pyruvic

Pyruvic acid is sometimes applied to the skin as a facial peel.

The sweet onion's higher water content also dilutes the pyruvic acid.

It is synthesized in plants via several steps starting from pyruvic acid.

Pyruvic acid facial peels seem to be safe when applied by a healthcare professional.

It may increase the amount of lactic acid and pyruvic acid within the blood.

The substrate (carbohydrate, fat, protein) is broken down into pyruvic acid (3C).

Pyruvic acid peels for the treatment of photoaging.

The reaction is reversible so that pyruvic acid and arginine can be regenerated.

Designing carbon fixation pathways to produce pyruvic acid.

All enterics initially produce pyruvic acid from glucose metabolism.

For example, the enzyme will convert L-alanine into pyruvic acid (2-oxopropanoic acid).

The researchers then spliced in two genes from a bacteria called zymomonas, which can convert pyruvic acid into ethanol.

Enterics that subsequently metabolize pyruvic acid to other acids lower the pH of the medium to 4.2.

An increased amount of oxygen is necessary to convert the lactic acid back to pyruvic acid at these locations.

Other names in common use include pyruvic oxidase, and phosphate-dependent pyruvate oxidase.

Final products of the reaction are indole, pyruvic acid, ammonia (NH) and energy.

It is also called 2-oxo-acid carboxylase, alpha-ketoacid carboxylase, and pyruvic decarboxylase.

Blame pyruvic acid.

Some people apply pyruvic acid, a liquid form of pyruvate, to the skin to reduce wrinkles and other signs of aging.

Grant in 1944 for research on the respiratory enzymes and the mechanism of the biological oxidation of pyruvic acid.

In plants and microorganisms, leucine is synthesised from pyruvic acid by a series of enzymes:

Phenylpyruvic acid is a pyruvic acid derivative.

Bromopyruvic acid, or bromopyruvate, is a synthetic brominated derivative of pyruvic acid.

Found in the form of pyruvic acid, pyruvate can be found in various foods including red apples, cheese, and red wine.

The Doebner reaction is the chemical reaction of an aniline with an aldehyde and pyruvic acid to form quinoline-4-carboxylic acids.