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60 Cards in this Set

  • Front
  • Back
Define Transposons
transposons are segments of DNA, 700-40,000 bp in length
they move from one location to another in a dna molecule or move to another molecule
Charactertistics of Transposons
the action of a transposon is transposition the frameshift insertion and recombination that needs no specific region.
importance of transposons
transposons are found in all prokaryotes,eukaryotes, and viruses. they vary in their nucleotide sequences but have palindrome sequence at end
types of transposons
Insertion sequences, complex transposons
Transposons:
insertion sequences
the simplest transposons consist of no more than two inverted repreats and has the gene that encodes the enzyme transposase that splits the dna molecule at the site and inserts the transposon and produces duplicate copy of the target site
Transposons: complex transposons
contain one or more genes not connected with transposition such as genes for antibiotic resistance r factors-plasmids that resist antibiotics often contain transposons
Plasmids definition
small, circular molecules of DNA that replicate independently of the chromosome.
Plasmid characteristics
circular and 1 to 5% the size of a bacterial chromosome each plasmid carries information required for its own replication
Factors of plasmids
Fertility, resistance, bacteriocin, virulence, cryptic
Plasmid- fertility factor
carry instruction for conjugation -transferting gentes from one bacterial cell to another
Plasmid- resistance factor
carry genes for restiance to antimicrobial druggs
Plasmid-bacteriocin factors
carry genes for proteinaceous toxins called bacteriocins which kill bacterial cells fo the same or similar species
Plasmid-Virulence plasmids
carry instructions for structures enzymes or toxins that enable a bacterium to become pathogenic
Plasmid- cryptic
no one knows
Bacterial genome
the genome of a cell or virus is its entire genetic complement including genes and nucleotide sequences that connect genes to one another
structure of nucleic acids
they are polymers of nucleotides that contain pentose sugar Deoxyribose and ribose, a phosphate, and one of the 5 nitrogenous bases gc at or u
dna replication process
an anabolic polymerization proces allows a cell to pass copies of its genome to descendants
dna replication require
they require monomers(building blocks) and energy triphosphate and deoxyribonucleotides 3 phosphate groups linked by two high energy bonds are functions in dna replication
structures in dna synthesis
guanosine triphosphate nucleotide (dGTP
in dATP it stores energy like ATP but with an RNA molecule
key to dna replication
complementary structure of the two strands
AG TC
initial process in dna replication
begins at specific sequence of nucleotides called origin. removes chromosomal proteins exposing DnAhelix
2. dna helicase unzip dna molecule by breaking the hydrogen bonds between complementary nucleotide bases.
next process in dna replication
after helicase untwist and expose replication fork other rpotein molecules stablizie single strands to prevent rejoining - dna polymerase binds to strands
5 kinds of dna polymerase
they synthesize dna by bonding to hydroxyl group at 3 prime and replicating 5 prime
strands
leading strand continuously synthesized while lagging strand is synthed in short segments latter joined
synthesis of leading strand
1. enzyme called primase synthesizes shor tna molecule and provides a 3 prime hydroxyl group to dna
2. triphosphate deoxyribonucleotides form hydrogen bonds with complements in parental strand
3 use energy in high energy bonds of triphosphate deoxyribonucleotides
4. dna polymerase proofreads removes incorrect pairs
5. another enzyme replaces rna primer with dna
Synthesis of the Lagging strand
1. primase sythezises rna
2. nucleotide pairs with complement at cg
3. dnapolymerase joins neighboring nucleotides and rpoffreads
4. another type of dna polymerase replaces rni primer with dna
5. dna ligase seals gaps btw ozaki frags(discontinuous segmentsin the lagging strand) and form a continuous dna strand
helicase
untwists dna
primase
synthesizes rna primer
DNA polymerase
joins neighboring nucleotides and proofreads
DNA ligase
seals gap btween adjacent okazaki fragments to form continuous dna strand
Polymerase chain reaction
is a scientific technique that produces a large number of identical molecules of DNA in vitro - for epidemiologists,
PCR is a repetitive process that separates and relpicates two strands of dna alternately
1. Denaturation - exposure to heat
2. priming- as temps cool dna will bind to primers to prevent rebinding
3. extension raising temp to 72 to increase rate of dna polymerase replicates each strand
required chemical compounds in polymerase chain reaction
DNA plymerase, primiers, and triphosphate deoxynucleotides
gel electrophoresis- purpose
isolates fragments of dna molecules that can be inserted into vectors and multiplied by pcr or preserved in library
gel electrophoresis- principle
dna molecules with negative charge are drawn through a gel(retards dna movement) by electric current towards positive electrode in chanber
components of rna nucleotides
transcription- copy dna info as rna nucleotide sequences - ribomes in rna synthesize polypeps called translation
dna is transcribed to rna that translates to form polypeptides
cells transcribe three types of rna from dna
messengerrna- carry genetic info from chromosomes to ribosomes
ribosomal rna- combine with ribosomal polypeps to form ribosomes -organelles that synthesize polypeps
transferrna- deliver amino acids to ribosomes
transcription occurs
in nucleoid region of cytoplasm in prokaryotes in eukaryotes it offurs in nucleus, mitochondria, and chloroplasts
steps in rna transcription
initiation of transcription
elongation of the rna transcript
termination of transcription
rna polymerase
enzyme that synthesizes rna
stages of translation: initiation
initiation
1. smaller ribosomal subunit attaches to mRNA at ribosomal recognition sequence with start codon at psite
2. tRNA attaches to ribosome 's p site, GTP supplies the energy required for binding
3. larger ribosomal subunit attaches to form complete initiation complex
stages of translation: elongation
1. transfer rna is escorted by elongation factor along with GTP to stabilize trna as it is added to A site
2. ribozyme formes peptide bond by dehydration synthesis and attaches polypeptide to tRNA occupying the A site
3. using energy supplied by moreGTP the ribosome moeves one codon down the mRNA moving trna down
4. ribosome releases empty trna from e site and it gets recharged
5. cycle repreats
stages of translation: termination
involves proteins called release factors to halt elongation
replication
duplicate cells genome
transcription
synthesize rna
translation
to synthesize polypeptides
mutation
a change in nucleotide base sequence of a genome in the genes
types of mutation
point mutation

frameshift mutation
point mutation
just one or a few nucleotide base paires are affected
substitution, insertion deletion
frameshift mutation
deletion or insertion that causes new sequences of codons altering polypeptide sequences dramatically
mutagen
mutations induced by physical or chemical agents
spontaneous mutation
error in replication and repari also recombination error
thimine dimers
nonionizing radiation from uv light causing adjacent tyhmine bases to bond with one another
horizontal gene transfer
prokaryotes acquire genes from other microbes of the same generation - a donor cell contributes part of its genome to recipient cell
3 types of horizontal gene transfer: transformation, transduction, bacterial conjugation
transformation- a recipient cell gets dna from environment
tranduction- transfer dna from one cell to another via replicating virus (bacteriophages)

Bacterial conjugation: donor cell remains alive- unlike other two,requires physical contact btw two cells- like sex
Bacterial
making cells competent for transformation
altering temp and salt content
competent
ability of cells to take up dna of their environment
Cojugation pili
sex pili are protenaecous rodlike structures
F+ F-
HFR and F-
gene coding for conjugation pili f plasmid- or f factor- cells with are F+ and give to F-
HFR moves around too much and is in the dna so F- doesnt get all info
compare transducing phage and normal phage
normally phages assmble around dna phage to form new phage particles but some mistaknly incormporat remaining fragments of bacterial dna to form transducing phages
transducing phage injects donor dna into host cell