biotin and pantothenic acid Flashcards

(34 cards)

1
Q

study reminder

A

be able to recognize biotin structure on an exam

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2
Q

what is free-biotin called

what is protein-bound biotin called

A
  • biotin

- biocytin

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3
Q

biotin and raw egg diet

A

avidin binds biotin tightly, causing a deficiency leading to symptoms

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4
Q

biotin is bound to ____ in foods

A

protein

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5
Q

what is the name of the enzyme that cleaves biocytin to biotin plus lysine

A

biotinidase

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6
Q

where does the cleavage and absorption of biotin occur?

A

intestine

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7
Q

what inhibits biotin absorption

A

avidin

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8
Q

what are the metabolic functions or biotin

A
  • functions as part of coenzyme for carboxylases
  • serves as CO2 donor to substrates
  • CO2 fixation reactions
  • 4 unique enzymes that depend on biotin..all involved in macronutrient and energy metabolism
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9
Q

list the 4 biotin dependent enzymes

A
  1. pyruvate carboxylase
  2. acetyl CoA carboxylase
  3. propionyl CoA carboxylase
  4. 3-methylcrotonyl CoA carboxylase

see OH for pathways
these all end in carboxylase so only need to remember first part

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10
Q

what is the biotin dependent enzyme pyruvate carboxylase used in

A
  • glucose metabolism
  • important step for gluconeogenesis
  • regenerates OAA for gluconeogenesis
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11
Q

what is the biotin dependent enzyme acetyl CoA carboxylase used for

A

FA synthesis

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12
Q

what is the biotin dependent enzyme propionyl CoA carboxylase used for

A

-source of energy; entry into TCA

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13
Q

what is the biotin dependent enzyme 3-methlycrotonyl used for

A

-AA metabolism; leucine degradation

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14
Q

what is the general term used to describe biotin-dependent enzymes

A

holocarboxylase

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15
Q

with all co-enzymes, there must be attachment to the enzyme. What is needed to attach biotin to the lysine residue of the enzyme

A

holocarboxylase synthase

once biotin is attached to the enzyme, the enzyme is classified as a holocarboxylase

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16
Q

how could a biotin deficiency occur

A
  • decreased intake
    • -> TPN solutions without biotin: bypass the gut and go right into blood
  • dec absorption (Avidib)
  • deficiency in key enzymes (genetic defects)
17
Q

egg white injury disease

A

once biotin-avidin complex forms, it is irreversible, and excreted in feces, preventing absorption

this causes deficiencies in animals (depression hallucinations, muscle pain, dermatitis)

18
Q

what happens to avidin when it is cooked

A

it is denatured and the affinity for biotin is therefore destroyed

19
Q

what are symptoms of biotin deficiency

A

neurological problems (depression, lethargy, hallucinations, paresthesia of extremeties)
thinning of hair
rash

20
Q

holocarboxylase synthase

A

attaches biotin to lysine of caboxylase enzymes

21
Q

holocarboxylase synthase deficiency

A

in children=immunodeficiency diseases

22
Q

biochemical results of biotin deficiency

A
  • dec in biotin-dependent enzymes
    • dec gluconeogenesis
    • inc pyruvate and lactate
    • less glucose produced
  • dec Acetyl CoA carboxylase
    • build up of acetyl CoA…risk of ketosis
    • impaired serum lipids
23
Q

biotin food sources

A
  • liver
  • whole grain cereals
  • nuts legumes, peanut butter
  • low in fruits and vegetables
24
Q

bacterial synthesis of biotin

A

biotin can be synthesized by intestinal bacteria

25
what affects biotin requirement
- large amounts of raw egg white - biotinidase deficiency (genetic) - drug interactions, anticonvulsants, biotin depletion - pregnancy
26
what are the two major coenzymes of pantothenic acid
Coenzyme A (CoA) Acyl Carrier Protein (ACP) both contains SH (thiol) group, which is where the actions of reactions happens
27
what is CoA synthesized from
pantothenic acid cysteine ATP
28
metabolic role of CoA
- transfer of Acetyl groups (2C) - connect to SH groups - central nutrient metbolism - many anabolic and catabolic fates
29
list 5 examples of CoA transferring acetyl groups
1. oxidative carboxylation - pyruvate-->acetyl CoA 2. FA oxidation - complete degradation of acetyl CoA 3. ketone body formation 4. other carboxylic reactions - AA catabolism 5. synthetic reactions - cholesterol synthesis
30
Acyl carrier protein (ACP)
another coenzyme form of pantothenic acid, also has a reactive SH group from cysteine
31
metabolic role of ACP (acyl carrier protein)
- FA synthesis - is an enzyme complex - pantothenic acid is a prosthetic group of ACP - ACP serves as chaperone for FA synthesis
32
Pantothenic acid deficiency
rare (since it is widespread in food) - ->pant=greek for every/all - burning feet syndrome!*
33
what is burning feed syndrome and what deficiency is it caused by
pain in toes and soles of feet common in: WWII prisoners of war poorly nourished in the Far East
34
what other uses does pantothenic acid serve
wound treatment -oral and topical (in rate) cholesterol-lowering