Formation of sedoheptulose-7-phosphate from enzymatically obtained "active glycolic aldehyde" and ribose-5-phosphate with transketolase.
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Aldehydes↗
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Results for “HEPTOSES”
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Evidence for two forms of fructose diphosphatase.
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Chemical Phenomena↗
Characterization of 3-deoxy-D-manno-octulosonic acid as a component of the cell wall lipoglycan from Escherichia coli (2101-R).
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Cell Wall↗
Mechanism of 3-deoxy-D-arabino-heptulosonate 7-phosphate (DAHP) synthetase.
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Arabinose↗
A regulatory mutation in tyrosine biosynthesis.
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Aldehyde-Lyases↗
Stereospecificity of the 3-deoxy-D-arabino-heptulosonate 7-phosphate synthetase reaction.
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Aldehyde-Lyases↗
Affinity chromatography of a regulatory enzyme based on specific interaction with the effector.
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Aldehyde-Lyases↗
Fate of 14C-D-mannoheptulose in the rat.
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Animals↗
Charge transfer interactions in transketolase-thiamine pyrophosphate complex.
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Binding Sites↗
Calcium: cofactor of transketolase from baker's yeast.
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Binding Sites↗
A complex of functionally-bound enzymes: transketolase and glyceraldehydephosphate dehydrogenase.
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Chromatography, Ion Exchange↗
Inhibition of transketolase by analogues of the coenzyme.
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Animals↗
A circular dichroism study of transketolase from baker's yeast.
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Alcohols↗
An unusual acidic polysaccharide produced by a rough strain of Escherichia coli.
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Animals↗
Appearance of sedoheptulose 1,7-diphosphatase activity on conversion of chloroplast fructose 1,6-diphosphatase from dimer form to monomer form.
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Chloroplasts↗
On the structure of the Escherichia coli C cell wall lipopolysaccharide core and on its phiX174 receptor region.
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Cell Wall↗
Pseudomonas diminuta LPS with a new endotoxic lipid A structure.
Lipid A that contains mainly 2,3-diamino-2,3-dideoxy-D-glucose, phosphate and fatty acids in the molar ratio 2:1:5-6 was found in Pseudomonas diminuta lipopolysaccharide. The lipid A was considered to have a diamino-sugar disaccharide structure that carries a nonglycosidic phosphomonoester group and amide-bound acyloxyacyl and 3-hydroxy fatty acyl groups. The lipopolysaccharide exhibited endotoxic activities including lethal toxicity, pyrogenicity, local Shwartzman activity, body weight-decreasing toxicity and Limulus activity. The free lipid A was also endotoxic.
Animals↗
Chromatography of sugars in body fluids. II. Paper chromatographic pattern of urinary sugars in five solvents.
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Acetates↗