Production of a novel mixture of mycosubtilins by mutants of Bacillus subtilis

Bioresour Technol. 2013 Oct:145:264-70. doi: 10.1016/j.biortech.2013.03.123. Epub 2013 Mar 26.

Abstract

Using promoter exchange and gene knock-out strategies, two mutant strains, the so-called BBG116 and BBG125, were constructed from Bacillus subtilis wild-type strain ATCC 6633, a surfactin and mycosubtilin producer. Compared to the parental strain, both mutants overproduced constitutively mycosubtilin, while BBG125 had lost the ability to synthesize surfactin. Surprisingly, BBG125 was found to produce about 2-fold less mycosubtilin than BBG116 despite an expected higher availability of the cytoplasmic precursors and cofactors pool for biosynthesis. Further physiological characterization of BBG125 also highlighted: (i) a strong influence of temperature on mycosubtilin biosynthesis in BBG125 with a maximal productivity observed at 22°C, compared to 15 and 30°C; (ii) substantial changes in fatty acid profiles and thereby in mycosubtilin isoforms, compared to the wild-type strain; and (iii) the presence of five novel mycosubtilin isoforms. The antifungal activities of the new mix were higher than or equal to those of purified isoforms.

Keywords: Antifungal activity; Bacillus subtilis; Mycosubtilin; Novel isoforms; Spreading.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antifungal Agents*
  • Bacillus subtilis / genetics
  • Bacillus subtilis / metabolism*
  • Bioreactors*
  • Biotechnology / methods*
  • Chromatography, High Pressure Liquid
  • Escherichia coli
  • Gene Knockout Techniques
  • Lipopeptides / genetics*
  • Lipoproteins / biosynthesis
  • Peptides, Cyclic / genetics*
  • Plasmids / genetics
  • Protein Isoforms / biosynthesis*
  • Species Specificity
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Tandem Mass Spectrometry
  • Temperature

Substances

  • Antifungal Agents
  • Lipopeptides
  • Lipoproteins
  • Peptides, Cyclic
  • Protein Isoforms
  • mycosubtiline
  • surfactin peptide