Seventy-four catalase protein sequences, including 29 bacterial, 8 fun
gal, 7 animal, and 30 plant sequences, were compiled, and 70 were used
for phylogenetic reconstruction. The core of the resulting tree revea
led unique, separate groups of plant and animal catalases, two groups
of fungal catalases, and three groups of bacterial catalases. The only
overlap of kingdoms occurred within one branch and involved fungal an
d bacterial large-subunit enzymes. The other fungal branch was closely
linked to the group of animal enzymes. Group I bacterial catalases we
re more closely related to the plant enzymes and contained such divers
e taxa as the Gram-positive Listeria seeligeri, Dein-ocococcus radiodu
rans, and gamma-proteobacteria. Group III bacterial sequences were mor
e closely related to fungal and animal sequences and included enzymes
from a broad range of bacteria including high-and low-GC Gram positive
s, proteobacteria, and a bacteroides species. Group TI was composed of
large-subunit catalases from diverse sources including Gram positives
(low-GC Bacilli and high-GC Mycobacteria), proteobacteria, and specie
s of the filamentous fungus Aspergillus. These data can be interpreted
in terms of two gene duplication events that produced a minimum of th
ree catalase gene family members that subsequently evolved in response
to environmental demands. Horizontal gene transfer may have been resp
onsible for the group II mixture of bacterial and fungal large-subunit
catalases.