Mycosubtilin overproduction by Bacillus subtilis BBG100 enhances the organism's antagonistic and biocontrol activities

被引:232
作者
Leclère, V
Béchet, M
Adam, A
Guez, JS
Wathelet, B
Ongena, M
Thonart, P
Gancel, F
Chollet-Imbert, M
Jacques, P
机构
[1] Univ Sci & Technol Lille, Polytech Lille, Lab Microbial Bioproc, F-59655 Villeneuve Dascq, France
[2] Univ Liege, Ctr Wallon Biol Ind, B-4000 Liege, Belgium
[3] Agr Univ Gembloux, Unite Chim Biol Ind, B-5030 Gembloux, Belgium
关键词
D O I
10.1128/AEM.71.8.4577-4584.2005
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A Bacillus subtilis derivative was obtained from strain ATCC 6633 by replacement of the native promoter (if he mycosubtilin operon by a constitutive promoter originating from the replication gene repU of the Staphylococcus aureus plasmid pUB110. The recombinant strain, designated BBG100, produced up to 15-fold more mycosubtilin than the wild type produced. The overproducing phenotype was related to enhancement of the antagonistic activities against several yeasts and pathogenic fungi. Hemolytic activities were also clearly increased in the modified strain. Mass spectrometry analyses of enriched mycosubtilin extracts showed similar patterns of lipopeptides for BBG100 and the wild type. Interestingly, these analyses also revealed a new form of mycosubtilin which was more easily detected in the BBG100 sample. When tested for its biocontrol potential, wild-type strain ATCC 6633 was almost ineffective for reducing a Pythium infection of tomato seedlings. However, treatment of seeds with the BBG100 overproducing strain resulted in a marked increase in the germination rate of seeds. This protective effect afforded by mycosubtilin overproduction was also visualized by the significantly greater fresh weight of emerging seedlings treated with BBG100 compared to controls or seedlings inoculated with the wild-type strain.
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收藏
页码:4577 / 4584
页数:8
相关论文
共 41 条
  • [1] Influence of culture conditions on lipopeptide production by Bacillus subtilis
    Akpa, E
    Jacques, P
    Wathelet, B
    Paquot, M
    Fuchs, R
    Budzikiewicz, H
    Thonart, P
    [J]. APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 2001, 91-3 (1-9) : 551 - 561
  • [2] SUBTILOSIN-A, A NEW ANTIBIOTIC PEPTIDE PRODUCED BY BACILLUS-SUBTILIS-168 - ISOLATION, STRUCTURAL-ANALYSIS, AND BIOGENESIS
    BABASAKI, K
    TAKAO, T
    SHIMONISHI, Y
    KURAHASHI, K
    [J]. JOURNAL OF BIOCHEMISTRY, 1985, 98 (03) : 585 - 603
  • [3] BACKMAN PA, 1997, BACTERIA BIOL CONTRO
  • [4] Biocontrol of Bacillus subtilis against infection of Arabidopsis roots by Pseudomonas syringae is facilitated by biofilm formation and surfactin production
    Bais, HP
    Fall, R
    Vivanco, JM
    [J]. PLANT PHYSIOLOGY, 2004, 134 (01) : 307 - 319
  • [5] Kodiak(R) - a successful biological-control product for suppression of soil-borne plant pathogens of cotton
    Brannen, PM
    Kenney, DS
    [J]. JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY, 1997, 19 (03) : 169 - 171
  • [6] Predictive, structure-based model of amino acid recognition by nonribosomal peptide synthetase adenylation domains
    Challis, GL
    Ravel, J
    Townsend, CA
    [J]. CHEMISTRY & BIOLOGY, 2000, 7 (03): : 211 - 224
  • [7] Altered srf expression in Bacillus subtilis resulting from changes in culture pH is dependent on the Spo0K oligopeptide permease and the ComQX system of extracellular control
    Cosby, WM
    Vollenbroich, D
    Lee, OH
    Zuber, P
    [J]. JOURNAL OF BACTERIOLOGY, 1998, 180 (06) : 1438 - 1445
  • [8] Dennis J J, 1995, Methods Mol Biol, V47, P125
  • [9] The mycosubtilin synthetase of Bacillus subtilis ATCC6633:: A multifunctional hybrid between a peptide synthetase, an amino transferase, and a fatty acid synthase
    Duitman, EH
    Hamoen, LW
    Rembold, M
    Venema, G
    Seitz, H
    Saenger, W
    Bernhard, F
    Reinhardt, R
    Schmidt, M
    Ullrich, C
    Stein, T
    Leenders, F
    Vater, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (23) : 13294 - 13299
  • [10] Handelsman J, 1996, PLANT CELL, V8, P1855, DOI 10.1105/tpc.8.10.1855