Evidence map›Paper›PMID 29156585›Full record

ArticleMicroorganisms2017

Pan-Cellulosomics of Mesophilic Clostridia: Variations on a Theme.

Bareket Dassa, Ilya Borovok, Vincent Lombard, Bernard Henrissat, Raphael Lamed, Edward A Bayer, Sarah Moraïs

Abstract read
In one paragraph

Article in Microorganisms, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Mapping the deformability of natural and designed cellulosomes in solution.Biotechnology for biofuels and bioproducts · 2022
    Article
  8. Article
  9. Article
  10. Secretomic analyses ofBiotechnology for biofuels · 2019
    Article
  11. Article
  12. 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.

Bareket DassaDepartment of Biomolecular Sciences, The Weizmann Institute of Science, Rehovot 7610001, Israel. bareket.dassa@weizmann.ac.il.
Ilya BorovokDepartment of Molecular Microbiology and Biotechnology, Tel Aviv University, Ramat Aviv 6997801, Israel. ilyabo@tauex.tau.ac.il.ORCID 0000-0003-1602-4499
Vincent LombardArchitecture et Fonction des Macromolecules Biologiques, CNRS and Universite Aix-Marseilles I & II, Marseilles 13288, France. vincent.lombard@afmb.univ-mrs.fr.
Bernard HenrissatArchitecture et Fonction des Macromolecules Biologiques, CNRS and Universite Aix-Marseilles I & II, Marseilles 13288, France. bernard.henrissat@afmb.univ-mrs.fr.
Raphael LamedDepartment of Molecular Microbiology and Biotechnology, Tel Aviv University, Ramat Aviv 6997801, Israel. lamedr@post.tau.ac.il.
Edward A BayerDepartment of Biomolecular Sciences, The Weizmann Institute of Science, Rehovot 7610001, Israel. ed.bayer@weizmann.ac.il.
Sarah MoraïsDepartment of Biomolecular Sciences, The Weizmann Institute of Science, Rehovot 7610001, Israel. sarahv@weizmann.ac.il.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The bacterial cellulosome is an extracellular, multi-enzyme machinery, which efficiently depolymerizes plant biomass by degrading plant cell wall polysaccharides. Several cellulolytic bacteria have evolved various elaborate modular architectures of active cellulosomes. We present here a genome-wide analysis of a dozen mesophilic clostridia species, including both well-studied and yet-undescribed cellulosome-producing bacteria. We first report here, the presence of cellulosomal elements, thus expanding our knowledge regarding the prevalence of the cellulosomal paradigm in nature. We explored the genomic organization of key cellulosome components by comparing the cellulosomal gene clusters in each bacterial species, and the conserved sequence features of the specific cellulosomal modules (cohesins and dockerins), on the background of their phylogenetic relationship. Additionally, we performed comparative analyses of the species-specific repertoire of carbohydrate-degrading enzymes for each of the clostridial species, and classified each cellulosomal enzyme into a specific CAZy family, thus indicating their putative enzymatic activity (e.g., cellulases, hemicellulases, and pectinases). Our work provides, for this large group of bacteria, a broad overview of the blueprints of their multi-component cellulosomal complexes. The high similarity of their scaffoldin clusters and dockerin-based recognition residues suggests a common ancestor, and/or extensive horizontal gene transfer, and potential cross-species recognition. In addition, the sporadic spatial organization of the numerous dockerin-containing genes in several of the genomes, suggests the importance of the cellulosome paradigm in the given bacterial species. The information gained in this work may be utilized directly or developed further by genetically engineering and optimizing designer cellulosome systems for enhanced biotechnological biomass deconstruction and biofuel production.

Indexed as

cellulosomescohesindockeringlycoside hydrolasesscaffoldin

Identifiers

PMID29156585
PMCPMC5748583

What OpenQuestion holds

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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.