glyoxylate


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glyoxylate

/gly·ox·y·late/ (gli-ok´sĭ-lāt) a salt, anion, or ester of glyoxylic acid.

glyoxylate

a carbohydrate precursor.

glyoxylate pathway
a pathway for the direct incorporation of acetate into a glucose precursor; operates in plants but not identified as an animal process.
References in periodicals archive ?
DCA is dehalogenated to glyoxylate by the cytosolic zeta-1 family isoform of glutathione transferase (GSTzl), which is identical to maleylacetoacetate isomerase (MAAI), the penultimate enzyme in the phenylalanine/tyrosine catabolic pathway [see Supplemental Material, Figure 2 (doi:10.
This mixture catalyzes the glyoxylate ene reaction to give higher enantioselectivities, higher yields and a more general catalyst.
Now a group from The Scripps Research Institute has shown the plausibility of an alternative pathway to those sugars called the glyoxylate scenario, which may push the field of pre-life chemistry past the formose reaction hurdle.
2001) reported that EG decreased the ATP content of proximal tubular segments isolated from the mouse kidney via their metabolites, glyoxylate and glycoaldehyde.
Primary hyperoxaluria (PH) is a metabolic disorder caused by deficiency of either the liver-specific enzyme alanine:glyoxylate aminotransferase (AGT) for PH type 1 (PH1) or glyoxylate reductase/hydroxypyruvate dehydrogenase (GR/HPR) for PH type 2 (PH2).
coli, dubbed SBS550MG, that contains six genetic alterations that allow it to produce succinate anaerobically from two different routes--the glyoxylate pathway and the fermentation route.
tuberculosis gets its energy from a pathway called the glyoxylate shunt.
The production of formate, a substrate for methanogenesis, from compounds related with the glyoxylate cycle by mixed ruminal microbes.
Primary hyperoxaluria type 1 (PH1) [1] (OMIM 259900) is an autosomal recessive disorder of glyoxylate metabolism caused by deficiency of alanine:glyoxylate aminotransferase (AGT; EC 2.
4 AA892799 Similar to glyoxylate reductase/hydroxypyruvate reductase -3.