Developing DNA barcodes of harmful marine microalgae in Malaysia

Morphological identification of microalgae species are required expertise in the taxonomy and well-trained skills in advanced microscopy. A new molecular tool, DNA barcode is widely used as molecular-based identification system that aims to identify biological species and to group them to a given s...

Full description

Saved in:
Bibliographic Details
Main Author: Cheng, Sue Lin.
Format: Final Year Project Report
Language:English
Published: Universiti Malaysia Sarawak (UNIMAS) 2014
Subjects:
Online Access:http://ir.unimas.my/id/eprint/23721/2/Developing%20DNA%20barcodes%20of%20harmful%20marine%20microalgae%20in%20Malaysia%20%28fulltext%29.pdf
http://ir.unimas.my/id/eprint/23721/
Tags: Add Tag
No Tags, Be the first to tag this record!
id my.unimas.ir.23721
record_format eprints
spelling my.unimas.ir.237212023-01-30T07:47:31Z http://ir.unimas.my/id/eprint/23721/ Developing DNA barcodes of harmful marine microalgae in Malaysia Cheng, Sue Lin. Q Science (General) QH Natural history Morphological identification of microalgae species are required expertise in the taxonomy and well-trained skills in advanced microscopy. A new molecular tool, DNA barcode is widely used as molecular-based identification system that aims to identify biological species and to group them to a given species. Harmful microalgae are harmful and toxic to the marine lifes. Human being also affected by the intoxication of harmful algal blooms (HABs). In this study, DNA barcoding is developed to characterize the species of harmful microalgae to ease the monitoring purposes. The second internal transcribed spacer (ITS2) of the nuclear encoded ribosomal DNA (rDNA) is used as the potential barcode coupled with its secondary structural information. In brief, the study involved plankton sampling that is undertaken by plankton net hauls from the coastal waters of Malaysia and Singapore in order to establish new cultures of harmful marine microalgae species found in both waters. Preserved plankton samples are examined by using scanning electron microscope and light microscope to obtain morphology of the species. Single-cell PCR is performed using saline ethanolpreserved natural samples. Clonal cultures are established from live samples collected. Gene amplification is performed to amplify the ITS region on culture samples. Homologous modeling and free energy minimization approaches are used to model the ITS2 secondary structure of the harmful microalgae found in Malaysian waters. Sequence signatures of species found is assigned for DNA barcoding. In the end of this study, detailed morphology of the harmful microalgae as well as their DNA barcode are obtained. Universiti Malaysia Sarawak (UNIMAS) 2014 Final Year Project Report NonPeerReviewed text en http://ir.unimas.my/id/eprint/23721/2/Developing%20DNA%20barcodes%20of%20harmful%20marine%20microalgae%20in%20Malaysia%20%28fulltext%29.pdf Cheng, Sue Lin. (2014) Developing DNA barcodes of harmful marine microalgae in Malaysia. [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)
QH Natural history
spellingShingle Q Science (General)
QH Natural history
Cheng, Sue Lin.
Developing DNA barcodes of harmful marine microalgae in Malaysia
description Morphological identification of microalgae species are required expertise in the taxonomy and well-trained skills in advanced microscopy. A new molecular tool, DNA barcode is widely used as molecular-based identification system that aims to identify biological species and to group them to a given species. Harmful microalgae are harmful and toxic to the marine lifes. Human being also affected by the intoxication of harmful algal blooms (HABs). In this study, DNA barcoding is developed to characterize the species of harmful microalgae to ease the monitoring purposes. The second internal transcribed spacer (ITS2) of the nuclear encoded ribosomal DNA (rDNA) is used as the potential barcode coupled with its secondary structural information. In brief, the study involved plankton sampling that is undertaken by plankton net hauls from the coastal waters of Malaysia and Singapore in order to establish new cultures of harmful marine microalgae species found in both waters. Preserved plankton samples are examined by using scanning electron microscope and light microscope to obtain morphology of the species. Single-cell PCR is performed using saline ethanolpreserved natural samples. Clonal cultures are established from live samples collected. Gene amplification is performed to amplify the ITS region on culture samples. Homologous modeling and free energy minimization approaches are used to model the ITS2 secondary structure of the harmful microalgae found in Malaysian waters. Sequence signatures of species found is assigned for DNA barcoding. In the end of this study, detailed morphology of the harmful microalgae as well as their DNA barcode are obtained.
format Final Year Project Report
author Cheng, Sue Lin.
author_facet Cheng, Sue Lin.
author_sort Cheng, Sue Lin.
title Developing DNA barcodes of harmful marine microalgae in Malaysia
title_short Developing DNA barcodes of harmful marine microalgae in Malaysia
title_full Developing DNA barcodes of harmful marine microalgae in Malaysia
title_fullStr Developing DNA barcodes of harmful marine microalgae in Malaysia
title_full_unstemmed Developing DNA barcodes of harmful marine microalgae in Malaysia
title_sort developing dna barcodes of harmful marine microalgae in malaysia
publisher Universiti Malaysia Sarawak (UNIMAS)
publishDate 2014
url http://ir.unimas.my/id/eprint/23721/2/Developing%20DNA%20barcodes%20of%20harmful%20marine%20microalgae%20in%20Malaysia%20%28fulltext%29.pdf
http://ir.unimas.my/id/eprint/23721/
_version_ 1756688304406790144
score 13.188404