澳门路氹湿地芦苇氮磷含量的季节变化

为探讨芦苇（Phragmites communis）的生长规律及其在湿地生态系统中的作用,对澳门路毡湿地芦苇氮磷含量变化进行了6次调查。结果表明：芦苇地上部分和地下茎的氮、磷含量都在秋冬达到最大值,在春夏达到最低值,其中叶氮、磷含量最高值分别为37．5和4．0g·kg^-1,最低值为28．0和3．5g·kg^-1;茎中部氮、磷含量最高值分别为14．1和2．0g·kg^1,最低值为11．5和1．6g·kg^1;地下茎氮、磷含量最高值分别为10．2和0．9g·kg^1,最低值为6．6和0．8g·kg^-1。各季节芦苇不同部位的氮、磷含量大小顺序均为叶〉地上茎〉地下茎。氮、磷没有在芦苇体不同器官或部位之间发生转移。     

东北地区芦苇植硅体形态的空间差异

笔者对东北地区12个样点的芦苇叶片的植硅体进行了分析,探讨了芦苇植硅体在空间上的分布规律,揭示芦苇植硅体的环境指示意义,为定量恢复古环境提供参考。实验结果表明:12个样点中芦苇植硅体基本类型相同,共有5种主要植硅体类型,即中鞍型、帽型、芦苇扇型、尖型和棒型;但芦苇植硅体的浓度随着纬度的变化而相应的发生变化。总体来说,纬度较低的样点芦苇植硅体的浓度较大,而纬度较高的样点芦苇植硅体的浓度相对较小;随着纬度的变化,芦苇的特征植硅体中鞍型的浓度也呈现波状变化,牡丹江以南的几个样点中鞍型植硅体浓度相对较大,9、10两个月牡丹江以北的几个样点中鞍型植硅体浓度迅速减少。芦苇扇型植硅体则呈现出纬度较高的样点植硅体浓度较大,纬度较低的样点植硅体浓度较小的特点,芦苇扇型植硅体的空间变化规律与扇型植硅体的不同。     

Antimicrobial and Cytotoxic Activity of Extracts of Ferula heuffelii Griseb. ex Heuff. and Its Metabolites

The antimicrobial and cytotoxic activities of isolates (CHCl₃ and MeOH extracts and selected metabolites) obtained from the underground parts of the Balkan endemic plant Ferula heuffelii Griseb . ex Heuff . were assessed. The CHCl₃ and MeOH extracts exhibited moderate antimicrobial activity, being more pronounced against Gram‐positive than Gram‐negative bacteria, especially against Staphylococcus aureus (MIC=12.5 μg/ml for both extracts) and Micrococcus luteus (MIC=50 and 12.5 μg/ml, resp.). Among the tested metabolites, (6E)‐1‐(2,4‐dihydroxyphenyl)‐3,7,11‐trimethyl‐3‐vinyldodeca‐6,10‐dien‐1‐one ( 2 ) and (2S*,3R*)‐2‐[(3E)‐4,8‐dimethylnona‐3,7‐dien‐1‐yl]‐2,3‐dihydro‐7‐hydroxy‐2,3‐dimethylfuro[3,2‐c]coumarin ( 4 ) demonstrated the best antimicrobial activity. Compounds 2 and 4 both strongly inhibited the growth of M. luteus (MIC=11.2 and 5.2 μM , resp.) and Staphylococcus epidermidis (MIC=22.5 and 10.5 μM , resp.) and compound 2 additionally also the growth of Bacillus subtilis (MIC=11.2 μM ). The cytotoxic activity of the isolates was tested against three human cancer cell lines, viz., cervical adenocarcinoma (HeLa), chronic myelogenous leukemia (K562), and breast cancer (MCF‐7) cells. The CHCl₃ extract exhibited strong cytotoxic activity against all cell lines (IC₅₀<11.0 μg/ml). All compounds strongly inhibited the growth of the K562 and HeLa cell lines. Compound 4 exhibited also a strong activity against the MCF‐7 cell line, comparable to that of cisplatin (IC₅₀=22.32±1.32 vs. 18.67±0.75μM ).     

Proteomic characterization of Phragmites communis in ecotypes of swamp and desert dune

Phragmites communis Trin. (common reed) is a recognized model plant for studying its adaptation to contrasting and harsh environments. To understand the inherent molecular basis for its remarkable resistance to combined stresses, we performed a comprehensive proteomic analysis of the leaf proteins from two ecotypes, i.e. swamp and desert dune, naturally growing in the desert region of northwestern China. First, a proteome reference map of Phragmites was established based on the swamp ecotype. Proteins were resolved by 2‐D/SDS‐PAGE and identified by MALDI‐TOF/TOF MS. In total, 177 spots were identified corresponding to 51 proteins. The major proteins identified are proteins involved in photosynthesis, glutathione and ascorbic acid metabolism as well as protein synthesis and quality control. Second, the 2‐DE profiles of the two ecotypes were compared quantitatively via DIGE analysis. Compared with swamp ecotype, 51 proteins spots are higher‐expressed and 58 protein spots are lower‐expressed by twofold or more in desert dune ecotype. Major differences were found for the proteins involved in light reaction of photosynthesis, protein biosynthesis and quality control and antioxidative reactions. The physiological significance of such differences is discussed in the context of a flow of complex events in relation to plant adaptation to combined environmental stresses.     

Anopheles gambiae feeding and survival on honeydew and extra-floral nectar of peridomestic plants

It is widely believed that the malaria vector Anopheles gambiae Giles (Diptera: Culicidae) rarely or never feeds on sugar in nature. If so, the need for supplemental blood-feeding may be increased and this would help to explain why it is such an efficient malaria vector. Nonetheless, both sexes of this mosquito species readily imbibe and digest sugar solutions, and sugar is a staple of laboratory colonies. In this study, we investigated whether An. gambiae will feed on the extra-floral nectar of three common peridomestic plants in Africa, and on honeydew of the mealybug Pseudococcus longispinus (Targioni-Tozetti) (Hemiptera: Homoptera: Pseudococcidae), and how this affects survivorship. We found that both males and females of An. gambiae provided with vegetative parts of cassava (Manihot esculenta Crantz) survived as well (x = 26.3 and 19.2 days, respectively) as they did on 50% sucrose solution (x = 29.7 and 24.3 days, respectively) and much longer than they did on water alone (x = 1.8 days, both sexes). Females provided with mealybug honeydew also lived substantially longer (x = 16.5 days) than those on water alone. Males and females provided with vegetative parts of castorbean (Ricinus communis L.) also survived much longer (x = 12.7 and 7.8 days, respectively) than on water, but those provided with flowering lantana (Lantana camara L.) did not. Anthrone tests of females after one night of exposure to these potential energy sources confirmed that they obtained fructose from cassava, from mealybug honeydew, and from non-flowering castorbean, but not from lantana or from castorbean lacking its petiolar nectaries. Previous laboratory studies had shown that sugar availability affects the survival and biting frequency of An. gambiae. It now appears that this mosquito can locate natural sources of plant sugar readily and utilize them effectively. Nectar-producing plants in the domestic environment may play a significant role in this mosquito's energy budget and malaria vectorial capacity.     

The Structure of Uncommon Lipid A from the Marine Bacterium <Emphasis Type="Italic">Marinomonas communis</Emphasis> ATCC 27118<Superscript>T</Superscript>

Lipid A was obtained in a high yield (27%) by the hydrolysis of lipopolysaccharide from the marine gamma proteobacterium Marinomonas communis ATCC 27118^T with 1% AcOH. Using chemical analysis and 1D and 2D NMR spectroscopic and fast atom bombardment mass spectrometric methods, it was shown to be β-1′,6-linked D-glucosaminobiose 1-phosphate acylated with (R)-3-dodecanoyl- or (R)-3-decanoyloxydecanoic acid, (R)-3-{(R)-3-hydroxydecanoyloxy)]decanoic acid and (R)-3-hydroxydecanoic acid at the C2, C2′ and C3 positions, respectively. Uncommon structural peculiarities (a low acylation and phosphorylation degree) of the M .communis lipid A in comparison with those of terrestrial bacteria may be of pharmacological interest. The potential physiological meaning of this lipid A and compounds of similar structure are discussed.__________Translated from Bioorganicheskaya Khimiya, Vol. 31, No. 4, 2005, pp. 404–413.Original Russian Text Copyright © 2005 by Vorob’eva, A. Dmitrenok, P. Dmitrenok, Isakov, Krasikova, Solov’eva.The article was translated by the authors.     

The Effects of Boric Acid and Gibberellic Acid on the Growth of Fiber of Phragmites cormmuhis Trin

Water-cultured young plants of Phragmites communis Trin. were used in this experiment. They were treated with boric acid and gibberellic acid, separately or in combination, by method of foliage spraying. The results are summarized as follows: 1. In comparation with the controls, the length of the fibre cells was remarkably increased following the treatment with boric acid at concentrations ranging from 1 to 200 μmol/l. The optimum concentration of boric acid was found to be 100 μmol/l. Gibberellic acid alone at the concentration of 50 μmol/l also enhanced the length of the fibre cells. However, the best result was obtained in the group treated with a combination of boric acid and gibmberellic acid at a ratio of 200:50 μmol/l. A maximum increasement of fibre length and a greater ratio of length to width were observed in this experimental group. 2. Microscopic study indicates that the increase in both the number of the fibre cells and ,the thickness of the fibre layer are apparent in histological preparation. 3. In addition, The authors have also found that the incorporation of H3-glucose into the fibre cell wall was greatly enhanced by such combination treatment. 4. In conclusion, it has been demonstrated clearly that the boric acid and the gibberellic acid, when used in combination, produces an augmentative effect on both the growth and the development of the fibre cells of Phragmites communis Trin.     

盐胁迫下芦苇叶肉细胞超微结构的研究

对青藏高原柴达木盆地柯柯盐湖边盐碱地上生长的芦苇叶肉细胞的超微结构进行了研究,并以西宁地区非盐碱地上生长的芦苇作对照。结果表明：西宁地区的芦苇叶肉细胞的叶绿体呈椭圆形,其膜系统完整,基粒片层和基质片层发育良好。在盐碱地上生长的芦苇叶肉细胞的叶绿体呈圆形,叶绿体内出现较大的淀粉粒,并发现有线粒体嵌入叶绿体的现象。叶绿体的类囊体膨大,线粒体的嵴也有膨大的现象。在盐湖水中生长的芦苇叶肉细胞,叶绿体的类囊体排列紊乱、扭曲、松散。类囊体膜局部被破坏,部分类囊体膜解体,空泡化,甚至消失,一些溶解了的类囊体流进细胞质中。综上所述,芦苇叶肉细胞超微结构的变化是该植物适应柯柯盐湖地区盐渍、低温、低气压、强辐射等环境因子的结果。     

Prior temperature exposure affects subsequent chilling sensitivity

The chilling sensitivity of small discs or segments of tissue excised from chillingsensitive species was significantly altered by prior temperature exposure subsequent to holding the tissue at chilling temperatures as measured by a number of physiological processes sensitive to chilling. This temperature conditioning was reversible by an additional temperature exposure before chilling, and mature-green and red-ripe tomato tissue exhibit similar chilling sensitivities. Exposing pericarp discs excised from tomato fruit (Lycopersicon esculentum Mill. cv. Castelmart), a chilling-sensitive species, to temperatures from 0 to 37°C for 6 h before chilling the discs at 2.5°C for 4 days significantly altered the rate of ion leakage from the discs, but had no effect on the rate of ion leakage before chilling and only a minimal effect on discs held at a non-chilling temperature of 12°C. Exposing chillingsensitive tissue to temperatures below that required to induce heat-shock proteins but above 20°C significantly increased chilling sensitivity as compared to tissue exposed to temperatures between 10 and 20°C. Rates of ion leakage after 4 days of chilling at 2.5°C were higher from fruit and vegetative tissue of chilling-sensitive species (Cucumis sativus L. cv. Poinsett 76, and Cucurbita pepo L. cv. Young Beauty) that were previously exposed for 6 h to 32°C than from similar tissue exposed to 12°C. Exposure to 32 and 12°C had no effect on the rate of ion leakage from fruit tissue of chilling tolerant species (Malus domestica Borkh. cv. Golden Delicious, Pyrus communis L. cv. Bartlett). Ethylene and CO₂ production were higher and lycopene synthesis was lower in chilled tomato pericarp discs that were previously exposed for 6 h to 32°C than the values from tissue exposed to 12°C for 6 h before chilling. Increased chilling sensitivity induced by a 6 h exposure to 32°C could be reversed by subsequent exposure to 12°C for 6 h.     

Novel Cytotoxic Sesquiterpene Ester Derivatives from the Roots of Ferula mervynii

This study is the first chemical investigation of Ferula mervynii M. Sağıroğlu & H. Duman, an endemic species to Eastern Anatolia. The isolations of nine compounds including six previously undescribed sesquiterpene esters, 8-trans-cinnamoyltovarol ( 1 ), 8-trans-cinnamoylantakyatriol ( 3 ), 6-acetyl-8-trans-cinnamoyl-3-epi-antakyatriol ( 5 ), 6-acetyl-8-trans-cinnamoylshiromodiol ( 6 ), 6-acetyl-8-trans-cinnamoylfermedurone ( 7 ), and 6-acetyl-8-trans-cinnamoyl-(1S),2-epoxyfermedurone ( 8 ), were described along with three known sesquiterpene esters, 6-acetyl-8-benzoyltovarol ( 2 ), 6-acetyl-8-trans-cinnamoylantakyatriol ( 4 ), and ferutinin ( 9 ). The structures of novel compounds were elucidated through extensive spectroscopic analyses and quantum chemistry calculations. The putative biosynthetic pathways for compounds 7 and 8 were discussed. The extracts and isolated compounds were tested for cytotoxic activity against the COLO 205, K-562, MCF-7 cancer cell lines, and Human Umbilical Vein Endothelial Cell (HUVEC) lines using MTT assay. Compound 4 showed the highest activity against the MCF-7 cell lines with an IC₅₀ value of 16.74±0.21 μM.