SciFom Macromolecules

  1. List the 4 biomolecules.
    Carbs, Lipids, Protein, nucleic acids
  2. What is the general structure for all carbs?
    CH2O
  3. What weight of the cell do carbs compose?
    2-3%
  4. What are the three classes of carbs?
    Monosaccarides, Disaccarides, Polysaccarides
  5. Sugars are held together as dimers or polymers by...
    alpha or beta glycosidic linkages
  6. Sucrose is composed of...and bound via
    glucose and fructose, alpha linkage
  7. Lactose is composed of...and bound via...
    glucose and lactose, beta linkage
  8. Lactose intolerance is cause by...
    lack of lactase due to repression of mcm6 (lactase regulatory element) gene after weaning. Microbial metabolism creates symptoms.
  9. Lactose persistence is cause by...
    mutation in Mcm6 allows for continued lactase production.
  10. Starch is found in ______ as ________ and ______ and has _______ linkage
    Plants, amyose, amylopectin, alpha
  11. Glycogen is found in _______ . It is ________ every _______ sugars.
    animals, branched, 10 sugars
  12. Cellulose is found in _______ has ________ linkage, requires ________ for metabolism.
    plants, beta, cellulase
  13. Chitin is found in ________ has ______linkage, is digested by _________
    hard shell animals, beta, chitinase
  14. Chitin is hard when ____ is added and causes _____ when _________.
    Calcium carbonate, allergies when chitinase breaks down too much of it.
  15. Mucopolysaccarides are also called _______ and are made of ________ and _________. They are also very _________
    glucosaminoglycans (GAG), amino sugar and uronic sugar OR galactose. Polar
  16. GAG sugar subunits can be _________ or _________ and __________ or ___________ or
    N-acetylglucoseamine or N-acetylgalactosamine and glucouronic acid oriduronic acid or galactose
  17. Lipids are ________ and soluble in _________ and contain __________
    non polar, ether (organic solvents), C, O, N, phosphorus
  18. Basic units of a lipid are...
    alcohol and fatty acid
  19. What are the 4 groups of lipids?
    triglycerides, phospholipids, waxes, steriods
  20. What are triglycerides?
    glycerol + 3 fatty acids
  21. Basic structure of glycerol is...
    3 carbon alcohol, 3 OH groups
  22. basic structure of a fatty acid is...
    long hydroC chain with COOH at one end.
  23. Which end of a fatty acid is the Ω end, and which is the α end?
    COOH is alpha
  24. How does one make a triglyceride?
    link 3 fatty acids to glycerol via condensation rxn. IE the OH groups + the OH groups on the fatty acids → and ester bond R-O-R + H2O.
  25. What is the difference between a saturated and unsaturated fat?
    saturated fats are saturated with Hydrogens.
  26. What is a phospholipid?
    glycerol + 2 fatty acids + phosphate + variable group
  27. Which is more rare in nature, trans fat or cis fat?
    trans. straight is hard to metabolize
  28. Which kind of cholesterol do trans fats raise? What does this put one at risk for?
    increases LDL, risk of coronary heart disease.
  29. ______is more common in ________ while _________is more common in __________.
    phosphatidylcholine, humans, phosphatidiylethanolamine, bacteria
  30. Basic structure of a steroid...
    core 4 ring body and a variable hydroC tail.
  31. What form of lipids store energy?
    Triglycerides
  32. Name 6 biological functions of lipids and examples for them.
    Stored energy(triglyc), Cell structure(membrane), protection(lipid cushions), Chemical regulators (steroid hormones), digestion (bile salts), Insulation
  33. What are lung surfactants for?
    allows for easy expansion and contraction
  34. What is SDD or RDS?
    • Surfactant dificency disorder, Respiratory distress syndrome
    • When newborns have a difficency of dipalmitoylphosphatidylcholine, the hyaline membrane in the lungs fills the alveoli, the lungs collapse, and breathing goes to crap.
    • Treat with inhailer or O2
  35. What is an L/S ratio? What levels are normal, and what is at risk?
    lecithin sphingomyelin ratio in amniotic fluid. 2 is normal, less than 1.5 is at risk.
  36. Glycine is...
    smallest AA, found in inner collagen helix
  37. Alanine is...
    hydrophobic, membrane associated
  38. Tyrosine, Tryptophan, phenylalanine are...
    involved in neurotransmitter creation, aromatic
  39. Lysine and arginine are...
    positively charged groups, histone tables
  40. Glutamic acid, aspartic acid are...
    negatively charged, important in early embryo brain development.
  41. Proline can...
    bend and turn
  42. Cysteine forms...
    disulfide bonds → Cystine
  43. Essential amino acids are...
    Those that the body cannot synthesize.
  44. A polypeptide is _____ long.
    3 - 50 AA
  45. What is the smallest protein?
    Insulin - 51 AAs
  46. Alpha helix is held together by...
    H bonds every 4th AA.
  47. Beta pleated sheet is held together by...
    H bond between every 4th AA
  48. What is a motif? What is an example?
    A supersecondary structure. zinc finger, commonly found in TFs.
  49. Describe Alzheimer Disease molecular pathology via APP
    Amyloid Precursor protein is cleaved by the wrong secretase (beta instead of alpha) and leaves the cell where it polymerizes and forms plaues by interfereing with cell functions causing apoptosis of surrounding cells.
  50. Describe Alzheimer Disease molecular pathology via TP
    Tau Protein is hyperphosphorylated and forms aggregates, leading to degeneration of axons.
  51. Describe the molecular pathology of Parkinson disease
    alpha synuclein forms aggregates called Lewy Bodies which impair cell function and lead to neuron degradation.
  52. What are prions? Describe molecular pathology of prionic diseases.
    small infectious proteins. creates plaques in the brain tissue. Normal Protein Prion-Cellular misfolds to Protein Prion-Scrapie. Aggregates form and interfere with cell functions.
  53. What are the biological functions of proteins?
    Immediate energy, Structural (collagen most abundant), Transport, Protection, Membrane, Enzyme, !!Buffers!!
  54. What are the parts of a nucleotide?
    Ribose, nitrogenous base, phosphate
  55. Which are the purine bases?
    Adenosine and Guanine (2 rings)
  56. What are the pyrimidines?
    Thymine, Uracil and Cystosine (1 ring)
  57. What are the functions of nucleic acids?
    Genetic material, !!Enzyme!!, gene regulation
  58. Which carbons are the nitrogenous base, the reactive OH group, and phosphate group on?
    NB - 1, OH -3, Phos - 5
  59. Describe A, B and Z form DNA
    A, dehydrated, B normal, Z oppositely twisted
  60. Where do most TFs bind to on DNA?
    The major groove.
  61. What is the Central Dogma of Molecular Biology?
    DNA ↔ RNA → Protein
  62. Describe a bacterial genome.
    circular, no protein associated, smaller than eukar,
  63. Describe a prokaryotic gene
    operon, which consists of a operator, promotor, and structural genes. No introns, little noncoding DNA, fewer TFs.
  64. What is a promotor? Operator?
    where sigma factor binds, where the repressor binds to.
  65. What is a polycistronic gene?
    Only in prokaryotes, multiple genes on one mRNA transcript, transcribed all at once.
  66. Describe the human genome
    6x10^9 bp. 46 homologus pairs, linear, lots of non-coding and transpositional genes. about 20,000 protein coding genes. Associated with histones
Author
jdespain
ID
322456
Card Set
SciFom Macromolecules
Description
SciFom test 1
Updated