麻疯树种子中佛波酯的提取及对菜青虫的杀虫活性

佛波酯是麻疯树种子中的主要毒性物质之一.麻疯树种子经乙醇浸提、液液萃取和柱层析,获得佛波酯富集物.以TPA为外标,通过高效液相色谱(HPLC)定量分析佛波酯的含量,同时检测其对菜青虫的毒杀和拒食活性.结果显示,富集物中佛波酯含量达到0.817 35 mg mg-1.佛波酯富集物对3龄菜青虫具有显著的毒杀和拒食活性:毒杀活性表现为胃毒作用,胃毒活性具有明显的剂量效应和时间效应,48、72、120 h的佛波酯半致死浓度(LC50)分别为73.86、16.99、5.26μg mL-1;24、48 h的非选择拒食中浓度(AFC50)分别为9.81、5.39μg mL-1.图3表3参24     

Sequestration of phorbol esters by aposematic larvae of Hyles euphorbiae (Lepidoptera: Sphingidae)?

Summary. The larvae of the hawkmoth species Hyles euphorbiae have a conspicuous aposematic colouration and show gregarious behaviour. It has thus been suggested that they sequester phorbol esters from their food plants which include different species of the genus Euphorbia (Euphorbiaceae) for chemical protection against predators. To test this hypothesis in more detail, we fed larvae an artificial diet with three doses of 12-tetradecanoyl-phorbol-13-acetate (TPA), then examined the faeces and the larval tissues, such as integument, haemolymph and gut of the caterpillars for the presence of TPA. In order to determine the ability of the larvae to detoxify phorbol esters, other larvae were directly injected with a TPA solution and analysed in the same manner. Our study indicates that the larvae of Hyles euphorbiae do not sequester phorbol esters. Upon oral application TPA was not found in the larval integument or the haemolymph. Instead, it was mostly metabolised (about 70–90%). Nevertheless, about 10-30% were retained and recovered in the faeces. The larvae were also able to metabolise and thus detoxify the phorbol ester when TPA was injected directly into the body. These hawkmoth caterpillars are relatively large and have a gut full of plant material, which they regurgitate into the direction of the predator when attacked in nature. Since phorbol esters are very potent toxins and irritants, we postulate that the gut content (and especially the plant slurry disgorged as regurgitant from the anterior gut) alone could be aversive for a potential predator, even if some metabolism has taken place. Thus, although H. euphorbiae caterpillars do not actively sequester phorbol esters, their aposematic colouration appears to be based on chemical defence through phorbol esters retained in the gut.     

Sequestration of phorbolesters by the aposematically coloured bug Pachycoris klugii (Heteroptera: Scutelleridae) feeding on Jatropha curcas (Euphorbiaceae)

Summary. The phorbol ester DHPB has been detected in 5th instars and adults of Pachycoris klugii which feed on Jatropha curcas, a producer of phorbol esters with mollusc-, insect-, and vertebrate toxicity. DHPB from Pachycoris activates protein kinase C (PKC) which appears to be the main molecular target for phorbol esters. Phorbol esters of J. curcas exhibit a wide range of acute toxic effects in vertebrates and insects. It is therefore likely that the sequestration of DHPB, which would explain the aposematic colouration of the bugs, confers chemical protection to P. klugii against vertebrate predators. Received 26 April 2000; accepted 31 May 2000     

麻疯树种仁油粕脱毒

为获得经冷榨脱油后麻疯树油粕最佳的脱毒方法,采用超声提取,运用四因素三水平正交实验,考察了脱毒温度、脱毒时间、脱毒次数以及脱油后种仁与乙醇料液比对脱毒效果的影响.结果显示,最佳的脱毒方法为料液比8:1,40℃,超声3次,每次20 min.该方法处理后麻疯树油粕中佛波酯含量为0.011 mg g-1.脱毒后的麻疯树油粕对小鼠的急性毒性实验显示,小鼠无死亡,体重增长正常,未出现中毒症状,初步表明脱毒方法有效.图2表3参9     

Nativ-basierte Grundöle für die Produktion von Kühlschmierstoffen

Aims and Scope

Compared to mineral oil products, cooling lubricants based on fatty acid esters have technological advantages. Moreover, they are more environmentally compatible and make a contribution to a sustainable economy. Nevertheless, they are rarely applied in practice, because of their comparably high price, that is based on raw-material and synthesis costs. Alternatives concerning raw-materials and synthesis pathways are considered and properties of resulting ester products are compared.

Methods

The investigations aimed at three fatty acid-2-ethyl-hexylesters that were synthesized in an enzymatic-catalytic routine based on peanut oil, suet, and waste edible fat and at esters that were conventionally produced from animal and plant fats and 2-ethyl-1-hexanol. Physical properties, fatty acid patterns, contents of free fatty acids, as well as oxidative and hydrolytic stabilities were determined. Thermolysis experiments were performed.

Results

The physical properties of the seven esters, density, viscosity, pourpoint, and flash point, were comparable and gave reason for the assumption, that the products could be used as basis oils in lubricant formulations. Hydrolysis stabilities of the esters were high and thermal stress did not point at high potential of hazardous compounds formation. Especially the enzymatic-catalytically produced esters showed deficits concerning oxidation stabilities and free fatty acid contents.

Outlook

For practice it will be necessary to define minimum qualities for raw-materials and resulting ester oils to be used as lubricant basis oils. Moreover, processes have to be developed, that yield high quality ester products from waste edible and animal fats without loosing the advantage of low-cost raw-materials by high production and refinement costs. Surely, one contribution is the further development of the energy-saving enzymtic alcoholysis for ester production.     

Application of heterogeneous catalysis to biodiesel synthesis using microalgae oil

• Microalgae oil application for biodiesel synthesis is discussed. • Catalytic effectiveness of ferment preparations and chemical catalyst is disputed. • Application of heterogeneous catalysts for biodiesel synthesis is reviewed. • Possibilities of catalyst regeneration is shown. Recently, there is a growing interest in the use of microalga in various fields. Microalgae have properties such as rapid reproduction and high biomass accumulation, and under certain conditions, some are able to accumulate a large amount of oil. However, microalgae oil often contains more free fatty acids than the vegetable oil and is therefore unsuitable for biodiesel synthesis using alkaline catalysts. For this reason, some authors suggest the application of heterogeneous catalysis. A particular interest in the use of immobilized enzymes has developed. Other solid substances can also be used as heterogeneous catalysts are usually metal oxides, carbonates or zeolites. The use of these catalysts results in simpler biodiesel synthesis, especially purification processes, a cleaner end product and a less polluted environment. The molar ratio of alcohol to oil is lower during enzymatic transesterification, and more than 90% ester yield is obtained using a molar ratio of alcohol to oil of 3:1 to 4.5:1. The alcohols do not have a negative effect on the effectiveness of chemical catalysts, so it is possible to use alcohols in molar ratio from 4:1 to 12:1. The optimal temperature of enzymatic process is 30℃‒50℃. An ester yield of more than 95% was obtained in 12‒48 h. Using chemical catalysts, greater than a 95% yield of esters was obtained at higher temperatures in a shorter time. Material costs of enzymatic catalysis can be reduced by reusing the catalysts directly or after regeneration.     

Studies on the digestive lipase of the surf clam Spisula solidissima

Crude molluscan lipase was prepared by homogenizing in tris buffer either fresh or lyophilized crystalline styles of Spisula solidissima. Both preparations showed specific activities less than 2% of standard hog pancreatic lipase, and pH and temperature optima of 8.0 and 20°C, respectively. When compared with mammalian hog pancreatic lipase, the clam lipase was found to be the more versatile enzyme on primary wax esters as well as methyl esters. Neither lipase was capable of hydrolyzing the oleate or palmitate esters of the secondary alcohols of glycerol, cholesterol or isopropyl alcohol; however, both showed activity on the oleate ester of isobutyl alcohol, a primary alcohol. S. solidissima lipase, hog pancreatic lipase, and a lipase isolated from the pancreas of the skate Raja erinacea, all demonstrated an inability to hydrolyze the methyl esters of eicosatetraenoic, eicosapentaenoic and docosahexaenoic acids. The lipase-resistant polyunsaturated fatty acid esters are discussed in terms of their role in the lipid biochemistry of marine organisms.     

Determination of Phthalate Esters in Samples from the Marine Environment Using Gas Chromatography Mass Spectrometry

Phthalate esters have been extracted from water, sediment and biota samples using a single solvent system, dichloromethane, and clean up by alumina column chromato-graphy. Analysis for dimethyl, diethyl, di-iso-butyl, di-n-butyl, di-n-heptyl, di-(2-ethylhexyl) and di-n-nonyl phthalates was carried out by gas chromatography and mass spectrometry. Phthalate esters were quantified using multiple ion detection, focussed on m/z 163 and m/z 149.

The procedure was tested on samples of water, sediment, bivalves and fish from the estuary of the River Crouch. The method gave satisfactory sensitivity for the determination of phthalate ester levels above the commonly found blank values of 1 to 20 nanograms per gram of solid or litre of water.

Comparative samples of fish from the heavily industrialised Tees Bay area did not show greatly elevated levels of phthalate esters.     

Determination of Phthalate Esters in Samples from the Marine Environment Using Gas Chromatography Mass Spectrometry

Phthalate esters have been extracted from water, sediment and biota samples using a single solvent system, dichloromethane, and clean up by alumina column chromato-graphy. Analysis for dimethyl, diethyl, di-iso-butyl, di-n-butyl, di-n-heptyl, di-(2-ethylhexyl) and di-n-nonyl phthalates was carried out by gas chromatography and mass spectrometry. Phthalate esters were quantified using multiple ion detection, focussed on m/z 163 and m/z 149.

The procedure was tested on samples of water, sediment, bivalves and fish from the estuary of the River Crouch. The method gave satisfactory sensitivity for the determination of phthalate ester levels above the commonly found blank values of 1 to 20 nanograms per gram of solid or litre of water.

Comparative samples of fish from the heavily industrialised Tees Bay area did not show greatly elevated levels of phthalate esters.     

Protein kinase C and ion transport in the posterior gills of the Chinese crabEriocheir sinensis

The possible involvement of protein kinase C in control of ion transport was investigated on a preparation of isolated, perfused posterior gills of the Chinese crabsEriocheir sinensis (collected in 1989 from lakes near Emden, northern Germany) acclimated to fresh water. 1-oleyl-2-acetyl-sn-glycerol (OAG) and phorbol 12-myristate 13-acetate (PMA), two activators of protein kinase C, when added to the perfusion saline, induced depolarisation of the transepithelial potential difference (PD) and an increase in transepithelial Na⁺ influx. The observed increase was proportional to OAG concentration up to 250µM, with a 2.5× accelerated Na⁺ influx. OAG and PMA remained without effect on Cl^– fluxes. The observed effects were in agreement with an activation, via protein kinase C, of the Na⁺/K⁺ ATPase located on the serosal side of the epithelium.     

Biosynthesis of wax esters in oceanic crustaceans

Slices from the hepatopancreas of various oceanic curstaceans incorporated radioactivity into wax esters from ¹⁴C glucose and ¹⁴C aspartic acid to a lesser extent and from ¹⁴C palmitic acid to a much greater extent. Radioactivity was incorporated from ¹⁴C palmitic acid into both fatty acid and fatty alcohol moieties of wax esters, the percentage of total radioactivity present in alcohol moieties being greater in deep-living than in shallow-living species. Cell-free preparations from the hepatopancreas but not from muscle, supplemented with ATP and reduced pyridine nucleotides, incorporated radioactivity from 1-¹⁴C palmitoyl Coenzyme A into both fatty alcohol and fatty acid moieties of wax esters. Incorporation into fatty alcohol was NADPH- rather than NADH-specific. Preparations from deep-living species had a greater percentage of total radioactivity in the fatty alcohol moieties of wax esters than preparations from shallow-living species. We conclude that the level of wax esters in a given species is correlated with the rate at which the species biosynthesises these lipids de novo; deep-living species have higher rates of wax ester biosynthesis and higher levels of wax esters than shallow-living species. The results support the thesis that wax esters in oceanic crustaceans are derived largely from the animals' internal biosynthetic activities, presumably in response to particular biochemical and/or physiological requirements, rather than from their diets.     

The occurrence of wax esters in crustaceans from the North-east Atlantic Ocean

The lipids of 2 species and 1 group of copepods, 4 species of euphausiids, 2 species of mysids, and 6 species of decapods, taken from different depths in the North-eastern Atlantic Ocean and Western Mediterranean Sea, have been analysed specifically for their wax ester content. The mid-water animals living below 500 m contained large amounts of wax ester (30 to 80% total lipid), while those animals living in the upper 600 to 700 m or on the sea floor had only small wax ester fractions (5 to 10% total lipid). It is suggested that the wax esters are laid down by those animals living in areas of low food density, where energy conservation is important, partly to achieve a more neutral buoyancy. In addition, it would appear that wax esters can function as energy reserves.     

Role of esters in egg removal behaviour in honeybee (Apis mellifera) colonies

In queen-right honeybee colonies workers detect and eat the vast majority of worker-laid eggs, a behaviour known as worker policing. However, if a colony becomes permanently queen-less then up to 25% of the worker population develops their ovaries and lay eggs, which are normally reared into a final batch of males. Ovary development in workers is accompanied by changes in the chemical secretion of the Dufour's gland with the production of queen-like esters. We show that ester production increases with the period that the colony is queen-less. The increased ester production also corresponds to an increase in persistence of worker-laid eggs in queen-right colonies, since the esters somehow mask the eggs true identity. However, in a rare queen-less colony phenotype, workers always eat eggs indiscriminately. We found that the egg-laying workers in these colonies were unusual in that they were unable to produce esters. This apparently maladaptive egg eating behaviour is also seen in queen-less colonies prior to the appearance of egg-laying workers, a period when esters are also absent. However, the indiscriminate egg eating behaviour stops with the appearance of ester-producing egg-laying workers. These observations suggest that esters are providing some contextual information, which affects the egg eating behaviour of the workers.     

Distribution and sources of phthalate esters in the topsoils of Beijing,China

Phthalate esters in the topsoil samples collected from Beijing were determined by derivatization and gas chromatography–mass spectrometry techniques. The results showed that diethyl phthalate (DEP), diisobutyl phthalate ester (DIBP), dibutyl phthalate ester (DBP), dibutyl (2-ethyl hexyl) phthalate (DEHP), and dimethyl phthalate (DMP) were found in the topsoils. The total concentrations of the five phthalate esters varied from 2.30 to 24.71 μg g^?1. According to phthalate esters (PAEs) control standards in soil of the USA, the standard exceeding rates of DMP, DBP, and DEHP were 100 %, 100 %, and 4.84 % in soils of Beijing, respectively. The rate of DBP exceeding soil remediation standard was 12.9 %. Overall, concentrations of PAEs in Beijing were at a high level in China. The concentrations of DBP, DEHP, and DIBP were high, and the total concentrations of all the phthalate esters were higher in the areas with intensive human activities than in the other areas, which may be related to the use of phthalate compounds (such as the use of plastic products). The total and individual concentrations of phthalate compounds were relatively low in the areas that used plastic films compared with other samples due to the diffusion of atmospheric motion, categories, and amounts of plastic products and other factors. The greatest contributor may be the usage amount of plastic products in people’s daily lives.     

海洋破囊壶菌△~5-延长酶和△~4-脱饱和酶在酿酒酵母中的共表达

二十二碳六烯酸(Docosahexaenoic acid,DHA C22:6n-3)是具有各种重要生理功能的高度不饱和脂肪酸.分别以质粒pYTFD5和pYFAD4为模板,扩增获得860 bp的△5-延长酶基因(elo5)和1 600 bp的△4-脱饱和酶基因(fad4).利用重叠延伸PCR构建elo5-fad4融合基因,Hind Ⅲ/Sph Ⅰ双酶切后连接到经同样处理过的pYES2.0载体,构建重组表达质粒pYEL05-FAD4.转化酿酒酵母尿嘧啶缺陷型菌株INVScl,通过缺少尿嘧啶的选择性培养基筛选阳性克隆子.添加外源脂肪酸C20:5底物.半乳糖诱导表达.气相色谱-质谱分析表明,重组酵母总脂肪酸中出现了DHA(二十二碳六烯酸,C22:6n-63)新产物,融合基因elo5-fad4在酿酒酵母中得到了表达.图7表1参18     

西南部分地区麻疯树种子油的理化性质及脂肪酸组成分析

从西南6个地区采集了麻疯树种子并分析比较了其生物学性状和种子油的理化性质及脂肪酸组成.所有样品的百粒重范围为41.80~71.39g,出仁率60.02%~81.43%,种仁含油率51.76%~57.93%,种子含油率31.07%~47.17%,不饱和脂肪酸含量74.89%~79.68%.其中永胜产麻疯树的种子品质最好,其出仁率为81.43%,种仁含油率57.93%,种子含油率47.17%,不饱和脂肪酸含量79.68%.攀枝花和宁南产麻疯树的种子品质次之.双柏和罗甸麻疯树的种子油酸值为0.81,在所有样品(0.81~9.46)中最低.对麻疯树种子及种子油性质的相关数据进行方差分析,结果表明,产地不同,麻疯树种子的生物学性质、种子油理化性质和脂肪酸组成都有一些差异.图2表3参18     

Metabolic relationships between fatty alcohol and fatty acid in the liver of Squalus acanthias

The high speed supernatant fraction of a homogenate of Squalus acanthias L. liver catalyses the oxidation of oleyl alcohol to oleic acid by an NAD-dependent process. Reduction of fatty acid to fatty alcohol could not be demonstrated. Liver lipids of S. acanthias contain about 60 and 40% of triglycerides and diacyl glyceryl ethers, respectively, with only traces of wax esters. Serum lipids contain 28, 15 and 26% of triglycerides, diacyl glyceryl ethers and wax esters, respectively. Cell-free fractions of S. acanthias liver catalyse the formation of wax esters by an ATP¹-dependent process. The bulk of wax ester synthesis occurs in the high-speed supernatant fraction of liver. The rate of formation of the ester bond in wax esters is comparable to the rate of synthesis of ester bonds in triglycerides, and greatly exceeds the rate of formation of the ether bond in diacyl glyceryl ethers. Results are discussed in terms of possible factors controlling the levels of neutral lipids in S. acanthias.     

Identification of calanoid copepod prey species via molecular detection of carbon fixation genes

Zooplankton and their phytoplankton prey form the basis of the marine food web, yet historically it has been difficult to discern species-specific trophic interactions. Molecular techniques provide opportunities to obtain taxonomic data where the traditional methodologies for gut content analysis lack resolution. The large subunit gene of RubisC/O, rbcL, was utilized as a molecular marker for the identification of prey species in calanoid copepods. Clone libraries were generated from DNA extracted from seawater and whole copepods during a transect cruise on the northern Gulf of Mexico shelf. Sequence data analysis provided evidence of diatoms, nanoplankton-sized chlorophytes, and cyanobacteria in DNA extracted from whole copepods. These data demonstrate that rbcL can be a useful marker for the identification of copepod phytoplankton prey. Combining the described approach with quantitative techniques such as quantitative PCR will provide opportunities for the assessment of species-specific predator–prey interactions.     

Extraction,chemical compositions,and cytotoxic activities of essential oils of Thevetia peruviana

Abstract

In this study, The essential oil of flowers, fruits, and leaves of Thevetia peruviana, which were collected in Vietnam, were being reported for the first time. The essential oil of flowers was extracted by different methods: n-hexane extraction, distillation water, and supercritical CO₂ extraction. The compositions of essential oil of different parts of Thevetia peruviana were analyzed by GC-FID and GC/MS systems. Major chemical compositions of essential oil were identified as monoterpenes, sesquiterpenes, terpenoids, and sterol. The activities of total essential oil extracts of the Thevetia peruviana exhibit inhibitory activities against five cancer cell lines.     

马莲鞍的化学成分研究

从马莲鞍根的乙醇提取物中分离得到3个具有细胞毒活性的化合物杠柳苷元(1)、杠柳苷元-3β-乙酸酯(2)和periplogenin3-O-β-D-glucopyranoside(3),此外,还得到了乌沙苷元(4)、α-香树脂醇乙酸酯(5)、α-香树脂醇十三酸酯(6)、乌苏酸(7)、9,19-环阿尔廷-25-烯-3β,24R-二醇(8)、9,19-环阿尔廷-25-烯-3β,24S-二醇(9)、环桉烯醇(10)、9,19-环阿尔廷-23E-烯-3β,25-二醇(11)、25-甲氧基-9,19-环阿尔廷-23E-烯-3β-醇(12)、11α,12α-epoxytaraxer-14-en-3β-ace-tate(13)、齐墩果酸(14)、β-谷甾醇(15)和β-胡萝卜苷(16).通过波谱学方法鉴定了它们的结构.通过X单晶衍射确证了13的结构.化合物1、2和3抗MDA-MB-231细胞株的GI50值分别为2.13×10-5molL-1,2.04×10-5molL-1和2.30×10-6molL-1.图2表5参17