Evidence map›Paper›PMID 28733934›Full record

ArticleMarine biotechnology (New York, N.Y.)2017

Draft Genome Sequence of the Deep-Sea Bacterium Moritella sp. JT01 and Identification of Biotechnologically Relevant Genes.

Robert Cardoso de Freitas, Estácio Jussie Odisi, Chiaki Kato, Marcus Adonai Castro da Silva, André Oliveira de Souza Lima

Abstract read
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In one paragraph

Article in Marine biotechnology (New York, N.Y.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Draft Genome Sequences of the Lipid-Degrading BacteriaMicrobiology resource announcements · 2021
    Article
  2. 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

5 authors at 2 institutions in 2 countries.

Robert Cardoso de FreitasTechnological Science Center of Earth and Sea, UNIVALI, R Uruguai 458, Itajai, SC, 88302-202, Brazil.
Estácio Jussie OdisiTechnological Science Center of Earth and Sea, UNIVALI, R Uruguai 458, Itajai, SC, 88302-202, Brazil.
Chiaki KatoDepartment of Marine Biodiversity Research, JAMSTEC, Natsushima-cho 2-15, Yokosuka, Kanagawa, 237-0061, Japan.
Marcus Adonai Castro da SilvaTechnological Science Center of Earth and Sea, UNIVALI, R Uruguai 458, Itajai, SC, 88302-202, Brazil.
André Oliveira de Souza LimaTechnological Science Center of Earth and Sea, UNIVALI, R Uruguai 458, Itajai, SC, 88302-202, Brazil. andreolima@gmail.com.
Universidade do Vale do Itajaí · BRJapan Agency for Marine-Earth Science and Technology · JP

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 565062/2010-7Coordenação de Aperfeiçoamento de Pessoal de Nível Superior CAPES/JSPS 02/13Fundação de Amparo à Pesquisa e Inovação do Estado de Santa Catarina 3422/2012
6 · The paper itself

Abstract

Deep-sea bacteria can produce various biotechnologically relevant enzymes due to their adaptations to high pressures and low temperatures. To identify such enzymes, we have sequenced the genome of the polycaprolactone-degrading bacterium Moritella sp. JT01, isolated from sediment samples from Japan Trench (6957 m depth), using a Illumina HiSeq2000 sequencer (12.1 million paired-end reads) and CLC Genomics Workbench (version 6.5.1) for the assembly, resulting in a 4.83-Mb genome (42 scaffolds). The genome was annotated using Rapid Annotation using Subsystem Technology (RAST), Protein Homology/analogY Recognition Engine V 2.0 (PHYRE2), and BLAST2Go, revealing 4439 protein coding sequences and 101 RNAs. Gene products with industrial relevance, such as lipases (three) and esterases (four), were identified and are related to bacterium's ability to degrade polycaprolactone. The annotation revealed proteins related to deep-sea survival, such as cold-shock proteins (six) and desaturases (three). The presence of secondary metabolite biosynthetic gene clusters suggests that this bacterium could produce nonribosomal peptides, polyunsaturated fatty acids, and bacteriocins. To demonstrate the potential of this genome, a lipase was cloned an introduced into Escherichia coli. The lipase was purified and characterized, showing activity over a wide temperature range (over 50% at 20-60 °C) and pH range (over 80% at pH 6.3 to 9). This enzyme has tolerance to the surfactant action of sodium dodecyl sulfate and shows 30% increased activity when subjected to a working pressure of 200 MPa. The genomic characterization of Moritella sp. JT01 reveals traits associated with survival in the deep-sea and their potential uses in biotechnology, as exemplified by the characterized lipase.

Indexed as

Genome, BacterialAquatic OrganismsBacterial ProteinsCold TemperatureEscherichia coliEsterasesLipaseMoritellaPolyestersPressureSequence Analysis, DNASodium Dodecyl SulfateBacterial ProteinsEsterasesLipasepolycaprolactonePolyestersSodium Dodecyl SulfateBioprospectingGenomicHeterologous expressionLipaseMarine bacteria

Identifiers

PMID28733934
OpenAlexW2736585214

What OpenQuestion holds

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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.