Module 4.4 Flashcards

1
Q

DNA In prokaryotes v Eukaryotes

A

Pro
- Naked
- Circular
- No introns

Euk
- bound to proteins
- linear
- introns

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2
Q

Organelles in Pro v Euk

A

Pro
- no nucleus
- no membrane bound organelles
- 70s ribosome

Euk
- nucleus
- membrane bound organelles
- 70 and 80s ribosomes

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3
Q

reproduction in pro v euk

A

pro
- binary fission
- single chromosome

euk
- mitosis and meiosis
- paired chromosomes

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4
Q

5 functions of mitochondria

A

generate ATP via ox phos
biffer Ca2+
Fe-S cluster biogenesis
apoptosis
immune signalling

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5
Q

protein transport in bacteria

A

BAM , YiC

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6
Q

protein transport in mitochondria

A

SAM , OCA1

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7
Q

How many genes in mitochondrial DNA and what do they form

A

37
2 rRNA
22 tRNA
13 protein

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8
Q

how do nuclear encoded proteins get to mitochondria

A
  1. nuclear encoded proteins are synthesises on cytosolic ribosomes
  2. precursor proteins have targeting sequences that deliver them to the mitochondria
  3. at the mitochondria, translocates mediate the protein entry to organelle
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9
Q

4 mitochondria translocates

A

TOM
TIM
SAM
OXA1

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10
Q

what is the proteome

A

entire set of proteins that can be expressed by a. genome, cell or tissue at a given point

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11
Q

what is the mitochondrial proteome

A

entire set of proteins that can be expressed by the genome targeted to the mitochondria

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12
Q

glycolysis

A

glucose + 2ATP -> fructose-1,6-biphosphate + 2ADP -> 2 GA3P + 4 ADP + 2 NAD+ -> 2 pyruvate + 2NADH + 4 ATP

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13
Q

Krebs cycle products

A

2 ATP
6NADH
2 FADH2
4CO2

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14
Q

Krebs cycle intermediate products formed

A

2 pyruvate
acetyle CoA
citrate
4C + 2CO2
Oxeloacetate

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15
Q

oxidative phosphorylation products

A

32-34 ATP
10 NAD+
2FAD
6H2O

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16
Q

2 processes in ox phos

A
  1. electron transport chain
  2. chemiosmosis
17
Q

what is mito

A

= when mitochondria fail to produce sufficient energy

18
Q

clinical presentation of mito

A

nueropathes
ischaemia
monoclinic epilepsy
myopathy
cardiomyopathy

19
Q

2 types of mito

A

primary
secondary

20
Q

primary mito

A

= mutation in gene directly linked to ETC

21
Q

secondary mito

A

= mutation in genes with an indirect function on ETC

22
Q

how do blood tests detect mito

A

detect levels of lactate and pyruvate

23
Q

how do urine tests detect mito

A

detect CSP, specific amino and organic acids

24
Q

how are genetic tests used for mito

A

= studies mitochondria and nuclear DNA

25
examples of mito genetic tests
genomics transcripomics proteomics metabolomics
26
what is homoplasmy
= uniformly absence of mitochondria
27
what is heteroplasmy
= mixture of normal and abnormal mitochondria
28
what is MELAS
mitacondrial encephalomyopathy lactic acidosis and stroke like episodes
29
what causes MELAS
mutations in MT-TL1 gene
30
'mito' cocktail
ubiquinone L carnitine thiamine riboflamine folic acid vitamins and minerals
31
what does ubiquinone do
electron carrier and antioxidant
32
what does L carnitine do
transport large folic acid
33
what does thiamine do
PDH complex cofactor
34
what does riboflamine do
cofactors for OXPHOS complex 1 and 2
35
what does folic acid do
treats folic deficiency
36
how does MTR help with MD
1. mother with disease donates egg 2. father donates sperm to 1 and 3 3. donor with healthy mita donates egg 4, nuclei from mother put in donor egg