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BCHM 270 Final Exam With Correct Answers, Exams of Biochemistry

BCHM 270 Final Exam With Correct Answers

Typology: Exams

2024/2025

Available from 03/12/2025

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BCHM 270 Final Exam With
Correct Answers
Acute Pancreatitis - ANSWER - pancreatic duct obstruction
- enzymes activate inside pancreas, attacking pancreatic tissue
- can be caused by CF
- pancreatic secretion deficiency
cystinuria - ANSWER - high concentrations of cysteine in urine
- stones in kidney, ureter and gall bladder
hyperammonemia - ANSWER - ammonia is highly toxic
- elevated levels
- liver or urea cycle diseases
- symptoms: tremors, slurred speech, blurred vision
PKU - ANSWER - amino acid metabolism error
- phenylalanine hydroxylase deficiency
- symptoms: elevated Phe and Phe metabolites, hypopigmentation (Tyr
deficiency), developmental delays
- treatment: low Phe diet
Albinism - ANSWER - Tyrosinase deficiency
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BCHM 270 Final Exam With

Correct Answers

Acute Pancreatitis - ANSWER - pancreatic duct obstruction

  • enzymes activate inside pancreas, attacking pancreatic tissue
  • can be caused by CF
  • pancreatic secretion deficiency cystinuria - ANSWER - high concentrations of cysteine in urine
  • stones in kidney, ureter and gall bladder hyperammonemia - ANSWER - ammonia is highly toxic
  • elevated levels
  • liver or urea cycle diseases
  • symptoms: tremors, slurred speech, blurred vision PKU - ANSWER - amino acid metabolism error
  • phenylalanine hydroxylase deficiency
  • symptoms: elevated Phe and Phe metabolites, hypopigmentation (Tyr deficiency), developmental delays
  • treatment: low Phe diet Albinism - ANSWER - Tyrosinase deficiency

MSUD - ANSWER - branched-chain a-keto acid dehydrogenase deficiency

  • symptoms: metabolic acidosis--> maple syrup pee smell
  • lethal if untreated
  • treatment: low protein diet, reduce branched aa intake Jaundice - ANSWER - yellow tinge to skin
  • caused by bilirubin deposits --> hyperbilirubinemia
  • caused by high rate of RBC destruction, liver dysfunction, bile duct obstruction
  • common in newborns who have low levels of the catabolic enzyme gout - ANSWER - hyperuricemia due to overproduction of uric acid or ingestion of too many purine-rich foods
  • form of arthritis
  • uric acid crystals build up in joints
  • treatment: xanthine oxidase lipid malabsorption - ANSWER - symptoms: increased lipids in feces (steatorrhea)
  • leads to fat-soluble vitamin deficiencies
  • may result from: CF, liver disease CF - ANSWER - secretion thickening and buildup
  • lung damage/disease, lipid malabsorption, pancreatic damage (diabetes)

oxidized lipoproteins - ANSWER - LDL accumulation oxidized by free radicals

  • atherosclerosis plaques Atherosclerosis - ANSWER - blockage or rupture of artery
  • vascular damage
  • heart attack & stroke PK deficiency - ANSWER - defective activity --> changes Vmax or Km for substrate or coenzymes, altered gene expression, abnormal response to activator
  • hemolytic anemia

G6PD deficiency - ANSWER - PPP regulator

  • hemolytic anemia
  • inability to detoxify ROS (NADPH deficiency)
  • increased resistance to malaria

hemolytic anemia - ANSWER - causes: oxidant drug treatment (e.g. antibiotics), favism, infection

Hypoglycemia - ANSWER - blood glucose deficiency

  • symptoms: CNS symptoms, odd behavior, coma
  • medical emergency
  • quick response to glucose ingestion

importance of plasma aminotransferases - ANSWER - elevated levels in blood indicates cell damage (usually intracellular)

  • usually seen connected to liver injury
  • can be seen in heart attack and muscle disorders

Bilirubin vs aminotransferases in liver damage - ANSWER aminotransferases higher first bilirubin levels increase later, after initial damage

Type I diabetes - ANSWER - Laura!

  • child/tween onset
  • immune attack on pancreatic B-cells--> no insulin production
  • "triggered" by smth
  • genetic
  • hyperglycemia
  • ketosis
  • hypertriglyceridemia

Nucleotide components - ANSWER - nitrogenous base

  • 5-C sugar
  • phosphate group

purines - ANSWER - 2 rings

  • A & G

Pyrimidines - ANSWER - 1 ring

  • C, T & U

Central Dogma - ANSWER info flows from DNA -> RNA -> Protein

silent mutation - ANSWER base changes, aa doesn't

missense mutation - ANSWER base changes, aa changes

nonsense mutation - ANSWER base changes, premature STOP codon

frameshift mutation - ANSWER base insertion or deletion that shifts reading frame

Restriction endonucleases - ANSWER an enzyme that cuts DNA at specific sites, producing small fragments used in genetic engineering. (DNA biotech)

Gel electrophoresis - ANSWER - Procedure used to separate and analyze DNA fragments by size

  • Placing a mixture of DNA fragments at one end of a porous gel and applying an electrical voltage to the gel (DNA biotech)

DNA cloning - ANSWER isolating DNA sequences and inserting them into other cells that will copy those sequences (e.g. plasmids, viruses) (DNA biotech)

DNA Probes - ANSWER Single stranded DNA fragment complement to the target of interest labeled with radioisotopes or dyes (DNA biotech)

Southern blot - ANSWER blotting separated DNA fragments from gel electrophoresis onto membrane so they can be labeled with DNA probes and studied

cDNA microarray - ANSWER cDNA labeled with dye to discover gene expression in cells (RNA biotech)

SDS-PAGE - ANSWER gel electrophoresis for proteins (polyacrylamide gel) (Protein biotech)

Antibodies - ANSWER - High specificity for their antigens

  • tagged antibodies (fluorescence or dye) to detect the presence of certain proteins (Protein biotech)

Western blots - ANSWER blotting for proteins (Protein biotech)

Direct ELISA - ANSWER - Wells coated with antigen of interest

  • Detects for antibodies

Sandwich ELISA - ANSWER - wells coated with "capture" antibody

  • antigen-containing samples added to wells
  • enzyme-labeled antibody used to detect antigen presence

ELISA - ANSWER - Detect protein-protein or protein-antigen interactions

Adenine - ANSWER

Cytosine - ANSWER

Guanine - ANSWER

Thymine - ANSWER

Uracil - ANSWER

Hydrogen bonding - ANSWER Weak bonds; occurs when a hydrogen atom in one molecule is attracted to an electronegative atom in another molecule

amphipathic - ANSWER having both a hydrophilic region and a hydrophobic region

Basic amino acids - ANSWER - lysine, arginine, histidine

  • positively charged at most pH's
  • can form salt bridges

Aromatic side chains for amino acids - ANSWER - Phenylalanine, tryptophan, tyrosine

  • can cause steric hinderance
  • can deeply affect structure of resulting peptide with gain or loss

Alanine - ANSWER Ala, A, nonpolar

Glycine - ANSWER Gly, G, nonpolar

Leucine - ANSWER Leu, L, nonpolar

Valine - ANSWER Val, V, nonpolar

Isoleucine - ANSWER Ile, I, nonpolar

Phenylalanine - ANSWER Phe, F, nonpolar, aromatic

Tryptophan - ANSWER Trp, W, nonpolar, aromatic

Methionine - ANSWER Met, M, nonpolar

Proline - ANSWER Pro, P, nonpolar

Serine - ANSWER Ser, S, uncharged polar

Threonine - ANSWER Thr, T, uncharged polar

Tyrosine - ANSWER Tyr, Y, uncharged polar, aromatic

Asparagine - ANSWER Asn, N, uncharged polar

Glutamine - ANSWER Gln, Q, uncharged polar

Cysteine - ANSWER Cys, C, uncharged polar

what enzymes add phosphate groups - ANSWER kinases

what enzymes remove phosphate groups - ANSWER phosphatases

phosphorylation - ANSWER turns proteins on and off attaches phosphate to a hydroxyl group

Sickle cell anemia results from... - ANSWER protein aggregation resulting from an amino acid change (E -> V)

Primary protein - ANSWER linear sequence of amino acids

Secondary protein - ANSWER max. H bonding alpha helix or beta pleated sheets

tertiary protein - ANSWER - determined by R-group interactions

  • stabilizing interactions occur

Quaternary protein - ANSWER binding of 2+ chains or subunits stabilized with noncovalent interactions

Misfolded proteins - ANSWER - degraded quickly by body

  • if not degraded, can lead to serious conditions

Alzheimer's disease - ANSWER - peptide cleaved incorrectly leading to aggregation

  • neurotoxic plaques build up and cause neuron death

Prion Disease - ANSWER - affects nervous system

  • caused by Prion proteins that when folded incorrectly, cause others to fold incorrectly as well
  • e.g. a-helices -> pleated sheets

Globular proteins - ANSWER - spherical, water-soluble proteins.

  • transporters, storage, enzymes

Fibrous proteins - ANSWER - long multimer chains

  • stabilized through disulfide bonds
  • structural supports

Osteogenesis Imperfecta - ANSWER Gly-X-Y sequences mutated into bulky amino acids preventing assembly of helices into a collagen fiber

Cofactors - ANSWER inorganic molecules that bind to enzymes, aiding in catalytic activity

Coenzymes - ANSWER Organic molecules that bind to enzymes, aiding in catalytic activity

2 components of an active site - ANSWER 1) Binding site for substrate

  1. Catalytic site for reaction

Lock & key model - ANSWER - enzyme & substrate fit perfectly

  • not entirely accurate

Induced fit model - ANSWER - enzyme will mold around substrate for a tighter fit

Isozymes - ANSWER multiple enzymes capable of catalyzing the same reaction

isoforms - ANSWER slightly different versions of the same protein

Blood Plasma - ANSWER - non-cell liquid portion

  • has anticoagulent

Blood Serum - ANSWER - Blood that's been allowed to clot

delta G - ANSWER - Gibbs free E

  • when -ve, rxn is spontaneous
  • when +ve, rxn is not spontaneous
  • when 0, rxn @ equilibrium

exergonic - ANSWER releases energy

endergonic - ANSWER requires energy

Factors affecting enzyme rate - ANSWER 1) Temperature

  1. pH
  2. Substrate Concentration