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Journal of Bacteriology, February 2001, p. 1284-1295, Vol. 183, No. 4
Institut de Génétique et
Microbiologie, Université Paris-Sud, Centre d'Orsay, F-91405
Orsay Cedex, France
Received 9 August 2000/Accepted 16 November 2000
The sodA gene encoding the Corynebacterium
melassecola manganese-cofactored superoxide dismutase (SOD) has
been cloned in Escherichia coli and sequenced. The gene is
transcribed monocistronically; the predicted polypeptide is 200 amino
acids long and associates in a homotetrameric, manganese-dependent
form, able to complement an SOD-deficient E. coli mutant. A
second open reading frame, coding for a putative 217-amino-acid protein
with high homology to peptide methionine sulfoxide reductases from
various origins, has been identified immediately upstream of
sodA in the opposite transcription orientation. The
sodA gene was inactivated by insertion of an integrative
vector carrying a kanamycin resistance gene. The growth rate of the
SOD-deficient integrant was only slightly affected in BHI rich medium
as well as in BMCG chemically defined medium, but was strongly affected
by the presence of the redox-cycling agent paraquat. The SOD deficiency
had, on the other hand, a deleterious effect on viability as soon as
the culture entered the stationary phase of growth in BHI medium.
Surprisingly, SOD deficiency was able to rescue the dramatic loss of
viability observed for the wild-type strain in BMCG synthetic medium
when glucose was not the limiting growth factor.
0021-9193/01/$04.00+0 DOI: 10.1128/JB.2001.183.4.1284-1295.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Cloning of the sodA Gene from
Corynebacterium melassecola and Role of Superoxide Dismutase
in Cellular Viability
*
Corresponding author. Mailing address: Institut de
Génétique et Microbiologie, Bat. 360, Université
Paris-Sud, Centre d'Orsay, F-91405 Orsay Cedex, France. Phone: 33 (0)1
69 15 63 41. Fax: 33 (0)1 69 15 63 34. E-mail:
armel{at}igmors.u-psud.fr.
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