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3 Biotech

, 9:149 | Cite as

Docking analysis of hexanoic acid and quercetin with seven domains of polyketide synthase A provided insight into quercetin-mediated aflatoxin biosynthesis inhibition in Aspergillus flavus

  • Shraddha Tiwari
  • Sonia K. Shishodia
  • Jata ShankarEmail author
Original Article
  • 110 Downloads

Abstract

Studies on phytochemicals as anti-aflatoxigenic agents have gained importance including quercetin. Thus, to understand the molecular mechanism behind inhibition of aflatoxin biosynthesis by quercetin, interaction study with polyketide synthase A (PksA) of Aspergillus flavus was undertaken. The 3D structure of seven domains of PksA was modeled using SWISS-MODEL server and docking studies were performed by Autodock tools-1.5.6. Docking energies of both the ligands (quercetin and hexanoic acid) were compared with each of the domains of PksA enzyme. Binding energy for quercetin was lesser that ranged from − 7.1 to − 5.25 kcal/mol in comparison to hexanoic acid (− 4.74 to − 3.54 kcal/mol). LigPlot analysis showed the formation of 12 H bonds in case of quercetin and 8 H bonds in hexanoic acid. During an interaction with acyltransferase domain, both ligands showed H bond formation at Arg63 position. Also, in product template domain, quercetin creates four H bonds in comparison to one in hexanoic acid. Our quantitative RT-PCR analysis of genes from aflatoxin biosynthesis showed downregulation of pksA, aflD, aflR, aflP and aflS at 24 h time point in comparison to 7 h in quercetin-treated A. flavus. Overall results revealed that quercetin exhibited the highest level of binding potential (more number of H bonds) with PksA domain in comparison to hexanoic acid; thus, quercetin possibly inhibits via competitively binding to the domains of polyketide synthase, a key enzyme of aflatoxin biosynthetic pathway. Further, we propose that key enzymes from aflatoxin biosynthetic pathway in aflatoxin-producing Aspergilli could be explored further using other phytochemicals as inhibitors.

Keywords

Aspergillus flavus Docking Polyketide synthase A Aflatoxin biosynthesis Quercetin Hexanoic acid 

Abbreviations

qRT-PCR

Quantitative real-time PCR

PksA

Polyketide synthase A

AF

Aflatoxin

KS

Ketoacyl synthase

AT

Acyltransferase

ACP

Acyl carrier proteins

KR

Ketoreductase

DH

Dehydratase

ER

Enol reductase

CYC

Cyclase

MT

Methyltransferase

Notes

Acknowledgements

Authors are thankful to the Department of Biotechnology and Bioinformatics, Jaypee University of Information Technology, Solan, Himachal Pradesh, India, for providing facilities and financial support to Ph.D. student ST and SKS.

Author contributions

ST and JS conceived and designed the experiments. ST and SKS performed the experiments. ST, SKS and JS analyzed the data. JS contributed reagents/materials/analysis tools. ST and JS contributed to writing the manuscript.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

Supplementary material

13205_2019_1675_MOESM1_ESM.tif (278 kb)
Supplementary material 1 (TIF 278 KB)
13205_2019_1675_MOESM2_ESM.docx (13 kb)
Supplementary material 2 (DOCX 12 KB)
13205_2019_1675_MOESM3_ESM.docx (15 kb)
Supplementary material 3 (DOCX 15 KB)

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Copyright information

© King Abdulaziz City for Science and Technology 2019

Authors and Affiliations

  1. 1.Genomic laboratory, Department of Biotechnology and BioinformaticsJaypee University of Information TechnologySolanIndia

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