Changes in the proton potential and the cellular energetics of Escherichia coli during growth by aerobic and anaerobic respiration or by fermentation
Abstract
The energetic parameters of Escherichia coli were analyzed for the aerobic/anaerobic transition. The electrochemical proton potential (Δ p) across the cytoplasmic membrane was determined in the steady state of respiration with O 2, nitrate, fumarate, dimethylsulfoxide (Me 2 SO), and for fermentation. With O 2, a proton potential of −160 mV was obtained. For anaerobic respiration with nitrate, fumarate or Me 2 SO, Δ p decreased only slightly by about 20 mV in contrast to earlier assumptions, whereas Δ p dropped by approximately 40 mV during fermentation. Under all conditions, the membrane potential (Δ @KY) contributed the major portion to Δ p. The cellular ATP levels were highest for aerobic growth (about 13 μmol/g dry cells) and decreased to 3−6 μmol/g in anaerobic metabolism. Δ .cf2.G.cf2..cf1..es.cf1.′.cf5..rb.eiPhos.rb, however, was constant due to equivalent changes of the ADP contents. Transition to the stationary growth phase caused a massive drop in the ATP content. It is concluded that, during anaerobic respiration, the energetic situation for the bacteria is very similar to that for aerobic growth with respect to Δ .cf2.G.cf2..cf1..es.cf1.′.cf5..rb.eiPhos.rb and Δ p whereas, for fermentation, a significant decrease in Δ p was observed. The consequences for the cellular energetics and for the regulation of the aerobic/anaerobic transition are discussed.
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Serpentinization gives rise to inorganic microcompartments and proton gradients of the right polarity and of sufficient magnitude to support chemiosmotic ATP synthesis by the rotor-stator ATP synthase.
“In addition, it gives rise to inorganic microcompartments and proton gradients of the right polarity and of sufficient magnitude to support chemiosmotic ATP synthesis by the rotor-stator ATP synthase.”
From Serpentinization as the source of energy, electrons, organics, catalysts, nutrients and pH gradients for the origin of LUCA and life (2023) · cites this paper as Tran and Unden, 1998
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“At the vent-ocean interface, this generated a natural proton gradient of roughly three pH units, a far greater gradient than the roughly one pH unit or less that modern cells require to power their rotor-stator ATP synthetase (Tran and Unden, 1998; Silverstein, 2014).”
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- Authors
- Tran, Q. H., & Unden, G.
- Affiliations
- Johannes Gutenberg University Mainz (DE)
- ORCID
- Unden, Gottfried
- Venue
- European Journal of Biochemistry
- Publisher
- Wiley
- Published
- 1998-01
- Volume
- 251
- Issue
- 1-2
- Pages
- 538-543
- ISSN
- 0014-2956 (ISSN-L)
- 1432-1033
- OpenAlex
- W2094618690
- Cited by
- 201
- References
- 0
- Citations by year
- 2026: 7 · 2025: 8 · 2024: 9 · 2023: 9 · 2022: 6 · 2021: 13 · 2020: 14 · 2019: 14 · 2018: 8 · 2017: 14 · 2016: 8 · 2015: 12 · 2014: 8 · 2013: 7 · 2012: 4
- FWCI
- 2.87
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- European Journal of Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › ATP Synthase and ATPases Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Microbial metabolism and enzyme function
- Keywords
- Escherichia coli, proton potential, membrane potential, cellular energetics, aerobic-anaerobic transition, anaerobic respiration, nitrate respiration, fumarate respiration, fermentation, ATP levels, ADP, stationary phase, plasma membrane
- MeSH terms
- Adenosine Diphosphate, Adenosine Triphosphate, Aerobiosis, Anaerobiosis, Edetic Acid, Energy Metabolism, Escherichia coli, Fermentation, Membrane Potentials, Phosphorylation, Protons
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