In Vitro Antimicrobial Activity of The Filtrate Crude Extract Produced by Aspergillus niger
Introduction: Aspergillus niger represents one of the fungi that can produce the secondary metabolites, including antimicrobial agents, industrial and biotechnological products. Methodology: A. niger was tested against Candida albicans on the same petri dish of potato dextrose agar at room temperatu...
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University of Thi-Qar
2019-05-01
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Series: | مجلة علوم ذي قار |
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Online Access: | http://jsci.utq.edu.iq/index.php/main/article/view/253 |
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author | Dhurgham A.H. Alhasan Husein A. Husein Ahmed Q. Dawood |
author_facet | Dhurgham A.H. Alhasan Husein A. Husein Ahmed Q. Dawood |
author_sort | Dhurgham A.H. Alhasan |
collection | DOAJ |
description | Introduction: Aspergillus niger represents one of the fungi that can produce the secondary metabolites, including antimicrobial agents, industrial and biotechnological products. Methodology: A. niger was tested against Candida albicans on the same petri dish of potato dextrose agar at room temperature. A. niger was cultured in potato dextrose broth at 27 °C for 7 days. The fungal filtrate was separated from mycelia, and the filtrate was extracted for getting a crude blackish-brown extract. The GC-MS analysis used to identify the constituents of the extract. Results: The filtrate crude extract of A. niger exhibited the antimicrobial effects against Staphylococcus aureus, Streptococcus mutans, Escherichia coli, and Candida albicans.GC-MS analysis revealed that the extract contains [(5-methyl-2-phenylindolizine), (thiocarbamic acid, N,N-dimethyl, S-1,3-diphenyl-2-butenyl ester) and (22-beta.-acetoxy-3.beta.,16.alpha.-dihydroxy-13,28epoxyolean-2)].The extract had the toxic effect on a solution of the human red blood cells by using 300 µL of 10 mg/ml after 5 minutes while 100 µL and 200 µL of the same concentration did not appear the toxic effects during 1 hour of the testing time period. Conclusions: The extract of A. niger has the ability to produce the antimicrobial activity, so it very needs to separate its constituents into pure compounds for elucidating their chemical structure by using techniques of spectrometry. Then, the compounds can be separately testing against microbial pathogens, human normal cell to determine half lethal concentration (LC50)), and application of other biological tests such as test of LD50. Finally, the identified and purified compounds will be tested by volunteers in order to identify the side effects and toxicity of these compounds to be implemented as drugs for treating diseases in the hospitals. |
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format | Article |
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issn | 1991-8690 2709-0256 |
language | English |
last_indexed | 2024-03-09T02:51:58Z |
publishDate | 2019-05-01 |
publisher | University of Thi-Qar |
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series | مجلة علوم ذي قار |
spelling | doaj.art-2a8f426929a144a9b58c2e162df699fb2023-12-05T09:57:31ZengUniversity of Thi-Qarمجلة علوم ذي قار1991-86902709-02562019-05-0171In Vitro Antimicrobial Activity of The Filtrate Crude Extract Produced by Aspergillus nigerDhurgham A.H. Alhasan0Husein A. Husein1Ahmed Q. Dawood2College of Veterinary Medicine/University of Thi-Qar, IraqCollege of Pharmacy/University of Thi-Qar, IraqCollege of Veterinary Medicine/University of Thi-Qar, IraqIntroduction: Aspergillus niger represents one of the fungi that can produce the secondary metabolites, including antimicrobial agents, industrial and biotechnological products. Methodology: A. niger was tested against Candida albicans on the same petri dish of potato dextrose agar at room temperature. A. niger was cultured in potato dextrose broth at 27 °C for 7 days. The fungal filtrate was separated from mycelia, and the filtrate was extracted for getting a crude blackish-brown extract. The GC-MS analysis used to identify the constituents of the extract. Results: The filtrate crude extract of A. niger exhibited the antimicrobial effects against Staphylococcus aureus, Streptococcus mutans, Escherichia coli, and Candida albicans.GC-MS analysis revealed that the extract contains [(5-methyl-2-phenylindolizine), (thiocarbamic acid, N,N-dimethyl, S-1,3-diphenyl-2-butenyl ester) and (22-beta.-acetoxy-3.beta.,16.alpha.-dihydroxy-13,28epoxyolean-2)].The extract had the toxic effect on a solution of the human red blood cells by using 300 µL of 10 mg/ml after 5 minutes while 100 µL and 200 µL of the same concentration did not appear the toxic effects during 1 hour of the testing time period. Conclusions: The extract of A. niger has the ability to produce the antimicrobial activity, so it very needs to separate its constituents into pure compounds for elucidating their chemical structure by using techniques of spectrometry. Then, the compounds can be separately testing against microbial pathogens, human normal cell to determine half lethal concentration (LC50)), and application of other biological tests such as test of LD50. Finally, the identified and purified compounds will be tested by volunteers in order to identify the side effects and toxicity of these compounds to be implemented as drugs for treating diseases in the hospitals.http://jsci.utq.edu.iq/index.php/main/article/view/253Aspergillus nigerAntimicrobial ActivityGC-MS |
spellingShingle | Dhurgham A.H. Alhasan Husein A. Husein Ahmed Q. Dawood In Vitro Antimicrobial Activity of The Filtrate Crude Extract Produced by Aspergillus niger مجلة علوم ذي قار Aspergillus niger Antimicrobial Activity GC-MS |
title | In Vitro Antimicrobial Activity of The Filtrate Crude Extract Produced by Aspergillus niger |
title_full | In Vitro Antimicrobial Activity of The Filtrate Crude Extract Produced by Aspergillus niger |
title_fullStr | In Vitro Antimicrobial Activity of The Filtrate Crude Extract Produced by Aspergillus niger |
title_full_unstemmed | In Vitro Antimicrobial Activity of The Filtrate Crude Extract Produced by Aspergillus niger |
title_short | In Vitro Antimicrobial Activity of The Filtrate Crude Extract Produced by Aspergillus niger |
title_sort | in vitro antimicrobial activity of the filtrate crude extract produced by aspergillus niger |
topic | Aspergillus niger Antimicrobial Activity GC-MS |
url | http://jsci.utq.edu.iq/index.php/main/article/view/253 |
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