A) E. coli DNA polymerase I is unusual in that it possesses only a 5' 3' exonucleolytic activity.
B) Endonucleases degrade circular but not linear DNA molecules.
C) Exonucleases degrade DNA at a free end.
D) Many DNA polymerases have a proofreading 5' 3' exonuclease.
E) Primases synthesize a short stretch of DNA to prime further synthesis.
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A) are extraordinarily efficient energetically.
B) are generally absent, except in egg and sperm cells.
C) can repair deletions, but not mismatches.
D) can repair most types of lesions except those caused by UV light.
E) normally repair more than 99% of the DNA lesions that occur.
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A) chains.
B) independently replicating segment.
C) origins.
D) replication forks.
E) termination points.
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A) DnaB (helicase)
B) DnaG (primase)
C) Dam methylase
D) DNA ligase
E) DnaA (a AAA+ ATPase)
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A) Serines in the protein active site become covalently attached to the nucleic acids during the mechanism.
B) The reaction is an ATP-dependent process.
C) The reaction steps are successive tranesterifications.
D) The integrase can be classified as a hydrolase.
E) The target DNA sequence for this protein is nonspecific.
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A) A specific recombinase enzyme is required.
B) The energy of the phosphodiester bond is preserved in covalent enzyme-DNA linkage.
C) Recombination sites have non-palindromic sequences.
D) Formation of Holliday intermediates is required.
E) Insertions or deletions can result from site-specific recombination.
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A) one
B) two
C) three
D) four
E) five
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A) eukaryotic chromosomes cannot usually replicate bidirectionally.
B) eukaryotic genomes are not usually circular, like the bacterial chromosome is.
C) the processivity of the eukaryotic DNA polymerase is much less than the bacterial enzyme.
D) their replication rate is much slower, and it would take too long with only a single origin per chromosome.
E) they have a variety of DNA polymerases for different purposes, and need a corresponding variety of replication origins.
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A) The enzyme would become more processive.
B) The enzyme would be more error prone.
C) The enzyme would become more efficient in base excision repair.
D) The enzyme would become more processive and more error-prone.
E) None of these is a potential outcome.
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A) R sites only
B) I sites only
C) DUE sites only
D) both R and I sites
E) both R and DUE sites
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A) of the leading strand requires multiple primers.
B) is mostly 3'to 5'.
C) always finishes at a conserved terminator sequence.
D) requires DNA-dependent RNA synthesis.
E) does not require the action of topoisomerases.
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A) a double strand break
B) cleavage of two crossover events
C) alignment of homologous chromosomes
D) formation of a single Holliday intermediate
E) exposed 3ʹ ends invade the intact duplex DNA of the homolog
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A) not mutagenic.
B) an antibiotic.
C) an amino acid.
D) lethal at high enough concentrations.
E) not taken up by bacteria.
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A) can initiate replication without a primer.
B) is efficient at nick translation.
C) is the principal DNA polymerase in chromosomal DNA replication.
D) represents over 90% of the DNA polymerase activity in E. coli cells.
E) requires a free 5'-hydroxyl group as a primer.
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