carb metabolism Flashcards

1
Q

Km

A

Thesubstrate concentration at which the reaction is half maximal. If a reaction has a low Km it suggests that the substrates have a strong affinity for the enzyme and the reaction will go at low substrate concentrations

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2
Q

Vmax

A

maximum rate of reaction catalyzed by enzyme

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3
Q

Describe the common features that make a particular step in a linked enzyme pathway a “key step”.

A

Key steps may include one where a molecule changes location (ie. entering cell), where body invests energy in transition from on molecular state to another to activate precursor, and/or any rate limiting steps

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4
Q

Primary function of glycolysis

A

generation of energy and useful chemical intermediates from the breakdown of glucose

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5
Q

key steps in glycolysis

A

Glucose enters cell through glucose transporters > glucose converted to glucose-6-phosphate and is trapped in cell b/c charge (requires ATP) > G-6-P transformed into fructose 1,6 bisphosphate by phospho-fructo-kinase (PFK- rate limiting) > final product is pyruvate

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6
Q

Net result of glycolysis

A

net production of energy in the form of ATP and NADH which can be produced in the absence of oxygen and mitochondria Also, pyruvate, the final product, has a lot of stored energy

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7
Q

compare the fate of pyruvate in aerobic vs anaerobic environment

A

aerobic: pyruvate enters TCA cycle and is oxidized into CO2 and water (or synthesized into fatty acids). Anaerobic: ie. hypoxia, intense exercise, or in RBC which lacks mitochondria- pyruvate will be converted to lactate and exported from the cell

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8
Q

Primary function of TCA/electron transport system

A

produces energy from pyruvate

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9
Q

key steps in TCA cycle

A

pyruvate > Acetyl CoA > oxidized to CO2 with release of energy stored in GTP, NADH and FADH2

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10
Q

compare TCA cycle in energy surplus vs energy deficit

A

Surplus: Acetyl-CoA from glycolysis can enter the TCA cycle and then leave without being oxidized to be used in fatty acid synthesis. Deficit: acetyl CoA, can continue around the TCA cycle to release energy through the conversion of NAD and FAD to NADH and FADH2 with the subsequent generation of ATP.

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11
Q

key steps in electron transport chain

A

NADH and FADH2 from TCA cycle enter the electron transport system on the inner membrane of the mitochondria in a process that couples oxygen consumption with ATP generation. Results in conversion of O2 to H2O and ADP to ATP (oxidative phosphorylation)

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12
Q

primary function of gluconeogenesis

A

During fasting, the liver (and to lesser extent the kidney) produce glucose

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13
Q

What are the substrates used for gluconeogenesis

A

lactate produced by glycolysis in muscle or red blood cells, amino acids derived from protein breakdown in muscle, or glycerol from triglyceride breakdown in adipose tissue.

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14
Q

key steps in gluconeogenesis

A

pyruvate converted to oxaloacetate then phosphoenol pyruvate via enzymes Pyruvate Carboxylase and Phospho-Enol-Pyruvate Carboxy-Kinase (PEPCK) > fructose 1,6 bis phosphonate converted to fructose-6-P by fructose 1,6 bisphosphatase > glucose-6-phosphate converted to free glucose by glucose-6-phosphatase

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15
Q

Name the organs that can produce/export glucose into the circulation

A

liver and kidney only b/c they can undergo gluconeogenesis

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16
Q

when does glycolysis vs gluconeogenesis occur?

A

When glucose is abundant in a liver cell, glycolysis predominates. When glucose is in short supply, gluconeogenesis predominates

17
Q

What compound is an important node in glucose metabolism

A

glucose-6-phosphate: it can go down pathway of glycolysis to be oxidized for energy or go towards storage in process of glycogen synthesis

18
Q

Function of glyogen synthesis

A

Forms a rapidly available source of glucose for acute oxidative needs

19
Q

key steps in glycogen synthesis

A

glucose-6-P converted to glucose-1-P then to UDP-glucose (this is the committed step) > glycogen synthase adds UDP-glucose to growing glycogen molecule > glycogen phosphorylase can remove glucose from glycogen.

20
Q

When is glycogen synthesized vs broken down?

A

glycogen synthesis is stimulated when the liver/skeletal muscle is in positive energy balance, and glycogen breakdown is activated when the body is in negative energy balance.

21
Q

structure of glycogen

A

Highly branched polymer- this allows rapid release of many glucose molecules when needed. This also means that an enzyme is required to create branch points when building glycogen

22
Q

function of pentose phosphate pathway

A

when glucose is abundant it is used for generation of NADPH and for generation of 5-carbon sugars used for nucleotide synthesis

23
Q

Pentose phosphate pathway key steps

A

oxidation of glucose-6-phosphate to 6-phosphogluconolactone by Glucose-6-Phosphate Dehydrogenase (G6PD) is the key regulated step in this pathway.

24
Q

function of NADPH

A

source of energy for a variety of synthetic reactions. These include fatty acid biosynthesis, cholesterol biosynthesis, defense against oxidative stress and white cell function

25
Q

what factors determine flux through a pathway

A

amount of substrate available, amount of key enzymes available, allosteric regulation and covalent modification of a key enzyme (ie. phosphorylation)

26
Q

Things that can affect levels of key enzymes available in gluconeogenesis

A

PEPCK is a key enzyme in gluconeogenesis and isnulin can decrease transcription of this enzyme, resulting in reduced flux through the pathway

27
Q

what is allosteric regulation

A

This is where another molecule (sometimes a substrate for or product of the reaction or an intermediate in a different pathway) alters the activity of a key enzyme in a pathway by altering the Km or Vmax.

28
Q

Give example of allosteric regulation in pentose phosphate pathway

A

NADPH/NADP+ (present when the pentose phosphate pathway has been active) reduces the activity of G6PD (the key regulated step in the pathway)

29
Q

describe hormonal regulation of carbohydrate metabolism

A

In fed state, insulin is high and glucagon/ catecholamines/ growth hormone/ cortisol are low resulting in glycolysis and glycogen synthesis. In fasting state, insulin is low and counterhormones are high, reuslting in gluconeogenesis and glycogen breakdown.