Phosphorylations, enzymic methods,

Simple procedures for the preparation of NMN+ by chemical or enzymic methods have been reported and although the phosphorylating agent metaphosphoric acid used in the chemical phosphorylation of nicotinamide 2, 3 -0-isopropylidene ribofuranoside is relatively imsophisticated, the synthesis can be carried out on a large scale with moderate yields. The stereo-... 

The most widely used and best developed enzyme-catalyzed phosphorylations are the ones that are coupled to ATP regeneration systems. Sugar phosphates, nucleoside phosphates and glycerides are the major classes of compounds prepared with these methods. 

Methods have been developed for the synthesis of essentially any oxygen chiral phosphate ester of biological importance, and the P-NMR methods described and illustrated in this chapter provide a convenient method for determining their configurations and elucidating the stereochemical consequences of enzyme-catalyzed phosphoryl and nucleotidyl transfer reactions. 

CK catalyzes the reversible phosphorylation of creatine in the presence of ATP and magnesium. When creatine phosphate is the substrate, the resulting creatine can be measured as the ninhydrin fluorescent compound, as in the continuous flow Auto Analyzer method. Kinetic methods based on coupled enzymatic reactions are also popular. Tanzer and Gilvarg (40) developed a kinetic method using the two exogenous enzymes pyruvate kinase and lactate dehydrogenase to measure the CK rate by following the oxidation of NADH. In this procedure the main reaction is run in a less favorable direction. 

However, the most common and important method of synthesis of chiral non-racemic hydroxy phosphoryl compounds has been the resolution of racemic substrates via a hydrolytic enzyme-promoted acylation of the hydroxy group or hydrolysis of the 0-acyl derivatives, both carried out under kinetic resolution conditions. The first attempts date from the early 1990s and have since been followed by a number of papers describing the use of a variety of enzymes and various types of organophosphorus substrates, differing both by the substituents at phosphorus and by the kind of hydroxy (acetoxy)-containing side chain. 

McDermott et al used rotational resonance, a then newly developed solid-state NMR method, for structural studies of an inhibited complex formed by reaction of D-alanine D-alanine ligase, ATP, and the aminoalkyl dipeptide analogue. The measured NMR coupling properties indicate that the two species are bridged in a P—O—P linkage, with a P—P through-space distance of 2.7 0.2 A. This work unambiguously demonstrated that the inactivation mechanism involves phosphorylation of enzyme-bound inhibitor by ATP to form a phos-phoryl-phosphinate adduct. ... 

Selected entries from Methods in Enzymology [vol, page(s)] Types of organophosphorus inhibitors, 11,686-688 toxicity hazards, 11,688 purity and analysis, 11,688 solutions of organophosphorus compounds, 11,689 estimation of specific radioactivity of organophosphorus compounds, 11,689-690 method for estimating phosphorus content, 11,691 reactions with enzymes, 11,691 -701 [rate constants, 11,692 phosphorylation of chymotrypsin, 11, 694-696 identification of phosphoryl and phosphonyl peptides,... 

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