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A-D-Glucose I-phosphate

Glucose derivatives. a-D-Glucose i-phosphate can be prepared by the action of potato phosphorylase on starch or synthesized from acetobromo glucose and trisilver phosphate or silver diphenyl phosphate . [Pg.135]

This enzyme [EC 2.4.1.1], also called phosphorylase, catalyzes the reaction of [(l,4)-o -D-glucosyl] with orthophosphate to produce [(l,4)-o -D-glucosyl] -i and a-D-glucose 1-phosphate. The name to be used with this enzyme is dependent on the naturally occurring substrate for example, glycogen phosphorylase, starch phosphorylase, maltodextrin phosphorylase, etc. [Pg.321]

A number of hexose phosphates have been isolated from natural sources. Of these oTructose 1,6-diphosphate (Harden-Young ester) (I), D-fructose 6-phosphate (Neuberg ester) (II), D-glucose 6-phosphate (Robison ester) (III), and a-D-glucose 1-phosphate (IV) are of particular biochemical importance in the processes of fermentation and glycolysis. These hexose phosphates are interconvertible in the presence of the proper enzymes and cofactors. [Pg.179]

This enzyme [EC 2.7.1.63], also known as polyphosphate-glucose phosphotransferase, catalyzes the reaction of [phosphatejn with o-glucose to yield [phosphate] ( i) and D-glucose 6-phosphate. The enzyme requires the presence of a neutral salt (such as potassium chloride) for maximum activity. Glucosamine can also serve as a substrate. [Pg.567]

Inositol is synthesized by the same route in all cells. D-Glucose-6-phosphate (d-G-6-P) is converted to L-mvo-inositol-1 -phosphate (l-I- 1 -P), which can also be termed D-myo-inositol-3-phosphate. The L-I-l-P is then hydrolyzed to myoinositol by a relatively specific phosphatase. As we will see, enzymes that do these reactions in bacteria and archaea can have quite different characteristics from the eukaryotic enzymes. [Pg.110]

Figure 3.92 Proposed biosynthetic pathway for the kedarcidin chromophore. (a) 1-Mycarose and kedarosamine from D-glucose-1-phosphate (b) (i )-2-aza-3-chloro-p-tyrosine from 2-aza-l-phenylalanine. Figure 3.92 Proposed biosynthetic pathway for the kedarcidin chromophore. (a) 1-Mycarose and kedarosamine from D-glucose-1-phosphate (b) (i )-2-aza-3-chloro-p-tyrosine from 2-aza-l-phenylalanine.
Acetamido-2-deoxyglucose i>-form 1,3,4-Tri-Ac, 6-phosphate, A-8 2-Acetamido-2-deoxy-a-D-glucose l-(dihydrogen phosphate). A-271... [Pg.1246]


See other pages where A-D-Glucose I-phosphate is mentioned: [Pg.35]    [Pg.179]    [Pg.179]    [Pg.35]    [Pg.179]    [Pg.179]    [Pg.44]    [Pg.142]    [Pg.1154]    [Pg.1154]    [Pg.1368]    [Pg.1368]    [Pg.1351]    [Pg.1351]    [Pg.1364]    [Pg.1364]    [Pg.168]    [Pg.46]    [Pg.647]    [Pg.378]    [Pg.59]    [Pg.287]    [Pg.33]    [Pg.239]    [Pg.13]    [Pg.107]    [Pg.207]    [Pg.302]    [Pg.107]    [Pg.160]    [Pg.329]    [Pg.306]    [Pg.1423]    [Pg.217]    [Pg.250]    [Pg.29]    [Pg.221]    [Pg.1154]    [Pg.68]    [Pg.158]    [Pg.320]    [Pg.112]    [Pg.319]    [Pg.441]   
See also in sourсe #XX -- [ Pg.1006 ]




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A-D-Glucose

A-Glucose

A-glucose 1-phosphate

D Glucose 6 phosphate

Glucose 1-phosphate

Glucose-6-Phosphat

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