Literature DB >> 11889103

The pyrimidine nucleotide reductase step in riboflavin and F(420) biosynthesis in archaea proceeds by the eukaryotic route to riboflavin.

Marion Graupner1, Huimin Xu, Robert H White.   

Abstract

The Methanococcus jannaschii gene MJ0671 was cloned and overexpressed in Escherichia coli, and its gene product was tested for its ability to catalyze the pyridine nucleotide-dependent reduction of either 2,5-diamino-6-ribosylamino-4(3H)-pyrimidinone 5'-phosphate (compound 3) to 2,5-diamino-6-ribitylamino-4(3H)-pyrimidinone 5'-phosphate (compound 4) or 5-amino-6-ribosylamino-2,4(1H,3H)-pyrimidinedione 5'-phosphate (compound 7) to 5-amino-6-ribitylamino-2,4(1H,3H)-pyrimidinedione 5'-phosphate (compound 5). Only compound 3 was found to serve as a substrate for the enzyme. NADPH and NADH functioned equally well as the reductants. This specificity for the reduction of compound 3 was also confirmed by using cell extracts of M. jannaschii and Methanosarcina thermophila. Thus, this step in riboflavin biosynthesis in these archaea is the same as that found in yeasts. The absence of the other genes in the biosynthesis of riboflavin in Archaea is discussed.

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Year:  2002        PMID: 11889103      PMCID: PMC134922          DOI: 10.1128/JB.184.7.1952-1957.2002

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  17 in total

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Authors:  A Bacher; S Eberhardt; M Fischer; S Mörtl; K Kis; K Kugelbrey; J Scheuring; K Schott
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Journal:  Methods Enzymol       Date:  1986       Impact factor: 1.600

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Journal:  J Bacteriol       Date:  1997-11       Impact factor: 3.490

5.  Purification and properties of guanosine triphosphate cyclohydrolase II from Escherichia coli.

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9.  A novel bifunctional transcriptional regulator of riboflavin metabolism in Archaea.

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