Journal of Bacteriology, March 1999, p. 1939-1943, Vol. 181, No. 6
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Department of Biotechnology,
Received 8 September 1998/Accepted 12 January 1999
We constructed a sodA-disrupted mutant of
Bacillus subtilis 168, BK1, by homologous recombination.
The mutant was not able to grow in minimal medium without Mn(II). The
spore-forming ability of strain BK1 was significantly lower in
Mn(II)-depleted medium than that of the wild-type strain. These
deleterious effects caused by the sodA mutation were
reversed when an excess of Mn(II) was used to supplement the medium.
Moreover, the growth inhibition by superoxide generators in strain BK1
and its parent strain was also reversed by the supplementation with
excess Mn(II). We therefore estimated the Mn-dependent
superoxide-scavenging activity in BK1 cells. Whereas BK1 cells have no
detectable superoxide dismutase (Sod) on native gel, the
superoxide-scavenging activity in crude extracts of BK1 cells grown in
Mn(II)-supplemented LB medium (10 g of tryptone, 5 g of yeast
extract, and 5 g of NaCl per liter) was significantly detected by
the modified Sod assay method without using EDTA. The results obtained
suggest that Mn, as a free ion or a complex with some cellular
component, can catalyze the elimination of superoxide and that both
SodA and Mn(II) are involved not only in the superoxide resistance of
vegetative cells but also in sporulation.
*
Corresponding author. Mailing address: Department of
Biotechnology, Kansai University, Yamate-cho, Suita 564-8680, Japan. Phone: 81-6-6368-1121. Fax: 81-6-6388-8609. E-mail:
ymatsu{at}ipcku.kansai-u.ac.jp.
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