Please use this identifier to cite or link to this item: http://ir.mu.ac.ke:8080/jspui/handle/123456789/9041
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dc.contributor.authorRamkat, Rose C.-
dc.contributor.authorOnyango, David Miruka-
dc.date.accessioned2024-04-30T07:26:38Z-
dc.date.available2024-04-30T07:26:38Z-
dc.date.issued2024-
dc.identifier.urihttps://doi.org/10.1007/978-1-0716-3782-1_23-
dc.identifier.urihttp://ir.mu.ac.ke:8080/jspui/handle/123456789/9041-
dc.description.abstractEarly monitoring of Microcystis, a cyanobacterium that produces microcystin, is paramount in order to confirm the presence of Microcystis spp. Both phenotypic and genotypic methods have been used. The phenotypic methods provide the presence of the microcystis but do not confirm its species type and toxin produced. Additionally, phenotypic methods cannot differentiate toxigenic from non-toxigenic Microcystis. Therefore, the current protocol also describes genetic methods based on PCR to detect toxigenic Microcystis spp. based on microcystin synthetase E (mcy E) gene and 16-23S RNA genes for species-specific identification, which can effectively comprehend distinct lineages and discrimination of potential complexity of microcystin populations. The presence of these microcystin toxins in blood, in most cases, indicates contamination of drinking water by cyanobacteria. The methods presented herein are used to identify microcystin toxins in drinking water and blood.en_US
dc.language.isoenen_US
dc.publisherSpringer linken_US
dc.subjectQuantification of cyanobacteriaen_US
dc.subjectGenotypic methodsen_US
dc.titlePhenotypic and genotypic methods for the identification and quantification of cyanobacteria in lake wateren_US
dc.typeArticleen_US
Appears in Collections:School of Biological and Physical Sciences

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