Characterisation of Synthetic Dye Decolourising Genes and their Enzymes Produced by an Endophytic Fungus Marasmius cladophyllus UMAS MS8

Wide spectrum usage of synthetic dyes particularly by the textile and dyestuff industry has caused serious pollution of rivers and lake due to insufficient treatment of dye containing wastewater by current known wastewater treatment methods. Endophytic fungi were therefore isolated from Melastoma ma...

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Main Author: Ngieng, Ngui Sing
Format: Thesis
Language:English
Published: unimas 2017
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Online Access:http://ir.unimas.my/id/eprint/20968/1/Ngieng%20Ngui%20Sing%20ft.pdf
http://ir.unimas.my/id/eprint/20968/
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Institution: Universiti Malaysia Sarawak
Language: English
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spelling my.unimas.ir.209682023-05-18T08:01:53Z http://ir.unimas.my/id/eprint/20968/ Characterisation of Synthetic Dye Decolourising Genes and their Enzymes Produced by an Endophytic Fungus Marasmius cladophyllus UMAS MS8 Ngieng, Ngui Sing Q Science (General) QH Natural history QH301 Biology Wide spectrum usage of synthetic dyes particularly by the textile and dyestuff industry has caused serious pollution of rivers and lake due to insufficient treatment of dye containing wastewater by current known wastewater treatment methods. Endophytic fungi were therefore isolated from Melastoma malabathricum (local name: Senduduk) to test for their ability to decolourise synthetic dyes. Screening on agar plate for synthetic dye decolourisation has enabled the identification of an isolate MS8 that is capable of decolourising all the synthetic dye tested. Synthetic dye decolourisation in liquid medium by MS8 further confirmed the ability of the fungus to decolourise both azo and anthraquinone dyes. Comparing the ITS sequence with NCBI GenBank identified the fungus to be Marasmius cladophyllus. Study on the dye decolourising mechanism of M. cladophyllus in liquid medium using RBBR dye showed the fungus degradative capability in decolourising the dye with no dye adsorption on the fungal mycelium. Further ligninolytic enzyme assay revealed that the presence of RBBR dye induced a 70 folds increase in laccase activity by M. cladophyllus. This laccase enzyme after precipitation by ammonium sulphate can also decolourise 90.2% of RBBR dye, 80.0% of Methyl red, 59.1% of Congo red and 56.1% of Orange G in just 24 hours thus indicating that laccase is the dye decolourising enzyme. unimas 2017 Thesis NonPeerReviewed text en http://ir.unimas.my/id/eprint/20968/1/Ngieng%20Ngui%20Sing%20ft.pdf Ngieng, Ngui Sing (2017) Characterisation of Synthetic Dye Decolourising Genes and their Enzymes Produced by an Endophytic Fungus Marasmius cladophyllus UMAS MS8. PhD thesis, UNIMAS.
institution Universiti Malaysia Sarawak
building Centre for Academic Information Services (CAIS)
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Sarawak
content_source UNIMAS Institutional Repository
url_provider http://ir.unimas.my/
language English
topic Q Science (General)
QH Natural history
QH301 Biology
spellingShingle Q Science (General)
QH Natural history
QH301 Biology
Ngieng, Ngui Sing
Characterisation of Synthetic Dye Decolourising Genes and their Enzymes Produced by an Endophytic Fungus Marasmius cladophyllus UMAS MS8
description Wide spectrum usage of synthetic dyes particularly by the textile and dyestuff industry has caused serious pollution of rivers and lake due to insufficient treatment of dye containing wastewater by current known wastewater treatment methods. Endophytic fungi were therefore isolated from Melastoma malabathricum (local name: Senduduk) to test for their ability to decolourise synthetic dyes. Screening on agar plate for synthetic dye decolourisation has enabled the identification of an isolate MS8 that is capable of decolourising all the synthetic dye tested. Synthetic dye decolourisation in liquid medium by MS8 further confirmed the ability of the fungus to decolourise both azo and anthraquinone dyes. Comparing the ITS sequence with NCBI GenBank identified the fungus to be Marasmius cladophyllus. Study on the dye decolourising mechanism of M. cladophyllus in liquid medium using RBBR dye showed the fungus degradative capability in decolourising the dye with no dye adsorption on the fungal mycelium. Further ligninolytic enzyme assay revealed that the presence of RBBR dye induced a 70 folds increase in laccase activity by M. cladophyllus. This laccase enzyme after precipitation by ammonium sulphate can also decolourise 90.2% of RBBR dye, 80.0% of Methyl red, 59.1% of Congo red and 56.1% of Orange G in just 24 hours thus indicating that laccase is the dye decolourising enzyme.
format Thesis
author Ngieng, Ngui Sing
author_facet Ngieng, Ngui Sing
author_sort Ngieng, Ngui Sing
title Characterisation of Synthetic Dye Decolourising Genes and their Enzymes Produced by an Endophytic Fungus Marasmius cladophyllus UMAS MS8
title_short Characterisation of Synthetic Dye Decolourising Genes and their Enzymes Produced by an Endophytic Fungus Marasmius cladophyllus UMAS MS8
title_full Characterisation of Synthetic Dye Decolourising Genes and their Enzymes Produced by an Endophytic Fungus Marasmius cladophyllus UMAS MS8
title_fullStr Characterisation of Synthetic Dye Decolourising Genes and their Enzymes Produced by an Endophytic Fungus Marasmius cladophyllus UMAS MS8
title_full_unstemmed Characterisation of Synthetic Dye Decolourising Genes and their Enzymes Produced by an Endophytic Fungus Marasmius cladophyllus UMAS MS8
title_sort characterisation of synthetic dye decolourising genes and their enzymes produced by an endophytic fungus marasmius cladophyllus umas ms8
publisher unimas
publishDate 2017
url http://ir.unimas.my/id/eprint/20968/1/Ngieng%20Ngui%20Sing%20ft.pdf
http://ir.unimas.my/id/eprint/20968/
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