and dicarboxylate metabolism 16 i 0.
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.
However, quantification of anaplerotic reactions and glyoxylate
shunt on the growth of C.
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
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
The production of formate, a substrate for methanogenesis, from compounds related with the glyoxylate
cycle by mixed ruminal microbes.
Primary hyperoxaluria type 1 (PH1)  (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.