scholarly journals Effect of adenine on the synthesis of purine derivatives in wheat seedlings

2015 ◽  
Vol 41 (2) ◽  
pp. 283-288 ◽  
Author(s):  
Hanna Rybacka

The effect of adenine and other purine derivatives on the "de novo" purine synthesis was investigated in young wheat schoots. Adenine, adenosine and AMP inhibited strongly this biosynthesis, whereas hypoxanthine had no effect. The incorporation of each of the used precursors; [l-<sup>14</sup>C] glycine, [<sup>14</sup>C] formate and [<sup>14</sup>C] carbonate was inhibited by adenine in the same extent.

1971 ◽  
Vol 18 (1) ◽  
pp. 33-44 ◽  
Author(s):  
J. Pourquié ◽  
H. Heslot

SUMMARYIn the fission yeastSchizosaccharomyces pombe, growth responses of mutants strains in the de novo purine synthesis pathway, in the purine interconversion system, and of various double mutants, have been studied upon different purine-supplemented media. The results show that exogenous purine utilization as nucleotide source is based exclusively upon pyrophosphorylation of purine bases, and they make it possible to identify most of the enzymic steps acting, in this organism, upon a purine ring to give another purine ring.A scheme of the interconversion system inSchizosaccharomyces pombeis given.


1989 ◽  
Vol 264 (1) ◽  
pp. 328-333 ◽  
Author(s):  
G P Beardsley ◽  
B A Moroson ◽  
E C Taylor ◽  
R G Moran

1990 ◽  
Vol 10 (11) ◽  
pp. 5679-5687
Author(s):  
C K Barlowe ◽  
D R Appling

In eucaryotes, 10-formyltetrahydrofolate (formyl-THF) synthetase, 5,10-methenyl-THF cyclohydrolase, and NADP(+)-dependent 5,10-methylene-THF dehydrogenase activities are present on a single polypeptide termed C1-THF synthase. This trifunctional enzyme, encoded by the ADE3 gene in the yeast Saccharomyces cerevisiae, is thought to be responsible for the synthesis of the one-carbon donor 10-formyl-THF for de novo purine synthesis. Deletion of the ADE3 gene causes adenine auxotrophy, presumably as a result of the lack of cytoplasmic 10-formyl-THF. In this report, defined point mutations that affected one or more of the catalytic activities of yeast C1-THF synthase were generated in vitro and transferred to the chromosomal ADE3 locus by gene replacement. In contrast to ADE3 deletions, point mutations that inactivated all three activities of C1-THF synthase did not result in an adenine requirement. Heterologous expression of the Clostridium acidiurici gene encoding a monofunctional 10-formyl-THF synthetase in an ade3 deletion strain did not restore growth in the absence of adenine, even though the monofunctional synthetase was catalytically competent in vivo. These results indicate that adequate cytoplasmic 10-formyl-THF can be produced by an enzyme(s) other than C1-THF synthase, but efficient utilization of that 10-formyl-THF for purine synthesis requires a nonenzymatic function of C1-THF synthase. A monofunctional 5,10-methylene-THF dehydrogenase, dependent on NAD+ for catalysis, has been identified and purified from yeast cells (C. K. Barlowe and D. R. Appling, Biochemistry 29:7089-7094, 1990). We propose that the characteristics of strains expressing full-length but catalytically inactive C1-THF synthase could result from the formation of a purine-synthesizing multienzyme complex involving the structurally unchanged C1-THF synthase and that production of the necessary one-carbon units in these strains is accomplished by an NAD+ -dependent 5,10-methylene-THF dehydrogenase.


2015 ◽  
Vol 14 (4) ◽  
pp. 1079-1092 ◽  
Author(s):  
Martial Boutchueng-Djidjou ◽  
Gabriel Collard-Simard ◽  
Suzanne Fortier ◽  
Sébastien S. Hébert ◽  
Isabelle Kelly ◽  
...  

1969 ◽  
Vol 47 (9) ◽  
pp. 839-845 ◽  
Author(s):  
D. Trachewsky ◽  
R. M. Johnstone

In extracts of Ehrlich ascites cells the synthesis of α-N-formylglycinamide ribonucleotide (FGAR), an early intermediate in de novo purine synthesis, is enhanced by the presence of ammonium ions. Under these experimental conditions glutamine participation in FGAR formation is not obligatory. Ribonucleotides, deoxyribonucleotides, and purine analogues which inhibit glutamine-dependent FGAR synthesis also inhibit ammonium-ion-dependent FGAR synthesis. 3′-Ribonucleotides do not inhibit purine precursor formation from ammonium ions or from glutamine.


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