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pubmed-article:16657821pubmed:dateCreated2010-6-29lld:pubmed
pubmed-article:16657821pubmed:abstractTextEnzymic formation of (14)C-kaurene from 2-(14)C-mevalonate was carried out with a cell-free system of Cucurbita pepo L. It was shown that either heating of the enzyme system or the addition of the growth retardants (2-chloroethyl)-trimethylammonium chloride and 2'-isopropyl-4' (trimethylammonium chloride)-5'-methylphenyl piperidine-1-carboxylate prevented the synthesis of (14)C-kaurene. Experiments in which (14)C-kaurene was applied to seedlings of Pharbitis nil revealed that the kaurene is converted to at least two compounds present in the acidic ethyl acetate fraction, containing free gibberellins, as well as in the second acidic ethyl acetate fraction, containing the released bound gibberellins. One of the compounds cochromatographed with gibberellic acid; the other compound is possibly a break-down product of gibberellic acid with no biological activity.lld:pubmed
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pubmed-article:16657821pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:16657821pubmed:monthOctlld:pubmed
pubmed-article:16657821pubmed:issn0032-0889lld:pubmed
pubmed-article:16657821pubmed:authorpubmed-author:COXF MFMlld:pubmed
pubmed-article:16657821pubmed:authorpubmed-author:BarendseG WGWlld:pubmed
pubmed-article:16657821pubmed:issnTypePrintlld:pubmed
pubmed-article:16657821pubmed:volume48lld:pubmed
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pubmed-article:16657821pubmed:pagination476-9lld:pubmed
pubmed-article:16657821pubmed:dateRevised2010-9-15lld:pubmed
pubmed-article:16657821pubmed:year1971lld:pubmed
pubmed-article:16657821pubmed:articleTitleIncorporation of C-Kaurene into the Gibberellin of a Higher Plant (Pharbitis nil Chois).lld:pubmed
pubmed-article:16657821pubmed:affiliationDepartment of Botany, University of Nijmegen, The Netherlands.lld:pubmed
pubmed-article:16657821pubmed:publicationTypeJournal Articlelld:pubmed