Inhibitory effect of a bioactivity-guided fraction from Rheum undulatum on the acid production of Streptococcus mutans biofilms at sub-MIC levels

Rheum undulatum root has been used traditionally in Korea for the treatment of dental diseases. The purpose of this study was to separate a fraction from R. undulatum showing anti-acid production activity against Streptococcus mutans biofilms and identify the main components in that fraction. Methanol extract of R. undulatum root and its fractions were prepared. To select a fraction exhibiting anti-acid production activity, suspension glycolytic pH-drop assay was performed. Among the fractions tested, dichloromethane fraction exhibited the strongest activity in a dose-dependent manner. To examine the effect of the selected fraction on the anti-acid production of S. mutans biofilms, 74 h old S. mutans biofilms were used. The selected fraction reduced the initial rate of acid production of S. mutans biofilms at sub-minimum inhibitory concentration (MIC) levels. HPLC qualitative analysis of the selected fraction indicated that the presence of anthraquinone derivatives, such as aloe-emodin, emodin, chrysophanol and physcion, as main components.     

Ent-trachyloban-19-oic acid isolated from Iostephane heterophylla as a promising antibacterial agent against Streptococcus mutans biofilms

From the roots of Iostephane heterophylla, six known compounds, namely, ent-trachyloban-19-oic acid (1), the mixture of ent-kaur-16-en-19-oic acid (2) and ent-beyer-15-en-19-oic acid (3), xanthorrhizol (4), 16α-hydroxy-ent-kaurane (5) and 16α-hydroxy-ent-kaur-11-en-19-oic acid (6) were isolated using a bioassay-guided fractionation method. The known compounds (1-6) were identified by comparison of their spectroscopic data with reported values in the literature. In an attempt to increase the resultant antimicrobial activity of 1 and 4, a series of reactions was performed on ent-trachyloban-19-oic acid (1) and xanthorrhizol (4), to obtain derivatives 1a, 1b, and 4a-4d. All the isolated compounds (1-6) and the derivatives 1a, 1b, and 4a-4d were evaluated for their antimicrobial activity against two oral pathogens, Streptococcus mutans and Porphyromonas gingivalis associated with caries and periodontal disease, respectively. Compounds 1, 1b, 2+3, 4 and 4d inhibited the growth of S. mutans with concentrations ranging from 4.1 μg/mL to 70.5 μg/mL. No significant activity was found on P. gingivalis except for 4 with an MIC of 6.8 μg/mL. The ability of 1, 1b, 2+3, 4 and 4d to inhibit biofilm formation by S. mutans was evaluated. It was found that 1, 1b, 4 and 4d interfered with the establishment of S. mutans biofilms, inhibiting their development at 32.5, 125.0, 14.1 and 24.4 μg/mL, respectively.     

Pistagremic acid,a glucosidase inhibitor from Pistacia integerrima

Pistacia integerrima Stewart in traditionally used as folk remedy for various pathological conditions including diabetes. In order to identify the bioactive compound responsible for its folk use in diabetes, a phytochemical and biological study was conducted. Pistagremic acid (PA) was isolated from the dried galls extract of P. integerrima. Strong α-glucosidase inhibitory potential of PA was predicted using its molecular docking simulations against yeast α-glucosidase as a therapeutic target. Significant experimental α-glucosidase inhibitory activity of PA confirmed the computational predictions. PA showed potent enzyme inhibitory activity both against yeast (IC₅₀: 89.12 ± 0.12 μM) and rat intestinal (IC₅₀: 62.47 ± 0.09 μM) α-glucosidases. Interestingly, acarbose was found to be more than 12 times more potent an inhibitor against mammalian (rat intestinal) enzyme (having IC₅₀ value 62.47 ± 0.09 μM), as compared to the microbial (yeast) enzyme (with IC₅₀ value 780.21 μM). Molecular binding mode was explored via molecular docking simulations, which revealed hydrogen bonding interactions between PA and important amino acid residues (Asp60, Arg69 and Asp 70 (3.11 Å)), surrounding the catalytic site of the α-glucosidase. These interactions could be mainly responsible for their role in potent inhibitory activity of PA. PA has a strong potential to be further investigated as a new lead compound for better management of diabetes.     

Ganoderic acid Df,a new triterpenoid with aldose reductase inhibitory activity from the fruiting body of Ganoderma lucidum

Ganoderic acid Df, a new lanostane-type triterpenoid, was isolated from the fruiting body of Ganoderma lucidum. Its structure was characterized as 7β, 11β-dihydroxy-3, 15, 23-trioxo-5α-lanosta-8-en-26-oic acid by 1D- and 2D-NMR spectra. This compound exhibited potent human aldose reductase inhibitory activity, with an IC₅₀ of 22.8 μM in vitro. A carboxyl group of this compound's side chain is essential for eliciting inhibitory activity because its methyl ester is much less active.     

New triterpene saponins from the root of Ilex pubescens

Two new triterpene glycosides named ilexpublesnin A (1) and ilexpublesnin B (2) were isolated from the root of Ilex pubescens. Their structures were determined as 3-O-(β-d-xylopyranosyl)-28-O-(β-d-glucopyranosyl)-3β, 19α-dihydroxyurs-23-oxo-12-en-28-oic acid (1) and 28-O-(β-d-xylopyranosyl-(2 → 1)-β-d-glucopyranosyl)-3β, 19α-dihydroxyurs-23-oxo-12-en-28-oic acid (2) on the basis of chemical and spectroscopic methods.     

松墨天牛对云南松的分解作用分析

为探索松墨天牛取食对林木的分解作用,本文通过对松墨天牛幼虫及成虫取食量的测定,寄主云南松韧皮组织及松墨天牛幼虫排泄物成分对比分析,并与资源利用相同的木材微生物分解能力进行对比,阐明了松墨天牛作为分解者的重要分解作用。研究表明,松墨天牛幼虫期(约为55 d)取食分解林木生物量平均为12.42 g(24.40 cm3),成虫期取食分解林木生物量平均为12.87 g(25.28 cm3);松墨天牛幼虫对糖类物质的利用度很高,具有较强的纤维分解利用能力,取食分解后总糖减少83.58%,粗纤维减少23.87%,1头松墨天牛幼虫期分解的林木粗纤维质量为1.93 g,分解利用率为0.008 g.d-1。松墨天牛对林木的分解证明,天牛作为一种重要的林木分解的先驱者,可以分解林木,更重要的是松墨天牛攻击亚健康林木,为微生物分解林木提供了容易入侵的途径,加速了亚健康林木的分解与循环,在森林生态系统物质分解与循环中具有重要的促进作用。     

Photosynthetic characteristics of Fagus sylvatica and Quercus robur established for stand conversion from Picea abies

Efforts in Europe to convert Norway spruce (Picea abies) plantations to broadleaf or mixed broadleaf-conifer forests could be bolstered by an increased understanding of how artificial regeneration acclimates and functions under a range of Norway spruce stand conditions. We studied foliage characteristics and leaf-level photosynthesis on 7-year-old European beech (Fagus sylvatica) and pedunculate oak (Quercus robur) regeneration established in open patches and shelterwoods of a partially harvested Norway spruce plantation in southwestern Sweden. Both species exhibited morphological plasticity at the leaf level by developing leaf blades in patches with an average mass per unit area (LMA) 54% greater than of those in shelterwoods, and at the plant level by maintaining a leaf area ratio (LAR) in shelterwoods that was 78% greater than in patches. However, we observed interspecific differences in photosynthetic capacity relative to spruce canopy openness. Photosynthetic capacity (A₁₆₀₀, net photosynthesis at a photosynthetic photon flux density of 1600 μmol photons m⁻² s⁻¹) of beech in respect to the canopy gradient was best related to leaf mass, and declined substantially with increasing canopy openness primarily because leaf nitrogen (N) in this species decreased about 0.9 mg g⁻¹ with each 10% rise in canopy openness. In contrast, A₁₆₀₀ of oak showed a weak response to mass-based N, and furthermore the percentage of N remained constant in oak leaf tissues across the canopy gradient. Therefore, oak photosynthetic capacity along the canopy gradient was best related to leaf area, and increased as the spruce canopy thinned primarily because LMA rose 8.6 g m⁻² for each 10% increase in canopy openness. These findings support the premise that spruce stand structure regulates photosynthetic capacity of beech through processes that determine N status of this species; leaf N (mass basis) was greatest under relatively closed spruce canopies where leaves apparently acclimate by enhancing light harvesting mechanisms. Spruce stand structure regulates photosynthetic capacity of oak through processes that control LMA; LMA was greatest under open spruce canopies of high light availability where leaves apparently acclimate by enhancing CO₂ fixation mechanisms.     

neo-Clerodane diterpenes from Ajuga decumbens and their inhibitory activities on LPS-induced NO production

A phytochemical investigation of the whole plants of Ajuga decumbens led to the isolation of three new (1, 2a, and 2b) and three known (3a−3c) neo-clerodane diterpenes. Their structures were elucidated by spectroscopic data analysis (IR, ESIMS, HR-ESIMS, 1D and 2D NMR), and the structure of 1 was confirmed by X-ray crystallography. The inhibitory activities on LPS-induced NO production of the six diterpenes were evaluated and compounds 2a, 2b, and 3a showed inhibitory effects.     

马尾松谷胱甘肽过氧化物酶PmGPX6基因cDNA克隆及转化拟南芥耐旱性初步研究

[目的]克隆马尾松谷胱甘肽过氧化物酶基因,并对其进行功能研究。[方法]采用RACE技术克隆基因c DNA序列,实时荧光定量PCR检测基因在马尾松干旱胁迫下的表达模式,花序浸泡法转化拟南芥,并对转基因与野生型拟南芥的生长表型和根系生长进行分析。利用荧光显微镜技术对转基因拟南芥不定根进行GFP荧光检测。[结果]克隆到1个871 bp的GPX基因全长c DNA序列,命名为Pm GPX6。Pm GPX6包括513 bp的完整开放阅读框,编码170个氨基酸残基。Pm GPX6蛋白与油松Pt GPX蛋白同源性达95%。Pm GPX6在马尾松根中高表达,茎、叶中表达量低。在干旱胁迫下,Pm GPX6在根、茎、叶中的表达量均在第15天达到最大,随后出现下降趋势。过表达Pm GPX6与野生型拟南芥植株在正常水分条件下表型与根长差异不大,但在干旱胁迫下,转基因植株根系更长。转基因拟南芥根在蓝色光激发下能发出强烈的绿色荧光,表明Pm GPX6基因能高效表达。[结论]推测Pm GPX6可能参与马尾松干旱胁迫应答。     

Stand level estimation of root respiration for two subtropical plantations based on in situ measurement of specific root respiration

In this study, the stand level root respiration was estimated for two monoculture plantations: Acacia crassicarpa and Eucalyptus urophylla, based on in situ measurement of specific root respiration using simplified root chamber method. The respiration rates of fine roots (<5 mm) were significantly higher than those of coarse roots (>5 mm) for both A. crassicarpa and E. urophylla species. The root respiration of A. crassicarpa showed a clear seasonal pattern with a higher value in the wet season. For E. urophylla, the seasonal pattern was observed for fine roots but not for coarse roots. After determining the biomass of fine roots and coarse roots and their specific rates of respiration at different time points, root respiration at the stand level (R_a) was estimated using a direct up-scaling model. We found that the R_a accounted for 14% and 19% of total soil respiration (R_s) for A. crassicarpa and E. urophylla, respectively. The fine (R_Tf) and coarse (R_Tc) root respiration at the stand level accounted for about 47% and 53% of the R_a for A. crassicarpa, and accounted for 58% and 42% for E. urophylla. This suggests that coarse root respiration cannot be ignored when estimating the root respiration at the stand level. Our results showed that the Q₁₀ values were more accurate in representing the temperature dependence when the confounding effect of soil moisture was considered. This study introduces an alternative approach to estimate stand level root respiration, but its reliability is largely dependent on the accuracy of root biomass quantification.     

一种新的白蜡虫寄生蜂体内Wolbachia的wsp基因分子检测及序列分析

采用Wolbachia的通用引物、A大组和B大组的特异性引物对一种新的白蜡虫寄生蜂--长尾啮小蜂(Aprostocetus sp.)体内Wolbachia的wsp基因进行分子检测,所获得的基因片段分别命名为wApr、wAprB和wAprB,长度分别为620、566和463bp;基因序列分析表明:wApA、wAprB与w...     

赤桉GAPDH家族基因的克隆及其序列分析

GAPDH is a typical structural protein in eukaryote organism, which plays an important role involved in the biosynthesis of cell composition and the expression of genetic information. In order to reveal the biological function of GAPDH in the growth and development of Eucalyptus, 3 genes were obtained and named as EC-GAP1, EC-GAP2 and EC-GAP3 by amplification with primers for GAPDH genes conserved regions and RACE method from the young leaf of Eucalyptus camaldulensis. The bioinformatics analysis suggested that the proteins encoded by corresponding genes owned the typical conserved domains of GAPDH and showed high homology with those of other plant species.     

Effects of defoliation by Eucalyptus weevil, Gonipterus scutellatus, and chrysomelid beetles on growth of Eucalyptus globulus in southwestern Australia

Plantations of Eucalyptus globulus in southwestern Australia are defoliated by Eucalyptus weevil, Gonipterus scutellatus, and a complex of chrysomelid and scarab beetles, yet there is no information on the impact of beetle defoliation to tree growth in southwestern Australia. To address this shortcoming, we used insect exclusion trials, to compare growth of insecticide treated (and thus relatively undamaged) trees with untreated (and thus defoliated) trees to determine whether defoliation by G. scutellatus and other beetles reduced the growth and harvest volume of E. globulus trees. Our results showed some evidence of beetle defoliation reducing growth of E. globulus. Mean defoliation levels of the growing tip of untreated trees ranged from 18% to 33% across the duration of the study and were significantly greater than mean defoliation levels of 5–16% on insecticide treated trees. Seasonal peaks in defoliation of 30–80% to the growing tip of untreated trees were recorded between late spring and early autumn. The greatest impact of defoliation on tree growth was evident during the 2.5 year period of insect exclusion, when higher relative growth rates were recorded for insecticide treated trees, which were significantly different from relative growth rates of untreated trees at two of the four plantations. However, our results showed only a limited impact of beetle defoliation on the total volume at harvest. Initially small trees tended to suffer more severe defoliation than initially large trees. Effects of insect exclusion treatment on harvest volume were modified by the initial tree size and the relationship between the initial tree size and levels of defoliation.     

Phenylpropionic acid derivates from the bark of Cerbera manghas

Two new phenylpropionic acid derivates, cerberic acids A (1) and B (2), were isolated from the bark of Cerbera manghas. Their structures were established on the basis of spectroscopic methods including IR, ESI-FT-ICR-MS, 1D and 2D NMR. Primary bioassays showed that compound 1 possessed weak cytotoxic activity against HepG2, MCF-7, and HeLa cell lines with IC₅₀ values of 44.7, 52.3, 48.7 μg/ml, respectively.     

杜仲1-脱氧-D-木酮糖-5-磷酸还原异构酶基因cDNA全长克隆与序列分析

以杜仲叶片cDNA为模板,采用反转录RCR及RACE技术分离出DXR基因cDNA全长。序列分析结果表明该基因序列全长1 814 bp,共编码478个氨基酸,推导的蛋白质分子量为51.71 kD,理论等电点5.79,命名为EuDXR。推导的EuDXR蛋白质序列具有植物DXR酶的5个典型基序,并预测出26个潜在的功能位点。系统进化树分析表明EuDXR蛋白与玉米、水稻亲缘关系最近,其次为橡胶、拟南芥、烟草。     

麻疯树磷酸烯酮式丙酮酸羧化酶em>pepc基因全长cDNA克隆及序列分析

应用RT-PCR和RACE法从麻疯树总RNA中分离出pepc基因全长cDNA,长度为3 142 bp,阅读框2 898 bp,编码965个氨基酸,在GenBank中登录,序列号为EU069413。它的氨基酸序列与蓖麻、陆地棉、橙、大豆、花生、烟草、油菜、拟南芥的氨基酸同源性分别为94.94%、92.46%、90.60%、90.50%、90.50%、88.33%、84.61%、82.44%。该基因编码了pepc基因家族中的pepc1,蛋白属于C₃型PEPC。推测了pepc编码蛋白分子量为110.6 kD,并对其稳定性、二级结构、疏水性等特性进行了分析,最后确定了该蛋白的功能位点和结构域。     

New withanolides from Mandragora officinarum: First report of withanolides from the Genus Mandragora

Two new withanolides named mandragorolide A (1) and mandragorolide B (2) were isolated from the MeOH extract of the whole plant of Mandragora officinarum of Jordanian origin, along with five known withanolides namely larnaxolide A (3), withanolide B (4), datura lactone 2 (5), withanicandrin (6) and salpichrolide C (7). Compound 3 has been reported only once before, from the leaves of Larnax glabra. This is the first report of withanolides of different biogenetic types from the genus Mandragora. Isolation of known fatty compounds, coumarins, sterols and tropane alkaloids was also achieved in this study.     

不同生长调节剂处理对卡特兰开花的影响

通过花鞘注射生长调节剂的方法,研究不同浓度的生长调节剂对卡特兰开花和开花性状的影响,结果表明:注射GA₃浓度为60、120 mg·kg^-1,卡特兰盛花期显著提前13.34、22.34 d,萼片、花瓣、花柄和花葶的长度显著增加;注射10 mg·kg^-1的NAA能够使花期提前,花朵显著增大;注射ABA对卡特兰的花期没有影响,注射ABA浓度为40 mg·kg^-1时,开花率下降,花朵缩小。注射60 mg·kg^{-1相似文献}   

Regeneration, in vitro glycoalkaloids production and evaluation of bioactivity of callus methanolic extract of Solanum tuberosum L.

Callus and differentiated shoots initiated from Solanum tuberosum L. on MS media containing BA, IAA, and Kin. Glycoalkaloids are produced in callus and shoots in concentrations higher than original tubers using HPLC. Callus methanolic extract had promising anticancer activity with low IC₅₀ values against human carcinoma cell lines of breast, lymphoplastic leukemia, larynx, liver, cervix, colon, and brain, IC₅₀ (µg/mL) were 2.7, 3.7, 6, 6.7, 10, 13.6, and 22.3 respectively. Antioxidant capacity of the extract (76.4%) performed using ESR. Preliminary screening showed that the extract exhibited in vitro virucidal activity against Herpes simplex. The extract possessed in vitro schistomicidal and fasciolicidal activity.