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CBE551 Genetics And Molecular Biology UITM Assignment Answer Malaysia

CBE551 Genetics And Molecular Biology” at UITM in Malaysia introduces students to various tools and techniques used in genetic engineering and recombinant DNA technology. It covers topics such as recombinant DNA enzymes, cloning strategies, and bacterial transformation methods. 

The CBE551 course also includes DNA amplification and analysis techniques, as well as cloning and expression of mammalian and plant genes in bacteria. Practical applications of genetic engineering and biotechnology are explored throughout the course.

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Assignment Task 1 : Demonstrate an understanding of the principles of genetic engineering, biotechnology and recombinant DNA technology.

Genetic engineering is a branch of biotechnology that involves the deliberate manipulation of an organism’s genetic material to modify its characteristics or transfer desirable traits between organisms. Recombinant DNA technology is a key tool in genetic engineering, enabling the insertion of foreign DNA into an organism’s genome. Here are the key principles:

  • DNA Structure: The fundamental building block of genetic engineering is deoxyribonucleic acid (DNA), a double-stranded molecule comprising nucleotides. The sequence of nucleotides determines an organism’s genetic information.
  • Restriction Enzymes: These are specialized proteins used in recombinant DNA technology to cut DNA at specific recognition sites, generating fragments with “sticky ends” that facilitate DNA recombination.
  • DNA Ligase: An enzyme that catalyzes the joining of DNA fragments by creating phosphodiester bonds, essential for recombining DNA pieces.
  • Plasmids: Circular DNA molecules found in bacteria, which can be used as vectors to carry foreign DNA into host cells.
  • Gene Cloning: The process of isolating and making copies of a specific gene, which can be inserted into other organisms.
  • Polymerase Chain Reaction (PCR): A technique used to amplify a specific segment of DNA, producing millions of copies for further analysis or manipulation.
  • Genetic Transformation: The process of introducing foreign DNA into a host organism, altering its genetic makeup and potentially expressing new traits.
  • Gene Editing: Techniques like CRISPR-Cas9 enable precise modifications to specific genes, allowing for targeted alterations in the DNA sequence.

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Assignment Task 2 : Show a basic level of competency in problem solving, data processing and analysis associated with the field of genetic engineering

Problem-solving and data analysis are crucial aspects of genetic engineering. Researchers use these skills to identify genetic targets, optimize experimental conditions, and analyze outcomes. Here’s a basic overview:

  • Problem Identification: Define the research question or objective in genetic engineering, such as modifying a specific gene or improving an organism’s traits.
  • Experimental Design: Plan the steps and procedures needed to achieve the desired outcome. This may involve selecting suitable vectors, designing primers, and setting up control experiments.
  • Data Collection: Conduct experiments and gather data, which may include DNA sequences, PCR results, protein expression levels, or phenotypic observations.
  • Data Processing: Analyze and organize the collected data to identify patterns, correlations, or anomalies.
  • Data Analysis: Interpret the results using statistical methods and compare experimental groups to draw conclusions.
  • Troubleshooting: Address any issues that arise during experiments, such as failed amplifications, contamination, or unexpected outcomes.

Assignment Task 3 : Utilise and provide information on techniques used to manipulate living cells and overview genetic engineering methods

Various techniques are used to manipulate living cells and achieve genetic engineering goals. Here are some commonly employed methods:

  • DNA Cloning: Isolating a gene of interest and inserting it into a plasmid or vector, which is then introduced into a host organism.
  • Polymerase Chain Reaction (PCR): Amplifying specific DNA sequences in vitro, enabling their further analysis or manipulation.
  • CRISPR-Cas9: A revolutionary gene-editing tool that uses RNA-guided Cas9 proteins to cut specific DNA sequences and introduce targeted genetic modifications.
  • RNA Interference (RNAi): Silencing genes by introducing small interfering RNAs (siRNAs) to block gene expression.
  • DNA Sequencing: Determining the precise order of nucleotides in a DNA molecule, enabling the identification of genes and mutations.
  • Gel Electrophoresis: Separating DNA, RNA, or proteins based on size and charge to analyze and compare samples.
  • Transgenic Organisms: Introducing foreign DNA into an organism to express specific traits or proteins.
  • Gene Synthesis: Constructing artificial genes with desired sequences for various applications.
  • Site-Directed Mutagenesis: Introducing specific mutations into DNA sequences to study gene function or create desired changes.
  • Gene Expression Analysis: Assessing the level of gene expression using techniques like reverse transcription PCR (RT-PCR) or RNA sequencing.

These techniques and principles form the foundation of genetic engineering and biotechnology, enabling researchers to manipulate living organisms for various beneficial purposes.

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