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OH • AMP

The Sephadex was soaked for 2k hours in the experimental solvent, and the fines decanted before being packed in the columns by pumping the swollen gel from a packing reservoir with the chromatographic eluent at 2 ml/min. Calibration standards of each of the Br AMP, OH-AMP and NH2 AMP derivatives were obtained. Solutions of each were made up in the experimental buffer, at concentrations between 50 and 150 ppm, and chromatographed. The calibration curves are shown in Figure 2. [Pg.298]

Figure 4. Recovery experiments for OH AMP at 110, 50, and 20 ppm in the absence (-----) and presence (-----) of polymeric dyes (1 g/dL) (ordinate absorb-... Figure 4. Recovery experiments for OH AMP at 110, 50, and 20 ppm in the absence (-----) and presence (-----) of polymeric dyes (1 g/dL) (ordinate absorb-...
Nucleotides are phosphoric acid esters of nucleosides Those derived from adenosine of which adenosine 5 monophosphate (AMP) is but one example are especially promi nent AMP is a weak diprotic acid with s for ionization of 3 8 and 6 2 respectively In aqueous solution at pH 7 both OH groups of the P(0)(0H)2 unit are ionized... [Pg.1160]

Plasmid Vectors for Facile Introduction of Passenger DNA and Selection of Recombinants. The map of a commonly used plasmid vector, pUC19 (7), is shown in Figure 2. Three parts of the vector are key to its utility. The origin sequence, oh, allows the repHcation of plasmid DNA in high copy number relative to the chromosome. A gene, amp, encoding the enzyme beta-lactamase, which hydrolyzes penicillin compounds, allows... [Pg.229]

In a nickel-cadmium battery (Nicad), cadmium is oxidized to Cd(OH)2 at the anode, while Ni203 is reduced to Ni(OH)2 at the cathode. A portable CD player uses 0.175 amp of current. How many grams of Cd and Ni203 are consumed when the CD player is used for an hour and a half ... [Pg.510]

Amp K. Chandra, Tyre Technology—Recent Advances and Future Trends, (Paper no. 40) presented at the Fall 170th Technical Meeting of the Rubber Division, American Chemical Society, Cincinnati, OH, 10-12 October, 2006. [Pg.933]

A similar reaction mechanism was proposed by Chin et al. [32] for the hydrolysis of the biological phosphate monoester adenosine monophosphate (AMP) by the complex [(trpn) Co (OH2)]2+ [trpn = tris(ami-nopropyl)amine]. Rapid cleavage is observed only in the presence of 2 equiv metal complex. It is evident from 31P NMR spectra that on coordination of 1 equiv (trpn)Co to AMP a stable four-membered chelate complex 4 is formed. The second (trpn)Co molecule may bind to another oxygen atom of the substrate (formation of 5) and provide a Co-OH nucleophile which replaces the alkoxy group. The half-life of AMP in 5 is about 1 h at pD 5 and 25 °C. [Pg.219]

Fig. 9. The transacetylase ribozyme. A Secondary structure of the clone 11 transacylase ribozyme based on the Zuker RNA folding algorithm Mfold. The oligonucleotide substrate is shaded in gray. The 2 -OH group of cytosine 147 (arrow) is the site of modification of the oligonucleotide substrate. B Reaction catalyzed by the clone 11 transacylase ribozyme. Note that the equilibrium of the reaction lies strongly on the side of the Bio-Phe-AMP substrate... Fig. 9. The transacetylase ribozyme. A Secondary structure of the clone 11 transacylase ribozyme based on the Zuker RNA folding algorithm Mfold. The oligonucleotide substrate is shaded in gray. The 2 -OH group of cytosine 147 (arrow) is the site of modification of the oligonucleotide substrate. B Reaction catalyzed by the clone 11 transacylase ribozyme. Note that the equilibrium of the reaction lies strongly on the side of the Bio-Phe-AMP substrate...
Lee YS, Kim WS, Kim KH, Yoon MJ, Cho HJ, Shen Y, Ye JM, Lee CH, Oh WK, Kim CT, Hohnen-Behrens C, Gosby A, Kraegen EW, James DE, Kim JB. (2006) Berberine, a natural plant product, activates AMP-activated protein kinase with beneficial metabolic effects in diabetic and insulin-resistance states. Diabetes 55 2256-2264. [Pg.585]

In our synthesis (57) of the arsonomethyl analogue of AMP, we developed a method (Fig. 12) for converting an alcohol, R—CH2—OH, into the arsonomethyl analogue, R—CH2—CH2—As03H2, of its phosphate, R—CH2— —P03H2. In this pathway the Meyer reaction is used on a 2-halocarboxylic acid, so that the reactant will be soluble in aqueous... [Pg.213]

Attack at the /3 phosphate of ATP displaces AMP and transfers a pyrophosphoiyl (not pyrophosphate) group to the attacking nucleophile (Pig. 13-10b). For example, the formation of 5 -phosphoribosyl-1-pyrophosphate (p. XXX), a key intermediate in nucleotide synthesis, results from attack of an —OH of the ribose on the /3 phosphate. [Pg.502]


See other pages where OH • AMP is mentioned: [Pg.298]    [Pg.298]    [Pg.299]    [Pg.301]    [Pg.302]    [Pg.203]    [Pg.504]    [Pg.398]    [Pg.421]    [Pg.1050]    [Pg.1090]    [Pg.609]    [Pg.33]    [Pg.1032]    [Pg.534]    [Pg.534]    [Pg.37]    [Pg.133]    [Pg.1050]    [Pg.1090]    [Pg.335]    [Pg.6]    [Pg.6]    [Pg.333]    [Pg.381]    [Pg.384]    [Pg.99]    [Pg.934]    [Pg.288]    [Pg.298]    [Pg.298]    [Pg.299]    [Pg.301]    [Pg.302]    [Pg.12]    [Pg.236]    [Pg.155]    [Pg.353]    [Pg.384]    [Pg.388]    [Pg.398]    [Pg.117]    [Pg.246]    [Pg.282]    [Pg.535]    [Pg.565]    [Pg.676]    [Pg.246]    [Pg.22]    [Pg.131]    [Pg.330]    [Pg.201]    [Pg.576]   
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5 -AMP

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