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Enzymatic Textile Dyes Decolorization by In vitro and In silico Studies.

Identifieur interne : 000283 ( Main/Exploration ); précédent : 000282; suivant : 000284

Enzymatic Textile Dyes Decolorization by In vitro and In silico Studies.

Auteurs : Sridevi Ayla [Inde] ; Monika Kallubai [Inde] ; Suvarnalatha Devi Pallipati [Inde] ; Golla Narasimha [Inde]

Source :

RBID : pubmed:31241023

Descripteurs français

English descriptors

Abstract

BACKGROUND

Laccase, a multicopper oxidoreductase (EC: 1.10.3.2), is a widely used enzyme in bioremediation of textile dye effluents. Fungal Laccase is preferably used as a remediating agent in the treatment and transformation of toxic organic pollutants. In this study, crude laccase from a basidiomycetes fungus, Phanerochaete sordida, was able to decolorize azo, antroquinone and indigoid dyes. In addition, interactions between dyes and enzyme were analysed using molecular docking studies.

METHODS

In this work, a white rot basidiomycete's fungus, Phanerochaete sordida, was selected from forest soil isolates of Eastern Ghats, and Tirumala and lignolytic enzymes production was assayed after 7 days of incubation. The crude enzyme was checked for decolourisation of various synthetic textile dyes (Vat Brown, Acid Blue, Indigo, Reactive Blue and Reactive Black). Molecular docking studies were done using Autodock-4.2 to understand the interactions between dyes and enzymes.

RESULTS

Highest decolourisation efficiency was achieved with the crude enzyme in case of vat brown whereas the lowest decolourisation efficiency was achieved in Reactive blue decolourisation. Similar results were observed in their binding affinity with lignin peroxidase of Phanerochaete chrysosporium through molecular docking approach.

CONCLUSION

Thus, experimental results and subsequent in silico validation involving an advanced remediation approach would be useful to reduce time and cost in other similar experiments.


DOI: 10.2174/1872208313666190625123847
PubMed: 31241023


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<term>Biodegradation, Environmental (MeSH)</term>
<term>Coloring Agents (analysis)</term>
<term>Coloring Agents (isolation & purification)</term>
<term>Coloring Agents (metabolism)</term>
<term>Fungal Proteins (chemistry)</term>
<term>Fungal Proteins (metabolism)</term>
<term>Laccase (chemistry)</term>
<term>Laccase (metabolism)</term>
<term>Molecular Docking Simulation (MeSH)</term>
<term>Phanerochaete (enzymology)</term>
<term>Phanerochaete (isolation & purification)</term>
<term>Soil Microbiology (MeSH)</term>
<term>Textile Industry (MeSH)</term>
<term>Water Pollutants, Chemical (analysis)</term>
<term>Water Pollutants, Chemical (isolation & purification)</term>
<term>Water Pollutants, Chemical (metabolism)</term>
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<term>Agents colorants (analyse)</term>
<term>Agents colorants (isolement et purification)</term>
<term>Agents colorants (métabolisme)</term>
<term>Dépollution biologique de l'environnement (MeSH)</term>
<term>Industrie textile (MeSH)</term>
<term>Laccase (composition chimique)</term>
<term>Laccase (métabolisme)</term>
<term>Microbiologie du sol (MeSH)</term>
<term>Phanerochaete (enzymologie)</term>
<term>Phanerochaete (isolement et purification)</term>
<term>Polluants chimiques de l'eau (analyse)</term>
<term>Polluants chimiques de l'eau (isolement et purification)</term>
<term>Polluants chimiques de l'eau (métabolisme)</term>
<term>Protéines fongiques (composition chimique)</term>
<term>Protéines fongiques (métabolisme)</term>
<term>Simulation de docking moléculaire (MeSH)</term>
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<term>Coloring Agents</term>
<term>Water Pollutants, Chemical</term>
</keywords>
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<term>Laccase</term>
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<term>Water Pollutants, Chemical</term>
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<term>Laccase</term>
<term>Water Pollutants, Chemical</term>
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<term>Agents colorants</term>
<term>Polluants chimiques de l'eau</term>
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<term>Laccase</term>
<term>Protéines fongiques</term>
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<keywords scheme="MESH" qualifier="enzymologie" xml:lang="fr">
<term>Phanerochaete</term>
</keywords>
<keywords scheme="MESH" qualifier="enzymology" xml:lang="en">
<term>Phanerochaete</term>
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<keywords scheme="MESH" qualifier="isolation & purification" xml:lang="en">
<term>Phanerochaete</term>
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<term>Agents colorants</term>
<term>Phanerochaete</term>
<term>Polluants chimiques de l'eau</term>
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<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Agents colorants</term>
<term>Laccase</term>
<term>Polluants chimiques de l'eau</term>
<term>Protéines fongiques</term>
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<term>Biodegradation, Environmental</term>
<term>Molecular Docking Simulation</term>
<term>Soil Microbiology</term>
<term>Textile Industry</term>
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<term>Dépollution biologique de l'environnement</term>
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<p>
<b>BACKGROUND</b>
</p>
<p>Laccase, a multicopper oxidoreductase (EC: 1.10.3.2), is a widely used enzyme in bioremediation of textile dye effluents. Fungal Laccase is preferably used as a remediating agent in the treatment and transformation of toxic organic pollutants. In this study, crude laccase from a basidiomycetes fungus, Phanerochaete sordida, was able to decolorize azo, antroquinone and indigoid dyes. In addition, interactions between dyes and enzyme were analysed using molecular docking studies.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>In this work, a white rot basidiomycete's fungus, Phanerochaete sordida, was selected from forest soil isolates of Eastern Ghats, and Tirumala and lignolytic enzymes production was assayed after 7 days of incubation. The crude enzyme was checked for decolourisation of various synthetic textile dyes (Vat Brown, Acid Blue, Indigo, Reactive Blue and Reactive Black). Molecular docking studies were done using Autodock-4.2 to understand the interactions between dyes and enzymes.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>Highest decolourisation efficiency was achieved with the crude enzyme in case of vat brown whereas the lowest decolourisation efficiency was achieved in Reactive blue decolourisation. Similar results were observed in their binding affinity with lignin peroxidase of Phanerochaete chrysosporium through molecular docking approach.</p>
</div>
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<p>
<b>CONCLUSION</b>
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<p>Thus, experimental results and subsequent in silico validation involving an advanced remediation approach would be useful to reduce time and cost in other similar experiments.</p>
</div>
</front>
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