Asexual Prokaryotes Flashcards
(34 cards)
Mutations
Permanent change in the DNA sequence of an organism.
Mutant
Resulting organism of a mutation may have a recognizable change in phenotype compared to wild type
Wild type
Phenotype most commonly observed in nature.
Point mutation
Affects a single base and most commonly occurs when one base is substituted or replaced by another.
Insertion
Addition of one or more bases in mutation
Deletion
Removal of one or more bases in mutations
Silent mutation
Sequence change having no effect on the proteins structure.
Missense mutations
Results in a different amino acid being incorporated into the resulting polypeptide. The effect depends on how chemically different the new amino acid is from the wild type amino acid. Location of the changed amino acid in the protein is also important.
Conditional mutations
Effects of missense mutations may be only apparent under certain environmental conditions.
Nonsense mutations
Point mutation that converts to a codon encoding an amino acid (sense codon) into a stop codon (nonsense codon). Result in synthesis of proteins that are shorter than the wild type and typically not functional.
Frameshift mutations
Causes by insertions or deletions of a number of nucleotides that aren’t a multiple of 3 are problematic because a shift in the reading frame results. Can change every amino acid after the point of mutation. Always nonfunctional
Spontaneous mutations
Caused by mistakes in the process of DNA replication
Induced mutations
Caused by exposure to mutagens which are various types of chemical agents or radiation
Carcinogens
Mutagen agents that cause cancer
Nucleoside analogs
Chemicals structurally similar to normal nucleotide bases and can be incorporated into DMA during replications.
Intercalating agents
These molecules slide between stacked nitrogenous bases of the DNA double helix, distorting the molecules and creating atypical spacing between nucleotide base pairs. As a result, In DNA replication, DNA polymerase may have insertion or deletion.
Strong ionizing radiation
Like x rays and gamma rays can cause single and double stranded breaks in the DNA backbone through formation of hydroxyl radicals or radiation exposure. Can also modify bases
Used to kill microbes to sterilize medical devices and food.
Nonionizing radiation
Like UV light can induce dimer formation between 2 adjacent pyramidine bases, commonly 2 thymines with a nucleotide strand.
Thymine dimer
During formation the 2 adjacent thymine become covalently linked and if left I repaired both DNA replication and transcription are stalled at this point. DNA polymerase may proceed and replicate the dimer incorrectly, potentially leading to frameshift or point mutations.
Proofreading
Dna polymerase reads the newly added base ensuring that it’s complimentary to the corresponding base in the template strand before adding the next one. if an incorrect base has been added, the enzyme makes a cut to relax the wrong nucleotide and a new base is added.
Mismatch repair
A mechanism where enzymes recognize the incorrectly added nucleotide, excise it and replace it with the correct base.
Nucleotide excision repair
Enzymes remove the pyramidine dimer and replace it with the correct nucleotide
Direct repair
Of thymine dimers occurs through the
Process of photoreactivation in the presence of visible light.
Replica plating
Technique used to identify bacterial mutants used to identify nutritional mutants called auxotrophs