B. Kafala et A. Sasarman, ISOLATION OF THE STAPHYLOCOCCUS-AUREUS HEM CDBL GENE-CLUSTER CODING FOR EARLY STEPS IN HEME-BIOSYNTHESIS, Gene, 199(1-2), 1997, pp. 231-239
We have recently reported [Kafala, B., Sasarman, A., 1994. Can. J. Mic
robiol. 40, 651-657] the cloning and sequencing of the Staphylococcus
aureus hemB gene. This gene purportedly encodes the delta-aminolevulin
ic acid dehydratase of the heme pathway. In this present communication
, we report the sequences and identities of three putative hem genes.
Two of these genes are located immediately upstream from hemB. Complem
entation analysis of Escherichia coli and Salmonella typhimurium hemC
and hemD mutants and the comparison of the Sa nucleotide sequences wit
h those of Bacillus subtilis and Ec showed that these two open reading
frames, ORF1 and ORF2, are likely to be the hemC gene coding for porp
hobilinogen deaminase and the hemD gene coding for uroporphyrinogen II
I synthase, respectively. The third hem gene, hemL, is located immedia
tely downstream of hemB, and encodes glutamate 1-semialdehyde 2,1-amin
otransferase. Sequencing of the region which extends past hemL indicat
es that no further hem genes are located downstream of hemL. In Sa, he
mC, hemD hemB and hemL are proposed to constitute a hem cluster encodi
ng enzymes required for the synthesis of uroporphyrinogen III from glu
tamate 1-semialdehyde (GSA). (C) 1997 Elsevier Science B.V.