New Isopropyl Chromone and Flavanone Glucoside Compounds from the Leaves of Syzygium cerasiforme (Blume) Merr. & L.M.Perry and Their Inhibition of Nitric Oxide Production

A new isopropyl chromone ( 1 ) and a new flavanone glucoside ( 2 ) together with eleven known compounds ( 3–13 ) were isolated from the leaves of Syzygium cerasiforme (Blume) Merr. & L.M.Perry. Their structures were elucidated as 5,7-dihydroxy-2-isopropyl-6,8-dimethyl-4H-chromen-4-one ( 1 ), 5,7-dihydroxyflavanone 7-O-β-D-(6′′-O-galloylglucopyranoside) ( 2 ), strobopinin ( 3 ), demethoxymatteucinol ( 4 ), pinocembrin-7-O-β-D-glucopyranoside ( 5 ), (2S)-hydroxynaringenin-7-O-β-D-glucopyranoside ( 6 ), afzelin ( 7 ), quercetin ( 8 ), kaplanin ( 9 ), endoperoxide G3 ( 10 ), grasshopper ( 11 ), vomifoliol ( 12 ), litseagermacrane ( 13 ) by the analysis of HR-ESI-MS, NMR, and CD spectral data. Compounds 1 , 2 , 5 , 6 and 10 inhibited NO production on LPS-activated RAW264.7 cells with IC₅₀ values of 12.28±1.15, 8.52±1.62, 7.68±0.87, 9.67±0.57, and 6.69±0.34 μM, respectively, while the IC₅₀ values of the other compounds ranging from 33.38±0.78 to 86.51±2.98 μM, compared to that of the positive control, N^G-monomethyl-L-arginine acetate (L-NMMA) with an IC₅₀ value of 32.50±1.00 μM.     

激素对樱桃番茄两种外植体诱导再生植株的影响

以 MS为基本培养基 ,附加不同浓度的 6-BA、IAA和 NAA培养樱桃番茄两种外植体以诱导再生植株。结果表明 :含 NAA的 MS+6-BA2 mg/L(单位下同 ) +NAA0 .2培养基诱导的叶片愈伤组织 ,经继续培养无芽的分化 ,含 IAA的 MS+6-BA2 +IAA0 .2培养基诱导的愈伤组织 ,经继续培养诱导芽的分化 ;含 NAA或IAA的 MS+6-BA2 +NAA0 .2和 MS+6-BA2 +IAA0 .2培养基利于下胚轴愈伤组织的诱导 ,而不含生长素的 MS+6-BA1 .0培养基可直接诱导芽的分化。     

NaCl胁迫对醋栗番茄、樱桃番茄和番茄幼苗生长、叶片气体交换和离子平衡的影响

以醋栗番茄( Solanum pimpinellifolium Linn.)、樱桃番茄品种‘秦皇贵妃红’( S. lycopersicum var. cerasiforme‘Qinhuangguifeihong’)和番茄品种‘浙粉202’(S. lycopersicum‘Zhefen 202’)幼苗为材料,研究了0(对照)、100、200 mmol·L-1 NaCl胁迫对其生长、叶片气体交换参数和离子平衡的影响。结果表明：在100和200 mmol·L-1 NaCl胁迫下,‘秦皇贵妃红’和‘浙粉202’幼苗单株总干质量的降幅较大,醋栗番茄的降幅较小。 NaCl胁迫明显增加醋栗番茄幼苗的根冠比,但不同胁迫条件下‘秦皇贵妃红’和‘浙粉202’幼苗的根冠比差异不显著。与对照相比,在100 mmol·L-1 NaCl胁迫下,醋栗番茄幼苗叶片的净光合速率( Pn)、胞间CO2浓度( Ci)和蒸腾速率( Tr)的降幅明显低于‘秦皇贵妃红’和‘浙粉202’,而醋栗番茄幼苗叶片气孔导度(Gs)的降幅明显高于后二者;在200 mmol·L-1 NaCl胁迫下,三者叶片Pn、Gs、Ci和Tr值的降幅接近。在100和200 mmol·L-1 NaCl胁迫下,醋栗番茄、‘秦皇贵妃红’和‘浙粉202’幼苗叶片的水分利用效率和气孔限制值均较各自对照显著升高,其中‘秦皇贵妃红’的增幅最大。在100和200 mmol·L-1 NaCl胁迫下,醋栗番茄、‘秦皇贵妃红’和‘浙粉202’幼苗根、茎和叶中Na+含量均较各自对照显著升高,而K+含量和K+/Na+比总体上较各自对照显著降低。与对照相比,经不同浓度NaCl处理后醋栗番茄幼苗根、茎和叶的Na+含量增幅以及K+含量降幅在供试3种植物中均最小,而其不同部位的K+/ Na+比总体上较高。上述研究结果表明：醋栗番茄的耐盐性较强,‘秦皇贵妃红’次之,‘浙粉202’较弱。 NaCl胁迫显著抑制‘秦皇贵妃红’和‘浙粉202’幼苗根的生长,但显著促进醋栗番茄幼苗根的生长,使其维持较强的耐盐性,且NaCl胁迫下醋栗番茄对Na+的吸收和运输减少,以维持体内的离子平衡及较强的光合作用。     

4种(变种)辣椒的核型研究

本文研究了辣椒属4种(变种)的核型,各个种的核型可简式为小米辣2n=24=23m+1sm:簇生辣2n=24=20m+2sm+2st:樱桃辣2n=24=20m+4sm(2SAT):“印度辣”2n=24=22m+2st。按照Stebbins的核型分类,小米辣为2A型;簇生辣和樱桃辣为2A型,印度辣为2B型。     

1-甲基环丙烯采后处理对樱桃番茄果实成熟过程的影响

研究了不同浓度(0、0.035、0.07和0.11μL/L)的乙烯受体竞争性抑制剂1-甲基环丙烯(1-MCP)采后处理对绿熟期樱桃番茄的乙烯合成、果实软化、果实色素(叶绿素、茄红素、β-胡萝卜素)含量消长的影响.0.07 μL/L及其以上浓度的1-MCP降低了前期乙烯合成,同时推迟了乙烯释放高峰,但0.035 μL/L浓度的1-MCP处理并不能抑制内源乙烯合成.1-MCP显著延迟了果实软化和叶绿素降解,但并不影响这两个过程的启动.茄红素合成的启动和积累均受到了1-MCP抑制,而1-MCP并不推迟β-胡萝卜素合成的启动,只抑制其积累.这些结果提示了乙烯调节成熟生理过程的不同机制.对于绿熟期的樱桃番茄,0.07～0.11μL/L的1-MCP是实用的有效处理浓度.1-MCP有效浓度可能用于了解果实的乙烯受体水平和乙烯敏感性.     

番茄种质资源遗传多样性分析与RAPD应用

对我们种质库中的29份番茄材料的观察结果,证明其中至少保存有10对以上的形态学基因的变异,10对基因将可提供不同基因重组的巨大可能性,在一定程度上反映出种质资源库保存遗传多样性的潜力。对取自种质库中的6份樱桃番茄材料所配制的7个F1代果实品质的性状调查结果初步显示,有些品质性状存在优于市场上销售品的可能。用18个引物对6个樱桃番茄亲本及其所配制的8个F1进行RAPD扩增的结果,有12个引物可以扩增,不同引物能显示被检测种质多态性的相对能力也不相同。既能在多数材料中扩增,又能够有效的显示多态性的引物分别是：A11,K05,C15和A17,其中K05和A11能产生最多的扩增带。另外,引物A11和C19可用于2013B,B11可用于2018A杂交种的纯度检验。并初步探讨了双引物扩增的结果。     

Environmental factors predict adaptive phenotypic differentiation within and between two wild Andean tomatoes

Environmental variation is widely viewed as a major force driving morphological change and speciation. Although many environmental attributes are potentially critical for adaptive responses within and between species, the individual and relative importance of these diverse attributes remain poorly understood. Here we combine a geographical information systems (GIS)-based analysis of environmental variation with a multipopulation analysis of phenotypic, physiological, and genetic variation, to generate and test hypotheses of environmental factors likely driving adaptive divergence within and between two wild Andean plant species. First, we document large environmental differences between population locations of the two species, and among regions within species. Second, we show evidence for inter- and intraspecific differences in genetically based phenotypic and physiological variation. Third, combining these data, we report evidence for trait-environment associations both among populations within species, and between species, that are strongly indicative of recent and rapid adaptive responses. Finally, we show that these trait-environment associations cannot be simply explained by genetic relatedness within species, reinforcing our inference that local, regional, and species-wide environmental conditions are responsible for phenotypic and physiological diversification. The strongest trait-environment associations involve temperature and precipitation gradients, suggesting these climatic factors are predominant drivers of adaptive diversification in these species.     

Species-specific DNA sequences for identification of somatic hybrids between Lycopersicon esculentum and Solanum acaule

Summary Species-specific highly repeated DNA sequences can be used to screen the progeny of protoplast fusions combining different species. Such probes are easy to clone and can be detected by fast methods, e.g., hybridization to total genomic DNA. Furthermore, due to their high copy number, hybridization signals are strong and represent more than one locus, unlike isozymes or resistance markers. After cloning and screening for species-specific DNA sequences we characterized the highly repeated DNA sequences of the solanaceous species Solanum acaule and Lycopersicon esculentum var. gilva. DNA sequencing and hy ridization revealed a prominent, tandemly arranged satellite DNA repeat of 162 bp in Lycopersicon esculentum and a different satellite repeat of 183 bp, also tandemly organized, in Solanum acaule. Each repeat is absent in the respective other species. Therefore, we have used these DNA repeats as markers to distinguish regenerated interspecific somatic hybrids from the respective fusion partners. These hybrids were clearly identified by Southern hybridization and dot-blot assays to the respective ³²P-labelled satellite DNA.     

毛酸浆(Physalis pubescens)花形态特征与小孢子发育

许多重要蔬菜和水果隶属于茄科(Solanaceae),植物花发育是物种延续和产品形成关键决定因子。茄科毛酸浆(Physalispubescens)是药食同源半野生浆果,目前其花发育研究不多。为了从不同视角了解茄科植物花发育,本研究采用比较生物学方法从花的形态特征和解剖学层面解析了毛酸浆(P.pubescens)和茄科模式植物番茄(Solanum lycopersicum var. cerasiforme)花器特征和小孢子发育进程。结果显示,开花后毛酸浆花萼迅速生长包被果实、花瓣有紫色斑纹、花药顶颈可育及背部开裂散粉特征与番茄花萼生长缓慢、黄色花瓣、花药顶颈不育及腹缝开裂散粉方式截然不同,展示了茄科植物遗传多样性。毛酸浆小孢子发育,在“四分体”之前迟于番茄,而“四分体”之后期却快于番茄。特别是番茄药隔组织在“四分体”时期开始向药室异常内突,并在花粉成熟期占据药室近1/2空间,而未在毛酸浆中观察到。该研究为开发茄科新的模式植物和从不同视角理解庞大茄科植物花发育提供了重要信息。     

Symptomatic Evidence for Differential Root Invasion by Fusarium Crown and Root Rot Pathogens Between Common Tomato Lycopersicon esculentum and Its Varieties

The pathogenic isolates (Kin2001a, Kin2001b and Kin2003) of Fusarium oxysporum f. sp. radicis‐lycopersici were obtained from hydroponically cultured seedlings of pear tomato (Lycopersicon esculentum var. pyriforme) infected at different times and their pathogenicity examined in an in vitro assay system on cotyledonal seedlings of pear tomato, cherry tomato (L. esculentum var. cerasiforme) and common tomato (L. esculentum). With the in vitro assay, infection and subsequent disease progress could be microscopically observed. Pear and cherry tomatoes suppressed invasion by all isolates at the junctions of epidermal cells along the root, comparable with the resistant cultivars of common tomato. The pathogen entered pear and cherry tomatoes at the tips of lateral roots and tap roots, in contrast to infection of susceptible cultivars of common tomato. In Kin2003‐inoculated roots, the top of the lateral rootlets first became discoloured, followed by the cortical parenchyma, central xylem vessel and finally the crown. This dark‐brown discolouration expanded rapidly and severe rot developed in the discoloured regions. In contrast, the dark‐brown discolouration in Kin2001b‐infected roots expanded into the cortical parenchyma cells abutting the originally infected lateral rootlets and at a much slower rate. Kin2001a was in a new group that entered via the cortical cleavage formed by the emergence of lateral rootlets, in addition to the tips of taproots and lateral roots. In this in vitro assay system, the Japanese pathogenic isolates collected from different districts of Japan were characterized and classified by the mode of host invasion. Of 13 isolates, four were placed with Kin2003, six with Kin2001a and three with Kin2001b.