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Journal of Bacteriology, January 2001, p. 287-291, Vol. 183, No. 1
University of Nebraska, Lincoln,
Nebraska,1 and Northern Arizona
University, Flagstaff, Arizona2
Received 23 May 2000/Accepted 6 October 2000
Few antibiotics targeting members of the archaeal domain are
currently available for genetic studies. Since bacterial antibiotics are frequently directed against competing and related organisms, archaea by analogy might produce effective antiarchaeal antibiotics. Peptide antibiotic (halocin) preparations from euryarchaeal halophilic strains S8a, GN101, and TuA4 were found to be toxic for members of the
hyperthermophilic crenarchaeal genus Sulfolobus. No
toxicity was evident against representative bacteria or eukarya.
Halocin S8 (strain S8a) and halocin R1 (strain GN101) preparations were cytostatic, while halocin A4 (strain TuA4) preparations were cytocidal. Subsequent studies focused on the use of halocin A4 preparations and
Sulfolobus solfataricus. Strain TuA4 cell lysates were not toxic for S. solfataricus, and protease (but not nuclease)
treatment of the halocin A4 preparation inactivated toxicity,
indicating that the A4 toxic factor must be a secreted protein.
Potassium chloride supplementation of the Sulfolobus assay
medium potentiated toxicity, implicating use of a salt-dependent
mechanism. The utility of halocin A4 preparations for genetic
manipulation of S. solfataricus was assessed through the
isolation of UV-induced resistant mutants. The mutants exhibited stable
phenotypes and were placed into distinct classes based on their levels
of resistance.
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.1.287-291.2001
Secreted Euryarchaeal Microhalocins Kill
Hyperthermophilic Crenarchaea

*
Corresponding author. Mailing address: E234 Beadle
Center for Genetics, University of Nebraska, Lincoln, NE 68588-0666. Phone: (402) 472-2769. Fax: (402) 472-8722. E-mail:
pblum{at}biocomp.unl.edu.
Present address: Section of Microbiology, University of
California
Davis, Davis, CA 95616.
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