Evidence map›Paper›PMID 28002476›Full record

ArticlePloS one2016

Bg10: A Novel Metagenomics Alcohol-Tolerant and Glucose-Stimulated GH1 ß-Glucosidase Suitable for Lactose-Free Milk Preparation.

Elisângela Soares Gomes-Pepe, Elwi Guillermo Machado Sierra, Mariana Rangel Pereira, Tereza Cristina Luque Castellane, Eliana Gertrudes de Macedo Lemos

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

5 citing papers in PubMed, 24 citations in OpenAlex.

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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

5 authors at 1 institution in 2 countries.

Elisângela Soares Gomes-PepeDepartment of Technology, São Paulo State University (Unesp), School of Agricultural and Veterinarian Sciences, Jaboticabal. Via de Acesso Prof. Paulo Donato Castellane S/N, km 5, CEP, Jaboticabal, São Paulo State, Brazil.
Elwi Guillermo Machado SierraDepartment of Technology, São Paulo State University (Unesp), School of Agricultural and Veterinarian Sciences, Jaboticabal. Via de Acesso Prof. Paulo Donato Castellane S/N, km 5, CEP, Jaboticabal, São Paulo State, Brazil.
Mariana Rangel PereiraDepartment of Technology, São Paulo State University (Unesp), School of Agricultural and Veterinarian Sciences, Jaboticabal. Via de Acesso Prof. Paulo Donato Castellane S/N, km 5, CEP, Jaboticabal, São Paulo State, Brazil.
Tereza Cristina Luque CastellaneDepartment of Technology, São Paulo State University (Unesp), School of Agricultural and Veterinarian Sciences, Jaboticabal. Via de Acesso Prof. Paulo Donato Castellane S/N, km 5, CEP, Jaboticabal, São Paulo State, Brazil.
Eliana Gertrudes de Macedo LemosDepartment of Technology, São Paulo State University (Unesp), School of Agricultural and Veterinarian Sciences, Jaboticabal. Via de Acesso Prof. Paulo Donato Castellane S/N, km 5, CEP, Jaboticabal, São Paulo State, Brazil.ORCID http://orcid.org/0000-0002-1119-7748
MRC Laboratory of Molecular Biology · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

New ß-glucosidases with product (glucose) or ethanol tolerances are greatly desired to make industrial processes more marketable and efficient. Therefore, this report describes the in silico/vitro characterization of Bg10, a metagenomically derived homodimeric ß-glucosidase that exhibited a Vmax of 10.81 ± 0.43 μM min-1, Kcat of 175.1± 6.91 min-1, and Km of 0.49 ± 0.12 mM at a neutral pH and 37°C when pNP-ß-D-glucopyranoside was used as the substrate, and the enzyme retained greater than 80% activity within the respective pH and temperature ranges of 6.5 to 8.0 and 35 to 40°C. The enzyme was stimulated by its product, glucose; consequently, the Bg10 activity against 50 and 100 mM of glucose were increased by 36.8% and 22%, respectively, while half of the activity was retained at 350 mM. Moreover, the Bg10 was able to hydrolyse 55% (milk sample) and 100% (purified sugar) of the lactose at low (6°C) and optimum (37°C) temperatures, respectively, suggesting the possibility of further optimization of the reaction for lactose-free dairy production. In addition, the enzyme was able to fully hydrolyse 40 mM of cellobiose at one hour and was tolerant to ethanol up to concentrations of 500 mM (86% of activity), while a 1 M concentration still resulted in 41% residual activity, which could be interesting for biofuel production.

Indexed as

Animalsbeta-GlucosidaseCellobioseEthanolGlucoseHydrogen-Ion ConcentrationHydrolysisKineticsLactoseMetagenomicsMilkPhylogenyProtein StabilityProtein Structure, TertiaryRecombinant ProteinsSubstrate Specificitybeta-GlucosidaseCellobioseEthanolGlucoseLactoseRecombinant Proteins

Identifiers

PMID28002476
PMCPMC5176175
OpenAlexW2567773633

What OpenQuestion holds

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LicenceCC BY
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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.