IMMS Flashcards

1
Q

Stages Of glycolysis

A

1)Glucose is converted into Glucose-6-Phosphate using enzyme HEXOKINASE and 1 mol of ATP
2)Glucose-6-Phosphate is converted to isomer Fructose-6-phosphate using enzyme PHOSPHOGLUCOISOMERASE
3)Fructose-6-Phosphate becomes phosphorylated using enzyme PHOSPHOFRUCTOKINASE(PFK-1) and 1 mol ATP making fructose-1,6-biphosphate
4)Fructose-1,6-biphosphate using enzyme ADOLASE forms 2x glyceraldehyde-3-phosphate
5)G3P converted into 2x1,3 Biphosphoglycerate using enzyme GLYCERALDEHYDE 3-PHOSPHATE DEHYROGENASE
5)This takes the Hydrogen from G3P and gives to NAD+ to form NADHx2
6)PHOSPHOGLYCERATE KINASE removes phosphate from 1,3BPG and gives to ADP to form 2xATP and 2x3phosphoglycerate
7)MUTASE moves phosphate group down to form 2x2phosphoglycerate
8)ENOLASE removes H2O and makes 2xphosphoenolpyruvate
9)PYRUVATE KINASE removes phosphate to form ATP from ADP and makes 2xpyruvate

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2
Q

Products of Glycolysis

A

-2xATP
-2xNADH
-2xPyruvate

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3
Q

Where does Glycolysis occur?

A

Occurs in the cytoplasm under both Aerobic and Anaerobic Conditions

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4
Q

Regulation Of Glycolysis

A

-PFK-1 is the rate limiting step–>rate at which PFK-1 converts to fructose-1,6-biphosphate determines speed at which glycolysis occurs.
-PFK-2 can also Phopshorylate fructose-6-phosphate but adds phosphate on second carbon making fructose-2,6-Biphosphate–>This increases amount of PFK-1 enzymes

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5
Q

Regulation of glycolysis 2

A

PFK is regulated by ATP, an ADP derivative called adenosine monophosphate (AMP), citrate and Fructose 2, 6 bisphosphates

ATP: is an inhibitor of PFK1
AMP: is an activator of PFK-1. When ATP is used, ADP accumulates and is converted to AMP by Adenylate kinase reaction to generate ATP. 2ADP = ATP + AMP

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6
Q

Regulation of glycolysis 3

A

-Increase in level of cells energy=increase ATP and Citrate=PFK-1 inhibited
-PFK-2 activity varies depending on level of glucose in the blood –>-glucose level increase=insulin increase=increase in PFK-2=Increase in fructose-2,6-Biphosphate=Increase in PFK-1
-Glucose levels decrease=Increase in glucagon=Inhibits PFK-2=Less FRUCTOSE-2,6-Biphosphate=Inhibits PFK-1=slows glycolysis down

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7
Q

Glycolysis

A

Anaerobic conditions-
-Lactate formation is catalysed by lactate dehydrogenase
-Regeneration of NAD

Aerobic conditions-
-Enters mitochondria and converted to acetyl-CoA and carbon dioxide by pyruvate dehydrogenase

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8
Q

Stages of krebs cycle

A

1)Pyruvate becomes oxidized to form acetyl-CoA using PYRUVATE DEHYDROGENASE COMPLEX forms NADH and CO2
2)Acetyl-CoA combines with oxaloacetate via CITRATE SYNTHASE to make Citrate+CoA
3)citrate–>isocitrate via ACONITASE
4)isocitrate is oxidized to form Alpha-ketoglutarate via ISOCITRATE DEHYDROGENASE and NADH +CO2 is produced
5)Alpha-ketoglutarate–>succinyl CoA via ALPHAKETOGLUTARATE DEHYDROGENASE and NADH +CO2 produced
6)succinyl CoA –>succinate via SUCCINATE CoA DEHYDROGENASE and molecule of GTP is formed
7)Succinate–>Fumrate via SUCCINATE DEHYDROGENASE and molecule of QH2 is formed which is used for production of FADH2
8)Fumrate –>Malate via FUMRASE
9)Malate –>Oxaloacetate via MALAGE DEHYDROGENASE and one molecule of NADH is formed.

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9
Q

products of krebs cycle

A

-cycle occurs 2x so products double as there is 2xpyruvate
-3xNADH
-1xFADH2
-1xGTP
-2xCO2

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10
Q

Where does the krebs cycle take place?

A

Occurs in the mitochondrial matrix

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11
Q

Nucleus

A

storage and transmission of genetic information

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12
Q

Mitochondria

A

Site of oxidative phosphorylation

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13
Q

Golgi Apparatus

A

Processes and modifies macromolecules

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14
Q

Cis-golgi

A

nuclear facing -recieves from rough ER protein phosphorylation occurs here

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15
Q

Medial Golgi

A

Forms oligosaccharides by ading sugars to lipids and protein

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16
Q

Trans Golgi

A

Proteolysis of peptides into active forms and sorting molecules into vesicles

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17
Q

Rough ER

A

Protein synthesis

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18
Q

Smooth ER

A

Lipid synthesis

19
Q

Ribosomes

A

protein synthesis attached to rough ER

20
Q

Cytoplasm

A

site og glycolysis

21
Q

Vesicles

A

Small spherical membrane-bound organelles that transports and store materials

22
Q

Nucleolus

A

Site of DNA transcription

23
Q

Lysosomes

A

Contain digestive enzymes

24
Q

peroxisomes

A

Small membrane-bound organelles which oxidise long chain fatty acids

25
Q

Tight Junctions

A

Seals neighbouring cells together to prevent leakage

26
Q

Gap junctions

A

Allows movement of small water soluble ions and molceules

27
Q

Desmosomes

A

joins intermediate filaments in one cell to a neighbour

28
Q

Adherens

A

Joins actin bundle in one cells to another to similar bundle in another cell

29
Q

Autocrine

A

messenger molecules bind with receptors in the cell where they are produced

30
Q

Paracrine

A

Messengers in ECF

31
Q

Endocrine

A

Secretions into blood

32
Q

Body fluid compartments of 70kg man

A

Total volume =42L
Extracellular fluid=14L
–>Extravascular=11L
—>intravascular=3L
—>interstitial =10.5L
—->Trancellular=0.5L
Intracellular fluid =28L

33
Q

DNA REPLICATION

A

-Before cell division DNA topoisomerase unwinds DNA and DNA helicase breaks hydrogen bonds between complimentary base pairs=have two replication forks

-single stranded binding proteins bind to strand to prevent reannealing

-Primate enzyme synthesised short RNA primer as DNA polymerase can extend nucleotide chain not start one

-DNA polymerase joins free floating nucleotides via complimentary base pairing in 5’ 3’ direction

-RNASE H removes primers
-DNA polymerase fills in gaps left
-ligase enzyme joins short DNA pieces into one continuous strand

34
Q

DNA TRANSCRIPTION

A

-DNA topoisomerase relieves supercoils and DNA helicase breaky hydrogen bonds= 2 strands
-SSBS prevent reannealing
-TATA sequence recognition signal to start
-AUG start codon
-MRNA nucelotides line up and bind to complimentary bases on antisense strands
-RNA polymerase joins MRNA nucleotide
-Transcription stops at stop codons
-Splicing-introns removed(non coding sections)
MRNA leaved through nuclear pores

35
Q

DNA TRANSLATION

A

-MRNA attaches to ribosomes
-At ribosomes MRNA bind to complimentary TRNA at their anticodons via codons on MRNA
-TRNA attached to specific amino acids
-Enzymes remove amino acid from TRNA and amino acids linked via peptide bonds to create a polypeptide chain

36
Q

Genotype

A

Genetic constitution of an individual

37
Q

Phenotype

A

Appearance of an individual affected by the genotype and environment

38
Q

Allele

A

Different forms of a gene at a specific locus

39
Q

Polymorphism

A

Frequent hereditary variations at a locus

40
Q

Heterozygous

A

Alleles at a different locus

41
Q

Homozygous

A

Alleles at the same locus

42
Q

Penetrance

A

The % of individuals with a specific genotype showing the expected phenotype

43
Q

Gonadal mosaicism

A

a mutation that is limited to the gonads and can be transmitted to offspring