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. 2019 Jan 4;9:3163. doi: 10.3389/fmicb.2018.03163

Table 1.

Percentage of superdormant (SD) spores in various isolation conditions and proposed superdormancy mechanisms.

SD spore type Germination stimulus Species ca. % SD spores Proposed superdormancy mechanisms Reference
Valine (10 mM) B. subtilis 1.1 Chen et al., 2014
Valine (10 mM) B. subtilis 4 Zhang et al., 20121
Valine (10 mM) B. subtilis 3.8 Ghosh and Setlow, 2009
Valine (300 μM) B. subtilis 58 Ghosh and Setlow, 2009
10 × LB medium2 B. subtilis 0.7 Ghosh and Setlow, 2009
AGFK3 B. subtilis 12 Permanent cause: lower GR Ghosh and Setlow, 2009
AGFK4 B. subtilis 6 levels Transient cause: Zhang et al., 20121
Nutrient-SD Glucose (10 mM) B. megaterium 3.5 activation status Ghosh and Setlow, 2009
Glucose (200 μM) B. megaterium 38 (Ghosh et al., 2009, 2012; Ghosh and Setlow, 2009
10 × LB medium B. megaterium 0.5 Wei et al., 2010; Ghosh and Setlow, 2009
Alanine (50 mM) B. cereus 5.3 Zhang et al., 2012) Ghosh and Setlow, 2010
Inosine (5 mM) B. cereus 2.3 Ghosh and Setlow, 2010
Inosine (250 μM) B. cereus 12 Ghosh and Setlow, 2010
Inosine (5 mM, no heat activation) B. cereus 12 Ghosh and Setlow, 2010
Ca2+DPA-SD Ca2+-DPA (60 mM) B. subtilis 0.9 (0.5–1.6) Coat defect, low levels of CLE CwlJ Perez-Valdespino et al., 2013
Dodecylamine-SD Dodecylamine (1.2 mM) B. subtilis 0.4 (0.1–1.1) Not clear Perez-Valdespino et al., 2013
High pressure SD No reported isolation Different to nutrient superdormancy Wei et al., 2010

Unless stated otherwise, heat activation was applied prior to nutrient germination for different species: B. subtilis: 75°C, 30 min; B. megaterium: 60°C, 15 min; B. cereus: 65°C, 20 min. 1Spores were heat activated at 70°C for 30 min. SD spore percentages were calculated based on observation of >440 spore for listed cases; 2LB medium: Luria-Bertani medium; 3AGFK (12 mM L-asparagine, 13 mM D-glucose, 13 mM D-fructose, 12.5 mM KPO4 buffer [pH 7.4]); 4AGFK (10 mM L-asparagine, 10 mM D-glucose, 10 mM D-fructose, 10 mM KCl in 25 mM KPO4 buffer [pH 7.4]).