期刊文献+

一株生防圆突起链霉菌的分类鉴定 被引量:4

Taxonomy of the Streptomyces torulosus strain exhibiting potential for biological control
原文传递
导出
摘要 菌株SCY311是从河南省凤凰山土壤样品中分离到的,对多种植物病原真菌具有拮抗活性的一株放线菌。为了明确其分类地位,在形态特征、培养特征、生理生化特征、细胞壁组分测定等传统分类学方法的基础上,测定和分析了菌株的16S rRNA基因序列。结果表明,菌株SCY311在高氏一号培养基上生长良好,基内菌丝呈褐色;气生菌丝灰色至鼠灰色,不产生可溶性色素,无吸水现象;孢子链卷曲,末端形成闭合或开放螺旋;孢子椭圆或圆柱状,表面形成结节状突起;生理生化特征和在国际链霉菌计划(ISP)培养基上的培养特征与圆突起链霉菌Streptomyces torulosus基本一致;菌株SCY311的16S rRNA序列与S.torulosus的16S rRNA序列同源性为99.9%。因此,将菌株SCY311鉴定为圆突起链霉菌。 The actinomycete strain SCY311,which exhibited antifungal activity against various plant pathogenic fungi,was isolated from the soil samples collected from Fenghuang Mountain in Henan province in China.Identification of strain SCY311 was conducted by the methods of traditional and molecular biological taxonomy,including determination of morphological characteristics,cultural characteristics,physiological and biochemical properties,cell wall components and 16S rRNA se-quences analysis.Results showed that strain SCY311 grew well on Gause′s synthetic agar plate.The color of substrate mycelium appeared brown,while that of aerial mycelium went from gray to mouse gray.The strain SCY311 neither produced the soluble pigment nor exhibited hygroscopicity.Spores were arranged in coil chains and the branched spore chains formed open or closed spirals.Spores were oval or columned in ship and the spore wall ornamentation category was knobby.Physiological proper-ties and cultural characteristics of the strain SCY311 on the ISP media were in close agreement with that of the Streptomyces torulosus.The 16S rRNA gene sequence of strain SCY311 showed 99.9% similarity to that of S.torulosus.Based on the results above,the strain SCY311 was identified as S.torulosus.
出处 《微生物学通报》 CAS CSCD 北大核心 2011年第5期687-693,共7页 Microbiology China
基金 河南省公益性重大招标项目(No.081100911300) 河南省自然科学基金项目(No.2009B210015)
关键词 圆突起链霉菌 孢子形态 分类 拮抗活性 Streptomyces torulosus Spore morphology Taxonomy Antibiotic activity
  • 相关文献

参考文献17

  • 1Mullie CJ. Use of 16S rRNA gene sequence for the description of new species//Peter A, McNamara. Trends in RNA research[M]. New York: Nova Science Pub Inc, 2006: 270-272.
  • 2Stackebrandt E, Goebel BM. Taxonomic note: a place for DNA-DNA reassociation and 16S rRNA sequence analysis in the present species definition in bacteriology[J]. International Journal of Systematic and Evolutionary, 1994, 44(4): 846-849.
  • 3Nguimbi E, Li YZ, Gao BL, et al. 16S-23S ribosomal DNA intergenic spacer regions in cellulolytic myxobacteria and differentiation of closely related strains[J]. Systematic and Applied Microbiology, 2003, 26(2): 262-268.
  • 4Nagpal ML, Fox KF, Fox A. Utility of 16S-23S rRNA intergenic spacer region methodology: how similar are interspace regions within a genome and between strains for closely related organisms?[J]. Journal of Microbiological Methods, 1998, 33(3): 211-219.
  • 5Tresner HD, Davies MC, Backus EJ. Electron microscopy of Streptomyces spore morphology and its role in species differentiation[J]. Journal of Bacteriology, 1961, 81(1): 70-80.
  • 6Dietz A, Mathews J. Classification of Streptomyces spore surfaces into five groups[J]. Applied Microbiology, 1971, 21(3): 527-533.
  • 7Lyons A J, Pridham TG. Streptomyces torulosus sp. n., an unusual knobby-spored taxon[J]. Applied Microbiology, 1971, 22(2): 190-193.
  • 8Shirling EB, Gottlieb D. Methods for characterization of Streptomyces species[J]. International Journal of Systematic Bacteriology, 1966, 16(3): 313-340.
  • 9Angelini P, Pagiotti R, Granetti B. Effect of antimicrobial activity of Melaleuca alternifolia essential oil on antagonistic potential of Pleurotus species against Trichoderma harzianum in dual culture[J]. World J Microbiol Biotechnol, 2008, 24(2): 197-202.
  • 10王平.测定放线菌菌体中氨基酸和单糖的快速方法-薄层层析法.微生物学通报,1986,13:228-230.

二级参考文献7

  • 1郑维,权春善,朴永哲,范圣第.一种快速提取细菌总DNA的方法研究[J].中国生物工程杂志,2006,26(4):75-80. 被引量:35
  • 2Li X,De Boer S H.Selection of polymerase chain reaction primers from an RNA intergenic spacer region for specific detection of Clavibacter michiganensis subsp.sepedonicus[J].Phytopathol,1995,85 (8):837-842.
  • 3Atlas R M,Park L C.Handbook of Microbiological Media[M].CRC Press,Inc.,corporate Blvd.,N.W.,Boca Raton,Florida 2000,33431.
  • 4Hopwood D H,Bibb M J,Chater K F,et al.Genetic Manipulation of Actomyces A Laboratory manual.In Preparation of chromosomal,plasmid and phage DNA[M].Norwich:F1 Crowe & Sons Ltd.1985:79-801.
  • 5Orsini M,Romano-Spica V.A microwave-based method for nucletic acid isolation from environmental samples[J].Lett Appl Microbiol,2001,33:17-20.
  • 6徐平,李文均,徐丽华,姜成林.微波法快速提取放线菌基因组DNA[J].微生物学通报,2003,30(4):82-84. 被引量:171
  • 7马万里,Josquin Tibbits,Mark Adams.一种可用于PCR扩增的直接提取土壤细菌DNA的方法[J].土壤通报,2004,35(1):56-58. 被引量:9

共引文献121

同被引文献63

引证文献4

二级引证文献27

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