铜锈微囊藻两种表型的生长生理特性及毒素组成比较分析

雷腊梅, 宋立荣, 刘永定

雷腊梅, 宋立荣, 刘永定. 铜锈微囊藻两种表型的生长生理特性及毒素组成比较分析[J]. 水生生物学报, 2001, 25(3): 205-209.
引用本文: 雷腊梅, 宋立荣, 刘永定. 铜锈微囊藻两种表型的生长生理特性及毒素组成比较分析[J]. 水生生物学报, 2001, 25(3): 205-209.
LEI La-mei, SONG Li-rong, LIU Yong-ding. COMPARISON OF GROWTH AND TOXIN ANALYSIS IN TWO PHENOTYPE MICROCYSTIS AERUGINOSA[J]. ACTA HYDROBIOLOGICA SINICA, 2001, 25(3): 205-209.
Citation: LEI La-mei, SONG Li-rong, LIU Yong-ding. COMPARISON OF GROWTH AND TOXIN ANALYSIS IN TWO PHENOTYPE MICROCYSTIS AERUGINOSA[J]. ACTA HYDROBIOLOGICA SINICA, 2001, 25(3): 205-209.

铜锈微囊藻两种表型的生长生理特性及毒素组成比较分析

基金项目: 

国家自然科学基金项目资助(39730380)

COMPARISON OF GROWTH AND TOXIN ANALYSIS IN TWO PHENOTYPE MICROCYSTIS AERUGINOSA

  • 摘要: 从滇池蓝藻水华中分离得到的铜锈微囊藻群体在实验室无机营养中解聚成单细胞,结果表明,群体微囊藻的生长速度明显低于单细胞微囊藻;前者具明显可见的胞外酸性多糖胶鞘,而单细胞则几乎没有;按常规方法分析比较两种细胞形态的毒性大小和毒素组成,发现群体微囊藻主要含有三种微囊藻毒素的异构体,而单细胞以MCLR为主;且单细胞微囊藻的毒性约为群体的10倍.二者的LDH和PGM同工酶酶谱也有差异.本研究为解释毒素的合成和调控机理提供了新的证据.
    Abstract: Colonial Microcystis aeruginosa isolated from water-bloom of Dianchi Lake lost its colonial type and became single-celled type upon continuous subcultured in inorganic medium. It was observed that the growth rate of colonial M.aeruginosa was markedly lower than that of single cell; the extracellular acid polysaccharide capsule was obviously visible in the colonial type but was absent in the single-celled one; toxin analysis indicated that three microcystins isomers were produced in colonial M. aeruginosa, but in single-celled M. aeruginosa, only one major toxin-MC-LR was detected; sing celled M. aeruginosa had the LD 50 value almost ten times higher than colonial M. aeruginosa. Allozyme divergence was detected, too. The study has brought forward a new proof to explanation of mechanisms on regulation of microcystin synthesis.
  • [1] Botes D P,Tuiman A A,Wessels P L.The Structure of cyanoginosins-LA,a cyclic peptide from the cyanobacterium Microcystis aeruginosa [J].J.Chem.Soc.F Perkin Trans,1984,1:2311—2318[2] Lange W.Speculations on a possible essential function of the gelatinous sheath of blue-green algae [J].Can.J.Microbiol,1976,22:1181—1185[3] Shirai M,Matumaru K,Ohotake A,et.al.Development of a solid medium for growth and isolation of axenic Microcystis strains(Cyanobacteria)and improved procedure for purification of culture [J].Appl.Environ.Microbio1,1989,55:2569—2571[4] Bolch JSC,Blackburn IS.Isolation and purification of Australian isolates of the toxic cyanobacterium Microcystis aeruginosa Kütz.[J].J.Appl.Phycol.,1996,8:5—13[5] 宋立荣,雷腊梅,何振荣,等.滇池水华蓝藻铜锈微囊藻和绿色微囊藻的生长生理特性及毒素分析[J].水生生物学报,1999,23;402—407[6] 李敦海,宋立荣,刘永定.葛仙米光合活性对盐胁迫的反应[J].水生生物学报,1999,23;420—424[7] J.萨姆布鲁克,E.F.弗里奇,T.曼尼阿蒂斯著.分子克隆实验指南(第二版)[M].北京;科学出版社,1996[8] 胡能书,万贤国.同工酶技术及原理[M].长沙;湖南科学技术出版社,1985[9] Rippka R.Deruelles J,Waterbury J B,et al.Generic assignments,strain histories and properties of pure culture of cyanobacteria [J].J.Gen.Microbiol.,1979,111:1—61[10] Holm-Hansen O.Recent advance in the physiology of blue-green algae.Proceeding symposium on environmental requirement of blue-green algae [C].Fed.Water Pollut.Control Adm.,Pacific Northwest Water Lab.,Corvallis,Oregon.1967,87—96[11] Parker DL.Improved procedures for the cloning and purification of Microcystis cultures(Cyanophyta)[J].J.Phycol.,1982,18:471—477[12] Costerton J W.Structure and plasticity at various organization levels in the bacterial cell [J].Can.J.Microbiol.,1988,34:513—521[13] Plude J L,Parker D L,Schommer O J,et al.Chemical characterization of polysaccharide from the slime layer of the cyanobacterium Microcystis flos-aquae C3-40[J].Appl.Environ.Microbiol.,1991,57:1696—1700[14] Martin C,Codd G A,Siegelman H W,et al.Lipopolysaccharides and polysaccharides of the cell envelope of toxic Microcystis aeruginosa strains [J].Arch.Microbiol.,1989,152:90—94[15] Forni C,Telo F R,Caiola M G.Comparative analysis of the polysaccharides produces by different species of Microcystis(Chroococcales,Cyanophyts)[J].Phycologia,1997,36:181—185[16] Nakagawa M.,Takamera Y.,Yagi O.Isolation and characterization of the slime from a cyanobacterium Microcystis aeruginosa K-3A [J] Agric.Biol.Chem.,1987,51:329—337[17] Shi L,Carmichael W W,Miller I.Immuno-gold localization of hepatotoxins in cyanobacterial cells [J].Arch.Microbiol.,1995,163:7—15

    Botes D P,Tuiman A A,Wessels P L.The Structure of cyanoginosins-LA,a cyclic peptide from the cyanobacterium Microcystis aeruginosa [J].J.Chem.Soc.F Perkin Trans,1984,1:2311—2318[2] Lange W.Speculations on a possible essential function of the gelatinous sheath of blue-green algae [J].Can.J.Microbiol,1976,22:1181—1185[3] Shirai M,Matumaru K,Ohotake A,et.al.Development of a solid medium for growth and isolation of axenic Microcystis strains(Cyanobacteria)and improved procedure for purification of culture [J].Appl.Environ.Microbio1,1989,55:2569—2571[4] Bolch JSC,Blackburn IS.Isolation and purification of Australian isolates of the toxic cyanobacterium Microcystis aeruginosa Kütz.[J].J.Appl.Phycol.,1996,8:5—13[5] 宋立荣,雷腊梅,何振荣,等.滇池水华蓝藻铜锈微囊藻和绿色微囊藻的生长生理特性及毒素分析[J].水生生物学报,1999,23;402—407[6] 李敦海,宋立荣,刘永定.葛仙米光合活性对盐胁迫的反应[J].水生生物学报,1999,23;420—424[7] J.萨姆布鲁克,E.F.弗里奇,T.曼尼阿蒂斯著.分子克隆实验指南(第二版)[M].北京;科学出版社,1996[8] 胡能书,万贤国.同工酶技术及原理[M].长沙;湖南科学技术出版社,1985[9] Rippka R.Deruelles J,Waterbury J B,et al.Generic assignments,strain histories and properties of pure culture of cyanobacteria [J].J.Gen.Microbiol.,1979,111:1—61[10] Holm-Hansen O.Recent advance in the physiology of blue-green algae.Proceeding symposium on environmental requirement of blue-green algae [C].Fed.Water Pollut.Control Adm.,Pacific Northwest Water Lab.,Corvallis,Oregon.1967,87—96[11] Parker DL.Improved procedures for the cloning and purification of Microcystis cultures(Cyanophyta)[J].J.Phycol.,1982,18:471—477[12] Costerton J W.Structure and plasticity at various organization levels in the bacterial cell [J].Can.J.Microbiol.,1988,34:513—521[13] Plude J L,Parker D L,Schommer O J,et al.Chemical characterization of polysaccharide from the slime layer of the cyanobacterium Microcystis flos-aquae C3-40[J].Appl.Environ.Microbiol.,1991,57:1696—1700[14] Martin C,Codd G A,Siegelman H W,et al.Lipopolysaccharides and polysaccharides of the cell envelope of toxic Microcystis aeruginosa strains [J].Arch.Microbiol.,1989,152:90—94[15] Forni C,Telo F R,Caiola M G.Comparative analysis of the polysaccharides produces by different species of Microcystis(Chroococcales,Cyanophyts)[J].Phycologia,1997,36:181—185[16] Nakagawa M.,Takamera Y.,Yagi O.Isolation and characterization of the slime from a cyanobacterium Microcystis aeruginosa K-3A [J] Agric.Biol.Chem.,1987,51:329—337[17] Shi L,Carmichael W W,Miller I.Immuno-gold localization of hepatotoxins in cyanobacterial cells [J].Arch.Microbiol.,1995,163:7—15

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出版历程
  • 收稿日期:  2000-07-18
  • 修回日期:  2000-08-21
  • 发布日期:  2001-05-24

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