lactoflavine - traduzione in francese
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lactoflavine - traduzione in francese

CHEMICAL COMPOUND
Vitamin B2; Vitamin G; Vitamin B2 Deficiency; Riboflavin phosphate sodium; Ariboflavinosis; Vitamin B-2; Riboflavin deficiency; Riboflavin metabolism; Lactoflavin; Riboflavins; Vitamin B2 deficiency; Riboflavin biosynthesis; Vitamin B₂; C17H20N4O6; ATC code A11HA04; ATCvet code QA11HA04; List of foods containing Vitamin G; Aqua-Flave; Beflavin; Beflavine; Bisulase; Dermadram; Fiboflavin; Flavaxin; Flavin Bb; Flaxain; HSDB 817; Hyflavin; Hyre; Lactobene; Ovoflavin; Ribipca; Ribocrisina; Riboderm; Ribosyn; Ribotone; Ribovel; Vitaflavine; Vitasan B2; E101 (E number)
  • Riboflavin is the biosynthetic precursor of FMN and FAD
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  • Cultures of ''Micrococcus luteus'' growing on pyridine (left) and succinic acid (right). The pyridine culture has turned yellow from the accumulation of riboflavin.<ref name="Sims1992"/>
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lactoflavine      
n. lactoflavin, yellowish-orange crystalline compound essential to proper nutrition (found in meat, eggs, and dark green vegetables), riboflavin, vitamin B2

Definizione

riboflavin
Riboflavin is a vitamin that occurs in green vegetables, milk, fish, eggs, liver, and kidney.
N-UNCOUNT

Wikipedia

Riboflavin

Riboflavin, also known as vitamin B2, is a vitamin found in food and sold as a dietary supplement. It is essential to the formation of two major coenzymes, flavin mononucleotide and flavin adenine dinucleotide. These coenzymes are involved in energy metabolism, cellular respiration, and antibody production, as well as normal growth and development. The coenzymes are also required for the metabolism of niacin, vitamin B6, and folate. Riboflavin is prescribed to treat corneal thinning, and taken orally, may reduce the incidence of migraine headaches in adults.

Riboflavin deficiency is rare and is usually accompanied by deficiencies of other vitamins and nutrients. It may be prevented or treated by oral supplements or by injections. As a water-soluble vitamin, any riboflavin consumed in excess of nutritional requirements is not stored; it is either not absorbed or is absorbed and quickly excreted in urine, causing the urine to have a bright yellow tint. Natural sources of riboflavin include meat, fish and fowl, eggs, dairy products, green vegetables, mushrooms, and almonds. Some countries require its addition to grains.

Riboflavin was discovered in 1920, isolated in 1933, and first synthesized in 1935. In its purified, solid form, it is a water-soluble yellow-orange crystalline powder. In addition to its function as a vitamin, it is used as a food coloring agent. Biosynthesis takes place in bacteria, fungi and plants, but not animals. Industrial synthesis of riboflavin was initially achieved using a chemical process, but current commercial manufacturing relies on fermentation methods using strains of fungi and genetically modified bacteria.