Evidence map›Paper›PMID 25947105›Full record

ArticleBMC microbiology2015

Influence of in situ progressive N-terminal is still controversial truncation of glycogen branching enzyme in Escherichia coli DH5α on glycogen structure, accumulation, and bacterial viability.

Liang Wang, Ahmed Regina, Vito M Butardo, Behjat Kosar-Hashemi, Oscar Larroque, Charlene M Kahler, Michael J Wise

Abstract read
In one paragraph

Article in BMC microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Characterization of glycogen-related glycoside hydrolaseFrontiers in cellular and infection microbiology · 2024
    Article
  3. The Structure of Maltooctaose-BoundMolecules (Basel, Switzerland) · 2023
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. 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

7 authors.

Liang WangSchool of Pathology and Laboratory Medicine, University of Western Australia, Perth, Australia. Liang.Wang@curtin.edu.au.
Ahmed ReginaCSIRO Agriculture Flagship, Canberra, Australia. Ahmed.Regina@csiro.au.
Vito M ButardoInternational Rice Research Institute, Los Baños, Philippines. v.butardo@irri.org.
Behjat Kosar-HashemiCSIRO Agriculture Flagship, Canberra, Australia. Behjat.Hashemi@csiro.au.
Oscar LarroqueCSIRO Agriculture Flagship, Canberra, Australia. Oscar.Larroque@csiro.au.
Charlene M KahlerSchool of Pathology and Laboratory Medicine, University of Western Australia, Perth, Australia. Charlene.Kahler@uwa.edu.au.
Michael J WiseSchool of Chemistry and Biochemistry, University of Western Australia, Perth, Australia. Michael.Wise@uwa.edu.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlycogen average chain length (ACL) has been linked with bacterial durability, but this was on the basis of observations across different species. We therefore wished to investigate the relationship between bacterial durability and glycogen ACL by varying glycogen average chain length in a single species. It has been shown that progressive shortening of the N-terminus of glycogen branching enzyme (GBE) leads to a lengthening of oligosaccharide inter-α-1,6-glycosidic chain lengths, so we sought to harness this to create a set of Escherichia coli DH5α strains with a range of glycogen average chain lengths, and assess these strains for durability related attributes, such as starvation, cold and desiccation stress resistance, and biofilm formation.

resultsA series of Escherichia coli DH5α mutants were created with glgB genes that were in situ progressively N-terminus truncated. N-terminal truncation shifted the distribution of glycogen chain lengths from 5-11 DP toward 13-50 DP, but the relationship between glgB length and glycogen ACL was not linear. Surprisingly, removal of the first 270 nucleotides of glgB (glgBΔ270) resulted in comparatively high glycogen accumulation, with the glycogen having short ACL. Complete knockout of glgB led to the formation of amylose-like glycogen containing long, linear α1,4-glucan chains with significantly reduced branching frequency. Physiologically, the set of mutant strains had reduced bacterial starvation resistance, while minimally increasing bacterial desiccation resistance. Finally, although there were no obvious changes in cold stress resistance or biofilm forming ability, one strain (glgBΔ180) had significantly increased biofilm formation in favourable media.

conclusionsDespite glgB being the first gene of an operon, it is clear that in situ mutation is a viable means to create more biologically relevant mutant strains. Secondly, there was the suggestion in the data that impairments of starvation, cold and desiccation resistance were worse for the strain lacking glgB, though the first of these was not statistically significant. The results provide prima facie evidence linking abiotic stress tolerance with shorter glycogen ACL. However, further work needs to be done, perhaps in a less labile species. Further work is also required to tease out the complex relationship between glycogen abundance and glycogen structure.

Indexed as

Microbial ViabilitySequence Deletion1,4-alpha-Glucan Branching EnzymeBiofilmsCold TemperatureDesiccationEscherichia coliGlycogenStress, Physiological1,4-alpha-Glucan Branching EnzymeGlycogen

Identifiers

PMID25947105
PMCPMC4433092

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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.