Wellcome Building for Biocatalysis, Biosciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, United Kingdom.
Felix MüllerCorporate Innovation, Evonik Industries AG, Essen, Germany.
Jacky L SnoepDepartment of Biochemistry, University of Stellenbosch, Matieland, South Africa.
Christopher BräsenMolecular Enzyme Technology and Biochemistry, Environmental Microbiology and Biotechnology, Centre for Water and Environmental Research (CWE), University of Duisburg-Essen, Essen, Germany.
Bettina SiebersMolecular Enzyme Technology and Biochemistry, Environmental Microbiology and Biotechnology, Centre for Water and Environmental Research (CWE), University of Duisburg-Essen, Essen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extremolytes - unique compatible solutes produced by extremophiles - protect biological structures like membranes, proteins, and DNA under extreme conditions, including extremes of temperature and osmotic stress. These compounds hold significant potential for applications in pharmaceuticals, healthcare, cosmetics, and life sciences. However, despite their considerable potential, only a limited number of extremolytes - most notably ectoine and hydroxyectoine - have achieved commercial relevance, primarily due to the absence of efficient production strategies for the majority of other extremolytes. Cyclic 2,3-diphosphoglycerate (cDPG), a unique metabolite found in certain hyperthermophilic methanogenic Archaea, plays a key role in thermoprotection and is synthesized from 2-phosphoglycerate (2PG) through a two-step enzymatic process involving 2-phosphoglycerate kinase (2PGK) and cyclic-2,3-diphosphoglycerate synthetase (cDPGS). In this study, we present the development of an efficient

Indexed as

2-phosphoglycerate kinasearchaeacompatible solutescyclic-2,3-diphosphoglycerate synthetaseextremolyteshyperthermophilesstress responsethermoprotection

Identifiers

PMID40469723
PMCPMC12136491

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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.