• Title/Summary/Keyword: Microcystins

검색결과 57건 처리시간 0.023초

남조류 독소 정량을 위한 스트립분석법과 HPLC 분석법의 비교 (Comparison of strip analysis and HPLC analysis for the quantitative analysis of cyanobacterial toxin)

  • 표동진;임미연
    • 분석과학
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    • 제28권3호
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    • pp.168-174
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    • 2015
  • 남조류 독소인 마이크로시스틴은 여름철 우리나라 여러 호수들에 존재하여 물고기와 가축 그리고 인간에게 강한 독성을 나타내는 독소이다. 본 논문에서는 이러한 수중 남조류 독소, 마이크로시스틴을 정량분석하는 두가지 방법, 즉 고성능 액체크로마토그래피(HPLC) 분석법과 최근 우리 실험실에서 개발한 스트립분석법의 비교를 시도하였다. 두 분석법의 측정가능농도범위가 많이 달라 HPLC 법으로 먼저 측정한 후 시료를 물로 희석시켜 스트립분석법에 적용하였다. 서로 다른 농도의 마이크로시스틴을 함유한 7가지 물시료들을 사용하여 HPLC분석법과 스트립 분석법으로 남조류 독소 총량을 측정하였다. 그 결과 두 분석법의 정량측정결과가 매우 잘 일치하는 것을 볼 수 있었다. 두 분석법의 상관분석 결과 r 값은 0.99998 이었으며 통계적인 유의성을 나타내는 p 값은 0.00001 이었다.

오존산화에 의한 정수장의 Microcystin제거 특성에 관한 연구 (A Study on the Removal Characteristics of Microcystin in the Water Treatement Plant by Ozonation)

  • 김민규;권재현;조영하;이진애;권오섭
    • 한국환경보건학회지
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    • 제29권1호
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    • pp.74-83
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    • 2003
  • Microcystin, stable compounds with circular heptapeptides, is presented inside cyanobacterial cell. So far, over 30 types have been known to exist and microcystin-LR, RR among them are the most potent toxin compound. By this reason, a strong oxidant, ozone was used in this study to remove the microcystins produced by cyanobacteria. Removal efficiency of microcystin at M water treatment plant was also evaluated. Microcystin concentration was determined by protein phosphatase inhibition assay. The results showed that dissolved microcystin in raw water detected in the range of 0.011-0.028 ㎍ Microcystin-RR equivalent/l. Above 98% of microcystin was removed through overall treatment system. Therefore, the water treatability of M treatment plant seemed to be excellent. Removal efficiency of microcystin according to unit process varied as characteristics of raw water such as DOC, UV/sub 254/ and turbidity. Removal efficiency of microcystin by ozonation was investigated in laboratory according to contact time and ozone dose. Dissolved microcystin was increased by twice fold according to ozone contact time, but increased by fifth fold according to ozone dose. So, changing of ozone dose more affected microcystin release than changing of ozone contact time. Behavior of microcystin by ozonation was similar to that of DOC, and residual ozone concentration gave influence to removal ratio of microcystin. In conclusion, single ozone treatment wasn't effective on microcystin removal in case of water containing a lot of cells. Therefore, it's more effective to use ozonation process after the removal of cyanobacterial cells in advance.

분자생물학적 방법에 의한 남조류의 독성 생성능의 확인 (Detection of Toxigenicity of Cyanobacteria by Molecular Method)

  • 이경락;정원화;김종민;김한순
    • 생태와환경
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    • 제40권1호
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    • pp.149-154
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    • 2007
  • 남조류의 독성 잠재력을 확인하기 위해 microcystins 합성 유전자인 mcyB에 특이적으로 작용하는 TOX2P/TOX2M primer쌍을 이용한 whole-cell PCR을 실시하였다. 환경시료를 대상으로 한 실험 결과에서 TOX2P/TOX2M primer쌍은 약 1,000 $cells{\cdot}mL^{-1}$의 낮은 밀도에서 효과적으로 mcyB 유전자의 증폭에 성공하였으며, mcyB유전자를 지닌 종들은 모두 ELISA분석에 의해 microcystins의 생성이 확인되었다. 따라서, TOX2P/TOX2M primer쌍은 국내의 수체에서 독성 남조류의 신속하고 효과적인 검출을 위한 유용한 probe로 판단되었다.

남조류의 대량배양 및 남조류 독소의 스트립분석법 연구 (A study on the massive cultivation of cyanobacteria and strip analysis of cyanobacterial toxin)

  • 표동진;임미연;김어진
    • 분석과학
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    • 제25권6호
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    • pp.388-394
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    • 2012
  • 남조류 독소인 마이크로시스틴은 여름철 우리나라 여러 호수들에 존재하여 물고기와 가축 그리고 인간에게 강한 독성을 나타내는 독소이다. 지금까지는 남조류독소인 마이크로시스틴을 분석하기 위하여 HPLC를 사용하거나 ELISA 분석법을 이용하였으나 본 연구에서는 대량배양을 통해서 얻어진 남조류들 속에 미량존재하는 마이크로시스틴을 분석하기 위해 스트립을 이용하는 새로운 분석방법을 시도하였다. 이 분석법은 항원-항체기술을 이용하여 높은 특이도(specifisity)와 테스트 스트립(test strip)의 신속성, 그리고, 형광리더(reader)의 고감도(sensitivity) 분석능력 등의 장점을 이용하였다. 따라서 새로 개발된 분석법을 이용하면 다양한 물시료속에 존재하는 마이크로시스틴을 독소 표준품 없이 단시간에 고감도로 분석할 수 있다.

Microcystin Production by Microcystis sp. under N or P Limitation

  • Oh Hee-Mock;Kim Jee-Hwan
    • 한국미생물학회:학술대회논문집
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    • 한국미생물학회 2001년도 추계학술대회
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    • pp.113-120
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    • 2001
  • The production of microcystins from Microcystis aeruginosa was investigated in a P-limited continuous culture and a batch culture. The microcystin content of M aeruginosa was higher at a lower $\mu$, whereas the microcystin (MC)-producing rate was linearly proportional to $\mu$. The ratios of the MC-producing rate to the C-fixation rate were higher at a lower $\mu$. Consequently, increases in the microcystin content per dry weight along with the production of the more toxic form, MC-LR, were both observed under more P-limited conditions. The microcystin content of M. aeruginosa exhibited a high correlation with the total N content regardless of N-fixed or P-fixed culture. The microcystin concentration was investigated from spring to autumn in 1999 in the Daechung Reservoir, Korea. The dominant species in the algal blooming season was Microcystis. When the microcystin concentration exceeded about 100 ng $1^{-1}$ the ratio of particulate to dissolved total nitrogen (TN) or total phosphorus (TP) interestingly converged at a value of 0.6. The microcystin concentration was lower than 50 ng $1^{-1}$ at a particulate N:P ratio below 8, whereas the microcystin concentration varied quite substantially from 50 ng $1^{-1}$ to 250 ng $1^{-1}$ at a particulate N:P ratio> 8.

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洛東江 하류 수계의 毒性 Microcystis 生態 연구 (Ecological Study on the Toxic Microcystis in the Lower Nakdong River)

  • 최애란;오희목;이진애
    • ALGAE
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    • 제17권3호
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    • pp.171-185
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    • 2002
  • The standing crop of genus Microcystis, microcystin concentrations and environmental factors were monitored at stations of the lower reaches of the Nakdong River in 1998 and 1999 during the periods of its occurrence. The Microcystis were observed from May to Octorber, and the cell density was highest at Station Seonam up to 250,000 cells${\cdot}ml^{-1}$ forming scum over the water surface. There were signigicant relationships between the standing crop of Microcystis and nitrate nitrogen, total phosphorus concentrations and Ph. Presumably these parameters were important in the succession to Microcystis dominated phytoplankton community in the summer period in the river. However, Ammonium nitrogen, phosphate phosphorus concentrations and N/P ratio were not critical factors. The Microcystis bloom was notable above $25^{\circ}C$ of surface water temperature. Microcystins were detected from May to November in the algal materials from the river. The 84.2% of algal materials with Microcystis exhibited the microcystin with the maximum of 1711.8 ${\mu}g{\cdot}g^{-1}$ dw. The microcystin concentrations in the algal materials were significantly related to the stading crop of Microcystis, which was the primary determinant factor in the toxin levle of algal materials. The concentrations were also significantly related to pH of the water column in the positive pattern.

대청호 조류발생에 따른 경보제 운영 및 개선 방안 고찰 (A study on the management and improvement of alert system according to algal bloom in the Daecheong Reservoir)

  • 정동환;이재정;김교영;이대희;홍선화;윤조희;홍석영;김태승
    • 환경영향평가
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    • 제20권6호
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    • pp.915-925
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    • 2011
  • Following the industrialization and urbanization in Korea, algal bloom causes aesthetic displeasure and many other problems such as taste and odor, coloration, scum, increase in pH, filter-bed blockage. There were some cases involving human death by microcystins during summertime in foreign countries. In Korea, Harmful cyanobacteria such as Microcystis and Anabaena develop in summer in the Daecheong reservoir, one of the main water resources, with the retention time of above 200 days. To better control algal bloom, the Ministry of Environment has been running algal bloom alert system from 1998 for the Daecheong reservoir, which needs to be improved to reflect the characteristics of river-type lakes. For this reason, we try to find new measures to improve an algal bloom alert system for each water zone considering the characteristics of harmful cyanobacteria in this study.

Identification and toxigenic potential of a Nostoc sp.

  • Nowruzi, Bahareh;Khavari-Nejad, Ramezan-Ali;Sivonen, Karina;Kazemi, Bahram;Najafi, Farzaneh;Nejadsattari, Taher
    • ALGAE
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    • 제27권4호
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    • pp.303-313
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    • 2012
  • Cyanobacteria are well known for their production of a multitude of highly toxic and / or allelopathic compounds. Among the photosynthetic microorganisms, cyanobacteria, belonging to the genus Nostoc are regarded as good candidate for producing biologically active secondary metabolites which are highly toxic to humans and other animals. Since so many reports have been published on the poisoning of different animals from drinking water contaminated with cyanobacteria toxins, it might be assumed that bioactive compounds are found only in aquatic species causes toxicity. However, the discovery of several dead dogs, mice, ducks, and fish around paddy fields, prompted us to study the toxic compounds in a strain of Nostoc which is most abundant in the paddy fields of Iran, using polymerase chain reaction and liquid chromatography coupled with a diode array detector and mass spectrophotometer. Results of molecular analysis demonstrated that the ASN_M strain contains the nosF gene. Also, the result of ion chromatograms and $MS^2$ fragmentation patterns showed that while there were three different peptidic compound classes (anabaenopeptin, cryptophycin, and nostocyclopeptides), there were no signs of the presence of anatoxin-a, homoanatoxin-a, hassallidin or microcystins. Moreover, a remarkable antifungal activity was identified in the methanolic extracts. Based on the results, this study suggests that three diverse groups of potentially bioactive compounds might account for the death of these animals. This case is the first documented incident of toxicity from aquatic cyanobacteria related intoxication in dogs, mice, and aquatic organisms in Iran.

나노크리스탈 Quantum-dot을 적용한 남조류 독소 Microcystin 탐지 연구 (Application of Quantum-dot Nanocrystals for Cyanobacterial Toxin-Microcystin Detection)

  • 이진욱;유혜원;김인수
    • 한국물환경학회지
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    • 제23권5호
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    • pp.705-711
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    • 2007
  • Green quantum-dot nanocrystal (QD525) with anti-microcystin monoclonal antibody was applied for detection of microcystin, a monocyclic peptide hepatotoxin, extracted from the culture of Microcystis aeruginosa. The presence of microcystin in the cell lysate was verified by HPLC analysis with UV absorbance at 238 nm. Microcystis cell extract exhibited fluorescence emission spectra, which peak was around 460 nm because of their complex organic substances. When a spherical QD525 antibody conjugates (10~20 nm in diameter) were bound to the microcystins in the Microcystis cell lysate, the fluorescence intensity of the primary peak at 525 nm diminished while the secondary emission peak at 460 nm slightly increased intensities. It is due to energy transfer from the primary (major) to the secondary (minor) peak, resulting from physical deformation of QD525 and different environmental factors. On the other hand, other cell extracts did not show any fluorescence emission change. This study is very available for detecting and monitoring the microcystin because it is one step assay without washing step and portable spectrophotometer makes on-site measurement possible. For health risk assessment of the microcystin, the reliable and rapid system to detect and quantify microcystin is seriously required.

화학적 산화제를 이용한 남조류 독소, 마이크로시스틴 LR의 분해연구 (A Study on the Degradation of Cyanobacterial Toxin, Microcystin LR Using Chemical Oxidants)

  • 표동진;김은정
    • 대한화학회지
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    • 제48권5호
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    • pp.467-472
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    • 2004
  • 남조류 독소인 마이크로시스틴은 여름철 우리나라 여러 호수들에 존재하여 물고기와 가축 그리고 인간에게 강한 독성을 나타내는 독소이다. 본 연구에서는 화학적 산화제인 염소($Cl_2$), 과망간산칼륨($KMnO_4$), 과산화수소수($H_2O_2$)를 이용하여 마이크로시스틴중 가장 독성이 강한 마이크로시스틴 LR의 분해실험을 시도하였다. 수중 마이크로시스틴LR의 농도 측정은 마이크로시스틴 LR의 단일클론항체를 이용한 효소면역흡착분석법으로 측정하였다. 실험결과 염소는 마이크로시스틴 LR의 농도 800 pg/mL, $Cl_2$의 농도 12 ppm, 암소방치시간 40분, pH 7에서 가장 잘 분해되었으며, 또한 pH 8 이상에서는 독소 파괴가 눈에 띄게 감소하였다. 과망간산칼륨의 경우 마이크로시스틴 LR의 농도 2000 pg/mL, $KMnO_4$의 농도 1.2 ppm, 암소방치시간 60분, pH 7에서 가장 잘 분해되었다. 그러나 과산화수소수에 의한 마이크로시스틴 LR의 분해는 느린 화학 반응 속도 때문에 효과적이지 못함을 알수 있었다.