首页> 外文期刊>Water Research >Study on characteristics of biocometabolic removal of omethoate by the Aspergillus spp
【24h】

Study on characteristics of biocometabolic removal of omethoate by the Aspergillus spp

机译:曲霉菌生物催化去除氧化乐果的特性研究

获取原文
获取原文并翻译 | 示例
           

摘要

A strain Aspergillus spp. F1 which could effectively metabolized omethoate was screened out in this study. F1 tended to form granula with diameter 4-5 mm after 5 days culture in shaker. The pH range from 4.5 to 6.5 was the suitable pH range for growth and metabolism of Aspergillus spp. Fl. The maximum omethoate removal rate was about 3.0mg/ (h L), and the removal fraction of omethoate reached 90% after 8 days culture when initial concentrations of omethoate were not more than 2000 mg/L in medium. There was no obvious relativity between cell growth and cometabolism of omethoate. Starch was the best carbon source for omethoate removal and the result after 3 days reached 56.6% removal. Fl could use omethoate to metabolize as single nitrogen or phosphate source. The residual fragments in medium after treatment with the Aspergillus spp. Fl were determined by gas chromatography-mass spectrometry. The analysis results showed that only fragment o,o,s,-trimethyl phosphorothioate (TEP) containing phosphorus was available and the fragment containing nitrogen was consumed by Fl thoroughly in culture process. But no accumulations of TEP were observed in the omethoate bioremediation process. Fl could effectively remove omethoate in complex nutritional environment safely.
机译:菌株曲霉属。在这项研究中筛选出可以有效代谢氧化乐果的F1。在摇床上培养5天后,F1倾向于形成直径4-5 mm的颗粒。 pH范围为4.5至6.5是曲霉属菌生长和代谢的合适pH范围。图最大氧化乐果去除率约为3.0mg /(h L),培养8天后,当培养基中氧化乐果的初始浓度不超过2000 mg / L时,氧化乐果的去除率达到90%。氧化乐果的细胞生长与新陈代谢之间没有明显的相关性。淀粉是去除氧化乐果的最佳碳源,3天后去除率达到56.6%。 F1可以使用氧化乐果作为单一氮或磷酸盐源进行代谢。用曲霉属菌种处理后培养基中的残留片段。通过气相色谱-质谱法测定F1。分析结果表明,在培养过程中,只有含磷的邻,间,三硫代磷酸三甲酯(TEP)片段可用,而含氮片段被Fl完全消耗。但是在氧化乐果的生物修复过程中未观察到TEP的积累。 Fl可以在复杂的营养环境中有效地去除氧化乐果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号