Evidence map›Paper›PMID 35013471›Full record

ArticleScientific reports2022

Relationship between delayed luminescence emission and mitochondrial status in Saccharomyces cerevisiae.

Miao Tian, Qing Li, Yang Liu, Peng Zheng, Danyu Li, Yanpeng Zhao, Bing Wang, Chenhao Li, Jing Wang, Peng Gao and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2022. 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
–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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Ultra weak photon emission-a brief review.Frontiers in physiology · 2024
    Review
  4. Article
  5. Non-chemical signalling between mitochondria.Frontiers in physiology · 2023
    Article
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

13 authors.

Miao Tian *ENNOVA Institute of Life Science and Technology, ENN Group, South District of ENN Industrial Park, Langfang, 065001, Hebei, China.
Qing Li *ENNOVA Institute of Life Science and Technology, ENN Group, South District of ENN Industrial Park, Langfang, 065001, Hebei, China.
Yang LiuENNOVA Institute of Life Science and Technology, ENN Group, South District of ENN Industrial Park, Langfang, 065001, Hebei, China.
Peng ZhengENNOVA Institute of Life Science and Technology, ENN Group, South District of ENN Industrial Park, Langfang, 065001, Hebei, China.
Danyu LiENNOVA Institute of Life Science and Technology, ENN Group, South District of ENN Industrial Park, Langfang, 065001, Hebei, China.
Yanpeng ZhaoENNOVA Institute of Life Science and Technology, ENN Group, South District of ENN Industrial Park, Langfang, 065001, Hebei, China.
Bing WangENNOVA Institute of Life Science and Technology, ENN Group, South District of ENN Industrial Park, Langfang, 065001, Hebei, China.
Chenhao LiENNOVA Institute of Life Science and Technology, ENN Group, South District of ENN Industrial Park, Langfang, 065001, Hebei, China.
Jing WangENNOVA Institute of Life Science and Technology, ENN Group, South District of ENN Industrial Park, Langfang, 065001, Hebei, China.
Peng GaoENNOVA Institute of Life Science and Technology, ENN Group, South District of ENN Industrial Park, Langfang, 065001, Hebei, China.
Qing TangENNOVA Institute of Life Science and Technology, ENN Group, South District of ENN Industrial Park, Langfang, 065001, Hebei, China.
Xiaochun ZhangENNOVA Institute of Life Science and Technology, ENN Group, South District of ENN Industrial Park, Langfang, 065001, Hebei, China.
Hong WuENNOVA Institute of Life Science and Technology, ENN Group, South District of ENN Industrial Park, Langfang, 065001, Hebei, China. wuhong@enn.cn.

Funding

ENN Research Fund 202105
6 · The paper itself

Abstract

Delayed luminescence (DL) is gradually used in various detection of biological systems as a rapid detection technique, however, its biological mechanism was still not clear. In this study, a new model of DL detection system for liquid biological samples is established to investigate the DL emission of Saccharomyces cerevisiae cells cultured in different glucose concentrations. We analyzed the relationship between the DL emission and cell growth, cell vitality, mitochondrial morphology, mitochondrial DNA (mtDNA) copy number, adenosine triphosphate (ATP), oxygen consumption rate (OCR), as well as mitochondria membrane potential (MMP) in S. cerevisiae cells cultured with 0.01, 0.05, 0.15, 3, 10 and 20 g/L glucose respectively. It was found that the DL emission had strong correlation with mitochondrial morphology, OCR, and MMP. The results suggested that DL is an indicator of mitochondria status under different glucose supply conditions, and may be an effective method to detect mitochondrial metabolism related disorders.

Indexed as

Energy MetabolismAdenosine TriphosphateDNA, FungalDNA, MitochondrialGlucoseLuminescent MeasurementsMembrane Potential, MitochondrialMicroscopy, ConfocalMicroscopy, FluorescenceMitochondriaOxygen ConsumptionSaccharomyces cerevisiaeSpectrometry, FluorescenceTime FactorsAdenosine TriphosphateDNA, FungalDNA, MitochondrialGlucose

Identifiers

PMID35013471
PMCPMC8748773

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.