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. 2014 Nov 13;6(11):3157–3172. doi: 10.3390/toxins6113157

Table 2.

Effect of different nitrogen sources, tryptone concentrations and initial pH value on aflatoxin B1 degradation (%) by Aspergillus niger. The reactions were carried out at 32 °C with agitation at 200 rpm for 24 h. Sterile MTM was used to substitute microbial culture in the control. Results are expressed as means ± SEM of three replicates. In nitrogen sources group, means without a common letter denote significant differences according Least Significant Difference method (p < 0.05); in tryptone concentrations group and initial pH value group, means without a common letter denote significant differences according Least Significant Difference method (p < 0.01); SEM, standard error of the mean.

Nitrogen sources Aflatoxin B1 degradation (%) Concentrations of tryptone (%) Aflatoxin B1 degradation (%) Initial pH value Aflatoxin B1 degradation (%)
tryptone 50.7 ± 0.6 a 0.5 50.7 ± 0.6 A 6.0 58.2 ± 0.9 A
Acidicase peptone 47.0 ± 1.0 b 0.7 50.4 ± 0.4 A 6.5 50.7 ± 0.6 B
Proteose peptone 45.1 ± 1.5 b 0.9 49.8 ± 0.3 A 7.0 49.2 ± 1.0 B
Ammonium nitrate 39.1 ± 1.1 c 0.3 38.9 ± 1.6 B 7.5 47.9 ± 1.6 B
Mixed ammonium salt 37.0 ± 1.0 c 0.1 14.1 ± 0.9 C 8.0 47.1 ± 1.1 B
Beef extract peptone 33.3 ± 0.8 d - - 5.5 35.2 ± 0.9 C
Peptone 33.1 ± 1.6 d - - 5.0 27.4 ± 1.8 D
Beef extract 32.6 ± 1.1 d - - - -

a, b, c, d, indicate significant differences between treatments at the 5% level of probability (p < 0.05).

A, B, C, D, indicate significant differences between treatments at the 1% level of probability (p < 0.01).