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Capsomere
the viral protein subunit, capsid is made of these
Capsid
protein structure to house the genome
Nucleocapsid
single molecule of nucleic acid surround by a capsid, come in several shapes such as helical, complex, and icosohedral
Virion
virus outside of the host cell
Bacteriophage
virus that infects bacteria
Enveloped Virus
virus that has an outer lipoprotein or lipopolysaccharide coat that was acquired by budding through a cell membrane
Lysozyme
enzyme inside virion, makes holes in cell wall to allow nucleic acid entry, lyses bacterial cell to release new virions
Neuraminidases
destroy glycoproteins and glycolipids to allow liberation of viruses from the host cell
RNA Replicase
RNA-dependent RNA polymerases
Reverse Transcriptase
RNA-dependent DNA polymerase
Pinocytosis
active "cell drinking", non-enveloped viruses
Fusion
enveloped viruses, viral envelope fuses with plasma membrane
Latent Period
part of infection to assembly of virion
Virulent Bacteriophages
cause acute infections, only do lytic cycle, host cell supports multiplication and virion assembly
Temperate Bacteriophages
causes chronic infections, does both lytic and lysogenic cycles, host cell genetically altered during lysogeny to include viral genome
Eclipse Phase
genome replicated and virion proteins translated
Maturation
packaging of nucleic acids in capsids
Latent Period
eclipse phase + maturation phase
Release
cell lysis, budding, or excretion
Integration
the process of viral DNA being put into host DNA
Quiescence and cI
lambda repressors, keeps viral genome inside bacterial genome
cII and cIII
help cI
Cro
allows viral DNA to be expressed outside of genome
Lysogeny Cycle
a method of viral reproduction where the virus integrates its genetic material into the host cell's genome, remaining dormant as a prophage without immediately killing the host
Lytic Cycle
a rapid, 5-6 step viral reproduction process where a bacteriophage infects a host bacterium, replicates, and kills the host, releasing 100-300 new viruses
Antigenic Shift
an abrupt, major change in a virus's surface antigens, usually influenza, caused by the reassortment of genetic material when two different strains infect the same cell
Antigenic Drift
the gradual, continuous accumulation of small genetic mutations in influenza viruses (specifically HA and NA surface proteins) that alter their structure over time
Topoisomerase
insert and remove supercoils in DNA
DNA Gyrase
type of topoisomerase, introduces supercoils into DNA via double-strand breaks
Chromosome
main genetic element in prokaryotes, typically circular, "house-keeping" genes
Plasmids
usually circular, beneficial genes
Transposable Elements
small segments of DNA can move from one site to another on same or different DNA molecule
Replicon
portion of genome that contains the origin of replication (oriC)
Origin-Binding Protein
binds origin of replication to open double helix
Helicase Loader
loads helicase at origin
Helicase
unwinds double helix at replication fork
Primase
primes new strands of DNA
DNA Polymerase III
main polymerizing enzyme
Tau Protein
helds together the two core enzymes for the leading and lagging strands
DNA Polymerase
excises RNA primer and fills in gaps
DNA Ligase
seals nicks in DNA
Replisome
large replication complex of multiple proteins
Primosome
helicase and primase subcomplex within replisome
DNA Proofreading
DNA polymerase I and III can move backwards to replace previous bases, proofreads as it lays down bases
DNA-Dependent RNA Polymerase
only RNA-polymerizing enzymes in prokaryotes, requires sigma factor to transcrie selectively
Strong Promoters
promoters conforming most closely to consensus sequences more effective in binding RNA polymerase
Type I Secretion Systems
proteins moved outside the cell in 1 step
Type II Secretion System
uses Sec or Tat to move folded protein past inner membrane, then out the cell
Type V Secretion System
uses Sec or Tat to move unfolded protein past inner membrane, then folded protein out of cell
Type III Secretion System
moves protein straight into another cell in 1 step
Type IV Secretion System
moves viral DNA straight into host cell in 1 step
Type VI Secretion System
uses a sheath that can retract and contract to send protein straight into another cell
Mutations
heritable and lead to change in genome
Horizontal Gene Transfer
large change in genome
Selective Media
choosing population based on if they grow on plate or not
Differential Media
shows growth that has different characteristics that are visible
Selectable Mutations
have a known benefit (antibiotic resistance)
Nonselectable Mutations
no advantage even though they may lead to a phenotypic change
Auxotrophs
cannot grow without a certain nutrient that is required for their survival
Spontaneous Mutations
random change in the DNA due to errors in replication that occur without known cause
Induced Mutations
those made environmentally and deliberately, radiation or chemicals that chemically modify DNA
Point Mutations
mutations that change only one base pair, can lead to single amino acid change in a protein, an incomplete protein, or no change at all
Silent Mutations
does not affect phenotype at all, normally 3rd base pair
Missense Mutation
changes one nucleotide, changing the amino acid that is coded for, has potential to alter protein function
Nonsense Mutation
coding codon changes to a stop codon, ending translation early
Frameshift Mutations
shifts the readng frame, resulting in a completely different protein that will be nonfunctional
Mutagens
chemical, physical, or biological agents that increase mutation rates
Nucleotide Base Analogs
resemble nucleotidea but have faulty base-pairing, causing extra mutations, and structural issues
Alkylating Agents
introduce mutations in coding and noncoding DNA, allows for wrong base-pair substitutions
Intercalating Agents
insert between two DNA base pairs, push them apart, causing sungle base insertions and deletions
Nonionizing Radiation
UV radiation, causes pyrimidine dimers, causes DNA polymerase to misread it
Ionizing Radiation
X-rays, causes double-stranded and single-stranded breaks in the backbone of DNA
Ionizing Radiation
X-rays, causes double-stranded and single-stranded breaks in the backbone of DNA
SOS Repair System
a DNA repair system activated by DNA damage
LexA
represses the SOS system, represses error-prone DNA polymerase IV, error-free DNA repair, and error-prone DNA repair, and Lex A
RecA
activated by DNA damage to inactivate LexA