Chemical structure of Vitamin B12
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Vitamin B12 Deficiency

The term vitamin B12 (or B12 for short) is used in two different ways. In a broader sense it refers to a group of Co-containing compounds known as cobalamins - cyanocobalamin (an artefact formed as a result of the use of cyanide in the purification procedures), hydroxocobalamin and the two coenzyme forms of B12, methylcobalamin (MeB12) and 5-deoxyadenosylcobalamin (adenosylcobalamin - AdoB12). more...

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In a more specific way, the term B12 is used to refer to only one of these forms, cyanocobalamin, which is the principal B12 form used for foods and in nutritional supplements.

Pseudo-B12 refers to B12-like substances which are found in certain organisms, such as Spirulina spp. (blue-green algae, cyanobacteria). However, these substances do not have B12 biological activity for humans.

Structure

B12 is the most chemically complex of all the vitamins. B12's structure is based on a corrin ring, which, although similar to the porphyrin ring found in haem, chlorophyll, and cytochrome, has two of the pyrrole rings directly bonded. The central metal ion is Co (cobalt). Four of the six coordinations are provided by the corrin ring nitrogens, and a fifth by a dimethylbenzimidazole group. The sixth coordination partner varies, being a cyano group (-CN), a hydroxyl group (-OH), a methyl group (-CH₃) or a 5'-deoxyadenosyl group (here the C5' atom of the deoxyribose forms the covalent bond with Co), respectively, to yield the four B12 forms mentioned above. The covalent C-Co bond is the only carbon-metal bond known in biology. (p.32)

Synthesis

B12 cannot be made by plants or by animals, as the only type of organism that have the enzymes required for the synthesis of B12 are bacteria (eubacteria, archaebacteria).

Functions

Coenzyme B12's reactive C-Co bond participates in two types of enzyme-catalyzed reactions: (p.675)

  1. Rearrangements in which a hydrogen atom is directly transferred between two adjacent atoms with concomitant exchange of the second substituent, X, which may be a carbon atom with substituents, an oxygen atom of an alcochol, or an amine.
  2. Methyl (-CH₃) group transfers between two molecules.

In humans there are only two coenzyme B12-dependent enzymes:

  1. MUT which uses the AdoB12 form and reaction type 1 to catalyze a carbon skeleton rearrangement (the X group is -COSCoA). MUT's reaction converts MMl-CoA to Su-CoA, an important step in the extraction of energy from proteins and fats (for more see MUT's reaction mechanism)
  2. MTR, a methyl transfer enzyme, which uses the MeB12 and reaction type 2 to catalyzes the conversion of the amino acid Hcy into Met (for more see MTR's reaction mechanism).

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Oral treatment of vitamin B12 deficiency
From Nutrition Research Newsletter, 6/1/97

Vitamin [B.sub.12] deficiency is customarily treated by intramuscular injections of the vitamin. This type of therapy is expensive if the injections are administered by medical personnel, but some patients -- particularly the elderly -- may find it difficult to administer their own injections at home.

Several studies have indicated that oral treatment with large doses of vitamin [B.sub.12] may be effective in correcting vitamin B 12 deficiency. This study, conducted in Belgium, evaluated the efficacy of oral treatment in 94 elderly patients with subnormal serum vitamin [B.sub.12] levels not due to pemicious anemia. Patients of this type are believed to have difficulty absorbing protein-bound or food-bound [B.sub.12] despite normal intrinsic factor functioning. Patients were treated with 0.1 mg oral vitamin [B.sub.12] daily (10 mL of a solution of 1 mg [B.sub.12] in 100 mL water). Normalization of vitamin [B.sub.12] serum levels occurred rapidly; 69% of patients had levels within the normal range after 10 days of therapy, and 88% achieved them within one month.

These data indicate that for most older people with vitamin B 12 deficiency not due to a lack of intrinsic factor, oral vitamin [B.sub.12] supplementation is a practical, effective form of therapy.

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