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1
Levels of biology
o Biosphere- most regions of land that contain living organisms and organic
compounds.
o Ecosystem - all living things in a certain area and non-living things that interact with
life.
o Communities- a set of populations is an area.
o Populations- a set of individuals living w/in the bounds of a area- specific
o Organisms a uni or multi-cellular being that can functions basic of life.
o Organs and Organs systemo Organs- a group of tissue that have similar function.
o Organ system- a group of organs that also have similar function.
o Tissues- a group of cells with the same function.
o Cells- the fundamental unit of life.
o Organelles- parts of the cell
o Molecules- a chemical structure that have 2 or more atoms.
Major Biological Areas
o Orgasmic Area
1. Zoology
2. Botany
3. Microbiology
Comparative physiology- A) comparative discourse of the nature of organism
B) the comparative study of how living things function.
Organism- any multi or uni-cellular being capable of performing lifes basic function.
ARE MADE UP OF CELLS !!!!!!!!!!!!
Metabolism All the chemical reactions in the body. ( will be later studied)
o A+BC anabolism sum of all building reactions.
o CA+B catabolism sum of all decomposition/ break-down reactions.
Chemical Reactions
o Occurs when atoms combine w/other atoms to form molecules break-down.
Synthesis
Decomposition reaction
A+BC
AB A+B
CHEMICAL REATIONS CELLS ARE PART OF METABOLIC PATHWAYS
3 TYPES OF METABOLIC PATHWAYS
a) Simple linear pathway
b) Branch pathways
c) Cycle
In a feedback the enzyme report the amount of product of the reaction from the
beginning of the reaction to the end.
o HOWEVER IN A FEEDFOWARD the enzyme from the end of the reaction
report back to the beginning of the reaction.
o Negative- stops
o Positive- speeds up the reaction.
o
ACTIVATION ENERGY
0-6 is Acidic.
Acidic solution- the H+ (proton)
exceeds the amount of hydroxides (OHin a solution.
7= Neutral. OH- equals H+
8-14 is basic.
Basic solution the OH- exceeds the
amount of H+ in a solution.
as shown the head are hydrophiliclike water and the tail are hydrophobic.
Also the head are lipophobicdon like lipid and the tail is lipophilid.
when the lipids are put in water the head will be in the water and tail will be out
of the water. upside down
if there are many lipids the tails will attach to each other to block out the water.
TYPES OF FAT
A) Saturated fatthe hydrocarbons and Carbon are bonded BY SINGLE BONDS.
a. SOLID AT ROOM TEMP.
B) Unsaturated fat- the hydrocarbons and Carbons are bonded by Double Bonds.
a. LIQUID AT ROOM TEMP.
Steroids
A type of lipid
2) Secondary Structure
a. Beta pleated sheet
b. Alpha helix
3) Tertiary structure- BOTH AND COMPINATION beta pleated sheets and alpha
sheet.
TYPES OF PROTEINS
1. Enzymatic proteins- selective acceleration of chemical reaction.
2. Structural proteins- support
3. storage proteins- storage of amino acids
4. transport protein- transport of other substances
5. hormonal protein coordination of an organisms activities
6. receptor protein response of cell to chemical stimuli
7. motor protein- movement
8. defensive protein protection against disease
4) NUCLEIC ACIDS : DNA & RNA
o nucileotides- basic building block for nucleic acid.
o 2 TYPES OF NUCILETIC ACID
o Ribose- ribonucleic acid RNA
o Deoxyribonucleic DNA
4 TYPES OF NITROGENIOUS BASE
1. cytosine ( C) at
2.Thymine ( T) ake
3. adenine (A) pples
4. guanine
(G) oodies
c) ribosome
d) plasma membrane
e) cytoplasm
ANIMAL CELL
H. PEROXISOME
Peroxisome does metabolic functions
in lipid metabolism.
Mostly function as a detoxification.
PLANT CELL
A. cytoskeleton
B. ribosome
C. Endoplasmic Reticulum
o In a plant cell the ER extends the plasodesmata and enters into a neighboring cell.
D. Plasmodesmata- channels through cell ways to connect to another cell.
E. Nucleus 2 Membrane
F. Gogi Appartus
G. Mitochondrion- 2 Membrane
H. Peroxisome
I. Plasma Membrane
J. Cell wall
o The outer layer
o Maintains the cell shape & protects.
o Primary cell wall
o Middle lamella
o Secondary cell wall
K. Chloroplast 2 membranes
PROKARYOTIC CELL
Cell Cycles
in the process of mitosis the cell divide into 2 or more that becomes
tissues.
Mitosis- the dividing of cells
Meiosis- the diving of cells the daughter cell have half the
chromosomes.
o Tissue- a group of cells w/a common function, structure. That are able to
recognize and communicate with each other.
o 4 types of tissues
o EPITHELIAL- cover the outside of the organism or lining of the organs,
Epithelium- cells of an epithelial tissue shaped like dice
o CONNECTIVE TISSUE- bind and support other tissues.
6 types
1. Loose
2. cartilage
3. fibrious
4. adipose
5. blood
6. bone
o MUSCLE TISSUE
o body movement
o most abundant
o 3types
1. skeletal
2. cardiac
3. smooth muscle
o NERVOUS TISSUE
o Sense stimuli and transmit signal neuron- nerve cell
o Glial cells or glia- nourish, insulate, and replenish the neurons
o Brain- the concentration of nerves.
AS TISSUE MUTIPLE IT FORMES ORGANS --- WHICH THEN TURN TO ORGAN
SYSTEM
ORGAN SYSYTEM
1. DIGESTIVE- mouth, pharynx, stomach, intestines, liver, pancreas, anus
a. Function: food processing
2. CIRCULATORY- heart, blood vessels, and blood
a. Function: distribution of materialsoxygen
3. RESPIRATORY- lungs, trachea
a. Function: gas exchange
4. IMMUNE AND LYMPHATIC- bone marrow. Lymph nodes, thymus, white
blood cells, and lymph vessels
a. Function: body defense
5. EXCRETORY- kidney, bladder.
a. function: disposal of metabolic waste
6. ENDOCRINE- pituitary, thyroid, pancreas, and other glands
a. Function: coordination of body activities.
7. REPRODUCTIVE- ovaries or testes
a. function: reproduce
8. NERVOUS- brain, spinal cord, nerves, sensory organs
a. Function: to sense things
9. INTEGUMENTARY- skin and it parts
a. Function: protects against injury, infection, drying out
10. SKELETAL- skeleton
a. Function: body support, movement, protection of internal organs
11. MUSCULAR- skeletal muscle
a. Function: locomotion and other movement
COORDINATION AND CONTROL
o Animals tissues, organ, and organ system must act in
conjunction w/ others.
o They can use hormones
o Hormones- signal molecules broadcast throughout the body by
the endocrine system.
o Diff, hormones have difference effects and slow-acting
Cells can also interact with each other through intercellular junction- ONLY
ANIMAL CELLS
o TIGHT JUCTIONS
o the cells in the phloem & xylem are dead cells (kinda)
o kinda b/c it still contain a plasma membrane BUR NO NUCLEUS
o WHY ARE THE CELLS DEAD?
As states before diffusion can be use to transport nutrients through
cells BUT THIS A LONG PROCESS B/C OF THE
ORGANELLS IN THE WAY.
THEREFORE, the xylem and phloem has to be as open as possible
so the transport would be easy as possible.
The xylem & phloem are surrounded by living cells.
o REMEMBER CELLS CAN COMMUCATE THROUGH CHEMCAL &
ELECTRICAL MEANS.
STEMS- an organ consisting of an alternating system of nodes MAIN FUNCTION IS
THE TRANSPORT OF NUTRIENTS
o Nodes- where the leaves are attach
o Internode- the place bet. The nodes
o Auxiliary bud- structure that can form a lateral shout known as a branch
METABOLISM
Sum of all catabolism & anabolism in biological entity. FOR ALL CHEMICAL
RECACTIONS
ENYMES
Is a protein ( all enzyme are protein) that work as a catalyst in a chemical reaction
o Speed up metablic reactions. NOT consume by the reaction.
ACTIVATION ENERGY BARRIER
Activation energy- the amount of energy that reactants most absorb before a
chemical reaction happens.
o the energy comes from the breaking of the bonds.
SUBSTRATE SPECIFY OF ENZYMES
substrate- the reactant an enzyme works on
enzyme-substrate complex- a TEMPORARY complex action when an enzymes binds its
substrate molecules.
While the enzyme and substrate are joined the catalytic action begins and a
product is produce.
Enzymes is VERY SPECIFICa enzyme can recognize its SPECIFIC substrate
OR something LIKE IT.
Active site the region where the substrate joins to the enzymes and the catalysis
occurs.
o temp. and pH are factors in the activity of an enzyme
MANY ENZYMES REQUIRE NONPROTIEN HELP FOR CATALYTIC ACTIVITY.
a) cofactor- any NON-PROTEIN molecule or ion that is required for the functioning of
an enzyme.
How does co-factors works
o they bind tightly or loosely to the enzyme or bind to the substrate
o crucial function in the catalysis.
b) coenzyme- an ORGANIC molecule serving as a cofactor.
competitive inhibitors- look alike substrate that compete for admission into the
active site. enters the active site and prevents the CORRECT substrate of doing
it job.
Non-competitive inhibitors- does not bind in the active site but rather another
part of the enzyme- to stop the reaction.
REGULATION
Allosteric Regulation- change an enzymes shape and the functioning of it active
site by binding elsewhere
Covalent regulation- a molecule that covalently binds to the enzyme ex- PO43o Phosphorlation- adding an PO43- to an molecule.
CANNOT HAPPEN ON IT OWN it need a catalyst
This catalyst s called kinase- do phosphorlation reaction.
o Dephosphoryaltion- take off the phosphalation & perform by enzymePhosphatase
STORAGE OF ENERGY
energy is need for reactions
free energy- the portion of a system energy that can perform work when temp and
pressure are uniform throughout the system.
ATP ( adensine triphophate) contains a nucleic base, sugar, and three PO43o the break of the three bonds in the triphophate gives off energy.
o WHY?
The bond bet. Them is negative so it takes energy to keep them
together so when the bond is broken PLENTY of energy is give
off.
ATPADP
--before the pyruvate enters the Krebs cycle it is Decarboxlation happens in the
mitochondria
o Decarboxlation- in the presence of Oxygen.
o Takes off one CO2 from an organic molecule.
o It removes the carboxyl group and adds the acetyl CoA in it place. (coenzymes)
o Acetyl CoA- the entry compound for the citric cycle or Kerbs cycle.
The carboxyl group is remove from the pyruvate and Acetyl CoA is put in it place
this is deoboxiation.
IF THIS REACTION IS W/O OXYGEN IT IS FERMATIONIN THE CYTOSOL.
2. CITRIC CYCLE (KREBS CYCLE) take place in the mitochondrial matrix
While pyruvate is entering the
mitochondrion it is changes to
acetyl CoA
NEEDS O2 B/C OF THE EACCTCEPTOR SO THIS DOES
NOT HAPPEN IN
FERMENTATION.
1 ATP PER C2 entering the Krebs
cycle. BUT THERE ARE 2 C2 in
the Krebs cycle 2 ATP. ( diagram
shows one C2 because one is down
per cyclewhen the 1st is done it
goes to the next. )
-2ATP GLYCOLYSIS
+4ATP GLYCOLYSIS
+2ATP KREBS CYCLE
.
NET = 4ATP IN BOTH GLYCOLISIS AND KREBS CYCLE
2 NADH= GLYCOLOSIS
2NADH= DECORBOXYTION
6 NADH= KREBS CYCLE
.
10 NADH2
o IN A COMPLETE CYLCE ABOUT 30 ATP IS USE
o THAT ATP IS FROM THE NADH2.
o Will be explain in the electron transport chain
2FAD IN KREBS
CYCLE
3) OXIDATIVE PHOSPHORYLATION CHEMIOMOISIS COUPLES ETRANSPORT TO ATP SYNTHESIS- HAPPENS IN THE CRISTAE
Oxidation phosphorlation-( process one to make ATP) ATP synthase- located in the cell
membrane
First let explain e- transport chain since this occurs in the oxidation phosphorlation.
o The e- transport chain is a collection of molecules that are embedded INNER
MEMBRANE of the mitochondrion in eukaryotic ( in prokaryotic in the plasma
membrane)
o In chain exist in multi-protein complexes 1 to 4.
o Bound to them is prosthetic groups (non-protein components for the
catalytic functions of certain enzymes)
THE IMAGE BELOW CONTAIN BOTH THE E- TRANSPORT & ATP SYNATANSE
o In the e- transport exchange the proton H+ are delivered upward ( remember the fluid
between the two membranes of the mitochondria has a low pH (high acid)
o The NADH from the citric acid cycle is transfer to the Complex ONE.
o The proton and e- is remove is from the NADH. ( 2 e- and 2 proton are
removed if it is NADH2)
o CONTIUNING IN COMPLEX ONE the proton that was removed is then
move upward to the matrix bet. The two membranes in the mitochondria.
o The e- is then carried from COMPLEX ONE by the UBIQUINONE (Q) ( the
Q can carry up to two e-)
o The Q carry the electron to Complex THREE
o In COMPLEX THREE also shuffle H+ upwards. HOWEVER the e- is then
brought to the cytochromes.
o Cytochromes- an iron containing protein and a component of the e- transport
Chain in the mitochondria and chloroplast.
o Cytochrome pass the e- to the COMPLEX FOUR where the e- is pass to
oxygen.
o Each oxygen atom also picks up a pair of Hydrogen from the aqueous
solution forming water.
SO HOW MANY ATP CAN BE MADE FROM NADH?
3 ATP CAN BE FROM 1 NADH
BACK TO COMBINATION OF GLOCYLOSIS, DECORBOXYTION, &
CREBS CYCLE
ALL 2GETHER THEY MADE 10 NADHTHEREFORE 30 NADH IS MADE
FROM CELLULAR RESPIRATION.
SO WHAT HAPPENS IN COMPLEX 2
ATP SYNTHASE- a complex of several membrane proteins that provide a port through
which proton diffuse.
o Make ATP from ADP
o ATP synthase use the energy is from the difference of in concentration of
H+ ( delta pH or gradientREMEMBER THE SPACE BETWEEN THE
TWO MEMBRANE IS ACIDIC THE MATRIX IS BASIC.)
This process is called e- gradient or chemiosome(process two)
o Chemiosome- an energy-coupling mechanism that uses energy stored in
the form of hydrogen ions gradient across a membrane
H+ enter the stator the stator is in the
membrane.
Then the H+ enter the binding site within the
rotor (Fo unit) changing the shape of each
subunit so the rotor spin within the
membrane.
Each H+ make one complete turn before
leaving Fo unit through a exit channel. That
then leaves to the other side of the
membrane.
The spinning of the Fo also cause the internal
rod to spin also.
ALL TOGETHER.
Review
Glycolysis- +2 ATP
Citric cycle- +2 ATP
Oxidative and chemiomois- + 32 or 34 ATP. (from the total amount of NADH)
REVIEW OF PROCESS
In the process called glycolosis ( that takes place in the cytosol) the C6 molecule,
glucose, is split in two. & and is further processed to 2 NADH2 , 4 MOLECULE OF
ATP, 2 MOLECULES OF PRRUVATE.
--But if there is no oxygen in the process FERMENTATION, which also happens in the
CYTOSOL, Fermentation regulate the concentration of NADH+
CHAPTER 10PHOTOSYNTHESIS- the conversion of light into energy
--The chloroplast of plants capture light energy from the sun and convert it chemical
Energy stored in sugars.
Break down to two reactions
o Light hit the pigment molecule and the chlorophyll get excited and pass it on
to other chlorophyll ( as stated before)
o Then that energy reaches the special pair in PHTOSYSTEM 2( is call
photosystem 2 because it was discovered 2nd )
o The special pair in Phtosystem 2 is call P680 it absorbed light at 680
wavelength very well.
o P680 then get excited and give off an eo ALSO HAPPENING THE PS2 an enzymes is catalyzes the splitting of water
into 2 e-
The ATP ( that was produce from the synthesis) & the NADPH+ (from the PS) goes to the
Calvin cycle (dark reactions)
Calvin cycle formula ( a shorter version of the previous formula)
6CO2 + H2O 2C3 C6
the Calvin cycle uses ATP and NADPH to convert CO2 to sugars.
The Calvin cycle is anabolic builds sugars from smaller molecules and comes
energy
o Unlike the cirtic or krebs cycle that break down sugar.
Exocytosis the cell gets rid of a molecule by fusing a vesicle to the plasma membrane.
Membrane selectivity
o a biological membrane in very selective of what goes through.
o Factors for movement across the membrane
Charge
Size
If there a need of energy
o Materials that need helpers proteins to transport them.
o The amount of material that need to transport affect the time
2 types of transport
1. Passive transport- diffusion of molecule trough the membrane that DOES NOT
require any energy.
o Goes down the gradient from high to low.
2. Active Transport- diffusion of molecule through the membrane that REQUIRES
Energy (ATP)
o Goes AGAINST the gradient that why energy is used.
o ANYTHING THAT GOES AGAINST THE GRADIENT NEED
ENERGY
o Secondary Active Transport- does not use ATP but uses the gradient as it
engery use to proform the transport.
WHAT IS DIFFUSION?
o Diffusion- the movement of substances DOWN the gradient
o Teacher defa random mixing of substances that occur in a solution b/c
of the substance kinetic energy.
WHAT IS CONCENTRATION GRADIENT?
Concentration gradient a region along which the density of a chemical substance
increases or decreases
osmosis- movement of water DOWN the concentration gradient. ( passive transport)
CLASSES OF PROTEINS
1. CHANNEL- membrane pores
2. CARRIERS- carries the substances from one side to the other
3. PUMPS- use energy to go against the gradient ( primary active transport)
a. Found in hearing
WHAT IS MEMBRANE POTENTIAL ?
Membrane potential- the diff. of electrical charge across the cell plasma membrane
ACTION POTENTAL not in chapter 7
Resting Membrane Potential (Vrest)
the membrane potential of non-conducting excitable cell w/the inside of the cell
more NEGATIVE than the OUTSIDE
Graded Potential
SMALL CHANGES in the resting potential
o By opeining Ligand-gated channels
Depolarization adding SMALL POSITIVE charges to the INTERIOR of the cell
o Also ligand-gated channel
o Na+ and K+ ion rush in. (neuron with sodium potassium pumps)
Action Potential
a DRAMATIC , LARGE, AND FAST, change in the membrane potential
o Voltage-gated channel (REMEMBER THEY ALL OPEN AT ONCE)
Repolarization
the phase when the cell tries to get back to it resting potential
o the inside get more negative.
o Tries to get rid of Na+ and K+ ions (neuron with sodium potassium pumps
o Voltage-gated are close ant lock
Hyper polarization
Adding SMALL NEGATIVE charges to the interior of the cell
o The cell get to negative and is under the resting potential.
o It uses pumps in order to go back to the resting potential.
PHASES OF ACTION POTENTIAL
Phase 1- resting potential
Phase 2- depolarization- small changes to getting more positive
Phase 3- Action potential
Phase 4- repolarization
Extra Notes
Cytoplasmic streaming- movement of fluid within a animal and plants cell.