Affiliation:
1. Research Institute for Biological Sciences Okayama (RIBS), Okayama 716-1241, Japan
Abstract
ABSTRACT
We developed a simple and sensitive screening method to investigate the distribution of microbes producing an antimicrobial poly(amino acid), ε-poly-
l
-lysine (ε-PL), in microflora. An acidic dye, Poly R-478, incorporated in an agar plate detected ε-PL producers by electrostatic interaction with the secreted basic polymers. All ε-PL producers, isolated after careful and sufficient screening of soil microflora, belonged exclusively to two groups of bacteria of the family
Streptomycetaceae
and ergot fungi. They were characterized based on the density and diameter of the concentric zone formed by the secreted polymers. The density depended on each isolate. The increase in the diameter of the concentric zone per unit of time varied among isolates and was negatively correlated with the molecular weight. Although the distribution of ε-PL producers was extremely limited, their products were structurally varied. The molecular masses of the secreted polymers among the isolates ranged from 0.8 to 2.0 kDa. There were also isolates producing unknown polymers inconsistent with the correlation or producing a mixture of polymers with original and modified structures. A chemically modified polymer was an ε-PL derivative, as determined by mass spectrometry. Since the structural variations had no relation to the phylogenetic position of the isolates, it is possible that enzymes involved in the synthesis diversified after putative horizontal transfers of relevant genes.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Reference14 articles.
1. Ashiuchi, M., K. Soda, and H. Misono. 1999. A poly-γ-glutamate synthetic system of Bacillus subtilis IFO 3336: gene cloning and biochemical analysis of poly-γ-glutamate produced by Escherichia coli clone cells. Biochem. Biophys. Res. Commun.263:6-12.
2. Breukink, E., C. van Kraaij, R. A. Demel, R. J. Siezen, O. P. Kuipers, and B. de Kruijff. 1997. The C-terminal region of nisin is responsible for the initial interaction of nisin with the target membrane. Biochemistry36:6968-6976.
3. Fujii, G., M. E. Selsted, and D. Eisenberg. 1993. Defensins promote fusion and lysis of negatively charged membranes. Protein Sci.2:1301-1312.
4. Hiraki, J., M. Hatakeyama, H. Morita, and Y. Izumi. 1998. Improved ε-poly-l-lysine production of an S-(2-aminoethyl)-l-cysteine resistant mutant of Streptomyces albulus. Seibutsu-Kogaku76:487-493.
5. Kirk, T. K., E. Schultz, W. J. Connors, L. F. Lorenz, and J. G. Zeikus. 1978. Influence of culture parameters on lignin metabolism by Phanerochaete chrysosporium. Arch. Microbiol.117:277-285.
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