BIOCHEM INTEGRATED Flashcards
<p>Process that releases energy.
-delta G</p>
<p>Exergonic Reaction</p>
<p>Process that requires energy
\+delta G</p>
<p>Endergonic Reaction</p>
<p>Site of ATP production</p>
<p>Cytoplasm and Mitochondria</p>
<p>Loss of electrons
| (Substance becomes more positive)</p>
<p>Oxidation</p>
<p>Gain of electrons
| (Substance becomes more negative)</p>
<p>Reduction</p>
<p>Product of de novo purine synthesis
| (Precursor of Guanine and Adenosine residues)</p>
<p>Inosine Monophosphate (IMP)</p>
<p>1st committed step of purine synthesis</p>
<p>Ribose-5-phosphate to PRPP
| (Thru action of PRPP synthetase and ATP)</p>
<p>Xanthine oxidase inhibitor</p>
<p>Allopurinol</p>
<p>Disease where there is deficiency in HGPRT</p>
<p>Lesch-Nyhan syndrome</p>
<p>Pyrimidine ring structure is formed by...</p>
<p>Carbamoyl phosphate and Aspartate</p>
<p>Rate limiting enzyme in Glycolysis</p>
<p>Phosphofrucktokinase-1 (PFK-1)</p>
<p>Glycogen synthetase : Glycogenesis
| \_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_ : Glycogenolysis</p>
<p>Glycogen phosphorylase</p>
<p>Rate limiting enzyme of gluconeogenesis</p>
<p>Fructose-2,6-bisphosphatase</p>
<p>Vitamin D deficiency in adults</p>
<p>Osteomalacia</p>
<p>pH at which zwitterion is predominant</p>
<p>Isoelectric pH (IpH)</p>
<p>This enzyme in glycolysis is inhibited when cell is rich in ATP</p>
<p>Phosphofructokinase-1</p>
<p>Number of ATP formed in one molecule of Acetyl CoA</p>
<p>10</p>
<p>Enzyme deficient in von Gierke's disease</p>
<p>Glucose-6-phosphatase</p>
<p>Carrier of TAGs and other dietary lipids from the INTESTINES to the LIVER and ADIPOSE TISSUE</p>
<p>Chylomicrons</p>
<p>Carrier of newly synthesized TAGs from liver to adipose tissue</p>
<p>Very Low Density Lipoproteins (VLDL)</p>
<p>Type of reaction
ATP to ADP or AMP</p>
<p>Hydrolysis</p>
<p>Products of Aldolase action on Fructose-1,6-bisphosphate</p>
<p>Dihydroxyacetone phosphate (DHAP) and Glyceraldehyde-3-phosphate (G3P)</p>
<p>Irreversible steps in Glycolysis</p>
<p>Step 1: Glucose ---> Glucose-6-phosphate (hexokinase or glucokinase)
Step 3: Fructose-6-phosphate ---> Fructose-1,6-bisphosphate (Phosphodructokinase-1)
Step 10: Phosphoenolpyruvate ---> Pyruvate (Pyruvate kinase)</p>
<p>Rate limiting enzyme of:
1. Ketogenesis
2. Cholesterol synthesis</p>
<p>1. HMG CoA synthase
| 2. HMG CoA reductase</p>
<p>Non-insulin requiring organs</p>
<p>Brain (except hypothalamus), RBCs, intestinal cells, kidneys</p>
<p>Converts pyruvate to Acetyl CoA</p>
<p>Pyruvate dehydrogenase</p>
<p>Product of anaerobic glycolysis</p>
<p>Lactate / lactic acid</p>
<p>PFK-1 is inhibited by \_\_\_\_\_ and activated by \_\_\_\_\_\_</p>
<p>ATP and Citrate; AMP</p>
<p>Fates of pyruvate</p>
<p>Lactate dehydrogenase ---> Lactate Pyruvate dehydrogenase ---> Acetyl CoA Pyruvate carboxylase ---> Oxaloacetate Pyruvate kinase ---> PEP to Pyruvate Yeast, bacteria ---> ethanol</p>
<p>Only amino acid with no chiral center / chiral carbon
Chiral center: Carbon with 4 unique substituenta attached to it</p>
<p>Glycine (2 Hydrogens attached to it)</p>
<p>Sulfur containing amino acids</p>
<p>Cysteine (Cys, C)
| Methionine (Met, M)</p>
<p>Acidic amino acids</p>
<p>Aspartic acid / Aspartate (Asp, D)
| Glutamic acid / Glutamate (Glu, E)</p>
<p>Branched chain amino acids</p>
<p>Leucine (Leu, L)
Isoleucine (Ile, I)
Valine (Val, V)</p>
<p>Smallest amino acid</p>
<p>Glycine</p>
<p>Products of PPP</p>
<p>Ribose-5-phosphate and NADPH</p>
<p>Another name for Glycolysis</p>
<p>Embden-Meyerhof pathway</p>
<p>INITIAL Electron carriers of ETC</p>
<p>NADH & FADH2</p>
Give the two ways in which your cells produce ATP
Oxidative Phosphorylation
Substrate Level Phosphorylation
Anaerobic glycolysis
Substrate Level Phosphorylation
Coupled with the electron transport chain
Oxidative Phosphorylation
Only method of ATP production for RBCs
Substrate Level Phosphorylation
Resting skeletal muscle and cardiac muscle, well-oxygenated neurons
Oxidative Phosphorylation
Fatigued skeletal muscle, cardiac muscle during acute MI, and neurons during ischemic stroke
Substrate Level Phosphorylation
Predominant hormone in the well fed state
Insulin
Hormone that helps maintain blood glucose levels during starvation
Glucagon
Exert effects similar to glucagon
Epinephrine
Cortisol
Growth Hormone
Ratio of carbon dioxide produced/oxygen consumed
Respiratory Quotient
Main metabolic fuel of neurons and erythrocytes
Glucose
Main metabolic fuel of heart muscle
Fatty Acids
Main fuel of the skeletal and heart muscle, and alternative fuel of the brain during a fast
Ketone Bodies
Percentage of the brain’s energy requirement that can be met by ketone bodies
20%
Product of aerobic glycolysis
Pyruvate
Product of anaerobic glycolysis
Lactate
Product of glycogenolysis in liver
Glucose
Product of glycogenolysis in muscle
Glucose-6-Phosphate
Building block of fatty acids and cholesterol
Acetyl CoA
Main substrate used for gluconeogenesis during a fast
Amino Acids
Intermediate that can never be used for gluconeogenesis
Acetyl CoA
During the first 18 to 24 hours of starvation, which pathway is responsible in maintaining blood glucose levels?
Glycogenolysis
After 24 hours of starvation, which pathway is mainly responsible for maintaining blood glucose levels?
Gluconeogenesis
Percentage of gluconeogenesis that occurs in the kidney during a prolonged fast
40%
Hours of fasting before glycogen stores are exhausted
18 hours
Cause of death in prolonged starvation
Catabolism of essential proteins
Amino acid that performs a central role in removal of nitrogen from most other amino acids
Glutamate
Transports ammonia from muscle to the liver
Alanine
Transports ammonia from peripheral tissues to the liver and kidney
Glutamine
Metabolic effects of uncontrolled diabetes mellitus
Glucagon»_space; insulin
↑ Gluconeogenesis from amino acids
↑ Lipolysis in adipose tissue
↑ Ketogenesis in liver
Metabolic effects of acute alcohol intoxication
Lactic acidosis
Ketoacidosis
Hypoglycemia
Massive increase of this molecule leads to metabolic effects of alcohol intoxication
NADH
Intermediate in alcohol metabolism that causes flushing, tachycardia, hyperventilation, andnausea
Acetaldehyde
Ketoacidosis with hyperglycemia
Diabetic Ketoacidosis
Ketoacidosis with hypoglycemia
Alcoholism
Prolonged starvation
Critical intermediate necessary to maintain TCA cycle activity usually depleted in prolonged starvation and alcohol intake
Oxaloacetate
TCA intermediate that is depleted during hyperammonemia
α-ketoglutarate
TCA intermediate that links it to the urea cycle
Fumarate
On ketogenic diet, these pathways that remain active in the liver even during the fed state
Gluconeogenesis
Ketogenesis