Results 41 to 50 of about 2,114,876 (117)
Direct reaction of [Zn(OH)(L)]+, L =cis,cis-1,3,5-tris[(E,E)-3-(2-furyl)acrylideneamino]cyclohexane, with methanol gives a mixture of the starting material and [Zn(OMe)(L)]+; structural analysis of the complexes shows that they are models of reactive ...
Cronin, L., Walton, P.H.
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The isoxazoline obtained by 1,3-dipolar cycloaddition of 2,2-diethoxyacetonitrile N-oxide to furan was converted into enantiomerically pure (-)-(3aS,5S,6S,6aR)- and (+)-(3aR,5R,6R,6aS)-3a,5,6,6a-tetrahydro-5,6-isopropylidenedioxyfuro [2,3-d]isoxazole-3 ...
Vogel, P., Schaller, C., Jager, V.
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Malic acid is a potential biomass-derivable "building block" for chemical synthesis. Since wild-type Saccharomyces cerevisiae strains produce only low levels of malate, metabolic engineering is required to achieve efficient malate production with this ...
Van Maris, A.J.A. (author) +23 more
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L-mandelate dehydrogenase from Rhodotorula graminis:comparisons with the L-lactate dehydrogenase (flavocytochrome b2) from Saccharomyces cerevisiae [PDF]
L-Lactate dehydrogenase (L-LDH) from Saccharomyces cerevisiae and L-mandelate dehydrogenase (L-MDH) from Rhodotorula graminis are both flavocytochromes b2. The kinetic properties of these enzymes have been compared using steady-state kinetic methods. The
Reid, Graeme A +4 more
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Teleological role of L-2-hydroxyglutarate dehydrogenase in the kidney [PDF]
L-2-hydroxyglutarate (L-2HG) is an oncometabolite found elevated in renal tumors. However, this molecule might have physiological roles that extend beyond its association with cancer, as L-2HG levels are elevated in response to hypoxia and during ...
Tennessen, Jason M. +17 more
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Regulation of 3β-Hydroxysteroid Dehydrogenase/∆5-∆4 Isomerase: A Review
This review focuses on the expression and regulation of 3β-hydroxysteroi ddehydrogenase/Δ5-Δ4 isomerase (3β-HSD), with emphasis on the porcine version. 3β-HSD is often associated with steroidogenesis, but its function in the metabolism of both steroids ...
Martin Krøyer Rasmussen +7 more
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l-2-hydroxyglutaric aciduria (l-2-HGA) is a rare inherited autosomal recessive neurometabolic disorder caused by mutations in the gene encoding l-2-hydroxyglutarate dehydrogenase.
Hahn, Andreas +59 more
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We identified the non-phosphorylated l-rhamnose metabolic pathway (Rha_NMP) genes that are homologous to those in the thermoacidophilic archaeon Thermoplasma acidophilum in the genome of the thermoacidophilic bacterium Sulfobacillus thermosulfidooxidans.
Bae, J, Kim, SM, Lee, SB
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Yue-Long Xu,1 Yuan-Yuan Hu,2 Ji-Wei Li,1 Lan Zhou,3 Li Li,1 Yu-Ming Niu21Department of Neurology, Linyi Central Hospital, Linyi 276400, Shandong Province, People’s Republic of China; 2Department of Stomatology and Center for Evidence-Based Medicine
Zhou L +5 more
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6-Phosphogluconate dehydrogenase (6PGDH) converts 6PG to ribulose 5-phosphate and concomitantly provides NADPH, inside the pentose phosphate pathway. Its presence has been shown essential for growth of bloodstream form Trypanosoma brucei, a parasite ...
Montin, Katy
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