2.1 cell structure and microscopes Flashcards

1
Q

name the four types of microscopes

A

light microscope
transmission electron microscope
scanning electron microscope
laser scanning microscope

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2
Q

what is the difference between magnification and resolution?

A

magnification is the process of enlarging the apparent size

resolution is the ability to distinguish 2 objects as separate

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3
Q

what is the maximum magnification and resolution of a light microscope

A

magnification 1500x
resolution 200nm

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4
Q

what is the maximum magnification and resolution of an SEM

A

magnification 200.000x
resolution 0.1nm

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5
Q

what is the maximum magnification and resolution of a TEM

A

magnification 2millionx
resolution 0.1nm

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6
Q

what is the maximum magnification and resolution of a laser scanning microscope

A

magnification 1000x
resolution 180nm-500nm

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7
Q

how is the beam focused in a light microscope

A

light beam is focused through glass lenses

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8
Q

how is the beam focused in an SEM

A

an electron beam is focused with electromagnetic coils

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9
Q

how is the beam focused in a TEM

A

an electron beam is focused with electromagnetic lenses

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10
Q

how is the beam focused in a laser scanning microscope

A

a laser beam through a light source is focused with objective glass lenses

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11
Q

which microscopes have a sectional or external view of the specimen

A

light - both
TEM - sectional
SEM - external
Laser - both

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12
Q

what is an application of a light microscope

A

can be used to provide information about the activity of cells

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13
Q

what is an application of a TEM

A

internal view of organelles and cells

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14
Q

what is an application of an SEM

A

external 3D viewing of cells

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15
Q

what is an application of a laser scanning microscope

A

medical progression

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16
Q

why is the maximum magnification of a light microscope limited to 1500x

A

the wavelength of visible light ranges from 400-700nnm so structures closer than 200nm will appear as one object.

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17
Q

state advantages of light microscopes

A

cheap
easy to use
able to study live specimens

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18
Q

state disadvantages of light microscopes

A

limited resolution due to wavelength of light

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19
Q

state advantages of SEM

A

high resolution
high magnification
produces 3D images

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20
Q

state disadvantages of SEM

A

inability to analyze live specimens
costly
training is required
black and white images only

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21
Q

state advantages of TEM

A

high magnification
high resolution
provides information on the internal structures of cells

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22
Q

state disadvantages of TEM

A

inability to analyze live specimens
costly
training required
black and white images only

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23
Q

explain why a vacuum is needed for electron microscopes

A

they prevent the electrons from being scattered by air particles

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24
Q

explain in terms of staining how electron microscopes differ

A

in an SEM the metal salt stain sits on top of the specimen whereas on a TEM the metal salt stain passes through the specimen

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25
use a named example to explain why staining is needed for light microscopes.
the main reason for staining is to highlight cells and parts of cells for a better visual, for example, acetic orcein stains DNA and chromosomes in cells dark red
26
briefly describe how to use a light microscope
put the slide on the STAGE and clip it in place turn on the power supply and light source look through the EYEPIECE and make sure the OBJECTIVE LENS is on the lowest magnification adjust your FINE and COARSE focus as well as IRIS DIAPHRAGM
27
describe how to change between units
mm -> microm =*1000 micromm-> mm=/1000 microm -> nm=*1000 nm ->microm /1000
28
what is the formula for magnification
magnification = image size/actual size
29
what is the difference between prokaryotic and eukaryotic cells
prokaryotic cells contain a cell wall and plasmids in the cytoplasm. However, it doesn't have a nucleus and membrane-bound organelles
30
describe the 10 structures of a prokaryotic cell
they contain: a waxy protective capsule peptidoglycan cell wall plasma membrane mesosome plasmid pili ribosomes cytoplasm DNA loop flagella
31
describe the endosymbiotic theory
the idea that eukaryotes arose from prokaryotes- that organelles were once prokaryotes ingested by a larger bacteria
32
what is the difference between the nucleus and the nucleolus
the nucleolus is inside the nucleus
33
describe the structure of the nucleus
the nucleus is surrounded by a double membrane called the nuclear envelope that contains pores the outer membrane joins up to the endoplasmic reticulum it is the largest organelle 10-20micro metres in diameter the nucleoplasm contains chromatin
34
describe the function of the nucleus
contains nearly of all a cells genetic material; instructions for making proteins and makes mRNA for protein synthesis
35
describe the structure of the nucleolus
not surrounded by a membrane the dense spherical structure inside the nucleus
36
describe the function of the nucleolus
makes RNA and ribosomes that pass into the cytoplasm through the nuclear pores
37
describe the structure of the ribosomes
non-membrane bound small spherical organelle that is about 20nm in diameter made of ribosomal RNA made in the nucleolus as two separate sub-units which pass through the nuclear envelope into the cytoplasm and then combine (40s and 60s sizes )
38
describe the function of ribosomes
ribosomes that bind to the exterior of the endoplasmic reticulum are mainly used for synthesising proteins that will be exported outside the cell ribosomes that are free in the cytoplasm, either singly or in clusters are primarily the site of assembly of proteins that will be used inside the cell
39
describe the structure of rough ER
system of membranes containing fluid-filled cavities (cisternae) that are continuous with the nuclear membranes coated in ribosomes
40
describe the function of rough ER
it is the intracellular transport system: the cisternae form channels for transporting systems from one area of a cell to another provides a large surface area for ribosomes which assemble amino acids into proteins - these proteins then actively pass through the membrane into the cisternae and are transported to the Golgi body for modification and packaging
41
describe the structure of smooth ER
system of membranes with fluid-filled cavities (cisternae)that are continuous with the nuclear membrane no ribosomes
42
describe the function of smooth ER
contains enzymes that catalyse reactions involved with lipid metabolism such as: -synthesis of cholesterol - synthesis of steroid hormones it is involved with absorption synthesis and transportation of lipids (from the gut)
43
describe the structure of the Golgi apparatus
consists of stacks of membrane-bound flattened sacs secretary vesicles bring materials to and from the Golgi body
44
describe the function of the Golgi apparatus
proteins are modified for example: -adding sugar molecules to make glycoproteins -adding lipid proteins to make lipoproteins -being folded into their 3D shape then proteins are packaged into vesicles that are then pinched off and : -stored in the cell or -moved into the plasma membrane, either to be incorporated into the plasma membrane or exported outside the cell
45
describe the structure of the mitochondria
they may be spherical or rod-shaped or branched and are 2-5 micrometers long they are surrounded by two membranes with a fluid-filled space between them. The inner membrane is highly folded into cristae the inner part of the mitochondrion is a fluid-filled matrix
46
describe the function of the mitochondria
site of ATP during aerobic respiration self-replicating so mare can be made if the cell needs more energy they are abundant in cells where much metabolic activity occurs
47
describe the structure of chloroplasts
these are large organelles that are 4-10 micrometers long they are surrounded by a double membrane or envelope the inner membrane is continuous with stacks of flattened membrane sacks called thylakoids which contain chloroplasts. Each stack of thylakoids is called a granum the fluid-filled matrix is called stroma
48
describe the function of chloroplasts
chloroplasts are the site of photosynthesis during the first stage of photosynthesis, when light energy is trapped by chlorophyll and used to make ATP occurs in the grana, water is also split to supply hydrogen ions
49
describe the structure of lysosomes
these are small bags formed from the Golgi apparatus and each is surrounded by a single membrane they contain powerful hydrolitic (digestive) enzymes
50
describe the function of lysosomes
they keep powerful hydrolitic enzymes separate from the rest of the cells they engulf old organelles or foreign matter, digest them and return the digested components to the cell for reuse they are abundant in phagocytic cells such as white blood cells and neutrophills
51
describe the function of the plasma membrane
separate contents of the cell from the outside permeable so it allows solutions to pass-through
52
describe the structure of the plasma membrane
a thin flexible layer of phospholipids
53
describe the structure of the cellulose cell wall
on the outside of the plasma membrane made from bundles of cellulose fibers
54
describe the function of the cellulose cell wall
strong and prevents plant cell from bursting when turgid provides strength and support maintains the cells shape permeable and allows solutions to pass through
55
describe the structure of the vacuole
surrounded by a membrane called the tonoplast and contains fluid
56
describe the function of the vacuole
filled with water and solutes and maintains cell stability because when full it pushes against the cell wall and makes the cell turgid
57
describe the structure of the vesicle
made from phospholipids
58
describe the function of the vesicle
used for transportation
59
how does the function of ribosomes that are free and those on the RER differ
Free ribosomes are mainly concerned with assembling proteins to be used within the cell. Ribosomes on RER mainly assemble proteins that are exported out of the cell.
60
how are chloroplasts moved nearer the surface on a dull day
Motor proteins drag chloroplasts along cytoskeleton threads or ‘tracks’.
61
name one substance that passes into the nucleus
mRNA
62
suggest why hydrolytic enzymes need to be inside a vesicle
To prevent them from digesting/breaking down the cell components.
63
describe the structure of centrioles
consists of two bundles of microtubules at right angles to each other the microtubules are made of tubulin protein subunits arranged to form a cylinder
64
describe the function of centrioles
before the cell divides the spindle, made of threads of tubulin, forms from the centrioles. Then chromosomes attach to the middle part of the spindle and motor proteins walk along the tubulin threads and pull the chromosomes apart involved in the formation of cilia and undulipodia
65
describe the structure of microfilaments
they are 7nm in diameter and made of subunits of the protein actin
66
describe the function of microfilaments
they are within the cytoplasm and give support and mechanical strength to keep the cell's shape stable and allow cell movement
67
describe the structure of intermediate filaments
10nm in diameter made of a variety of proteins
68
describe the function of intermediate filaments
they anchor the nucleus within the cytoplasm extend between cells in some tissues between special junctions enabling cell-cell communication and allowing cells to adhere to a basement membrane stabilising the tissue
69
describe the structure of microtubules
18-30nm in diameter made of protein subunits called tubulin
70
describe the function of microtubules
also, provide shape and support to cells and help organelles/substances move through the cytoplasm they form the track along which motor proteins (kinesin) walk and drag organelles from one part of the cell to another they form the spindle before a cell divides and these spindle threads enable a chromosome to be moved within the cell
71
why are some human cells ciliated
to waft mucus
72
name a type of human cell that can move and explain why that is important for its function
phagocytes the can move so that they can engulf pathogens
73
How do you use a graticule
lace a stage micrometer on the stage of the microscope. Line up one of the divisions on the eyepiece graticule with a fixed point on the stage micrometer. Count the number of divisions on the eyepiece graticule that correspond with a set measurement on the stage micrometer. Calculate the distance in micrometres of one division on the eyepiece graticule.