New Eudesmane Sesquiterpenoids from Salvia plebeia R. Br.

Three new sesquiterpenoids, salplebeones A – C ( 1  –  3 ), were isolated from the ethanol‐soluble extract of the aerial part of Salvia plebeia R. Br . Their structures were established by detailed analysis of NMR and MS spectra. Salplebeone A was an eudesmane lactone, while salplebeones B and C were rare eudesmane sesquiterpenoids, containing 12,8‐lactam groups. Antiproliferative activities of salplebeones A – C to myeloid leukemia cell lines were evaluated.     

Diversity of essential oil glands of clary sage (Salvia sclarea L., Lamiaceae)

The Lamiaceae is rich in aromatic plant species. Most of these species produce and store essential oils in specialised epidermal oil glands, which are responsible for their specific flavour. Two types of glands producing essential oil and possessing different morphological structure can be found in Salvia sclarea : peltate and capitate glands. The content of single oil glands from different positions on the plant (corolla, calyx and leaf) were sampled using an SPME fibre and analysed by gas chromatography in order to study variability of the essential oil composition. It was found that the composition of terpenoids is quite variable within an individual plant. Capitate oil glands mainly produce three essential oil compounds: the monoterpenes linalool and linalyl acetate, and the diterpene sclareol. Peltate oil glands, however, accumulate noticeable concentrations of sesquiterpenes and an unknown compound (m/z = 354). Furthermore, the oil composition varies within each gland type according to the plant organ. Linalool and linalyl acetate are characteristic substances of flowers, whereas the sesquiterpenes occur in higher proportions in leaves. Even within one gland type on a single leaf, the chemical variability is exceedingly high.     

Secondary metabolites from the aerial parts of Salvia palaestina Bentham

Three sesterterpenes (1-3), one triterpene (4) and five diterpenes (5-9) were isolated from the aerial parts of Salvia palaestina Bentham (Lamiaceae), together with two sesquiterpenes, 10 known diterpenes, three triterpenes, and rosmarinic acid. Their structural elucidation was accomplished by extensive spectroscopic methods including 1D ((1)H, (13)C, (13)C DEPT, TOCSY, NOESY) and 2D NMR experiments (DQF-COSY, HSQC, HMBC, ROESY) as well as ESIMS analysis and chemical analysis.     

The signaling role of extracellular ATP and its dependence on Ca2+ flux in elicitation of Salvia miltiorrhiza hairy root cultures

The application of a polysaccharide elicitor from yeast extract,YE, to Salvia miltiorrhiza hairy root cultures induced transientrelease of ATP from the roots to the medium, leading to a dose-dependentincrease in the extracellular ATP (eATP) level. The eATP levelrose to a peak (about 6.5 nM with 100 mg l^–1 YE) at about10 h after YE treatment, but dropped to the control level 6h later. The elicitor-induced ATP release was dependent on membraneCa²⁺ influx, and abolished by the Ca²⁺ chelator EGTA or thechannel blocker La³⁺. The YE-induced H₂O₂ production was stronglyinhibited by reactive blue (RB), a specific inhibitor of membranepurinoceptors. On the other hand, the application of exogenousATP at 10–100 µM to the cultures also induced rapidand dose-dependent increases in H₂O₂ production and medium pH,both of which were effectively blocked by RB and EGTA. The non-hydrolyzableATP analog ATPS was as effective as ATP, but the hydrolyzedderivatives ADP or AMP were not so effective in inducing thepH and H₂O₂ increases. Our results suggest that ATP releaseis an early event and that eATP plays a signaling role in theelicitation of plant cell responses; Ca²⁺ is required for activationof the elicitor-induced ATP release and the eATP signal transduction.This is the first report on ATP release induced by a fungalelicitor and its involvement in the elicitor-induced responsesin plant cells.     

In vitro cytotoxicity of Tanshinones isolated from Salvia miltiorrhiza Bunge against P388 lymphocytic leukemia cells

The cytotoxic effect of four tanshinones isolated from the dried root of Salvia miltiorrhiza Bunge (Lamiaceae) were studied in vitro using P388 lymphocytic leukemia cells. Tanshinone I and tanshinone IIA were shown to be quite strongly cytotoxic against the cells (86.76% and 56.05% cell inhibition at 25 microg/ml). Dihydrotanshinone I and cryptotanshinone, which lack of saturation at C-15, showed little cytotoxicity (13.71% and 39.21% cell inhibition at 25 microg/ml). The results also revealed a structure activity relationship. We suggest that the unsaturation at C-15 and saturation on ring A may be critical structural components for cytotoxicity in these diterpenes.     

高速逆流色谱法分离纯化丹参并尝试制订中药指纹图谱

用国产高速逆流色谱（HSCCC）分离纯化中草药——丹参,选用正己烷乙醇水体系,固定相保留率达到788%。采用分步洗脱,3个产地丹参各分离得到12个洗脱组分,经高效液相色谱仪和紫外光谱仪检测证明3张HSCCC洗脱图谱中对应洗脱峰为同一组分。HSCCC洗脱图谱不包含非共有峰,并且对应洗脱峰保留时间的相对标准偏差RSD<3%,符合国家标准关于制订指纹图谱方法学考察资料的技术参数。因此,HSCCC作为制订指纹图谱的方法之一具有可行性。     

丹参氮、磷肥效效应及最佳施肥模式研究

在陕西省商州市山阳县不同肥力土壤上,采用N、P二因素五水平最优设计,进行了丹参氮、磷优化配方施肥模式研究的多点田问试验。根据田间试验结果,求得不同土壤肥力水平下的N、P肥效反应方程,根据方程提出丹参不同产量水平的N、P合理配比和肥料用量。寻优结果表明,在山阳低肥力土壤目标产量10000～11500kg／hm^2之间的施氮为88．17～165．7kg／hm^2,施磷(P2O4)为88．18～165．7kg／hm^2;中肥力土壤目标产量在11000～14000kg／hm^2之间的施N量为108．5～187．4kg／hm^2,施磷(P2O5)为105．1～179．5kg／hm^2;高肥力土壤目标产量在20000～25000kg／hm^2之间的施N量为85．4～173．1kg／hm^2,施磷(P2O5)为121．95～179．01kg／hm^2。合理施用N、P肥有利于提高丹参产量,但过量施肥会造成丹参减产。     

固沙树种梭梭在不同水分梯度下的光合生理特征

对不同水分梯度下梭梭光合作用的研究发现,地下水位、土壤含水量、灌水量对梭梭的光合具有明显的影响。在1．4m、2．4m、3．4m地下水位下,梭梭的光合速率、呼吸作用、量子效率随水位的降低而降低,光补偿点随水位的降低而增大;在滴灌供水时,梭梭的光合速率较对照明显提高,且灌水量越大,梭梭的光合速率越高;半流动沙丘、丘间低地、粘土沙障固定沙丘退化梭梭的光合作用的强弱同其林地土壤水分的高低基本一致。7月,不同水分梯度下的梭梭光合作用均表现出午休现象,9月只有立地条件较差的梭梭发生光合午休,而且9月光合作用要强于7月,说明9月环境条件更有利于梭梭生长。     

短毛柽柳不同部位中总黄酮含量及稳定性研究

目的：比较短毛柽柳中不同部位总黄酮的含量差异,研究黄酮化合物保存的条件,方法：采用超声波乙醇浸提法,在正交优先的最佳条件（料液比为1∶15,超声处理时间为40min,乙醇浓度为45%,超声温度50℃,提取3次）下提取不同部位总黄酮,并测定不同条件下其吸光度的变化。结果：柽柳花、叶、茎中总黄酮得率分别为24.585mg/g、25.623mg/g、41.726mg/g,柽柳中提取的黄酮溶液在光照、高温、高浓度蔗糖溶液和Na＋存在条件下不稳定;pH 4~7条件下较稳定;氧化剂对其稳定性的影响不大。结论：柽柳茎中总黄酮含量明显高于其他两个部位。柽柳黄酮保存时应避免接触碳水化合物和盐离子,在避光、常温、中性条件下保存。     

Revised karyotyping and gene mapping of the Biomphalaria glabrata embryonic (Bge) cell line

The fresh water snail Biomphalaria glabrata (2n = 36) belongs to the taxonomic class Gastropoda (family Planorbidae) and is integral to the spread of the human parasitic disease schistosomiasis. The importance of this mollusc is such that it has been selected as a model molluscan organism for whole genome sequencing. In order to understand the structure and organisation of the B. glabrata’s genome it is important that gene mapping studies are established. Thus, we have studied the genomes of two B. glabrata embryonic (Bge) cell line isolates 1 and 2 grown in separate laboratories, but both derived from Eder L. Hansen’s original culture from the 1970s. This cell line continues to be an important tool and model system for schistosomiasis and B. glabrata. Using these cell line isolates, we have investigated the genome content and established a revised karyotype based on chromosome size and centromere position for these cells. Unlike the original karyotype (2n = 36) established for the cell line, our investigations now show the existence of extensive aneuploidy in both cell line isolates to the extent that the total complement of chromosomes in both greatly exceeds the original cell line’s diploid number of 36 chromosomes. The isolates, designated Bge 1 and 2, had modal chromosome complements of 64 and 67, respectively (calculated from 50 metaphases). We found that the aneuploidy was most pronounced, for both isolates, amongst chromosomes of medium metacentric morphology. We also report, to our knowledge for the first time using Bge cells, the mapping of single-copy genes peroxiredoxin (BgPrx4) and P-element induced wimpy testis (piwi) onto Bge chromosomes. These B. glabrata genes were mapped onto pairs of homologous chromosomes using fluorescence in situ hybridization (FISH). Thus, we have now established a FISH mapping technique that can eventually be utilized for physical mapping of the snail genome.