Test 3 - Lecture 24 Flashcards

(63 cards)

1
Q

Lysosomes:

A

membrane - enclosed organelles that contain enzymes to break down all types of biological polymers.

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

Lysosomes are the ______ system of the cell

A

diestive

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

Lysosomes can vary in _____ and _____ depending on the materials that have been taken up for ______.

A

size
shape
digestion

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

Lysosomes contain about ___different degradative enzymes

A

60

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

Mutations n genes that encode these enzymes result in _____ _____ ______ - undergraded material accumulated in the lysosomes of affected individuals

A

lysosomal
storage
diseases

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

______ ______ : The enzyme deficiency in ______ ______ prevents the hydrolysis of __________ to glucose and ceramide.

A

Gaucher Disease
Gaucher Disease
glucosylceramide

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

Gaucher Disease:
In the most common form of the disease, _____ are the only cells affected. Their function is to eliminate aged and damaged cells by _________.

A

macrophages

phagocytosis

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

Most lysosomal enzymes are ____ _______ - active at pH 5 in lysosomes, but not in the _______ (pH 7.2)

A

acid hydrolases

cytoplasm

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

This prevents uncontrolled digestion of cell contents if the _______ ________ breaks down.

A

lysosome membrane

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

To maintain the acidic pH, a ______ ______ in the lysosomal membrane actively transports protons into the lysosome.

A

proton pump

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

Lysosomes digest material taken up from outside the cell by _______

A

endocytosis

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

Lysosomes are formed when transport vesicles from the ____ - _____ network fuse with a late endosome.

A

trans - Golgi

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

Three types of endosomes: ______, _______, and ______ endosomes

A

early
recycling
late

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

Early endosomes receive _______ vesicles directly from the plasma memebrane

A

endocytic

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

They separate molecules targeted for ______ from those destines for _______ in lysosomes.

A

reclycling

degradation

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

The molecules to be recycled are passed to ______ endosomes and back to the plasma membrane

A

recycling

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

Molecules destined for degradation are transported to mulitvesicular bodies ad then to ______ endosomes

A

late

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

Transport vesicles carrying ____ ______ from the trans - Golgi network then fuse with late endosomes, which mature into _______

A

acid hydrolases

lysosomes

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

____ _______ are targeted to late endosomes by mannose - 6 - phosphate residues, whic are recognozed by mannose - 6 - phosphate receptors in the trans Golgi network ans packaged into _____ - _____ vesicles

A

Acid hydrolases

clathrin - coated

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

Phagocytosis:

A

specialized cells such as macrophages take up and degrade large particles, including bacteria, cell debris , and aged cells.

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

The particles are taken up in phagocytic vacuoles (__________), which fuse with lysosomes to become __________

A

phagosomes

phagolysosomes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Autophagy:

A

turnover of the cell’s own componenets

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Autophagy -

Important in embryonic development and programmed cell _____

A

death

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

A small area of cytoplasm or organelle is enclosed in a vesicle (_________) which fuses with a lysosome, and its contents are digested

A

autophagosome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Autophagy leads to continuous ________ of cellular constituents
turnover
26
Autophagy - It can also be regulated during development in response to ______ It nutrient _______ occurs, autophagy degrades nonessential macromolecules so their components can be ______ Autophagy also plays an important role in programmed cell death
stress starvation reutilized
27
1. The generation of ________ energy is a major activity of all cells
metabolic
28
2. _______ generate energy from breakdown of lipids and carbohydrates
Mitochondria
29
3. _______ use sunlight energy to generate ATP and reducing power to synthesize carbohydrates form CO2 and H2O
Choloropasts
30
4. _______ contain enzymes involved in a variety of metabollic
Peroxisomes
31
Mitochondria, Chloroplasts and Peroxisomes - | Proteins are synthesized on _____ ribosomes and imported to these organelles as completed ________
free | polypeptides
32
1. Mitochondria and chloroplasts also have their own _______, including some genes that are transcribed and translated within the organelle
genomes
33
2. Mitochondria are surrounded by a _______ - ________ system
double - membrane
34
Mitochondria - | Inner and outer membranes are separated by an _________ space
intermembrane
35
Mitochondria - | The inner membrane has numerous folds (______), which extend into the interior (______)
cristae | matrix
36
Mitochondria - | 1. The matrix : contains _______ system and ______ for oxidative metabolism
genetic | enzymes
37
Mitochondria - 2. _______ (form glycolysis) is transported to mitochondria, (1) complete oxidation to CO2; (2) yields the bulk of energy (ATP)
Pyruvate
38
Mitochondria - 3. The enzymes of the citric acid cycle are in the mitochondrial _____ Glycolysis occurs in the cytosol: pyruvate is transported into mitochondria, where its complete _______ to CO2 yields the bulk of usable energy (ATP) obtained from _______ ________
matrix oxidation glucose metabolism
39
Glycolysis takes place in the ______
cytosol
40
In eukaryotic cells, pyruvate is then transported into ________, where it is completely oxidized
mitochondria
41
Pyruvate undergoes oxidative decarboxylation in the presense of ______ _ (____ - __), forming ______ ____; generation of _____
coenzyme A (CoA - SH) acetyl CoA 2NADH
42
Acetyl CoA enter the ____ _____ cycle (_____ cycle)
citric acid | Krebs
43
The 2 - carbon acetyl group combines with oxaloacetate ( ___ carbons) to yield ____ ( 6 carbons)
4 | citrate
44
In the remaining reactions, 2 carbons of citrate are completely ______ to CO2 and oxaloacetate is _______
oxidized | regenerated
45
2 carbons of citrate:
``` 2 CO2 1 oxaloacetate 1 GTP 3 NADH and 1 FADH2 ```
46
Oxidation of glucose:
6 molecules of CO2, 4 ATP, 10 NADH, 2 FADH2
47
Total ATP yields from oxidation of glucose: 38 ( in some cells 36) Glycolysis: _ ____ + 2 NADH Citric acid cycle: 2 ATP + _ _____ + 2 FADH2 Oxdative phophorylation: each NADH yields _ ATP, each _____ yields 2 ATP Total: 2 ATP + 2 ATP + 10*3 (NADH) + 2*2 (FADH2) = 38
2 ATP 8 NADH 3 FADH2
48
1. _______ _ receives _______ from the citric acid cycle intermediate succinate
Complex II | electrons
49
2. These electrons are transferred to FADH2, rather than NADH, and then to _______ _
coenzyme Q
50
True/False: | The first step of transfer does not yield free energy
True
51
Mitochondria - | 1. The enzymes of the ____ _____ _____ are in the mitochondrial matrix
citric acid cycle
52
Mitochondria - 2. Most of the energy is produced by _________ _________, takes place in the ______ mitochondrial membrane
oxidative phosphorylation | inner
53
Mitochondria - 3. _____ - energy electrons form NADH and FADH2 are transferred through a series of carries in the _______ to molecular oxygen
High | membrane
54
Mitochondria - | 4. The energy derived from this is converted to potential energy stored in a ______ ______, which drives ATP synthesis
proton gradient
55
Mitochondria - 1. The inner membrane The principal site of ____ _______ Surface area is increased by _______ into cristae Contains a high percentage of _______ involved in oxidative metabolism and transport ________ to most ions and small molecules - this helps maintain the proton gradient
ATP generation folding proteins impermrable
56
Mitochondria - 2. The outer mitochondrial membrane ______ permeable to ______ molecules Contains _______, which form channels that allow the free diffusion of small molecules Composition of the intermembrane space is similar to the ______
Highly small porins cytosol
57
Mitochondria - | 3. Position; often near locations of ____ - _____ use, such as synapses in nerve cells
high - energy
58
In most mitochondria form an ___________ network, and are constantly ______ and _______ to remodel this network, and modify mitochondrial ________ and function
interconnected fusing dividing morphology
59
Mitochondrial genomes usually ______ DNA molecules, present in ________ copies encode only a few proteins that are essential for ________ __________ encode all the _____ and most of the _____ needed for translating the protein - coding sequences
``` circular multiple oxidative phosphorylation rRNAs tRNAs ```
60
The human mitochondrial genome encodes __ proteins involved in _______ _______ and oxidative phosphorylation The sequences are designed as _________ ________ I, II, III, IV or V Plus ___ and 12S rRNAs; and 22 _____, which are required for translation of the proteins
``` 13 electron transport respiratory complexes 16S tRNAs ```
61
True/False: | The mitochondrial genetic code is the same form the universal code
False - | It is different
62
U in the tRNA anticodon can pair with any of the four bases in the ____ codon position of mRAN; thus four codons are recognized by a _____ ______
third | single tRNA
63
Some codons specify different amino acids in ________ than in the universal code
mitochondrua