Identification and purification of a protein that induces production of the Lactobacillus acidophilus bacteriocin lactacin B

Author:

Barefoot S F1,Chen Y R1,Hughes T A1,Bodine A B1,Shearer M Y1,Hughes M D1

Affiliation:

1. Department of Food Science, Clemson University, South Carolina 29634.

Abstract

Lactacin B is a heat-stable bacteriocin produced by Lactobacillus acidophilus N2 that is active against closely related lactobacilli, including Lactobacillus delbrueckii subsp. lactis (formerly Lactobacillus leichmannii) ATCC 4797. Pure producer cultures propagated in MRS broth (initial pH 6.5) contain no lactacin B; it is detected only in cultures maintained at pH 5.0 to 6.0 and produced optimally at pH 6.0 S. F. Barefoot and T. R. Klaenhammer, Antimicrob. Agents Chemother. 26:328-334, 1984). Associative growth of producer and indicator, L. delbrueckii subsp. lactis ATCC 4797, resulted in production of an inhibitor identical to lactacin B. Associative growth increased lactacin B production from nondetectable levels (< 100 activity units [AU]/ml) to between 3,200 and 6,400 AU/ml in MRS broth (initial pH 6.5) and resulted in early but equal production of lactacin B (approximately 25,600 AU/ml) in broth maintained at pH 6.0. Indicator cells, but not spent culture filtrates, induced lactacin B production. Indicator cells disrupted by a French pressure cell yielded cell-free filtrates containing inducing activity. Chromatofocusing and gel filtration high-performance liquid chromatography of cell-free filtrates yielded a protein with a pI of 4.1 and a molecular size of approximately 58 kDa that induced lactacin B production. Analytical isoelectric focusing yielded a single protein band. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis gels contained a 28-kDa protein suggesting a two-subunit structure. Protein sequencing identified an N-terminal serine and 18 additional amino acids. To our knowledge, there are not previous descriptions of proteins that induce bacteriocin production in lactic acid bacteria.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference38 articles.

1. Primary structure of triosephosphate isomerase from Bacillus stearothermophilus;Artavanis-Tsakonas S.;Eur. J. Biochem.,1980

2. Detection and activity of lactacin B, a bacteriocin produced by Lactobacillus acidophilus;Barefoot S. F.;Appl. Environ. Microbiol.,1983

3. Purification and characterization of the Lactobacillus acidophilus bacteriocin lactacin B;Barefoot S. F.;Appl. Environ. Microbiol.,1984

4. Barefoot S. F. C. G. Nettles and Y. R. Chen. 1994. Lactacin B a bacteriocin produced by Lactobacillus acidophilus p. 353-376. In L. De Vuyst and E. J. Vandamme (ed.) Bacteriocins of lactic acid bacteria. Blackie Academic and Professional London.

5. Bio-Rad. 1982. Protease substrate gel tablets bulletin 1111. Bio-Rad Laboratories Hercules Calif.

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