I'm so screwed Flashcards
(145 cards)
0
Q
What are two ways of determining the actual size of a specimen?
A
- proportion of field of view by the specimen -use the equation size of specimen=amount of field taken up (decimal)x field of view
- use an ocular micrometer- actual size of cell=# of ocular divisions x length of ocular division
1
Q
How do you calculate magnification?
A
Magnification of drawing=size of drawing/ actual size of the specimen
2
Q
What does reducing the amount of light change for your microscope?
A
The contrast
3
Q
What does switch itching from a 40X objective lens (40/0.65) to 100X lens (100/1.25) do for your microscope?
A
Change in resolution and magnification
4
Q
What does the use of immersion oil do for your microscope?
A
Change in Resolution
5
Q
What does staining the specimen help with?
A
Contrast
6
Q
What does changing the light source from a 400nm to a 500 NMR light help with for the microscope?
A
Contrast
7
Q
What does changing the light source from a 500nm to a 400 nk light do for the microscope?
A
Helps with resolution
8
Q
True or false a plant cell will become plasmolyzed when placed in a hypotonic solution.
A
False it will remain turgid
9
Q
Hypotonic
A
There is less solute in the cell than the surrounding solution
10
Q
Hypertonic
A
There is more solute in the cell than the surrounding solution
11
Q
Isotonic
A
Net osmosis is 0
12
Q
True or false- A hypertonic solution has a higher concentration of solutes than found in side the cell
A
True
13
Q
Interpupillary distance
A
Distance between the centre of the pupils of the eyes
14
Q
Ocular micrometer
A
A ruler on the eye piece of the microscope that can be used to measure the actual size of the specimen
15
Q
Parfocal
A
When switching magnification the microscope stays in focus
16
Q
Turgid
A
When the cell fills with water and swells
17
Q
Plasmolyzed
A
When water leaves the cell and the plasma membrane pulls away from the cell wall
18
Q
Flaccid
A
If to much water is lost the plant cell will wilt
19
Q
You have been asked to test the 5 second rule. To do this you: place candies on the floor for 5 seconds, press the candies to the agar plates, incubate the plates and look for microbial growth
What is the independent variable, dependent variable, experimental group and constants? What’s missing from the exp?
A
Whether or not the candy touched the ground, the amount of microbial growth on the agar, pieces of candy touched the floor for 5 seconds, (time the agar is incubated and type of candy on the floor) there is no control group
20
Q
Explain why grocery stores spray their products with water
A
So the plants don’t go into plasmolysis because they are dried out. The spray has little solute in it so it is hypertonic and water goes into the cell
21
Q
Why was distilled water used as a blank?
A
.
22
Q
For the experimental question “what is the effect of acetylcholine on heart rate in humans?”
a. independent variable
b. dependent variable
c. experimental group
d. control group
A
Ind. acetylcholine, dep. heart rate, exp group. Acetylcholine present control acetylcholine absent
23
Q
The 10x, 40x and 100x objectives on the compound microscopes you used during the term are par focal. The fact that the microscopes are par focal implies:
a. When you look through both eye pieces, you only see one image
b. There are three lens systems on the compound microscope
c. the condenser lens must be focused before you use the microscope
d. you only need to adjust the fine focus when switching between objective lens
e. each of the objective lenses has a corresponding position on the annular condenser
A
D
24
Interpupillary distance on a microscope accounts for the differences between individuals who wear glasses and those that do not
False. Interpupillary distance accounts for the distance between individual's pupils
25
True or false. An animal cell with an internal solute concentration of 0.25M will shrink when placed in a solution with a solute concentration of 1.0M
True
26
Your partner streaked an agar plate with a mixed bacterial culture. He placed a freshly flamed loop into a culture tube and made an initial streak on the surface of the agar. He then reclaimed the loop and without plunging the loop into the again streaked a portion of the first streak to make a second streak. Why did the bacteria not grow in the normal growth pattern?
Because the loop was still hot it killed the cells in the second streak
27
# Choose the one correct order of signal transmission in the Spectronic 20 spectrophotometer.
a. light source, transmitted light, sample, incident light, meter
b. light source, photometer, transmitted light,sample, incident light, meter
c. light source, incident light, sample,transmitted light, photometer, meter
e. light source, incident light, sample, photometer, transmitted light, meter
C
28
In lab 2 why did you set the wavelength at 525nm to measure your samples?
Because betacyanin absorbs maximally at 525nm
29
In lab 2 what did you use to calibrate the meter on the spectrophotometer, why?
We used water as our blank because that was the solution the betacyanin was extracted in
30
A cell contains a red pigment in the cytoplasm and a blue pigment in the vacuole. After an irradiating treatment, the plasma membrane of the cells were damaged by that tonoplast remained in tasted what colour did the solution turn?
After the treatment the solution should appear red because the cell membrane was damaged the red would seep out however the blue in the vacuole would remain intact end because the vacuole remained intact
31
True or False. Absorb acne of light by pigment increases with concentration of pigment
True
32
What is the purpose of Safranin, what is the purpose of Gram iodine?
Safrine is a counter stain used to stain bacterial cells that were decolourized with ethanol during gram stain. Gram iodine forms a complex with crystal violet making it difficult to remove crystal violet stain from gram positive cells
33
In lab 8 during the alkali lysis mini prep procedure, it was critical not to vortex your tube after the addition of solution II (which contained SDS and NaOH) because vortexing will:
a. shear the plasma DNA causing it to denature
b. cause RNA to precipitate thus removing RNA from prep
c. break the bacterial genomic DNA into small pieces
d. beak the cells open causing the lays ate to become very viscous
e. cause RNA to remain in the solution, thus contaminating the plasmid DNA with RNA
C
34
In Lab 3 what characteristics did you use to identify the bacteria in the culture?
Gram stain reaction, colony morphology, cell morphology, O2 requirements, glucose fermentation, endosperm formation and mobility
35
Which of the following statements is false?
a. Iodine complexes with crystal violet
b. Safranin is the differential step in the Gram stain
c. Gram positive cells have a thick peptidoglycan layer
d. Safranin stains gram-negative cells pink
e. Ethanol washes crystal violet out of Gram negative cells
B
36
```
All of the following are cell morphology characteristics except for:
a length
b shape
c edge
d gram reaction
e motile structures
```
C
37
You are concerned about bacterial contain inaction in the water from the drinking fountain opposite of the Bio 107 Labs, you get a sample of the drinking water from the fountain and streak it onto a PCA plate
a. What is the objective of streaking the cells onto solid medium
b. For colonies grow on the plate. Three colonies have identiacal colony morphology and one has different what can you conclude?
c. how would you confirm your answer in B?
A. To obtain single colonies
B.there are at least two diff species because diff characteristics means diff species. There could be more because identical cell morphology does not necessarily mean the same species.
C.preform further tests such as gram stain, determine cell morphology and various biochemical tests.
38
Your TA gives you a mixed culture of 2 bacteria in a liquid medium and asks you to preform a gram stain for each. What must you do at the beginning of the gram stain?
B. You notice that bacteria A is a negative bacillus but your stain for bacterium B has both gram negative A bacillus and Gram positive cocci. Explain the results.
A. Streak the cells on the plate to obtain isolated colonies
B. Possible contamination of bacterium B with cells of bacterium A, either due to shaking hands when picking up colony or improper isolation of colonies
39
True or False. The positive result for bacteria that produce endospores is turbid culture following following heating to 80C for 10 minutes and adequate incubation at optimal temperature
True
| Turbid: cloudy
40
In one sentence briefly describe the purpose of using Detain
Impedes the movement of cells
41
Some you add cholchicine, a drug that effectively inhibits the function of microtubules to Pelomyxa Carolinensis. What effect would manipulation have on the mobility of this organism
No effect as the mobility of this organism is due to interactions between the microfilament cytoskeleton and the cytoplasm
42
Moltility via pseudopodia is achieved using which components?
I. Actin filaments II. Tubulidentata filaments III. Intermediate filaments IV. Flagellin V. Chromatin VI. Dynein
Tumblin filaments
43
Three ways to increase contrast in order to view a cell
Stain cell, adjust condenser diaphragm, use phase contrast microscope
44
True or false. The function of the contractile vacuole is single celled eukaryotic organisms is to pump waste particle out of the cell
False. The function of the contractile vacuole in single celled eukaryotic organisms is to pump water out of the cell
45
True or false. Enzymes are proteins that are composed of glucose molecules.
False enzymes are composed of amino acids
46
There were 2 controls in lab 6 photosynthesis. Describe what assumptions they were designed to test.
They were both dark controls-assumes that light is necessary for photosynthesis
47
True or false. Cellular respiration consumes oxygen and produces CO2
True
48
Glycolysis is a pathway that precedes:
I. Alcoholic fermentation II. The Krebs cycle III photosynthesis IV latic acid fermentation V the Calvin cycle
A.I, II,IV B.I,IV C.II only D.III,V E.All of the above F none of the above
A
49
Yeast in the Durham tube were undergoing anaerobic respiration
False fermentation
50
In lab 7 sugar metabolism in yeast you incubated yeast with glucose and varying amounts of ethanol inDurham tubes and obtained CO2 production. What do you think would happen to the rates of CO2 production if you incubated the tubes at 50C?
The rate of production would be less because the temp is much higher than the optimal temp of 30C
51
Bacteria genomic DNA:
a. Contains between 2 and 25 genes
b. Is a circular molecule anchored to the plasma membrane
c. is contained in the nucleus
d. exists in supercoiled conformation
e. is not necessary for the cell survival
B
52
True or False. Solution II (SDS and NaOH) is used in the plasmid mini-prep procedure to denature proteins disrupt the plasma membrane and cause hydrogen bonds in the DNA to re-form
False. Causes the hydrogen bonds to break
53
In lab 8 DNA extraction, when performing the mini-plasmid prep, after addition of which does plasma precipitate.
a. T buffer b. Solution II c. 70% ethanol d.95% ethanol e.solution III f.Solution I
D
54
You used micro pipettes as a tool to accurately measure small volumes of liquid
a. Briefly describe the function of the first two stops of the button on top of the pipettor
b. why is it important to touch the tip to the side of the receiving vessel when expelling liquid?
A. Stop 1 measures volume of the liquid in the selected window, stop 2 blows out the last few drops from the tip
B. The capillary action draws the last few drops out of the tip
55
In lab 8 during the alkali lysis mini-prep and during the preparation of HMW salmon sperm DNA, you precipitated the DNA with 95% ethanol, then washed the DNA pellet with 70% ethanol. What was the purpose of the 70% ethanol?
a. to remove lipids which will interfere with subsequently reactions
b. To remove salts and to add a bit of water to the pellet, making it easier to resuspend
c. to remove Mg2+ ions and therefore inhibit any DNAse activity
d. To remove medium and bacterial debris that inhibit the activity of restriction enzymes
e. to disrupt the plasma membrane and denature proteins
B
56
Gram positive cells
Have a thin layer of peptidoglycan and second phospholipid bilayer
57
Which of the following is true about plate count method?
I. It is an indirect way to determine cell count
II.it can be used to determine the # of competent cells in solution
III.it only considers plates between 30 and 300 to be accurate
IV. It takes into account the volume of the cells used
V.it I'd traditionally preformed using a petroff-hausser counting chamber
II,III, IV
58
Aseptic technique
(Sterile technique) sterilizing surfaces, working quickly to avoid contaimination
59
If you transformed antibiotic sensitive competent D. aureus with a las mid containing a tetracycline resistance gene and a chloramphenicol resistance gene, on which plates would you expect growth?
A.LB B. LB+tetracycline C.LB+chloramphenicol+tetracycline D.LB and chloramphenicol E all the above F none of the above
E
60
Gram negative cells
Have a cell wall with a thick layer of peptidoglycan that surrounds the plasma membrane
61
Stock solution
A concentrated solution of a solute with a known concentration
62
Standard curve
A graph that shows the relationship between absorb acne and concentration
63
Formula for dilution
Dilution= volume of original solution/volume of original solution + volume of solvent
64
Tonoplast
Large central vacuole surrounded by membrane
65
Betacyanin
Beets characteristic red pigment
66
What is a hypothesis based on?
Prior knowledge and review of published literature
67
Independent variable
Variable of interest being manipulated
68
Resolution
The capacity to distinguish two adjacent points as being distinct
69
Ocular lens
Magnifies the image
70
Objective lens
Varying lens mounted to the nose piece (gather light, project image)
71
Dependent variable
The measured results of the manipulation
72
What are the steps of the scientific method?
1.formulate a hypothesis 2. Test you hypothesis 3. Draw a conclusion from data 4 from hypothesis to theory
73
Peptidoglycan
A sugar and peptide polymer that gives prokaryotic cell wall
74
Differential stain
Divides bacteria into two groups
75
Crystal violet
A basic purple dye
76
Iodine solution
Is the mordant
77
Mordant
Increases affinity to the dye of the structure it is staining
78
Differential step
Step that distinguishes the gram positive from gram negative
79
Safranin
A pink dye
80
Colony morphology
The characteristic size, shape, edge ,texture ,degree of opacity and colour of a colony
81
Cell morphology
Characteristic shape of cells
82
Cocci
Spherical shape
83
Bacilli
Shaped like rods or cylinders
84
Spirilla
Resembles a corkscrew (spiral)
85
Motile
Able to move
86
1mm= ? Micro meters
1000
87
1 cm = ? mm
10
88
1 m = ? cm = ? nm
100 cm 1000nm
89
Obligate anaerobes
Requires no O2 in order to grow
90
Obligate Aeorbe
Requires O2 in order to grow
91
Facultative anaerobes
Non-motile growth with or without O2
92
Facultative Aerobes
Motile growth with or without O2
93
How do you calculate resolution
R=0.61landa/ N.A.
94
In the formula for calculating resolution what is R, lands and N.A.
R: resolution value, distance between distinguishable points, landa: wavelength of light, N.A.: numerical aperture of the lens
95
What was the counter stain used in lab 3?
Safranin
96
What step is the counter stain in lab 3?
When the gram negative cells are decolourized by ethanol
97
What does the cell use microtubules for?
Motile structures flagella and cilia can also be used to propel food towards it
98
What does the cell use microfilaments for?
Amoeboid movement (allows pseudopods to move by assembling and disassembling networks of microfilaments)
99
Plasmagel and plasmol
Plasmagel viscous regions of the cytoplasm. Plasmol liquid regions of the cytoplasm.
100
What does the cell use intermediate filaments for?
Structural roles an example of this is that intermediate filaments make up the meshwork that gives the nucleus it's shape. During mitosis the nuclear lamina is dissembled and the nuclear envelope fragments
101
What are vital stains? Why do they seldom work?
Vital stains are stains applied to a live specimen but they almost always eventually kill the cells and they do not stain very intensely
102
What is a bright field microscope?
In a bright field microscope a condenser lens focuses light on the specimen making the microscope field appear brighter
103
Why can a bright field (light) microscope not be used for transparent cells?
Because in a transparent medium such as water the cell appears invisible because the intensity of the light passing through the cell and medium are the same
104
Phase contrast microscopes
Phase contrast microscopes causes areas of higher refractive index to appear dark and areas of lower refractive index to appear lighter
105
Flouroesence microscopes
Allows you to observe specimens that are able to fluoresce when exposed to light
106
Autofluoresce
Able to fluorescence (glow when exposed to light) without being stained
107
Paramecium Caudatum
A single celled protist
108
Congo red
A pH indicator dye that is red in colour at neutral pH and yellow-orange at an acidic pH
109
Oral groove
Collects food until it can be sweeped into into the cell mouth
110
Cilia in a paramecium
Helps to move and sweeps food to the oral groove
111
After Pyruvate is oxidized which process does it enter?
Citric Acid cycle
112
Exogonic reactions
Products require energy to progress
113
Exergonic reactions
Reactants higher energy than products (can occur spontaneously)
114
Pelomyxa Carolinensis
An ameoba
115
Which process results in ATP, NADH and pyruvate?
Glycolysis
116
Glycolysis
(Cytoplasm) glucose is hydrolyzed in a multistep process to form pyruvate
117
How many steps is the citric acid cycle? What are the products?
Eight steps. Produces ATP, NADH, FADH2 and CO2
118
What is the formula for cellular respiration?
Glucose+ O2 -> CO2 + H2O + ATP
119
What are the products of Oxidative phosphorylation?
ATP and H2O
120
Electron transport chain
N oxidative phosphorylation NADH and FADH2 transfer their electrons to a chain of proteins called the electron transport chain, the e- are then passed down the chain this releases energy at the end of the chain the electrons are transferred to oxygen and form water
121
What are the phases of cellular respiration?
Glycolysis, Citric acid cycle, Oxidative phosphorylation
122
Where do light reactions occur?
Thylakoid membranes
123
What happens in the light reactions?
Light pigments in photosystem II causing the loss of an electron. The e is passed along an electron transport chain releasing energy which is used to pump protons to make ATP. At the end of the chain the e is transferred to NADP+ to form NADPH.
124
How is the electron "hole" filled in light reactions?
The lysing of water, releasing O2
125
Where does the Calvin cycle occur?
The stroma
126
What are the phases of Photosynthesis?
Light reactions and the Calvin cycle
127
How do you calculate z score?
Z= data point-mean/SD
128
What is the overall reaction for photosynthesis?
H2O +light +CO2-> glucose and O2
129
What does the Calvin cycle do?
It uses ATP and NADPH to fix CO2 to glucose
130
What process occurs in the Krebs cycle?
Glycolysis
131
What are the products of the Krebs cycle?
CO2 and ethanol
132
What are the elements of a physiological curve?
Lag, log, stationary, death
133
How is the rate measured of the physiological curve?
During the linear portion of the log phase
134
Bacterial genomic DNA
Is a double stranded DNA helix arranged in a circle that is anchored to the plasma membrane
135
Bacterial plasmid DNA
Floats freely in the cytoplasm of the bacterial cell, almost all are circular -> can assume a supercoiled conformation (the double helix is twisted upon itself)
136
Eukaryotic DNA
Arranged in linear strands called chromosomes located in the nucleus of the cell
137
HMW
High molecular weight DNA (eukaryotic DNA because it is large in size)
138
Who did a similar experiment to lab 9?
Avery, MacLeod and McCarty (1944)
139
Selectable marker
Allows you to select for or against a certain type
140
How do you calcule cell concentration?
Cu=Cd/D
| Culture undiluted= culture diluted/ dilution
141
How do you calculate percent transformation?
Determine the # of cells that could be transformed and that were transformed using (Cu=Cd/D) to find Cu for both and divide the number of cells that could be transformed by the cells transformed x100
142
What are the base parings?
A-T (for mRNA T turns to U)
| C-G
143
What is the mRNA base pairing for TTC AGG GTC
AAG UCC CAG
144
What are the 3 kinds of genetic mutation?
Silent (same AA is made), Missense (Diff AA is made) Nonsense (no AA is made)
