Evidence map›Paper›PMID 35906439›Full record

ArticleApplied microbiology and biotechnology2022

Evaluation of a bacterial group 1 LEA protein as an enzyme protectant from stress-induced inactivation.

Enrique Raga-Carbajal, Guadalupe Espin, Marcela Ayala, Julieta Rodríguez-Salazar, Liliana Pardo-López

Abstract read
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In one paragraph

Article in Applied microbiology and biotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 28% 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

3 citing papers in PubMed, 9 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 2 institutions in 1 country.

Enrique Raga-CarbajalDepartamento de Microbiología Molecular, Instituto de Biotecnología, UNAM, Av. Universidad #2001, Col. Chamilpa, 62210, Cuernavaca, Morelos, Mexico.
Guadalupe EspinDepartamento de Microbiología Molecular, Instituto de Biotecnología, UNAM, Av. Universidad #2001, Col. Chamilpa, 62210, Cuernavaca, Morelos, Mexico.
Marcela AyalaDepartamento de Ingeniería Celular Y Biocatálisis, Instituto de Biotecnología, UNAM, Av. Universidad #2001, Col. Chamilpa, 62210, Cuernavaca, Morelos, Mexico.
Julieta Rodríguez-SalazarDepartamento de Microbiología Molecular, Instituto de Biotecnología, UNAM, Av. Universidad #2001, Col. Chamilpa, 62210, Cuernavaca, Morelos, Mexico. sjulietars@gmail.com.ORCID http://orcid.org/0000-0003-1565-8027
Liliana Pardo-LópezDepartamento de Microbiología Molecular, Instituto de Biotecnología, UNAM, Av. Universidad #2001, Col. Chamilpa, 62210, Cuernavaca, Morelos, Mexico. liliana.pardo@ibt.unam.mx.
Universidad Americana de Morelos · MXUniversidad Autónoma del Estado de Morelos · MX

Funding

PAPIIT DGAPA IN207019
6 · The paper itself

Abstract

Late embryogenesis abundant (LEA) proteins are hydrophilic proteins that lack a well-ordered tertiary structure and accumulate to high levels in response to water deficit, in organisms such as plants, fungi, and bacteria. The mechanisms proposed to protect cellular structures and enzymes are water replacement, ion sequestering, and membrane stabilization. The activity of some proteins has a limited shelf-life due to instability that can be caused by their structure or the presence of a stress condition that limits their activity; several LEA proteins have been shown to behave as cryoprotectants in vitro. Here, we report a group1 LEA from Azotobacter vinelandii AvLEA1, capable of conferring protection to lactate dehydrogenase, catechol dioxygenase, and Baylase peroxidase against freeze-thaw treatments, desiccation, and oxidative damage, making AvLEA a promising biological stabilizer reagent. This is the first evidence of protection provided by this LEA on enzymes with biotechnological potential, such as dioxygenase and peroxidase under in vitro stress conditions. Our results suggest that AvLEA could act as a molecular chaperone, or a "molecular shield," preventing either dissociation or antiaggregation, or as a radical scavenger, thus preventing damage to these target enzymes during induced stress. KEY POINTS: • This work expands the basic knowledge of the less-known bacterial LEA proteins and their in vitro protection potential. • AvLEA is a bacterial protein that confers in vitro protection to three enzymes with different characteristics and oligomeric arrangement. • The use of AvLEA as a stabilizer agent could be further explored using dioxygenase and peroxidase in bioremediation treatments. AvLEA1 protects against freeze-thaw treatments, desiccation, and oxidative damage on three different enzymes with biotechnological potential.

Indexed as

Bacterial ProteinsDioxygenasesEmbryonic DevelopmentPeroxidasesPlant ProteinsWaterBacterial ProteinsDioxygenasesPeroxidasesPlant ProteinsWaterAzotobacter vinelandiiCryoprotectionDesiccationExcipientsOxidative inactivation

Identifiers

PMID35906439
OpenAlexW4288685649

What OpenQuestion holds

Textmetadata
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.