Liang Dandan, Xing Fuguo, Selvaraj Jonathan Nimal, Liu Xiao, Wang Limin, Hua Huijuan, Zhou Lu, Zhao Yueju, Wang Yan, Liu Yang
Inst. of Food Science and Technology, Chinese Academy of Agricultural Sciences, Key Laboratory of Agro-products Processing, Ministry of Agriculture, Beijing, 100193, P. R. China.
J Food Sci. 2015 Dec;80(12):M2917-24. doi: 10.1111/1750-3841.13144. Epub 2015 Nov 10.
In order to reveal the inhibitory effects of cinnamaldehyde, citral, and eugenol on aflatoxin biosynthesis, the expression levels of 5 key aflatoxin biosynthetic genes were evaluated by real-time PCR. Aspergillus flavus growth and AFB1 production were completely inhibited by 0.80 mmol/L of cinnamaldehyde and 2.80 mmol/L of citral. However, at lower concentration, cinnamaldehyde (0.40 mmol/L), eugenol (0.80 mmol/L), and citral (0.56 mmol/L) significantly reduced AFB1 production with inhibition rate of 68.9%, 95.4%, and 41.8%, respectively, while no effect on fungal growth. Real-time PCR showed that the expressions of aflR, aflT, aflD, aflM, and aflP were down-regulated by cinnamaldehyde (0.40 mmol/L), eugenol (0.80 mmol/L), and citral (0.56 mmol/L). In the presence of cinnamaldehyde, AflM was highly down-regulated (average of 5963 folds), followed by aflP, aflR, aflD, and aflT with the average folds of 55, 18, 6.5, and 5.8, respectively. With 0.80 mmol/L of eugenol, aflP was highly down-regulated (average of 2061-folds), followed by aflM, aflR, aflD, and aflT with average of 138-, 15-, 5.2-, and 4.8-folds reduction, respectively. With 0.56 mmol/L of citral, aflT was completely inhibited, followed by aflM, aflP, aflR, and aflD with average of 257-, 29-, 3.5-, and 2.5-folds reduction, respectively. These results suggest that the reduction in AFB1 production by cinnamaldehyde, eugenol, and citral at low concentration may be due to the down-regulations of the transcription level of aflatoxin biosynthetic genes. Cinnamaldehyde and eugenol may be employed successfully as a good candidate in controlling of toxigenic fungi and subsequently contamination with aflatoxins in practice.
为揭示肉桂醛、柠檬醛和丁香酚对黄曲霉毒素生物合成的抑制作用,通过实时荧光定量PCR评估了5个关键黄曲霉毒素生物合成基因的表达水平。0.80 mmol/L的肉桂醛和2.80 mmol/L的柠檬醛可完全抑制黄曲霉生长和AFB1产生。然而,在较低浓度下,肉桂醛(0.40 mmol/L)、丁香酚(0.80 mmol/L)和柠檬醛(0.56 mmol/L)可显著降低AFB1产生,抑制率分别为68.9%、95.4%和41.8%,而对真菌生长无影响。实时荧光定量PCR显示,肉桂醛(0.40 mmol/L)、丁香酚(0.80 mmol/L)和柠檬醛(0.56 mmol/L)可下调aflR、aflT、aflD、aflM和aflP的表达。在肉桂醛存在下,AflM高度下调(平均下调5963倍),其次是aflP、aflR、aflD和aflT,平均下调倍数分别为55、18、6.5和5.8倍。在0.80 mmol/L丁香酚作用下,aflP高度下调(平均下调2061倍),其次是aflM、aflR、aflD和aflT,平均下调倍数分别为138、15、5.2和4.8倍。在0.56 mmol/L柠檬醛作用下,aflT完全被抑制,其次是aflM、aflP、aflR和aflD,平均下调倍数分别为257、29、3.5和2.5倍。这些结果表明,低浓度的肉桂醛、丁香酚和柠檬醛降低AFB1产生可能是由于黄曲霉毒素生物合成基因转录水平下调所致。肉桂醛和丁香酚有望成功用于实际控制产毒真菌及随后的黄曲霉毒素污染。