Intermediacy of iridodial in the biosynthesis of some iridoid glucosides

Administration of MVA-[2-¹⁴C] to Lamium applexicaule and Deutzia crenata as well as of 11-hydroxyiridodial glucoside-[10-³H] and 7-deoxyloganic acid-[10-³H] to the former plant suggested that, in contrast to secoiridoid-indole alkaloids, iridoid glucosides such as ipolamiide, lamiide, lamioside, deutzioside and scabroside in these plants are biosynthesized via iridodial. Iridodial as a precursor for the biosynthesis of asperuloside was also suggested from the results of the administration of MVA-[2-¹⁴C] to Galium spurium var. echinospermon.     

Application of capillary-scale NMR for the structure determination of phytochemicals

Employing a capillary-scale NMR probe enables the miniaturisation of structure determination and de-replication of purified natural products from plants using only 5-100 microg of material. Approximately 5 microg are required to perform one-dimensional proton and two-dimensional homonuclear (COSY and NOESY) NMR experiments; some 30 microg are needed to acquire HMQC- or HSQC-NMR spectra; ca. 75-100 microg are necessary to measure HMBC-NMR spectra; and around 200 microg of a compound are needed to perform 13C- and DEPT-NMR experiments. In order to illustrate the integration of the outputs from high-throughput natural product chemistry methods with the capabilities of the state-of-the-art CapNMR technology, the preparation of a natural product library from the extract of Penstemon centranthifolius, and the subsequent isolation, purification and structure determination of six known iridoid glycosides with 25-300 microg of material are presented.     

The phylogenetics and biochemistry of host-plant specialization in Melitaeine butterflies (Lepidoptera: Nymphalidae)

Butterflies in the tribe Melitaeini (Lepidoptera: Nymphalidae) are known to utilize host plants belonging to 16 families, although most host-plant records are from four families. Of the 16 host-plant families, 12 produce secondary plant metabolites called iridoids. Earlier studies have shown that larvae of several melitaeine species use iridoids as feeding stimulants and sequester these compounds for larval defense. I investigate the evolutionary history of host-plant use in the tribe Melitaeini by testing a recent phylogenetic hypothesis of 65 species representing the four major species groups of the tribe. By simple character optimization of host-plant families and presence/absence of iridoids in the host plants, I find that plant chemistry is a more conservative trait than plant taxonomy. The ancestral host plant(s) of the entire tribe most likely contained iridoids and were likely to be in the plant family Plantaginaceae. A major host shift from plants containing iridoids to plants not containing iridoids has happened three times independently. The results show that the evolution of host-plant use in melitaeines has been (and still is) a dynamic process when considering plant taxonomy, but is relatively stable when considering host-plant chemistry.     

栀子兰色素可能为栀子粉末外用抗炎消肿时的活性物质

传统中药山栀子中的环烯醚萜成分及尼平（ｇｅｎｉｐｉｎ）与甘氨酸反应可形成兰色素,初步药理实验显示,该兰色色素对小鼠具有抗炎和镇痛作用,推测栀子兰色素可能为民间将栀子粉末外用抗炎消肿时的活性物质。     

Structural studies on 10-hydroxygeraniol dehydrogenase: A novel linear substrate-specific dehydrogenase from Catharanthus roseus

Conversion of 10-hydroxygeraniol to 10-oxogeranial is a crucial step in iridoid biosynthesis. This reaction is catalyzed by a zinc-dependent alcohol dehydrogenase, 10-hydroxygeraniol dehydrogenase, belonging to the family of medium-chain dehydrogenase/reductase (MDR). Here, we report the crystal structures of a novel 10-hydroxygeraniol dehydrogenase from Catharanthus roseus in its apo and nicotinamide adenine dinucleotide phosphate (NADP⁺) bound forms. Structural analysis and docking studies reveal how subtle conformational differences of loops L1, L2, L3, and helix α9' at the orifice of the catalytic site confer differential activity of the enzyme toward various substrates, by modulating the binding pocket shape and volume. The present study, first of its kind, provides insights into the structural basis of substrate specificity of MDRs specific to linear substrates. Furthermore, comparison of apo and NADP⁺ bound structures suggests that the enzyme adopts open and closed states to facilitate cofactor binding.     

紫丁香花蕾化学成分研究

采用硅胶柱色谱和半制备高效液相色谱等从紫丁香花蕾乙酸乙酯溶液中分离得到8个单体化合物,经理化性质和波谱方法分别鉴定为:丁香苦素B(1)、齐墩果酸(2)、乌苏酸(3)、羽扇豆酸(4)、羽扇豆醇(5)、对羟基苯丙醇(6)、对羟基苯乙醇(7)和β-谷甾醇(8)。其中化合物6首次从该种植物中分离得到,其余均为首次从该植物花蕾中分离得到。     

Detrimental effects of plant compounds on a polyembryonic parasitoid are mediated through its highly polyphagous herbivore host

Plant defensive compounds can have sometimes severe deleterious effects on both herbivores and their natural enemies. Iridoid glycosides (IGs) are defensive compounds that are well established as deterrent to several generalist herbivores and generalist predators. Trichoplusia ni Hübner (Lepidoptera: Noctuidae) is exceptional among generalist herbivores for its ability to tolerate and thrive when feeding upon IG‐producing plant species; however, it is not known whether the compounds themselves have a harmful effect on T. ni and whether the effects in turn affect its oligophagous endoparasitoid Copidosoma floridanum Ashmead (Hymenoptera: Encyrtidae). To examine these effects, a semi‐purified extract of the IG‐containing plant Plantago lanceolata L. (Plantaginaceae), containing the IGs aucubin and catalpol, was added to artificial diets at 0, 1, 5, or 10% diet dry weight. These diets were fed to both C. floridanum‐parasitized and unparasitized T. ni. Diets higher in IGs tended to be more toxic to both parasitized and unparasitized larvae: host larvae that did survive were slightly smaller and took longer to develop on higher IG diets and total clutch size and survival of the parasitoid C. floridanum were greatly reduced as the host's dietary intake of IGs increased. Only small amounts of aucubin were detected inside the T. ni hemocoel, suggesting that the negative effect of these compounds on C. floridanum is due to nutritional quality of the host being reduced rather than direct toxic effects of the compounds.     

Iridoid aglycones from Deutzia scabra

Scabrogenin and deutziogenin, the stable aglycones of known iridoid glucosides scabroside and deutzioside, have been isolated from Deutzia scabra. Their structures and mutarotational equilibria were investigated by detailed analysis of ¹H NMR and ¹³C NMR data.     

5,7-Bisdeoxycynanchoside,an iridoid glucoside from Macfadyena cynanchoides

A new iridoid glucoside from Macfadyena cynanchoides leaves has been identified by spectral (¹H and ¹³C NMR) and chemical procedures as 5,7