On the occurrence of tuliposides in the liliiflorae

Approximately 200 samples of liliiflorous plants were investigated for the presence of tuliposides. Appreciable amounts of tuliposide A were detected in all species of Erythronium, Tulipa, Gagea, Bomarea and Alstroemeria. Large amounts of tuliposide B seem to be restricted to Erythronium and Tulipa. The occurrence of identical post-inhibitins in Tulipa and allied taxa and in Alstroemeria and allied taxa is interpreted as indicating a close relationship between Lilioideae and Alstroemeriaceae. At the same time the allergenic potentialities of all taxa of Alstroemeria are stressed.     

Content and vacuole/extravacuole distribution of neutral sugars, free amino acids, and anthocyanin in protoplasts

Neutral sugar, free amino acid, and anthocyanin levels and vacuole/extravacuole distribution were determined for Hippeastrum and Tulipa petal and Tulipa leaf protoplasts. Glucose and fructose, the predominant neutral monosaccharides observed, were primarily vacuolar in location. Glutamine, the predominant free amino acid found, was primarily extravacuolar. γ-Methyleneglutamate was identified as a major constituent of Tulipa protoplasts. Qualitative characterization of Hippeastrum petal and vacuole organic acids indicated the presence of oxalic, malic, citric, and isocitric acids. Data are presented which indicate that vacuoles obtained by gentle osmotic shock of protoplasts in dibasic phosphate have good purity and retain their contents.     

Molecular analysis of species of Tulipa L. from Iran based on ISSR markers

Molecular characterization of Tulipa L. species can elucidate the relationships among the species and provide more information about the taxonomy of this valuable genus. In this study, the genetic relationship among 39 Tulipa accessions from Khorassan and Yazd Provinces, located in east and northeast Iran, were analyzed using inter-simple sequence repeat (ISSR) primers. Ten selected ISSR primers from 20 screened primers generated a total of 97 polymorphic DNA bands. Unweighted pair-group method of cluster analysis based on Dice similarity values separated the accessions into nine groups. Seven species were recognized within these groups, and T.?micheliana Hoog was the most frequently encountered species. The subgroups formed within both T.?micheliana and T.?lehmanniana Merckl. revealed a low level of diversity within these species. T.?biebersteiniana Schultes & Schultes fil. and T.?biflora Pallas accessions made a separate clusters. The grouping of accessions was generally consistent with principal coordinate analysis (PCA) and clearly showed the position of species in the subgenera and sections of Tulipa. These results clearly showed the usefulness of DNA fingerprinting for identification of Tulipa accessions, and it is imperative to collect and characterize more genetic variability from the other distribution areas of this genus.     

Subcellular localization of enzymes of anthocyanin biosynthesis in protoplasts

Flavanone synthase, chalcone-flavanone isomerase and UDP-glucose; anthocyanidin-3-O-glucosyltransferase activities of protoplasts and subcellular fractions of protoplasts of Hippeastrum and Tulipa were investigated. Subcellular fractions studied were intact vacuoles, cytosol and particulate components of protoplasts less the vacuole. The cytosol fraction had the highest activity of the three enzymes studied. Results similar to those found for Hippeastrum were obtained with fractions from leaves and petals of Tulipa. The increase in flavanone synthase activity in the cytosol fraction from petals of Hippeastrum during development paralleled the increase in anthocyanin content of the petals.     

Membrane-bound ATPase of intact vacuoles and tonoplasts isolated from mature plant tissue

Intact vacuoles were isolated from petals of Hippeastrum and Tulipa (Wagner G.J. and Siegelman, H.W. (1975) Science 190, (1298–1299). The ATPase activity of fresh vacuole suspensions was found to be 2–3 times that of protoplasts from the same tissue. 70–80% of the ATPase activity of intact vacuoles was recovered in tonoplast preparations. The antibiotic Dio-9 at 6 μg/10⁶ vacuoles or protoplasts causes 40% inhibition. However, only the protoplast ATPase is sensitive to oligomycin. N,N′-dicyclohexylcarbodiimide (DCCD) slightly stimulates ATPase activity in both vacuole and protoplast suspensions, whereas ethyl-3-(3-dimethylaminopropyl carbodiimide) (EDAC) strongly inhibits.Spectrophotometric studies show that in the petal the vacuolar contents have a pH of 4.0 for Tulipa and 4.3 for Hippeastrum, whereas the intact isolated vacuole has an internal pH of 7.0 (in pH 8.0 buffer) for Tulipa and about 7.3 for Hippeastrum. Internal ion concentrations of 150, 46, 30, 30 and 6 mM were found for K⁺, Na⁺, Mg²⁺, Cl^?, and Ca²⁺ respectively, which are about the same as those in protoplasts.     

Anthocyanin content of Tulipa species and cultivars and its impact on tepal colours

Flowers of tulips (17 species and 25 cultivars) were subjected to qualitative and relative quantitative examination for anthocyanins. Altogether five anthocyanins were identified as the 3-O-(6″-O-α-rhamnopyranosyl-β-glucopyranoside) of delphinidin (1), cyanidin (2) and pelargonidin (3), and the 3-O-[6″-O-(2‴-O-acetyl-α-rhamnopyranosyl)-β-glucopyranoside] of cyanidin (4) and pelargonidin (5). The pigments 1–5 represented 7%, 43%, 12%, 2% and 31%, respectively, of the total anthocyanin amount in the tepals of the Tulipa species, and 20%, 37%, 30%, 6% and 4%, respectively, in the cultivar tepals. Nearly 50% of the samples contained acetylated anthocyanins. The colours of the freeze-dried tepals described by the CIELab coordinates, hue angle (h_ab), saturation (C*), and lightness (L*) together with the anthocyanin content were subjected to multivariate analysis. All tepals classified with hue angles described as “blue nuances” were from cultivars. They contained 1 as the major anthocyanin, and no or just traces of pelargonidin derivatives. The species and cultivars having “magenta nuances” showed similar anthocyanin content with increased relative proportions of 2 at the expense of 1. Orange coloured tepals were to a large extent correlated with high relative proportions of the pelargonidin derivatives, 3 and 5. Acetylation of anthocyanins furnished a weak colour effect opposite to the bluing effect previously reported for anthocyanins with aromatic acyl groups. All six species belonging to the section Eichleres (subgenus Tulipa) were after principal component analysis grouped closely together. They were characterized by high concentrations of the pelargonidin derivatives 3 and 5, and orange petal nuances. However, within section Tulipa (subgenus Tulipa), considerable anthocyanin variation was observed. Species in the subgenus Eriostemones were generally characterized by the two anthocyanins 1 and 2, and no pelargonidin derivatives.     

Species identification of the medicinal plant Tulipa edulis (Liliaceae) by DNA barcode marker

Tulipa edulis (Liliaceae) is the botanical origin of the traditional Chinese medicine (TCM) “Guangcigu”. Due to overexploitation that induced a decline in natural sources, many dried bulbs from other species of Tulipa have been used, adulterating the medicine in recent years. This practice may cause a series of inconsistent therapeutic effects and quality control problems in the herbal medicine industry. Hence, three DNA regions (matK, psbA-trnH and rbcL) were evaluated as barcodes for identifying T. edulis and its adulterants. All candidate DNA barcodes were successfully amplified from leaf samples. Based on the sequence divergences, rbcL and psbA-trnH can assign T. edulis and its adulterants to the correct genus, while matK can accurately differentiate T. edulis and its adulterants. Thus, at the DNA level, the matK intergenic region is a more suitable, accurate and applicable identification of T. edulis and its adulterants than rbcL and psbA-trnH.     

Molecular phylogenetic analysis of Tulipa (Liliaceae) based on noncoding plastid and nuclear DNA sequences with an emphasis on Turkey

We investigated the phylogenetic relationships in Tulipa in Turkey using DNA sequences from the plastid trnL‐trnF region and the internal transcribed spacer (ITS) of nuclear ribosomal DNA. We generated trnL‐trnF and nuclear ITS sequences for 11 Tulipa spp. from Turkey and compared the utility of trnL‐trnF and ITS sequences for phylogenetic analysis. Neighbor‐joining, Bayesian and maximum parsimony methods were implemented using the same matrices. Our study of Tulipa based on molecular data revealed congruent results with previous studies. Despite the relatively lower resolution of trnL‐trnF than that of ITS, both sequence matrices generated similar results. Three clades were clearly distinguished, corresponding to subgenera Tulipa, Eriostemones and Orithyia. It is not fully resolved whether Clusianae should be recognized as a separate section of subgenus Tulipa or a distinct subgenus. © 2013 The Linnean Society of London, Botanical Journal of the Linnean Society, 2013, 172 , 270–279.     

Reassessment of diversity and analysis of distribution in Tulipa (Liliaceae) in Uzbekistan

The diversity and distribution of the genus Tulipa in Uzbekistan are discussed; 34 taxa of Tulipa are recognized in Uzbekistan. The taxa were mapped using GIS software and their distributions were analyzed. Six species are endemic to the country. A national check‐list of Tulipa was created based on the classification developed by Zonneveld (2009). ‘Hot spot’ areas of tulip diversity in Uzbekistan are western Tien‐Shan (18 taxa), the western Pamir–Alay mountains (18 taxa) and the Turan lowland (5 taxa). An assessment of rare tulip species according to IUCN red list categories and criteria was performed for the first time for Uzbekistan. Evaluation of the latest classification of Tulipa clearly shows that further studies are required to arrive at a natural classification of the genus.     

Tulip allergens in Alstroemeria and some other liliiflorae

A study has been made of the occurrence of tulip allergens (tuliposides) among several plant genera belonging to the Liliiflorae. All species of the genera Alstroemeria, Erythronium and Tulipa can be considered potentially allergenic (tuliposide-A). Tuliposide-B is more generally distributed and occurs in Lilium, Notholirion and Calochortus as well. Small amounts of both tuliposides are found in Fritillaria. A brief discussion is given of the systematic implications of the results.     

Crossability analysis in subgenus Tulipa of the genus Tulipa L.

A range of almost 1400 cross combinations has been carried out between 31 species of Tulipa subgenus Tulipa. Most of the sections are well separated reproductively from each other. The designated species aggregates in section Clusianae appeared to be intersterile. Also in section Kolpakowskianae the species, as far as used, cannot be combined. Some crosses between species of section Tulipanum succeeded. The species of sections Eichleres and Tulipa (including the cultivated tulip T gesneriana) could be combined in various ways, although the highest level of seed set was achieved within either section. The crossability data support the current taxonomic division. The level of reproductive isolation between sympatric species is discussed, and the importance of crossability studies for plant breeding in Tulipa pointed out briefly.     

Spatial and temporal flowering patterns of the monocarpic dwarf bamboo Sasa veitchii var. hirsuta

In order to clarify spatial and temporal patterns in the flowering process of S. veitchii var. hirsuta, the authors investigated the flowering of the species at a regional level in a mountainous area of Kyoto City, and at population/individual culm levels at experimental forest stations within the same municipal region. S. veitchii var. hirsuta flowered in several separate areas spanning ranges between several and more than 10?km north?Csouth and east?Cwest from 2004 to 2007. Sporadic flowering occurred the year before mass flowering. In the mass-flowering year, 98% of the culms in an S. veitchii var. hirsuta population flowered, and the other 2% or so flowered in the years before and after mass flowering. These results show a spatiotemporal synchronous flowering pattern (with most culms of populations gregariously flowering in a year over a large area) and an asynchronous flowering pattern (with a small percentage of the culms of populations flowering before and after the mass-flowering year) for S. veitchii var. hirsuta. It was also clarified that the year and scale of mass flowering differ by area, and that mass flowering occurs in individual areas in successive years. The survey performed at the individual culm level revealed that the mean numbers of open florets and attached seeds per culm showed two peaks from April to July, suggesting that S. veitchii var. hirsuta flowering events occur twice a year.     

Contributions to the pollen morphology and taxonomy of the Liliaceae

Pollen of 34 species from 7 genera of the Liliaceae were examined by LM and SEM with respect to the taxonomy of the family. Detailed pollen­morphological characteristics are given for all genera in the family on the basis of the results presented here together with data from the literature. The genera Tulipa and Lilium are heterogeneous in both aperture type and exine ornamentation. Pollen of Tulipa is monosulcate, 3-aperturate or inaperturate, with a microreticulate-striate, reticulate-implecto-striate, scabrate, perforate-rugulate, perforate-striate exine surface. Pollen of Lilium is monosulcate and 3-porate with a macroreticulate exine. The other genera are homogeneous in possessing of single longitudinal aperture (type monosulcate). The pattern of exine ornamentation and the structure of the aperture and its membrane are peculiar features for species and genera. Pollen of Erythronium and Tulipa are occasionally operculate, while in other representatives of the Liliaceae an operculum is lacking. Pollen morphological data support the division of the family into 3 tribes, namely Lloydieae, Lilieae, and Tulipeae.     

Heterologous Expression of Wheat VERNALIZATION 2 (TaVRN2) Gene in Arabidopsis Delays Flowering and Enhances Freezing Tolerance

The vernalization gene 2 (VRN2), is a major flowering repressor in temperate cereals that is regulated by low temperature and photoperiod. Here we show that the gene from Triticum aestivum (TaVRN2) is also regulated by salt, heat shock, dehydration, wounding and abscissic acid. Promoter analysis indicates that TaVRN2 regulatory region possesses all the specific responsive elements to these stresses. This suggests pleiotropic effects of TaVRN2 in wheat development and adaptability to the environment. To test if TaVRN2 can act as a flowering repressor in species different from the temperate cereals, the gene was ectopically expressed in the model plant Arabidopsis. Transgenic plants showed no alteration in morphology, but their flowering time was significantly delayed compared to controls plants, indicating that TaVRN2, although having no ortholog in Brassicaceae, can act as a flowering repressor in these species. To identify the possible mechanism by which TaVRN2 gene delays flowering in Arabidopsis, the expression level of several genes involved in flowering time regulation was determined. The analysis indicates that the late flowering of the 35S::TaVRN2 plants was associated with a complex pattern of expression of the major flowering control genes, FCA, FLC, FT, FVE and SOC1. This suggests that heterologous expression of TaVRN2 in Arabidopsis can delay flowering by modulating several floral inductive pathways. Furthermore, transgenic plants showed higher freezing tolerance, likely due to the accumulation of CBF2, CBF3 and the COR genes. Overall, our data suggests that TaVRN2 gene could modulate a common regulator of the two interacting pathways that regulate flowering time and the induction of cold tolerance. The results also demonstrate that TaVRN2 could be used to manipulate flowering time and improve cold tolerance in other species.     

Species relationships and taxonomy inTulipa subg.Tulipa (Liliaceae)

Principal component and canonical variate analyses were used to analyse the variation of 34 morphological characters measured in 98 accessions ofTulipa subg.Tulipa, formerly known as sect.Leiostemones. In addition 43 accessions were analysed cytogenetically by means of C-banding methods. Based on the encountered variation and on geographical distribution data 30 species in five sections were recognized, of which the synonymy is stated. Seven new series in two different sections have been designated.     

Studies on the expression patterns of the circadian rhythm regulated genes in mango

Mango, an important fruit crop of the tropical and subtropical regions shows alternate bearing in most varieties causing a financial loss to the farmer. Genetic reasons for this undesirable trait have not been studied so far. In our attempts to investigate the genetic reasons for alternate bearing we have initiated studies on genes associated with the induction, repression and regulation of flowering in mango. We have previously identified and characterized FLOWERING LOCUS T (FT) genes that induce flowering and two TERMINAL FLOWER1 (TFL1) genes that repress flowering. In this communication, we have explored the association of GI-FKF1-CDF1-CO module with the regulation of flowering in mango. The role of this module in regulating flowering has been well documented in photoperiod sensitive plants. We have characterized these genes and their expressions during flowering in Ratna variety as also their diurnal fluctuations and tissue specific expressions. The data taken together suggest that GI-FKF1-CDF1-CO module may also be employed by mango in regulating its flowering. Further, we suggest that the temperature dependent flowering in mango is probably associated with the presence of temperature sensitive elements present in the promoter region of one of the GIGANTEA genes that have been shown to be closely associated with floral induction.Supplementary InformationThe online version contains supplementary material available at 10.1007/s12298-021-01053-8.     

Role of SEPALLATA3 (SEP3) as a downstream gene of miR156-SPL3-FT circuitry in ambient temperature-responsive flowering

SEPALLATA3 (SEP3) is important in determining flowering time as well as floral organ identity. Although much is known about the regulation of floral organ identity by SEP3, its role as a downstream gene of FLOWERING LOCUS T (FT) for the regulation of ambient temperature-responsive flowering is poorly understood. Here, we show that SEP3 as a downstream gene of SQUAMOSA PROMOTER BINDING PROTEIN-LIKE3 (SPL3) and FT modulates the flowering time in response to different ambient temperatures. SEP3 overexpression showed temperature-insensitive flowering at 23°C and 16°C. This suggests that altered SEP3 activity affects ambient temperature-responsive flowering. However, a lesion in SEP3 did not obviously affect ambient temperature-responsive flowering. SEP3 expression was affected by altered SPL3 and FT activities in the leaf and shoot apical regions at different temperatures. These results suggest that the miR156-SPL3-FT circuitry directly or indirectly regulates SEP3 expression for the regulation of ambient temperature-responsive flowering in Arabidopsis.