Structure elucidation of transformed metabolites from bioactive compounds using microbial transformations as a green synthetic tool / Mohd Zaimi Mohd Noor

Biotransformation is considerably one of the foundational pillars of green chemistry practice. Chemical modification through biotransformation are performed in mild condition, room temperature, in water based syntheses pot and can provide efficient alternative to chemical syntheses as the microbial...

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Main Author:	Mohd Noor, Mohd Zaimi
Format:	Thesis
Language:	English
Published:	2014
Subjects:	Botanical chemistry Phytochemicals Nutrition
Online Access:	https://ir.uitm.edu.my/id/eprint/34883/1/34883.pdf
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spelling	my-uitm-ir.348832022-07-06T04:16:19Z Structure elucidation of transformed metabolites from bioactive compounds using microbial transformations as a green synthetic tool / Mohd Zaimi Mohd Noor 2014 Mohd Noor, Mohd Zaimi Botanical chemistry. Phytochemicals Nutrition Biotransformation is considerably one of the foundational pillars of green chemistry practice. Chemical modification through biotransformation are performed in mild condition, room temperature, in water based syntheses pot and can provide efficient alternative to chemical syntheses as the microbial transformation can reduce the use and generation of hazardous substances. Biotransformation is an important tool for modification of organic compounds, especially natural product with complex structures like steroids. Microorganisms whole cell based biotransformation have been carried out by using steroidal compounds as starting point and few range of fungi have been screened in this bioconversion activity. This research has been focused on the structural modifications of steroids mediated by fungi, in order to investigate the effect of culture on substrate. In the study we have chosen to investigate the effect of Trichothecium roseum and SSW endophyte and it has been carried out for the first time. Biotransformation of tibolone by fungal Trichothecium roseum yielded five metabolites. The hydroxylations were mainly undergone in rings A, B and C, especially at C-3, C-6 and C-12 positions. The structural modification of an antiinflammatory drug, prednisolone by a marine endophytic fungus coded as SSW isolated from marine algae sea weed was reported for the first time. The biotransformation led to the formation of a known compound named 20p-hydroxy prednisolone. Transformation of 21-acetylprednisolone was done in parallel with prednisolone in order to see the effect of side chain of prednisolone in biotransformation. Endophytic fungus Penicilium lapidosum (SSW) also gave a positive result on deacetylation of 21-acetylprednisolone to prednisolone in two days fermentation and finally transformed to 20P-hydroxyprednisolone after six days fermentation. The absolute configuration of 20p-hydroxyprednisolone was also confirmed first time by both experimental and calculated chemical coupling constants and ECD spectra. The isolation and identification of marine endophytic fungus SSW was successfully performed in this study. The SSW strain sequence was blasted in National Centre for Biological Information (NCBI) Genebank. The blast showed 99% homology with Penicilium lapidosum database sequence. 2014 Thesis https://ir.uitm.edu.my/id/eprint/34883/ https://ir.uitm.edu.my/id/eprint/34883/1/34883.pdf text en public masters Universiti Teknologi MARA Faculty of Pharmacy Sultan, Sadia (Dr)
institution	Universiti Teknologi MARA
collection	UiTM Institutional Repository
language	English
advisor	Sultan, Sadia (Dr)
topic	Botanical chemistry Phytochemicals Nutrition
spellingShingle	Botanical chemistry Phytochemicals Nutrition Mohd Noor, Mohd Zaimi Structure elucidation of transformed metabolites from bioactive compounds using microbial transformations as a green synthetic tool / Mohd Zaimi Mohd Noor
description	Biotransformation is considerably one of the foundational pillars of green chemistry practice. Chemical modification through biotransformation are performed in mild condition, room temperature, in water based syntheses pot and can provide efficient alternative to chemical syntheses as the microbial transformation can reduce the use and generation of hazardous substances. Biotransformation is an important tool for modification of organic compounds, especially natural product with complex structures like steroids. Microorganisms whole cell based biotransformation have been carried out by using steroidal compounds as starting point and few range of fungi have been screened in this bioconversion activity. This research has been focused on the structural modifications of steroids mediated by fungi, in order to investigate the effect of culture on substrate. In the study we have chosen to investigate the effect of Trichothecium roseum and SSW endophyte and it has been carried out for the first time. Biotransformation of tibolone by fungal Trichothecium roseum yielded five metabolites. The hydroxylations were mainly undergone in rings A, B and C, especially at C-3, C-6 and C-12 positions. The structural modification of an antiinflammatory drug, prednisolone by a marine endophytic fungus coded as SSW isolated from marine algae sea weed was reported for the first time. The biotransformation led to the formation of a known compound named 20p-hydroxy prednisolone. Transformation of 21-acetylprednisolone was done in parallel with prednisolone in order to see the effect of side chain of prednisolone in biotransformation. Endophytic fungus Penicilium lapidosum (SSW) also gave a positive result on deacetylation of 21-acetylprednisolone to prednisolone in two days fermentation and finally transformed to 20P-hydroxyprednisolone after six days fermentation. The absolute configuration of 20p-hydroxyprednisolone was also confirmed first time by both experimental and calculated chemical coupling constants and ECD spectra. The isolation and identification of marine endophytic fungus SSW was successfully performed in this study. The SSW strain sequence was blasted in National Centre for Biological Information (NCBI) Genebank. The blast showed 99% homology with Penicilium lapidosum database sequence.
format	Thesis
qualification_level	Master's degree
author	Mohd Noor, Mohd Zaimi
author_facet	Mohd Noor, Mohd Zaimi
author_sort	Mohd Noor, Mohd Zaimi
title	Structure elucidation of transformed metabolites from bioactive compounds using microbial transformations as a green synthetic tool / Mohd Zaimi Mohd Noor
title_short	Structure elucidation of transformed metabolites from bioactive compounds using microbial transformations as a green synthetic tool / Mohd Zaimi Mohd Noor
title_full	Structure elucidation of transformed metabolites from bioactive compounds using microbial transformations as a green synthetic tool / Mohd Zaimi Mohd Noor
title_fullStr	Structure elucidation of transformed metabolites from bioactive compounds using microbial transformations as a green synthetic tool / Mohd Zaimi Mohd Noor
title_full_unstemmed	Structure elucidation of transformed metabolites from bioactive compounds using microbial transformations as a green synthetic tool / Mohd Zaimi Mohd Noor
title_sort	structure elucidation of transformed metabolites from bioactive compounds using microbial transformations as a green synthetic tool / mohd zaimi mohd noor
granting_institution	Universiti Teknologi MARA
granting_department	Faculty of Pharmacy
publishDate	2014
url	https://ir.uitm.edu.my/id/eprint/34883/1/34883.pdf
_version_	1783734282541334528

Structure elucidation of transformed metabolites from bioactive compounds using microbial transformations as a green synthetic tool / Mohd Zaimi Mohd Noor

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