2018
DOI: 10.1016/j.aquatox.2018.05.003
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Dynamics of paralytic shellfish toxins and their metabolites during timecourse exposure of scallops Chlamys farreri and mussels Mytilus galloprovincialis to Alexandrium pacificum

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Cited by 34 publications
(28 citation statements)
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“…and dcSTX, respectively, may occur in the presence of a carbamoylase enzyme, through the hydrolysis of the benzoate group . In addition, the conversion of C1+2 and C3+4 into M1 and M7 toxins, respectively, by desulfation of the 11-hydroxysulfate group and the conversion of GTX5 into M1, by hydroxylation of the same group, should also be considered (Qiu et al, 2018;Ding et al, 2017;Li et al, 2012;Vale, 2010).…”
Section: Discussionmentioning
confidence: 99%
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“…and dcSTX, respectively, may occur in the presence of a carbamoylase enzyme, through the hydrolysis of the benzoate group . In addition, the conversion of C1+2 and C3+4 into M1 and M7 toxins, respectively, by desulfation of the 11-hydroxysulfate group and the conversion of GTX5 into M1, by hydroxylation of the same group, should also be considered (Qiu et al, 2018;Ding et al, 2017;Li et al, 2012;Vale, 2010).…”
Section: Discussionmentioning
confidence: 99%
“…The most studied analogues are divided into three families, according to their side chains: carbamoil (saxitoxin-STX, neosaxitoxin-NEO and gonyautoxins-GTX1 to GTX4), N-sulfocarbamoil (GTX5, GTX6 and C1 to C4) and decarbamoil (dcGTX1 to dcGTX4, dcSTX and dcNEO) (Oshima, 1995a). Other families have been identified, such as deoxydecarbamoil (doSTX, doGTX2 and doGTX3), hydroxy-and sulfate-benzoate toxins (GC toxins), and hydroxylated saxitoxins (M toxins), whose origin and biosynthesis pathway is not yet fully understood (Qiu et al, 2018;Ding et al, 2017;Li et al, 2012;Vale, 2010;Wiese et al, 2010;Dell'Aversano et al, 2008;Negri et al, 2007Negri et al, , 2003. Bivalves as filter feeding organisms may accumulate and biotransform those compounds in their tissues during toxic algal blooms (Bricelj and Shumway, 1998).…”
Section: Introductionmentioning
confidence: 99%
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“…More recently, some new C-11 hydroxyl analogs of PSTs have been reported in shellfish such as scallops, mussels, cockles and clams [3][4][5][6][7]. These new analogs are generally considered to be metabolites of PSTs in shellfish and are called "M-toxins" (Figure 1) [3,[6][7][8]. Recently, trace amounts of several M-toxins were also reported in the PST-producing dinoflagellates Alexandrium spp.…”
Section: Introductionmentioning
confidence: 99%
“…Recently, trace amounts of several M-toxins were also reported in the PST-producing dinoflagellates Alexandrium spp. [8,9] and cyanobacteria of the genus Aphanizomenon [10]. They have also been formed through chemical degradation, [7] adding further uncertainty and complexity to their origin and formation.…”
Section: Introductionmentioning
confidence: 99%