Bioelectroanalytical Detection of Lactic Acid Bacteria

Lactic acid bacteria (LAB) are an industrial important group of organisms that are notable for their inability to respire without growth supplements. Recently described bioelectroanalytical detectors that can specifically detect and enumerate microorganisms depend on a phenomenon known as extracellu...

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Main Authors: Evelina Jing Ying Han, Lola Gonzalez Olias, Stefan Wuertz, Jamie Hinks
Format: Article
Language:English
Published: MDPI AG 2022-01-01
Series:Applied Sciences
Subjects:
Online Access:https://www.mdpi.com/2076-3417/12/3/1257
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author Evelina Jing Ying Han
Lola Gonzalez Olias
Stefan Wuertz
Jamie Hinks
author_facet Evelina Jing Ying Han
Lola Gonzalez Olias
Stefan Wuertz
Jamie Hinks
author_sort Evelina Jing Ying Han
collection DOAJ
description Lactic acid bacteria (LAB) are an industrial important group of organisms that are notable for their inability to respire without growth supplements. Recently described bioelectroanalytical detectors that can specifically detect and enumerate microorganisms depend on a phenomenon known as extracellular electron transport (EET) for effective detection. EET is often described as a type of microbial respiration, which logically excludes LAB from such a detection platform. However, members of the LAB have recently been described as electroactive with the ability to carry out EET, providing a timely impetus to revisit the utility of bioelectroanalytical detectors in LAB detection. Here, we show that an LAB, <i>Enterococcus faecalis</i>, is easily detected bioelectroanalytically using the defined substrate resorufin-β-<span style="font-variant: small-caps;">d</span>-galactopyranoside. Detection is rapid, ranging from 34 to 235 min for inoculum sizes between 10<sup>7</sup> and 10<sup>4</sup> CFU mL<sup>−1</sup>, respectively. We show that, although the signal achieved by <i>Enterococcus faecalis</i> is comparable to systems that rely on the respiratory EET strategies of target bacteria, <i>E. faecalis</i> is not dependent on the electrode for energy, and it is only necessary to capture small amounts of an organism’s metabolic energy to, in this case 1.6%, to achieve good detection. The results pave the way for new means of detecting an industrially important group of organisms, particularly in the food industry.
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spelling doaj.art-7a14fa11e4e44200af0c75364eaf53032023-11-23T15:54:33ZengMDPI AGApplied Sciences2076-34172022-01-01123125710.3390/app12031257Bioelectroanalytical Detection of Lactic Acid BacteriaEvelina Jing Ying Han0Lola Gonzalez Olias1Stefan Wuertz2Jamie Hinks3Singapore Centre for Environmental Life Sciences Engineering (SCELSE), Nanyang Technological University, 60 Nanyang Drive, Singapore 637551, SingaporeCentre for Biosensors, Bioelectronics and Biodevices (C3Bio), Department of Chemical Engineering, University of Bath, Bath BA2 7AY, UKSingapore Centre for Environmental Life Sciences Engineering (SCELSE), Nanyang Technological University, 60 Nanyang Drive, Singapore 637551, SingaporeSingapore Centre for Environmental Life Sciences Engineering (SCELSE), Nanyang Technological University, 60 Nanyang Drive, Singapore 637551, SingaporeLactic acid bacteria (LAB) are an industrial important group of organisms that are notable for their inability to respire without growth supplements. Recently described bioelectroanalytical detectors that can specifically detect and enumerate microorganisms depend on a phenomenon known as extracellular electron transport (EET) for effective detection. EET is often described as a type of microbial respiration, which logically excludes LAB from such a detection platform. However, members of the LAB have recently been described as electroactive with the ability to carry out EET, providing a timely impetus to revisit the utility of bioelectroanalytical detectors in LAB detection. Here, we show that an LAB, <i>Enterococcus faecalis</i>, is easily detected bioelectroanalytically using the defined substrate resorufin-β-<span style="font-variant: small-caps;">d</span>-galactopyranoside. Detection is rapid, ranging from 34 to 235 min for inoculum sizes between 10<sup>7</sup> and 10<sup>4</sup> CFU mL<sup>−1</sup>, respectively. We show that, although the signal achieved by <i>Enterococcus faecalis</i> is comparable to systems that rely on the respiratory EET strategies of target bacteria, <i>E. faecalis</i> is not dependent on the electrode for energy, and it is only necessary to capture small amounts of an organism’s metabolic energy to, in this case 1.6%, to achieve good detection. The results pave the way for new means of detecting an industrially important group of organisms, particularly in the food industry.https://www.mdpi.com/2076-3417/12/3/1257lactic acid bacteriaextracellular electron transfermicrobial detection<i>E. faecalis</i>redox mediator
spellingShingle Evelina Jing Ying Han
Lola Gonzalez Olias
Stefan Wuertz
Jamie Hinks
Bioelectroanalytical Detection of Lactic Acid Bacteria
Applied Sciences
lactic acid bacteria
extracellular electron transfer
microbial detection
<i>E. faecalis</i>
redox mediator
title Bioelectroanalytical Detection of Lactic Acid Bacteria
title_full Bioelectroanalytical Detection of Lactic Acid Bacteria
title_fullStr Bioelectroanalytical Detection of Lactic Acid Bacteria
title_full_unstemmed Bioelectroanalytical Detection of Lactic Acid Bacteria
title_short Bioelectroanalytical Detection of Lactic Acid Bacteria
title_sort bioelectroanalytical detection of lactic acid bacteria
topic lactic acid bacteria
extracellular electron transfer
microbial detection
<i>E. faecalis</i>
redox mediator
url https://www.mdpi.com/2076-3417/12/3/1257
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AT lolagonzalezolias bioelectroanalyticaldetectionoflacticacidbacteria
AT stefanwuertz bioelectroanalyticaldetectionoflacticacidbacteria
AT jamiehinks bioelectroanalyticaldetectionoflacticacidbacteria