Literature DB >> 22240061

Bacteriocin formation by dominant aerobic sporeformers isolated from traditional maari.

Donatien Kaboré1, Line Thorsen, Dennis Sandris Nielsen, Torben Sune Berner, Hagrétou Sawadogo-Lingani, Bréhima Diawara, Mamoudou Hama Dicko, Mogens Jakobsen.   

Abstract

The antimicrobial activity of 8 Bacillus spp. and 2 Lysinibacillus spp. representing the predominant aerobic sporeformers during traditional maari fermentations, a traditional fermented baobab seeds product from Burkina Faso, was investigated. The antimicrobial activity was assessed against a total of 31 indicator organisms representing various Gram-negative and positive pathogens. The screening showed that 3 Bacillus subtilis strains (B3, B122 and B222) in particular had antimicrobial activity against some Gram-positive organisms and were selected for further studies. It was found that the antimicrobial substances produced were heat stable, in-sensitive to catalase, sensitive to protease and trypsin but resistant to the proteolytic action of papain and proteinase K and equally active at pH values ranging from 3 to 11. Bacteriocin secretion started in late exponential growth phase and maximum activity was detected during the stationary growth phase. The production of bacteriocin by B. subtilis B3, B122 and B222 was dependent on the aeration conditions. Maximum production of bacteriocin was observed under reduced aeration. Specific primers were used to screen isolates B3, B122 and B222 for genes involved in the synthesis of the bacteriocins subtilosin A, subtilin, sublancin and ericin. Amplicons of the expected sizes were detected for iywB, sboA, sboX, albA and spaS involved in the biosynthesis of subtilosin and subtilin, respectively. The translated nucleotide sequences had 100% identity to the YiwB, SboX and SboA amino acid sequences of the subtilosin A producing B. subtilis subsp. subtilis strain 168. Interestingly there was a 3 amino acid deletion at the N-terminal part of AlbA in B3, B122 and B222 that probably alters the activity of this enzyme. Analysis of the spaS gene sequences of B3, B122 and B222, encoding a subtilin precursor peptide, showed that the translated nucleotide sequence had 98% identity with the corresponding SpaS amino acid sequence of subtilin producing B. subtilis subsp. spizizenii strain ATCC6633.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 22240061     DOI: 10.1016/j.ijfoodmicro.2011.12.003

Source DB:  PubMed          Journal:  Int J Food Microbiol        ISSN: 0168-1605            Impact factor:   5.277


  4 in total

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Authors:  Yérobessor Dabiré; Namwin Siourimè Somda; Marius K Somda; Clarisse B Compaoré; Iliassou Mogmenga; Lewis I Ezeogu; Alfred S Traoré; Jerry O Ugwuanyi; Mamoudou H Dicko
Journal:  BMC Microbiol       Date:  2022-09-29       Impact factor: 4.465

3.  Characterization and Quantitative Determination of a Diverse Group of Bacillus subtilis subsp. subtilis NCIB 3610 Antibacterial Peptides.

Authors:  Angeliki Karagiota; Hara Tsitsopoulou; Rafail Nikolaos Tasakis; Varvara Zoumpourtikoudi; Maria Touraki
Journal:  Probiotics Antimicrob Proteins       Date:  2020-09-12       Impact factor: 4.609

4.  Stability of Bacteriocin-Like Inhibitory Substance (BLIS) Produced by Pediococcus acidilactici kp10 at Different Extreme Conditions.

Authors:  Nurul Lyana Md Sidek; Murni Halim; Joo Shun Tan; Sahar Abbasiliasi; Shuhaimi Mustafa; Arbakariya B Ariff
Journal:  Biomed Res Int       Date:  2018-09-27       Impact factor: 3.411

  4 in total

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