Evidence map›Paper›PMID 31601209›Full record

ArticleMicrobial cell factories2019

Optimization of Saccharomyces cerevisiae α-galactosidase production and application in the degradation of raffinose family oligosaccharides.

María-Efigenia Álvarez-Cao, María-Esperanza Cerdán, María-Isabel González-Siso, Manuel Becerra

Open access · goldAbstract read
In one paragraph

Article in Microbial cell factories, 2019. 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
3.8field-weighted citation impact, top 7% 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, 37 citations in OpenAlex.

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  6. 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

4 authors at 1 institution in 1 country.

María-Efigenia Álvarez-CaoDepartamento de Bioloxía, Facultade de Ciencias, Centro de Investigacións Científicas Avanzadas (CICA), Universidade da Coruña. Grupo EXPRELA, A Coruña, Spain.
María-Esperanza CerdánDepartamento de Bioloxía, Facultade de Ciencias, Centro de Investigacións Científicas Avanzadas (CICA), Universidade da Coruña. Grupo EXPRELA, A Coruña, Spain.
María-Isabel González-SisoDepartamento de Bioloxía, Facultade de Ciencias, Centro de Investigacións Científicas Avanzadas (CICA), Universidade da Coruña. Grupo EXPRELA, A Coruña, Spain.
Manuel BecerraDepartamento de Bioloxía, Facultade de Ciencias, Centro de Investigacións Científicas Avanzadas (CICA), Universidade da Coruña. Grupo EXPRELA, A Coruña, Spain. manu@udc.es.ORCID http://orcid.org/0000-0003-0913-9749
Universidade da Coruña · ES

Funding

Consellería de Economía, Emprego e Industria, Xunta de Galicia (ES) ED431C 2016-012Fundación Pedro Barrié de la Maza (ES), Fondo de Investigación en Ciencia Bio-alfa-gal
6 · The paper itself

Abstract

backgroundα-Galactosidases are enzymes that act on galactosides present in many vegetables, mainly legumes and cereals, have growing importance with respect to our diet. For this reason, the use of their catalytic activity is of great interest in numerous biotechnological applications, especially those in the food industry directed to the degradation of oligosaccharides derived from raffinose. The aim of this work has been to optimize the recombinant production and further characterization of α-galactosidase of Saccharomyces cerevisiae.

resultsThe MEL1 gene coding for the α-galactosidase of S. cerevisiae (ScAGal) was cloned and expressed in the S. cerevisiae strain BJ3505. Different constructions were designed to obtain the degree of purification necessary for enzymatic characterization and to improve the productive process of the enzyme. ScAGal has greater specificity for the synthetic substrate p-nitrophenyl-α-D-galactopyranoside than for natural substrates, followed by the natural glycosides, melibiose, raffinose and stachyose; it only acts on locust bean gum after prior treatment with β-mannosidase. Furthermore, this enzyme strongly resists proteases, and shows remarkable activation in their presence. Hydrolysis of galactose bonds linked to terminal non-reducing mannose residues of synthetic galactomannan-oligosaccharides confirms that ScAGal belongs to the first group of α-galactosidases, according to substrate specificity. Optimization of culture conditions by the statistical model of Response Surface helped to improve the productivity by up to tenfold when the concentration of the carbon source and the aeration of the culture medium was increased, and up to 20 times to extend the cultivation time to 216 h.

conclusionsScAGal characteristics and improvement in productivity that have been achieved contribute in making ScAGal a good candidate for application in the elimination of raffinose family oligosaccharides found in many products of the food industry.

Indexed as

alpha-GalactosidaseKineticsRaffinoseSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSubstrate Specificityalpha-GalactosidaseRaffinoseSaccharomyces cerevisiae ProteinsBiochemical characterizationProduction optimizationRaffinose family oligosaccharidesSaccharomyces cerevisiaeα-Galactosidase

Identifiers

PMID31601209
PMCPMC6786279
OpenAlexW2979805961

What OpenQuestion holds

Textmetadata
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.