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J. Biol. Chem., Vol. 269, Issue 20, 14386-14390, 05, 1994
G Rieder, MJ Merrick, H Castorph and D Kleiner
A mutant of the enterobacterium Klebsiella pneumoniae with a defect in the
hisF gene (in the histidine biosynthesis pathway) was isolated, which can
only grow with high but not low ammonia concentrations. The mutated hisF
product can use ammonia for the formation of the imidazole ring of
histidine but not glutamine provided by the hisH product. Site- directed
insertional mutagenesis of hisH led to the same dependence of prototrophic
growth on high ammonia levels. The nucleotide sequence of K. pneumoniae
hisF is almost identical to that of hisF from other enterobacteria.
Similarities of the hisF product with the hisA product and of HisH
sequences with the glutamine binding domains of TrpG-type amidotransferases
provide additional evidence for the functions of the hisF and hisH products
in histidine biosynthesis, namely that HisF catalyzes the ammonolytic
cleavage of N'-(5'-phosphoribulosyl)- formimino-5-
aminoimidazole-4-carboxamide ribonucleotide either utilizing free ammonia
or deriving the ammonia moiety from glutamine bound to HisH.
Function of hisF and hisH gene products in histidine biosynthesis
Lehrstuhl Mikrobiologie der Universitat, Bayreuth, Federal Republic of Germany.
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