Spores of Bacillus subtilis: their resistance to and killing by radiation, heat and chemicals

• Published in: Journal of applied microbiology 2006-09, Vol.101 (3), p.514-525
• Main Author: Setlow, P
• Format: Article
• Language: English
• Subjects: Bacillus; Bacillus subtilis; Bacillus subtilis - drug effects; Bacillus subtilis - physiology; Bacillus subtilis - radiation effects; Biological and medical sciences; Cell Death - drug effects; Cell Death - radiation effects; Cell Membrane Permeability - physiology; DNA Damage; DNA, Bacterial; Drug Resistance, Bacterial - physiology; Fundamental and applied biological sciences. Psychology; Gamma Rays; Hot Temperature; Microbiology; Radiation, Ionizing; Spores, Bacterial - drug effects; Spores, Bacterial - physiology; Spores, Bacterial - radiation effects; Ultraviolet Rays; Water
• ISSN: 1364-5072; 1365-2672
• DOI: 10.1111/j.1365-2672.2005.02736.x

A number of mechanisms are responsible for the resistance of spores of Bacillus species to heat, radiation and chemicals and for spore killing by these agents. Spore resistance to wet heat is determined largely by the water content of spore core, which is much lower than that in the growing cell protoplast. A lower core water content generally gives more wet heat-resistant spores. The level and type of spore core mineral ions and the intrinsic stability of total spore proteins also play a role in spore wet heat resistance, and the saturation of spore DNA with α/β-type small, acid-soluble spore proteins (SASP) protects DNA against wet heat damage. However, how wet heat kills spores is not clear, although it is not through DNA damage. The α/β-type SASP are also important in spore resistance to dry heat, as is DNA repair in spore outgrowth, as Bacillus subtilis spores are killed by dry heat via DNA damage. Both UV and γ-radiation also kill spores via DNA damage. The mechanism of spore resistance to γ-radiation is not well understood, although the α/β-type SASP are not involved. In contrast, spore UV resistance is due largely to an alteration in spore DNA photochemistry caused by the binding of α/β-type SASP to the DNA, and to a lesser extent to the photosensitizing action of the spore core's large pool of dipicolinic acid. UV irradiation of spores at 254 nm does not generate the cyclobutane dimers (CPDs) and (6-4)-photoproducts (64PPs) formed between adjacent pyrimidines in growing cells, but rather a thymidyl-thymidine adduct termed spore photoproduct (SP). While SP is formed in spores with approximately the same quantum efficiency as that for generation of CPDs and 64PPs in growing cells, SP is repaired rapidly and efficiently in spore outgrowth by a number of repair systems, at least one of which is specific for SP. Some chemicals (e.g. nitrous acid, formaldehyde) again kill spores by DNA damage, while others, in particular oxidizing agents, appear to damage the spore's inner membrane so that this membrane ruptures upon spore germination and outgrowth. There are also other agents such as glutaraldehyde for which the mechanism of spore killing is unclear. Factors important in spore chemical resistance vary with the chemical, but include: (i) the spore coat proteins that likely react with and detoxify chemical agents; (ii) the relative impermeability of the spore's inner membrane that restricts access of exogenous chemicals to the spore core; (iii) the prote