2000
DOI: 10.1584/jpestics.25.117
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Reversible Conversion between Teasterone and Its Ester Conjugates in Lily Cell Cultures

Abstract: Metabolisms of both teasterone and its 3-myristate were studied using lily cell cultures. Teasterone was metabolized to two ester conjugates, teasterone-3-myristate and teasterone-3-laurate, which have been identified from the lily pollen. On the other hand, teasterone-3-myristate was metabolized to teasterone. The same reversible conversion was suggested during the course of brassinolide biosynthesis in the lily pollen. It was considered that the conjugates are the reversible storage forms during the biosynth… Show more

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Cited by 17 publications
(15 citation statements)
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“…Notably BL levels have not been measured for many BR mutants due to its very low abundance, thus it is difficult to assess how general these apparent discrepancies are. BRs are thought to act locally within the tissue [61] and we suspect that PIZ overexpression may cause stronger down-regulation of BRs only in a subset of cells where BRs primarily function. Such local changes might be masked in our bulk analysis.…”
Section: Discussionmentioning
confidence: 99%
“…Notably BL levels have not been measured for many BR mutants due to its very low abundance, thus it is difficult to assess how general these apparent discrepancies are. BRs are thought to act locally within the tissue [61] and we suspect that PIZ overexpression may cause stronger down-regulation of BRs only in a subset of cells where BRs primarily function. Such local changes might be masked in our bulk analysis.…”
Section: Discussionmentioning
confidence: 99%
“…For example, 3,24鈥恉iepiCS and 3,24鈥恉iepiBL were found to be conjugated to 3鈥恖aurate, 3鈥恗yristate or 3鈥恜almitate ester in serradella cells ( Ornithopus sativus ) (Kolbe et al ., , ). TE and its derivatives may be conjugated to 3鈥恖aurate and 3鈥恗yristate, creating several acyl metabolites in lily ( Lilium longiflorum ) cell cultures (Abe et al ., ; Asakawa et al ., , ; Kolbe et al ., ; Soeno et al ., ,b). These acyl BRs are easily converted to free TE, CS and BL intermediates by hydrolysis.…”
Section: Discussionmentioning
confidence: 99%
“…Conjugated BRs, such as glycosylated or acylated compounds that are well known from several species (Fujioka and Yokota, 2003;Bajguz, 2007), may serve as reversibly inactivated storage forms, which can be mobilized enzymatically when hormone synthesis and accumulation are required. Such a reversible reaction is C-3 myristylation of teasterone that was described in lily (Lilium longiflorum), and was suggested to support BL synthesis during pollen development (Asakawa et al, 1996;Soeno et al, 2000). Conjugative reactions, rather than catabolic breakdown, can be responsible for the rapid decrease of the total BR content in fully developed pea seeds (Nomura et al, 2007).…”
Section: Discussionmentioning
confidence: 97%