BioChem Flashcards

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1
Q

Glycolysis input/output

A

Input: Glucose + 2NAD + 2P + 2 ADP Output: 2 pyruvate + 2NADH + 2H + 2H2O + 2ATP

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2
Q

glycolysis happens in cytoplasm. how does pyruvate get into mitochondria?

A

pyruvate translocase

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3
Q

function of PDC

A

pyruvate dehydrogenase complex oxidizes pyruvate into acetyl coA + CO2 + NADH

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4
Q

PDC regulation

A

stimulated by high ADP/ATP ratio

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5
Q

Krebs output per glucose

A

6NADH 2FADH2 2GTP 2CO2

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6
Q

Krebs substrates

A

A Cougar I ate said: sugar, fuck me only acetyl coA>citrate>isocitrate>alphaketoglutarate>succynyl coA>succinate>fumarate>malate>oxaloacetate

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7
Q

thiamine pyrophosphate

A

thio-vitamine vitamin B involved in PDC complex involved in alpha-ketoglutarate dehydrogenase complex

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8
Q

definition of prosthetic group

A

nonprotein molecule covalently bound to an enzyme as part of the enzymes active site

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9
Q

definition of cofactor

A

various organic and inorganic substances necessary to the function of an enzyme but which never actually interact with the enzyme

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10
Q

describe ETC electron carrier organization

A

1) NADH dehydrogenase (aka coenzyme Q reductase) oxidizes NADH and eventually passes those 2 electrons to ubiquinone (aka coenzyme Q). 2) Coenzyme Q is a mobile electron carrier that takes the electrons to the next carrier, cytochrome C reductase. 3) cytochrome C reductase obtains electrons from ubiquinone. cytochrome C reductase transfers electrons to… you guessed it… cytochrome C 4) cytochrome C is another mobile electron carrier. cytochrome C delivers electrons to cytochrome C oxidase. 4) cytochrome C oxidase passes the electrons to the final electron acceptor>usually oxygen

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11
Q

ubiquinone receives electrons from these three sources:

A

1) traditional ETC chain, ubiquinone receives 2 elecrons from NADH dehydrogenase/NADH oxidized 2) FADH2 delivers electrons directly to coenzyme Q, bypassing NADH dehydrogenase 3) NADH produced in cytosol is delivered to mitochrondria via glycerol phosphate shuttle. The NADH from cytosol delivers electrons directly to ubquinone (I presume due to its ability to receive electrons from cytosol side of mitochondrial matrix)

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12
Q

of hydrogens pumped across mitochondrial matrix per NADH molecule oxidized (traditional full ETC involvement)

A

about ten hydrogens are pumped across the mitochondrial matrix per NADH oxidized

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13
Q

of hydrogens required to produce an ATP in the ETC

A

It requires 3 hydrgoens to create the ATP but 1 extra hydrogen to transport the incoming phosphate therefore, it take 4 hydrogens to create an ATP

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14
Q

how many ATP are created by NADH oxidized via traditional ETC

A

NADH oxidation: 10 hydrogens pumped across membrane ATP synthesis: 4 hydrogens/ATP therefore, 2.5 ATP created/ NADH oxidized

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15
Q

How many hydrogens pumped across membrane/FADH2 reduced

A

6 hydrogens are pumped across the mitochondrial membrane per FADH2 oxidized. This Is because FADH2 skips NADH dehydrogenase and is oxidized by ubiquinone

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16
Q

total ATP produced per glucose in eukaryotes

A

30

17
Q

total ATP produced per glucose in eukaryotes. why is this different from prokaryotes

A
  1. prokaryotes don’t have to waste energy trying to shuttle NADH across mitochondria. Prokaryotic ATP synthase is located in their plasma membrane
18
Q

where is glycogen stored

A

liver and muscle

19
Q

where does gluconeogenesis occur

A

liver only. muscle doesn’t have necessary enzymes

20
Q

what are the products of amino acid catabolism

A

alpha ketoacid and urea

and ketone bodies and glucose

21
Q

describe pentose phosphate pathway

A

means of diverting glucose-6-phosphate to uses other than glycolysis such as: Gluc-6-P>Ribose-6-P> Nucleotides and NADPH

22
Q

Krebs cycle regulation: Enzyme, positive regulator, negative regulator

A

enzyme: isocitrate dehydrogenase :positive regulator: ADP Negative regulator: ATP,NADH

23
Q

glycolysis regulation: enzyme, positive regulator, negative regulator

A

enzyme: phosphofructokinase positive regulators: fructose 2,6 bisphosphate negative regulators: ATP

24
Q

gluconeogenesis regulation: enzyme, positive regulator, negative regulator

A

enzyme: fructose 1,6 bisphosphatase posititve regulator- X negative regulator: Fructose 2,6 bisphosphatase

25
Q

metabolic response to low blood sugar

A

low blood sugar detected, glucagon released from alpha cells of pancrerase, binds to cell surface receptor because glucagon is peptide hormone, increases cAMP, activates protein kinase, protein kinase phosphorylates PFK-2/F-2,6-Bisphosphatase, phosphorylated F-2,6,BPase deactivates PFK-1 and deactivates F-2,6-BP deactivation of F-2,6BP increases F-1,6BPase which pushes metablism towards gluconeogenisis.. F-1,6BPase catalyzes a large energy reverse step in glycolysis: F-1,6BP > F6P and pushes back toward gluconeogenesis

26
Q

describe glycogenolysis in the liver and muscle in response to glucagon and epinepherine

A

Liver responds to glucagon and epinepherine by increasing glycogenolysis Muscle response ONLY to epinepherine

27
Q

describe fat digestion describe fatty acid metabolism

A

1) fats eaten and sent to stomach. In the stomach, they ar mixed with acid. In the stomach, fatty acids don’t digest they just make a immiscible solution and float on top of other materials. Once the pyloric sphincter opens, fats travel into the duodenum. Presence of food in the small intestine stimultaes cholecystokynin release. CCK activates the gallbladder to release bile. Further, CCK stimulates the pancrease to release pancreatic lipase. Biile emulsifies fats into micelles which allows pancreatic lipase to begin hydrolyzing the triglycerides into fatty acids. Fatty acids can diffuse into small intestine epithelium where they reform into tryglycerides and are pulled into chylomicrons. chylomicrons are take up via lacteals of the lymphatic system where they are eventually drained back into veinous blood supply near the neck. chylomicrons can now travel to the liver, adipocytes,etc 2) The first step in breaking down fats to use them for energy is to hydrolize triglycerides into FFA’s. Then, FFA’s can be attached to acyl-coA (requires 2ATP), bound to carnitine and shuttled into the mitochondria for beta-oxidation. Beta oxidation is a set of reactions that ultimately cleaves the bond beta alpha and beta carbons on the Fatty acid. This produces an acetyl-Coa, 1FADH2, and 1NADH for each round of Beta oxidation.

28
Q

FA synthesis

A

initial activation requires Acetyl-Coa carboxylase to catalyze acetyl-Coa into malonyl coA. malonyl coA is the molecule used by fatty acid synthase to tranfer two carbon units to the growing chain of molecules on the fatty acid Fatty acid synthesis requires NADPH

29
Q

common monosacharides

A
30
Q

Polar, Neutral amino acids

A

tyrosine

asparigine

glutamine

threonine

cysteine

serine

31
Q

Polar, Basic Amino Acids

A

Basic H.A.L

Histidine

Arginine

Lysine

32
Q

polar, acidic amino acids

A

apartic acid

glutamic acid

33
Q

Nonpolar, neutral

amino acids

A

glycine

leucine

isoleucine

tryptophan

proline

methionine

phenylalalnine

alnanine

valine

34
Q

where is NADPH made?

Where is NADPH used?

A

NADPH is made as a side product in the pentose phosphate pathway

NADPH is used in fatty acid synthesis. Think about it. something has to reduce the acetyl coA into a reduced fatty acid chain. what is going to do all of the reducing? NADPH!

NADPH is also used to create reactive oxygen species that is used in peroxisomes to destroy stuff