Evidence map›Paper›PMID 23950181›Full record

ArticleThe Journal of biological chemistry2013

A bacterial glucanotransferase can replace the complex maltose metabolism required for starch to sucrose conversion in leaves at night.

Christian Ruzanski, Julia Smirnova, Martin Rejzek, Darrell Cockburn, Henriette L Pedersen, Marilyn Pike, William G T Willats, Birte Svensson, Martin Steup, Oliver Ebenhöh and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

14 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  4. Production of Large-Ring Cyclodextrins by Amylomaltases.Molecules (Basel, Switzerland) · 2022
    Review
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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

12 authors at 5 institutions in 3 countries.

Christian RuzanskiFrom the John Innes Centre, Norwich Research Park, Norwich NR4 7UH, United Kingdom.
Julia Smirnova
Martin Rejzek
Darrell Cockburn
Henriette L Pedersen
Marilyn Pike
William G T Willats
Birte Svensson
Martin Steup
Oliver Ebenhöh
Alison M Smith
Robert A Field
John Innes Centre · GBTechnical University of Denmark · DKUniversity of Copenhagen · DKUniversity of Potsdam · DEUniversity of Aberdeen · GB

Funding

Biotechnology and Biological Sciences Research Council BB/C507361/1Biotechnology and Biological Sciences Research Council BB/J004561/1Biotechnology and Biological Sciences Research Council BBS/E/J/00000020Biotechnology and Biological Sciences Research Council BBS/E/J/000C0618
6 · The paper itself

Abstract

Controlled conversion of leaf starch to sucrose at night is essential for the normal growth of Arabidopsis. The conversion involves the cytosolic metabolism of maltose to hexose phosphates via an unusual, multidomain protein with 4-glucanotransferase activity, DPE2, believed to transfer glucosyl moieties to a complex heteroglycan prior to their conversion to hexose phosphate via a cytosolic phosphorylase. The significance of this complex pathway is unclear; conversion of maltose to hexose phosphate in bacteria proceeds via a more typical 4-glucanotransferase that does not require a heteroglycan acceptor. It has recently been suggested that DPE2 generates a heterogeneous series of terminal glucan chains on the heteroglycan that acts as a "glucosyl buffer" to ensure a constant rate of sucrose synthesis in the leaf at night. Alternatively, DPE2 and/or the heteroglycan may have specific properties important for their function in the plant. To distinguish between these ideas, we compared the properties of DPE2 with those of the Escherichia coli glucanotransferase MalQ. We found that MalQ cannot use the plant heteroglycan as an acceptor for glucosyl transfer. However, experimental and modeling approaches suggested that it can potentially generate a glucosyl buffer between maltose and hexose phosphate because, unlike DPE2, it can generate polydisperse malto-oligosaccharides from maltose. Consistent with this suggestion, MalQ is capable of restoring an essentially wild-type phenotype when expressed in mutant Arabidopsis plants lacking DPE2. In light of these findings, we discuss the possible evolutionary origins of the complex DPE2-heteroglycan pathway.

Indexed as

DarknessArabidopsisBuffersCytosolEscherichia coliEscherichia coli ProteinsEvolution, MolecularGlucosyltransferasesMaltoseMetabolomicsMutationOligosaccharidesPhenotypePlant LeavesPlants, Genetically ModifiedProtein Structure, TertiaryBuffersEscherichia coli ProteinsGlucosyltransferasesMaltoseOligosaccharidesRecombinant ProteinsStarchSucroseCarbohydrate MetabolismComputer ModelingGlucanotransferaseLeaf CellMaltose MetabolismMetabolic RegulationOligosaccharidePlant BiochemistryStarch Degradation

Identifiers

PMID23950181
PMCPMC3789958
OpenAlexW2081518479

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.