BIOE Exam 1 Chapter 1 Flashcards

1
Q

What is the central dogma of biology?

A

DNA => transcription => RNA => translation => Protein

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2
Q

When was the first cell thought to have arisen?

A

at least 3.8 billion years ago by the
enclosure of self-replicating RNA in a phospholipid membrane

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3
Q

What is metabolism?

A

the set of life-sustaining chemical reactions in organisms including energy conversion, biosynthesis, and waste elimination.

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4
Q

All cells use what as their primary energy source?

A

Adenosine 5’-triphosphate (ATP)

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5
Q

What are the three main metabolic pathways?

A

Glycolysis, Photosynthesis, and Oxidative Metabolism

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6
Q

What is glycolysis?

A

A metabolic pathway that breaks down glucose into pyruvate, producing ATP and NADH. Occurs in the cytoplasm

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7
Q

What is the purpose of photosynthesis?

A

To convert light energy into chemical energy (glucose) using CO₂ and H₂O. Occurs in the chloroplasts of plants

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8
Q

What is oxidative metabolism

A

The process of producing ATP through cellular respiration, using oxygen to break down glucose in the mitochondria

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9
Q

What are the key differences between prokaryotic and eukaryotic cells?

A

Prokaryotic cells: No nucleus, small, simple structure, single circular chromosome.

Eukaryotic cells: Have a nucleus, organelles, multiple linear chromosomes.

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10
Q

What structures do prokaryotic cells have?

A

Cell wall (contains peptidoglycan in bacteria, absent in archaea)

Plasma membrane (separates the cell from the environment)

Nucleoid (region where DNA is located)

Ribosomes (protein synthesis)

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11
Q

Bacteria and Archaea are what type of cells?

A

Prokaryotic ( They lack a nucleus and membrane-bound organelles

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12
Q

How do Bacteria and Archaea differ?

A

Bacteria: Have peptidoglycan in their cell walls, use formyl-methionine as the initiator tRNA.

Archaea: Lack peptidoglycan, use methionine as the initiator tRNA, have unique membrane lipids

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13
Q

What are the key organelles found in both plant and animal eukaryotic cells?

A

Both have a nucleus, mitochondria, endoplasmic reticulum, Golgi apparatus, cytoskeleton, and plasma membrane.

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14
Q

What unique structures are found in plant cells that are absent in animal cells?

A

Plant cells have a cell wall (made of cellulose), chloroplasts for photosynthesis, and a large central vacuole for storage.

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15
Q

What are some features unique to animal cells compared to plant cells?

A

Animal cells typically have lysosomes and centrosomes and lack a rigid cell wall, which allows for more flexible cell shapes.

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16
Q

What are the key functions of the nucleus?

A

Stores DNA, directs synthesis of ribosomes and proteins.

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17
Q

What is the role of mitochondria?

A

ATP production via cellular respiration.

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18
Q

What is the function of the endoplasmic reticulum (ER)?

A

Rough ER: Modifies proteins.

Smooth ER: Synthesizes lipids, detoxifies chemicals.

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19
Q

What is the function of the Golgi apparatus?

A

Modifies, sorts, and packages proteins and lipids for transport.

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20
Q

What are the two prokaryotic domains of life?

A

Archaea and
Bacteria

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21
Q

The evolution of
eukaryotic cells (Eukarya)
from the Archaea involved
the formation of
mitochondria by what?

A

endosymbiosis

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22
Q

What is Endosymbiosis

A

one cell living
inside another

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23
Q

What are the simplest eukaryotes?

A

Yeasts
(Saccharomyces cerevisiae)

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24
Q

What is a germ layer?

A

a primary layer of cells that forms
during embryonic development

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25
Q

What are the three primary germ layers formed during embryonic development and what do they become?

A

Endoderm (internal layer): Forms internal organs such as the digestive tract, lungs, and liver.

Mesoderm(middle layer): Gives rise to muscles, bones, the circulatory system, and connective tissues.

Ectoderm(external layer) : Develops into the skin, nervous system, and parts of the sensory organs.

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26
Q

What is cell formation during embryonic development?

A

Cell formation, or embryogenesis, is the process where a fertilized egg (zygote) divides and differentiates into various cell types, ultimately forming tissues and organs.

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27
Q

What does cell culture of animal cells allow us to do?

A

Study metabolic functions

28
Q

What was the first Human Cell Line?

A

HeLa Cells, cultured from a biopsy of a cervicale cancer taken from 30 yr-old Henrietta Lacks (February 1951)

29
Q

What is the 293 T Human Cell Line

A

an epithelial-like cell
that was isolated from the
kidney of a patient

30
Q

What is the U87 Glioblastoma Human Cell Line ?

A

U-87 MG is a cell line with
epithelial morphology that was
isolated from malignant gliomas
from a male patient, likely with
Glioblastoma.

31
Q

What are primary cell cultures?

A

Primary cell cultures are cells directly isolated from living tissue that are cultured in the lab for research purposes. These cells have a limited lifespan and more closely resemble cells in vivo

32
Q

What is the difference between primary cells and cell lines?

A

Primary Cells: Directly isolated from living tissue, have a limited lifespan, and maintain closer resemblance to in vivo conditions.

Cell Lines: Cultured cells that can proliferate indefinitely, often from transformed or immortalized cells (e.g., HeLa cells). They may not accurately reflect the behavior of primary cells.

33
Q

What are the advantages of using primary cells in research?

A

-Closer to in vivo behavior
-Better mimic human disease models
-Retain tissue-specific functions and structures

34
Q

What are the disadvantages of using primary cells in research?

A

Limited lifespan and proliferation potential
Expensive and difficult to obtain
Variability between samples

35
Q

What are the advantages of using cell lines in research?

A

Can be cultured indefinitely (immortalized)
Easier to maintain and handle
Provide consistency between experiments and batches

36
Q

What are the disadvantages of using cell lines in research?

A

-Lack of tissue-specific characteristics
-May not accurately reflect in vivo cell behavior
-Can mutate over time and lose original traits

37
Q

Plant cell culture has several advantages over animal cell culture. What is one main advantage?

A

In many instances, an entire adult plant capable of reproduction can be regenerated from cells in plant tissue culture

38
Q

What is a limit of light microscopy?

A

It isn’t powerful enough to reveal fine details of cell structure, for which resolution

39
Q

How does light microscopy work?

A

Light is focused on the
specimen by the
condenser lens and
then collected by the
objective lens of the
microscope

40
Q

What is the refractive index of the medium used in light microscopy?

A

Air or oil

41
Q

What are the different types of Light Microscopy?

A

Brightfield : Produces an image on a bright background ( used as the standard microscopy)

Darkfield: Useful for viewing live specimens. Produces a bright image on a darker background

Phase Contrast : Creates high-contrast, high-res images useful for viewing live specimen and structures such as endospores and organelles.

Differential interference contrast (DIC) : Produces high-contrast images of living organisms with 3-D appearance, useful in distinguishing structures in live-unstained specimens. Images reveal detailed structures within cells

Fluorescence : Uses fluorescent stains to produce images. Used to identify pathogens, find particular species, distinguish living from dead cells or find locations of particular molecules within cells. Used for immunofluorescence

Confocal: Uses a laser to scan multiple z-planes. Useful for examining thick specimens such as biofilms.

Two-photon: Uses scanning technique, fluorochromes and wavelength light (infrared) to penetrate into thick specimens

42
Q

What causes an electron to transition to a higher excited energy state?

A

Excitation of a fluorophore entails absorption of light energy of a particular wavelength

43
Q

What is the result after an excited electron returns to its ground state?

A

The emission of light at a longer wavelength.

44
Q

What is DAPI ?

A

A DNA specific probe which forms a fluorescent complex by attaching in the minor grove of A-T sequences of DNA

45
Q

What is Confocal microscopy used for?

A

Sharpening the focus and seeing cells deeper within living tissue

46
Q

In multiphoton excitation microscopy, what is the specimen illuminated by?

A

A wavelength twice the excitation wavelength of the fluorophore

47
Q

What does excitation of the fluorophore require?

A

Simultaneous absorption of two or more photons

48
Q

What is the range of the super-resolution microscopy?

49
Q

What does Super-resolution microscopy use to improve resolution?

A

Fluorescent probes.

50
Q

To who was the 2014 Nobel Prize in Chemistry awarded to?

A

Eric Betzig, Stefan Hell and William Moerner, for the development of super-resolution microscopy.

51
Q

What is STORM and when was it developed?

A

Developed in 2006, stands for stochastic optical reconstruction microscopy. Has a resolution of 20 nm. Produces high res images by compiling individual images from thousands to millions of individual fluorescent molecules.

52
Q

In Conventional fluorescence microscopy…

A

all of the fluorescent molecules in a
sample fluoresce at the same time resulting in a blurred image

53
Q

in STORM…

A

only a small random fraction of the probes are fluorescent at any one time

54
Q

What is the practical limit of resolution of the electron microscope?

55
Q

What is the main difference between SEM and TEM?

A
  • SEM creates an image by detecting reflected or knocked-off electrons
  • TEM uses transmitted electrons (electrons passing through the sample) to create an image. TEM also requires the samples to be thin while SEM doesn’t
56
Q

What is subcellular fractionation?

A

process where cells are lysed and their components are separated using differential centrifugation.

57
Q

What is the purpose of differential centrifugation?

A

To separate subcellular components based on their size and density through successive centrifugation steps.

58
Q

What happens after each centrifugation step?

A

The organelles that sediment to the bottom form the pellet, while the remaining solution (supernatant) is recentrifuged at a higher speed.

59
Q

What is the pellet in differential centrifugation?

A

It is the solid material at the bottom of the tube that contains the organelles separated by centrifugation.

60
Q

How are organelles separated in differential centrifugation?

A

By increasing centrifugation speeds, allowing larger organelles to sediment first and smaller ones later.

61
Q

How can a greater degree of purification be achieved?

A

By density-gradient centrifugation in which organelles are separated by sedimentation through a gradient of dense substance (sucrose)

62
Q

How are subcellular components separated in density gradients?

A

on the basis of their buoyant density, independent of their size and shape

63
Q

In equilibrium centrifugation, how is the sample centrifuged?

A

It is centrifuged in a gradient containing a high concentration of sucrose or cesium chloride

64
Q

What occurs in velocity centrifugation?

A

Particles are separated based on their sedimentation rate or “velocity” in a centrifuge. Larger or denser particles will pellet first

65
Q

In equilibrium centrifugation, where does sedimentation stop and where can the purified organelles be collected at?

A

At the equilibrium position :)