Академический Документы
Профессиональный Документы
Культура Документы
2012
Atomic Structure
An atom is the smallest particle of an element that has the same chemical
properties of that element. Atoms of the same element are all identical.
An atom is made of three types of subatomic particle. These are the proton,
the neutron and the electron. The proton and neutron are in the centre of the atom
and electrons spin around the nucleus.
Nuclide notation
In nuclide notation, there are two important terms: mass number and atomic
number. The mass number is basically the mass of the atom in atomic mass units (i.e.
number of neutrons + number of protons), and the atomic number is the number of
protons.
The nuclide notation is basically the structure of the atom being written in
symbol form:
Isotopes
Isotopes are atoms of the same element with the same number of protons but
a different number of neutrons. Therefore, they have the same atomic number but a
different mass number. Isotopes of the same element have similar chemical
properties (chemical reactions) but different physical properties (melting point,
boiling point, density, etc.).
Isotopes are usually expressed in the form {element – mass number}. Some
examples are carbon-12, carbon-13, carbon-14, uranium-235, uranium-239, etc. They
can also be expressed in nuclide notation. Some isotopes, such as the isotopes for
hydrogen, even have special names (hydrogen-1 is protium, hydrogen-2 is
deuterium and hydrogen-3 is tritium).
Electronic configuration
The reason why this only applies for the first 20 elements is because of
subshells. In an atom, there are not only shells; there are also the subshells s, p, d and
f. The first shell only has subshell 1s, the second shells has 2s and 2p, the third shell has
3s, 3p and 3d, while the fourth shell has 4s, 4p, 4d and 4f. After we factor in these
subshells, we then can actually derive a formula for the maximum number of
electrons in each shell – 2(shell number)2. This means that the first shell can hold 2
electrons, the second can hold 8, the third can hold 18, and the fourth can hold 32.
It then follows that s subshells can hold 2 electrons, p subshells can hold 6, d subshells
can hold 10 and f subshells can hold 14. These subshells also require different energy
levels to fill up. 1s is the easiest to fill up, followed by 2s, 2p, 3s, 3p, 4s then 3d.
(Mnemonic: We can assume the amount of energy needed to fill up a subshell as 1
+ the letter, where s is 1.4, p is 2.3, d is 3.2 and f is 4.1. Then 1s would require 2.4, 2s
would require 3.4, 2p would require 4.3 and so on. It then applies that 4s requires 5.4,
while 3d requires 6.2, followed by 4p which requires 6.3.) This then shows that 4s is
easier than 3d to fill up, and will be filled up before 3d. In the first 20 elements, 3d
isn’t filled up (it is only filled up from element 21) since 1s, 2s, 2p, 3s, 3p and 4s must
be filled up with exactly 20 electrons. :D
The subshell configuration is given by 1snumber of electrons here, 2snumber of electrons here
and so on.
Atomic orbitals
The quantum theory says that electrons are not found in fixed orbits, but can
appear randomly in a 3D probability field. These probability fields, called atomic
orbitals, are different for different subshells, and actually look quite cool :P
Periodic Table
The periodic table is probably one of the most useful things in chemistry. It is a
way of arranging and classifying the elements, which are arranged in order of
proton number.
As the group number increases, the elements become less and less metal-like
(their metallic characteristics/properties decrease). A zigzag staircase can be drawn
through the periodic table, from boron downwards to polonium. This line divides
metals and non-metals. Some of the elements which are touched by this line are
metalloids, which exhibit properties of both metals and non-metals.
Going back to the three important groups, elements of these groups have
notable characteristics that are important.
There are basically three types of bonding – ionic bonding, covalent bonding
and metallic bonding. Of the two, only ionic bonding and covalent bonding are
tested.
Ionic bonding
In ionic compounds, the ions are packed closely together in a regular pattern.
The positive and negative ions are strongly attached to one another by ionic bonds
and arranged into a giant lattice structure.
Covalent bonding
Ionic
Covalent
Bases
- A base is a substance that reacts with an acid to form a salt and water only.
- It can be any metal oxide or hydroxide.
- Soluble bases are called alkalis.
- Alkalis dissociate to produce hydroxide ions (OH-) when dissolved in water.
- There are strong bases (highest pH) and weak bases (higher pH – above 7).
Strong bases include potassium hydroxide (KOH) and sodium hydroxide
(NaOH), and weak bases include aqueous ammonia.
- Properties of a base
Bitter taste.
Slippery and soapy feel.
Turn red litmus paper blue.
pH value is more than 7.
Good conductor of electricity.
Chemical Formulae
Basically, positive ions react with negative ions such that the overall charge
becomes 0. However, you have to memorize the charges of some elements.
1 Sodium (Na)
Potassium (K)
Bromide (Br)
Iodide (I)
Silver (Ag) Hydroxide (OH)
Ammonium (NH4) Nitrate (NO3)
Magnesium (Mg) Oxide (O)
Calcium (Ca) Sulfide (S)
Barium (Ba) VS
2 Zinc (Zn) Sulfate (SO4)
Lead (II) (Pb) Carbonate (CO3)
Copper (II) (Cu)
Iron (II) (Fe)
3 Aluminium (Al)
Iron (III) (Fe)
Phosphate (PO4)
Most of this stuff can actually be derived from the periodic table except the
stuff in green.
Anyway, now that we know the charges, we can mix and match according
to the name of the chemical to make the charge 0.
For example, silver (+1) nitrate (-1) is AgNO3, sulfuric (-2) acid (acid =
hydrogen, which is +1) is H2SO4 (number of hydrogen atoms must be doubled as
Now that we know how to convert substances into their chemical formulae,
we can now write chemical equations :D
Step 2: Convert the chemicals in the word equation to chemical formulae (which
you can get from the periodic table and the table above).
Step 3: Balance the equation (make sure that the left side has exactly the same
number of atoms of each element as the right side) by adding numbers at the
left side of the chemical formula (e.g. 2H2O = 2 water molecules = 4 hydrogen
atoms + 2 oxygen atoms).
Step 4: Write down the state symbols. (solid, liquid, gas, aqueous)
1. Optics
Light
Pinhole cameras
Reflection
Drawing reflection diagrams
Geometrical properties used in this topic
Refraction and Snell’s Law
Total internal reflection and critical angle
2. Nuclear physics
Types of decay
Nuclear reactions and atomic notation
Half life
Applications of radioactivity
Nuclear fission
Nuclear power plants
Optics
What is light?
Light is a form of energy. Light travels in a straight line. It is both a wave (EM
waves) and a particle (photons) – wave-particle duality, which has to do with
quantum mechanics. In this whole topic, however, light will be represented as a ray.
The direction of this light ray will be represented by arrows drawn on the ray.
1. =
2. As the size of the hole increases, the image become brighter but blurrier.
3. The image is inverted and real.
Reflection
Reflection is basically the object reflecting light that is shone on it. Reflection is
how we see things – light is cast onto the thing and is reflected into our eyes.
There are two laws of reflection – the incident ray, the reflected ray and the
normal (the imaginary line perpendicular to the surface; in a circle, this is a line from
the centre of the circle) lie on the same plane, and the angle of incidence is equal
to the angle of reflection.
There are two types of reflection. These are regular reflection and diffuse
reflection. Regular reflection involves all the light rays striking a smooth, regular
The reflected image has certain properties – it is laterally inverted and is virtual
(cannot be captured on a screen; opposite of real). The distance of the reflected
image from the mirror is always the same as the distance of the real object from the
mirror. There are some special cases however, which involve having two mirrors
placed at a certain angle. In these cases, a greater number of images can be seen,
with the angle between the mirrors, α, determining the number of images formed.
This number is -1. The distance from the object to the place where the mirrors
meet and the distance from the images to this point is equidistant, and the object
and images themselves are also equidistant. In these cases, not all the reflections
are laterally inverted. All of them are still virtual, however.
1. Reflect the object into the mirror (i.e. draw the image in the mirror). This image
has the same distance from the mirror as the object.
2. Draw lines from the image to the eye. You will have to draw two rays to the
top and bottom of the eye, and these rays should both be straight.
3. The rays in the mirror should be dotted lines, while the lines out of the mirror
should be solid lines. Draw 2 more solid lines to the place where the dotted
lines hit the mirror from the object.
4. Draw the normal for both these light rays.
1. Triangles
Formulae:
Similar triangles:
Isosceles triangle:
If point F is drawn in line with AB, and angle BAD = angle BFD, then triangle AFD is an
isosceles triangle. In this case, AD = FD and AB = BF.
Refraction
The optical density of a medium can be determined by its refractive index (n).
The refractive index indicates how much light slows down compares to when light is
in a vacuum (i.e. if the refractive index is greater, the light slows down more). When
a light travels from medium A to medium B, the incident ray will bend towards the
normal if medium B has a higher refractive index, and will bend away from the
normal if medium B has a lower refractive index.
1. Snell’s Law
n1 1 = n2 2 (this is like the most important law of refraction and almost all
When a light ray travels from an optically denser medium (with a greater
refractive index) to an optically less dense medium (with a smaller refractive index),
the light ray will bend away from the normal. When the angle of the refracted ray
from the normal becomes 90 , the angle from the incident ray to the normal is the
critical angle. When the angle from the incident ray to the normal surpasses the
critical angle, there will be total internal reflection. The reflected ray in total internal
reflection follows the normal laws of reflection. Theoretically, if the two surfaces are
parallel, a ray that has experienced total internal reflection will never get out from
the interior of the optically denser medium (such as in optical fibers).
The formula for the critical angle, which can be derived using Snell’s Law, is:
sin-1( )*
Refraction extras :D
When a light ray enters a certain set of mediums at n , it will escape from that
set of mediums at n away from the normal assuming the mediums are all parallel.
Types of decay
Ionizing power: The power to ionize gas, or to make molecules in gas lose an
electron to become ions, and thus become ionized.
Penetrating power: The power to pass through blockage. For example, alpha
particles have low penetrating power as they can be blocked by 1-2 sheets
of paper, beta particles have medium penetrating power as they can only
be blocked by 5mm of aluminum, while gamma rays need a few cm of lead
to be blocked.
Nuclear equations
So, what is the equation like in nuclear decay? Let’s first look at the nuclide
notation of the various particles.
The nuclide notation for beta particles is a bit trickier. In beta decay, although
the electron is emitted, it is actually caused by a neutron turning into a proton and
an electron, and the emission of the electron. Therefore, the notation is:
Since gamma rays are only photons, they have no nuclide notation. Gamma
rays are basically given out when there is extra energy in the nucleus after one of
the other decays.
Anyway, now that we know the nuclide notations, we can determine what
will happen to the mass and atomic number of an atom after a certain type of
decay.
Examples
Alpha decay:
Beta decay:
Half life
Half life is basically the average time taken for half of the nuclei in a sample of
a radioactive isotope to undergo decay. It is a probability, so the amount left after a
half life may not be half, although it probably will be half.
There are x grams of an element with half life y minutes. How much is left after
z minutes? Answer: x/2z/y.
For some questions, however, the numbers they give may not be nice powers
of two. So, what do you do? There are 3 options:
1. Approximate to the nearest power of 2. This is the easiest but least accurate
solution. And what if it can’t be approximated properly?
2. Draw the graph of time against amount left based on the information. Then
find the point that you want. This is darn irritating and nobody will ever waste
time doing this. Might as well lose the 2 or so marks…
3. Formula. Yes, there is actually a formula linking original amount, amount left
and time. You can utilize the equation to suit your purposes. However, the
math involved is challenging (involves “e” and “In”, don’t use formula if you
can’t utilize this!). Nevertheless, just dumping all the values into the equation is
reasonably simple. The equation is (in a few forms):
Nt is the remainder.
N0 is the original.
t is the time that has passed.
λ is the disintegration constant. (only for
that element)
For half life OR disintegration constant, use
equation 1 and take Nt/N0 = ½ (assuming
you know either one).
Tracing – weak radioisotopes are injected into the body as tracers to trace
their motion, usually caused by the body’s motions.
Sterilizing – radioactivity can be used to kill bacteria in syringes and in food.
Thickness control – Beta radiation can be used to check how thick an object
is by seeing how much can pass through.
Radiotherapy – used to kill malignant cancer cells.
Nuclear fission
This is the main process used to produce nuclear energy as the temperatures
required for nuclear fusion are currently unachievable.
Nuclear power plants are powered by the heat produced from the energy
generated in nuclear fission.
In the reactor vessel, water is superheated and flows through a pipe system.
This pipe system is in contact with water in a steam generator. When the
superheated water flows through the pipe system, it will heat up the water in the
steam generator, and will then lose heat and flow back into the reactor vessel. The
water in the steam generator, after being heated, will boil, and the steam would
turn a turbine, which turns a generator, generating electricity. The steam will then
travel through a pipe system into a condenser and will condense and flow back into
the steam generator.
This cycle will then continue to produce huge amounts of electricity, while
leaving behind some nuclear waste.
1. Human reproduction
Puberty
Parts of the human reproductive system
The menstrual cycle
Pregnancy
Assisted Reproductive Technologies (ARTs)
Birth control methods
Abortion
STIs
2. Heredity
Key terms
Mitosis and meiosis
Variation
Monohybrid inheritance
3. DNA
Structure of DNA
DNA replication
Central dogma
Genetic engineering
Human reproduction
Puberty
These some important parts of the male and female reproductive systems and
their functions:
Corpus luteum in the ovary produces the hormone progesterone, which helps to
maintain the uterine lining.
If fertilization does not occur (what usually happens), the corpus luteum begins
to degenerate, and the production of progesterone ceases.
Oestrogen and progesterone levels decline.
Uterine lining begins to degenerate.
NOTE: Teachers may troll and make Day 1 of the menstrual cycle different from the
first day of the month in the question. Day 1 is ALWAYS when menstruation starts. So
don’t get trolled and throw marks away. :D
Pregnancy
During the menstrual cycle, there is a short period called the fertile period.
This period is Day 11-17 of the menstrual cycle. It can be found by taking into account
the ovulation stage (Day 13-15) in menstrual cycle. Since the ovum is able to survive for
1-2 days in the woman, the sperms are able to fertilize it as late as Day 17. The sperms
are able to survive for about 3 days waiting in the oviduct and thus can start waiting
from Day 11.
Gametes
During fertilization, the nuclei of the male and female gametes fuse to form a
zygote. The zygote then divides and develops into an embryo over about 3-5 days in a
process known as embryo development in the oviduct. Finally, after all of this
development, implantation of the embryo (not the zygote) in the uterine lining occurs,
in which the embryo simply attaches itself to into the uterine lining of the uterus.
After this, pregnancy occurs.
Pregnancy
During pregnancy, the embryo basically develops into a fetus, and then finally is
born as a baby. There are some important parts involved in pregnancy:
1. Placenta: It is basically a disc for the transport of nutrients to the fetus and
the removal of waste material from fetus. It is the place where exchange of
materials takes place between the mother’s and fetus’ blood, and is made up of
the villi and the uterine wall. The waste materials consist of carbon dioxide and
urea, while the nutrients consist of dissolved food substances and oxygen.
2. Umbilical cord: The fetus is attached to the placenta by the umbilical cord. The
cord contains the umbilical artery, which transports waste materials, and the
Extra – twins
Identical twins are formed when the zygote divides into two identical zygotes,
which then divide separately to form two identical embryos, which develop and
gradually become identical twins.
Fraternal twins are formed when two eggs are fertilized to form two different
zygotes, which then develop into two different fetuses and gradually become fraternal
twins. This can also be caused by IVF, in which two or more eggs may implant into the
uterine lining and lead to fraternal twins.
These are placed in the woman’s urine to detect certain hormones. Monoclonal
antibodies are used in these kits to detect human chorionic gonadotropin (HCG) which
is produced as soon as an embryo implants into the uterus. If HCG is detected, the
woman is probably pregnant.
Some couples simply cannot have children due to a problem with the
reproductive system of either parent – they are infertile. Infertility is defined as the
inability to conceive after a year of regular unprotected intercourse. Therefore, ARTs,
which are methods used to achieve pregnancy by artificial or partial artificial means,
are used to help them to get a child. There are many different types of ART:
ART Details
IVF In-vitro fertilization.
Firstly, fertility drugs are used to stimulate the ovaries to
superovulate (release multiple ova).
Secondly, an operation using ultrasound is used to retrieve the
ova.
Thirdly, sperm obtained using ejaculation is placed together with
the ova and fertilization occurs.
Some people want to have children but can’t, but others can have children but
don’t want to. These people would then use birth control methods. Birth control
methods are classified into these categories: natural, chemical/ mechanical, hormonal,
intrauterine devices, and sterilization.
Natural
Name Details (how it works, how it’s used, cost, effectiveness,
duration and limitations)
Rhythm method Avoid having unprotected sex during ‘fertile period’ of the female.
Keep sperm out of vagina on fertile days of the female. 3 methods to
track fertile period:
Chemical/mechanical
Name Details
Condom Male: Thin cover that fits snugly over erect penis
Female: Plastic tube with flexible ring at each end to help stay in
place in the vagina
Condoms acts as a barrier to prevent sperms from entering the
vagina during sexual intercourse; protects against STIs.
$1 per male condom
$4 per female condom
~80%
Use and dispose with each act of intercourse
Irritation due to latex allergy and spermicide allergy, requires
cooperation from both partners to be effective
Diaphragm Flexible rubber cup inserted into vagina and fit snugly over cervix
Can only be obtained by prescription from healthcare provider.
Diaphragm acts as a barrier to prevent sperms from entering the
uterus
$15 - $75 (lasts up to 2 years)
~80%
Use with each act of intercourse, reusable
Irritation due to latex allergy
Increased risk of vaginal infection
Spermicide Comes in a few forms: Cream, Foam, Gel, Suppository, Film
Kills or inactivates sperms, preventing them from fertilising the egg
~$8 per package
~71%
Use with each act of intercourse
Nonoxynol-9, a common ingredient, is known to increase risk of HIV
& other STI transmission; Frequent use can induce lesions and
Hormonal
Name Details
Emergency Hormones in pill stop ovulation and cause cervical mucus to thicken,
contraception preventing sperm from entering uterus
$10-$77 for consultation/prescription
~80%
Use after unprotected intercourse
Nausea & vomiting
Abdominal pain, sore breasts, irregular bleeding, headaches
“Pill” Hormones in pill prevent ovulation and thicken cervical mucus to
block sperm from entering uterus
$15-$50 every month
92%
Taken daily for 21 days (rest 7 days)
Nausea & vomiting; Abdominal pain, tender breasts, irregular
bleeding, headaches; Easy to forget taking pills daily
Sterilization
Name Details
Vasectomy Simple outpatient procedure where healthcare provider numbs the
area round the scrotum and makes a small incision into the scrotum
to cut and tie the vas deferens.
The sperm ducts are tied, cut or sealed to prevent sperms from
entering the semen.
$350-$1000 for consultation/procedure
99%
Permanent
Possible short-term tenderness or bruising after procedure;
Permanent/irreversible
Tubal Ligation Fallopian tubes are tied, cut or sealed, through incisions into the
Abortion
As seen above, the success rate is not 100%. If a woman really becomes
pregnant, but does not want to, she has to remove the fetus through a process called
abortion.
Abortion is basically the gruesome process of destroying the unborn fetus and
sucking the dismembered parts out of the mother’s uterus using a vacuum. It is
extremely controversial since it is like murder (gruesome murder) and there are many
ethical issues related to abortion. Also, it may cause harm to the mother’s uterus,
disallowing her from having children even when she wants to. Therefore, it’s obviously
not recommended.
STIs
During intercourse, even with birth control (except for condoms) some
infections can be passed on from one partner to the other. They are called STIs
(Sexually Transmitted Infections), and are transmitted by the exchange of bodily fluid,
for example through blood, saliva, semen, vaginal secretion or breast milk. STIs are
quite severe and not easy to get rid of. The only way to prevent them is by using the
aforementioned condom, or, even better, don’t have multiple sexual partners.
Heredity
Mitosis and meiosis
Before we even start on this topic, we need to understand a few key terms:
Mitosis is a type of cell division that takes place during cell growth in asexual
reproduction. It results in the production of 2 daughter cells from 1 parent cell. The
number and type of chromosomes in the nuclei of the daughter cells are identical to
that of the parent cell. The daughter cells have a diploid number of chromosomes. In
this process, the chromosomes are duplicated with sister chromatids and then they are
split and form 2 identical cells.
Meiosis, however, is another type of cell division that results in the production
of gametes for sexual reproduction. 4 haploid daughter cells are produced from 1
diploid parent cell. In this process, the chromosomes are duplicated and homologous
chromosomes are paired up through the centromere and crossing over (swap of alleles
at a chiasma [crossing-over point]) takes place. They then separate and split into 2 non-
identical (due to crossing over) daughter cells with the sister chromatids remaining
together. Finally, the sister chromatids are separated into 4 haploid cells.
Variation
Human beings belong to the same species, but look different from each other.
These differences are called variations. Genes determine the inherited characteristics
of an individual and are carried on a specific locus (position) in a given chromosome, and
thus cause these variations.
There are two main types of variation: continuous and discontinuous variation:
Monohybrid inheritance
Genetic diagram
1. Let big letter be allele for dominant trait, small letter be allele for recessive
trait.
2. Parental phenotype: Father’s phenotype x Mother’s phenotype.
3. Parental genotype: Father’s genotype x Mother’s genotype.
4. Gametes: From the genotype, just split the two letters and circle them.
5. Draw lines from gamete 1, 3 to F1 genotype 1, 1,4 to F1 genotype 2 and so on. (1,3;
1,4; 2,3; 2,4).
6. F1 genotype (should have 4 of these, as derived from the line-drawing.
7. F1 phenotype: Write the phenotype of the offspring based on the genotype.
Remember that heterozygous always follows the dominant allele.
8. Phenotypic ratio: Always 3:1, 1:1 or all of a certain phenotype. Put in simplest
terms.
This is a method for rough working. Firstly, draw a 2x2 square. Then draw the
gametes of one parent above the square and the gametes of the other parent at the
left of the square. Circle the gametes. Then, in the 1x1 squares in the 2x2 square, write
the genotypes of the offspring based on the allele in the gamete to the direct left and
directly above the 1x1 square. You have just derived the genotypes :D
Cheat sheet
Sex-linked traits
Sex-linked traits are traits associated with the sex chromosomes. In humans,
the X chromosome usually carries the allele, and these traits are usually diseases like
colour-blindness and haemophilia (causing you to bleed to death). Before you start
cackling with joy about how only females get these diseases, think again. Males have
the genotype XY. The alleles for these traits are recessive. This means that once a
male gets one recessive allele for the disease, he’s screwed, while a female (XX) can
have one recessive allele but would have the dominant allele to mask it, and she would
be defined as a carrier. There are some questions associated with these sex-linked
traits and how they are passed over to the offspring so here’s the cheat sheet:
Normal mother x Normal father = All normal children. (you don’t say)
Normal mother x Diseased father = 100% carrier daughters, 100% normal sons.
Carrier mother x Normal father = 50% normal daughters, 50% carrier daughters, 50%
normal sons, 50% diseased sons.
Carrier mother x Diseased father = 50% carrier daughters, 50% diseased daughters,
50% normal sons, 50% diseased sons.
Diseased mother x Normal father = 100% carrier daughters, 100% diseased sons.
Diseased mother x Diseased father = All diseased children. (you don’t say)
This may be tested for genetic diagrams, and drawing these will still be the
same as in the normal genetic diagrams.
Pedigree chart
Test cross
This involves crossing an organism with a dominant trait with another organism
with a recessive trait to determine the genotype of the organism with the dominant
trait (homozygous dominant or heterozygous). If some offspring have the recessive
trait, the genotype of that parent is heterozygous, whereas if no offspring have the
recessive trait, the genotype of that parent is homozygous dominant.
Co-dominance is when both traits are shown in the organism which has both the
dominant alleles of the same thing.
Incomplete dominance, on the other hand, is when a fusion of the traits is shown.
Co- dominance: Red + White = Red spots on white/white spots on red. Like a cow.
Implication: if one parent has the blood group AB, he or she cannot have an
offspring with blood group O.
This may be tested for genetic diagrams, and drawing these will still be the
same as in the normal genetic diagrams.
DNA
DNA Structure
DNA (deoxyribonucleic acid) is the essence of life. Without it, life as we know it
probably would not exist. DNA is normally found in the nuclei of cells, in the
chromosomes. In each chromosome, DNA is coiled around histones (some proteins, we
don’t need to know) and compacted into a chromosome.
DNA is a double helix. That means it looks something like the picture at the
extreme left. However, in exams, for simplification, DNA is usually drawn like the
diagram next to the nice-looking double-helix.
In the diagram, you will notice that some colors are always paired with other
bases. This is called complementary based pairing. DNA basically has 4 different
nitrogenous bases – Adenine, Thymine, Cytosine and Guanine. Adenine bonds with
Thymine, and Cytosine pairs with Guanine. Therefore, the percentage of Adenine is
around that of Thymine, and the percentage of Guanine is around the same as that of
Cytosine. Note that this is very important and without this complementary base pairing,
nothing would work the way we are used to.
DNA Replication
Obviously, DNA must replicate itself for stuff like mitosis and meiosis, which
are essential for life. So, how does it do this?
Remember that DNA has 2 strands, and that the strands are complementary to
each other. Also note that the strands are antiparallel, i.e. one of them runs from the 3’
to 5’ direction and the other from the 5’ to 3’ direction.
In DNA replication, the 2 strands must basically be split to form 2 new double
helixes, each with 1 old and 1 new strand.
First, the double helix is unzipped into 2 strands so it can be photocopied. This
process is greatly sped up by an enzyme called helicase, and is done with relative speed
and ease due to the weak hydrogen bonds holding the bases together.
Secondly, the single strands of DNA act as templates for their complementary
bases to attach onto. The free nucleotides will basically find a complementary base to
attach to, and these nucleotides will form the new DNA strand. The main enzyme
speeding up this process is DNA polymerase.
NOTE: You don’t need to know the info in the rest of this section.
On the lagging strand, primase joins RNA nucleotides into a primer. From the
primer, DNA polymerase III adds DNA nucleotides to the primer until it reaches the
next primer, forming an Okazaki fragment. Finally, the RNA primer is replaced by DNA
by DNA polymerase I and is added to the 3’ ends of the neighboring Okazaki fragment.
Finally, DNA ligase joins up the gaps between the fragments of DNA, which forms the
strand of DNA complementary to the lagging strand. Note that this actually happens
just as quickly as the synthesis of the complementary strand to the leading strand.
Telomeres
Due to the method in which the lagging strand is replicated, it cannot be fully
replicated due to one of the primers having no 3’ end to bind to. Basically, small bits of
DNA at the tips of the DNA strand will be gone as the DNA replicates itself. To
counter this, DNA has junk ends with a rubbish sequence. These are called telomeres.
As the DNA replicates, instead of having important bits of DNA cut out, the telomeres
are shortened instead, prolonging the life of the cells.
Central dogma
Now that we know how DNA is replicated, we can now see how DNA is used.
First, however, we must understand another important acid – ribonucleic acid (RNA).
DNA RNA
Contains deoxyribose. Contains ribose.
Double-stranded. Single-stranded.
Contains the four bases Adenine, Thymine, Contains the four bases Adenine, Uracil,
Guanine and Cytosine. Guanine and Cytosine.
Uracil basically replaces Thymine as the
base to be complementary to Adenine.
Now that we know what RNA is, we can go into the central dogma, which explains
how genes in DNA are read to produce proteins and then make up life.
Transcription
Translation
After the mRNA leaves the cell, it is processed by a ribosome. In this process,
another type of RNA called transfer RNA (tRNA). tRNA basically has an amino acid
attached to one end of it and an anticodon on the other end. This anticodon is
complementary to a codon on the mRNA that codes for the certain amino acid.
Anyway, this set of three codons basically has a tRNA attach to it in the
ribosome from the anticodon through complementary base pairing. The amino acid then
detaches itself from the tRNA and starts a polypeptide chain from the ribosome.
After the first tRNA leaves, the next codon is then bonded to by the tRNA and the
next amino acid detaches and joins the first amino acid, continuing the chain. This
process continues until a stop codon, which basically has no anticodon coding for a
protein that can attach to it. From this process, a polypeptide chain, and later proteins,
will be formed, and the proteins can be used to repair cells, make enzymes and so on,
allowing the organism to survive.
Note that key structures that have been highlighted are required to be labeled
in the exam, and may even have to have their function described.
Restriction enzyme: These enzymes act like scissors. They recognize certain
sequences of bases and cut the DNA at these portions.
Sticky end: The single-stranded ends of DNA that has just been cut by a
restriction enzyme. Note that sticky ends cut by the same restriction enzyme
can join together through complementary base pairing.
DNA ligase: This enzyme acts like a glue for DNA. It basically glues any bits of
DNA back together by repairing the sugar-phosphate backbone.
Plasmid: Circular DNA often found in bacteria that are outside of the
chromosomes, but influence the cell’s characteristics and can be replicated
independently.
Vector: A DNA molecule used as a carrier to transfer genetic material from one
cell to another.
cDNA: Complementary DNA, which is DNA synthesized from mRNA.
Reverse transcriptase: An enzyme that allows mRNA to be used for cDNA
synthesis.
1. mRNA is extracted from the organism from which you want to get the trait (e.g.
bioluminescence, insulin production, etc.)
2. Reverse transcriptase and DNA polymerase converts this mRNA to cDNA.
These two steps may seem a bit extra, but remember that DNA has a lot of
junk DNA in it. Only the useful bits for protein production are converted to
mRNA. Therefore, converting mRNA back to cDNA instead of just taking DNA
would result in a lot less junk that you have to sieve through to get the required
trait.
3. A plasmid is extracted from the bacterium.
4. cDNA and the plasmid are cut by the same restriction enzyme, allowing the
sticky ends to be complementary.
Note that the protein the bacteria produce is exactly the same as the protein
the cell you took the mRNA from produces. This only works because the genetic
code is universal. If not, if you take the human gene coding for insulin production
and insert it into an E. Coli, it may produce some poisonous protein and kill the
person this poison is injected into.
It is also worth noting that it is much easier to use this technology on bacteria
than other organisms, since editing the organism’s chromosomal DNA has a high
chance of causing that cell not to be able to divide due to the mutation.