Antimicrobial Isoflavones and Derivatives from Erythrina (Fabaceae): Structure Activity Perspective (Sar & Qsar) on Experimental and Mined Values Against <i>Staphylococcus Aureus</i>

Prenylated (iso)flavonoids, -flavans and pterocarpans from taxa in <i>Erythrina</i> are repeatedly flagged as potent antimicrobial compounds. In the current study, bark from <i>E. lysistemon</i> was extracted and seven isoflavone derivatives were purified: erybraedin A (<b...

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Main Authors: Nicholas J. Sadgrove, Tiago B. Oliveira, Gugulethu P. Khumalo, Sandy F. van Vuuren, Ben-Erik van Wyk
Format: Article
Language:English
Published: MDPI AG 2020-04-01
Series:Antibiotics
Subjects:
Online Access:https://www.mdpi.com/2079-6382/9/5/223
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spelling doaj-8fef021abd6645828465b12ce72510742020-11-25T03:31:15ZengMDPI AGAntibiotics2079-63822020-04-01922322310.3390/antibiotics9050223Antimicrobial Isoflavones and Derivatives from Erythrina (Fabaceae): Structure Activity Perspective (Sar & Qsar) on Experimental and Mined Values Against <i>Staphylococcus Aureus</i>Nicholas J. Sadgrove0Tiago B. Oliveira1Gugulethu P. Khumalo2Sandy F. van Vuuren3Ben-Erik van Wyk4Jodrell Science Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3AB, UKDepartment of Pharmacy, Federal University of Sergipe (UFS-SE), São Cristóvão 491000-000, BrazilDepartment of Botany and Plant Biotechnology, University of Johannesburg, P.O. Box 524, Auckland Park 2006, South AfricaDepartment of Pharmacy and Pharmacology, Faculty of Health Sciences, University of the Witwatersrand, 7 York Road, Park town 2193, South AfricaDepartment of Botany and Plant Biotechnology, University of Johannesburg, P.O. Box 524, Auckland Park 2006, South AfricaPrenylated (iso)flavonoids, -flavans and pterocarpans from taxa in <i>Erythrina</i> are repeatedly flagged as potent antimicrobial compounds. In the current study, bark from <i>E. lysistemon</i> was extracted and seven isoflavone derivatives were purified: erybraedin A (<b>1</b>), phaseollidin (<b>2</b>), abyssinone V-4’ methyl ether (<b>3</b>), eryzerin C (<b>4</b>), alpumisoflavone (<b>5</b>), cristacarpin (<b>6</b>) and lysisteisoflavone (<b>7</b>). Minimum inhibition concentration (MIC) values were determined against a range of species of bacteria (skin pathogens), then values for another 67 derivatives from <i>Erythrina</i>, only against <i>Staphylococcus aureus</i>, were mined from the literature. Of the seven isolates, MIC values widely ranged from 1–600 μg/mL, with no obvious pattern of selectivity for Gram-types. Nevertheless, using the mined and experimentally determined values against <i>S. aureus</i>, Klekota-Roth fragments (Structure Activity Relationship: SAR) were determined then used as molecular descriptors to make a ‘decision tree’ based on structural characters inspired by the classes of antimicrobial potency (classes A-D). Furthermore, to make quantitative predictions of MIC values (Quantitative SAR: QSAR) ‘pace regression’ was utilized and validated (R² = 0.778, Q² = 0.727 and P² = 0.555). Evidently, the position and degree of prenylation is important; however, the presence of hydroxyl groups at positions 5 and 7 in ring A and 4’ in ring B is associated with lower MIC values. While antimicrobial results continue to validate the traditional use of <i>E. lysistemon</i> extracts (or <i>Erythrina</i> generally) in therapeutic applications consistent with anti-infection, it is surprising that this class of compound is not being utilized more often in general industry applications, such as food or cosmetic preservation, or in topical antimicrobial creams. Prenylated (iso)flavonoids are derived from several other Genera, such as <i>Dorstenia</i> (Moraceae), <i>Ficus</i> (Moraceae), <i>Glycyrrhiza</i> (Fabaceae), <i>Paulownia</i> (Lamiales) or <i>Pomifera </i>(Moraceae).https://www.mdpi.com/2079-6382/9/5/223pterocarpanprenylated isoflavonoidtraditional medicineQSARMRSA
collection DOAJ
language English
format Article
sources DOAJ
author Nicholas J. Sadgrove
Tiago B. Oliveira
Gugulethu P. Khumalo
Sandy F. van Vuuren
Ben-Erik van Wyk
spellingShingle Nicholas J. Sadgrove
Tiago B. Oliveira
Gugulethu P. Khumalo
Sandy F. van Vuuren
Ben-Erik van Wyk
Antimicrobial Isoflavones and Derivatives from Erythrina (Fabaceae): Structure Activity Perspective (Sar & Qsar) on Experimental and Mined Values Against <i>Staphylococcus Aureus</i>
Antibiotics
pterocarpan
prenylated isoflavonoid
traditional medicine
QSAR
MRSA
author_facet Nicholas J. Sadgrove
Tiago B. Oliveira
Gugulethu P. Khumalo
Sandy F. van Vuuren
Ben-Erik van Wyk
author_sort Nicholas J. Sadgrove
title Antimicrobial Isoflavones and Derivatives from Erythrina (Fabaceae): Structure Activity Perspective (Sar & Qsar) on Experimental and Mined Values Against <i>Staphylococcus Aureus</i>
title_short Antimicrobial Isoflavones and Derivatives from Erythrina (Fabaceae): Structure Activity Perspective (Sar & Qsar) on Experimental and Mined Values Against <i>Staphylococcus Aureus</i>
title_full Antimicrobial Isoflavones and Derivatives from Erythrina (Fabaceae): Structure Activity Perspective (Sar & Qsar) on Experimental and Mined Values Against <i>Staphylococcus Aureus</i>
title_fullStr Antimicrobial Isoflavones and Derivatives from Erythrina (Fabaceae): Structure Activity Perspective (Sar & Qsar) on Experimental and Mined Values Against <i>Staphylococcus Aureus</i>
title_full_unstemmed Antimicrobial Isoflavones and Derivatives from Erythrina (Fabaceae): Structure Activity Perspective (Sar & Qsar) on Experimental and Mined Values Against <i>Staphylococcus Aureus</i>
title_sort antimicrobial isoflavones and derivatives from erythrina (fabaceae): structure activity perspective (sar & qsar) on experimental and mined values against <i>staphylococcus aureus</i>
publisher MDPI AG
series Antibiotics
issn 2079-6382
publishDate 2020-04-01
description Prenylated (iso)flavonoids, -flavans and pterocarpans from taxa in <i>Erythrina</i> are repeatedly flagged as potent antimicrobial compounds. In the current study, bark from <i>E. lysistemon</i> was extracted and seven isoflavone derivatives were purified: erybraedin A (<b>1</b>), phaseollidin (<b>2</b>), abyssinone V-4’ methyl ether (<b>3</b>), eryzerin C (<b>4</b>), alpumisoflavone (<b>5</b>), cristacarpin (<b>6</b>) and lysisteisoflavone (<b>7</b>). Minimum inhibition concentration (MIC) values were determined against a range of species of bacteria (skin pathogens), then values for another 67 derivatives from <i>Erythrina</i>, only against <i>Staphylococcus aureus</i>, were mined from the literature. Of the seven isolates, MIC values widely ranged from 1–600 μg/mL, with no obvious pattern of selectivity for Gram-types. Nevertheless, using the mined and experimentally determined values against <i>S. aureus</i>, Klekota-Roth fragments (Structure Activity Relationship: SAR) were determined then used as molecular descriptors to make a ‘decision tree’ based on structural characters inspired by the classes of antimicrobial potency (classes A-D). Furthermore, to make quantitative predictions of MIC values (Quantitative SAR: QSAR) ‘pace regression’ was utilized and validated (R² = 0.778, Q² = 0.727 and P² = 0.555). Evidently, the position and degree of prenylation is important; however, the presence of hydroxyl groups at positions 5 and 7 in ring A and 4’ in ring B is associated with lower MIC values. While antimicrobial results continue to validate the traditional use of <i>E. lysistemon</i> extracts (or <i>Erythrina</i> generally) in therapeutic applications consistent with anti-infection, it is surprising that this class of compound is not being utilized more often in general industry applications, such as food or cosmetic preservation, or in topical antimicrobial creams. Prenylated (iso)flavonoids are derived from several other Genera, such as <i>Dorstenia</i> (Moraceae), <i>Ficus</i> (Moraceae), <i>Glycyrrhiza</i> (Fabaceae), <i>Paulownia</i> (Lamiales) or <i>Pomifera </i>(Moraceae).
topic pterocarpan
prenylated isoflavonoid
traditional medicine
QSAR
MRSA
url https://www.mdpi.com/2079-6382/9/5/223
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