BIOL302 Class 17 Flashcards

1
Q

nitrogenous bases

A
  • pyrimidine
  • purine
  • both are weakly basic
  • both are flat/planar molecules (useful to form hydrogen bonds between bases & provides a 3D structure)
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2
Q

Purines

A

Adenine & Guanine

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3
Q

Pyrimidines

A

Cytosine, Uracil, Thymine

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4
Q

Nucleic Acid Polymers

A

DNA: ATG
RNA: UGC
5 prime to 3 prime

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5
Q

nucleosides are building blocks for numerous biological molecules

A

examples such as cyclic AMP & cGMP are important signaling molecules

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6
Q

NTPS (not just ATP)

A

Important sources of energy for enzymatic catalysis in metabolism (energizing compounds for chemical transfers)

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7
Q

AMP

A

a structural component of important coenzymes like NAD(P), coenzyme A, and FAD

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8
Q

cAMP/cGMP and GTP

A

are important metabolic regulators and signaling molecules (PKA, G-Proteins, etc)

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9
Q

metabolic requirements for nucleotides are met by

A

1) recycling/salvage pathways
2) dietary intake
3) de novo synthesis from pre-existing metabolites

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10
Q

metabolic fates of dietary nitrogenous bases overlaps with salvage pathways of bases during normal “tunover”

A
  • free bases and 5-P-Ribose can be used to rebuild NTPS (salvage pathways)
  • Ribose-P can be synthesized from glucose via Pentose Phosphate Pathway
  • there is a constant and rapid turn-over of nucleic acids in a cell, so salvage is essential
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11
Q

PRPP Kinase

A
  • ADP and GDP are negative regulators (PRPP is the limiting substrate in purine synthesis)
  • NOT the commitment step since PRPP has multiple metabolic fates (such as the salvage pathway)
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12
Q

where does Ribose-5-Phosphate come from? under what conditions would this sugar become available?

A
  • comes from Pentose Phosphate pathway
  • becomes available when there’s a high energy demand & when RNA and DNA need to be made
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13
Q

Purine Biosynthesis

A
  • step by step building of the base onto the activated ribose PRPP
  • the eventual cyclization yields Inosine monophosphate (IMP) which is the direct precursor to both AMP and GMP
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14
Q

committed step for purine biosynthesis

A

Gln-PRPP Amidotransferase

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15
Q

why does it make sense for AMP and GMP to be negative regulators?

A

They’re the end products **

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16
Q

once inosine is made it is converted to GMP and AMP

A
  • if you dont have sufficient AMP you cant make GMP, if you dont have sufficient GMP you cant make AMP
17
Q

what do amino acids provide to nucleotide synthesis?

A

nitrogens

18
Q

uric acid

A

anything causing a build up of uric acid concentration in blood or urine past its solubility in these liquids can lead to its precipitation

19
Q

gout

A

painful accumulation of uric acid crystal needles
- clogs arteries, especially at the joints

20
Q

inhibition of xanthine oxidase by allopurinol

A

prevents uric acid production and allows for xanthine and hypoxanthine to be excreted instead

21
Q

purine salvage

A

purines are a major metabolic investment so salvage pathways collect free adenine, hypoxanthine, and guanine bases and convert them back to useful forms (nucleotides) via PRPP

22
Q

HGPRT is essential for the purine salvage pathways

A
  • disruption of the enzyme by heritable mutation causes lesch-nyhan syndrome (a sex-linked trait since HGPRT is on the x)
  • results in build up of uric acid –> gouty arthritis, severe mental retardation and/or behavioral abnormalities at worse
23
Q

pyrimidine biosynthesis

A
  • unlike purines, the pyrimidine ring is assembled first, and then added to PRPP as a unit
  • initial step uses CPSII to make carbamoyl phosphate; built from HCO3- and amide from glutamine
  • end-product regulation targets CPSII
  • synthesis is essentially coupling of carbamoyl-P to Aspartate, followed by cyclization and transfer to PRPP
24
Q

Tetrahydrofolate

A

the methyl carrier for methylation of dUMP by thymidylate synthase

25
Q

folate deficiency

A

can cause anemia in adults and insufficiency during pregnancy that can lead to birth defects like Spina Bifida (failure to close neural tube)