Methodological improvement of the protein phosphatase inhibition assay for the detection of okadaic acid in mussels.

R Della Loggia, S Sosa, A Tubaro
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引用次数: 23

Abstract

A simplified procedure for the enzyme inhibition assay to measure okadaic acid and DTX-1 in mussels, based on the use of a commercially available enzyme preparation, is presented. The detection limit is 10 ng of toxin per g of digestive glands. Using Certified Reference Material (MUS-2), high accuracy and good precision is demonstrated for contamination levels higher than 32 ng g(-1). Twenty samples can be processed in about 9 h by one operator, at the cost of US$ 10 per sample. Some possibilities for further enhancing the sensitivity and reducing the processing time are discussed and a monitoring example is presented.

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贻贝中冈田酸蛋白磷酸酶抑制法的方法学改进。
一个简化的程序酶抑制测定,以测量冈田酸和DTX-1在贻贝,基于使用市售酶制剂,提出。检测限为每g消化腺10 ng毒素。使用认证标准物质(MUS-2),高准确度和良好的精度证明污染水平高于32 ng g(-1)。一个操作员可以在大约9小时内处理20个样品,每个样品的成本为10美元。讨论了进一步提高灵敏度和缩短处理时间的可能性,并给出了一个监测实例。
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Erratum: Alfonso D, Johnson HA, Colman-Saizarbitoria T, Presley CP, McCabe GP, McLaughlin JL (1996): SARs of annonaceous acetogenins in rat liver mitochondria. Nat Toxins 4:181-188. Advances in detection methods for fungal and algal toxins. HPLC/MS analysis of fusarium mycotoxins, fumonisins and deoxynivalenol. Neuronal binding of tetanus toxin compared to its ganglioside binding fragment (H(c)). A new type sandwich immunoassay for microcystin: production of monoclonal antibodies specific to the immune complex formed by microcystin and an anti-microcystin monoclonal antibody.
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