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26 Cards in this Set

  • Front
  • Back

Two parts to riboflavin structure

Flavin and Ribitol (sugar alcohol)

RDA for Riboflavin

M- 1.3mg/day


F- 1.1mg/day

Three forms of Riboflavin

Free form,


FMN (Flavin mononucleotide)


FAD (Flavin Adenine Dinucleotide)

FAD = _____ + _____

FMN + AMP

Enzymes involved in Riboflavin to FAD

Flavokinase


FAD Synthase

Riboflavin is only absorbed in ____ form in ____ and _____

Free


Duodenum


Jejunum

True or False: Digestion is needed for absorption of Riboflavin

True

FAD ----> FMN ----> Riboflavin enzymes

FAD Pyrophosphatase, FMN Phosphatase

Riboflavin transport features

Energy-dependent


Sodium-independent carrier mediated


Riboflavin transporters RFTs/RFVTs

Found in the basolateral membrane of enterocytes

RFVT1

Found in intracellular vesicles and basolateral membrane. Ubiquitously expressed -all tissues

RFVT2

Main transporter found in apical membrane of enterocytes

RFVT3

Group of membrane proteins include over 300 members organized in 52 families


Transport variety of substrates including glucose, minerals, AA etc.

Solute Carrier

Riboflavin transport is mediated by

Facilitated diffusion

RF, FMN, and FAD are bound to proteins like albumin, only free RF enters cells. In blood or tissues?

Blood

RF rich in liver, kidney, heart. Converted to FMN and FAD inside cells (trapped). FMN major form (60-95%). In blood or tissues?

Tissue

FMN and FAD form part of enzymes called ___ that are involved in redox reactions

Flavoproteins

FMD and FAD are ____ agents and accept e- and protons

Oxidizing

FMN/FAD = _____ form


FMNH2 or FADH2 ____ form

Oxidized


Reduced

Measure of tendency of molecule to accept e- and thereby be reduced

Redox potential

FADH2 enters the ETC at complex ___


NADH enters the ETC at complex ___


2


1

One molecule of FADH2 generates ___ ATP

2

Catalyzes the transfer of e- from NADH to coenzyme Q10. Generates 4H+ for each NADH. What form of RF is required?

Complex I, FMN

Deficiency of RF is known as

Ariboflavinosis

Symptoms of Ariboflavinosis

Inflammation of tongue, can inhibit syn. of niacin and B6 metab.

Rare neurological genetic disorder of mutation of rf transporter

Brown-Vialetto-Van Laere syndrome