Adenosine enzymic synthesis

S. R. Kornberg (1957a). Adenosine triphosphate synthesis from polyphosphate by an enzyme from... 

Espada, J. 1962. Enzymic synthesis of adenosine diphosphate glucose from glucose 1-phosphate and adenosine triphosphate. J. Biol. Chem. 237, 3577-3581. 

Atovaquone is an antiprolozoal agent (750 mg p.o. t.i.d for 21 days), that inhibits mitochondrial electron transport in metabohc enzymes of microorganisms. This may cause inhibition of nucleic acid and adenosine triphosphate synthesis. Atovaquone is indicated in the treatment of mild to moderate Pneumocystis carinii pneumonia in patients who cannot tolerate trimethoprimsulfamethoxazole, and in acute oral treatment of mild to moderate PCP in patients who are intolerant to trimethoprimsulfamethoxazole. 

Secrist, J. A., Barrio, J. R.. and Leonard, N. I., 1972, A fluorescent modification of adenosine triphosphate with activity In enzyme synthesis 1, -ethenoadenosine triphosphate. Science 175 646-647. 

The almost universal presence of adenosine 3 , 5 cyclic phosphate (cAMP) as a biologic regulator in microbial and hormone-sensitive animal tissues raises the question of whether this nucleotide might mediate the steroid hormone effect on specific enzyme synthesis. This possibility is made especially attractive because certain enzymes known to be induced by the steroids can also be induced by the cyclic nucleotide. Thus, several enzymes which are induced in the prostate or seminal vesicles by (dihydro) testosterone can also be induced by cAMP (Singhal et al., 1970). Likewise, tyrosine aminotransferase is inducible in embryonic and adult liver by the cyclic nucleotide as well as by the glucocorticoids (Wicks, 1968). 

A simple enzymic synthesis of barium glucose 6-phosphate from starch has appeared. Ths use of 2-methylthio-4 -l,3,2-benzodioxaphosphorin-2-oxide (MTBO) (see M. Eto et al.. Tetrahedron Letters, 1971, 4263) continues to receive attention. A study of twenty amines as catalysts has shown that primary n-alkyl and alicyclic amines are the most effective, followed by secondary and tertiary amines. Increasing the branching reduced the catalytic efficacy while cyclic imines gave low yields. MTBO has been used to synthesize adenosine 2, 3 -cyclic phosphate in 50% yield from 5 -0-acetyladenosine (Scheme 5). o-Arabinose 5-phosphate and o-xylose 5-phosphate have been... 

Finally, a brief word about cyclic AMP. Activation of the enzyme adenyl cyclase which catalyses cyclic 3, 5 -adenosine monophophate synthesis constitutes the initial molecular event in the target cells of several mammalian hormones. The nucleotide then initiates a series of events leading to a final response characteristic of the hormone. Despite numerous studies on the barley aleurone layer there is no convincing evidence that GA action is mediated via cyclic AMP [73] in fact the weight of evidence is against this nucleotide playing an important role in any plant tissue [7]. 

There is also support for a role of PGD2 in sleep control and homeostasis (Hayaishi, 2002). PGD2 is synthesized in the subarachnoid space ventral to the POA. Administration of PGD2 in the subarachnoid space induces normal sleep, and inhibition of synthesis or receptors suppresses sleep. Sleep rebound after deprivation is reduced in mice in which the synthetic enzyme is knocked out. Administration of PGD2 to the subarachnoid space also induces c-Fos in the VLPO as well as dorsal POA neurons (Scammel et a ., 1998). The hypnogenic actions of PGD2 seem to be mediated by an adenosine A2a pathway (Satoh et al, 1966). 

T. brucei is unable to synthesize purines de novo and, as such, is dependent upon salvage mechanisms from the host. A number of transporters and enzymes are used by T. brucei to accomplish this task, and inhibition of these targets offers promise for development of trypanocides [39]. This strategy has been validated by demonstration that cordycepin (34), a substrate for T. brucei adenosine kinase (TbAK), which terminates RNA synthesis and parasite growth, can cure stage 2 HAT infections in mice when coadministered with deoxycoformycin (35), an adenosine deaminase inhibitor [40]. 

The initial conversion of light into chemical energy takes place in the thylakoid membrane. Besides the chlorophylls and series of electron carriers, the thylakoid membrane also contains the enzyme adenosine triphosphate (ATP) synthase. The enzymes that are responsible for the actual fixation of C02 and the synthesis of carbohydrate reside in the stroma that surround the thylakoid membrane. The stroma also contains deoxyribonucleic acid (DNA), ribonucleic acid (RNA), and ribosomes that are essential for protein synthesis [37]. 

Adenosine triphosphate (ATP) is one of the most important cofactors involved in many of the synthetic reactions going on within the cell. Its recent large scale in vitro enzymatic synthesis from adenosine and acetylphosphate is of particular interest. Three enzymes immobilized in polyacrylamide gel were used adenosine kinase, adenylate kinase and acetate kinase (lip. ... 

Phosphoribosylpyrophosphate (PRPP) synthetase is one of the very few enzymes which transfer a pyrophosphoryl group from ATP in one step. When the synthesis is carried out in lsO-enriched water, lsO is incorporated into the PRPP, but not into AMP.91 The lsO in the PRPP arises from a pre-exchange between the H2180 and the ribose phosphate, and hence the results confirm that fission of the /5-P—O bond takes place. PRPP and ATP are starting materials in the biosynthesis of histidine, and Ai-(5 -phospho-D-ribosyl)adenosine triphosphate (29) is an intermediate. The... 

Mitochondria are found in the cell body and all processes of the neuron. They possess a double membrane and their own DNA and they play a role in cellular respiration and energy synthesis. Mitochondria contain enzymes essential for energy production in the form of adenosine triphosphate (ATP). 

The cytochrome b(6)f complex mediates electron transfer between the PSI and PSII reaction centers by oxidizing hpophUic plastoquinol (PQH2) (see Figure 7.24) and reducing the enzymes plastocyanin or cytochrome Ce. The electronic connection also generates a transmembrane electrochemical proton gradient that can support adenosine triphosphate (ATP) synthesis instead of electron transport. 

During the past 15 years data from experiments with different types of animal tissues and micro-organisms, using intact cells, crude extracts or purified enzymes, have firmly established the general occurrence of nucleotide reductases and have stressed their importance for DNA synthesis in essentially all types of rapidly growing cells [54]. It has been proposed that ribonucleotide diphosphates lose a hydroxide ion from C-2 to form a carbonium ion which is then stero-specifically reduced by a hydride ion derived from thioredoxin [54]. Adenosine diphosphate and guanosine diphosphate (as well as uridine and cytidine diphosphates) are reduced in this manner. 

The first step of this sequence, which is not unique to de novo purine nucleotide biosynthesis, is the synthesis of 5-phosphoribosylpyrophosphate (PRPP) from ribose-5-phosphate and adenosine triphosphate. Phosphoribosyl-pyrophosphate synthetase, the enzyme that catalyses this reaction [278], is under feedback control by adenosine triphosphate [279]. Cordycepin interferes with thede novo pathway [229, 280, 281), and cordycepin triphosphate inhibits the synthesis of PRPP in extracts from Ehrlich ascites tumour cells [282]. Formycin [283], probably as the triphosphate, 9-0-D-xylofuranosyladenine [157] triphosphate, and decoyinine (LXXlll) [284-286] (p. 89) also inhibit the synthesis of PRPP in tumour cells, and this is held to be the blockade most important to their cytotoxic action. It has been suggested but not established that tubercidin (triphosphate) may also be an inhibitor of this reaction [193]. 

Carbamoyl phosphate synthetase formation in liver taken from tadpoles treated with thyroxine is enhanced by the addition of orotic acid, uracil or uridine (cytosine and adenosine had no effect). The synthesis of this enzyme is not affected by these pyrimidines in untreated animals. This indicates that there is a relative pyrimidine deficiency during thyroxine-induced metamorphosis [140]. 

The answer is D. Impaired immune function in severe combined immunodeficiency (SCID) is the direct result of blocked DNA synthesis due to inadequate supplies of de-oxyribonucleotides in B and T cells. This effect arises by dATP-induced allosteric inhibition of ribonucleotide reductase, which catalyzes reduction of the 2 -hydroxyl groups on ADP and GDP to form dADP and dCDP. The ultimate cause of many cases of SCID is adenosine deaminase deficiency, which leads to accumulation of dATP and consequent inhibition of ribonucleotide reductase. Although the other enzymes mentioned are also involved in purine nucleotide metabolism, their deficiencies do not lead to SCID. 

---