Fluorescence‐based analysis of the intracytoplasmic membranes of type I methanotrophs

Summary Most methanotrophic bacteria maintain intracytoplasmic membranes which house the methane‐oxidizing enzyme, particulate methane monooxygenase. Previous studies have primarily used transmission electron microscopy or cryo‐electron microscopy to look at the structure of these membranes or lipid...

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Main Authors: Kyle T. Whiddon, Ravindra Gudneppanavar, Theodore J. Hammer, Destiny A. West, Michael C. Konopka
Format: Article
Language:English
Published: Wiley 2019-09-01
Series:Microbial Biotechnology
Online Access:https://doi.org/10.1111/1751-7915.13458
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spelling doaj-c7b155f47f5146268f6eb2ef983ae54e2020-11-25T02:57:49ZengWileyMicrobial Biotechnology1751-79152019-09-011251024103310.1111/1751-7915.13458Fluorescence‐based analysis of the intracytoplasmic membranes of type I methanotrophsKyle T. Whiddon0Ravindra Gudneppanavar1Theodore J. Hammer2Destiny A. West3Michael C. Konopka4Department of Chemistry The University of Akron Akron OH USADepartment of Chemistry The University of Akron Akron OH USADepartment of Chemistry The University of Akron Akron OH USADepartment of Chemistry The University of Akron Akron OH USADepartment of Chemistry The University of Akron Akron OH USASummary Most methanotrophic bacteria maintain intracytoplasmic membranes which house the methane‐oxidizing enzyme, particulate methane monooxygenase. Previous studies have primarily used transmission electron microscopy or cryo‐electron microscopy to look at the structure of these membranes or lipid extraction methods to determine the per cent of cell dry weight composed of lipids. We show an alternative approach using lipophilic membrane probes and other fluorescent dyes to assess the extent of intracytoplasmic membrane formation in living cells. This fluorescence method is sensitive enough to show not only the characteristic shift in intracytoplasmic membrane formation that is present when methanotrophs are grown with or without copper, but also differences in intracytoplasmic membrane levels at intermediate copper concentrations. This technique can also be employed to monitor dynamic intracytoplasmic membrane changes in the same cell in real time under changing growth conditions. We anticipate that this approach will be of use to researchers wishing to visualize intracytoplasmic membranes who may not have access to electron microscopes. It will also have the capability to relate membrane changes in individual living cells to other measurements by fluorescence labelling or other single‐cell analysis methods.https://doi.org/10.1111/1751-7915.13458
collection DOAJ
language English
format Article
sources DOAJ
author Kyle T. Whiddon
Ravindra Gudneppanavar
Theodore J. Hammer
Destiny A. West
Michael C. Konopka
spellingShingle Kyle T. Whiddon
Ravindra Gudneppanavar
Theodore J. Hammer
Destiny A. West
Michael C. Konopka
Fluorescence‐based analysis of the intracytoplasmic membranes of type I methanotrophs
Microbial Biotechnology
author_facet Kyle T. Whiddon
Ravindra Gudneppanavar
Theodore J. Hammer
Destiny A. West
Michael C. Konopka
author_sort Kyle T. Whiddon
title Fluorescence‐based analysis of the intracytoplasmic membranes of type I methanotrophs
title_short Fluorescence‐based analysis of the intracytoplasmic membranes of type I methanotrophs
title_full Fluorescence‐based analysis of the intracytoplasmic membranes of type I methanotrophs
title_fullStr Fluorescence‐based analysis of the intracytoplasmic membranes of type I methanotrophs
title_full_unstemmed Fluorescence‐based analysis of the intracytoplasmic membranes of type I methanotrophs
title_sort fluorescence‐based analysis of the intracytoplasmic membranes of type i methanotrophs
publisher Wiley
series Microbial Biotechnology
issn 1751-7915
publishDate 2019-09-01
description Summary Most methanotrophic bacteria maintain intracytoplasmic membranes which house the methane‐oxidizing enzyme, particulate methane monooxygenase. Previous studies have primarily used transmission electron microscopy or cryo‐electron microscopy to look at the structure of these membranes or lipid extraction methods to determine the per cent of cell dry weight composed of lipids. We show an alternative approach using lipophilic membrane probes and other fluorescent dyes to assess the extent of intracytoplasmic membrane formation in living cells. This fluorescence method is sensitive enough to show not only the characteristic shift in intracytoplasmic membrane formation that is present when methanotrophs are grown with or without copper, but also differences in intracytoplasmic membrane levels at intermediate copper concentrations. This technique can also be employed to monitor dynamic intracytoplasmic membrane changes in the same cell in real time under changing growth conditions. We anticipate that this approach will be of use to researchers wishing to visualize intracytoplasmic membranes who may not have access to electron microscopes. It will also have the capability to relate membrane changes in individual living cells to other measurements by fluorescence labelling or other single‐cell analysis methods.
url https://doi.org/10.1111/1751-7915.13458
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