scholarly journals TheSaccharomyces cerevisiae RIB4Gene Codes for 6,7-Dimethyl- 8-ribityllumazine Synthase Involved in Riboflavin Biosynthesis

1995 ◽  
Vol 270 (40) ◽  
pp. 23801-23807 ◽  
Author(s):  
José J. García-Ramírez ◽  
Maria A. Santos ◽  
José L. Revuelta
2016 ◽  
Vol 88 (5) ◽  
pp. 705-716 ◽  
Author(s):  
Na Sa ◽  
Renu Rawat ◽  
Chelsea Thornburg ◽  
Kevin D. Walker ◽  
Sanja Roje

1967 ◽  
Vol 22 (7) ◽  
pp. 755-758 ◽  
Author(s):  
F. Lingens ◽  
O. Oltmanns ◽  
A. Bacher

Using various riboflavin deficient mutants of S. cerevisiae, we have found two intermediates of the riboflavin biosynthesis. 6.7-Dimethyl-8-ribityl-lumazine was isolated from the culture fluid of two mutants. The formation of 4-ribitylamino-5-amino-uracil by two other mutants was proved by trapping the product with glyoxal or diacetyl, leading to the formation of 8-ribityl-lumazine or 6,7-dimethyl-8-ribityl-lumazine and riboflavin respectively. These mutants were able to grow in riboflavin free medium supplemented with diacetyl.6,7-Dimethyl-8-ribityl-lumazine promoted the growth of adequately blocked mutants.


1979 ◽  
Vol 25 (3) ◽  
pp. 380-389 ◽  
Author(s):  
W. J. E. Gardner ◽  
R. A. Woods

Mutants of yeast which are auxotrophic for guanine have been isolated from two prototrophic haploid strains, one of which carried the suppressor of purine excretion, su-pur, and the other carried the alternative allele, su-pur+. The mutants were allocated to three genes, gua1, gua2, and gua3, between which no close linkage was demonstrable. Mutants of all three genes were recessive and showed normal Mendelian segregation in crosses. The gene gua1 was shown by an in vivo enzyme assay procedure to specify guanosine 5′-phosphate (GMP) synthetase, the second enzyme involved in the biosynthesis of GMP from inosine 5′-phosphate (IMP). Mutants of this gene excrete large amounts of purine derivatives, predominantly xanthosine, into guanine-free, but not into guanine-supplemented, medium. The gene gua2 is probably involved in the biosynthesis of riboflavin from guanine nucleotides; the phenotype of these mutants suggests a possible interaction between aromatic amino acid metabolism and riboflavin biosynthesis. No role for gua3 can be assigned on the evidence so far available, but it is not involved in the specification of IMP dehydrogenase, the first enzyme involved in the synthesis of GMP and IMP.


2011 ◽  
Vol 10 (5) ◽  
pp. 2590-2601 ◽  
Author(s):  
Jorge Rodríguez-Celma ◽  
Giuseppe Lattanzio ◽  
Michael A. Grusak ◽  
Anunciación Abadía ◽  
Javier Abadía ◽  
...  

2019 ◽  
Vol 39 (4) ◽  
pp. 1338-1371 ◽  
Author(s):  
Biswajit Kundu ◽  
Dipayan Sarkar ◽  
Namrata Ray ◽  
Arindam Talukdar

2013 ◽  
Vol 82 (1) ◽  
pp. 393-404 ◽  
Author(s):  
Andrew L. Garfoot ◽  
Olga Zemska ◽  
Chad A. Rappleye

ABSTRACTDuring infection of the mammalian host,Histoplasma capsulatumyeasts survive and reside within macrophages of the immune system. Whereas some intracellular pathogens escape into the host cytosol,Histoplasmayeasts remain within the macrophage phagosome. This intracellularHistoplasma-containing compartment imposes nutritional challenges for yeast growth and replication. We identified and annotated vitamin synthesis pathways encoded in theHistoplasmagenome and confirmed by growth in minimal medium thatHistoplasmayeasts can synthesize all essential vitamins with the exception of thiamine. Riboflavin, pantothenate, and biotin auxotrophs ofHistoplasmawere generated to probe whether these vitamins are available to intracellular yeasts. Disruption of theRIB2gene (riboflavin biosynthesis) prevented growth and proliferation of yeasts in macrophages and severely attenuatedHistoplasmavirulence in a murine model of respiratory histoplasmosis. Rib2-deficient yeasts were not cleared from lung tissue but persisted, consistent with functional survival mechanisms but inability to replicatein vivo. In addition, depletion of Pan6 (pantothenate biosynthesis) but not Bio2 function (biotin synthesis) also impairedHistoplasmavirulence. These results indicate that theHistoplasma-containing phagosome is limiting for riboflavin and pantothenate and thatHistoplasmavirulence requiresde novosynthesis of these cofactor precursors. Since mammalian hosts do not rely on vitamin synthesis but instead acquire essential vitamins through diet, vitamin synthesis pathways represent druggable targets for therapeutics.


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