Impact of Zero-Valent Iron Nanoparticles and Ampicillin on Adenosine Triphosphate and Lactate Metabolism in the Cyanobacterium <i>Fremyella diplosiphon</i>

In cyanobacteria, the interplay of ATP and lactate dynamics underpins cellular energetics; their pronounced shifts in response to zero-valent iron (nZVI) nanoparticles and ampicillin highlight the nuanced metabolic adaptations to environmental challenges. In this study, we investigated the impact of...

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Main Authors: Yavuz S. Yalcin, Busra N. Aydin, Viji Sitther
Format: Article
Language:English
Published: MDPI AG 2024-03-01
Series:Microorganisms
Subjects:
Online Access:https://www.mdpi.com/2076-2607/12/3/612
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author Yavuz S. Yalcin
Busra N. Aydin
Viji Sitther
author_facet Yavuz S. Yalcin
Busra N. Aydin
Viji Sitther
author_sort Yavuz S. Yalcin
collection DOAJ
description In cyanobacteria, the interplay of ATP and lactate dynamics underpins cellular energetics; their pronounced shifts in response to zero-valent iron (nZVI) nanoparticles and ampicillin highlight the nuanced metabolic adaptations to environmental challenges. In this study, we investigated the impact of nZVIs and ampicillin on <i>Fremyella diplosiphon</i> cellular energetics as determined by adenosine triphosphate (ATP) content, intracellular and extracellular lactate levels, and their impact on cell morphology as visualized by transmission electron microscopy. While a significant increase in ATP concentration was observed in 0.8 mg/L ampicillin-treated cells compared to the untreated control, a significant decline was noted in cells treated with 3.2 mg/L nZVIs. ATP levels in the combination regimen of 0.8 mg/L ampicillin and 3.2 mg/L nZVIs were significantly elevated (<i>p</i> < 0.05) compared to the 3.2 mg/L nZVI treatment. Intracellular and extracellular lactate levels were significantly higher in 0.8 mg/L ampicillin, 3.2 mg/L nZVIs, and the combination regimen compared to the untreated control; however, extracellular lactate levels were the highest in cells treated with 3.2 mg/L nZVIs. Visualization of morphological changes indicated increased thylakoid membrane stacks and inter-thylakoidal distances in 3.2 mg/L nZVI-treated cells. Our findings demonstrate a complex interplay of nanoparticle and antibiotic-induced responses, highlighting the differential impact of these stressors on <i>F. diplosiphon</i> metabolism and cellular integrity.
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spelling doaj.art-0e31c24cfe884b15b569fb2ccbfedc9e2024-03-27T13:56:00ZengMDPI AGMicroorganisms2076-26072024-03-0112361210.3390/microorganisms12030612Impact of Zero-Valent Iron Nanoparticles and Ampicillin on Adenosine Triphosphate and Lactate Metabolism in the Cyanobacterium <i>Fremyella diplosiphon</i>Yavuz S. Yalcin0Busra N. Aydin1Viji Sitther2Department of Biology, Morgan State University, 1700 E. Cold Spring Lane, Baltimore, MD 21251, USADepartment of Biology, Morgan State University, 1700 E. Cold Spring Lane, Baltimore, MD 21251, USADepartment of Biology, Morgan State University, 1700 E. Cold Spring Lane, Baltimore, MD 21251, USAIn cyanobacteria, the interplay of ATP and lactate dynamics underpins cellular energetics; their pronounced shifts in response to zero-valent iron (nZVI) nanoparticles and ampicillin highlight the nuanced metabolic adaptations to environmental challenges. In this study, we investigated the impact of nZVIs and ampicillin on <i>Fremyella diplosiphon</i> cellular energetics as determined by adenosine triphosphate (ATP) content, intracellular and extracellular lactate levels, and their impact on cell morphology as visualized by transmission electron microscopy. While a significant increase in ATP concentration was observed in 0.8 mg/L ampicillin-treated cells compared to the untreated control, a significant decline was noted in cells treated with 3.2 mg/L nZVIs. ATP levels in the combination regimen of 0.8 mg/L ampicillin and 3.2 mg/L nZVIs were significantly elevated (<i>p</i> < 0.05) compared to the 3.2 mg/L nZVI treatment. Intracellular and extracellular lactate levels were significantly higher in 0.8 mg/L ampicillin, 3.2 mg/L nZVIs, and the combination regimen compared to the untreated control; however, extracellular lactate levels were the highest in cells treated with 3.2 mg/L nZVIs. Visualization of morphological changes indicated increased thylakoid membrane stacks and inter-thylakoidal distances in 3.2 mg/L nZVI-treated cells. Our findings demonstrate a complex interplay of nanoparticle and antibiotic-induced responses, highlighting the differential impact of these stressors on <i>F. diplosiphon</i> metabolism and cellular integrity.https://www.mdpi.com/2076-2607/12/3/612antibioticATPinter-thylakoid distancelactatenZVIs
spellingShingle Yavuz S. Yalcin
Busra N. Aydin
Viji Sitther
Impact of Zero-Valent Iron Nanoparticles and Ampicillin on Adenosine Triphosphate and Lactate Metabolism in the Cyanobacterium <i>Fremyella diplosiphon</i>
Microorganisms
antibiotic
ATP
inter-thylakoid distance
lactate
nZVIs
title Impact of Zero-Valent Iron Nanoparticles and Ampicillin on Adenosine Triphosphate and Lactate Metabolism in the Cyanobacterium <i>Fremyella diplosiphon</i>
title_full Impact of Zero-Valent Iron Nanoparticles and Ampicillin on Adenosine Triphosphate and Lactate Metabolism in the Cyanobacterium <i>Fremyella diplosiphon</i>
title_fullStr Impact of Zero-Valent Iron Nanoparticles and Ampicillin on Adenosine Triphosphate and Lactate Metabolism in the Cyanobacterium <i>Fremyella diplosiphon</i>
title_full_unstemmed Impact of Zero-Valent Iron Nanoparticles and Ampicillin on Adenosine Triphosphate and Lactate Metabolism in the Cyanobacterium <i>Fremyella diplosiphon</i>
title_short Impact of Zero-Valent Iron Nanoparticles and Ampicillin on Adenosine Triphosphate and Lactate Metabolism in the Cyanobacterium <i>Fremyella diplosiphon</i>
title_sort impact of zero valent iron nanoparticles and ampicillin on adenosine triphosphate and lactate metabolism in the cyanobacterium i fremyella diplosiphon i
topic antibiotic
ATP
inter-thylakoid distance
lactate
nZVIs
url https://www.mdpi.com/2076-2607/12/3/612
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AT vijisitther impactofzerovalentironnanoparticlesandampicillinonadenosinetriphosphateandlactatemetabolisminthecyanobacteriumifremyelladiplosiphoni