Vol. 180, Issue 13, 3339-3344, July 1, 1998
1 Unité de Régulation de
l'Expression Génétique, Complementation of an Escherichia coli cya mutant with
a genomic library from Aeromonas hydrophila allowed
isolation of clones containing two different cya genes.
Whereas one of these genes (cyaA) coded for an adenylyl
cyclase (AC1) belonging to the previously described class I adenylyl
cyclases (ACs), the second one (cyaB) coded for a protein
(AC2) that did not match any previously characterized protein when
compared to protein sequence databases. In particular, it did not align
with any of members of the three known classes of ACs. The purified AC2
enzyme exhibited remarkable biochemical characteristics, namely, an
optimum activity at a high temperature (65°C) and at an alkalinic pH
(9.5). In order to investigate the functions of both cyclases in
A. hydrophila, each gene was inactivated in the chromosome
and the resulting mutant strains were examined for physiological
alterations. It was shown that, in contrast to cyaA, the
cyaB gene was not expressed under usual laboratory growth
conditions. However, introduction of a plasmid harboring the
cyaB gene in a cyaA mutant, as well as in a
cyaA cyaB mutant, allowed cyclic AMP production. AC2 is the
first member of a new class of previously unrecognized ACs, and to
date, no functional counterpart has been demonstrated in other
organisms. However, scanning databases revealed a significant
similarity between AC2 and the gene product of three hyperthermophilic
archaebacteria: Methanobacterium thermoautotrophicum,
Archaeglobus fulgidus, and Methanococcus
jannaschii. The possibility of a gene transfer between such
phylogenetically divergent bacteria is discussed.
Copyright © 1998 by American Society for Microbiology
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