bio112 Flashcards

(52 cards)

1
Q

prokaryotes can be divided into which 2 domains

A

bacteria and archaea

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

biological applications for extremophiles

A

pcr
biofuels
biomining
carotenoid production
detergents

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

components of prokaryotic cells

A

nucleiod , ribosomes , plasma membrane , cell wall , capsule

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

magnification

A

ratio of objects image size to real size

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

resolution

A

measure of minimum distance of two distinguishable points

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

contrast

A

visible differences in brightness or colour between parts of the sample

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Deconvolution microscopy

A

Algorithms remove out of focus light and this sharpens the image and improves resolution

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Super resolution

A

gathers light from individual fluorescent molecules and records their position. Combining information from these individual molecules breaks the resolution limit

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

scanning electron microscope

A

electrons reflected on surface and collected by electron detector and converted into electron signal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

uses for cell fractionation

A

Protein Enrichment
•Enrich target proteins and improve detection of low abundance protein
Protein Characterization
•Identify the subcellular localization of a protein
Protein Translocation
Monitor translocation of cell signalling molecules from the cytoplasm to the nucleus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

lipid molecules form what in aqueous envieonments

A

micelles or bilayers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

smooth endoplasmic reticulum

A

phospholipid , fat and steriod manufacturer
carbohydrate metabolism
breaks down stored glycogen to release glucose
detoxifies lipid soluble drugs such as barbiturates

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

sarcoplsdmic reticulum

A

found in muscle cells
network of tubular sacs
transmits electrical signals
sequesters calcium ions from systole
level of intereceullar calcium regales muscle contractions. in cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

myofibrils

A

composed of repetitive arrangements of filaments called a sarcomere ( a region where myosin and acton filaments overlap )

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

H line

A

only myosin
shortens during contraction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

A line

A

region containing length of dingle myosin filament

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

RER

A

protein synthesissecreted glyocsylated lysosomal enzymes membrane bound proteins

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

protein synthesis in the RER

A

ribosome synthesiseing Poetin w specific signal peptide attaches to RER
N terminus of proteins contains a signal peptide
signal recognition particle attaches to signal peptide and stops tranlastio in cystol
SRP docks to its receptor om membrane and translation starts again
hydrophobic signal peptide passes thru membrane and loops back thru membrane and is cleaved off . erst of peptide passes thru membrane and into ER lumen .

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

glyoclisation inn the RER

A

addition of sugars
oligosaccharide added in RER . composed of N - acetylglucosamine , mannose and glucose resides containing 124 sugar residues and transfers to the proteins in RER

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

endosymbiotic theory of mitochondrial origin

A

•Own circular genome
•Double membrane
•Similar in size to prokaryotic cell
•Divide by binary fission

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Prokaryotic Cell

A

Prokaryotic cells are unicellular organisms lacking membrane-bound organelles and a true nucleus. Their DNA is located in a nucleoid region.

22
Q

Domains of Prokaryotes

A

Two main domains: Bacteria and Archaea. Bacteria: medically/economically significant. Archaea: often extremophiles, thriving in harsh environments.

23
Q

Key Structural Features of Prokaryotic Cells

A

Plasma membrane, cytoplasm, nucleoid, ribosomes. Optional structures: cell wall, flagella, pili, capsule. DNA is circular; additional genes may be on plasmids.

24
Q

Bacterial Cell Shapes

A

Cocci - spherical, Bacilli - rod-shaped, Spirochetes - spiral-shaped.

25
Prokaryotic Cell Wall Types
Gram-positive: Thick peptidoglycan wall, teichoic acids present. Stains purple, more antibiotic susceptible. Gram-negative: Thin peptidoglycan layer, outer membrane with lipopolysaccharides. Stains pink, more resistant to antibiotics.
26
Prokaryotic Modes of Nutrition
Photoautotrophs: Light + CO₂, Chemoautotrophs: Inorganic molecules + CO₂, Photoheterotrophs: Light + organic compounds, Chemoheterotrophs: Organic compounds for energy and carbon.
27
Archaea and Extremophiles
Archaea thrive in extreme conditions: high salt, temperature, or acidity. Example: Thermus aquaticus used in PCR due to heat-stable enzymes. Potential model for extraterrestrial life.
28
Viruses - Basic Structure
Not cells; not alive. Consist of nucleic acid (DNA/RNA) enclosed in a protein capsid made of capsomers. Some have a lipid envelope (e.g., influenza, SARS-CoV-2).
29
Types of Viruses
Filamentous: e.g., Tobacco mosaic virus. Spheroid: e.g., Adenovirus. Enveloped: e.g., Coronaviruses. Tailed Spheroid: e.g., Lambda phage.
30
Bacterial Use in Biotechnology
Medical: Insulin production, drug screening. Agriculture: Genetically modified crops (e.g., purple tomatoes). Environment: Bioremediation. Industry: Lactic acid bacteria in food and wine production.
31
Light microscope sample preparation
Whole mounts: small relatively transparent specimens mounted directly onto slides Tissue sections: most tissues need to be sectioned before they can be examined Fixation: This involves using chemical fixatives to prevent cell autolysis and to preserve the structure of the tissue. Dehydration and clearing: This removes the water from the tissue in preparation for wax impregnation Embedding: The specimen is infiltrated with molten wax, after which it is transferred to a mould Sectioning: Thin sections approximately 5 microns thick are cut on a microtome, and collected onto a glass slides Staining: The wax is removed and the tissue stained with a coloured dye such as Eosin (cytoplasm) or haematoxylin (nuclei)
32
Advanced light microscopy
•Permits observation of transparent living cells•Light phase shifts induced by specimen are used to generate contrast •Phase contrast (refracted and unrefracted light)•Differential interference contrast (two light beams)
33
Deconvolution microscopy
•Algorithms remove out of focus light and this sharpens the image and improves resolution.
34
Super resolution
gathers light from individual fluorescent molecules and records their position. Combining information from these individual molecules breaks the resolution limit.
35
Membrane Proteins
Transmembrane proteins are amphipathic they have hydrophobic regions and hydrophilic regions Peripheral membrane proteins are only associated with the membrane by non-covalent linkages and are easily dislodged
36
Freeze-fracture electron microscopy
1)Fixation and preservation with glycerol2)Rapid Freezing – liquid nitrogen3)Fracturing – under pressure using a liquid nitrogen cooled microtome4)Replication5)Replica cleaning
37
Membrane Proteins have Many Functions
Transport protein. E.g. the sodium/potassium ATPase pump which pumps 3 sodium ions out of the cell and 2 potassium ions into the cell Receptor sites: the exterior region of a transmembrane protein may act as a receptor for a chemical messenger such as a hormone or growth factor. Structural roles: Membrane proteins called Integrins allow the cell to attach to the extracellular matrix Cell junctions: Tight junctions are present between some cell types. They act to separate the apical and basal membranes which have different functions.
38
The Endomembrane System
A network of membrane-bound structures unique to eukaryotic cells, including the nuclear envelope, smooth and rough ER, Golgi apparatus, lysosomes, and vesicles.
39
Smooth Endoplasmic Reticulum (SER)
Interconnected tubules lacking ribosomes. Functions: Lipid and steroid synthesis, carbohydrate metabolism, detoxification, and calcium storage (in hepatocytes and muscle cells).
40
Sarcoplasmic Reticulum (SR)
A specialized SER found in muscle cells. Stores and releases calcium ions, which trigger muscle contraction by binding to troponin, causing tropomyosin to shift and expose actin-binding sites.
41
Rough Endoplasmic Reticulum (RER)
Studded with ribosomes. Functions: Synthesis of secreted proteins, membrane-bound proteins, lysosomal enzymes, and glycoproteins.
42
Signal Mechanism for ER Targeting
Signal peptide at N-terminus of proteins directs them to RER. Recognized by signal recognition particle (SRP), which pauses translation. SRP docks to ER, translation resumes, peptide enters lumen, and signal is cleaved by signal peptidase.
43
Ribosomes and Polyribosomes
Ribosomes synthesize proteins by translating mRNA. Polyribosomes: Multiple ribosomes attached to a single mRNA strand, increasing translation efficiency.
44
Glycosylation in the RER
Oligosaccharides (14 residues long) are added to proteins. Composed of N-acetylglucosamine, mannose, and glucose. Essential for proper protein folding and function.
45
Golgi Apparatus
Receives proteins from RER via vesicles. Modifies (mainly glycosylates), sorts, and ships proteins to final destinations: secretion, plasma membrane, or organelles like lysosomes.
46
Mannose-6-Phosphate (M6P) Pathway
In cis-Golgi, lysosomal enzymes are tagged with M6P. M6P receptors in the trans-Golgi direct them to lysosomes.
47
Glycosylation in the Golgi
Adds complex sugar chains to proteins. Essential for forming mucins, large glycoproteins in mucus. Defective glycosylation linked to cystic fibrosis.
48
Lysosomes
Membrane-bound organelles containing ~60 hydrolytic enzymes. Functions: Autophagy: recycling organelles, Phagocytosis: engulfing pathogens, Apoptosis: programmed cell death.
49
Lysosomal Storage Diseases
Caused by defective enzymes leading to accumulation of undegraded materials. Example: Tay-Sachs disease - deficiency in hexosaminidase A, causes ganglioside build-up in neurons.
50
Exocytosis
Vesicles fuse with the plasma membrane to export materials like hormones, mucus, and proteins. Important in secretion and cell communication.
51
Types of Endocytosis
Phagocytosis: Engulfing large particles or pathogens. Pinocytosis: Non-specific uptake of extracellular fluid. Receptor-mediated endocytosis: Specific uptake using clathrin-coated vesicles (e.g., transferrin or SARS-CoV-2).
52
Clathrin and Endocytosis
In receptor-mediated endocytosis, clathrin polymerizes around forming vesicles, creating a cage-like structure that enables selective internalization of macromolecules.