• Title/Summary/Keyword: microcystin

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

  • 김민규;권재현;조영하;이진애;권오섭
    • Journal of Environmental Health Sciences
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    • v.29 no.1
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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.

A Novel Microcystin-degrading Bacterium, Microbacterium sp. MA21 (Microcystin을 분해하는 신균주 Microbacterium sp. MA21)

  • Ko, So-Ra;Lee, Young-Ki;Oh, Hee-Mock;Ahn, Chi-Yong
    • Korean Journal of Environmental Biology
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    • v.31 no.2
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    • pp.158-164
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    • 2013
  • A microcystin-degrading bacterium was isolated from Daechung reservoir, Korea. The isolated bacterium was identified as Microbacterium sp. by 16S rRNA gene sequence analysis, and designated as Microbacterium sp. MA21. This strain degraded cyanobacterial hepatotoxin, microcystin-LR, over 80% when incubated at $30^{\circ}C$ for 12 hr in R2A medium. Two unknown metabolites of microcystin were also identified during the degradation process. Although only Sphinogomonas and Actinobacteria have been known to degrade microcystin previously, this is the first report that Microbacterium sp. MA21 could degrade microcystin.

Isolation of Microcystin-LR and Its Potential Function of Ionophore

  • Kim, Gilhoon;Han, Seungwon;Won, Hoshik
    • Journal of the Korean Magnetic Resonance Society
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    • v.19 no.2
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    • pp.67-73
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    • 2015
  • The microcystin is a cyclic heptapeptide from metabolites of cyanobacteria in the genera mycrocystis, anabaeba as a result of eutrophication. It has been known that microcystin-LR is a potent inhibitor of the catalytic subunits of protein phosphatase-1 (PP-1) as well as powerful tumor promoter. The active site of microcystin actually has two metal ions $Fe^{2+}/Zn^{2+}$ close to the nucleophilic portion of PP-1-microcystin complex. We report the isolation and purification of this microcystin-LR from cyanobacteria (blue-green algae) obtained from Daechung Dam in Chung-cheong Do, Korea. Microcystin-LR was extracted from solid-phase extraction (SPE) sample preparation using a CN cartridge. The cyanobacteria extract was purified to obtain microcystin-LR by HPLC method and identified by LC/MS. The detail structural studies that can elucidate the possible role of monovalent and divalent metal ions in PP-1-microcystin complexation were carried out by utilizing molecular dynamics. Conformational changes in metal binding for ligands were monitored by molecular dynamic computation and potential of mean force (PMF) using the method of the free energy perturbation. The microcystin-metal binding PMF simulation results exhibit that microcystin can have very stable binding free energy of -10.95 kcal/mol by adopting the $Mg^{2+}$ ion at broad geometrical distribution of $0.5{\sim}4.5{\AA}$, and show that the $K^+$ ion can form a stable metal complex rather than other monovalent alkali metal ions.

Microcystin Production by Microcystis sp. under N or P Limitation

  • Oh Hee-Mock;Kim Jee-Hwan
    • Proceedings of the Microbiological Society of Korea Conference
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    • 2001.11a
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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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Evaluation of the Potential Human Health Risk Associated with the Microcystin Bioaccumulation in the Freshwater Fish from Lake Yeongcheon and Lake Daecheong (영천호와 대청호에서 담수어류의 microcystin 농축에 따른 인체 건강위해성 평가)

  • Lee, Kyung-Lak;Jheong, Weon-Hwa;Kang, Young-Hoon;Kim, Han-Soon
    • Korean Journal of Ecology and Environment
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    • v.42 no.3
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    • pp.331-339
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    • 2009
  • This study evaluated the potential human health risk on the basis of the level of bioaccumulation and EDI (Estimated Daily Intake) of microcystin-LR, one of hepatotoxic, in organs, including liver, muscle, viscera and gill, of fish from Lake Yeongeheon and Lake Daecheong when the cyanobacterial water-blooms broke out. The result has confirmed that Carassius cuvieri from Lake Yeongcheon contains higher level of microcystin-LR in its organs including liver. In Lake Daecheong, omnivorous Hemibarbus labeo and phytoplanktivorous Carassius cuvieri have shown high microcystin-LR level on average, especially higher for viscera, and Carassius cuvieri has appeared to contain higher level of microcystin-LR in the liver and the gill compared with other species. As a result of comparison between EDI of microcystin-LR from each organs and TDI (Tolerable Daily Intake) of WHO (Chorus and Bartram, 1999) to evaluate human health risk, the EDI levels from Carassius cuvieri's organs except museles have exceeded TDI level at the both lakes. Consequently, the study has proved that microcystin was bioaccumulated in the various parts of fish, and it can be ingested by human resulting in risking human health. Continuous monitoring and reducing consumption of fish, especially Carassius cuvieri, during the cyanobacterial water-blooming period will be needed to protect human health.

Occurrence of Microcystin-Containing Toxic Water Blooms in Central India

  • Agrawal Manish K.;Ghosh Shubhro K.;Bagchi Divya;Weckesser Juergen;Erhard Marcel;Bagchi Suvendra N.
    • Journal of Microbiology and Biotechnology
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    • v.16 no.2
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    • pp.212-218
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    • 2006
  • Three out of fourteen Microcystis-dominant cyanobacterial blooms in Central India were found to be toxic to mice ($LD_{50}$ ranging from 35-450 mg bloom dry mass/kg body weight). The liver architecture of the treated mice showed characteristic symptoms of hepatotoxicity relative to the untreated controls, with increased enzyme activities of serum lactate dehydrogenase (LDH), serum glutamate oxaloacetate transaminase (SGOT), alkaline phosphatase (ALP), and serum glutamate pyruvate transaminase (SGPT). RP-HPLC revealed the presence of microcystin-LR, microcystin-RR, and desmethyl microcystin-RR in the given region to maximum amounts of 390, 1,030, and $860{\mu}g/g$ bloom dry weight, respectively, corresponding to a maximum of 2.8 mg/l microcystin-LR in the lake water. Further confirmation of the microcystin variants was conducted using a MALDI-TOF MS analysis.

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

  • Pyo, Dong-Jin;Kim, Eun-Jung
    • Journal of the Korean Chemical Society
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    • v.48 no.5
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    • pp.467-472
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    • 2004
  • Cyanobacterial toxins, microcystins which exist in korean lakes show strong toxicity to fish, cattles and human. In this study, we tried to degrade microcystin LR using various chemical oxidants, Chlorine, Potassium permanganate and Hydrogen Peroxide. The detection method for the concentrations of microcystin LR in water samples was Enzyme-Linked Immunosorbent Assay (ELISA) method using the monoclonal antibody of microcystin. Chlorine degraded microcystin LR effectively at the concentration of 800 pg/mL microcystin LR and 12 ppm chlorine. The reaction took 40 minutes at pH 7. Potassium Permanganate also degraded microcystin LR successfully at the concentration of 2000 pg/mL microcystin LR and 1.2 ppm chlorine. The degradation reaction took 60 minutes at pH 7. In the case of hydrogen peroxide, the degradation rate of microcystin LR was very slow because of the slow reaction rate.

Dynamics of Cyanobacterial Toxins in the Downstream River of Lake Suwa (Suwa호 하류하천에서의 남조류 독소의 동태)

  • Kim, Bom-Chul;Park, Ho-Dong;Katagami, Yukimi;Hwang, Soon-Jin;Kim, Ho-Sub
    • Korean Journal of Ecology and Environment
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    • v.34 no.1 s.93
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    • pp.45-53
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    • 2001
  • Transport of cyanobacterial toxins (microcystin-LR, -RR, -YR) were assessed from a eutrophic lake, Lake Suwa, through the outflowing river, the Tenryu River, and its irrigation channel branch. Temporal variation of phytoplankton species composition in the river coincided with those of the lake; Microcystis ichthyoblabe dominated from June to July, and M. viridis dominated from August to September. When cyanobacterial bloom occurred, microcystins were continuously detected at the concentration of $0.3{\sim}3.2\;{\mu}g/l$ even at 32 km downstream. The change of the content of three microcystin variants were related both with the total cell density of Microcystis and with the change of Microcystis species composition. When Microcystis ichthyoblabe dominated during July, only microcystin-RR (MC-RR) and -LR (MC-LR) were detected, while when Microcystis viridis dominated between August and October, microcystin-RR,-YR (MC -YR) and -LR were detected. Along 29 km flowing distance (flow time 11 hours) between site 2 and site 5 in the Tenryu River, cyanobacterial density and microcystin concentration were reduced by 73% and 72%, respectively, which is mostly contributed by the dilution effect of tributary waters (61% and 57%, respectively) . In the artificial irrigation channel microcystins and cyanobacterial cells were decreased less than in the natural river. The results indicate that cyanobacterial toxins can be transported far downstream without much removal and give hazards to water usage in downstream of eutrophic lakes with cyanobacterial blooms.

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

  • Lee, Jinwook;Yu, Hye-Weon;Kim, In S.
    • Journal of Korean Society on Water Environment
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    • v.23 no.5
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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.

Studies on the Structure and Biological Activity of Microcystins Produced from Korean Cyanobacteria, Microcystis Species (한국산 남조류 Microcystis로부터 생산된 microcystin 구조와 생물활성에 관한 연구)

  • Choi, Byoung Wook;Noh, Young Ho;Lee, Jong-Soo
    • Applied Chemistry for Engineering
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    • v.8 no.4
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    • pp.610-616
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    • 1997
  • Hepatotoxic cyanobacteria, Microcystis species, were collected from the Nakdong River and we could isolate hepatotoxins, microcystin-LR and microcystin-RR, which are also strong inhibitors of protein phosphatase 1 and 2A. From the microcystins, several microcystin derivatives were synthesized and tested on the mouse toxicity in order to establish the structure-activity relationship. Esterification od carboxyl groups of Glu and MeAsp residue produced nontoxic compounds. However, when we reduced the Mdha residue with sodium borohydride into Ala residue, toxicity was still maintained. Also, the change of guanidyl moiety of Arg residue in microcystin-LR into dimethylpyrimidyl moiety did not change the toxicity of microcystins as well. Thus the carboxyl groups seem to play important roles in binding with protein phosphatase 1 and 2A, whereas Mdha residue and the guanidyl moiety of Arg residue do not.

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