Abstract
Microalgae has been widely known as a natural sources of highly potential of bioactive compounds that are valuable in many factors such as food, cosmetics and even biopharmaceutical application. Previous research found out that microalgae has beneficial properties that make this species useful in the pharmaceutical product such antioxidant, antimicrobial and anticancer properties. However, current methodologies for microalgae identification are very laborious and time-consuming. The requirement of many reagents and steps involved in the microalgae identification leads to a large investment of money needed; the researchers are more susceptible to chemical exposure and lead to a very time-consuming process. These factors cause microalgae identifications are very challenging which concurrently influence the utilization of microalgae. Rapid and simple methods for microalgae identification that are able to eliminate these challenges are in demand. New rapid methods are derived in this study by eliminating the reagents involved in the conventional method. Rapid Method 1 requires addition of Tris-EDT A with physical mean while Rapid Method 2 requires physical mean only for DNA extraction. The conventional PROMEGA method is included in this study to allow comparison to be made between conventional method and rapid method. Three samples of microalgae were subjected with different parameters of microalgae identification to identify the most effective method for microalgae identification. Rapid Method 2 shows the bright amplification band similar to the conventional PROMEGA kit which indicated these methods is able to yield the PCR product. However, Rapid Method 1 did not show any amplification band which is not suitable for the microalgae identification. This finding helps in the development of new rapid and simple method in the microalgae identification. Thus, promote microalgae research thus utilization of microalgae for their benefits is increasing.
Metadata
Item Type: | Thesis (Degree) |
---|---|
Creators: | Creators Email / ID Num. Ahmad, Erra Fazira UNSPECIFIED |
Contributors: | Contribution Name Email / ID Num. Thesis advisor Ahmad, Norazlina UNSPECIFIED |
Subjects: | Q Science > QK Botany Q Science > QP Physiology R Medicine > RB Pathology > Clinical pathology. Laboratory technique |
Divisions: | Universiti Teknologi MARA, Selangor > Puncak Alam Campus > Faculty of Pharmacy |
Programme: | Bachelor of Pharmacy |
Keywords: | PCR, Malaysian microalgae |
Date: | 2015 |
URI: | https://ir.uitm.edu.my/id/eprint/116288 |
Download
![[thumbnail of 116288.PDF]](https://ir.uitm.edu.my/style/images/fileicons/text.png)
116288.PDF
Download (1MB)
Digital Copy
Physical Copy

ID Number
116288
Indexing

