cell structure- chapter 3 Flashcards
what is the magnification equation
size of image/size of real object
what is the resolution
the minimum distance apart that two objects can be in order for them to appear as separate items
what is cell fractionation
the process where cells are broken up and the different organelles that they contain are separated out
before cell fractionation, why is the tissue placed in a cold buffered solution of the same water potential as the tissue
cold= reduce enzyme activity that might break down the organelles
same water potential= prevent organelles bursting or shrinking as a result of osmotic gain or loss of water
buffered= so the pH doesn’t fluctuate, as any change in pH could alter the structure of organelles or affect the functioning enzymes
what are the two stages to cell fractionation and explain them
homogenation= cells are broken up by a homogeniser (blender) which releases the organelles from the cell. the resultant fluid, known as homogenate, is then filtered to remove any complete cells and large pieces of debris
ultracentrifugation= process by which the fragments in the filtered homogenate are separated in a machine called a centrifuge. This spins tubes of homogenate at very high speeds in order to create a centrifugal forces
what is the process of ultracentrifugation of animal cells
- the tube of filtrate is placed in the centrifuge and spun at a slow speed
- the heaviest organelles, the nuclei, are forced to the bottom of the tube, where they form a thin sediment or pellet
- the fluid at the top of the tube (supernatant) is removed, leaving the sediment of the nuclei
- the supernatant is transferred to another tube and spun in the centrifuge at a faster speed than before
- the next heaviest organelles, the mitochondria, are forced to the bottom of the tube
- the process is continued this way so that, at each increase in speed, the next heaviest organelle is sedimented and separated out
what are two advantages of the electron microscope
- the electron beam has a very short wavelength and the microscope can therefore resolve objects as well- high resolving power
- as electrons are negatively charged the beam can be focused using electromagnets
what are the two types of electron microscope
TEM (transmission electron microscope) and SEM (scanning electron microscope)
what is a TEM microscope
- consists of an electron gun that produces a beam of electrons that is focused onto the specimen by a condenser electromagnet
- the beam passes through a thin section of the specimen
- parts of the specimen absorb electrons and therefore appear darker
- other parts allow electrons to pass through and so appear bright
- an image is produced on a screen and this can be photographed to give a photomicrograph
why cant the resolving power of the TEM is 0.1nm always be achieved
- difficulties preparing the specimen limit the resolution that can be achieved
- a higher energy electron beam is required and this may destroy the specimen
what are the main limitations of TEM
- the whole system must be in a vacuum and therefore living specimens cannot be observed
- a complex ‘staining’ process is required and even then the image is not in colour
- the specimen must be extremely thing
- the image may contain artefacts- theyre things that result from the way the specimen is prepared, artefacts may appear on the finished photomicrograph but are not part of the natural specimen
what are the limitations of an SEM
all the same as TEM except that the specimens need to not be extremely thin as electrons do no penetrate
explain an SEM
- directs a beam of electrons on to the surface of the specimen from above, rather than penetrating it from below
- the beam is then passed back and forth across a portion of the specimen in a regular pattern
- the electrons are scattered by the specimen and the pattern of this scattering depends on the contours of the specimen surface
- you can build up a 3-D image by computer analysis of the pattern of scattered electrons and secondary electrons produces
- the basic SEM had a lower resolving power than a TEM
what is an eyepiece graticule
- can measure the size of objects
- the graticule is a glass disc that is placed in the eyepiece of a microscope
- a scale is etched on the glass disc
what is a stage micrometer
needed to calibrate an eyepiece graticule
what does the nucleus contain
the hereditary material and controls the cells activities
what are 5 structures in the nucleus
nuclear envelope, nuclear pores, nucleoplasm, chromosomes and nucleolus
what does the nuclear envelope do
- is a double membrane that surrounds the nucleus
-Its outer membrane is continuous with the endoplasmic reticulum of the cell and often has ribosomes on its surface - It controls the entry and exit of materials in and out of the nucleus and contains the reactions taking place within it
what do the nuclear pores do
- allow the passage of large molecules, such as messenger RNA, out of the nucleus
- There are typically around 3000 pores in each nucleus
what is the nucleoplasm do
the granular, jelly-like material that makes up the bulk of the nucleus
what are the chromosomes in the nucleus
consists of protein-bound, linear DNA
what is the nucleolus
- a small spherical region within the nucleoplasm
- It manufactures ribosomal RNA and assembles the ribosomes
- There may be more than one nucleolus in a nucleus.
what are the 3 functions of the nucleus
- act as the control centre of the cell through the production of mRNA and tRNA and hence protein synthesis
- retain the genetic material of the cell in the form of DNA and chromosomes
- manufacture ribosomal RNA and ribosomes
what structures are within the mitochondrion
double membrane
cristae
matrix