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Chapter 13

Frederick Griffith discovered that a harmless strain of bacteria could be transformed into a pathogenic strain by exposure to heat-killed pathogenic bacteria. Oswald Avery found that this transforming principle was DNA, not protein. In 1953, Watson and Crick discovered the double helix structure of DNA, consisting of two strands coiled around each other and held together by hydrogen bonds between complementary nucleotide base pairs of adenine-thymine and guanine-cytosine. DNA replication is semiconservative, producing two DNA molecules each containing one original and one new strand through unwinding of the helix and synthesis of new strands according to the base pairing rules.

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0% found this document useful (0 votes)
97 views9 pages

Chapter 13

Frederick Griffith discovered that a harmless strain of bacteria could be transformed into a pathogenic strain by exposure to heat-killed pathogenic bacteria. Oswald Avery found that this transforming principle was DNA, not protein. In 1953, Watson and Crick discovered the double helix structure of DNA, consisting of two strands coiled around each other and held together by hydrogen bonds between complementary nucleotide base pairs of adenine-thymine and guanine-cytosine. DNA replication is semiconservative, producing two DNA molecules each containing one original and one new strand through unwinding of the helix and synthesis of new strands according to the base pairing rules.

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DNA Structure and

Function
Chapter 13
Hunt for Fame, Fortune and
DNA
• Researchers first believed that proteins held the key for
heritable information, because they were so diverse.
• Frederick Griffith wanted to develop a vaccine against the
bacterium Streptococcus pneumoniae
• The colonies of one strain had a rough surface appearance,
and the other colony seemed to be smooth. Griffin gave
them the name of R and S.
• The steps of Griffin experiment.
– First he injected mice with live R cells. The mice did not
develop pneumonia. The R strain was harmless.
– Second he injected other mice with lice S cells. The mice
died. The S strain was pathogenic, it caused the disease.
– Third he killed S cells by exposing them to high
temperature. The mice injected with dead S cells did not
die.
– Fourth he mixed live R cells with heat-killed S cells and
injected it into the mice. The mice died. Their blood
showed live S cells.
– Heat had killed the S cells but did not destroy their
hereditary material.
Cont.
• Oswald Avery was intrigued by Griffith’s
discovery.
• He transformed harmless bacteria by mixing
them with extracts of killed pathogenic cells.
• He found that adding protein-digesting enzymes
to the extracts had to effect, cell were still
transformed.
• He then added a DNA-digesting enzyme to
extracts which prevented transformation.
• After Avery experiments many other scientist
started using bacteriophages in their
experiments.
• Bacteriophages- only infect bacteria.
– Consist only of DNA and a coat of protein.
Cont.
• Linus Pauling deducted the structure
of protein (collagen).
• In 1953 Watson and Crick built a
model of DNA. They discovered the
structure of DNA.
Discovery of DNA
• Nucleotide- is found in DNA and it consist of a five-
carbon sugar, a phosphate group, and a nitrogen-
containing base.
• The nitrogen-containing bases are adenine (A),
guanine (G), thymine (T), and cytosine (C).
• T and C are pyrimidines with a backbone of carbon
and nitrogen that forms a single ring.
• A and C are purines which are larger molecules having
two rings.
• The amount of adenine to thymine is the same and
the amount of guanine to cytosine is the same.
• The nucleotides in DNA are joined to one another by
way of condensation reactions that form long chains.
• Scientist Rosalind Franklin made x-ray diffraction
images of DNA.
Cont.
• Pauling who discovered proteins made a big
mistake by making all of the negatively charged
phosphate groups pointing inward facing each
other. They should have been facing outward so
that they do not repel each other.
• Watson and Crick came to the conclusion that
DNA must consist of two strands held together
by hydrogen bonds.
• The bonds form when the two strands are
running in opposite directions of each other and
twist to form a double helix.
• Only two kinds of base paring form along the
molecules length A-T and G-C.
• All DNA molecules show the same bonding
pattern.
• The constancy in DNA’s bonding pattern is the
DNA Replication and Repair
• Semiconservative Replication
– Enzymes easily break the hydrogen bonds
between 2 nucleotide strands of DNA.
– When the enzymes and proteins act on the
DNA strand it unwinds and exposes the
nucleotide bases.
– Each of the parent strands stays intact and
a companion strand is assembled according
to paring rule of A-T and G-C.
– As soon as the strand is done being coded
the old strand and the new strand bind
together and form a double helix.
– Each parent cell is conserved during
Cont.
• Replication Enzyme
– Molecules that are over the cell cycle activate replication
enzymes
– Helicases unzip the hydrogen bonds which are
individually weak and easy to break.
– The 2 parent cells are prevented from winding back
together because small proteins temporarily bind with
them.
– DNA polymerase catalyze the formation of two brand-
new strands of DNA from free nucleotides.
– They can only assemble in the 5’ to 3’ direction.
– For the parent cells that runs in the opposite direction
the nucleotides are assembled in short stretches on the
parent strand and DNA ligases seal the stretches
together in a continuous strand.
– This complementary strand winds up with the old strand.
– A free nucleotide has a tail of three phosphate groups
dangling from the 5’ carbon end.
Cont.
• AN individual may not survive if something
changes in its DNA.
• The wrong nucleotide may be base-paired with
the parent template and unless this is fixed it
can weaken the functions of the genes or
protein products.
• DNA proofreading mechanisms- fix most errors
in replication and most of the strands breaks.
– When they can not replication is arrested and
control over the cell cycle come into play.
– Mismatches that slip past the proofreaders are only
one type of DNA damage.
– Repair enzymes- can repair some changes; they
recognize and snip out damaged site or

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