Flavonoids of Astilbe and Rodgersia compared to Aruncus

The flavonoid profiles of Astilbe (four taxa studied) and Rodgersia (two taxa studied) are based on simple flavonol glycosides. Astilbe has 3-O-mono-, 3-O-di-, and 3-O-triglycosides of kaempferol, quercetin, and myricetin, while Rodgersia has only mono- and diglycosides of kaempferol and quercetin. Astilbe×arendsii was also shown to accumulate dihydrochalcone glycosides. The flavonoid profile of Rodgersia is the simplest recorded so far in the herbaceous Saxifragaceae. The flavonoids of two species of Aruncus were shown to be based upon kaempferol and quercetin 3-O-mono- and 3-O-diglycosides. One of the species also exhibited an eriodictyol glycoside. The triglycoside differences were not considered important, but the differences in myricetin occurrences were taken as evidence against derivation of Saxifragaceae from an Aruncus-like ancestor. Should such an event be proposed, however, serious consideration would have to be given to the current pattern of myricetin occurrence in the two families.     

Variations in flavonoid patterns within the genus Chondropetalum (restionaceae)

HPLC and chemical analyses of the flavonoids in culms of 11 Chondropetalum species divide the genus into two groups: seven, with glycosides of myricetin larycitin and syringetin; and four, with glycosides of kaempferol, quercetin, gossypetin, gossypetin 7-methyl ether and herbacetin 4′-methyl ether. This chemical dichotomy is correlated with anatomical differences and confirms the view that the genus requires taxonomic revision. HPLC measurements on those species with myricetin derivatives show that taxa with a qualitatively similar pattern of glycosides can be readily separated on quantitative grounds. Syringetin 3-arabinoside and a glycoside of herbacetin 4′-methyl ether are reported for the first time from the genus.     

Malonylated flavonol glycosides from the petals of Clitoria ternatea

Three flavonol glycosides, kaempferol 3-O-(2"-O-alpha-rhamnosyl-6"-O-malonyl)-beta-glucoside, quercetin 3-O-(2"-O-alpha-rhamnosyl-6"-O-malonyl)-beta-glucoside, and myricetin 3-O-(2",6"-di-O-alpha-rhamnosyl)-beta-glucoside were isolated from the petals of Clitoria ternatea cv. Double Blue, together with eleven known flavonol glycosides. Their structures were identified using UV, MS, and NMR spectroscopy. They were characterized as kaempferol and quercetin 3-(2(G)- rhamnosylrutinoside)s, kaempferol, quercetin, and myricetin 3-neohesperidosides, 3-rutinosides, and 3-glucosides in the same tissue. In addition, the presence of myricetin 3-O-(2"-O-alpha-rhamnosyl-6"-O-malonyl)-beta-glucoside was inferred from LC/MS/MS data for crude petal extracts. The flavonol compounds identified in the petals of C. ternatea differed from those reported in previous studies.     

Chemosystematic studies in the chrysobalanaceae. I. Flavonoids in Parinari

A survey of flavonoids in 31 Asian, African and Neotropical species of Parinari showed a predominance of flavonol glycosides based on myricetin, quercertin, and kaemp-ferol. The African taxa split into two groups based on the presence or absence of myricetin glycosides. The Neotropical taxa, a complex of closely related species, are chemically very similar to each other and lack myre?etin, as does one group of African species. The Asian taxa are similar to the Neotropical ones in their flavonoid patterns and lack of myricetin glycosides. The presence of myricetin considered a primitive flavonoid character, suggest that te African species pro-ducing this flavonol represent a primitive nucleus eastward and westward ex-pansion to two myricetin-lacking phytogeographic lines. This hypothesis is in agreement with current proposals for geographic evolution in the Chrysobalanaceae.     

Flavonoids of the Hydrangeaceae Dumortier

Fourteen species representing nine genera of the Hydrangeaceae Dumortier were surveyed for their flavonoid pigments. All taxa exhibited profiles based upon common flavonols. Myricetin was seen in two genera: Jamesia and Decumaria. Jamesia was further distinguished by the absence of kaempferol or its glycosides. A complex array of 3-O-mono-, 3-O-di- and 3-O-triglycosides was observed, although not all species had all levels of glycosylation. Decumaria barbara was unique within the species studied in its possession of 3,7-di- and 3,7-triglycosides. The overall pattern of flavonol glycosides observed for the Hydrangeaceae closely resembles that found in herbaceous genera of Saxifragaceae. The comparatively low frequency of myricetin contrasts with its high occurrence in herbaceous genera.     

紫荆族的脉序研究

本文对代表豆科云实亚科紫荆族全部五个属．即紫荆属、腺叶紫荆属、格里芬豆属、拟羊蹄甲属和羊蹄甲属的几乎全部系或亚组的１３４个种或种下分类单元的叶脉序进行了研究,并描述了本族２０个基本脉序类型．在紫荆族中,腺叶紫荆属和拟羊蹄甲属的脉序式样非常相似;紫荆属的种类的脉式样以全绿叶,一级脉不及绿等特征组合有别于本族其它属;格里芬豆属的脉序高度特化,有别于紫荆亚族的所有类群;羊蹄甲属是叶脉序式样最多样化的类群．在羊蹄甲属中,羊蹄甲亚属和显托亚属的脉序式样非常多样化．Ｅｌａｙｕｎａ亚属的两个组和Ｂａｒｋｌｙａ亚属的脉序式样非常相似．Ｂａｒｋｌｙａ亚属的仅有种了香叶羊蹄甲的脉序仅以其叶全缘区别于Ｅｌａｙｕｎａ亚属．脉序性状支持把Ｃａｎｓｅｎｉａ系、白花羊蹄甲系、羊蹄甲系、绿花羊蹄甲亚组、总状花羊蹄甲亚组、Ｅｌａｙｕｎａ亚属、伞房系、Ｃｈｌｏｒｏｘａｎｔｈａｅ系、棒花系、掌叶组和萼管组等作为自然类群的观点．在本族植物的脉序类型中,一级脉及缘、全缘叶、发育完好的脉岛等性状常相关出现;另一方面,一级脉不及缘,具二小叶或叶深裂,脉岛发育不完善及盲脉多分枝等性状常相关出现．如同形态和花粉性状,脉序性状能为紫荆族的分类提供另一方面的佐     

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

A survey of leaf hydrolysates of 52 species in section Vireya of Rhododendron showed that the flavonols kaempferol, quercetin and myricetin were commonly present. However, other more characteristic Rhododendron flavonol derivatives were either rare (caryatin, azaleatin) or absent (gossypetin). A study of the glycosides in four representative species showed that quercetin and kaempferol were present as the 3-rhamnoside, 3-glucoside, 3-galactoside or 3-rutinoside. The pattern in section Vireya is thus simpler than that in other Rhododendron species. This is in keeping with its geographical isolation, most species being endemic to the mountains of the Malesian-Australian region.     

Synthesis of flavonol 3-O-glycoside by UGT78D1

Glycosylation is an important method for the structural modification of various flavonols, resulting in the glycosides with increased solubility, stability and bioavailability compared with the corresponding aglycone. From the physiological point of view, glycosylation of plant flavonoids is of importance and interest. However, it is notoriously complicated that flavonols such as quercetin, kaempferol and myricetin, are glucosylated regioselectively at the specific position by chemical method. Compared to the chemical method, enzymatic synthesis present several advantages, such as mild reaction condition, high stereo or region selectivity, no protection/deprotection and high yield. UGT78D1 is a flavonol-specific glycosyltransferase, responsible for transferring rhamnose or glucose to the 3-OH position in vitro. In this study, the activity of UGT78D1 was tested against 28 flavonoids acceptors using UDP-glucose as donor nucleoside in vitro, and 5 acceptors, quercetin, myricetin, kaempferol, fisetin and isorhamnetin, were discovered to be glucosylated at 3-OH position. Herein, the small-scale 3-O-glucosylated quercetin, kaempferol and myricetin were synthesized by UGT78D1 and their chemical structures were confirmed by (1)H and (13)C nuclear magnetic resonance (NMR) and high resolution mass spectrometry (HRMS).     

Phylogeny of Cercis based on DNA sequences of nuclear ITS and four plastid regions: implications for transatlantic historical biogeography

The disjunct genus Cercis has been used to test models of Northern Hemisphere historical biogeography. Previous phylogenetic estimates employing DNA sequences of the ITS region and (in one study) those of ndhF recovered a well supported clade of North American and western Eurasian species that was nested within a paraphyletic group of Chinese species. Resolution and clade support within the tree were otherwise low and the monophyly of Cercis canadensis was uncertain. Here we conduct a phylogenetic analysis of Cercis with a higher number of regions (ITS, ndhF, rpoB-trnC, trnT-trnD, and trnS-trnG) and samples than in previous studies. Results corroborate the initial divergence between the Chinese species Cercis chingii and the rest of the genus. Support is newly found both for a clade of the two North American species as sister to the western Eurasian species, and for the monophyly of C. canadensis. As in a previous study, divergence between North American and western Eurasian Cercis was estimated as mid-Miocene (ca. 13 million years ago), and the ancestor in which this divergence occurred was inferred to be xerophytic. Contrary to previous studies, however, our data infer strictly east-to-west vicariance. The timing of the transatlantic divergence in Cercis is too recent to be explained by a postulated continuous belt of semi-arid vegetation between North America and Europe in the Paleogene, suggesting instead the presence of a Miocene North Atlantic corridor for semi-arid plants. In the absence of strong evidence from other sources, the possibility that Cercis has been able to quickly adapt from mesophytic antecedents to semi-arid conditions whenever the latter have arisen in the Northern Hemisphere can be considered a plausible alternative, although parsimony optimization renders this scenario two steps longer.     

Degradation of the upper pulvinus in modern and fossil leaves of Cercis (Fabaceae)

Identification of fossil leaf impressions as Cercis has been questioned based upon the presence or absence of a pulvinus at the base of the lamina (upper pulvinus). In the present study, leaves of Cercis canadensis were examined before and after abscission to explore the degradation processes that could occur prior to fossilization, and the North American record for fossil foliage of Cercis was revised accordingly. Results for C. canadensis indicate that: (1) the pulvinus consists largely of tissues with nonlignified cells (a wide cortex, a nonlignified fiber sheath, phloem, and pith) that degrade rapidly after leaf abscission, (2) the lignified xylem tissue that remains in the pulvinus after degradation is in brittle strands, (3) the pulvinus degrades at a faster rate than the lamina or the petiole, and (4) the degraded pulvinus cushion leaves a semicircular pattern on the lamina. From examination of fossils as well as extant species, we: (1) demonstrated that in fossils, the upper pulvinus can show a greater degree of degradation than the adjoining petiole or lamina tissue, suggesting the degradation of upper pulvinus tissue is similar in modern vs. fossil specimens, (2) defined numerous other laminar characters that can be used in conjunction with, or in the absence of, an upper pulvinus to confirm the presence of Cercis in the fossil record, and (3) showed from those criteria that the earliest known North American fossil leaf record for Cercis, from a specimen newly reported in the present study, is from the middle Miocene Succor Creek flora of Oregon.     

Flavonoid glycosides and the chemosystematics of Eucalyptus camaldulensisis

Leaf flavonoid glycosides of Eucalyptus camaldulensis were identified as kaempferol 3-glucoside and 3-glucuronide; quercetin 3-glucoside, 3-glucuronide, 3-rhamnoside, 3-rutinoside and 7-glucoside, apigenin 7-glucuronide and luteolin 7-glucoside and 7-glucuronide. Two chemical races were observed based on the flavonoid glycosides. These races correspond to the northern and southern populations of species growing in Australia. The Middle Eastern species examined were found to belong to the southern Australian chemical race. The major glycosides of E. occidentalis proved to be quercetin and myricetin 3-glucuronide.     

Flavonol and drimane-type sesquiterpene glycosides of Warburgia stuhlmannii leaves

An investigation of methanolic extract of Warburgia stuhlmannii leaves has led to the isolation of two new drimane-type sesquiterpene glycosides characterized as mukaadial 6-O-beta-D-glucopyranoside, mukaadial 6-O-alpha-L-rhamnopyranoside together with two other novel flavonol glycosides identified as 3',5'-O-dimethylmyricetin 3-O-beta-D-2",3"-diacetylglucopyranoside and 3'-O-methylquercetin 3-O-beta-D-2",3",4"-triacetylglucopyranoside. The known compounds; mukaadial, deacetylugandensolide, quercetin, kaempferol, kaempferol 3-O-alpha-L-rhamnopyranoside, quercetin 3-O-beta-D-glucopyranoside, kaempferol 7-O-beta-D-glucopyranoside, myricetin 3-O-alpha-L-rhamnopyranoside, quercetin 3-O-alpha-L-rhamnopyranoside, quercetin 3-O-sophoroside and isorhamnetin 3-O-beta-D-glucopyranoside were also isolated from the same extract.     

A morphological and chemical study of Populus acuminata Rydberg

Evidence from morphology, flavonoid chemistry, and field observations suggests thatPopulus acuminata is of hybrid origin. The putative parents areP. angustifolia, the narrow leaf cottonwood, and deltoid leaved plants that are assigned toP. sargentii (P. deltoides var.occidentalis), P. fremontii, orP. wislizenii (P. fremontii var.wislizenii). Populus angustifolia exhibits a series of flavonol glycosides (kaempferol, quercetin, and myricetin) in its leaves. By contrast, the major leaf flavonoids of the broad leaved plants are flavone glycosides (apigenin and luteolin).Populus acuminata is intermediate between the suspected parents in morphological features. Additionally, the leaves of mostP. acuminata plants contain the exact summation of the flavonoid compounds characteristic of the putative parents. A diploid chromosome number of 2n = 38 was obtained for six plants, which confirms the one previous report for the species. Meiosis was regular in all cases. Correlated data indicate that the majority of plants ofP. acuminata represent F₁ hybrids and that complex hybridization is not common. Evidence from morphological and chemical studies is presented to show that in certain instances backcrossing to both parents has occurred. Results gathered in this study show thatP. ×andrewsii is undoubtedly “typical”P. acuminata, but the type specimen is from a sucker shoot, and thus has been interpreted as a backcross toP. sargentii. Populus acuminata var.rehderi is not considered worthy of taxonomic recognition.     

FLAVONOIDS AND TAXONOMY OF THE LIMNANTHACEAE

To help clarify relationships within the Limnanthaceae, all 19 taxa were compared on the basis of flavonoids occurring in all tissues, and 14 of these taxa were additionally compared on the basis of flavonoids occurring only in the petals. Of the 46 flavonol glycosides encountered, 35 were identified as derivatives of six flavonol aglycone types: syringetin, isorhamnetin, kaempferol, laricytrin (myricetin 3'-methyl ether), quercetin and myricetin, all glycosylated with combinations of glucose and rhamnose. Varimax Factor Analysis with rotation of the flavonoid data indicated that the family probably contains 3 phyletic lines, an observation inconsistent with the conventional 2-generic interpretation of the family. Mason's sectional treatment of Limnanthes is supported by petal flavonoid results, but not by whole-plant flavonoid results, indicating that petal flavonoids more clearly reflect natural relationships in Limnanthes. Evolution of whole-plant flavonoids of Limnanthes appears to be partly linked to changes in breeding system.     

FLAVONOIDS AND FLAVONOID EVOLUTION IN FUCHSIA (ONAGRACEAE)

A comprehensive survey of 225 populations of 80 taxa of Fuchsia showed flavonol monoglycosides, especially quercetin and kaempferol 3-O-glucosides, to be ubiquitous in all species examined. Flavonol diglycosides are unusual, however, and occur in just eight species in five of the nine sections of the genus. Flavone glycosides were found in only nine species belonging to five sections and are associated with primitive taxa, having been lost in more recently derived species or sections. Flavone sulphates are restricted to species of the disjunct sect. Skinnera from New Zealand. The limited presence of flavone glycosides and flavonol diglycosides in certain species can be effectively employed as chemical markers in determining the parentage of these species in fuchsia cultivars of unknown hybrid origin.     

The leaf flavonoids of the Zingiberales

A survey of flavonoids in the leaves of 81 species of the Zingiberales showed that, while most of the major classes of flavonoid are represented in the order, only two families, the Zingiberaceae and Marantaceae are rich in these constituents. In the Musaceae (in 9 species), Strelitziaceae (in 8 species) and Cannaceae (1 of 2 species) flavonol glycosides were detected in small amount and in the Lowiaceae no flavonoids were fully identified. In the Zingiberaceae kaempferol (in 22%), quercetin (72%) and proanthocyanidins (71%) are distributed throughout the family. The two subfamilies of the Zingiberaceae may be distinguished by the presence of myricetin (in 26%), isorhamnetin (10%) and syringetin (3%) in the Zingiberoideae and of flavone $\text{C-}\text{glycosides}$ (in 86% of taxa) in the Costoideae. A number of genera have distinctive flavonol profiles: e.g. Hedychium species have myricetin and quercetin. Roscoea species isorhamnetin and quercetin and Alpinia species kaempferol and quercetin glycosides. A new glycoside, syringetin 3-rhamnoside was identified in Hedychium stenopetalum. In the Zingiberoideae flavonols were found in glycosidic combination with glucuronic acid, rhamnose and glucose but glucuronides were not detected in the Costoideae or elsewhere in the Zingiberales. The Marantaceae is chemically the most diverse group and may be distinguished from other members of the Zingiberales by the occurrence of both flavone $\text{O-}$ and $\text{C-}\text{glycosides}$ and the absence of kaempferol and isorhamnetin glycosides. The distribution of flavonoid constituents within the Marantaceae does not closely follow the existing tribai or generic limits. Flavonols (in 50% of species). flavones (20%) and flavone $\text{C-}\text{glycosides}$ (40%) are found with similar frequency in the two tribes and in the genera Calathea and Maranta both flavone and flavonol glycosides occur. Apigenin- and luteolin-7-sulphates and luteolin-7,3′-disulphate were identified in Maranta bicolor and M. leuconeura var. kerchoveana and several flavone $\text{C-}\text{glycosides}$ sulphates in Stromanthe sanguinea. Anthocyanins were identified in those species with pigmented leaves or stems and a common pattern based on cyanidin-and delphinidin-3-rutinosides was observed throughout the group. Finally the possible relationship of the Zingiberales to the Commelinales, Liliales, Bromeliales and Fluviales is discussed.     

Flavonol and iridoid glycosides of Ajuga remota aerial parts

Six flavonol glycosides characterised as myricetin 3-O-alpha-rhamnosyl-(1'-->2')-alpha-rhamnoside-3'-O-alpha-rhamnoside, 5'-O-methylmyricetin 3-O-[alpha-rhamnosyl (1'-->2')][alpha-rhamnosyl (1'-->4')]-beta -glucoside-3'-O-beta-glucoside, 5'-O-methylmyricetin 3-O-alpha-rhamnosyl (1'-->2')-alpha-rhamnoside 3'-O-beta-galactoside, kaemferol 3-O-rutinoside-7-O-rutinoside, myricetin 3-O-rutinoside-3'-O-alpha-rhamnoside, myricetin 3-O-beta-glucosyl (1'-->2')-beta-glucoside-4'-O-beta-glucoside together with two iridoid glycosides identified as 6,8-diacetylharpagide and 6,8-diacetylharpagide-1-O-beta-(3',4'-di-O-acetylglucoside) have been isolated from extract of Ajuga remota aerial parts. Also isolated from the same extract were known compounds; kaempferol 3-O-alpha-rhamnoside, quercetin 3-O-beta-glucoside, quercetin 3-O-rutinoside, 8-acetylharpagide, ajugarin I and ajugarin II.     

Flavonol glycosides of Limnanthes douglasii

Eighteen flavonol glycosides were isolated from petal and leaf-stem of Limnanthes douglasii. There were six aglycones: kaempferol, quercetin, isorhamnetin, myriectin, syringetin and a new flavonol, myricetin 3′-methyl ether. Each occurred as the 3-rutinoside, 3-rhamnosylrutinoside and 3-rutinoside-7-glucoside.     

A chemotaxonomic survey of flavonoids in leaves of the Oleaceae

Leaves of 97 taxa representing all the genera at present recognized in the family Oleaceae were surveyed for flavonoids. Four flavonol glycosides were found to be common, the 3-glucmides and 3-rutinosides of quercetin and kaempferol, as were four flavone glycosides, namely the 7-glurosides arid 7-rutinosides of luteolin and apigenin. Among rarer constituents detected were luteolin 4'-glucoside, eriodictyol 7-glucoside, chrysoeriol 7-glucoside, an apigenin-di-C-glycoside and several higher glycosides of quercetin. The species and genera surveyed fell into two groups: those with flavonol glycosides alone; and those with both flavonol and flavone glycosides. The most striking correlation was with chromosome number (and subfamily division) since almost all taxa with a basic number of 11, 13 and 14 had only flavonol glycosides, whereas most taxa with x = 23 had both types of flavonoid. Evolutionary advancement in the family appears to involve the gradual replacement of flavonol by flavone glycosides. Indeed, a few tam, notably Nestegis apelala, Picconia excelsa and Tesserandra fluminense , lacked flavonol glycosides in the leaves completely. At the lower levels of classification, the distribution of flavonoids is of less interest. However, the patterns in Linociera and Chionanthus , two taxa recently made congeneric, are sufficiently different to suggest that this decision might have to be reconsidered when more is known of their chemistry. Otherwise leaf patterns generally fit in with the existing generic classification in the family.     

Systematic studies in sedum section ternata (Crassulaceae)

An investigation of flavonoid compounds, pollen grains, and seed coats of the four taxa of the genusSedum sectionTernata, S. nevii, S. glaucophyllum, S. pulchellum, andS. ternatum, was undertaken to resolve the taxonomic status ofS. glaucophyllum. Flavonoid compounds were tentatively identified utilizing UV spectroscopy and shift reagents. Both flavones and fla vonols, as apigenin, luteolin, quercetin, and kaempferol aglycones and glycosides, were detected. Pollen grains and seed coats were viewed and photographed with the aid of a scanning electron microscope. Pollen grains of all four taxa were uniformly tricolporate; interspecific variation was negligible. Seed coats of all four taxa differed significantly with respect to ornamentation. Phytochemical and morphological data both support the recognition ofS. glaucophyllum as a species distinct from S.nevii.