Evidence map›Paper›PMID 26879123›Full record

ArticleBMC genomics2016

Isolation and genome sequencing of four Arctic marine Psychrobacter strains exhibiting multicopper oxidase activity.

Morteza Shojaei Moghadam, Andreas Albersmeier, Anika Winkler, Lorenzo Cimmino, Kjersti Rise, Martin Frank Hohmann-Marriott, Jörn Kalinowski, Christian Rückert, Alexander Wentzel, Rahmi Lale

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
6.5field-weighted citation impact, top 4% 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

16 citing papers in PubMed, 38 citations in OpenAlex.

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  12. AdaptiveFrontiers in microbiology · 2019
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  16. Resistance of Permafrost and ModernBioMed research international · 2016
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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

10 authors at 3 institutions in 2 countries.

Morteza Shojaei MoghadamDepartment of Biotechnology, PhotoSynLab, Faculty of Natural Sciences and Technology, NTNU Norwegian University of Science and Technology, N-7491, Trondheim, Norway. morteza.s.moghadam@ntnu.no.
Andreas AlbersmeierTechnology Platform Genomics, Center for Biotechnology (CeBiTec), Bielefeld University, Sequenz 1, D-33615, Bielefeld, Germany. aalbersm@cebitec.uni-bielefeld.de.
Anika WinklerTechnology Platform Genomics, Center for Biotechnology (CeBiTec), Bielefeld University, Sequenz 1, D-33615, Bielefeld, Germany. awinkler@cebitec.uni-bielefeld.de.
Lorenzo CimminoDepartment of Biotechnology, PhotoSynLab, Faculty of Natural Sciences and Technology, NTNU Norwegian University of Science and Technology, N-7491, Trondheim, Norway. lore.cimmino@gmail.com.
Kjersti RiseDepartment of Biotechnology, PhotoSynLab, Faculty of Natural Sciences and Technology, NTNU Norwegian University of Science and Technology, N-7491, Trondheim, Norway. kjersti.rise@ntnu.no.
Martin Frank Hohmann-MarriottDepartment of Biotechnology, PhotoSynLab, Faculty of Natural Sciences and Technology, NTNU Norwegian University of Science and Technology, N-7491, Trondheim, Norway. martin.hohmann-marriott@ntnu.no.
Jörn KalinowskiTechnology Platform Genomics, Center for Biotechnology (CeBiTec), Bielefeld University, Sequenz 1, D-33615, Bielefeld, Germany. joern@cebitec.uni-bielefeld.de.
Christian RückertTechnology Platform Genomics, Center for Biotechnology (CeBiTec), Bielefeld University, Sequenz 1, D-33615, Bielefeld, Germany. cruecker@mit.edu.
Alexander WentzelDepartment of Biotechnology, SINTEF Materials and Chemistry, N-7465, Trondheim, Norway. Alexander.Wentzel@sintef.no.
Rahmi LaleDepartment of Biotechnology, PhotoSynLab, Faculty of Natural Sciences and Technology, NTNU Norwegian University of Science and Technology, N-7491, Trondheim, Norway. rahmi.lale@ntnu.no.
Norwegian University of Science and Technology · NOBielefeld University · DESINTEF · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMarine cold-temperature environments are an invaluable source of psychrophilic microbial life for new biodiscoveries. An Arctic marine bacterial strain collection was established consisting of 1448 individual isolates originating from biota, water and sediment samples taken at a various depth in the Barents Sea, North of mainland Norway, with an all year round seawater temperature of 4 °C. The entire collection was subjected to high-throughput screening for detection of extracellular laccase activity with guaiacol as a substrate.

resultsIn total, 13 laccase-positive isolates were identified, all belonging to the Psychrobacter genus. From the most diverse four strains, based on 16S rRNA gene sequence analysis, all originating from the same Botryllus sp. colonial ascidian tunicate sample, genomic DNA was isolated and genome sequenced using a combined approach of whole genome shotgun and 8 kb mate-pair library sequencing on an Illumina MiSeq platform. The genomes were assembled and revealed genome sizes between 3.29 and 3.52 Mbp with an average G + C content of around 42%, with one to seven plasmids present in the four strains. Bioinformatics based genome mining was performed to describe the metabolic potential of these four strains and to identify gene candidates potentially responsible for the observed laccase-positive phenotype. Up to two different laccase-like multicopper oxidase (LMCO) encoding gene candidates were identified in each of the four strains. Heterologous expression of P11F6-LMCO and P11G5-LMCO2 in Escherichia coli BL21 (DE3) resulted in recombinant proteins exhibiting 2,2'-azino-bis-3-ethylbenzothiazoline-6-sulphonic acid (ABTS) and guaiacol oxidizing activity.

conclusionsThirteen Psychrobacter species with laccase-positive phenotype were isolated from a collection of Arctic marine bacteria. Four of the isolates were genome sequenced. The overall genome features were similar to other publicly available Psychrobacter genome sequences except for P11G5 harboring seven plasmids. However, there were differences at the pathway level as genes associated with degradation of phenolic compounds, nicotine, phenylalanine, styrene, ethylbenzene, and ethanolamine were detected only in the Psychrobacter strains reported in this study while they were absent among the other publicly available Psychrobacter genomes. In addition, six gene candidates were identified by genome mining and shown to possess T1, T2 and T3 copper binding sites as the main signature of the three-domain laccases. P11F6-LMCO and P11G5-LMCO2 were recombinantly expressed and shown to be active when ABTS and guaiacol were used as substrates.

Indexed as

Genome, BacterialPhylogenyArctic RegionsBacterial Typing TechniquesBase CompositionBase SequenceCold TemperatureDNA, BacterialMolecular Sequence DataNorwayOxidoreductasesPsychrobacterRNA, Ribosomal, 16SSeawaterSequence Analysis, DNADNA, BacterialOxidoreductasesRNA, Ribosomal, 16S

Identifiers

PMID26879123
PMCPMC4754876
OpenAlexW2278340088

What OpenQuestion holds

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LicenceCC BY
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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.