Evidence map›Paper›PMID 40194273›Full record

ArticleAnalytical chemistry2025

Monitoring the Metabolic Activity of a Single Bacterial Cell Based on Scattering Intensity.

Akira Tokonami, Miya Kawanaka, Hikaru Ikeda, Shigeki Nishii, Takashi Kamegawa, Yojiro Yamamoto, Yasuhiro Sadanaga, Hiroshi Shiigi

Abstract read
In one paragraph

Article in Analytical chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Optical analysis of bacterial metabolic activity and spore germination via formazan formation.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2026
    Article
  2. 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

8 authors.

Akira TokonamiDepartment of Applied Chemistry, Osaka Metropolitan University, 1-2 Gakuen, Naka, Sakai, Osaka 599-8570, Japan.
Miya KawanakaDepartment of Applied Chemistry, Osaka Metropolitan University, 1-2 Gakuen, Naka, Sakai, Osaka 599-8570, Japan.
Hikaru IkedaDepartment of Applied Chemistry, Osaka Metropolitan University, 1-2 Gakuen, Naka, Sakai, Osaka 599-8570, Japan.
Shigeki NishiiDepartment of Applied Chemistry, Osaka Metropolitan University, 1-2 Gakuen, Naka, Sakai, Osaka 599-8570, Japan.
Takashi KamegawaDepartment of Applied Chemistry, Osaka Metropolitan University, 1-2 Gakuen, Naka, Sakai, Osaka 599-8570, Japan.
Yojiro YamamotoDepartment of Applied Chemistry, Osaka Metropolitan University, 1-2 Gakuen, Naka, Sakai, Osaka 599-8570, Japan.
Yasuhiro SadanagaDepartment of Applied Chemistry, Osaka Metropolitan University, 1-2 Gakuen, Naka, Sakai, Osaka 599-8570, Japan.
Hiroshi ShiigiDepartment of Applied Chemistry, Osaka Metropolitan University, 1-2 Gakuen, Naka, Sakai, Osaka 599-8570, Japan.ORCID 0000-0002-1664-7816

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell activity is evaluated using the number of colonies formed on a medium or the number of live cells in a suspension or by staining nuclei with fluorescent dyes to determine whether cells are dead. However, the culture methods generally require extended culturing times, and damage to the cell membranes observed using fluorescent dyes is not necessarily related to cell survival or activity. Hence, accurately determining the activities of individual cells is impossible. Therefore, we developed a method for quantitatively evaluating the metabolic activities of single cells by focusing on the optical and chemical properties of formazan dye, i.e., 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT). The oxidized form of MTT is soluble and highly permeable to cell membranes, but it is reduced to insoluble MTT formazan upon reaction with intracellular metabolic products. Single-cell observation using dark-field microscopy revealed that insoluble formazan aggregates within the cells formed particles that emitted characteristic scattered light. The formazan-derived scattered light component extracted via peak fitting was related to metabolic activity, demonstrating its usefulness as a parameter indicating the activity of an individual cell. This method enables the real-time evaluation of the activities of single cells, which should lead to not only the acceleration of bacterial screening and microbial control but also the development of antibiotics and suppression of drug-resistant bacteria.

Indexed as

Escherichia coliSingle-Cell AnalysisTetrazolium SaltsFormazansScattering, RadiationThiazolesFormazansTetrazolium SaltsThiazolesthiazolyl blue

Identifiers

PMID40194273
PMCPMC12019773

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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.