Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/6113
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dc.contributor.authorSydenham, Eric W
dc.contributor.authorThiel, Pieter G
dc.contributor.authorShephard, Gordon S
dc.contributor.authorKlaus, R Koch
dc.contributor.authorTherese, Hutton
dc.date.accessioned2017-11-10T06:53:47Z
dc.date.available2017-11-10T06:53:47Z
dc.date.issued1995
dc.identifier.issn0021-8561
dc.identifier.urihttp://pubs.acs.org/doi/pdf/10.1021/jf00057a016
dc.identifier.urihttp://hdl.handle.net/11189/6113
dc.description.abstractThe natural occurrence in corn of carcinogenic mycotoxins, the fumonisins, has prompted the development of potential decontamination procedures. Chemical treatment of fumonisin B1 (FBI)- contaminated corn with calcium hydroxide [Ca(OH)21 results in the base hydrolysis of FBI (the major naturally occurring fumonisin analogue) to yield its corresponding aminopentol (AP1) and tricarballylic acid (TCA) moieties. Complete hydrolysis proceeds in a sequential reaction involving the removal of one TCA group and the formation of a partially hydrolyzed moiety (PHI), which exists as an equilibrium mixture of the two possible monoesters. PHI was prepared by the treatment of Fusarium moniliforme culture material with Ca(OH12 and subsequently isolated and purified using chromatographic methods. PHI was also prepared, using similar methods, from pure FBI. The identity of the PHI moiety was determined by liquid chromatography-electrospray mass spectrometry.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/za/
dc.subjectFumonisin BIen_US
dc.subjectAlkaline hydrolysisen_US
dc.subjectPartially hydrolyzed fumonisin BIen_US
dc.subjectIsolationen_US
dc.titlePreparation and isolation of the partially Hydrolyzed Moiety of Fumonisin B1en_US
dc.typeArticleen_US
Appears in Collections:HWSci - Journal Articles (DHET subsidised)
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