期刊文献+

PCR-DGGE技术在厌氧反应器中的应用 被引量:4

Application of PCR-DGGE in the Anaerobic Reactor
下载PDF
导出
摘要 PCR-DGGE技术是现代分子生物学技术中一种很重要的分析手段,近年来在环境微生物领域发展迅速,与传统微生物培养鉴定方法相比,PCR-DGGE技术简便、快速、准确,并且对于难以培养的微生物也具有较好的分离效果,因此,在环境微生物领域中受到普遍重视。介绍了PCR-DGGE技术的基本原理、影响因素,以及在厌氧反应器中的应用,并对其应用前景做了展望。 PCR-DGGE technique is a very important tool in modem molecular biology techniques in recent years.It has a rapid development in the field of environmental microbiology, compared to traditional identification of bacterial culture, PCR-DGGE technique is simple, rapid, accurate, and has a better separation effect to difficult culture organisms. Therefore, PCR-DGGE technique has received wide attention in the field of environmental microbiology. The basic principle and influence factors of this technology were introduced as well as application in the anaerobic reactor, and its application prospect was put forward.
出处 《辽宁化工》 CAS 2010年第12期1263-1265,共3页 Liaoning Chemical Industry
基金 国家自然科学基金资助项目 项目号:50978118
关键词 PCR-DGGE 厌氧反应器 分子生物学 PCR-DGGE Anaerobic reactor Molecular biology
  • 相关文献

参考文献22

  • 1马溪平等..厌氧微生物学与污水处理[M],2005.
  • 2张自杰主编..排水工程 下 第4版[M].北京:中国建筑工业出版社,2000:637.
  • 3Muyzer,G.,.DGGE/TGGE a method for identifying genes from natural ecosystems[J].Curr.Opin.Microbiol.1999,2:317-322. 被引量:1
  • 4Muyzer,G.,E.C.de Waal,and A.G.Uitterlinden.Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction-amplified genes coding for 16S Rrna[J].Appl Environ Microbiol,1993,59:695-700. 被引量:1
  • 5Muyzer G,Smalla K.Application of denaturing gradient gel electrophoresis (DGGE) and temperature gradient gel electrophoresis (TGGE) inmicrobial ecology[J].AntonievanLeeuwenhoek,1998,73:127-141. 被引量:1
  • 6Muyzer G,Waal EC,Uitterlinden AG.Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction amplified genes encoding for 16S Rrna[J].Appl Environ Microbiol,1993,59:695-700. 被引量:1
  • 7Krsek M,Wellington EMH.Comparison of different methods for the isolation and purification of total community DNA from soil[J].Microbiol Methods,1999,39:1-16. 被引量:1
  • 8李鹏,毕学军,汝少国.DNA提取方法对活性污泥微生物多样性PCR-DGGE检测的影响[J].安全与环境学报,2007,7(2):53-57. 被引量:33
  • 9Myers RM,Fischer SG,Lerman LS,et al.Nearly all single base substitutions in DNA fragments joined to a GC-clamp can be detected by denaturing gradient gel electrophoresis[J].NucleicAcids Res,1985,13:3131-3145. 被引量:1
  • 10Sheffield V.C.,Cox D.R.,Myers RM.Attachment of a 40bp G+C rich sequence (GC clamp) to genomic DNA fragments by polymerase chain reaction results in improved detection of single-base changes[J].Proc NatlAcad Sci USA,1989,86:232-236. 被引量:1

二级参考文献62

共引文献138

同被引文献49

引证文献4

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部