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Branched-chain amino

Herbicides also inhibit 5- (9/-pymvylshikiniate synthase, a susceptible en2yme in the pathway to the aromatic amino acids, phenylalanine, tyrosine and tryptophan, and to the phenylpropanes. Acetolactate synthase, or acetohydroxy acid synthase, a key en2yme in the synthesis of the branched-chain amino acids isoleucine and valine, is also sensitive to some herbicides. Glyphosate (26), the sulfonylureas (136), and the imida2oles (137) all inhibit specific en2ymes in amino acid synthesis pathways. [Pg.45]

In the case of hyperphenylalaninaemia, which occurs ia phenylketonuria because of a congenital absence of phenylalanine hydroxylase, the observed phenylalanine inhibition of proteia synthesis may result from competition between T.-phenylalanine and L-methionine for methionyl-/RNA. Patients sufferiag from maple symp urine disease, an inborn lack of branched chain oxo acid decarboxylase, are mentally retarded unless the condition is treated early enough. It is possible that the high level of branched-chain amino acids inhibits uptake of L-tryptophan and L-tyrosiae iato the brain. Brain iajury of mice within ten days after thek bkth was reported as a result of hypodermic kijections of monosodium glutamate (MSG) (0.5—4 g/kg). However, the FDA concluded that MSG is a safe kigredient, because mice are bom with underdeveloped brains regardless of MSG kijections (106). [Pg.283]

In Parenteral and Enteral Nutrition. Amino acid transfusion has been widely used since early times to maintain basic nitrogen metaboHsm when proteinaceous food caimot be eaten. It was very difficult to prepare a pyrogen-free transfusion from protein hydrolysates. Since the advances in L-amino acid production, the crystalline L-amino acids have been used and the problem of pyrogen in transfusion has been solved. The formulation of amino acid transfusion has been extensively investigated, and a solution or mixture in which the ratio between essential and nonessential amino acid is 1 1, has been widespread clinically. Special amino acid mixtures (eg, branched chain amino acids-enriched solution) have been developed for the treatment of several diseases (93). [Pg.296]

J. Stetter (ed.), Herbicides Inhibiting Branched Chain Amino Acids Biosynthesis. Recent Development [Chemistry of Plant Protection, Vol. 10], Springer-Verlag, Berlin, 1994. [Pg.277]

Condensation of a series of methyl glycopyranosiduloses with nitromethane provides isomeric nitroaldol adducts, precursors of branched-chain amino sugars30. The isomers are separable by chromatography. [Pg.634]

THE INITIAL REACTIONS ARE COMMON TO ALL THREE BRANCHED-CHAIN AMINO ACIDS... [Pg.259]

METABOLIC DISORDERS OF BRANCHED-CHAIN AMINO ACID CATABOLISM... [Pg.259]

The catabolism of leucine, valine, and isoleucine presents many analogies to fatty acid catabolism. Metabolic disorders of branched-chain amino acid catabolism include hypervalinemia, maple syrup urine disease, intermittent branched-chain ketonuria, isovaleric acidemia, and methylmalonic aciduria. [Pg.262]

Skeletal muscle is the principal site of metabolism of branched-chain amino acids, which are used as an energy source. [Pg.576]

BCAA branched-chain amino acids DHA docosahexenoic acid... [Pg.1527]

The analysis of extraterrestrial matter is concentrated on the detection of nucleic acid and protein building blocks, i.e., N-heterocycles and amino acids. The search for such compounds began immediately after the fall of the Murchison meteorite. Twenty-two amino acids were detected in it as early as 1974 eight of them pro-teinogenic, ten which hardly ever occurred in biological material, and four which were unknown in the biosphere. Up to now, about 70 amino acids have been identified (Cronin, 1998), the most common being glycine and a-aminoisobutyric acid. The latter is a branched-chain amino acid with the smallest possible number of carbon atoms. The most frequently found amino acids occur in concentrations of... [Pg.69]

Singh BK, Shaner DL (1992) Carbon flow through branched-chain amino acid biosynthetic pathway lessons from acetohydroxy acid synthase inhibitors. In Singh BK, Flores HE, Shannon JC (eds) Biosynthesis and molecular regulation of amino acids in plants. American Society of Plant Physiologists, Maryland, p 354... [Pg.236]

Volume 166. Branched-Chain Amino Acids Edited by Robert Harris and John R. Sokatch... [Pg.22]

Volume 324. Branched-Chain Amino Acids (Part B)... [Pg.31]

Similar to the work described by Spohn et al. [34], a trienzyme sensor was developed recently for the determination of branched-chain amino acids (L-valine, L-leucine, and L-isoleucine). Leucine dehydrogenase, NADH oxidase, and peroxidase were coimmobilized covalently on tresylate-hydrophylic vinyl polymer beads and packed into a transparent PILL tube (20 cm X 1.0 id), which was used as flow cell. The sensor was free of interferences from protein and NH4+ and it was stable for 2 weeks. The sensor system was applied to the determination of branched-chain amino acids in plasma with recoveries ranging from 98 to 100% [36],... [Pg.577]

Maple syrup urine disease involves a congenital failure to oxidize the three branched-chain amino acids 671... [Pg.667]

Effective treatment of maple syrup urine disease involves the restriction of dietary branched-chain amino acids 672... [Pg.667]

Branched-chain Defective branched-chain Coma, convulsions, vomiting, respiratoryfailure Diet low in branched-chain amino... [Pg.668]

Many organic acidurias originate in the breakdown of the three branched-chain amino acids, leucine, isoleucine and valine (Fig. 40-1). Metabolism of the organic acids requires the presence of specific enzymes, congenital... [Pg.669]

Effective treatment of maple syrup urine disease involves the restriction of dietary branched-chain amino acids. Long-term treatment entails the dietary restriction of the BCAAs. This is accomplished by administration of a special formula from which these amino acids are removed. The outlook for intellectual development is favorable in youngsters in whom diagnosis is made early and who do not suffer recurrent, severe episodes of metabolic decompensation [17]. [Pg.672]

Elimination reactions (Figure 5.7) often result in the formation of carbon-carbon double bonds, isomerizations involve intramolecular shifts of hydrogen atoms to change the position of a double bond, as in the aldose-ketose isomerization involving an enediolate anion intermediate, while rearrangements break and reform carbon-carbon bonds, as illustrated for the side-chain displacement involved in the biosynthesis of the branched chain amino acids valine and isoleucine. Finally, we have reactions that involve generation of resonance-stabilized nucleophilic carbanions (enolate anions), followed by their addition to an electrophilic carbon (such as the carbonyl carbon atoms... [Pg.83]

Humans have a limited capacity to synthesize amino acids de novo, but extensive interconversions can occur. Those amino acids which cannot be formed within the body and must be supplied by the diet are called essential . Members of this group, which includes the branched chain amino acids leucine and valine, and also methionine and phenylalanine, are all dietary requirements. Such essential amino acids may be chemically converted, mainly in the liver, into the non-essential amino acids. The term non-essential does not equate with not biochemically important but simply means they are not strict dietary components. [Pg.172]

Transaminase enzymes (also called aminotransferases) specifically use 2-oxoglutarate as the amino group acceptor to generate glutamate but some have a wide specificity with respect to the amino donor. For example, the three branched-chain amino acids leucine, isoleucine and valine, all serve as substrates for the same enzyme, branched-chain amino acid transaminase, BCAAT ... [Pg.255]

In a muscle at rest, most of the 2-oxo acids produced from transamination of branched chain amino acids are transported to the liver and become subject to oxidation in reactions catalysed by branched-chain 2-oxo acid dehydrogenase complex. During periods of exercise, however, the skeletal muscle itself is able to utilize the oxo-acids by conversion into either acetyl-CoA (leucine and isoleucine) or succinyl-CoA (valine and isoleucine). [Pg.255]

Debono, M. and Molloy, R.M., Isolation and structure of the novel branched-chain amino sugar derived from antibiotic A35512B, J. Org. Chem., 45, 4685, 1980. [Pg.162]


See other pages where Branched-chain amino is mentioned: [Pg.156]    [Pg.157]    [Pg.45]    [Pg.45]    [Pg.282]    [Pg.608]    [Pg.176]    [Pg.1518]    [Pg.215]    [Pg.231]    [Pg.269]    [Pg.669]    [Pg.671]    [Pg.207]    [Pg.294]    [Pg.140]    [Pg.258]    [Pg.223]   
See also in sourсe #XX -- [ Pg.8 , Pg.29 ]




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Alanine and the Branched-Chain Amino Acids

Amino acid branched-chain synthesis

Amino acid branched-chain, degradation

Amino acids branch-chained

Amino acids branched chain

Branch-chained amino acids chemical structure

Branch-chained amino acids function

Branch-chained amino acids metabolic functions

Branch-chained amino acids oxidation

Branch-chained amino acids transamination

Branched Chain Amino Acid Biosynthesis

Branched chain

Branched chain amino acid disorders

Branched chain amino acid glutamate

Branched chain amino acid glutamate transaminase

Branched chain amino acids, catabolism

Branched chain amino acids, catabolism disorders

Branched-chain amino acid aminotransferase

Branched-chain amino acid metabolism

Branched-chain amino acid transaminase

Branched-chain amino acids accumulation

Branched-chain amino acids chemical structure

Branched-chain amino acids muscle metabolism

Branched-chain amino acids oxidation

Branched-chain amino aciduria

Branched-chain amino adds

Chain branching

Disorders of Branched-Chain Amino Acid Metabolism

Hepatic encephalopathy branched-chain amino acids

Isoleucine branched-chain amino acid

Isotopically labeled branched-chain amino acid

Metabolism amino acid, branched-chain, enzyme

Sugars branched-chain amino

Sugars branched-chain amino, preparation

The Aliphatic Branched-Chain Amino Acids

Thiamin branched chain amino acids

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