In silico Targeting, inhibition and analysis of polyketide synthase enzyme in Aspergillus ssp

Aflatoxins are toxic and carcinogenic components produced by some Aspergillus species such as Aspergillus flavus. Polyketide synthases enzyme (PKS) plays a central role in aflatoxin s biosynthesis of in Aspergillus flavus, especially the product template (PT) domain, which controls the aldol cycliza...

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Main Authors: Mai M. Labib, M.K. Amin, A.M. Alzohairy, M.M.A. Elashtokhy, O. Samir, I. Saleh, I.A. Arif, G.H. Osman, S.E. Hassanein
Format: Article
Language:English
Published: Elsevier 2020-12-01
Series:Saudi Journal of Biological Sciences
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Online Access:http://www.sciencedirect.com/science/article/pii/S1319562X20304976
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spelling doaj-3ae46213e5124f03b51629e32315378c2020-12-03T04:30:36ZengElsevierSaudi Journal of Biological Sciences1319-562X2020-12-01271231873198In silico Targeting, inhibition and analysis of polyketide synthase enzyme in Aspergillus sspMai M. Labib0M.K. Amin1A.M. Alzohairy2M.M.A. Elashtokhy3O. Samir4I. Saleh5I.A. Arif6G.H. Osman7S.E. Hassanein8Agriculture Genetic Engineering Research Institute (AGERI), Egypt; Corresponding authors at: Agriculture Genetic Engineering Research Institute (AGERI), Egypt (S. Hassanein).Faculty of Agriculture, Zagazig University, Department of GeneticsFaculty of Agriculture, Zagazig University, Department of GeneticsFaculty of Agriculture, Zagazig University, Department of GeneticsMisr University for Science and Technology (MUST), October 6, Al Jizah, EgyptBotany and Microbiology Department, Faculty of Sciences, King Saud University, Saudi ArabiaBotany and Microbiology Department, Faculty of Sciences, King Saud University, Saudi ArabiaDepartment of Biology, Faculty of Applied Sciences, Umm Al-Qura University, Makkah, Saudi Arabia; Research Laboratories Center, Faculty of Applied Science, Umm Al-Qura University, Mecca, Saudi Arabia; Microbial Genetics Department, Agricultural Genetic Engineering Research Institute (AGERI), ARC, 12619, Giza, EgyptAgriculture Genetic Engineering Research Institute (AGERI), Egypt; Misr University for Science and Technology (MUST), October 6, Al Jizah, Egypt; Corresponding authors at: Agriculture Genetic Engineering Research Institute (AGERI), Egypt (S. Hassanein).Aflatoxins are toxic and carcinogenic components produced by some Aspergillus species such as Aspergillus flavus. Polyketide synthases enzyme (PKS) plays a central role in aflatoxin s biosynthesis of in Aspergillus flavus, especially the product template (PT) domain, which controls the aldol cyclization of the polyketide forerunner during the biosynthesis of the aflatoxin pathway process. Here, we apply the in silico approaches to validate 623 natural components obtained from the South African Natural Compound Database (SANCDB), to distinguish the PT domain s prospected inhibitors. From the 623 compounds, docking results showed that there are 330 different compounds with energy binding lower than the natural substrate (palmitic acid or PLM) of the Product Templet domain (PT). Three factors were selected to determine the best 10 inhibiting components; 1) energy binding, 2) the strengthen chemical interactions, 3) the drug-likeness. The top ten inhibiting components are kraussianone 6, kraussianone 1, neodiospyrin, clionamine D, bromotopsentin, isodiospyrin, spongotine A, kraussianone 3, 14β-Hydroxybufa-3,5,20,22-tetraenolide and kraussianone 7. The chemical interactions between 3HRQ domain and the natural substrate in the active site amino acids are highly similar to the 3HRQ with the top ten components, but the main differences are in the binding energy which is the best in the top ten ligands. Those ten components give successful inhibition with PT domain which will lead to the formula to be used for inhibition and control aflatoxin contamination of agriculture crop yields and lessen the degree of harming and sicknesses that are coming about because of acquiring measures of aflatoxin.http://www.sciencedirect.com/science/article/pii/S1319562X20304976AflatoxinPKS enzymeAflatoxin B1PT domainDocking
collection DOAJ
language English
format Article
sources DOAJ
author Mai M. Labib
M.K. Amin
A.M. Alzohairy
M.M.A. Elashtokhy
O. Samir
I. Saleh
I.A. Arif
G.H. Osman
S.E. Hassanein
spellingShingle Mai M. Labib
M.K. Amin
A.M. Alzohairy
M.M.A. Elashtokhy
O. Samir
I. Saleh
I.A. Arif
G.H. Osman
S.E. Hassanein
In silico Targeting, inhibition and analysis of polyketide synthase enzyme in Aspergillus ssp
Saudi Journal of Biological Sciences
Aflatoxin
PKS enzyme
Aflatoxin B1
PT domain
Docking
author_facet Mai M. Labib
M.K. Amin
A.M. Alzohairy
M.M.A. Elashtokhy
O. Samir
I. Saleh
I.A. Arif
G.H. Osman
S.E. Hassanein
author_sort Mai M. Labib
title In silico Targeting, inhibition and analysis of polyketide synthase enzyme in Aspergillus ssp
title_short In silico Targeting, inhibition and analysis of polyketide synthase enzyme in Aspergillus ssp
title_full In silico Targeting, inhibition and analysis of polyketide synthase enzyme in Aspergillus ssp
title_fullStr In silico Targeting, inhibition and analysis of polyketide synthase enzyme in Aspergillus ssp
title_full_unstemmed In silico Targeting, inhibition and analysis of polyketide synthase enzyme in Aspergillus ssp
title_sort in silico targeting, inhibition and analysis of polyketide synthase enzyme in aspergillus ssp
publisher Elsevier
series Saudi Journal of Biological Sciences
issn 1319-562X
publishDate 2020-12-01
description Aflatoxins are toxic and carcinogenic components produced by some Aspergillus species such as Aspergillus flavus. Polyketide synthases enzyme (PKS) plays a central role in aflatoxin s biosynthesis of in Aspergillus flavus, especially the product template (PT) domain, which controls the aldol cyclization of the polyketide forerunner during the biosynthesis of the aflatoxin pathway process. Here, we apply the in silico approaches to validate 623 natural components obtained from the South African Natural Compound Database (SANCDB), to distinguish the PT domain s prospected inhibitors. From the 623 compounds, docking results showed that there are 330 different compounds with energy binding lower than the natural substrate (palmitic acid or PLM) of the Product Templet domain (PT). Three factors were selected to determine the best 10 inhibiting components; 1) energy binding, 2) the strengthen chemical interactions, 3) the drug-likeness. The top ten inhibiting components are kraussianone 6, kraussianone 1, neodiospyrin, clionamine D, bromotopsentin, isodiospyrin, spongotine A, kraussianone 3, 14β-Hydroxybufa-3,5,20,22-tetraenolide and kraussianone 7. The chemical interactions between 3HRQ domain and the natural substrate in the active site amino acids are highly similar to the 3HRQ with the top ten components, but the main differences are in the binding energy which is the best in the top ten ligands. Those ten components give successful inhibition with PT domain which will lead to the formula to be used for inhibition and control aflatoxin contamination of agriculture crop yields and lessen the degree of harming and sicknesses that are coming about because of acquiring measures of aflatoxin.
topic Aflatoxin
PKS enzyme
Aflatoxin B1
PT domain
Docking
url http://www.sciencedirect.com/science/article/pii/S1319562X20304976
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