Molecular study of psammobia rostratus (ambal goyang) from Buntal Bay, Sarawak

Pcannnohia rostratus (Antbai Govang) is one of the species of clams that spread along Buntal bay area. P. rostratus is filter feeders that plays important role in ecological services. They are harvested by local people from August to March during low tide either for domestic consumption or side inc...

Full description

Saved in:
Bibliographic Details
Main Author: Mohd Fazhan, Bin Mohd Hanafiah
Format: Final Year Project Report
Language:English
Published: Universiti Malaysia Sarawak (UNIMAS) 2009
Subjects:
Online Access:http://ir.unimas.my/id/eprint/23743/2/Molecular%20study%20of%20Psammobia%20rostratus%20%28Ambal%20Goyang%29...%28fulltext%29.pdf
http://ir.unimas.my/id/eprint/23743/
Tags: Add Tag
No Tags, Be the first to tag this record!
id my.unimas.ir.23743
record_format eprints
spelling my.unimas.ir.237432023-09-11T06:29:56Z http://ir.unimas.my/id/eprint/23743/ Molecular study of psammobia rostratus (ambal goyang) from Buntal Bay, Sarawak Mohd Fazhan, Bin Mohd Hanafiah Q Science (General) QR Microbiology Pcannnohia rostratus (Antbai Govang) is one of the species of clams that spread along Buntal bay area. P. rostratus is filter feeders that plays important role in ecological services. They are harvested by local people from August to March during low tide either for domestic consumption or side income. The aims of this study were to amplify and sequence the 16S rRNA gene, COI gene, ITS gene and ITS1 gene, documented the PCR-RFLP restriction profile of ITS gene. The modified CTAB DNA extraction method and modified Phenol Chloroform DNA extraction method were used to extract the total genomics DNA of about 33 samples of P. rostratus from Buntal bay area. In this study, the amplification of the mitochondrial gene, 16S rRNA gene generated fragment size approximately 550 bp whereas the COI gene only generated fragment approximately 350 bp. For nuclear DNA gene, the size of ITS gene are approximately 1000 bp and no positive result yielded for the amplification of ITS I gene. After PCR, the 16S rRNA gene, COI gene and ITS gene were purified and sent to commercial company for sequencing but the sequencing result was noisy and cannot be used for further analysis. The PCR product of ITS gene were subjected for PCR-RFLP analysis using 10 restriction enzymes (REs) namely Csp61, Hindlll, Tagl, Mholl, BsuRI, MnII, MspI (Hpall), Mbol, Ail and Rsal. Excluding Csp6I and Hindlll, all REs successfully revealed the restriction profile. Universiti Malaysia Sarawak (UNIMAS) 2009 Final Year Project Report NonPeerReviewed text en http://ir.unimas.my/id/eprint/23743/2/Molecular%20study%20of%20Psammobia%20rostratus%20%28Ambal%20Goyang%29...%28fulltext%29.pdf Mohd Fazhan, Bin Mohd Hanafiah (2009) Molecular study of psammobia rostratus (ambal goyang) from Buntal Bay, Sarawak. [Final Year Project Report] (Unpublished)
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)
QR Microbiology
spellingShingle Q Science (General)
QR Microbiology
Mohd Fazhan, Bin Mohd Hanafiah
Molecular study of psammobia rostratus (ambal goyang) from Buntal Bay, Sarawak
description Pcannnohia rostratus (Antbai Govang) is one of the species of clams that spread along Buntal bay area. P. rostratus is filter feeders that plays important role in ecological services. They are harvested by local people from August to March during low tide either for domestic consumption or side income. The aims of this study were to amplify and sequence the 16S rRNA gene, COI gene, ITS gene and ITS1 gene, documented the PCR-RFLP restriction profile of ITS gene. The modified CTAB DNA extraction method and modified Phenol Chloroform DNA extraction method were used to extract the total genomics DNA of about 33 samples of P. rostratus from Buntal bay area. In this study, the amplification of the mitochondrial gene, 16S rRNA gene generated fragment size approximately 550 bp whereas the COI gene only generated fragment approximately 350 bp. For nuclear DNA gene, the size of ITS gene are approximately 1000 bp and no positive result yielded for the amplification of ITS I gene. After PCR, the 16S rRNA gene, COI gene and ITS gene were purified and sent to commercial company for sequencing but the sequencing result was noisy and cannot be used for further analysis. The PCR product of ITS gene were subjected for PCR-RFLP analysis using 10 restriction enzymes (REs) namely Csp61, Hindlll, Tagl, Mholl, BsuRI, MnII, MspI (Hpall), Mbol, Ail and Rsal. Excluding Csp6I and Hindlll, all REs successfully revealed the restriction profile.
format Final Year Project Report
author Mohd Fazhan, Bin Mohd Hanafiah
author_facet Mohd Fazhan, Bin Mohd Hanafiah
author_sort Mohd Fazhan, Bin Mohd Hanafiah
title Molecular study of psammobia rostratus (ambal goyang) from Buntal Bay, Sarawak
title_short Molecular study of psammobia rostratus (ambal goyang) from Buntal Bay, Sarawak
title_full Molecular study of psammobia rostratus (ambal goyang) from Buntal Bay, Sarawak
title_fullStr Molecular study of psammobia rostratus (ambal goyang) from Buntal Bay, Sarawak
title_full_unstemmed Molecular study of psammobia rostratus (ambal goyang) from Buntal Bay, Sarawak
title_sort molecular study of psammobia rostratus (ambal goyang) from buntal bay, sarawak
publisher Universiti Malaysia Sarawak (UNIMAS)
publishDate 2009
url http://ir.unimas.my/id/eprint/23743/2/Molecular%20study%20of%20Psammobia%20rostratus%20%28Ambal%20Goyang%29...%28fulltext%29.pdf
http://ir.unimas.my/id/eprint/23743/
_version_ 1778166681452937216
score 13.214268