Bafana Amit, Jain Minakshi, Agrawal Gaurav, Chakrabarti Tapan
Environmental Biotechnology Division, National Environmental Engineering Research Institute, Nagpur, India.
Chemosphere. 2009 Mar;74(10):1404-6. doi: 10.1016/j.chemosphere.2008.11.043. Epub 2008 Dec 25.
Direct Red 28 (DR28) is a benzidine-based azo dye widely used in several countries. It has also been a subject of intense research for its anti-prion activity. Like other benzidine-based azo dyes, it is also carcinogenic and toxic. However, there are very few studies addressing its detoxification. In the present study, a Bacillus velezensis strain was used for detoxification of DR28. Toxicity was checked by a battery of highly sensitive genotoxicity assays like comet assay, DNA ladder formation, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling assay and flow cytometric Annexin V binding assay. HL-60 cell line was used as the test system. All the assays showed an initial increase in toxicity upon biodegradation due to release of mutagenic products, like benzidine and 4-aminobiphenyl, from the dye. These intermediates caused significant DNA damage and induced apoptosis in HL-60 cells. Then the culture degraded these mutagenic intermediates, due to which the toxicity was reduced gradually, finally resulting in nearly complete detoxification.
直接红28(DR28)是一种基于联苯胺的偶氮染料,在多个国家被广泛使用。因其抗朊病毒活性,它也一直是深入研究的对象。与其他基于联苯胺的偶氮染料一样,它也具有致癌性和毒性。然而,针对其解毒的研究非常少。在本研究中,一株贝莱斯芽孢杆菌被用于对DR28进行解毒。通过一系列高灵敏度的遗传毒性试验来检测毒性,如彗星试验、DNA梯状条带形成、末端脱氧核苷酸转移酶介导的dUTP缺口末端标记试验和流式细胞术膜联蛋白V结合试验。HL-60细胞系用作测试系统。所有试验均表明,由于染料中诱变产物如联苯胺和4-氨基联苯的释放,生物降解后毒性最初会增加。这些中间产物导致显著的DNA损伤并诱导HL-60细胞凋亡。然后培养物降解这些诱变中间产物,由此毒性逐渐降低,最终实现几乎完全解毒。