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54 Cards in this Set

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  • Back

What is the equation for magnification?

Magnification= size of object/size of image (real size)

Resolution

The minimum distance 2 objects can be from each other before they appear as one

What is the purpose of cell fractionation?

To break cells up into seperate organelles for scientific study

What is cholera?

Infectious disease caused by prokaryotic bacterium Vibrio cholerae

How does cholera cause diarrhoea?

Bacterium adheres to epithelium and secretes toxin CT which enters epithelial cells. Activates chloride ion channels in cell membrane. Cause chloride ions to diffuse out of cells into lumen. Lowers water potential in lumen. Water moves due to osmosis into lumen. Produces diarrhoea and dehydration

What is the treatment for diarrhoea?

Oral Rehydration Therapy


Drink solution of glucose and salt. Bind to sodium-glucose transport protein and are carried down concentration gradient into cell. Lowers epithelial water potential. Body is rehydrated as water moves by osmosis out of lumen

In cell fractionation, what kind of liquid do you place the broken up cell into and why?

cold (reduce enzyme activity)


isotonic (same water potential to prevent bursting or shrinking)


buffer (to maintain constant pH)

what is a homogenizer and a homogenate?

the blender to break up cells and the homogenate the leftover fluid which is later filtered to remove complete cells and debris

supernatant

the top fluid left after using an ultracentrifuge

what is the order in which cells are seperated/forced to bottom of ultracentrifuge?

nuclei, mitochondia, chloroplats, other membrane fragments, lysosomes, ribosomes

What are the advantages of a TEM?

very high resolving power


good for organelles and prokaryotes

What are the disadvantages of a TEM?

must be in a vacuum


only dead species


complex staining process -> artifacts?


only in black + white


specimen must be very thin

What are the advantages of a SEM?

3D image


you can see surfaces!


don't need thin sections


don't need to stain

What are the disadvantages of a SEM?

resolution not as good as TEM


can't see internal structures


ultrastructure

internal structure suiting cell job

eukaryotic

distinct nucleus and membrane bound organelles

prokaryotic

no distinct nucleus

endocytosis

import of molecules and particles into cell



vesicle internally folds around substrate and this is digested and transported into cytoplasm

exocytosis

materials exported out through secretory vessles



golgi packages materials into vesicle, vesicle fuses with plasma membrane



important for excretory products

nucleus (eukaryotic)

makes mRNA (for protein synthesis) and ribsomes and ribsomal RNA


nuclear envelope (eukaryotic)

in nucleus


double membrane contains reaction, outher membrane has ribosomes

nuclear pores (eukaryotic)

in nucleus


around 300


allow passage of large molecules

nucleoplasm (eukaryotic)

in nucleus


granular, jelly-like contains chromatin (diffuse form of chromosomes)

nucleolus (eukaryotic)

in nucleus


manufactures ribsomal RNA and ribosomes

mitochondria (eukaryotic)

facilitates certain stages of diffusion


makes ATP

double membrane of mitochondria

controls entry/exit



inner folds form cristae

cristae of mitochondria

extensions which provide large s.a. for attachment of enzymes during respiration

matrix of mitochondria

semi-ridgid material made of proteins, lipids, traces of DNA and enzymes

why would a cell have more mitochondria?

if cell has high metabolic activity e.g. muscle cells

endoplasmic reticulum

elaborate 3D system of membranes and flattened sacs (cisternae) throughout cytoplasm

RER

has ribosomes


synthesises proteins and glycoproteins


provides pathway for material transport

SER

no ribosomes


synethise, store and transport lipids + transport

Golgi

makes lysosomes, secretes, modifies, stores other stuuff

what cells would have a well developed ER?

cells that need to make and store lots of carbohydrates, protein, lipis e.g. liver

what cells would have a well developed golgi appartus?

secretory cells e.g. epithelial cells of intestine

ribsomes

found in RER or cytoplasm


SITES OF PROTEIN SYNTHESIS


have 2 subunits which fit into each other



contain ribosomal RNA and protein


super numerous!



80s type (eukaryotic)


70s type (prokaryotic)

lysosomes

formed from RER and Golgi (just vesicles containing cocktail of digestive enzymes)


when are lysosomes abundant?

in secretory cells e.g. phagocytic cells

what are lipids?

mixed ground of hyrdrophobic compounds containing carbon, hydrogen and oxygen



common lipis are triglycerides (fats and oils), phospholipids and waxes



insoluble in water, soluble in organic solvents e.g. alchohol

what are some functions of lipids?

plasma membrane


energy source


waterproofing


insulation fats


protection fats around delicate organs (adipose tissue)

what are triglycerides?

have 3 fatty acids with 1 glycerol


made in condensation reactions

what are fatty acids?

over 70 fatty acids


super long molecules



all have carboxyl acid group (-COOH) and a hydrocarbon chain (R group, variably lengthed chain)

what is glycerol?

small, 3 carbon molecule with 3 alcohol (OH) groups

small, 3 carbon molecule with 3 alcohol (OH) groups

How is a triglyceride formed?

a condensation polymerisation reaction!


 


1 glycerole joins with 3 fatty acids by ester bonds


 


'kicks out' 3 H20 molcules

a condensation polymerisation reaction!



1 glycerole joins with 3 fatty acids by ester bonds



'kicks out' 3 H20 molcules

saturated fats

no carbon-carbom double bonds



all carbons are joined to max. number of hydrogens

mono-unsaturated fats (oils)

a single carbon-carbon double bond

polyunsaturated fats (oils)

more than one double carbon-carbon bond



(double bonds cause molecules to bend, cannot pack themselves so closesly so are liquid at room temp.)

what are phospholipids?

same as triglycerides but with a phosphate group instead of fatty acid chain



hydrophobic tails (fatty acids)


hydrophilic head (glycerol and phosphate)

Describe the emulsion test

test for lipids!


test tube filled with sample and ethanol


shake to dissolve lipi


add equal amount of water


shake again


cloudy-white = LIPID




lipid is finely dispersed in water = emulsion. Light passing through is refracted as it passes from water to oil droplets = cloudy

whats the purpose of plasma membrane?

controls entry/exit


allows conditions to be different

what are purpose of phosholipids in plasma membrane?

keeps membrane flexible


allows lipid-soluble molecules to enter


not water-soluble molecules

extrinisic proteins

on surface or partially embedded

intrinsic proteins

spans entire bilayer

what is the purpose of proteins on the bilayer?

provide structural support


allow active transport with ion channels e.g. sodium or potassium


helps cells adhere together


form recognition sites (often glycoproteins)


act as receptors


enzymes