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. 2007 Jan 26;189(7):2813–2824. doi: 10.1128/JB.01701-06

TABLE 6.

Comparison of specific levels of enterotoxin production between the fnr mutant and its parent strain, B. cereus F4430/73a

Growth conditions Amt of enterotoxin (U g−1 [dry weight] of cells)
Hbl
Nhe
WT fnr WT fnr
Aerobic
    Glucose 1.0 ± 0.2 NZ 1.5 ± 0.3 NZ
Anaerobic
    Glucose 12.0 ± 2.0 NG 8.0 ± 1.0 NG
    Glucose and 20 mM fumarate 10.0 ± 2.0 NG 5.5 ± 0.5 NG
    Glucose and 20 mM nitrate 1.0 ± 0.2 NZ 2.1 ± 0.2 NZ
    Glycerol and 20 mM nitrate 0.16 ± 0.03 NZ 0.37 ± 0.03 NZ
    Glycerol and 60 mM nitrate NZ NZ NZ NZ
a

Hbl and Nhe levels were measured in culture supernatants at the end points for pH-regulated batch cultures. Cells were grown under aerobiosis or anaerobiosis on MOD medium supplemented with glucose (30 mM) or glycerol (60 mM) as a carbon source and with or without an external electron acceptor (nitrate or fumarate). Values are means ± standard deviations of three independent measurements. WT, wild type (B. cereus F4430/73); fnr, fnr mutant; NG, no growth; NZ, yield near zero or below 0.01.