蕾后期和花前期切花菊品种'神马'不同部位叶片光合作用和叶绿素荧光特性的比较

对蕾后期和花前期切花菊(Chrysanthemum morifolium Ramat.)品种'神马'('Jinba')不同部位叶片光合作用参数日变化、叶绿素荧光参数、光响应曲线及参数进行了研究.结果表明:蕾后期和花前期品种'神马'叶片蒸腾速率(Tr)、气孔导度(Gs)和净光合速率(Pn)的日变化均为单峰曲线,峰值出现在10:00或12:00;胞间CO2浓度(Ci)的日变化则先降低后升高,谷值出现在12:00.蕾后期和花前期品种'神马'叶片Tr、Ci和Gs值的平均值总体上随叶片位置降低而逐渐升高;蕾后期不同部位叶片Pn值的平均值差异较小,花前期叶片Pn值的平均值则随叶片位置降低而逐渐降低.随着叶片位置降低,蕾后期和花前期品种'神马'叶片的初始荧光(Fo)、最大荧光(Fm)、可变荧光(Fv)、表观量子效率(AQE)和最大净光合速率(Pmax)以及蕾后期的暗呼吸速率(Rd)均逐渐降低,而花前期的Rd值以及蕾后期和花前期的光补偿点(LCP)均逐渐升高.随着光合有效辐射(PAR)升高,蕾后期不同部位叶片以及花前期中部叶和下部叶的Pn值呈先急剧升高后趋于平稳的变化趋势,而花前期上部叶的Pn值则呈先急剧升高后逐渐下降的变化趋势.研究结果显示:在切花菊设施栽培过程中适当补充光照可提高切花菊品质.     

Light-dark regulation of carotenoid biosynthesis in pepper (Capsicum annuum) leaves

The carotenoid content in photosynthetic plant tissue reflects a steady state value resulting from permanent biosynthesis and concurrent photo-oxidation. The contributions of both reactions were determined in illuminated pepper leaves. The amount of carotenoids provided by biosynthesis were quantified by the accumulation of the colourless carotenoid phytoene in the presence of the inhibitor norflurazon. When applied, substantial amounts of this rather photo-stable intermediate were formed in the light. However, carotenoid biosynthesis was completely stalled in darkness. This switch off in the absence of light is related to the presence of very low messenger levels of the phytoene synthase gene, psy and the phytoene desaturase gene, pds. Other carotenogenic genes, such as zds, ptox and Icy-b also were shown to be down-regulated to some extent. By comparison of the carotenoid concentration before and after transfer of plants to increasing light intensities and accounting for the contribution of biosynthesis, the rate of photo-oxidation was estimated for pepper leaves. It could be demonstrated that light-independent degradation or conversion of carotenoids e.g. to abscisic acid is a minor process.     

Genetic studies of self incompatibility in the garden chrysanthemum,Chrysanthemum morifolium ramat

Summary Self incompatibility was investigated in the hexaploid garden chrysanthemum, a member of Compositae. Nine sibling clones selected from a highly compatible cross were all self incompatible. 14.8% of the crosses between these sibs in diallel were compatible, but one sib, 67-111-42, accounted for 10 of the 12 compatible crosses. 67-111-42 was also more compatible than the remaining 8 sibs in crosses to other closely related plants. Crosses of the 9 sibs to 12 unrelated tester clones indicated that none were male or female sterile. Inbreeding via pseudocompatibility was successful in increasing homozygosity at the S loci. The percentage of compatible crosses obtained in 3 sib diallels of I ₂ clones from crosses of 67-111-42I ₁ plants approached that of the original 9 × 9 diallel, but no one individual accounted for most of the compatible crosses. It was possible to separate the 9 sibs into 9 incompatibility patterns from the pollinations made in this study. The evidence suggests that the self-incompatibility reaction in the garden chrysanthemum is sporophytic and involves more than 1 locus.Scientific Journal Series Paper Number 7882 of the Minnesota Agricultural Experiment Station.Lyndon W. Drewlow was a National Science Foundation Trainee.     

MicroRNA Expression Profile during Aphid Feeding in Chrysanthemum (Chrysanthemum morifolium)

MicroRNAs (miRNAs) are important regulators of gene expression, affecting many biological processes. As yet, their roles in the response of chrysanthemum to aphid feeding have not been explored. Here, the identity and abundance of miRNAs induced by aphid infestation have been obtained using high-throughput Illumina sequencing platform. Three leaf small RNA libraries were generated, one from plants infested with the aphid Macrosiphoniella sanbourni (library A), one from plants with mock puncture treatment (library M), and the third from untreated control plants (library CK). A total of 7,944,797, 7,605,251 and 9,244,002 clean unique reads, ranging from 18 to 30 nucleotides (nt) in length, were obtained from library CK, A and M, respectively. As a result, 303 conserved miRNAs belonging to 276 miRNAs families and 234 potential novel miRNAs were detected in chrysanthemum leaf, out of which 80, 100 and 79 significantly differentially expressed miRNAs were identified in the comparison of CK-VS-A, CK-VS-M and M-VS-A, respectively. Several of the differentially abundant miRNAs (in particular miR159a, miR160a, miR393a) may be associated with the plant''s response to aphid infestation.     

Susceptibility of gerbera and chrysanthemum varieties (Gerbera jamesoni and Chrysanthemum morifolium) to Fusarium oxysporum f.sp. chrysanthemi

In 2002, gerbera plants (cv Kaliki) were observed exhibiting symptoms of a wilt in a soilless cultivation at Albenga area (Northern Italy). A similar wilt was also observed in the Sanremo area (Northern Italy) on cv Red Bull, Anedin and Gud finger grown in soil. The same observations were carried out in 2004 in SW Spain where gerbera plants showing wilt symptoms were observed in soilless crops. In all cases, the planting material originated from the Netherlands. Recently on the base of experimental trials F. oxysporum f. sp. chrysanthemi was recognized as the causal agent of wilts of gerbera both in Italy and in Spain. The aim of this experimental work was the evaluation of the resistance/susceptibility of available cultivars of chrysanthemum and gerbera to the Fusarium wilt. The pathogenicity of two isolates of Fusarium chrysanthemi obtained from infected gerbera (Gerbera jamesonii) and chrysanthemum (Chrysanthemum morifolium) plants was tested on several varieties both of gerbera and chrysanthemum in 2004-2006. In 2004 and 2005 respectively 54 and 30 cultivars of chrysanthemum and 57 and 55 of gerbera were tested, while in 2006 only 53 cultivars of gerbera were tested. The results showed that respectively in 2004 and 2005 67 and 33 % of chrysanthemum cultivars were highly resistant to F. chrysanthemi obtained from chrysanthemum while 57 and 53 % were highly resistant to strain isolated from gerbera. In 2004, 2005 and 2006 47, 65 and 75 % of gerbera cultivars were highly resistant to F. chrysanthemi obtained from chrysanthemum and 48, 56 and 72 % were highly resistant to the strain isolated from gerbera.     

Efficient,direct plant regeneration from stem segments of chrysanthemum (Chrysanthemum morifolium Ramat. cv. Royal Purple)

Direct plant regeneration was obtained from fresh chrysanthemum (Chrysanthemum morifolium Ramat. cv. Royal Purple) stem segments cultured on Murashige and Skoog's (1962) basal media supplemented with 6-benzylaminopurine (BAP, 0.5–2.0 mg/l) and -naphthaleneacetic acid (NAA, 0.2–2.0 mg/l). The morphogenetic potential varied with the developmental stage of the stem explant. The highest percentage of shoot formation (100%) and greatest average number of shoots per explant (14.6) were observed on stem segments taken from the top of the cutting. This organogenetic capacity decreases in the more mature stem. Normal, flowering plants were obtained three to four months after culture.     

Carotenoid composition in petals of chrysanthemum (Dendranthema grandiflorum (Ramat.) Kitamura)

Sixteen xanthophylls were isolated from the petals of chrysanthemum (Dendranthema grandiflorum (Ramat.) Kitamura). Among them, (3S,5S,6R,3'R,6'R)-5,6-dihydro-5,6-dihydroxylutein (1) and five di-Z geometrical isomers of lutein-5,6-epoxide, i.e., 9Z,13'Z (2), 13Z,9'Z (3), 9'Z,13'Z (4), 9Z,13Z (5), and 9Z,9'Z (7), had never before been identified as natural products. All of the carotenoids isolated from chrysanthemum, except for (9Z)-violaxanthin, are beta,epsilon-carotene (alpha-carotene) derivatives. The analyses indicate that carotenoids from the petals of chrysanthemum have a very characteristic composition.     

Genetic Mapping of Quantitative Trait Loci Underlying Flowering Time in Chrysanthemum (Chrysanthemum morifolium)

Flowering time is an important trait in chrysanthemum, but its genetic basis remains poorly understood. An intra-specific mapping population bred from the cross between the autumn-flowering cultivar ‘Yuhualuoying’ and the summer-flowering ‘Aoyunhanxiao’ was used to determine the number and relative effect of QTL segregating for five measures of flowering time. From flowering time data recorded over two consecutive seasons, 35 additive QTL were detected, each explaining between 5.8% and 22.7% of the overall phenotypic variance. Of these, 13 were detected in both years. Nine genomic regions harboring QTL for at least two of the five traits were identified. Ten pairs of loci epistatically determined the flowering time, but their contribution to the overall phenotypic variance was less than for the additive QTL. The results suggest that flowering time in chrysanthemum is principally governed by main effect QTL but that epistasis also contributes to the genetic architecture of the trait, and the major QTL identified herein are useful in our ongoing efforts to streamline the improvement of chrysanthemum via the use of molecular methodology.     

Regulation of carotenoid biosynthesis during tomato development.

Phytoene synthase (Psy) and phytoene desaturase (Pds) are the first dedicated enzymes of the plant carotenoid biosynthesis pathway. We report here the organ-specific and temporal expression of PDS and PSY in tomato plants. Light increases the carotenoid content of seedlings but has little effect on PDS and PSY expression. Expression of both genes is induced in seedlings of the phytoene-accumulating mutant ghost and in wild-type seedlings treated with the Pds inhibitor norflurazon. Roots, which contain the lowest levels of carotenoids in the plant, have also the lowest levels of PDS and PSY expression. In flowers, expression of both genes and carotenoid content are higher in petals and anthers than in sepals and carpels. During flower development, expression of both PDS and PSY increases more than 10-fold immediately before anthesis. During fruit development, PSY expression increases more than 20-fold, but PDS expression increases less than threefold. We concluded that PSY and PDS are differentially regulated by stress and developmental mechanisms that control carotenoid biosynthesis in leaves, flowers, and fruits. We also report that PDS maps to chromosome 3, and thus it does not correspond to the GHOST locus, which maps to chromosome 11.     

SRAP-based mapping and QTL detection for inflorescence-related traits in chrysanthemum (Dendranthema morifolium)

Chrysanthemum (Dendranthema morifolium) is an economically important ornamental species and comprises a large proportion of the flower industry in south-east Asian and European countries. In this study, a segregating population of 142 F₁ progeny of the cross between the two chrysanthemum cultivars ??Yuhualuoying?? and ??Aoyunhanxiao?? was used to construct two separate genetic linkage maps via a double pseudo-testcross mapping strategy. Genotyping was performed using 500 SRAP primer combinations, of which about 50% were informative. This allowed the definition of 896 SRAP loci, of which about 23% showed some segregation distortion. The ??Yuhualuoying?? map consisted of 333 testcross markers arranged into 57 linkage groups (LGs). It covered >1,900 cM with a mean inter-marker distance of 6.9 cM. The map constructed from ??Aoyunhanxiao?? comprised 342 test cross markers arranged into 55 LGs. It spanned nearly 1,900 cM, with a mean inter-marker distance of 6.6 cM. The markers were distributed rather uniformly along both maps. A quantitative trait loci analysis was conducted to investigate the pattern of inheritance of three inflorescence traits. This led to the detection of 12 putative loci at a LOD score >2.5, of which four each specified flower diameter, ray floret layer number, and ray floret length. This study provides molecular mapping information on marker-assisted selection programs for the improvement of multiple traits of interest.     

Polyamine metabolism,floral initiation and floral development in Chrysanthemum (Chrysanthemum morifolium Ramat.)

In the short-day plant Chrysanthemum (Chrysanthemum morifolium Ramat. variety Pavo) putrescine and spermidine conjugates appeared in the apical bud before the first observable transformation of the meristem into floral structures. These compounds accumulated on floral initiation and well before floral evocation. Spermidine conjugates were predominant during floral initiation whereas free amines did not accumulate to any significant extent. Different associations of amides were observed during floral initiation as compared with the reproductive phase. 3,4-Dimethoxyphenethylamine conjugates (water-insoluble compounds) were the predominant amine conjugates observed during flower development. These compounds decreased drastically after fertilization. In vegetative buds from plants grown in long days polyamine conjugates were very low and appeared as plants aged. We present evidence that ornithine decarboxylase (ODC) regulates putrescine biosynthesis during floral initiation and floral development. When ODC action was blocked by DFMO (-DL-difluoromethylornithine, a specific, irreversible inhibitor of ODC), flowering was inhibited, and free and conjugated polyamines were not detected. This treatment led to a slight enhancement of ADC activity. When putrescine was added, polyamine titers and flowering were restored. A similar treatment with DFMA (-DL difluoromethylarginine, a specific, irreversible inhibitor of ADC) did not affect flowering and the polyamine titers. The results suggest that ODC and polyamine conjugates are involved in regulating floral initiation in Chrysanthemum.Abbreviations ADC arginine decarboxylase - ODC ornithine decarboxylase - DFMA -DL-difluoromethylarginine - DFMO -DL-difluoromethylornithine     

Uptake and Distribution of Copper in Chrysanthemum morifolium

The effects of various levels of copper on the uptake and distributionof copper in Chrysanthemum morifolium grown in solution cultureand peat-sand have been examined. Whole plants growing in shortdays were sampled at regular intervals, divided into roots,stem, leaves and lateral shoots, and analysed for copper. Thepartitioning of copper between these tissues showed that a relativelylarge proportion (30–40 per cent) of the total plant copperwas accumulated in the roots of normal plants during the harvestingperiod, compared with approximately 10 per cent in the rootsof copper deficient plants. Whilst the copper content (ug g^–1) of leaves and stemfrom normal plants was negatively correlated with the amountof dry matter produced (P < 0·001), the correspondingcopper deficient tissues showed little variation in copper contentwith increases in tissue dry weight. A more detailed investigationof the copper content of leaves from normal plants showed thatgradients existed within the plant with respect to both leafposition and time of harvest which could be described by a singlecubic surface equation (P < 0·001).     

Color and chirality: carotenoid self-assemblies in flower petals

As a novel phenomenon, optical activity--often very strong--has been detected by circular dichroism (CD) spectroscopy in carotenoid-containing living flowers of several species belonging to different families. Using natural pure xanthophyll esters, very similar CD spectra were obtained in vitro, proving the ability of these molecules to form chiral self-assemblies. The relationship between the ultrastructure of the chromoplast, its chemical composition and the optical activity is discussed. The applicability of CD spectroscopy for studying intact plant tissue is emphasized.     

Daminozide Alters Anthocyanin Metabolism in Ray Florets of Bronze Chrysanthemum (Chrysanthemum morifolium Ramat.)

Daminozide is a well-known chemical inhibitor of the gibberellic acid biosynthesis pathway regulating the vegetative growth of potted chrysanthemums (Chrysanthemum morifolium Ramat.). However, the precise mechanism underlying daminozide-related floral color loss is unknown. To investigate the latter, in two separate greenhouse experiments, bronze flowering chrysanthemum cultivars ‘Baton Rouge’ and ‘Pelee’ were treated weekly with consecutive (0 or 5,000 mg l^?1) foliar daminozide spray applications at early, intermediate, and late stages during the short-day photoperiod. The ray florets of both cultivars were sampled, and the effect of daminozide application on anthocyanins and their biosynthetic precursors were determined by HPLC. Daminozide applied to ‘Baton Rouge’ plants at early developmental stages was correlated with partial loss of red color, and HPLC analysis determined that this was associated with a 75 % reduction in ray floret anthocyanins. Conversely, a near complete loss of red coloration in daminozide-sprayed ‘Pelee’ relative to control plants was associated with as much as a 98 % decline in anthocyanins, irrespective of the time of application. HPLC analysis determined that daminozide application was associated with a 22–50 % increase in the flavones apigenin 7-O-rutinoside, acacetin 7-O-rutinoside, diosmetin 7-O-rutinoside, and eupatorin, and a 68 % increase in the flavonol quercetin 3-O-glucoside, in ray florets of ‘Pelee’ relative to control plants. There was no relative change in ‘Baton Rouge’ flavone and flavonol levels. The accumulation of bronze C. morifolium flavones and flavonols following foliar daminozide application suggests that red color loss is associated with inhibition of anthocyanidin synthase of ‘Pelee’ ray florets.     

A comparison of the effects of a new quaternary ammonium growth retardant with those of other growth retarding chemicals on the pot chrysanthemum (Chrysanthemum morifolium)

A new quaternary ammonium growth retardant, i-allyl-i-(3,7-dimethyl-octyl)-piperidinium bromide (ADOPB), was compared with daminozide, ancymidol and chlorphonium chloride for its effectiveness in reducing lateral stem length in the pot chrysanthemum (Chrysanthemum morifolium). Single foliar sprays of ADOPB applied at 100 to 250 ppm active ingredient (a.i.) gave excellent height control without phytotoxicity in cv. Bright Golden Anne throughout the year. Similar results were obtained in two trials with cvs Purple Anne and Regal Anne. As much as 10 to 50 times this concentration of daminozide was required to achieve a similar degree of height control. However, under summer conditions even high concentrations of daminozide did not adequately reduce stem length. Foliar sprays of ancymidol (50–100 ppm a.i.) also gave good control of stem length but this chemical was more effective when applied as a compost drench. Compost drenches of ADOPB reduced stem extension but a greater quantity of a.i. was required compared to a foliar spray. Foliar sprays of dikegulac-sodium (100 to 5000 ppm a.i.) were very phytotoxic. Reductions in thelength of lateral stems were associated with marked decreases in their fresh and dry weights. Growth retardants delay the flowering of pot chrysanthemums by inducing a slower rate of flower bud development. Foliar sprays of ADOPB generally delayed flowering by 2–3 days more than did sprays of daminozide, but this was comparable with that associated with the use of compost drenches of chlorphonium chloride. High concentrations of all the retardants reduced the diameter of open flowers. Only daminozide caused a loss of flower colour in cv. Regal Anne. The results are discussed in relation to the mode of action of growth retardants, with particular reference to the effects of gibberellins on stem extension and flower development in the chrysanthemum.     

Regulation of carotenoid biosynthesis genes in response to light in Chlamydomonas reinhardtii

As we had found previously that thapsigargin, an endomembrane Ca2+-ATPase inhibitor, induces production of intracellular platelet-activating factor (PAF) [Br. J. Pharmacol. 116 (1995) 2141], we decided to investigate the possible roles of intracellular PAF in nuclear factor (NF)-kappaB activation of thapsigargin-stimulated rat peritoneal macrophages. When rat peritoneal macrophages were stimulated with thapsigargin, the level of inhibitory protein of NF-kappaB-alpha (IkappaB-alpha) was decreased and the nuclear translocation of NF-kappaB was increased. The thapsigargin-induced activation of NF-kappaB was inhibited by the PAF synthesis inhibitor SK&F 98625 and the PAF antagonist E6123. Structurally unrelated PAF antagonists such as E5880 and L-652,731 also inhibited the thapsigargin-induced activation of NF-kappaB. Lipopolysaccharide (LPS)-induced activation of NF-kappaB was also suppressed by these drugs. In a culture of rat peritoneal macrophages, exogenously added PAF did not induce degradation of IkappaB-alpha. These findings suggest that the intracellular PAF produced by the stimulation with thapsigargin or LPS is involved in activation of the NF-kappaB pathway.