Key Mechanisms Flashcards
Transcription mechanism
- The DNA helix is unwound by helicase enzyme which separates the hydrogen bonds between bases
- One of the exposed strands is the coding strand, which acts as a template for mRNA synthesis
- RNA Polymerase lines up the complementary nucleotides C-G and A-U and joins them together by condensation reactions to form phosphodiester bonds
- The mRNA is spliced before leaving the nucleus. Non-coding introns are removed and the exons are joined together.
- The mature mRNA leaves through a nuclear pore and enters the cytoplasm
- The mRNA attaches to a ribosome and is translated
- Pieces of the RER pinch off to form vesicles carrying the polypeptide to the Golgi body, where it is processed and packaged.
- The mature protein is pancaked into vesicles for storage or exocytosis
Translation mechanism
- The ribosome attaches to the mRNA strand
- The ribosome has two active sites into which tRNA molecules can enter
- The tRNA that enters the active site must have the correct anti-codon to match the codon being read.
- As the two tRNA are alongside each other, the amino acids they carry can be joined together by condensation reaction to form a peptide bond at the expense of ATP.
- One of the tRNA now exits the ribosome leaving a vacant active site. The ribosome moves along one codon, and then another tRNA brings the next amino acid and so on until the end of the mRNA strand, or until a STOP codon is reached.
DNA replication mechanism
- Happens during the synthesis phase of interphase
- The DNA molecules uses a gyrase enzyme to unwind its double helix and then uses a DNA helicase enzyme to break the hydrogen bonds between the complementary base pairs on order to ‘unzip’ the molecule
- this results in two exposed strands of nucleotides which act as a template for semi-conservative replication
- Complementary nucleotides free in the nucleolus match up with the exposed bases on the original two strands by forming hydrogen bonds between them and DNA polymerase catalyses the formation of phosphodiester bonds between nucleotides in the 5’ to 3’ direction
- This happens continuously for the leading strand but for the lagging strand, it is built as Okazaki fragments due to it being opposite to the leading strand.
- The Okazaki fragments in the lagging strand are then joined by ligase enzymes
- This process forms 2 identical DNA molecules which each contain 1 strand of the original parent DNA
- this makes DNA replication semi-conservative
Competitive inhibition mechanism
- The inhibitor has a shape similar to the substrate
- They both compete for the active site, consequently fewer Enzyme-Substrate complexes can be formed
- so the reaction rate is lower than normal
- at higher doses of substrate the inhibition can be overcome as the substrate will greatly outnumber the inhibitor molecule and most collisions will actually form Enzyme-Substrate complexes
Non-competitive inhibition mechanism
- This binds to the allosteric site away from the active site
- this causes the tertiary structure of the enzyme to change
- this changes the shape of the active site so it is no longer complementary to the substrate
- fewer Enzyme-Substrate complexes can form
- reaction rate is lowered
- higher substrate concentrations cannot overcome the inhibition because the limiting factor is the number of active sites
Cell Cycle and Division Mechanism
Interphase: (not part of mitosis)
Prophase:
- Chromosomes condense and become visible as DNA supercoils
- Nuclear envelope and nucleolus breaks down
- Centrioles divide and two new daughter centrioles move to opposite ends of the cell
- Mitotic spindle fibres form
Metaphase:
- pairs of chromatids attach to the spindle threads at equator region
- they attach by their centromeres
Anaphase:
- Centromere of each pair of chromatids splits
- Motor proteins pull each sister chromatid towards opposite poles
- Chromatids form chromosomes
Telophase:
- Separated chromosomes reach the poles
- New nuclear envelope forms around each set of chromosomes
- Cell now contains two new nuclei which are genetically identical to each other and to the parent cells they came from
Cytokinesis: (not part of mitosis)
- Cell splits into two
- each new cell contains a nucleus
- New plasma membrane forms around the two new cells
- Two daughter cells are formed
- They are genetically identical to each other and the parent cell
Meiosis mechanism
Prophase 1:
- Chromatin condenses and each chromosome supercoils
- Nuclear envelope breaks down
- Centrioles form
- Chromosomes come together in homologous pairs
- Each member of the pair consists of two chromatids
- Crossing over occurs - where non-sister chromatids wrap around each other and swap sections so that alleles are shuffled
Metaphase 1:
- Pairs of homologous chromosomes attach along the equator of spindles
- Each attached to a spindle thread by its centromere
- Independent Assortment occurs
- Where homologous pairs are arranged randomly and face opposite poles of the cell
Anaphase 1:
- Chromatids in each pair of homologous chromosomes are pulled apart by motor proteins across the spindle
- Centromeres don’t divide
- Crossed-over areas separate from each other
- This results in swapped areas of chromosomes and allele shuffling
Telophase 1:
- Two new nuclear envelopes from around each set of chromosomes
- Cell divides by cytokinesis
- Chromosomes uncoil during interphase
- Each new nucleus contains half the original number of chromosomes
- Each chromosome consists of two chromatids
- In plant cells, cell goes from anaphase 1 into prophase 2
Prophase 2:
- If nuclear envelopes have reformed, they then break down
- Chromosomes coil and condense, each one consisting of two chromatids
- Chromatids of each chromosome are no longer identical
- This is due to crossing over in Prophase 1
- Spindles form
Metaphase 2:
- Chromosomes attach to equator of the spindle by the centromeres
- Chromatids of each chromosome are randomly arranged
Anaphase 2:
- Centromeres divide
- Chromatids of each chromosome are pulled apart by motor proteins towards opposite poles
- Chromatids are therefore randomly segregated
Telophase 2:
- Nuclear envelopes from around each of the four haploid nuclei
- In animals, two cells divide to give four haploid cells
- In plants, a tetras of four haploid cells is formed
Interphase Mechanism
G1(Gateway 1)
Cells grow and increase in size. • Transcription of genes to make RNA occurs. • Organelles duplicate. • Biosynthesis, like protein synthesis, including making the enzymes needed for DNA replication in the S phase. • The p53 (tumour suppressor) gene helps control this phase.
S Phase(synthesis):
DNA replicates.
• When all chromosomes have been duplicated,
each one consists of a pair of identical sister
chromatids.
• This phase is rapid, and because the exposed
DNA base pairs are more susceptible to mutagenic agents, this reduces the chances of spontaneous mutations happening.
G2(Gateway 2):
Cells grow
M Phase(Mitosis):
Cell growth stops
Mitosis occurs
Cytokinesis follows to create two daughter cells identical to each other and the parent cell
Phagocytosis and Antigen Presentation Mechanisms
Phagocytosis:
- Receptor on phagocyte’s cell surface membrane binds to antigen on pathogen’s cell surface membrane
- Pathogen engulfed by endocytosis
- This produces a phagosome
- Lysosomes fuse with phagosome, releasing enzymes(lysins) into it
- The pathogen is digested into amino acids and fatty acids
- Products are absorbed into cytoplasm by diffusion
- Phagocyte can incorporate antigens into cell membrane to become an antigen-presenting cell
Antigen Presentation:
Antigen presenting cells move around body where can come into contact with specific cells and activate the immune response
These are B and T lymphocytes
The antigen-presenting cells increase chances that the lymphocytes will come into contact with pathogen
Pressure changes in mouth that cause water to move over gills mechanism
Fish opens its mouth, lowering the buccal cavity
The volume of the buccal cavity increases therefore decreasing the pressure causing water to be sucked in
When the fish closes its mouth, the buccal cavity is raised
This decreases the volume and increases the pressure
The increased pressure forces water out of the operculum cavity across gill filaments
This causes the operculum to open
This allows the water to move out of the gills down a pressure gradient.
Adaptations in fish gas exchange
Large surface area provided by gill filaments
Rich blood supply from lamallae
Thin walls - shorter diffusion pathway
Countercurrent flow - concentration gradient maintained by counter flow of water in opposite direction to blood flow, oxygen constantly moving into blood by diffusion along a concentration gradient . Happens as oxygen concentration in the water is always higher than oxygen concentration in the blood
Ventilation in insects
Air enters pores in their abdomen called spiracles
Air comes through a tube called trachea
These then split into tracheoles which branch very finely between all tissues
The ends of tracheoles are filled with tracheal fluid
The gases will diffuse in the tracheal fluid where it will diffuse into the cell
-When muscles use up oxygen they respire anaerobically
Lactic acid builds up ==> more negative water potential
Water moves by osmosis from tracheoles and into the muscle.
Increases the surface area of the exchange surface and so increased oxygen diffusion
Inspiration in the lungs
Signal is sent from the medulla oblongata / brain stem along the phrenic nerve
Rib External intercostal muscles contract causing the ribs to move up
The diaphragm muscles contract which makes the diaphragm move down and out
The volume of the lungs increase
The pressure of air decreases below atmospheric pressure
Air enters the lungs to equalise the pressure.
Expiration in the lungs
Ribs move down and in
Diaphragm muscles relax, causing diaphragm to move up from pressure of Liver
The volume of the lungs decreases
The pressure inside the lungs increases above atmospheric pressure and mainly
Elastic recoil of the lung tissue
Adaptations of alveoli
Good blood supply so gases can easily diffuse in and out of the blood and maintain a steep concentration gradient by rapid removal of Oxygen
Well ventilated - maintain steep concentration gradient of Oxygen with blood
Moist lining - gases can dissolve first before entering blood
Folded - increases their surface area, more oxygen from bronchioles can diffuse into blood
Contain a lung surfacant - stops alveoli collapsing and sticking together
Contain collagen and elastic fibres that can stretch out and recoil to squeeze air out, stops alveoli exploding
Squamous epithelium of alveoli - thinner walls for a shorter diffusion distance for gases
Squamous endothelium of the capillary - thinner walls for a shorter diffusion distance for gases into alveoli
Cardiac Cycle Mechanism
- SAN sends an electrical impulse across the atrial wall
- This causes the atria to contract
- The volume in the atria decreases and the pressure increases above ventricular pressure
- Blood is forced through the atrioventricular valves and into the ventricles
- A band of connective tissue is non-conductive and prevents the signal passing to the ventricles
- The AVN is stimulated and conveys signals to the apex of the heart through the Bundle of His
- These family into the purkyne fibres which rapidly and evenly disperse the impulse
- this causes a delayed ventricular contraction - Ventricular pressure increases
- Atrioventricular valves close and semi-lunar valves open - Blood leaves through the pulmonary artery and aorta
Enzyme induced fit hypothesis mechanism
- Enzymes have active sites complementary to the substrate molecule
- When the substrate molecules fit into the enzyme’s active site, the active site changes shape slightly to mould itself around the substrate
- An enzyme-substrate complex is formed, and non-covalent forces such as hydrogen bonds, ionic attractions, van der Waals forces and hydrophobic interactions, bind the substrate molecule to the enzyme’s active site.
- When the substrate molecules have been converted to the product molecules and these are still in the active site, they form an enzyme-product complex.
- As the product molecules have a slightly different shape from the substrate molecule, they detach from the active site.
- The enzyme molecule is now free to catalyse another reaction with another substrate molecule of the same type.
Formation of tissue fluid mechanism
Arteries branch into arterioles, and then into a network of capillaries
These link up with venules to carry blood to veins
Therefore blood flowing into an organ or tissue is contained in the capillaries
At arterial end of a capillary, blood is at relatively high hydrostatic pressure.
This pressure tends to push blood fluid out of capillaries through their walls - slit pores
The fluid can leave through tiny gaps between cells in capillary walls
Fluid that leaves the blood consists of plasma with dissolved nutrients and oxygen.
All RBCs, platelets and WBCs remain in the blood, as do the plasma proteins above RMM 69000
These are too large to be pushed out through the gaps in the capillary wall
Tissue fluid surrounds the body cells, so exchange of gases and and nutrients can occur across the plasma membrane.
Exchange occurs by diffusion, facilitated
diffusion, and active uptake
Oxygen and nutrients enter the cells; CO2 and other wastes leave the cells
Tissue fluid returning to the blood mechanism
The blood pressure(hydrostatic pressure) at the venous end of the capillary is much lower than oncotic pressure
This allows some of the tissue fluid to return to the capillary carrying carbon dioxide and other waste substances into the blood.
The proteins that remained in the blood exert a high negative water potential
Osmosis of water from tissue fluid into lumen
Some tissue fluid directed to another tubular system called lymphatic system
This drains excess tissue fluid out of tissues and returns it to blood system in left subclavian vein in chest
Fluid in lymphatic system called “lymph” and is similar in composition to tissue fluid
Contains more lymphocytes, as they are produced in the lymph nodes
A* low protein in the blood ==> fluid accumulates in tissue (see Kwaskiokor syndrome)
A* parasites can block lymph vessesl and cause tissue swelling ==> see elephantiasis / filiariasis ==> affects over 1 million worldwide )
How do xylem vessels form?
Lignin impregnates early xylem
Waterproofs and kills the cells
Long column of dead cells with no contents forms - called xylem vessel
This prevents vessel from collapsing
Lignin thickens and forms spiral in cell wall
This allows some flexibility to stem or branch
Where lignification is not complete, bordered pits form
These allow water to move sideways into cells
Transpiration stream mechanism
H
Translocation/Active loading mechanism
- H+ ions are actively pumped out of the companion cell
- This process requires the use of ATP
- This creates a concentration gradient outside the companion cell
- High concentration of H+ ions causes facilitated diffusion back into the companion cell
- Sucrose is carried with the H+ ions through cotransport proteins in the plasma membrane
- As the concentration of sucrose in the companion cell increases, facilitated diffusion occurs via contransport proteins in the membrane
- sucrose moves through the plasmodesmata into the sieve tube element
Test for Reducing Sugars
- Benedict’s reagent is heated to 80Degrees Celsius with a solution of the sample
- Reagent test strips can be used for semi-quantitative results
- On heating, if a reducing sugar is present, there will be a red or orange precipitate
- Intensity of colour depends on concentration of reducing sugars. If there is little it will be green, if there is a high conc. if will turn intense red.
- Use colorimetry and a calibration curve to quantify reducing sugars in a sample
Triggering immune response mechanism
- Antigens on pathogen’s surface communicate to body cells is foreign
- To initiate immune response, pathogens have to be detected by B and T lymphocytes with complementary receptors on pathogen’s antigens
- Infected cells sometimes get pathogen’s antigens on their surface - helps to select right B and T lymphocytes
- Macrophages in the lymph nodes engulf and digest pathogens. They separate the pathogen’s antigens and incorporate them into their own cell surface membrane. They are now antigen presenting cells ‐ they increase the chances of the correct T lymphocytes locating the foreign antigens.
• The selection of the correct lymphocytes with receptors complementary in shape to the antigens is call clonal selection.
• More of these lymphocytes are needed to fight the pathogens so they divide by mitosis in clonal expansion.