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Phosphate, inorganic requiring

It was shown previously (24) that KD0-8-phosphate was a weak end-product inhibitor of the synthase reaction. Both of the end products of this reaction, KDO and inorganic phosphate are weak mixed-function inhibitors of KD0-8-phosphate phosphatase. The reduced form of KD0-8-phosphate (the C-2 carbonyl was reduced to the corresponding diasterioisomeric alcohol with NaBH, Table V, 3 red.), an open chain analogue, was neither an inhibitor of KD0-8-phosphate synthase nor was it a substrate or inhibitor of the phosphatase reaction. These findings indicate that the mechanism of KD0-8-phosphate synthase does not involve the formation of a linear intermediate and that the KD0-8-phosphate phosphatase requires the phosphorylated substrate in the ring form rather than the linear form. [Pg.154]

Among activated forms of amino acids, mixed anhydrides with inorganic phosphate or phosphate esters require a special discussion because they are universally involved in peptide biosynthesis through the ribosomal and non-ribosomal pathways. These mixed anhydrides have stimulated studies in prebiotic chemistry very early in the history of this field. Amino acyl adenylates 18c have been shown to polymerize in solution [159,160] and in the presence of clays [139]. However, their participation as major activated amino acid species to the prebiotic formation of peptides from amino acids is unlikely for at least two reasons. Firstly, amino acid adenylates that have a significant lifetime in aqueous solution become very unstable as soon as either CO2 or bicarbonate is present at millimolar concentration [137]. Lacey and coworkers [161] were therefore conduced to consider that CO2 was absent in the primitive atmosphere for aminoacyl adenylate to have a sufficient lifetime and then to allow for the emergence of the modern process of amino acid activation and of the translation apparatus. But this proposition is unlikely, as shown by the analysis of geological records in favor of CO2 contents in the atmosphere higher than present levels [128]. It is also in contradiction with most studies of the evolution of the atmosphere of telluric planets [30,32], Secondly, there is no prebiotic pathway available for adenylate formation and ATP proved to be inefficient in this reaction [162]. [Pg.100]

Inorganic Requirements.—Various inorganic constituents must also be present in the fermenting liquor. Some of these, phosphates in particular, play a part in the mechanism of fermentation. Others are necessary to provide food for the yeast, nitrogen compounds, calcium, potassium and manganese, etc. In addition there is a still incompletely defined compound called bios which appears to be essential to success. Most of these are present in sufficient amounts in the raw materials of the fermentation industry although it is probable that close study of their occurrence might be rewarded by increased yields and/or improved products. [Pg.20]

The incorporation of inorganic phosphate into the transport protein, which is the initial step in the reaction sequence of ATP formation, presumably leads also to different phosphoprotein species. When calcium is removed from the internal as well as from the external calcium binding sites of the membranes, i.e. when no calcium gradient exists, saturation of phosphate incorporation requires the presence of high concentrations of magnesium and phosphate and the absence of monovalent cation [126,127], As mentioned before, the reaction proceeds endothermically with a heat of... [Pg.201]

Studies of this enzyme from Ehrlich ascites tumor cells, eiythrocytes, and Salmonella typhimurium have indicated a number of features which are at least potential mechanisms for the control of its activity. Thus, although Mg + is needed to form the actual substrate, MgATP, free Mg + also stimulates enzyme activity (36, 37). One of the most interesting effectors is inorganic phosphate, for which there is an absolute requirement. With the tumor cell enzyme, 50 mM phosphate is required for maximal activity with an apparent Michaelis constant of 3.3 mM (36, 40). A biphasic response of the bacterial enzyme to phosphate was observed with apparent Michaelis constants of 2.3 and 40 mM (37). In both cases, arsenate was a weak substitute. Wong and Murray (40) found that the Michaelis constant for ATP did not vary with phosphate concentration, whereas that for ribose-5-P did vary. Hershko et al. (4I) and others have also shown stimulation of enzyme activity by phosphate in intact erythrocytes and Ehrlich ascites tumor cells incubated in media containing varying concentrations of phosphate. [Pg.89]

Star-shaped molecules possessing similar properties have also been obtained by the action of muscle phosphorylase on intact amylopectin. Both the synthesis and the degradation of starch are regulated by the level of inorganic phosphate. The highest rates of starch synthesis by spinach chloroplasts in the light occurred at <0.25 mmole of phosphate, whereas a ten-fold higher concentration of phosphate is required for the breakdown of starch in the dark. [Pg.249]

Fig. 4. Requirements, substrates, and products of Mo-nitrogenase catalysis, where I is the MoFe protein II the Fe protein and Pi is inorganic phosphate. The generating system is composed of creatine phosphate and creatine phosphokinase to recycle the inhibitory MgADP produced during catalysis to... Fig. 4. Requirements, substrates, and products of Mo-nitrogenase catalysis, where I is the MoFe protein II the Fe protein and Pi is inorganic phosphate. The generating system is composed of creatine phosphate and creatine phosphokinase to recycle the inhibitory MgADP produced during catalysis to...
Flame retardants (qv) are incorporated into the formulations in amounts necessary to satisfy existing requirements. Reactive-type diols, such as A/ A/-bis(2-hydroxyethyl)aminomethylphosphonate (Fyrol 6), are preferred, but nonreactive phosphates (Fyrol CEF, Fyrol PCF) are also used. Often, the necessary results are achieved using mineral fillers, such as alumina trihydrate or melamine. Melamine melts away from the flame and forms both a nonflammable gaseous environment and a molten barrier that helps to isolate the combustible polyurethane foam from the flame. Alumina trihydrate releases water of hydration to cool the flame, forming a noncombustible inorganic protective char at the flame front. Flame-resistant upholstery fabric or liners are also used (27). [Pg.348]

TheNef reaction of primary nitro compounds gives iildehydes or carboxylic acids, depending on the reaction conditions. Each transformation provides an important tool in organic synthesis. Primary nitro compotmds are converted into carboxylic acids vrith concentrated mineriil acids. Because such harsh conditions iilso lead to side reactions, a milder method is required inorganic synthesis. Basic phosphate-buffered KMnO rapidly converts primary nitroalkanes into carboxylic acids in 90-99% yield fEq. 6.13. "... [Pg.162]

The type of membrane cleaning required depends on both the type and degree of fouling experienced, but typically it is either organic (bacterial slimes, natural organics, or process foulants and nutrients) or inorganic (silica, carbonate, sulfate, or phosphate deposits). [Pg.371]

Figure 11.3 Regulation of GAD during the synthesis of GABA. Active GAD (GAD-PLP) combines with glutamate (1) to form a complex (GAD-PLP-GLU). After decarboxylation (2) this yields GABA and GAD-PLP (3). The intermediate product (GAD-INT) can undergo an alternative reaction (4) to produce succinic semialdehyde (SSA) and pyridoxamine-5 -phosphate (PMP). PMP dissociates from GAD (5) leaving inactive enz5mie, which requires additional PLP to be reactivated (6), a process that is affected by ATP and inorganic phosphate... Figure 11.3 Regulation of GAD during the synthesis of GABA. Active GAD (GAD-PLP) combines with glutamate (1) to form a complex (GAD-PLP-GLU). After decarboxylation (2) this yields GABA and GAD-PLP (3). The intermediate product (GAD-INT) can undergo an alternative reaction (4) to produce succinic semialdehyde (SSA) and pyridoxamine-5 -phosphate (PMP). PMP dissociates from GAD (5) leaving inactive enz5mie, which requires additional PLP to be reactivated (6), a process that is affected by ATP and inorganic phosphate...
Substitution of Asn or Glu for Asp707 inhibited Ca transport both with ATP or acetylphosphate as energy donors the formation of E P from ATP in the presence of 0.1 mM Ca or from Pi in the absence of Ca was also inhibited [103]. This data is consistent with a requirement for Asp707 in the phosphorylation of the enzyme by ATP, acetylphosphate and inorganic phosphate. [Pg.81]


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Phosphate requirements

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