Evidence map›Paper›PMID 27009074›Full record

ArticleAMB Express2016

Marine-derived fungus Aspergillus cf. tubingensis LAMAI 31: a new genetic resource for xylanase production.

Juliana A Dos Santos, Juliana M F Vieira, Alexandre Videira, Lucas A Meirelles, André Rodrigues, Marta H Taniwaki, Lara D Sette

Open access · goldAbstract read
In one paragraph

Article in AMB Express, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 25 citations in OpenAlex.

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  6. Harnessing the sponge microbiome for industrial biocatalysts.Applied microbiology and biotechnology · 2020
    Review
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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

7 authors at 2 institutions in 1 country.

Juliana A Dos SantosDepartamento de Bioquímica e Microbiologia, Universidade Estadual Paulista Júlio de Mesquita Filho-UNESP, 24A, 1515, Rio Claro, SP, 13506-900, Brazil.
Juliana M F VieiraDepartamento de Bioquímica e Microbiologia, Universidade Estadual Paulista Júlio de Mesquita Filho-UNESP, 24A, 1515, Rio Claro, SP, 13506-900, Brazil.
Alexandre VideiraDepartamento de Bioquímica e Microbiologia, Universidade Estadual Paulista Júlio de Mesquita Filho-UNESP, 24A, 1515, Rio Claro, SP, 13506-900, Brazil.
Lucas A MeirellesDepartamento de Bioquímica e Microbiologia, Universidade Estadual Paulista Júlio de Mesquita Filho-UNESP, 24A, 1515, Rio Claro, SP, 13506-900, Brazil.
André RodriguesDepartamento de Bioquímica e Microbiologia, Universidade Estadual Paulista Júlio de Mesquita Filho-UNESP, 24A, 1515, Rio Claro, SP, 13506-900, Brazil.
Marta H TaniwakiInstituto de Tecnologia de Alimentos-ITAL, Campinas, SP, Brazil.
Lara D SetteDepartamento de Bioquímica e Microbiologia, Universidade Estadual Paulista Júlio de Mesquita Filho-UNESP, 24A, 1515, Rio Claro, SP, 13506-900, Brazil. larasette@rc.unesp.br.ORCID http://orcid.org/0000-0002-5980-3786
Universidade Estadual Paulista (Unesp) · BRInstituto de Tecnologia de Alimentos · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Marine-derived fungi have been reported as relevant producers of enzymes, which can have different properties in comparison with their terrestrial counterparts. The aim of the present study was to select from a collection of 493 marine-derived fungi the best producer of xylanase in order to evaluate the enzymatic production under different conditions. A total of 112 isolates produced xylanase in solid medium containing xylan as the carbon source, with 31 of them able to produce at least 10 U/mL of the enzyme. The best production (49.41 U/mL) was achieved by the strain LAMAI 31, identified as Aspergillus cf. tubingensis. After confirming the lack of pathogenicity (absence of ochratoxin A and fumonisin B2 production) this fungus was submitted to the experimental design in order to evaluate the effect of different variables on the enzymatic production, with the aim of optimizing culture conditions. Three experimental designs (two Plackett-Burman and one factorial fractional) were applied. The best condition for the enzymatic production was defined, resulting in an increase of 12.7 times in comparison with the initial production during the screening experiments. In the validation assay, the peak of xylanase production (561.59 U/mL) was obtained after 96 h of incubation, being the best specific activity achieved after 72 h of incubation. Xylanase from A. cf. tubingensis LAMAI 31 had optimum pH and temperature at 5.0 and 55 °C, respectively, and was shown to be stable at a range of 40-50 °C, and in pH from 3.6 to 7.0. Results from the present work indicate that A. cf. tubingensis LAMAI 31 can be considered as a new genetic resource for xylanase production.

Indexed as

Experimental designMarine biotechnologyMarine-derived fungiXylanase

Identifiers

PMID27009074
PMCPMC4805677
OpenAlexW2311270332

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.