Bacteriological Control of Cyanobacterial Bloom.

시안세균 수화의 세균학적 조절

  • 김철호 (진주산업대학교 미생물공학과) ;
  • 권오섭 (인제대학교 환경시스템학) ;
  • 이진애 (인제대학교 환경시스템학부)
  • Published : 2004.06.01

Abstract

A Gram (-), rod-shaped bacterium in size of 1.3∼$1.8{\times}0.35{\mu}m$ inhibiting the growth of cyanobacterium (Ana-baena cylindrica) was isolated and designated NG-2 in this manuscript. This isolate showed positive reactions for catalase and oxidase, and optimal growth conditions of 35∼TEX>$40<^{\circ}C$ and pH 9.0. In a mixed-culture of A. cylindrica and the isolate, each microorganism grew inverse-proportionally, and the cyanobacterial vegetative cells almost completely disappeared within 24 hours. NG-2 lysed A. cylindrica only under light, which means that lytic activity of NG-2 was dependent on the photosynthetic activity of host. When observed under phase contrast microscope, the isolate lysed vegetative cells of A. cylindrica in scattered state in a liquid medium, whereas het-erocysts have not been lysed. When cyanobacterial cell walls have been lysed partly, NG-2 attatched around A. cylindrica filament and formed colony, then encouraged complete lysis of cyanobacterial cells. The isolate showed similar lytic activity in natural water as in an artificial medium. And lytic activity of NG-2 was enhanced when attached on expandable polystyrene bead.

시안세균(Anabaena cylindrica)의 생장을 효과적으로 억제하는 세균을 분리하여 NG-2로 구분하였다. 이 세균은 그람 음성의 막대형 세균으로서 1.3∼$1.8{\times}0.35{\mu}m$ 정도의 크기를 보였으며, 카탈라제와 옥시다제 양성 반응을 나타내었고, 35∼$40^{\circ}C$아 pH 9.0의 적정생장 조건을 보였다. A.cylindrica의 NG-2를 JM 배지에서 혼합배양할 경우 두 미생물군은 서로 반비례적으로 성장하였으며, 24시간 이내에 A. cylindrica의 영양세포가 거의 완전히 소멸하였다. NG-2는 빛이 있는 조건에서만 효과적으로 A. cylindrica를 분해하였는데, 이는 NG-2의 A. cylindrica 분해활성이 숙주의 광합성 작용에 매우 의존적임을 의미한다. 분리세균의 A. cylindlica 분해작용을 현미경으로 관찰한 결과 NG-2는 숙주세포에 부착하지 않고 배지 내에 산재한 상태에서 영양세포를 분해하였으며, 이형세포는 분해되지 않았다. 또한 영양세포의 세포벽이 분해되면 분해세균들이 filament 주위에 집중적으로 부착하는 콜로니를 형성함으로써 A. cylindrica를 완전히 분해하는 것이 확인되었다. A. cylindrica에 대한 NG-2의 분해활성은 인공배지 뿐만 아니라 강물에서도 유사한 결과를 나타내었다. 또한 발포 polystyrene 재질의 bead에 세균을 부착함으로써 A. cylindrica 분해 효율을 더 상승시킬 수 있었다.

Keywords

References

  1. Mar.Ecol. Prog. Ser. v.153 Cell lysis and release of particulate polysac-charides in extensive marine mucilage assessed by lipid biomarkers and molecular probes Baldi F.;A.Minacci;A.Saliot;L.Mejanelle;P.Mozetic;V.Turk;A.Malej https://doi.org/10.3354/meps153045
  2. Arch. Microbiol. v.129 Entrapment and lysis of the cyanobacterium Phormidium luridum by aqueous colonies of Myxococcus xanthus PCO2 Burnham J.C.;S.A.Collart;B.W.Highison https://doi.org/10.1007/BF00414699
  3. J. Phycol. v.12 Extracellular lysis of the blue-green algae Phormidium luridum by Bdellovibrio bacteriovorus Burmham J.C.;T.Stetak;G.Locher
  4. Sci. Am. v.270 The toxins of cyanobacteria Carmichael W.W. https://doi.org/10.1038/scientificamerican0194-64B
  5. Ecological Engineering v.16 Cyanobacterial toxins, the perception of water quality and the prioritisation of eutrophication control Codd G.A.
  6. Water Treat. Exam. v.22 The occurrence of blue-green algae an lytic bacteria at a waterworks in Scotland Daft M.J.;S.McCord;W.D.P.Stewart
  7. Freshwater Biol. v.5 Ecological studies on algal-lysing bacteria in fresh waters Daft M.J.;S.B.McCord;W.D.P.Stewart https://doi.org/10.1111/j.1365-2427.1975.tb00157.x
  8. New Phytol. v.72 Light and electron microscope observations on algal lysi by bacterium CP-1 Daft M.J.;W.D.P.Stewart https://doi.org/10.1111/j.1469-8137.1973.tb02055.x
  9. J. Bacteriol. v.103 Composition of the cellular envelopes of Anabaena cylindrica Dunn J.H.;C.P.Wolk
  10. The Royal Society for Chemistry Health problems from exposure to cyanobacteria and proposed safety guidelines for drinking and recreational water Falconer I.R.;G.A.Codd(ed.);T.M.Jefferies(ed.);C.W.Keevil(ed.);E.Potter(ed.)
  11. Arch. Mikrobiol. v.84 Antimicrobial effects of Cellvibrio on blue-green algae Granhall,V.;B.Berg https://doi.org/10.1007/BF00425201
  12. Microbiology v.41 A flexibacter that lyses blue-green algae Gromov B.V.;O.G.lvanov;K.A.Mamkaeva;I.A.Avilova
  13. Appl. Environ. Microbiol. v.65 Changes in bacterial and eukaryotic community structure after mass lysis of filamentous cyanobacteria associated with viruses van Hannen E.J.;G.Zwart;M.P.van Agterveld;H.J.Gons;J.Ebert;H.J.Laanbroek
  14. New Engl. J. Med. v.338 Liver failure and death after exposure to microcystins at a haemodialysis center in Brazil Jochimsen E.M.;W.W.Carmichael;J.S.An;D.M.Cardo;S.T.Cookson;C.E.M.Holmes;M.D.Antunes;D.A.de Melo Filho;T.M.Lyra;C.S.V.Barreto;S.M.D.O.Azevedo;W.R.Jarvis https://doi.org/10.1056/NEJM199803263381304
  15. Korean J. Limnol. v.31 The effect of environmental factors on the lytic activity of Moraxella sp. CK-1 against Anabaena cylindrica Kim,C.H.;Y.K.Choi.
  16. Korean J. Limnol. v.36 Identification of alga-lytic bacteria AK-07 and its enzyme activities associated with degradability of cyanobacterium Anabaena cylindrica Kim,J.C.;M.S.Han
  17. Arch. Hydrobiol. v.121 Production and biodegradation of cyanobacterial toxins-a laboratory study Kiviranta J.;K.Sivonen;K.Lahti;R.Luukkainen;S.I.N.Helsinki
  18. Phycology(2nd ed.) Lee,R.E.
  19. Microbial Ecology Biological regulation of bloom-causing blue-green algae Martin E.L.;J.E.Leach;K.J.Kuo;M.W.Loutit(ed.);J.A.R.Miles(ed.)
  20. J. Phycol. v.28 Simazineinduced inhibition in photoacclimated populations of Anabaena circinalis(Cyanophyta) Millie D.F.;C.M.Hersh;C.P.Dionigi https://doi.org/10.1111/j.0022-3646.1992.00019.x
  21. Bull. JSME. v.2 Occurrence of blue-green algae and algal lytic bacteria in lake Biwa Mitsutani A.;A.Uchida;Y.Ishida
  22. Appl. Environ. Microbiol. v.55 Toxicity of Microcystis species isolated from natural blooms and purification of the toxin Ohtake A.;M.Shirai;T.Aida;N.Mori;K.Harada;K.Matsuura;M.Suzuki;M.Nakano
  23. Biol. Rev. v.50 Water-blooms Reynolds C.S.;A.E.Walsby https://doi.org/10.1111/j.1469-185X.1975.tb01060.x
  24. Aquaculture v.88 Cyanobacteria in fish ponds Reyssac S.J.;M.Pletikosic https://doi.org/10.1016/0044-8486(90)90315-E
  25. J. Appl. Phycol. v.6 Structure and biosynthesis of toxins from blue-green algae(cyanobacteria) Rinehart K.L.;M.Namikoshi;B.W.Choi https://doi.org/10.1007/BF02186070
  26. Microbios v.77 Lysis of cyanobacteria with Flexibacter spp. isolated from domestic sewage Sallal A.K.J.
  27. Biosensors and Bioelectronics v.16 Monitoring of phosphorus bioavailability in water by an immobilized luminescent cyanobacterial reporter strain Schreiter P.P.Y.;O.Gillor;A.Post;S.Belkin;R.D.Schmid;T.T.Bachmann https://doi.org/10.1016/S0956-5663(01)00224-X
  28. J. Bacteriol. v.104 Lysis of blue-green algae by Myxobacter Shilo M.
  29. Hydrobiologia v.190 Toxic cyanobacteria(blue-green algae) in finnish fresh and coastal waters Sivonen K.;S.I.Niemel$\"{a}$;R.M.Niemi;L.Lepist$\"{o}$;T.H.Luoma;L.A.R$\"{a}s\"{a}$nen https://doi.org/10.1007/BF00008195
  30. Arch. Mikrobiol. v.80 Algicidal non-fruiting myxobacteria with high G+C ratios Stewart J.R.;R.M.Brown https://doi.org/10.1007/BF00411882
  31. Advances in Aquatic Microbiology Microbial pathogens of cyanophycean blooms Stewart W.D.P.;M.J.Daft;Droop M.R.(ed.);H.W.Kannasch(ed.)
  32. Biological Control v.18 An aquatic bacterium that lyses cyanobacteria associated with off-flavor of channel cat-fish(Ictalurus punctatus) Walker H.L.;L.R.Higginbotham https://doi.org/10.1006/bcon.2000.0813
  33. App. Environ. Microbiol. v.66 β-Cyanoalanine production by marine bacteria on cyanide-free medium and its specific inhibitory activity toward cyanobacteria Yoshikawa K.;K.Adachi;M.Nishijima;T.Takadera;S.Tamaki;K.I.Harada;K.Mochida;H.Sano https://doi.org/10.1128/AEM.66.2.718-722.2000