Evidence map›Paper›PMID 34436794›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2021

Molecular Recognition of Natural and Non-Natural Substrates by Cellodextrin Phosphorylase from Ruminiclostridium Thermocellum Investigated by NMR Spectroscopy.

Valeria Gabrielli, Juan C Muñoz-García, Giulia Pergolizzi, Peterson de Andrade, Yaroslav Z Khimyak, Robert A Field, Jesús Angulo

Open access · hybridAbstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
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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

7 authors at 2 institutions in 2 countries.

Valeria GabrielliSchool of Pharmacy, University of East Anglia Norwich Research Park, Norwich, NR4 7TJ, UK.ORCID http://orcid.org/0000-0003-0475-5032
Juan C Muñoz-GarcíaSchool of Pharmacy, University of East Anglia Norwich Research Park, Norwich, NR4 7TJ, UK.
Giulia PergolizziDepartment of Biological Chemistry, John Innes Centre Norwich Research Park, Norwich, NR4 7TH, UK.ORCID http://orcid.org/0000-0003-0880-0179
Peterson de AndradeDepartment of Biological Chemistry, John Innes Centre Norwich Research Park, Norwich, NR4 7TH, UK.
Yaroslav Z KhimyakSchool of Pharmacy, University of East Anglia Norwich Research Park, Norwich, NR4 7TJ, UK.ORCID http://orcid.org/0000-0003-0424-4128
Robert A FieldDepartment of Biological Chemistry, John Innes Centre Norwich Research Park, Norwich, NR4 7TH, UK.ORCID http://orcid.org/0000-0001-8574-0275
Jesús AnguloSchool of Pharmacy, University of East Anglia Norwich Research Park, Norwich, NR4 7TJ, UK.ORCID http://orcid.org/0000-0001-7250-5639
University of East Anglia · GBJohn Innes Centre · GB

Funding

Biotechnology and Biological Sciences Research Council BB/M011216/1Biotechnology and Biological Sciences Research Council BB/P010660/1Biotechnology and Biological Sciences Research Council BBS/E/J/000C0618Biotechnology and Biological Sciences Research Council BBS/E/J/000PR9790Engineering and Physical Sciences Research Council EP/N033337/1Engineering and Physical Sciences Research Council IUK 4159000 442149Ministerio de Ciencia, Innovación y Universidades PID2019-109395GB-I00
6 · The paper itself

Abstract

β-1→4-Glucan polysaccharides like cellulose, derivatives and analogues, are attracting attention due to their unique physicochemical properties, as ideal candidates for many different applications in biotechnology. Access to these polysaccharides with a high level of purity at scale is still challenging, and eco-friendly alternatives by using enzymes in vitro are highly desirable. One prominent candidate enzyme is cellodextrin phosphorylase (CDP) from Ruminiclostridium thermocellum, which is able to yield cellulose oligomers from short cellodextrins and α-d-glucose 1-phosphate (Glc-1-P) as substrates. Remarkably, its broad specificity towards donors and acceptors allows the generation of highly diverse cellulose-based structures to produce novel materials. However, to fully exploit this CDP broad specificity, a detailed understanding of the molecular recognition of substrates by this enzyme in solution is needed. Herein, we provide a detailed investigation of the molecular recognition of ligands by CDP in solution by saturation transfer difference (STD) NMR spectroscopy, tr-NOESY and protein-ligand docking. Our results, discussed in the context of previous reaction kinetics data in the literature, allow a better understanding of the structural basis of the broad binding specificity of this biotechnologically relevant enzyme.

Indexed as

Acetivibrio thermocellusGlucosyltransferasesMagnetic Resonance SpectroscopyPolysaccharidescellodextrin phosphorylaseGlucosyltransferasesPolysaccharidescellodextrin phosphorylaseligand-based NMR spectroscopymolecular dockingprotein-ligand interactions

Identifiers

PMID34436794
PMCPMC9293210
OpenAlexW3193342942

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.