Morphological and phenotypical characterization of Bacillus sporothermodurans

J Appl Microbiol. 2004;97(4):802-9. doi: 10.1111/j.1365-2672.2004.02371.x.

Abstract

Aims: Enumeration of resistant bacteria in ultra-high temperature (UHT) treated milk; morphological characterization and phenotyping of resistant strains by traditional and nontraditional methods and their identification by molecular biology.

Methods and results: Modified standard plate count agar (PCA) and modified brain-heart infusion (BHI) agar were used for colony counts. Physiological culture traits were determined as suggested by Bergey's Manual of Systematic Bacteriology or in modified J-broth or in modified BHI agar. Scanning electron microscope (SEM) was used for microscopic examination. Strain identification was carried out by polymerase chain reaction (PCR). A total of 125 (62.81% of 199) samples were positive and the bacterial load was higher than 10(5) CFU ml(-1) in 46 samples (28.80% of 125). The 16S rRNA sequence of bacterial cultures obtained from UHT-treated milk was similar to that of Bacillus sporothermodurans M215 type strain((T)) and different biotypes were found by analysis of colony appearance, cell morphology and physiological traits.

Conclusions: Bacillus sporothermodurans was the predominant sporigenous micro-organisms in UHT milk.

Significance and impact of the study: BHI agar is more suitable than PCA for quality control of milk after UHT treatment. Modified J-broth medium is useful to determine selected physiological traits of B. sporothermodurans. The strains characterized and identified as B. sporothermodurans were significantly different compared with the type strain.

MeSH terms

  • Animals
  • Bacillus / genetics*
  • Bacillus / metabolism
  • Bacillus / ultrastructure
  • Colony Count, Microbial / methods
  • Culture Media
  • Food Microbiology*
  • Microscopy, Electron, Scanning / methods
  • Milk / microbiology*
  • Phenotype
  • Polymerase Chain Reaction / methods
  • RNA, Ribosomal, 16S / genetics
  • Sterilization
  • Temperature

Substances

  • Culture Media
  • RNA, Ribosomal, 16S