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嗜盐菌Halobacterium species NRC-1不同盐浓度下基因表达差异分析

Analysis on Differential Genes in Changing Salinity in The Halophile Halobacterium species NRC-1
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摘要 用RNA随机起始PCR(RAP-PCR)技术分析了盐杆菌NRC-1(Halobacterium NRC-1)不同NaCl盐度下基因表达的差异。81条引物用于比较17%、30%两种盐度下基因表达的差异,每条引物平均可以产生10条以上扩增条带,共得到15条在2种盐度下差异表达的条带,这些差异扩增条带的获得将有助从分子水平上了解Halobacterium NRC-1在高盐环境下的适应机制。 The RNA arbitrarily primed PCR (RAP-PCR) approach was used to identify those genes that are differentially expressed in response to changing salinity in Halobacterium NRC-1. 81 primers were used to scan two different RNA pools derived from cultures of 17% and 30% NaC1 concentrations. On average, each RT-PCR reaction yielded more than ten bands on the agrose gel. Of the approximately 900 bands that were generated by 81 RT-PCR reaction pairs, 15 differentially-expressed bands were obtained. The results would be useful to understand the adaptation raeehanism of Halobacterium NRC-1 to high salinity conditions.
作者 李鑫 刘军
出处 《微生物学杂志》 CAS CSCD 2009年第4期62-66,共5页 Journal of Microbiology
基金 湖北省自然科学基金资助项目(2005ABA094)
关键词 差异表达 盐杆菌NRC-1 RNA随机起始PCR Differential expression Halobacterium species NRC-1 RNA arbitrarily primed PCR (RAP-PCR)
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参考文献10

  • 1Ng WV, Kennedy SP, Mahairas GG, et al. Genome sequence of Halobacterium species NRC-1 [J]. PNAS, 2000, 97 (22) : 12 176-12 181.
  • 2Bidle KA. Differential expression of genes induced by changing salinity using RNA arbitrarily primed PCR in the archaeal halophile Haloferax volcanii[ J]. Extremophiles, 2003,7: 1-7.
  • 3Li SK, Xiao X, Li JY, et al. Identification of genes regulated by changing salinity in the deep-sea bacterium Shewanella sp. WP3 using RNA arbitrarily primed PCR [ J]. Extremophiles, 2006, 10:97-104.
  • 4Brzostowicz PC, Gibson KL, Thomas SM, et al. Simultaneous identification of two cyclohexanone oxidation genes from an environmental Brivibacterium isolate using mRNA differential display[ J]. Journal of Bacteriology, 2000,182:4 241-4 248.
  • 5Liang P, Pardee AB. Differential display of eukaryotic messenger mRNA by means of the polymerase chain reaction[ J]. Science, 1992, 257 : 967-971.
  • 6Welsh J, Chada K, Dalai SS, et al. Arbitrarily primed PCR fingerprinting of RNA [ J ]. Nucleic Acids Res. , 1992, 11 :4 965-4 970.
  • 7Fleming JT, Yao WH, Sayler GS. Optimization of differential display of prokaryotic mRNA : application to pure culture and soil microcosms [ J]. Applied and environmental microbiology, 1998, 64:3 698-3 706.
  • 8Bhaya D, Vaulot D, Amin P, et al. lsolation of regulated genes of the cyanobacterium Synechocystis sp. Strain PCC 6803 by differential display[ J]. Journal of Bacteriology, 2000, 182 (20) :5 692-5 699.
  • 9Brzostowicz PC, Waiters DM, Thomas SM, et al. mRNA differential display in a microbial enrichment culture: Simuhaneous identification of three eyelohexanone monooxygenases from three species [ J ]. Applied and environmental microbiology, 2003,69 : 334-342.
  • 10Wahers DM, Russ R, Knackmuss HJ, et al. High-density sampiing of a bacterial operon using mRNA differential display[ J]. Gene, 2001,273 : 305-315.

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