Suppr超能文献

土壤链霉菌对甲草胺的生物降解作用。

Biodegradation of alachlor by soil streptomycetes.

作者信息

Durães Sette L, Mendonça Alves Da Costa L A, Marsaioli A J, Manfio G P

机构信息

CPQBA/UNICAMP, CP 6171, SP CEP 13081-970, Campinas, Brazil.

出版信息

Appl Microbiol Biotechnol. 2004 Jun;64(5):712-7. doi: 10.1007/s00253-003-1494-1. Epub 2004 Jan 16.

Abstract

Streptomycetes resistant to the herbicide alachlor [2-chloro-2',6'-diethyl- N-(methoxymethyl) acetanilide] were used in degradation assays to characterize the products of alachlor biodegradation. Of six strains tested, Streptomyces sp. LS166, LS177, and LS182 were able to grow at an alachlor concentration of 144 mg l(-1) and degraded approximately 60-75% of the alachlor in 14 days, as evaluated by high performance liquid chromatography. The alachlor biodegradation products were identified by gas chromatography-mass spectrometry based on mass spectral data and fragmentation patterns. All compounds detected in these assays were similar for all streptomycetes strains tested, and involved dechlorination with subsequent N-dealkylation and cyclization of the remaining N-substituent with one of the ethyl groups to produce indole and quinoline derivatives. The enzymatic pathway used by Streptomyces sp. LS182 did not generate DEA (2',6'-diethylaniline), a carcinogenic derivative of alachlor reported in other studies. Given the high degradation rates observed here, the Streptomyces strains tested may be useful in the degradation/detoxification processes of alachlor.

摘要

对除草剂甲草胺[2-氯-2',6'-二乙基-N-(甲氧基甲基)乙酰苯胺]具有抗性的链霉菌被用于降解试验,以表征甲草胺生物降解的产物。在所测试的6个菌株中,链霉菌属的LS166、LS177和LS182能够在144 mg l(-1)的甲草胺浓度下生长,并在14天内降解约60-75%的甲草胺,这是通过高效液相色谱法评估得出的。基于质谱数据和裂解模式,通过气相色谱-质谱联用仪鉴定了甲草胺的生物降解产物。在这些试验中检测到的所有化合物对于所有测试的链霉菌菌株都是相似的,包括脱氯,随后是N-脱烷基化以及剩余N-取代基与其中一个乙基进行环化反应,从而生成吲哚和喹啉衍生物。链霉菌属的LS182所使用的酶促途径不会产生DEA(2',6'-二乙苯胺),DEA是其他研究中报道的甲草胺的致癌衍生物。鉴于此处观察到的高降解率,所测试的链霉菌菌株可能在甲草胺的降解/解毒过程中有用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验