Accession Number:

ADA513406

Title:

Effects of L-Alanine and Inosine Germinants on the Elasticity of Bacillus anthracis Spores

Descriptive Note:

Journal article

Corporate Author:

WORCESTER POLYTECHNIC INST MA DEPT OF CHEMICAL ENGINEERING

Report Date:

2010-01-22

Pagination or Media Count:

8.0

Abstract:

The surface of dormant Bacillus anthracis spores consists of a multilayer of protein coats and a thick peptidoglycan layer that allow the cells to resist chemical and environmental insults. During germination, the spore coat is degraded, making the spore susceptible to chemical inactivation by antisporal agents as well as to mechanical inactivation by high-pressure or mechanical abrasion processes. While chemical changes during germination, especially the release of the germination marker, dipicolinic acid DPA, have been extensively studied, there is as yet no investigation of the corresponding changes in the mechanical properties of the spore. In this work, we use atomic force microscopy AFM to characterize the mechanical properties of the surface of Bacillus anthracis spores during germination. The Hertz model of continuum mechanics of contact was used to evaluate the Youngs moduli of the spores before and after germination by applying the model to load-indentation curves. The highest modulus was observed for dormant spores, with average elasticity values of 197 - 81 MPa. The elasticity decreased significantly after incubation of the spores with the germinants L-alanine or inosine 47.5 - 41.7 and 35.4 - 15.8 MPa, respectively. Exposure of B. anthracis spores to a mixture of both germinants resulted in a synergistic effect with even lower elasticity, with a Youngs modulus of 23.5 - 14.8 MPa. The elasticity of the vegetative B. anthracis cells was nearly 15 times lower than that of the dormant spores 12.4 - 6.3 MPa vs 197.0 - 80.5 MPa, respectively. Indeed from a mechanical strength point of view, the germinated spores were closer to the vegetative cells than to the dormant spores. Further, the decrease in the elasticity of the cells was accompanied by increasing AFM tip indentation depths on the cell surfaces. Indentation depths of up to 246.2 nm were observed for vegetative B. anthracis compared to 20.5 nm for the dormant spores.

Subject Categories:

  • Biochemistry
  • Microbiology

Distribution Statement:

APPROVED FOR PUBLIC RELEASE