Phenols and lignans from Chenopodium album

Cinnamic acid, 4-hydroxy-cinnamic acid, ferulic acid, methyl ferulate, sinapic acid, methyl 3-(4-hydroxy-3-methoxyphenyl)propanoate, 4-(1-hydroxyethyl)-2-methoxyphenol, vanillyl alcohol, 4-(hydroxymethyl)-2-methoxyphenol, 4-hydroxy-3-methoxybenzoic acid, 4-vinylphenol, 4-methylbenzaldehyde, N-[2-(1H-indol-3-yl)ethyl]acetamide, pinoresinol, syringaresinol, lariciresinol, 5,5'-dimethoxy-lariciresinol, threo-guaiacylglycerol-3-beta-4-syringaresinol ether and two new sesquilignans, namely, threo-guaiacylglycerol-alpha-O-methyl-beta-O-4-syringaresinol ether and threo-syringylglycerol-alpha-O-methyl-beta-O-4-syringaresinol ether, were isolated and identified as components of Chenopodium album. Constitutions were established on the basis of spectroscopic data, including two-dimensional NMR analyses.     

福建橄榄18S-26S rRNA及其ITS片段的克隆与序列分析

利用18S-26S rRNA基因及其ITS片段的PCR扩增、克隆及测序分析,对福建14个橄榄品种进行分子标记及遗传分类。序列分析结果表明:14个品种可分为4个类别,以1号品种为参照,3、4、6、7、8、9、11号品种的ITS1、ITS2和5.8S共634个碱基序列完全一致,与1号仅ITS2上有1个碱基差异,2号和1号品种的ITS1和5.8S序列完全一致,仅ITS2上有2个碱基差异,归为第一类;5号和14号的序列完全一致,与1号在ITS1和ITS2上各有1个碱基差异,归为第二类;10号和12号序列完全一致,与1号在ITS1上有2个碱基差异,归为第三类;13号品种5.8S的序列与1号相同,但在ITS1上有1个碱基差异,在ITS2上有24个碱基差异,归为第四类。使用DNAMAN软件建立的同源关系树说明了不同橄榄品种的变异程度。将橄榄18S-26S rRNA基因及其ITS序列登陆GenBank,登陆号:DQ517524。     

昆诺阿藜链格孢叶斑病病原及其生物学特性

为明确昆诺阿藜链格孢叶斑病病原,在山西省昆诺阿藜种植区采集典型症状的标本分离病原菌,选择代表性菌株LGB-b和LGB-h对其形态学、分子生物学、致病性及生物学特性进行了研究。综合形态学和多基因系统发育(Alt a 1、endoPG 和OPA10-2)分析,确定昆诺阿藜链格孢叶斑病病原为Alternaria alternata。致病性测定发现接种6 d后病斑呈灰绿至黄绿色,表面具有灰棕至灰褐色霉层,周围具黄绿色晕圈,与田间症状基本一致。菌株LGB-b和LGB-h均可侵染昆诺阿藜、藜和台湾藜。菌株LGB-b菌丝生长的最适培养基为V8 蔬菜汁琼脂培养基(V8)、温度为25-30 ℃、水活度≥0.98、pH为6-7;分生孢子萌发的最适水活度≥0.98、pH为6-7。菌株LGB-h菌丝生长的最适培养基为马铃薯胡萝卜琼脂培养基(PCA)、温度为20-25 ℃、水活度≥0.98、pH为6-7;分生孢子萌发的最适水活度≥0.98、pH为7-8。     

Epidermal structures and composition of epicuticular waxes of Sedum album sensu lato (Crassulaceae) in Balkan Peninsula

Sedum album is a succulent plant, with phenotypic variability resulting in delimitation of a number of taxa with diverse taxonomic recognition. We analyzed the taxa from Sedum album in broad sense (S. album, S. micranthum, S. athoum and S. serpentini) from Balkan Peninsula, to check whether the variability of their epidermal structures and epicuticular wax composition corresponds to their taxonomic reliability. Epidermal structures and epicuticular waxes were analyzed using light and scanning electron microscopy, gas chromatography-mass spectrometry and gas chromatography-flame ionization detector chromatography and multivariate statistical techniques. Analyses of studied taxa have shown that significant systematic characters include adaxial epidermal and guard cell length, stomatal frequency and subsidiary cells area on abaxial epidermis. The content of n-alkanes C₂₉, C₃₀, C₂₇, C₃₂ and C₃₃ was shown to be valuable criterion for their phytochemical delimitation. The comparison of epicuticular wax microstructures has shown no significant differences. Results indicate presence of two (micromorphology) or three (phytochemistry) well-defined groups of populations, with S. serpentini manifesting a considerable level of separation toward the others. Sedum athoum have shown weak to moderate degree of differentiation, while S. micranthum has shown general resemblance to S. album.     

High content,size and distribution of single-stranded DNA in the mitochondria of Chenopodium album (L.)

Mitochondrial (mt) DNA of higher plants is unique in its large size and complexity. We report here a hitherto unknownfeature, the presence of large quantities of single-stranded (ss) DNA. About 2.0-8.5% of the chromosomal mtDNA from a suspension culture (depending on the growth stage) and 6.5% of the chromosomal mtDNA from whole plants of Chenopodium album were found to be in ss form by dot-blot hybridization after neutral transfer. Similar amounts of ss mtDNA were observed by binding of the single-strand binding (SSB) protein of Escherichia coli under the electron microscope. Significantly less ssDNA was found in plastids of C. album and in E. coli cells. We observed ss regions between 100 and 22 800 bases distributed in the mt genome spaced from 0.5-100 kb apart. After pulsed-field gel electrophoresis (PFGE), the well-bound fraction of mtDNA (found to consist of circular, sigma-shaped and rosette-like molecules), contained the major part of ssDNA as opposed to the migrating linear molecules. Digestion of mtDNA by ss-specific nucleases followed by PFGE mobilized all well-bound DNA and correspondingly increased the quantity of migrating linear DNA molecules. The implications of ssDNA for the structural organization on plant mt genomes are discussed.     

Applicability and limitations of optimal biomass allocation models: a test of two species from fertile and infertile habitats

BACKGROUND AND AIMS: The practical applicability of optimal biomass allocation models is not clear. Plants may have constraints in the plasticity of their root : leaf ratio that prevent them from regulating their root : leaf ratio in the optimal manner predicted by the models. The aim of this study was to examine the applicability and limitations of optimal biomass allocation models and to test the assumption that regulation of the root : leaf ratio enables maximization of the relative growth rate (RGR). METHODS: Polygonum cuspidatum from an infertile habitat and Chenopodium album from a fertile habitat were grown under a range of nitrogen availabilities. The biomass allocation, leaf nitrogen concentration (LNC), RGR, net assimilation rate (NAR), and leaf area ratio (LAR) of each species were compared with optimal values determined using an optimal biomass allocation model. KEY RESULTS: The root : leaf ratio of C. album was smaller than the optimal ratio in the low-nitrogen treatment, while it was almost optimal in the high-nitrogen treatment. In contrast, the root : leaf ratio of P. cuspidatum was close to the optimum under both high- and low-nitrogen conditions. Owing to the optimal regulation of the root : leaf ratio, C. album in the high-nitrogen treatment and P. cuspidatum in both treatments had LNC and RGR (with its two components, NAR and LAR) close to their optima. However, in the low-nitrogen treatment, the suboptimal root : leaf ratio of C. album led to a smaller LNC than the optimum, which in turn resulted in a smaller NAR than the optimum and RGR than the theoretical maximum RGR. CONCLUSIONS: The applicability of optimal biomass allocation models is fairly high, although constraints in the plasticity of biomass allocation could prevent optimal regulation of the root : leaf ratio in some species. The assumption that regulation of the root : leaf ratio enables maximization of RGR was supported.     

檀香种胚离体培养快速育苗研究

利用添加植物生长调节剂的培养基对檀香种胚进行离体培养,研究种胚萌发和成苗的影响因素以及种苗快速繁育技术。结果显示:生长调节剂GA₃和种胚成熟度都是影响檀香种胚萌发和成苗的重要因素,檀香成熟胚在含14 μmol/L GA₃的MS培养基上7~10 d即可萌发,45 d后成苗率达82.5%,檀香种胚离体培养是有效的快速育苗方法。     

Effects of elevated CO2 on the size structure in even-aged monospecific stands of Chenopodium album

To investigate the effect of elevated CO₂ on the size inequality and size structure, even‐aged monospecific stands of an annual, Chenopodium album, were established at ambient and doubled CO₂ with high and low nutrient availabilities in open top chambers. The growth of individual plants was monitored non‐destructively every week until flowering. Elevated CO₂ significantly enhanced plant growth at high nutrients, but did not at low nutrients. The size inequality expressed as the coefficient of variation tended to increase at elevated CO₂. Size structure of the stands was analyzed by the cumulative frequency distribution of plant size. At early stages of plant growth, CO₂ elevation benefited all individuals and shifted the whole size distribution of the stand to large size classes. At later stages, dominant individuals were still larger at elevated than at ambient CO₂, but the difference in small subordinate individuals between two CO₂ levels became smaller. Although these tendencies were found at both nutrient availabilities, difference in size distribution between CO₂ levels was larger at high nutrients. The CO₂ elevation did not significantly enhance the growth rate as a function of plant size except for the high nutrient stand at the earliest stage, indicating that the higher biomass at elevated CO₂ at later stages in the high nutrient stand was caused by the larger size of individuals at the earliest stage. Thus the effect of elevated CO₂ on stand structure and size inequality strongly depended on the growth stage and nutrient availabilities.