Biochemistry 1 Flashcards

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1
Q

Describe stored ATP

A

-stored in small amounts in the body (80-100g)

-immediate energy source

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2
Q

What is creatine phosphate used for?

A

-converts ADP back to ATP by direct phosphorylation

-immediate muscle energy store

-CP stores are limited -not effective in providing enough ATP

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3
Q

Define creatine kinase

A

an enzyme that catalyses direct phosphorylation

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4
Q

Where is CK found?

A

-found inside healthy muscle

-muscle damage causes CK to be lost into the blood stream

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5
Q

What is CK a marker for?

A

Myocardial infarction

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6
Q

define glycogenolysis

A

breakdown of glycogen stored in muscle or liver

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7
Q

Define gluconeogenesis

A

formation of glucose from other nutrients in the liver

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8
Q

what is the equation for the complete catabolisim of glucose?

A

C6H12O6 + 6O2
→ 6H2O + 6CO2 + 38 ATP + heat

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9
Q

Name the 3 linked metabolic pathways involved in the complete catabolism of glucose

A

-glycolysis
-krebs cycle
-Electron transport chain

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10
Q

describe the overall process of glycolysis

A

1) glucose is broken down into 2 pyruvic acid molecules in the cytoplasm

2)uses 2 ATP to activate the glucose, forms 4 ATP through pathway- Net gain of 2 ATP

3) intermediate metabolites are oxidised
H+ and e- are removed and picked up by a carrier NAD+ which is converted to 2NADH + H+

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11
Q

Describe the anaerobic outcome of glycolysis

A

in a lack of O2- pyruvic acid is converted to lactic acid-leads to muscle fatigue and acidosis

NADH+ H+ converted back to NAD+ anaerobic pathway- overall production of 2 ATP per glucose molecule

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12
Q

Describe the aerobic outcome of glycolysis

A

-in enough O2
-Pyruvic acid enters mitochondria for the krebs cycle
-potential production of 38ATP molecules per glucose molecule

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13
Q

Describe the transition process from pyruvate dehydrogenase to acetyl-co enzyme A

A

-pyruvate dehydrogenase converts each pyruvate into acetyl-coenzyme A

-redox reaction-hydrogens are removed, oxidation of pyruvate, picked up by NAD+ which is reduced to NADH + H+

1c removed as cO2 waste

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14
Q

Where does krebs cycle occur?

A

mitochondria

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15
Q

Describe the products when each acetyl-CoA enters the krebs cycle

A

-carbon atoms removed as CO2 waste

-3NAD+ are reduced to 3 NADH+H+

-another carrier FAD is reduced to FADH2

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16
Q

What is phase 1 of glycolysis?

A

-sugar activation
-glucose is activated by phosphorylation and converted to fructose-1-6-bisphosphate

17
Q

What is phase 2 of glycolysis?

A

-sugar cleavage
-fructose-1-6-bisphosphate is cleaved into two 3-carbon fragments

18
Q

What is phase 3 of glycolysis?

A

-sugar oxidation and formation of ATP

-the 3 carbon fragments are oxidised by removal of hydrogen and 4 ATP molecules are formed

19
Q

Where does glycolysis occur?

A

cytosol

20
Q

Define oxidation

A

addition of oxygen,removal of hydrogens and electrons

21
Q

Where is NAD and FAD derived from?

A

NAD- derived from the B vitamin niacin

FAD-derived from the B vitamin riboflavin

22
Q

What are the equations for NAD and FAD in there oxidized and reduced from?

A

NAD+ + 2H –> NADH + H+

FAD + 2H —> FADH2

lhs-oxidized form
rhs-reduced form

23
Q

where does oxidative phosphorylation occur?

A

Via the elctron transport chain

24
Q

Describe the events that occur in oxidative phosphorylation

A

1) NADH + H+ and FADH2 pass on their hydrogens and high energy e- to O2 as the final acceptor producing H2O

2) linked to high ATP production

3) Each NADH + H+ carriers leads to 3 ATP production

4) each FADH2 carrier leads to 2 ATP formed

NAD+ and FAD are regenerated at the same time so can accept another lot of e-/H+

25
Q

what is the ETC?

A

e- are transferred from complex to complex and some of their energy is used to pump protons into the intermembrane space, creating a proton gradient

26
Q

What is chemiosmosis?

A

ATP synthesis is powered by the flow of H+ back across the inner mitochondrial membreane through ATP synthase

27
Q

How is CO2 produced in the catabolism of glucose?

A

-produced in the conversion of pyruvate to acetyl-COA and oxidation of acetyl-COA via the kreb cycle

28
Q

Describe the catabolism of lipids

A

-glycerol can enter glycolysis, and if enough O2 is available, itll carry on into krebs and ETC

29
Q

describe how the 3 fatty acids that have 16c-18c are split up

A

2c split through a series of enzymatic reactions called beta-oxidation in the mitochondria

each 2c is coverted to acetyl-CoA

if enough O2 full catabolism of fat will occur through Kreb’s cycle and ETC

30
Q

When does ketoacididosis happen?

A

-high fat use, acetyl CoA converted to ketones, blood becomes acidic, due to reduced availability of carbohydrates

-low CHO
-starvation
-uncontrolled diabetes mellitus

31
Q

What are the effects of ketoacidiidosis?

A

-kussmauls respiration
-ketone breath
-ketones in urine
-eventually coma

32
Q

Describe the catabolism of protein

A

-used when other sources are unavailable, or during prolonged excersise

1) in the liver, NH2 is removed from AA= deamination. NH2 converted to NH3 then to urea

2)Remaining part of molecules may be converted to pyruvic acid or acetyl CoA
-carry on krebs and ETC

33
Q

Define Respiratory exchange ratio

A

used to determine the predominant energy source being used

oxygen consumed: CO2 produced