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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
20
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pubmed:dateCreated |
1991-7-2
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pubmed:abstractText |
A number of phosphorylated aminosugars have been prepared and tested as substrates for metabolic reactions. 6-Aminoglucose is a slow substrate for yeast hexokinase with a Vmax that is only 0.012% that for glucose. While Vmax is pH independent, V/K decreases below the pK of 9.0 of the amino group. 6-Aminoglucose is a competitive inhibitor vs glucose with a Ki value increasing below the pK of 9 but leveling off at 33 mM below pH 7.16. Thus, protonation decreases binding affinity by 2.4 kcal/mol and only the neutral amine is catalytically competent. 6-Aminoglucose-6-P was synthesized enzymatically with hexokinase. Its pK's determined by 31P NMR were 2.46 and 8.02 (alpha anomer) and 2.34 and 7.85 (beta anomer), with a beta:alpha ratio of 3.0. It is most stable at pH 12 (half-life 228 h at 22 degrees C), while as a monoanion its half-life is 3 h. The free energy of hydrolysis at 25 degrees C and pH 9.25 is -10.3 kcal/mol. The phosphorylated amino analogues of 6-P-gluconate, ribulose-5-P, fructose-6-P, fructose-1,6-bis-P (amino group at C-6 only), and glyceraldehyde-3-P were synthesized enzymatically. The 31P NMR chemical shifts of these analogues are 8-8.5 ppm at pH 9.5. Their relative stability is 6-aminogluconate-6-P greater than 3-aminoglyceraldehyde-3-P greater than 6-aminoglucose-6-P greater than 6-aminofructose-1,6-bis-P congruent to 6-aminofructose-6-P greater than 5-aminoribulose-5-P. These analogues were tested as substrates for their respective enzymes.(ABSTRACT TRUNCATED AT 250 WORDS)
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Alkaline Phosphatase,
http://linkedlifedata.com/resource/pubmed/chemical/Amino Sugars,
http://linkedlifedata.com/resource/pubmed/chemical/Glucose-6-Phosphate Isomerase,
http://linkedlifedata.com/resource/pubmed/chemical/Glucosephosphate Dehydrogenase,
http://linkedlifedata.com/resource/pubmed/chemical/Hexokinase,
http://linkedlifedata.com/resource/pubmed/chemical/Indicators and Reagents,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphofructokinase-1,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphoglucomutase,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphogluconate Dehydrogenase,
http://linkedlifedata.com/resource/pubmed/chemical/Sugar Phosphates
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0006-2960
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
21
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pubmed:volume |
30
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4978-84
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:1827991-Alkaline Phosphatase,
pubmed-meshheading:1827991-Amino Sugars,
pubmed-meshheading:1827991-Glucose-6-Phosphate Isomerase,
pubmed-meshheading:1827991-Glucosephosphate Dehydrogenase,
pubmed-meshheading:1827991-Hexokinase,
pubmed-meshheading:1827991-Indicators and Reagents,
pubmed-meshheading:1827991-Kinetics,
pubmed-meshheading:1827991-Magnetic Resonance Spectroscopy,
pubmed-meshheading:1827991-Mathematics,
pubmed-meshheading:1827991-Phosphofructokinase-1,
pubmed-meshheading:1827991-Phosphoglucomutase,
pubmed-meshheading:1827991-Phosphogluconate Dehydrogenase,
pubmed-meshheading:1827991-Substrate Specificity,
pubmed-meshheading:1827991-Sugar Phosphates,
pubmed-meshheading:1827991-Thermodynamics
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pubmed:year |
1991
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pubmed:articleTitle |
Phosphorylated aminosugars: synthesis, properties, and reactivity in enzymatic reactions.
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pubmed:affiliation |
Institute for Enzyme Research, University of Wisconsin, Madison 53705.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.
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