Evidence map›Paper›PMID 32941430›Full record

ArticlePloS one2020

Lignin induced iron reduction by novel sp., Tolumonas lignolytic BRL6-1.

Gina Chaput, Andrew F Billings, Lani DeDiego, Roberto Orellana, Joshua N Adkins, Carrie D Nicora, Young-Mo Kim, Rosalie Chu, Blake Simmons, Kristen M DeAngelis

Abstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
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

10 authors.

Gina ChaputDepartment of Microbiology, University of Massachusetts-Amherst, Amherst, MA, United States of America.ORCID 0000-0001-5612-5687
Andrew F BillingsDepartment of Microbiology, University of Massachusetts-Amherst, Amherst, MA, United States of America.
Lani DeDiegoDepartment of Microbiology, University of Massachusetts-Amherst, Amherst, MA, United States of America.
Roberto OrellanaDepartamento de Biología, Facultad de Ciencias Naturales y Exactas, Universidad de Playa Ancha, Playa Ancha, Valparaíso, Chile.
Joshua N AdkinsBiological Sciences Department, Pacific Northwest National Laboratory, Richland, Washington, DC, United States of America.
Carrie D NicoraBiological Sciences Department, Pacific Northwest National Laboratory, Richland, Washington, DC, United States of America.
Young-Mo KimBiological Sciences Department, Pacific Northwest National Laboratory, Richland, Washington, DC, United States of America.ORCID 0000-0002-8972-7593
Rosalie ChuEnvironmental and Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington, DC, United States of America.
Blake SimmonsU.S. Department of Energy Joint Genome Institute, Berkeley, California, United States of America.
Kristen M DeAngelisDepartment of Microbiology, University of Massachusetts-Amherst, Amherst, MA, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lignin is the second most abundant carbon polymer on earth and despite having more fuel value than cellulose, it currently is considered a waste byproduct in many industrial lignocellulose applications. Valorization of lignin relies on effective and green methods of de-lignification, with a growing interest in the use of microbes. Here we investigate the physiology and molecular response of the novel facultative anaerobic bacterium, Tolumonas lignolytica BRL6-1, to lignin under anoxic conditions. Physiological and biochemical changes were compared between cells grown anaerobically in either lignin-amended or unamended conditions. In the presence of lignin, BRL6-1 accumulates higher biomass and has a shorter lag phase compared to unamended conditions, and 14% of the proteins determined to be significantly higher in abundance by log2 fold-change of 2 or greater were related to Fe(II) transport in late logarithmic phase. Ferrozine assays of the supernatant confirmed that Fe(III) was bound to lignin and reduced to Fe(II) only in the presence of BRL6-1, suggesting redox activity by the cells. LC-MS/MS analysis of the secretome showed an extra band at 20 kDa in lignin-amended conditions. Protein sequencing of this band identified a protein of unknown function with homology to enzymes in the radical SAM superfamily. Expression of this protein in lignin-amended conditions suggests its role in radical formation. From our findings, we suggest that BRL6-1 is using a protein in the radical SAM superfamily to interact with the Fe(III) bound to lignin and reducing it to Fe(II) for cellular use, increasing BRL6-1 yield under lignin-amended conditions. This interaction potentially generates organic free radicals and causes a radical cascade which could modify and depolymerize lignin. Further research should clarify the extent to which this mechanism is similar to previously described aerobic chelator-mediated Fenton chemistry or radical producing lignolytic enzymes, such as lignin peroxidases, but under anoxic conditions.

Indexed as

AeromonadaceaeBacterial ProteinsBiomassIronLigninOxidation-ReductionSulfatasesBacterial ProteinsIronLigninSulfatases

Identifiers

PMID32941430
PMCPMC7497984

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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.