To Develop the Method for UHPLC-HRMS to Determine the Antibacterial Potential of a Central American Medicinal Plant

The development of antibiotic resistance by microbials has long been acknowledged. The major challenge worldwide is to develop novel, natural, and potent antibiotics against the multidrug resistant bacteria. In this study, our aim was to develop the method for a highly sensitive instrument, ultra-hi...

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Main Authors: Gaganpreet Kaur Monga, Anima Ghosal, Dil Ramanathan
Format: Article
Language:English
Published: MDPI AG 2019-07-01
Series:Separations
Subjects:
MIC
Online Access:https://www.mdpi.com/2297-8739/6/3/37
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spelling doaj-89e9b9dbe7f24a3ca4259f1855ea45d32020-11-24T21:30:42ZengMDPI AGSeparations2297-87392019-07-01633710.3390/separations6030037separations6030037To Develop the Method for UHPLC-HRMS to Determine the Antibacterial Potential of a Central American Medicinal PlantGaganpreet Kaur Monga0Anima Ghosal1Dil Ramanathan2New Jersey Center for Science, Technology and Mathematics—Kean University, Union, NJ 07083, USANew Jersey Center for Science, Technology and Mathematics—Kean University, Union, NJ 07083, USANew Jersey Center for Science, Technology and Mathematics—Kean University, Union, NJ 07083, USAThe development of antibiotic resistance by microbials has long been acknowledged. The major challenge worldwide is to develop novel, natural, and potent antibiotics against the multidrug resistant bacteria. In this study, our aim was to develop the method for a highly sensitive instrument, ultra-high performance liquid chromatograph-high resolution mass spectrometer (UHPLC-HRMS), to evaluate the antibacterial property of a natural product. <i>Aechmea magdalenae</i> (<i>Andre) Andre ex Baker</i>, a plant belonging to the family Bromeliaceae, a native of Central America was used in this study. Based on the available literature, it was hypothesized that <i>Aechmea magdalenae</i> has antibacterial activity. In addition, the profiling done on <i>A.</i> <i>magdalenae</i> using gas chromatography-mass spectrometry (GC-MS) also revealed the presence of medicinally important chemical compounds, such as acetic acid. Minimum inhibitory concentration (MIC) of dried Aechmea plant extract was determined for the first time using 96-well plate assay, followed by determination of antibacterial potential using LC-MS. The reason being that other dried methanolic plant extracts, such as <i>Vismia macrophylla</i>, lined up for antibacterial testing have dark extracts, for which determining the antibacterial potential and reading the results with the naked eye would be challenging. To overcome the situation of dark plant extracts, a generalized novel LC-MS method was developed that was used for the plant <i>A. magdalenae,</i> and would be used further for other plants. A blue indicator called resazurin was added to the wells; resazurin, upon incubation with the living cells, got reduced to resorufin (which was pink), while it remained blue with bacterial growth inhibition. The mass difference created due to reduction of resazurin to resorufin was detected by using LTQ Orbitrap Discovery in positive ion mode to determine the antibacterial activity of the plant extract. The sample preparation for LC-MS assay included centrifugation of the samples taken from 96-well plate, followed by filtration of the supernatant, before exposing them to C-18 column. The results obtained from full scan LC-MS spectrum consistently demonstrated the presence of resorufin from wells with bacterial growth, and resazurin from wells with inhibition through peaks of relevant masses.https://www.mdpi.com/2297-8739/6/3/37UHPLC-HRMSantibacterial activity<i>Aechmea magdalenae</i>MICmedicinal plant
collection DOAJ
language English
format Article
sources DOAJ
author Gaganpreet Kaur Monga
Anima Ghosal
Dil Ramanathan
spellingShingle Gaganpreet Kaur Monga
Anima Ghosal
Dil Ramanathan
To Develop the Method for UHPLC-HRMS to Determine the Antibacterial Potential of a Central American Medicinal Plant
Separations
UHPLC-HRMS
antibacterial activity
<i>Aechmea magdalenae</i>
MIC
medicinal plant
author_facet Gaganpreet Kaur Monga
Anima Ghosal
Dil Ramanathan
author_sort Gaganpreet Kaur Monga
title To Develop the Method for UHPLC-HRMS to Determine the Antibacterial Potential of a Central American Medicinal Plant
title_short To Develop the Method for UHPLC-HRMS to Determine the Antibacterial Potential of a Central American Medicinal Plant
title_full To Develop the Method for UHPLC-HRMS to Determine the Antibacterial Potential of a Central American Medicinal Plant
title_fullStr To Develop the Method for UHPLC-HRMS to Determine the Antibacterial Potential of a Central American Medicinal Plant
title_full_unstemmed To Develop the Method for UHPLC-HRMS to Determine the Antibacterial Potential of a Central American Medicinal Plant
title_sort to develop the method for uhplc-hrms to determine the antibacterial potential of a central american medicinal plant
publisher MDPI AG
series Separations
issn 2297-8739
publishDate 2019-07-01
description The development of antibiotic resistance by microbials has long been acknowledged. The major challenge worldwide is to develop novel, natural, and potent antibiotics against the multidrug resistant bacteria. In this study, our aim was to develop the method for a highly sensitive instrument, ultra-high performance liquid chromatograph-high resolution mass spectrometer (UHPLC-HRMS), to evaluate the antibacterial property of a natural product. <i>Aechmea magdalenae</i> (<i>Andre) Andre ex Baker</i>, a plant belonging to the family Bromeliaceae, a native of Central America was used in this study. Based on the available literature, it was hypothesized that <i>Aechmea magdalenae</i> has antibacterial activity. In addition, the profiling done on <i>A.</i> <i>magdalenae</i> using gas chromatography-mass spectrometry (GC-MS) also revealed the presence of medicinally important chemical compounds, such as acetic acid. Minimum inhibitory concentration (MIC) of dried Aechmea plant extract was determined for the first time using 96-well plate assay, followed by determination of antibacterial potential using LC-MS. The reason being that other dried methanolic plant extracts, such as <i>Vismia macrophylla</i>, lined up for antibacterial testing have dark extracts, for which determining the antibacterial potential and reading the results with the naked eye would be challenging. To overcome the situation of dark plant extracts, a generalized novel LC-MS method was developed that was used for the plant <i>A. magdalenae,</i> and would be used further for other plants. A blue indicator called resazurin was added to the wells; resazurin, upon incubation with the living cells, got reduced to resorufin (which was pink), while it remained blue with bacterial growth inhibition. The mass difference created due to reduction of resazurin to resorufin was detected by using LTQ Orbitrap Discovery in positive ion mode to determine the antibacterial activity of the plant extract. The sample preparation for LC-MS assay included centrifugation of the samples taken from 96-well plate, followed by filtration of the supernatant, before exposing them to C-18 column. The results obtained from full scan LC-MS spectrum consistently demonstrated the presence of resorufin from wells with bacterial growth, and resazurin from wells with inhibition through peaks of relevant masses.
topic UHPLC-HRMS
antibacterial activity
<i>Aechmea magdalenae</i>
MIC
medicinal plant
url https://www.mdpi.com/2297-8739/6/3/37
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