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History
Nucleic acids were discovered by Friedrich
Miescher in 1869. In the early
1880s Albrecht Kossel further purifies the
substance and discovers its highly acidic
properties. He later also identifies the
nucleobases. In 1889 Richard
Altmann creates the term nucleic acid.
In 1938 Astbury and Bell published the first
X-ray diffraction pattern of DNA.
In 1953 Watson and Crick determined
the structure of DNA. Experimental studies
of nucleic acids constitute a major part of
modern biological and medical research,
and form a foundation
for genome and forensic science, and
the biotechnology and pharmaceutical
industries.
Structure of DNA
DNA consists of 2 polynucleotide chains or
strands, wound around each other such
that they resemble a twisted ladder. This
structure is referred to as the double helix.
The backbone of each of these strands is a
repeating pattern of a 5-carbon sugar and a
phosphate group. Each sugar is attached to
one of the four nitrogen-containing bases:
A, T, G, or C.
The sugar present in the nucleotide is a
deoxyribose, hence the name
deoxyribonucleic acid (DNA). In the double
helix DNA structure, all four bases are
confined to the inside of the double helix,
held in place by hydrogen (H) bonds linking
complimentary bases on the two strands.
The sugar-phosphate backbones of DNA
are on the outside of the double helix.
DNA is the acronym for deoxyribonucleic
acid, usually 2'-deoxy-5'-ribonucleic acid.
DNA is a molecular code used within cells
to form proteins. DNA is considered a
genetic blueprint for an organism because
every cell in the body that contains DNA
has these instructions, which enable the
organism to grow, repair itself, and
reproduce.
DNA Structure
A single DNA molecule is shaped as a
double helix made up of two strands of
nucleotides that are bonded together. Each
nucleotide consists of a nitrogen base, a
sugar (ribose), and a phosphate group. The
same 4 nitrogen bases are used as the
genetic code for every strand of DNA, no
matter which organism it comes from. The
bases and their symbols are adenine (A),
thymine (T), guanine (G), and cytosine (C).
The bases on each strand of DNA
are complementary to each other. Adenine
always binds to thymine; guanine always
binds to cytosine.
These bases meet each other at the core of
the DNA helix. The backbone of each
strand is made of the deoxyribose and
phosphate group of each nucleotide. The
number 5 carbon of the ribose is covalently
bonded to the phosphate group of the
nucleotide. The phosphate group of one
nucleotide binds to the number 3 carbon of
the ribose of the next nucleotide. Hydrogen
bonds stabilize the helix shape.
The order of the nitrogenous bases has
meaning, coding for amino acids that are
joined together to make proteins. DNA is
used as a template to make RNA through
a process called transcription. The RNA
uses molecular machinery called
ribosomes, which use the code to make the
amino acids and join them to make
polypeptides and proteins. The process of
making proteins from the RNA template is
called translation.
Structure of RNA
RNA differs from DNA in three aspects.
First, the backbone of RNA contains ribose
rather than 2’-deoxyribose. That is, ribose
has a hydroxyl group at the 2’-position.
Second, RNA contains uracil in place of
thymine. Uracil has the same single-ringed
structure as thymine, except that it lacks the
5’-methyl group. Thymine is in effect 5’-
methyl-uracil. Third, RNA is usually found
as a single polynucleotide chain. Except for
the case of certain viruses, RNA is not the
genetic material and does not need to be
capable of serving as a template for its own
replication.
Pentose Sugar
Nitrogenous Bases
Uracil (C4H4O2N2), found in RNA molecules
only, is a white, crystalline pyrimidine base
with MW = 112.10 daltons and a m.p.
338°C.
Medical Therapies
Chemicals that mimic the constituents of
nucleic acids are being used as drugs today,
with further developments in this area
underway. For example, a slightly modified
form of uracil, 5-fluorouracil (5-FU), has been
used for decades to treat carcinoma of the
colon. It does this by imitating a true
nitrogenous base closely enough so that it
becomes inserted into newly manufactured
DNA. This ultimately leads to a breakdown in
protein synthesis.
Imitators of nucleosides (which, you may recall,
are a ribose sugar plus a nitrogenous base)
have been used in antibacterial and antiviral
therapies. Sometimes, it is the base portion of
the nucleoside that undergoes modification,
and at other times the drug targets the sugar
portion.
General characteristics of
nucleic acid
1. nucleic acids generally have beta N glycosidic
bond
2. they are polyfunctional acids
3. they absorb ultraviolet light close to 260nm
hence can be quantized
4. they serve diverse physiological functions -
like ATP is a biological transducer of free
energy, cAMP is a second messenger, help in
protein synthesis, UDP helps in carbohydrate
metabolism and detoxification... etc.
5. they have high group transfer potential
especially the nucleotide triphosphates
6. synthetic nucleotides are used for
chemotherapy, for research
7. polynucleotides are directional
macromolecules- like DNA has a 5'and 3' end