Organisms whose genetic material has been altered using genetic engineering techniques. This alteration can involve inserting, deleting, or modifying specific genes to achieve desired traits.
Transgenic organisms
A subset of GMOs where genetic material from one species is inserted into the genome of another species. This results in the expression of traits or characteristics from the inserted gene.
DNA Transfer
1. Transformation
2. Transduction
3. Conjugation
DNA arrangement in cells
In eukaryotic cells, chromosomes are found within the nucleus and are composed of chromatin (DNA and associated proteins)
Prokaryotic cells have a single, circular chromosome
Proteins
Large biomolecules made up of amino acids linked together by peptide bonds. They play critical roles in various cellular functions.
Protein structure
Primary (amino acid sequence)
Secondary (local folding patterns like alpha helices and beta sheets)
Tertiary (overall 3D structure)
Quaternary (arrangement of multiple protein subunits)
Transcription
The process by which RNA is synthesized from a DNA template.
Translation
The process by which proteins are synthesized using the mRNA template.
Proteomes
The entire set of proteins expressed by an organism.
Biochemical pathways
Sequences of chemical reactions occurring within a cell, often involving enzymes and substrates.
CRISPR-Cas9
A gene-editing tool derived from a bacterial immune system that allows precise editing of DNA sequences by targeting specific locations in the genome and introducing changes such as gene knockouts, insertions, or modifications.
Plasmids
Small, circular DNA molecules found in bacteria and used as vehicles to carry and transfer foreign genetic material between organisms.
Recombinant plasmid construction
Inserting foreign DNA fragments (e.g., genes) into plasmid vectors using restriction enzymes and ligases.
Enzymes in genetic engineering
Polymerases
Ligases
Restriction enzymes
PCR (Polymerase Chain Reaction)
1. Denaturation
2. Annealing
3. Extension
PCR players
DNA template
Primers (short DNA sequences)
DNA polymerase
Nucleotides (A, T, C, G)
Buffer solution
Gel electrophoresis
Separates DNA fragments based on size by applying an electric field to a gel matrix
Gelelectrophoresisplayers
Gel
DNA samples
Buffer solution
Electrodes
The separated DNA fragments appear as bands on the gel, with smaller fragments migrating faster and farther than larger ones. The pattern of bands can be analyzed to determine fragment sizes.
GMOs
Organisms whose genetic material has been altered in a way that does not occur naturally through mating or natural recombination
Transgenic organisms
A specific type of GMOs where genetic material from one species is inserted into the genome of another species
Transgenic organisms
Are a type of GMOs
All transgenic organisms are GMOs, but not all GMOs are transgenic organisms
DNA Transfer
DNA can be transferred between organisms through transformation, transduction, and conjugation
DNA arrangement in eukaryotic cells
DNA is arranged into chromosomes within the nucleus, composed of chromatin (DNA and associated proteins)
DNA arrangement in prokaryotic cells
DNA is a single, circular chromosome
Proteins
Large biomolecules made up of amino acids linked by peptide bonds, playing critical roles in cellular functions
Protein structure
Primary (amino acid sequence)
Secondary (local folding patterns)
Tertiary (overall 3D structure)
Quaternary (arrangement of multiple subunits)
Transcription
The process by which RNA is synthesized from a DNA template
Translation
The process by which proteins are synthesized using the mRNA template
Proteome
The entire set of proteins expressed by an organism
Biochemical pathways
Sequences of chemical reactions occurring within a cell, often involving enzymes and substrates
Understanding proteomes and biochemical pathways is important when developing GMOs, particularly transgenic organisms, to ensure desired traits are expressed without disrupting essential cellular functions
CRISPR-Cas9
A gene-editing tool derived from a bacterial immune system
CRISPR-Cas9
Allows precise editing of DNA sequences by targeting specific locations in the genome and introducing changes such as gene knockouts, insertions, or modifications
Valuable for its simplicity, efficiency, and versatility in genome editing, making it a powerful tool for research and applications in biotechnology and medicine
Plasmids
Small, circular DNA molecules found in bacteria and used as vehicles to carry and transfer foreign genetic material between organisms
Plasmid vectors
Engineered plasmids designed to carry specific DNA sequences (e.g., genes of interest) into target cells
Making a recombinant plasmid
Insert foreign DNA
Polymerases
Enzymes that catalyze the synthesis of DNA or RNA strands from nucleotide triphosphates
Ligases
Enzymes that catalyze the joining of DNA fragments by forming phosphodiester bonds