Hawari J, Halasz A, Beaudet S, Paquet L, Ampleman G, Thiboutot S
Biotechnology Research Institute, National Research Council, Montreal, PQ H4P 2R2, Canada.
Appl Environ Microbiol. 1999 Jul;65(7):2977-86. doi: 10.1128/AEM.65.7.2977-2986.1999.
The biotransformation of 2,4,6-trinitrotoluene (TNT) (175 microM) by Phanerochaete chrysosporium with molasses and citric acid at pH 4.5 was studied. In less than 2 weeks, TNT disappeared completely, but mineralization (liberated 14CO2) did not exceed 1%. A time study revealed the presence of several intermediates, marked by the initial formation of two monohydroxylaminodinitrotoluenes (2- and 4-HADNT) followed by their successive transformation to several other products, including monoaminodinitrotoluenes (ADNT). A group of nine acylated intermediates were also detected. They included 2-N-acetylamido-4,6-dinitrotoluene and its p isomer, 2-formylamido-4, 6-dinitrotoluene and its p isomer (as acylated ADNT), 4-N-acetylamino-2-amino-6-nitrotoluene and 4-N-formylamido-2-amino-6-nitrotoluene (as acetylated DANT), 4-N-acetylhydroxy-2,6-dinitrotoluene and 4-N-acetoxy-2, 6-dinitrotoluene (as acetylated HADNT), and finally 4-N-acetylamido-2-hydroxylamino-6-nitrotoluene. Furthermore, a fraction of HADNTs were found to rearrange to their corresponding phenolamines (Bamberger rearrangement), while another group dimerized to azoxytoluenes which in turn transformed to azo compounds and eventually to the corresponding hydrazo derivatives. After 30 days, all of these metabolites, except traces of 4-ADNT and the hydrazo derivatives, disappeared, but mineralization did not exceed 10% even after the incubation period was increased to 120 days. The biotransformation of TNT was accompanied by the appearance of manganese peroxidase (MnP) and lignin-dependent peroxidase (LiP) activities. MnP activity was observed almost immediately after TNT disappearance, which was the period marked by the appearance of the initial metabolites (HADNT and ADNT), whereas the LiP activity was observed after 8 days of incubation, corresponding to the appearance of the acyl derivatives. Both MnP and LiP activities reached their maximum levels (100 and 10 U/liter, respectively) within 10 to 15 days after inoculation.
研究了在pH 4.5条件下,用糖蜜和柠檬酸,黄孢原毛平革菌对2,4,6-三硝基甲苯(TNT)(175微摩尔)的生物转化。在不到2周的时间里,TNT完全消失,但矿化作用(释放出的14CO2)不超过1%。一项时间研究揭示了几种中间产物的存在,其特征是最初形成两种单羟基氨基二硝基甲苯(2-和4-HADNT),随后它们依次转化为其他几种产物,包括单氨基二硝基甲苯(ADNT)。还检测到一组九种酰化中间产物。它们包括2-N-乙酰氨基-4,6-二硝基甲苯及其对位异构体、2-甲酰氨基-4,6-二硝基甲苯及其对位异构体(作为酰化ADNT)、4-N-乙酰氨基-2-氨基-6-硝基甲苯和4-N-甲酰氨基-2-氨基-6-硝基甲苯(作为乙酰化DANT)、4-N-乙酰羟基-2,6-二硝基甲苯和4-N-乙酰氧基-2,6-二硝基甲苯(作为乙酰化HADNT),最后是4-N-乙酰氨基-2-羟基氨基-6-硝基甲苯。此外,发现一部分HADNT重排为其相应的酚胺(班伯格重排),而另一组二聚为氧化偶氮甲苯,氧化偶氮甲苯又转化为偶氮化合物并最终转化为相应的连氮衍生物。30天后,除了痕量的4-ADNT和连氮衍生物外,所有这些代谢产物都消失了,但即使将培养时间延长至120天,矿化作用也不超过10%。TNT的生物转化伴随着锰过氧化物酶(MnP)和木质素依赖性过氧化物酶(LiP)活性的出现。MnP活性在TNT消失后几乎立即被观察到,这一时期以最初的代谢产物(HADNT和ADNT)的出现为标志,而LiP活性在培养8天后被观察到,这与酰基衍生物的出现相对应。MnP和LiP活性在接种后10至15天内均达到最高水平(分别为100和10 U/升)。