Abstract
In a previous study (J. O'Rear, L. Alberti, and R. M. Harshey, J. Bacteriol. 174:6125-6137, 1992) we reported the isolation of several transposon mutants of Serratia marcescens 274 that were defective either in swarming alone or in both swimming and swarming motility. All the nonflagellate (Fla-) mutants, while defective in both types of motility, were able to spread rapidly on the surface of low-agar (0.35%) media. We show here that some of the swarming-defective mutants are defective in the production of serrawettin W1, an extracellular cyclic lipopeptide produced by S. marcescens 274. When combined with a Fla defect, the serrawettin (Swt) mutants are deficient in spreading on low-agar media. The spreading deficiency can be overcome by serrawettin supplied extracellularly. Introduction of Fla defects into chemotaxis mutants does not affect this mode of surface translocation. These results suggest that spreading may be a passive form of translocation. We also report that swarming defects in all mutants showing a Dps phenotype (able to swarm within the inoculated area but unable to move outward) in the earlier study can be overcome by changing the commercial source of agar.
MeSH Terms
Agar
Cell Movement/genetics
Culture Media
DNA Mutational Analysis
Depsipeptides
Flagella/physiology
Mutagenesis, Insertional
Peptides, Cyclic/genetics,pharmacology
Polysaccharides, Bacterial
Serratia marcescens/genetics,growth & development
Chemicals
Culture Media
Depsipeptides
Peptides, Cyclic
Polysaccharides, Bacterial
serratamolide
Agar
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Matsuyama T
Department of Bacteriology, Niigata University School of Medicine, Japan.
Bhasin A
Harshey R M
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