Information Package / Course Catalogue
Recombinant DNA Technology
Course Code: ZZO510
Course Type: Area Elective
Couse Group: Second Cycle (Master's Degree)
Education Language: Turkish
Work Placement: N/A
Theory: 3
Prt.: 0
Credit: 3
Lab: 0
ECTS: 6
Objectives of the Course

The primary objective of this course is to provide graduate students with a comprehensive understanding of the molecular principles, methodologies, and applications of recombinant DNA technology in animal science. The course covers the theoretical foundations and practical applications of fundamental molecular biology techniques, including DNA isolation, restriction enzymes, cloning vectors, polymerase chain reaction (PCR), gene cloning, DNA sequencing, gene expression analysis, genome editing technologies, and recombinant protein production. Emphasis is placed on the application of recombinant DNA technologies in animal breeding, molecular genetics, genomic selection, biotechnology, disease resistance, functional genomics, and sustainable livestock production systems. Upon successful completion of the course, students will be able to critically evaluate molecular biological techniques, select appropriate recombinant DNA methodologies for research purposes, interpret molecular data, and integrate contemporary biotechnological approaches into advanced research and innovation in animal science.

Course Content

1- Fundamental principles of recombinant DNA technology and its role in molecular biology. 2- Nucleic acid isolation, purification, and quality assessment methods. 3- Restriction enzymes, DNA ligases, and strategies for recombinant DNA construction. 4- Cloning vectors, host cell systems, and gene cloning techniques. 5- Polymerase Chain Reaction (PCR), quantitative real-time PCR (qPCR), and DNA amplification methods. 6- DNA sequencing technologies, next-generation sequencing (NGS), and genome analysis. 7- Gene expression analysis, recombinant protein production, and functional genomics applications. 8- Genome editing technologies (CRISPR/Cas systems) and their applications in animal biotechnology. 9- Applications of recombinant DNA technologies in animal breeding, genomic selection, disease resistance, and molecular genetics research. 10- Biosafety, ethical considerations, regulatory frameworks, and laboratory practices in recombinant DNA technology.

Name of Lecturer(s)
Learning Outcomes
1.Explain the fundamental principles of recombinant DNA technology, molecular biology techniques, and their applications in animal science.
2.Select and evaluate appropriate methodologies for DNA isolation, PCR, gene cloning, DNA sequencing, and gene expression analysis used in recombinant DNA research.
3.Interpret molecular data generated through recombinant DNA technologies and apply these data in animal breeding, molecular genetics, and biotechnology research.
4.Critically analyze genome editing technologies, particularly CRISPR/Cas systems, and recombinant protein production approaches, and evaluate their potential applications in animal biotechnology.
5.Apply appropriate laboratory practices by considering biosafety, ethical principles, and regulatory requirements in recombinant DNA technology, and critically evaluate recent scientific advances in the field.
Recommended or Required Reading
1.Gene Cloning and DNA Analysis: An Introduction, 6th Edition, T. Brown, Wiley-Blackwell, ISBN: 978-1-4051-8173-0,
2.From Genes to Genomes: Concepts and Applicaitons of DNA Technology, 2nd Edition, Dale, von Schantz, John Wiley & Sons, Ltd, ISBN: 978-0-470-01734-0, 2007
3.Principles of Gene Manipulation and Genomics, 7th Edition, Primrose, Twyman, Blackwell Publishing, ISBN: 978-1-4051-3544-3, 2006
Weekly Detailed Course Contents
Week 1 - Theoretical
Introduction to recombinant DNA technology, its historical development, and applications in animal science
Week 2 - Theoretical
Structure and organization of DNA and RNA, and fundamental principles of molecular biology
Week 3 - Theoretical
Nucleic acid isolation, purification, and quality assessment methods
Week 4 - Theoretical
Restriction enzymes, DNA ligases, and construction of recombinant DNA molecules
Week 5 - Theoretical
Cloning vectors, plasmids, bacteriophages, and host cell systems
Week 6 - Theoretical
Gene cloning techniques, transformation, and verification of recombinant DNA
Week 7 - Theoretical
Polymerase Chain Reaction (PCR), quantitative real-time PCR (qPCR), and DNA amplification techniques
Week 8 - Theoretical
DNA sequencing methods: Sanger sequencing and Next-Generation Sequencing (NGS) technologies
Week 9 - Theoretical
Gene expression analysis and transcriptomic approaches
Week 10 - Theoretical
Recombinant protein production, expression systems, and protein purification methods
Week 11 - Theoretical
Genome editing technologies: CRISPR/Cas systems, TALENs, and zinc-finger nucleases (ZFNs)
Week 12 - Theoretical
Applications of recombinant DNA technologies in animal breeding, genomic selection, and functional genomics
Week 13 - Theoretical
Biosafety, ethical aspects, and national/international regulatory frameworks for recombinant DNA technology
Week 14 - Theoretical
Recent advances in biotechnology, case studies, critical evaluation of scientific literature, and overall course review
Assessment Methods and Criteria
Type of AssessmentCountPercent
Assignment1%10
Quiz1%10
Assignment Examination1%10
Final Examination1%70
Workload Calculation
ActivitiesCountPreparationTimeTotal Work Load (hours)
Lecture - Theory143384
Assignment18311
Assignment Examination18311
Quiz18311
Final Examination128331
TOTAL WORKLOAD (hours)148
Contribution of Learning Outcomes to Programme Outcomes
PÇ-1
PÇ-2
PÇ-3
PÇ-4
PÇ-5
PÇ-6
PÇ-7
OÇ-1
5
OÇ-2
5
3
OÇ-3
5
3
OÇ-4
5
5
5
5
OÇ-5
5
5
5
Adnan Menderes University - Information Package / Course Catalogue
2026