Aquatic Microbiology

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Cyanotoxin of Blooming Microcystin

Oleh :
RENANDA BAGHAZ D.S.P.
Introduction

Enrichment nutrien

Blooming microcystis

cyanotoxin
Material and Method
Biomanipulation

Restocking
3 Fish pen size
Silver carp,
0,36 km2
Bighead carp

Sampling per
month , growth, plankton
gut
Material and Method
Sampling

30 silver carp and 30 bighead carp were randomly captured

examine individual body length and body weight

examine food items, 5 individuals of each carp and the guts removed
in each month

Intracellular microcystins were measured by a reverse-phase high-


performance liquid chromatography (HPLC)
Material and Method
Detoxification with Portulaca oleracea

P. oleracea cv. was grown under a germ-free condition on


MurashigeeSkoog medium (3% sucrose and 0.2% gellan gum)
in a culture bottle

The propagation of the aseptic plants was carried out


by stem cuttings on the same medium

the plantlets were pre-cultured I with various concentrations of MC-


LR, 0, 0.02, 0.2, or 2 mg/ml of MCLR, and after 7 days the amount of
MC-LR in the medium and plant extracts were determined

For the extraction of MC-LR from P. oleracea cv., freeze-dried


plant samples were grinded with a mortar The sample was centrifuged
at 140 0 g for 20 min, and the supernatant was collected and analyzed
with HPLC
Material and Method
Antimycobacterial activity of microcystins

m.aeruginosa Microcystin Evaluation of


Isolates
antimycobacterial
extracts analysis mycobacterium spp
activity

•the cells were • Analysis of microcystin • M. aeruginosa extract, • the assay is


obtained [D-Leu1] MC-LR, and accomplished on
dissolved in from Microcystis RST microcystin-LR toxins microplates (96 wells)
absolute methanol, 9501 was performed were tested against using resazurin as
•sonicated three using the HPLC the nontuberculous indicator of cellular
times and equipment Shimadzu mycobacteria: M. viability.
SCL-10AVP (Japan). terrae (ATCC15755), M. • Medium 7H9 enriched
centrifuged chelonae (ATCC 946) with 10 % OADC was
(10,000 × g) at 4°C, and M. employed. The
for ten minutes. kansasii(ATCC12478). extracts and pure
Extracts were microcystin were
evaporated at 40°C weighed, dissolved in
DMSO
• and the determination
of minimal inhibitory
concentration (MIC)
Result
Biomanipulation

Blue points represent inflow water; Red points represent outflow water.

Figure 4. Temporal changes of Microcystis biomass and MC concentration


in both the fish pens and the surrounding lake from April to November.
Result
Biomanipulation
Result
Detoxification with Portulaca oleracea

FIG. 1. Changes in MC-LR concentrations and protein phosphatases inhibition activities


in the medium treated with P. oleracea cv. The initial MC-LR concentration was 0.02
mg/ ml, and the medium was treated with P. oleracea cv. for 7 days. Open circle: MC-LR
concentration in the medium treated with P. oleracea cv., open triangle: MC-LR
concentration of control culture, closed circle: protein phosphatases inhibition activity
in the medium treated with P. oleracea cv., and closed triangle: protein phosphatases
inhibition activity of control culture.
Result
Antimycobacterial activity of microcystins
Result
Antimycobacterial activity of microcystins
Result
Antimycobacterial activity of microcystins
Conclusion

Biomanipulation using silver carp and Bighead


carp significantly can remove MC

Detoxification using Portulaca oleracea as


detoxificator able to decrease microcystins
through absorbtion when blooming in aquatic

Microcystin can use as antimicrobial because it


able to inhibition and inactivation activity of
bacteria
SEKIAN & TERIMA KASIH

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