Patel I R, Rao K K
Acta Microbiol Hung. 1984;31(4):359-64.
Microsomal metabolites of aflatoxin B1 (AFB1) causing induction of prophage in lysogenic strain of Pseudomonas aeruginosa SM was studied. Reduction of culture turbidity was determined at various concentrations of toxin. The effect of the toxin was also studied on deoxyribonucleic acid (DNA), ribonucleic acid (RNA) and protein synthesis. AFB1 at the concentration of 50 micrograms/ml reduced initial turbidity to approximately 90% in 4 h. DNA synthesis stopped completely in the first hour but reappeared due to induction of the temperate phage. Soon after induction both RNA and protein synthesis continued but later little or no net synthesis of these macromolecules occurred. Plaque forming units (pfu) were increased approximately 90 times at 2 h as compared to the control. Testing of the effect of AFB1 on the non-lysogenic, sensitive strain demonstrated that although there was no significant decrease in culture turbidity at 50 micrograms/ml concentration of AFB1, DNA synthesis stopped completely within 1 h, while RNA and protein synthesis were increasing throughout the test interval. It has been concluded that the liver microsomal fraction of AFB1 caused induction of prophage in lysogenic cells and inhibited DNA synthesis significantly in non-lysogenic cells.
对黄曲霉毒素B1(AFB1)的微粒体代谢产物进行了研究,该代谢产物可导致铜绿假单胞菌SM溶原性菌株中的前噬菌体诱导。在不同毒素浓度下测定培养物浊度的降低情况。还研究了毒素对脱氧核糖核酸(DNA)、核糖核酸(RNA)和蛋白质合成的影响。浓度为50微克/毫升的AFB1在4小时内将初始浊度降低至约90%。DNA合成在第一小时完全停止,但由于温和噬菌体的诱导而重新出现。诱导后不久,RNA和蛋白质合成继续,但后来这些大分子的净合成很少或没有发生。与对照相比,2小时时噬菌斑形成单位(pfu)增加了约90倍。对AFB1对非溶原性敏感菌株的作用测试表明,尽管在AFB1浓度为50微克/毫升时培养物浊度没有显著降低,但DNA合成在1小时内完全停止,而RNA和蛋白质合成在整个测试期间都在增加。得出的结论是,AFB1的肝脏微粒体部分在溶原性细胞中导致前噬菌体诱导,并在非溶原性细胞中显著抑制DNA合成。