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Metabolomic Fingerprints of Individual Algal Cells Using the Single-Probe Mass Spectrometry Technique

Traditional approaches for the assessment of physiological responses of microbes in the environment rely on bulk filtration techniques that obscure differences among populations as well as among individual cells. Here, were report on the development on a novel micro-scale sampling device, referred t...

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Autores principales: Sun, Mei, Yang, Zhibo, Wawrik, Boris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5936784/
https://www.ncbi.nlm.nih.gov/pubmed/29760716
http://dx.doi.org/10.3389/fpls.2018.00571
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author Sun, Mei
Yang, Zhibo
Wawrik, Boris
author_facet Sun, Mei
Yang, Zhibo
Wawrik, Boris
author_sort Sun, Mei
collection PubMed
description Traditional approaches for the assessment of physiological responses of microbes in the environment rely on bulk filtration techniques that obscure differences among populations as well as among individual cells. Here, were report on the development on a novel micro-scale sampling device, referred to as the “Single-probe,” which allows direct extraction of metabolites from living, individual phytoplankton cells for mass spectrometry (MS) analysis. The Single-probe is composed of dual-bore quartz tubing which is pulled using a laser pipette puller and fused to a silica capillary and a nano-ESI. For this study, we applied Single-probe MS technology to the marine dinoflagellate Scrippsiella trochoidea, assaying cells grown under different illumination levels and under nitrogen (N) limiting conditions as a proof of concept for the technology. In both experiments, significant differences in the cellular metabolome of individual cells could readily be identified, though the vast majority of detected metabolites could not be assigned to KEGG pathways. Using the same approach, significant changes in cellular lipid complements were observed, with individual lipids being both up- and down-regulated under light vs. dark conditions. Conversely, lipid content increased across the board under N limitation, consistent with an adjustment of Redfield stoichiometry to reflect higher C:N and C:P ratios. Overall, these data suggest that the Single-probe MS technique has the potential to allow for near in situ metabolomic analysis of individual phytoplankton cells, opening the door to targeted analyses that minimize cell manipulation and sampling artifacts, while preserving metabolic variability at the cellular level.
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spelling pubmed-59367842018-05-14 Metabolomic Fingerprints of Individual Algal Cells Using the Single-Probe Mass Spectrometry Technique Sun, Mei Yang, Zhibo Wawrik, Boris Front Plant Sci Plant Science Traditional approaches for the assessment of physiological responses of microbes in the environment rely on bulk filtration techniques that obscure differences among populations as well as among individual cells. Here, were report on the development on a novel micro-scale sampling device, referred to as the “Single-probe,” which allows direct extraction of metabolites from living, individual phytoplankton cells for mass spectrometry (MS) analysis. The Single-probe is composed of dual-bore quartz tubing which is pulled using a laser pipette puller and fused to a silica capillary and a nano-ESI. For this study, we applied Single-probe MS technology to the marine dinoflagellate Scrippsiella trochoidea, assaying cells grown under different illumination levels and under nitrogen (N) limiting conditions as a proof of concept for the technology. In both experiments, significant differences in the cellular metabolome of individual cells could readily be identified, though the vast majority of detected metabolites could not be assigned to KEGG pathways. Using the same approach, significant changes in cellular lipid complements were observed, with individual lipids being both up- and down-regulated under light vs. dark conditions. Conversely, lipid content increased across the board under N limitation, consistent with an adjustment of Redfield stoichiometry to reflect higher C:N and C:P ratios. Overall, these data suggest that the Single-probe MS technique has the potential to allow for near in situ metabolomic analysis of individual phytoplankton cells, opening the door to targeted analyses that minimize cell manipulation and sampling artifacts, while preserving metabolic variability at the cellular level. Frontiers Media S.A. 2018-04-30 /pmc/articles/PMC5936784/ /pubmed/29760716 http://dx.doi.org/10.3389/fpls.2018.00571 Text en Copyright © 2018 Sun, Yang and Wawrik. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Sun, Mei
Yang, Zhibo
Wawrik, Boris
Metabolomic Fingerprints of Individual Algal Cells Using the Single-Probe Mass Spectrometry Technique
title Metabolomic Fingerprints of Individual Algal Cells Using the Single-Probe Mass Spectrometry Technique
title_full Metabolomic Fingerprints of Individual Algal Cells Using the Single-Probe Mass Spectrometry Technique
title_fullStr Metabolomic Fingerprints of Individual Algal Cells Using the Single-Probe Mass Spectrometry Technique
title_full_unstemmed Metabolomic Fingerprints of Individual Algal Cells Using the Single-Probe Mass Spectrometry Technique
title_short Metabolomic Fingerprints of Individual Algal Cells Using the Single-Probe Mass Spectrometry Technique
title_sort metabolomic fingerprints of individual algal cells using the single-probe mass spectrometry technique
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5936784/
https://www.ncbi.nlm.nih.gov/pubmed/29760716
http://dx.doi.org/10.3389/fpls.2018.00571
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