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希瓦氏菌S12对偶氮萘胺磺酸染料苋菜红的还原及部分降解机制

Reduction and partial degradation mechanisms of naphthylaminesulfonic azo dye amaranth by Shewanella decolorationis S12.

作者信息

Hong Yiguo, Guo Jun, Xu Zhicheng, Mo Cuiyun, Xu Meiying, Sun Guoping

机构信息

Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, Guangdong Institute of Microbiology, Guangzhou, 510070, China.

出版信息

Appl Microbiol Biotechnol. 2007 Jun;75(3):647-54. doi: 10.1007/s00253-007-0838-7. Epub 2007 Jan 27.

Abstract

Reduction and biodegradation mechanisms of naphthylaminesulfonic azo dye amaranth using a newly isolated Shewanella decolorationis strain S12 were investigated. Under anaerobic conditions, amaranth was reduced by strain S12, and a stoichiometric amount of two reduction products RP-1 and RP-2 were generated. UV/visible spectrophotometric and high performance liquid chromatography (HPLC) analysis indicated that RP-1 and RP-2 were 1-aminenaphthylene -4-sulfonic acid and 1-aminenaphthylene-2-hydroxy-3, 6-disulfonic acid. The result strongly supports a mechanism of azo dye reduction by the process via the reductive cleavage of the azo bond to form corresponding aromatic amines. The result of HPLC analyses revealed that these aromatic amines were not able to be mineralized by strain S12 under anaerobic conditions. But after re-aeration of the decolorized culture, RP-2 was mineralized completely by this microorganism, but the consumption of RP-1 was not observed. Ames test showed that amaranth had mutagenic but no cytotoxic potential. The mutagenic potential was relieved after the anaerobic treatment with strain S12 as the mutagenic effect of the two reduction products from amaranth was not detected by Ames test. Thus, the ability of strain S12 to reduce and partially mineralize the naphthylaminesulfonic azo dye efficiently was demonstrated, which can potentially be used to biodegrade and detoxify wastewater containing azo dyes using an alternating anaerobic/aerobic treatment procedure.

摘要

研究了一种新分离的希瓦氏菌脱色希瓦氏菌菌株S12对萘胺磺酸偶氮染料苋菜红的还原和生物降解机制。在厌氧条件下,菌株S12将苋菜红还原,并生成化学计量的两种还原产物RP-1和RP-2。紫外/可见分光光度法和高效液相色谱(HPLC)分析表明,RP-1和RP-2分别为1-氨基萘-4-磺酸和1-氨基萘-2-羟基-3,6-二磺酸。该结果有力地支持了偶氮染料通过偶氮键的还原裂解形成相应芳香胺的过程进行还原的机制。HPLC分析结果表明,这些芳香胺在厌氧条件下不能被菌株S12矿化。但是,在对脱色培养物进行再曝气后,RP-2被该微生物完全矿化,但未观察到RP-1的消耗。艾姆斯试验表明,苋菜红具有诱变潜力但无细胞毒性潜力。在用菌株S12进行厌氧处理后,诱变潜力得到缓解,因为艾姆斯试验未检测到苋菜红的两种还原产物的诱变作用。因此,证明了菌株S12有效还原和部分矿化萘胺磺酸偶氮染料的能力,这有可能用于通过交替厌氧/好氧处理程序对含偶氮染料的废水进行生物降解和解毒。

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