Microbiology Module 3 Study Guide
Termini in questo insieme (31)
The flow of genetic material from DNA to RNA to protein.
RNA has a ribose sugar, uses uracil instead of thymine, and is usually single-stranded.
Both have a sugar, phosphate group, and nitrogenous base; DNA has deoxyribose, RNA has ribose.
DNA gyrase relieves supercoiling ahead of the replication fork by cutting and rejoining DNA strands.
Helicase unwinds and separates the two DNA strands at the replication fork.
DNA polymerase III synthesizes the new DNA strand by adding nucleotides in the 5' to 3' direction.
DNA polymerase I removes RNA primers and replaces them with DNA nucleotides.
Primase synthesizes short RNA primers to provide a starting point for DNA polymerase.
DNA ligase joins Okazaki fragments by forming phosphodiester bonds to complete the lagging strand.
DNA strands are antiparallel; replication is continuous on the leading strand and discontinuous on the lagging strand.
Short DNA fragments synthesized on the lagging strand during discontinuous replication.
Each new DNA molecule contains one original strand and one newly synthesized strand.
The Y-shaped region where DNA strands separate and replication occurs.
RNA polymerase synthesizes mRNA from DNA template starting at the promoter.
rRNA forms ribosomes, mRNA carries the code, and tRNA brings amino acids.
Codons are mRNA triplets; anticodons are complementary tRNA triplets.
Prokaryotes have coupled transcription and translation; eukaryotes have introns and exons and separate these processes.
Introns are non-coding sequences removed from mRNA; exons are coding sequences joined together.
An operon is a gene cluster controlled by one promoter; it allows coordinated regulation of related genes.
Inducible operons are off until activated; repressible operons are on until deactivated.
Reverse transcription converts RNA to DNA; used by retroviruses like HIV.
Mutations introduce genetic variation that can be acted on by natural selection.
Base analogs mimic bases causing mispairing; UV light causes thymine dimers disrupting DNA replication.
Deletion/insertion: add/remove bases; frameshift: shifts reading frame; silent: no amino acid change; nonsense: stop codon; missense: amino acid change.
To detect mutagenic potential of chemicals by observing mutations in bacteria.
A DNA repair process that removes damaged bases and replaces them to prevent mutations.
The exchange of genetic material between organisms leading to genetic diversity.
Conjugation transfers plasmids between bacteria, spreading genes like antibiotic resistance.
Transformation: bacteria can take up genetic material from dead cells and gain new traits.
Bacteriophages transfer random bacterial DNA between cells during infection.
Small circular DNA molecules that carry genes beneficial for survival and are used in genetic engineering.