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Citrulline

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citrulline [′si·trə‚lēn]
(biochemistry)
C6H13O3N3An amino acid formed in the synthesis of arginine from ornithine.

Citrulline 

(also called α-amino-δ-ureidovaleric acid), H2NCONH(CH2)3CH(NH2)COOH, a natural amino acid.

Citrulline exists in the optically active L- and D-forms and in the racemic DL-form. L-citrulline is found as a free compound in the juice of watermelons and a number of other plants, in the tubers of legumes, and in the tissues of mammals (liver, kidney, brain, muscles, and blood). Citrulline is not a component of natural proteins. Citrulline is separated from enzymatic hydrolysates of casein as a result of arginine splitting. In many organisms, citrulline participates in the ornithine cycle, in which it serves as an intermediate in the biosynthesis of arginine from ornithine. In plants, citrulline also participates in nitrogen fixation.

REFERENCES

Meister, A. Biokhimiia aminokislot. Moscow, 1961. (Translated from English.)
Lehninger, A. Biokhimiia: Molekuliarnye osnovy struktury i funktsii kletki. Moscow, 1976. (Translated from English.)


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Some of the amino acids used in these formulations include L-arginine, along with citrulline and other vitamin/mineral co-factors.
The urea cycle consists of five reactions, and citrulline is formed in the second of these.
It is biosynthesized from L-arginine and oxygen to citrulline by several nitric-oxide synthases, or NOS, enzymes and by the reduction of inorganic nitrate.
 
 
 
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