Isolation and identification of denitryifing from indegenous mircroorganism

The objective of this study was to isolate and identify novel potential denitrifying bacteria from two different Kuantan areas which are Jubli Perak Agricultural Park, Kuantan (3º50'49.6"N103º18'06.1"E) and Felda Lepar Hilir, Kuantan (3º40'41.4"N 103º03'24.7"E...

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Main Authors: Maizatul Farhain, Ismail, Nurul 'Azyyati, Sabri, Saiful Nizam, Tajuddin, Lee, Chin Mei, Siti Hatijah, Mortan, Ab. Rahim, Mohd-Hairul
Format: Article
Language:English
Published: The Official Publication of The Malaysian Society for Biochemistry & Molecular Biology (MSBMB) 2019
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Online Access:http://umpir.ump.edu.my/id/eprint/24871/1/Maizatul%20Farhain%20Ismail%20et%20al%20galley%20proof.pdf
http://umpir.ump.edu.my/id/eprint/24871/
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spelling my.ump.umpir.248712019-05-08T07:06:30Z http://umpir.ump.edu.my/id/eprint/24871/ Isolation and identification of denitryifing from indegenous mircroorganism Maizatul Farhain, Ismail Nurul 'Azyyati, Sabri Saiful Nizam, Tajuddin Lee, Chin Mei Siti Hatijah, Mortan Ab. Rahim, Mohd-Hairul T Technology (General) TP Chemical technology The objective of this study was to isolate and identify novel potential denitrifying bacteria from two different Kuantan areas which are Jubli Perak Agricultural Park, Kuantan (3º50'49.6"N103º18'06.1"E) and Felda Lepar Hilir, Kuantan (3º40'41.4"N 103º03'24.7"E). Indigenous Microorganisms (IMOs) available in the locations were cultivated by fermentation of steamed rice in the location together with brown sugar. Serial dilutions of the fermented medium were spread on Jensen’s agar and incubated at 30 ºC for eight days. A total of six colonies were subjected to various biochemical analysis including Gram staining, catalase, methyl red, carbohydrate fermentation and nitrate reduction tests. All bacterial isolates were subjected to genomic DNA extraction and PCR amplification of 16S rRNA genes using 27F and 1942R primers. All the amplified product of 16S rRNA genes from the bacterial isolates were purified and sent for sequencing. BLASTn and phylogenetic analysis based on 16S rRNA gene sequences shown all the isolates belong to Bacillus spp. and clustered into two main clusters. The Official Publication of The Malaysian Society for Biochemistry & Molecular Biology (MSBMB) 2019 Article PeerReviewed pdf en http://umpir.ump.edu.my/id/eprint/24871/1/Maizatul%20Farhain%20Ismail%20et%20al%20galley%20proof.pdf Maizatul Farhain, Ismail and Nurul 'Azyyati, Sabri and Saiful Nizam, Tajuddin and Lee, Chin Mei and Siti Hatijah, Mortan and Ab. Rahim, Mohd-Hairul (2019) Isolation and identification of denitryifing from indegenous mircroorganism. Malaysian Journal Of Biochemistry & Molecular Biology (1). pp. 17-21. ISSN ISSN: 1511-2616, E-ISSN 2600-9005, http://mjbmb.org
institution Universiti Malaysia Pahang
building UMP Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Pahang
content_source UMP Institutional Repository
url_provider http://umpir.ump.edu.my/
language English
topic T Technology (General)
TP Chemical technology
spellingShingle T Technology (General)
TP Chemical technology
Maizatul Farhain, Ismail
Nurul 'Azyyati, Sabri
Saiful Nizam, Tajuddin
Lee, Chin Mei
Siti Hatijah, Mortan
Ab. Rahim, Mohd-Hairul
Isolation and identification of denitryifing from indegenous mircroorganism
description The objective of this study was to isolate and identify novel potential denitrifying bacteria from two different Kuantan areas which are Jubli Perak Agricultural Park, Kuantan (3º50'49.6"N103º18'06.1"E) and Felda Lepar Hilir, Kuantan (3º40'41.4"N 103º03'24.7"E). Indigenous Microorganisms (IMOs) available in the locations were cultivated by fermentation of steamed rice in the location together with brown sugar. Serial dilutions of the fermented medium were spread on Jensen’s agar and incubated at 30 ºC for eight days. A total of six colonies were subjected to various biochemical analysis including Gram staining, catalase, methyl red, carbohydrate fermentation and nitrate reduction tests. All bacterial isolates were subjected to genomic DNA extraction and PCR amplification of 16S rRNA genes using 27F and 1942R primers. All the amplified product of 16S rRNA genes from the bacterial isolates were purified and sent for sequencing. BLASTn and phylogenetic analysis based on 16S rRNA gene sequences shown all the isolates belong to Bacillus spp. and clustered into two main clusters.
format Article
author Maizatul Farhain, Ismail
Nurul 'Azyyati, Sabri
Saiful Nizam, Tajuddin
Lee, Chin Mei
Siti Hatijah, Mortan
Ab. Rahim, Mohd-Hairul
author_facet Maizatul Farhain, Ismail
Nurul 'Azyyati, Sabri
Saiful Nizam, Tajuddin
Lee, Chin Mei
Siti Hatijah, Mortan
Ab. Rahim, Mohd-Hairul
author_sort Maizatul Farhain, Ismail
title Isolation and identification of denitryifing from indegenous mircroorganism
title_short Isolation and identification of denitryifing from indegenous mircroorganism
title_full Isolation and identification of denitryifing from indegenous mircroorganism
title_fullStr Isolation and identification of denitryifing from indegenous mircroorganism
title_full_unstemmed Isolation and identification of denitryifing from indegenous mircroorganism
title_sort isolation and identification of denitryifing from indegenous mircroorganism
publisher The Official Publication of The Malaysian Society for Biochemistry & Molecular Biology (MSBMB)
publishDate 2019
url http://umpir.ump.edu.my/id/eprint/24871/1/Maizatul%20Farhain%20Ismail%20et%20al%20galley%20proof.pdf
http://umpir.ump.edu.my/id/eprint/24871/
http://mjbmb.org
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score 13.18916