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利用定量杂交方法对几个人工和环境微生物样品的分析研究

Characterization of several synthetic and environmental microbial samples by quantitative hybridization.
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摘要 利用真细菌和真核生物两个域特异性探针 ,初步建立起 16SrRNA定量杂交的方法 ,并对几个人工RNA样品 (由提取自S .cerevisiae和P .fluorescens纯培养细胞的RNA按一定比例混和而成 )和一个提取自垃圾填埋场渗滤液的RNA样品进行了初步的定量分析 .结果表明该方法能从域的水平上对这些样品的组成作较精确的分析 。 Limitations of traditional techniques based on selective enrichment and pure culture isolation make it difficult to precisely characterize the natural microbial ecosystems. Molecular techniques are now being developed and used to address these limitations. Group specific 16S rRNAs targeted oligonucleotide probes of different phylogenetic levels are increasingly used to identify and quantify the microbial members in complex environmental samples. Two domain specific probes were used in this study to elementarily characterize the defined mixtures of RNAs extracted from pure culture (synthetic samples) and a RNA sample obtained from landfill leachate (environmental sample). The results demonstrated that 16S rRNA quantitative hybridization provided an excellent estimation of domain level community composition of these samples, and thus, had a huge potential of usefulness in microbial ecology studies.
出处 《应用生态学报》 CAS CSCD 2003年第3期405-408,共4页 Chinese Journal of Applied Ecology
基金 国家杰出青年基金项目 (3 95 2 5 0 0 7) 国家自然科学基金项目(3 9970 0 63 ) 广东省自然科学基金资助项目 (0 1112 0 )
关键词 16SrRNA 寡核苷酸探针 定量杂交 微生物生态 S rRNA, Oligonucleotide probes, Quantitative hybridization, Microbial ecology.
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参考文献15

  • 1[1]Alm EW, Oerther DB, Larsen N,et al. 1996. The oligonucleotide probe database.Appl Environ Microbiol, 62:3557~3559
  • 2[2]Amann RI, Krumholz L,Stahl DA. 1990. Fluorescent-oligonucleotide probing of whole cells for determinative, phylogenetic and environmental studies in microbiology.J Bacteriol,172:762~770
  • 3[3]Amann RI, Ludwig W,Schleifer KH. 1995. Phologenetic identification and in situ detection of individual microbial cells without cultivation.Microbiol Rev,59:143~169
  • 4[4]Atlas RM.1983.Use of microbial diversity measurements to assess environmental stress. In: Klug MJ and Reddy CA,eds. Current Perspectives in Microbial Ecology.Washington, D.C.:American Society for Microbiology.540~545
  • 5[5]Kogure K, Simidu U,Taga N. 1980. Distribution of viable marine bacterial in netrtic seawater around Japan.Can J Microbiol,26:318~323
  • 6[6]Raskin L,Capman WC, Sharp R,et al.1997. Molecular ecology of gastrointestinal ecosystems.In:Mackie RI, White BA, Issacson RE, eds. Gastrointestinal Microbiology 2.Gastrointestinal Microbes and Host Interactions.New York:Chanpman & Hall,243~298
  • 7[7]Raskin L, Poulse LK, Noguera DR,et al. 1994. Quantification of methanogenic groups in anaerobic biological reactors by oligonucleotide probe hybridization.Appl Environ Microbiol,60:1241~1248
  • 8[8]Raskin L, Stromley JM, Rittmann BE,et al. 1994. Group-specific 16S rRNA hybridization probes to describe natural communities of methanogens.Appl Environ Microbiol,60:1232~1240
  • 9[9]Sambrook J, Fritsch EF Maniatis T. 1989. Molecular Cloning, A Laboratory Manual.2nd ed.New York: Cold Spring Harbor Laboratory Press.
  • 10[10]Stahl DA, Flesher B, Mansfield HR,et al. 1988. Use of phylogenetically based hybridization probes for studies of ruminal microbial ecology.Appl Environ Microbiol,54:1079~1084

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