...
首页> 外文期刊>Polymer Degradation and Stability >RNA analysis of anaerobic sludge during anaerobic biodegradation of cellulose and poly(lactic acid) by RT-PCR-DGGE
【24h】

RNA analysis of anaerobic sludge during anaerobic biodegradation of cellulose and poly(lactic acid) by RT-PCR-DGGE

机译:RT-PCR-DGGE对纤维素和聚乳酸厌氧降解过程中厌氧污泥的RNA分析

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Here, we apply a method to evaluate the anaerobic biodegradability of bioplastics, such as poly-caprolactone and poly(lactic acid) (PLA), in aquatic (slurry) conditions at 55 C. Previous reports have suggested that some of the microorganisms participating in the anaerobic biodegradation of cellulose and PLA differ. however, polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) analysis was ineffective at detecting the microorganisms involved in the anaerobic biodegradation of cellulose and PLA. In this study, reverse transcription-PCR-DGGE analysis was employed instead. New DGGE bands appeared during the anaerobic biodegradation of cellulose and PLA, and some of these DGGE bands differed between the anaerobic biodegradation of cellulose and PLA, indicating that some of the microorganisms involved in these two processes differed. These results and those of our previous study therefore show that it is necessary to describe, not the anaerobic biodegradation rate of cellulose, as generally used at present, but the anaerobic biodegradation rate of plastic in the plastic anaerobic biodegradation test, to evaluate the sludge condition containing plastic anaerobic biodegradation activity in the sludge used in the anaerobic biodegradation test of plastics at 55 C.
机译:在这里,我们采用一种方法来评估生物塑料(如聚己内酯和聚乳酸(PLA))在水(泥浆)条件下于55℃下的厌氧生物降解性。以前的报告表明,某些微生物参与其中纤维素和PLA的厌氧生物降解有所不同。然而,聚合酶链反应-变性梯度凝胶电泳(PCR-DGGE)分析不能有效地检测出涉及纤维素和PLA厌氧生物降解的微生物。在这项研究中,采用了逆转录-PCR-DGGE分析。纤维素和PLA的厌氧生物降解过程中出现了新的DGGE谱带,其中某些DGGE谱带在纤维素和PLA的厌氧生物降解之间有所不同,表明这两个过程中涉及的某些微生物有所不同。因此,这些结果和我们先前研究的结果表明,有必要描述塑料的厌氧生物降解测试中的塑料厌氧生物降解率,而不是像目前通常使用的那样,而是描述塑料的厌氧生物降解率。在55°C下用于塑料厌氧生物降解测试的污泥中含有塑料厌氧生物降解活性。

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