Evidence map›Paper›PMID 42911328›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2027

Long-Term Cryopreservation of Pseudomonas spp. for Biobanking and Biotechnology Applications.

José Luis Aguirre-Noyola, José Daniel Chávez-González, Jeiry Toribio-Jiménez, Lorena Jacqueline Gómez-Godínez, Gustavo Cuaxinque-Flores

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2027. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

José Luis Aguirre-NoyolaCentro Nacional de Recursos Genéticos, INIFAP, Tepatitlán de Morelos, Jalisco, Mexico. jaguirrenoyola@outlook.com.
José Daniel Chávez-GonzálezEscuela superior de Ciencias de la Tierra, Doctorado en Recursos Naturales y Ecología. Universidad Autónoma de Guerrero, Guerrero, Mexico.
Jeiry Toribio-JiménezLaboratorio de Microbiología Molecular y Biotecnología Ambiental, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Chilpancingo, Guerrero, Mexico.
Lorena Jacqueline Gómez-GodínezCentro Nacional de Recursos Genéticos, INIFAP, Tepatitlán de Morelos, Jalisco, Mexico.
Gustavo Cuaxinque-FloresDoctorado en Recursos Naturales y Ecología. Universidad Autónoma de Guerrero, Guerrero, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The genus Pseudomonas encompasses one of the most metabolically versatile and ecologically diverse groups among Gram-negative bacteria, comprising over 300 validly described species distributed across virtually all ecosystems. Members of this genus are of considerable relevance in medicine, environmental science, and industrial biotechnology, owing to their capacity to produce a wide array of bioactive compounds, as well as their involvement in biodegradation of xenobiotics and plant growth promotion. Among the most extensively studied representatives are P. aeruginosa and P. putida, which serve as contrasting model strains in pathogenicity research and environmental biotechnology, respectively. Improper storage conditions may compromise key physiological traits of these strains, including pigment production and biosurfactant-synthesizing capacity, thereby limiting their utility in downstream applications. The long-term preservation of Pseudomonas strains in biobanks is therefore essential to safeguard biological material of scientific, biotechnological, and biomedical value. In this chapter, we describe a standardized glycerol-based cryopreservation protocol at -80°C for the long-term preservation of Pseudomonas strains, along with the evaluation of their functional stability following reactivation. The method relies on glycerol as a penetrating cryoprotectant, which minimizes cellular damage associated with ice crystal formation and osmotic stress while preserving cell viability, genetic integrity, and metabolic functionality. Post-reactivation validation includes the assessment of fluorescence emission and the capacity to produce biosurfactants. This protocol provides a reliable and reproducible tool for the preservation of biotechnologically relevant microbial genetic resources.

Indexed as

Biological Specimen BanksBiotechnologyCryopreservationPseudomonasBiosurfactantsCryoprotective AgentsGlycerolCryoprotective AgentsGlycerolBiosurfactantsGlycerolPseudomonas aeruginosaPseudomonas putida

Identifiers

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.