Evidence map›Paper›PMID 34613759›Full record

ArticleApplied and environmental microbiology2021

Removal of Toxic Volatile Compounds in Batch Culture Prolongs Stationary Phase and Delays Death of Escherichia coli.

Melisa G Osborne, Christopher J Geiger, Christopher H Corzett, Karin E Kram, Steven E Finkel

Open access · greenAbstract read
In one paragraph

Article in Applied and environmental microbiology, 2021. 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 24% 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, 10 citations in OpenAlex.

  1. Article
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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 1 institution in 1 country.

Melisa G Osborne *Molecular and Computational Biology Section, Department of Biological Sciences, University of Southern Californiagrid.42505.36, Los Angeles, California, USA.
Christopher J Geiger *Molecular and Computational Biology Section, Department of Biological Sciences, University of Southern Californiagrid.42505.36, Los Angeles, California, USA.
Christopher H CorzettMolecular and Computational Biology Section, Department of Biological Sciences, University of Southern Californiagrid.42505.36, Los Angeles, California, USA.
Karin E KramMolecular and Computational Biology Section, Department of Biological Sciences, University of Southern Californiagrid.42505.36, Los Angeles, California, USA.ORCID 0000-0001-8811-8449
Steven E FinkelMolecular and Computational Biology Section, Department of Biological Sciences, University of Southern Californiagrid.42505.36, Los Angeles, California, USA.ORCID 0000-0003-1715-6696
University of Southern California · US

Funding

US Army Research Office W911NF1010444
6 · The paper itself

Abstract

The mechanisms controlling entry into and exit from the death phase in the bacterial life cycle remain unclear. Although bacterial growth studies in batch cultures traditionally focus on the first three phases during incubation, two additional phases, the death phase and the long-term stationary phase, are less understood. Although there are a number of stressors that arise during long-term batch culture, including nutrient depletion and the accumulation of metabolic toxins such as reactive oxidative species, their roles in cell death are not well-defined. By manipulating the environmental conditions of Escherichia coli incubated in long-term batch culture through chemical and mechanical means, we investigated the role of volatile metabolic toxins in modulating the onset of the death phase. Here, we demonstrate that with the introduction of substrates with high binding affinities for volatile compounds, toxic by-products of normal cell metabolism, into the headspace of batch cultures, cells display a prolonged stationary phase and delayed entry into the death phase. The addition of these substrates allows cultures to maintain a high cell density for hours to days longer than cultures incubated under standard growth conditions. A similar effect is observed when the gaseous headspace in culture flasks is continuously replaced with sterile air, mechanically preventing the accumulation of metabolic by-products in batch cultures. We establish that toxic compound(s) are produced during the exponential phase, demonstrate that buildup of toxic by-products influence entry into the death phase, and present a novel tool for improving high-density growth in batch culture that may be used in future research or industrial or biotechnology applications.

Indexed as

Batch Cell Culture TechniquesEscherichia coliCell CycleIndustrial MicrobiologyVolatile Organic CompoundsVolatile Organic Compoundsculture viabilitylong-term survivalstationary phase

Identifiers

PMID34613759
PMCPMC8612265
OpenAlexW3204753111

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.