Phytochemical screening, cytotoxicity and antibacterial activities of two Bangladeshi medicinal plants

The objectives of the present study were to investigate phytochemical screening and to assay cytotoxicity and antibacterial activities of ethanolic extracts of leaves of two medicinal plants, Aglaonema hookerianum Schott (Family: Araceae) and Lannea grandis Engl. (Family: Anacardiaceae) available in Bangladesh. The brine shrimp lethality bioassay showed that the ethanolic extracts of Aglaonema hookerianum and Lannea grandis possessed cytotoxic activities with LC50 5.25 (microg mL(-1)) and 5.75 (microg mL(-1)) and LC90 10.47 (microg mL(-1)) and 9.55 (microg mL(-1)), respectively. Two extracts obtained from leaves were examined for their antibacterial activities against some gram positive bacteria such as Bacillus subtilis, Bacillus megaterium and Staphylococcus aureus, also gram negative strains of Pseudomonas aeruginosa, Escherichia coli, Shigella dysenteriae, Salmonella typhi, Salmonella paratyphi and Vibrio cholerae. Agar disc diffusion method was applied to observe the antibacterial efficacy of the extracts. Results indicated that both plant extracts (500 microg disc(-1)) displayed antibacterial activity against all of the tested microorganisms. These results were also compared with the zones of inhibition produced by commercially available standard antibiotic, Amoxicillin at concentration of 10 microg disc(-1). Observed antibacterial properties of the ethanolic extract of Aglaonema hookerianum Schott and Lannea grandis Engl. showed that both plants might be useful sources for the development of new potent antibacterial agents.     

Characteristics, efficacy and safety testing of standardized extract of Croton tiglium seed from Indonesia as laxative material

Identification and taxonomy analysis conducted at Herbarium Bogoriense at Research Centre for Biology, Indonesian Institute of Sciences Bogor. The name of the plant was C. tiglium L. The result of analysis on C. tiglium, ethanol extract as laxative material using the intestinal transit method showed treatment group that received dosage 0.06 mL/30 g b.wt. (72.5%) was significantly different compared to negative control (48.4%) or positive control (50.6%) which showed the weak effect as laxative at the dosage of 0.75 mL/30 g b.wt. It showed that ethanol extract of C. tiglium seed at dosage 0.06 mL/30 g is effective as laxative. The test result of the treatment using dosage 0.06, 0.04, 0.026 and 0.07 mL/28 g of body weight showed the mice population response 100, 60, 40 and 40% consecutively. The Thompson and Weil analysis result showed the ED50 was at 0.027 mL or equal to 639,5 g kg(-1) b.wt. The LD50 was at 0.0707 equals with 1674,5 mg kg(-1) b.wt. Safety limit is the range of dosage that cause the lethal effect and the dosage that gives the intended effect. The safety limit is represented by the comparison of LD50/ED50. Calculation result that the extract safety limit was LD50/ED50 = 0.0707/0.027 = 2.7.     

Study of some factors of conservation of pollens of two plant species (Callistemon rigidus and Hymenocardia acida) of bee flora of Adamawa (Cameroon)

To contribute to the preservation of the bee flora of Adamawa, a study to determine the optimal conditions for preservation of Callistemon rigidus and Hymenocardia acida pollens, two endangered bee species, was conducted from March 2006 to March 2007 in this region. The study began by anthers collection at the experimental site and they were brought to the laboratory where fresh pollens are collected and undergo in vitro germination and storage tests. These tests have required the installation of two solidified media culture: Brewbaker and Kwack (BK) and Heslop-Harrison (HH) media to evaluate pollens germination under the influence of some physiological factors and assess the influence of storage at + 10 and -20 degrees C with and without initial drying. The results show that sucrose concentrations of 10 and 15% on BK medium has produced respectively 60.69 +/- 3.1 and 04.49 +/- 0.21% as the highest values of germination percentage in Callistemon rigidus and Hymenocardia acida. Temperatures of 30 and 25 degrees C which produced 60.69 +/- 2.53 and 04.25 +/- 0.29% of germination and pH 5 with 55.14 +/- 4.14% and 6.8 with 04.54 +/- 0.6% were respectively favourable in the same order for the germination of both species of pollens. Time for a week of drying allowed the extension of storage time of both species of pollens as from +10 to -20 degrees C. The Callistemon rigidus pollens were generally more tolerant to the storage at-20 degrees C showing the critical period of storage exceeding 22 weeks while those of Hymenocardia acida were less tolerant to both temperatures with most critical period of storage established to 8 weeks.     

Free radical scavenging activity of selected medicinal plants of Eastern Botswana

Water and methanol extracts from roots of Ozoroa paniculosa (Anarcardiaceae); seeds of Colophospermum mopane (Caesalpiniaceae) and Cucumis metuliferus (Cucurbitaceae) ripe fruits were assessed for in vitro antioxidant activity. Free radical scavenging activity was measured spectrophotometrically as maximum fading power of DPPH at 525 nm. Water and methanol extracts of Ozoroa paniculosa exhibited higher scavenging potency than extracts of either Colophospermum mopane or Cucumis metuliferus at all tested concentrations. None of the extracts from Cucumis metuliferus exhibited any recognizable free radical scavenging activity. Above 50 microg mL(-1) both water and methanol extracts of Ozoroa paniculosa exhibited 91% scavenging activity similar to the control compounds L-ascorbic acid (91%) and (-) epicatechin (92%). Between 50-100 microg mL(-1), water and methanol extracts of Colophospermum mopane exhibited scavenging potency of < or = 70%. However, above 100 microg mL(-1), both water and methanolic extracts of C. mopane exhibited scavenging activity > 70%. Chloroform extracts of all the tested plants showed poor scavenging activity (< 30%). The order of scavenging potency for the tested samples was as follows: L-ascorbic acid > or = epicatechin > O. paniculosa (methanolic extract) > O. paniculosa (water extract) > O. paniculosa (ethylacetate extract) > C. mopane (methanolic extract) > C. mopane (water extract) > all extracts of C. metuliferus. These findings lend credence to the use of these plants as anti-inflammatory and antioxidant agents in folk medicine.     

Toxicity and repellence of aqueous and ethanolic extracts from Schinus molle on elm leaf beetle Xanthogaleruca luteola

Extracts of leaves of Schinus molle Rev L. (Anacardiaceae) obtained with water or ethanol as solvents were evaluated in the laboratory for their insecticidal effect on adults of the elm leaf beetle, Xanthogaleruca luteola Müller (Coleoptera: Chrysomelidae), at 2.5, 3.0, 4.3, and 5.6% w/v for the aqueous extracts and, 2.0, 2.5, 3.5, 4.3, and 4.7% w/v for the ethanol extracts. The extracts were applied onto leaves of elm trees (Ulmus sp., Ulmaceae) to observe the feeding of adults, and later their effectiveness and to obtain the LC₅₀. Both extracts were effective and caused mortalities greater than 97% with the ethanol extract at the two highest concentrations (4.3 and 4.7% w/v), and near 27% with water at 4.3 and 5.6% w/v. The LC₅₀ of the ethanol extract, calculated through Probit analysis, was 1.88% w/v on the 2nd day, lower than the LC₅₀ of 8.52% w/v on the 4^th day achieved by the aqueous extract. Additionally, the antifeeding effect of both extracts on adults was determined. The aqueous extract inhibited feeding completely (100%), whereas the ethanol extract did not cause any antifeeding effect.     

Optimization of process parameters influencing the submerged fermentation of extracellular lipases from Pseudomonas aeruginosa, candida albicans and Aspergillus flavus

The present study was aimed at optimization, production and partial purification of lipases from Pseudomonas aeruginosa, Candida albicans and Aspergillus flavus. Various nutritional and physical parameters affecting lipase production such as carbon and nitrogen supplements, pH, temperature, agitation speed and incubation time were studied. Refined sunflower oil (1% v/v) and tryptone at a pH of 6.2 favored maximum lipase production in Pseudomonas at 30 degrees C and 150 rpm, when incubated for 5 days. In C. albicans refined sunflower oil (3% v/v) and peptone resulted in maximum lipase production at pH 5.2, 30 degrees C and 150 rpm, when incubated for 5 days. In A. flavus coconut oil (3% v/v) and peptone yielded maximum lipase at pH 6.2, 37 degrees C, 200 rpm after an incubation period of 5 days. The lipases were partially purified by ammonium sulphate precipitation and dialysis. In P. aeruginosa enzyme activity of the dialyzed fraction was found to be 400 U mL-' and for C. albicans 410 U mL(-1). The dialysed lipase fraction from A. flavus demonstrated an activity of 460 U mL(-1). The apparent molecular weights of the dialyzed lipases were determined by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE). The dialyzed lipase fraction obtained from P. aeruginosa revealed molecular weights of 47, 49 and 51 kDa, whereas, lipases from C. albicans and A. flavus demonstrated 3 bands (16.5, 27 and 51 kDa) and one band (47 kDa), respectively. These extracellular lipases may find wide industrial applications.     

Influence of sprouting and elicitation on phenolic acids profile and antioxidant activity of wheat seedlings

Influence of germination and elicitation on nutraceutical potential of sprouted wheat was investigated. The seeds of three Polish winter wheat cultivars were elicited with 0.1% (w/v) of Saccacharomyces cerevisiae (SC) extract, 0.1% (v/v) Salix daphnoides (SD) bark extract and their combinations (SC/SD 1:1). Seeds were germinated for 4 day at 20 °C in darkness. For phenolic acids determination LC-ESI-MS/MS analysis was used. Antiradical ability, chelating power, reducing power and ability to prevent lipids against oxidation were determined. Bioaccessibility of antioxidative compounds was estimated using in vitro digestion method. Eleven phenolic acids (protocatechuic, p-hydroxybenzoic, vanillic, caffeic, syryngic, p-coumaric, cis- and trans-ferulic, salicylic, trans- and cis-synapinic) were identified. Sprouting increased p-hydroxybenzoic, syryngic and p-coumaric acids level. The most effective elicitor for improving antioxidant activity of potentially bioaccessible phytochemicals was SD. Especially high effect was obtained for antiradical activity, chelating power and ability to lipid prevention.     

Marine-Derived Quorum-Sensing Inhibitory Activities Enhance the Antibacterial Efficacy of Tobramycin against Pseudomonas aeruginosa

Bacterial epiphytes isolated from marine eukaryotes were screened for the production of quorum sensing inhibitory compounds (QSIs). Marine isolate KS8, identified as a Pseudoalteromonas sp., was found to display strong quorum sensing inhibitory (QSI) activity against acyl homoserine lactone (AHL)-based reporter strains Chromobacterium violaceum ATCC 12472 and CV026. KS8 supernatant significantly reduced biofilm biomass during biofilm formation (−63%) and in pre-established, mature P. aeruginosa PAO1 biofilms (−33%). KS8 supernatant also caused a 0.97-log reduction (−89%) and a 2-log reduction (−99%) in PAO1 biofilm viable counts in the biofilm formation assay and the biofilm eradication assay respectively. The crude organic extract of KS8 had a minimum inhibitory concentration (MIC) of 2 mg/mL against PAO1 but no minimum bactericidal concentration (MBC) was observed over the concentration range tested (MBC > 16 mg/mL). Sub-MIC concentrations (1 mg/mL) of KS8 crude organic extract significantly reduced the quorum sensing (QS)-dependent production of both pyoverdin and pyocyanin in P. aeruginosa PAO1 without affecting growth. A combinatorial approach using tobramycin and the crude organic extract at 1 mg/mL against planktonic P. aeruginosa PAO1 was found to increase the efficacy of tobramycin ten-fold, decreasing the MIC from 0.75 to 0.075 µg/mL. These data support the validity of approaches combining conventional antibiotic therapy with non-antibiotic compounds to improve the efficacy of current treatments.     

Hypolipidaemic effects of Ballota undulata in rabbits

The aim of to study the effect of Ballota undulata (70% EtOH) extract on lipid profile on Rabbits. The plant extract was orally administered to the atherogenic rabbits (atherogenic diet + cholesterol powder supplement 400 mg/kg/body weight/day dissolved in 5 mL coconut oil) at dose of 1.2 g kg(-1) body weight/day. During the overall period of the experiment blood was collected and serum was analyzed for lipid profile. Animals were sacrificed; the heart and the liver were collected and kept at -20 degrees C until assayed. Biochemical analysis of blood serum and tissue (liver and heart muscle) level were made for cholesterol, phospholipids and triglycerides. In addition blood serum was analyzed further for HDL-Cholesterol. All the results were statistically analyzed using students t-test. Hypolipidaemic nature of Ballota undulata (70% EtOH) extract was studied in hyperlipidaemic Rabbits. The increased cholesterol levels were brought to normal by administration of Ballota undulata. Serum cholesterol levels dropped from 940.7 to 230.41 (75.55%) and further to 119.2 (87.32%) by the end of the experiment. Similarly, phospholipids and triglycerides levels were observed to be also reduced. The tissues lipids profiles of liver and heart muscle showed similar changes in those noticed in serum lipids. Ballota undulata possesses active hypolipidaemic constituents.     

火炬树叶浸提液对小麦根尖细胞的遗传毒性

为了解入侵植物火炬树对小麦根尖细胞的遗传毒性,用不同浓度的火炬树叶浸提液(0.5‰、1‰、2‰、5‰、1%、3%、5%、7%、10%)处理萌发期的小麦根尖6、12、24和36h,观察其有丝分裂的变化和染色体行为的异常。结果表明,除低浓度(<2‰)浸提液外,火炬树叶浸提液对小麦根尖细胞产生了明显的毒害作用。随着处理浓度的升高和处理时间的延长,有丝分裂指数逐渐降低,同时诱发了微核、多核和染色体畸变的出现,畸变率随处理浓度的提高和处理时间的延长而逐渐升高。     

Total Phenolic Levels,In Vitro Antioxidant Properties,and Fatty Acid Profile of Two Microalgae,Tetraselmis marina Strain IMA043 and Naviculoid Diatom Strain IMA053, Isolated from the North Adriatic Sea

This work studied the potential biotechnological applications of a naviculoid diatom (IMA053) and a green microalga (Tetraselmis marina IMA043) isolated from the North Adriatic Sea. Water, methanol, and dichloromethane (DCM) extracts were prepared from microalgae biomass and evaluated for total phenolic content (TPC) and in vitro antioxidant properties. Biomass was profiled for fatty acid methyl esters (FAME) composition. The DCM extracts had the highest levels of total phenolics, with values of 40.58 and 86.14 mg GAE/g dry weight (DW in IMA053 and IMA043, respectively). The DCM extracts had a higher radical scavenging activity (RSA) than the water and methanol ones, especially those from IMA043, with RSAs of 99.65% toward 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid)diammonium salt (ABTS) at 10 mg/mL, and of 103.43% against 2,2-diphenyl-1-picrylhydrazyl (DPPH) at 5 mg/mL. The DCM extract of IMA053 displayed relevant copper chelating properties (67.48% at 10 mg/mL), while the highest iron chelating activity was observed in the water extract of the same species (92.05% at 10 mg/mL). Both strains presented a high proportion of saturated (SFA) and monounsaturated (MUFA) fatty acids. The results suggested that these microalgae could be further explored as sources of natural antioxidants for the pharmaceutical and food industry and as feedstock for biofuel production.     

Optimization of temperature, moisture content and inoculum size in solid state fermentation to enhance mannanase production by Aspergillus terreus SUK-1 using RSM

Optimization of three parameters, temperature (25-35 degrees C), moisture content (40% (w/v)-60% (w/v) and inoculum sizes (5% (w/v)-15% (w/v) were investigated and optimized by Response Surface Methodology (RSM) for optimal mannanase production by Aspergillus terreus SUK-1. A second order polynomial equation was fitted and the optimum condition was established. The result showed that the moisture content was a critical factor in terms of its effect on mannanase. The optimum condition for mannanase production was predicted at 42.86% (w/v) initial moisture (31 C) temperature and 5.5% (w/v) inoculum size. The predicted optimal parameter were tested in the laboratory and the mannanase activity 45.12 IU mL-1 were recorded to be closed to the predicted value (44.80 IU mL-1). Under the optimized SSF condition (31 degrees C, 42.86% moisture content (w/v) and 5.5% inoculum size (w/v)), the maximum mannanase production was to prevail about 45.12 IU mL-1 compare to before optimized (30 degrees C, 50% moisture content (w/v) and 10% inoculum size (w/v)) was only 34.42 IU mL-1.     

Antispasmodic effect of Piper nigrum fruit hot water extract on rat ileum

The aim of this study was to investigate the effect of black pepper fruit hot water extract (BPE) on rat ileum contractility and the mechanism(s) of its action. The extract was prepared by adding black pepper powder to boiling distilled water followed by evaporated the solvent. Ileum was dissected from male adult rat (Wistar) and in Tyrode solution the tissue contractions were recorded by an isotonic transducer under 1 g tension. The cumulative concentrations of the BPE (0.0625-1 mg mL(-1)) reduced the ileum contractions induced by KCl (60 mM) or carbachol (10 microM) concentration dependently (p<0.001). In Ca2+-free Tyrode solution with high potassium (60 mM), BPE, (0.0625-1 mg mL(-1)) attenuated the contractions induced by cumulative concentrations of CaCl2 (0.225-2.7 mM) concentration dependently (ANOVA, p<0.05). The incubation of the tissue preparation (20 or 30 min) with L-NAME (100 microM), naloxone (1 microM) or propranolol (1 microM) did not reduce the extract antispasmodic effect on KCl-induced ileum contraction. The extract spasmolytic effect was attenuated neither by glibenclamide (10 microM) nor by tetraethylammonium (1 mM). Present results suggest that the spasmolytic effect of the extract on rat ileum was possibly mediated via Ca2+ influx.     

猴耳环多酚的大孔树脂纯化工艺及其组分分析

建立并优化猴耳环多酚的纯化工艺并对其组分进行定性分析。本研究以猴耳环多酚粗提物为原料,以吸附及解吸附效果筛选了最优大孔树脂,再以吸附、解吸附和纯度为评价指标,考察各工艺参数对AB-8树脂纯化多酚的影响,最后采用超高效液相色谱-四级杆-飞行时间串联质谱（UPLC-Q-TOF-MS）法进行多酚组成定性分析。结果表明：优选 AB-8树脂,粗提物以质量浓度3 mg/mL、流速1 mL/min上样10 BV（柱体积：1 BV=10 mL）,水洗后,用60%乙醇5 BV以1 mL/min的流速洗脱。在此工艺条件下,多酚纯度达到58.64%。UPLC-Q-TOF-MS定性分析了纯化后猴耳环多酚14种组分。建立的猴耳环多酚的纯化工艺稳定可行,实现了其组分定性分析,为进一步研究提供了依据。     

Bioactive properties and chemical constituents of methanolic extract and its fractions from Jatropha curcas oil

The present work is designed to evaluate the bioactive properties of the crude methanolic extract of Jatropha curcas oil and its solvent fractions. The crude methanolic extract obtained was fractionated using a hydrophilic lipophilic balanced (HLB) cartridge and then eluted with different solvents in the order of hexane (F1), dichloromethane (F2), chloroform (F3), ethyl acetate (F4) and methanol (F5), respectively. Total phenolic content of the crude methanolic extract and its fractions was in the range of 0.19-4.5 mg/g as gallic acid equivalent. Antioxidant activity of the crude methanolic extract and its fractions were determined by two complementary test methods, namely, phenanthroline method and 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging method. All samples demonstrated weak antioxidant activity (150-851 μmol Fe/100 g of the extract and IC₅₀ of 1.05-13.5 mg/mL). When compared to butylated hydroxytoluene (BHT), a reference synthetic antioxidant, both showed weaker antioxidative potential. The evaluation of antimicrobial activity of the extracts was performed using a disc diffusion method and a micro-well dilution method against six economic plant disease bacteria. The results showed that all extracts possessed strong to moderate antibacterial activity with varying degrees of growth inhibition against the test bacteria. The minimum inhibitory concentrations (MIC) were in the range of 14.92-428.6 μg/mL. In addition, the chemical constituents in each fraction of the extract were subjected to analyze by gas chromatography-mass spectrometry (GC-MS). The eleven constituents were identified. Among them, 2,4-di-tert-butylphenol, methyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate and linoleic acid may be the main cause of its strong antibacterial activity. Therefore, this oil present in the methanolic extract had great potential as effective antibacterial sources.     

Vasorelaxant and hypotensive effects of Allium cepa peel hydroalcoholic extract in rat

The aim of present study was to investigate the effect of onion (Allium cepa) peel hydroalcoholic extract (OPE) on rat hypertension induced by high-fructose diet and aorta contractility. The OPE was prepared by maceration method using 70% ethanol. The thoracic aorta from male adult rat (Wistar) was dissected and suspended in Krebs-Henseleit solution under 1 g resting tension. Tissue preparation was contracted by KCl (80 mM) or phenylephrine (Phe, 1 microM) and then the extract was applied cumulatively (0.0625-2 mg mL(-1)). Hypertension was induced in negative control and three groups of rats by adding fructose (10% WN/V) in drinking water for 6 weeks but control group received tap water. Hypertensive groups received saline or OPE at 200, 400 and 800 mg kg(-1) daily for last 3 weeks by gavage. Results showed that OPE reduces aorta contractions induced by KCl or Phe in a concentration-dependent manner (p < 0.001). Removing aorta endothelium did not attenuate the OPE activity. Inhibition of nitric oxide, cGMP and prostaglandin synthesis by L-NAME (100 microM), methylene blue (10 microM) and indomethacin (10 microM), respectively, did not attenuate OPE activity. Atropine abolished ACh-induced relaxation in Phe precontracted aorta but not the OPE-induced relaxation. Although the extract did not change heart rate but after 3 weeks reduced the hypertension induced by fructose (p < 0.001). Present results indicated that OPE reduces aortic contractions possibly via inhibition of calcium influx but without involving NO, cGMP, endothelium and prostaglandins. The OPE hypotensive effect could be due to extract quercetin content, antioxidant activity and inhibiting vascular smooth muscle cells Ca2+ influx.     

鱼藤根提取物对假眼小绿叶蝉的防治

进行了鱼藤根提取物对茶树害虫假眼小绿叶蝉的室内生物活性和田间小区防治试验。结果表明,室内条件下,鱼藤根提取物对假眼小绿叶蝉具有拒食、触杀和毒杀作用,触杀作用很强,不具内吸活性。田间条件下,鱼藤根提取物的药效与毗虫味和阿克泰的防效相当,40 ug血L的鱼藤根提取物浓度即可满足田间防治假眼小绿叶蝉用药,药后5d的防效可达97.24%,鱼藤根提取物与毗虫咻混配的防效与毗虫琳单用的防效相当。     

Suppression of rice sheath blight disease using a heat stable culture filtrate from Streptomyces philanthi RM-1-138

Streptomyces philanthi RM-1-138, isolated from the rhizosphere soil of chili pepper in southern Thailand, was investigated for its antagonistic activity against phytopathogenic fungi. In dual culture on glucose yeast-malt extract (GYM) agar plates, this strain suppressed the mycelial growth of all seven plant pathogenic fungi tested (Rhizoctonia solani PTRRC-9, Pyricularia grisea PTRRC-18, Colletotrichum gloeosporioides NBCRSR-3, Colletotrichum capcisi NBCRSR-15, Ganoderma boninense NBCRSR-26, Fusarium fujikuroi PTRRC-16 and Bipolaris oryzae PTRRC-36) with an 82.2–89.2% inhibition and that was most pronounced on R. solani PTRRC-9. Heat treatment of the culture filtrate from growing R. solani PTRRC-9 at 40 °C, 60 °C, 80 °C, and 100 °C for 30 min and 121 °C for 15 min had no negative effect on the inhibitory activity against R. solani PTRRC-9 tested on both solid and liquid culture. The effective dose (>80% inhibition) of culture filtrate in liquid culture was at 5.0% (v/v) while it was at 10% (v/v) on the solid medium. This effectiveness was similar to those of the four chemical fungicides tested. The effect of S. philanthi RM-1-138 against R. solani PTRRC-9 was investigated using SEM and TEM. The compounds produced by S. philanthi RM-1-138 induced alterations to the cell-wall structure of R. solani PTRRC-9, that resulted in the loss of cytoplasm materials by partial lysis. The greenhouse experiment revealed that using either the culture filtrate or the autoclaved culture filtrate from S. philanthi RM-1-138 effectively suppressed rice sheath blight disease by up to 65.6 and 60.8%, respectively.     

大叶丁香丙酮提取物对皮氏叶螨的毒力及代谢酶活性的影响

采用叶片浸渍法和分光光度法研究了大叶丁香(Eugenia caryophyllata Thunb)丙酮提取物对皮氏叶螨(Tetranychus piercei McGrvgor)的毒力及其代谢酶活性的影响。试验结果表明:大叶丁香丙酮提取物对皮氏叶螨具有良好的毒杀作用,处理后72 h LC50值为4.31 mg/mLL;其13.33 mg/mL对皮氏叶螨的48 h和72 h校正死亡率分别为81.82％和95.35％,其6.67 mg/mL对皮氏叶螨的72 h校正死亡率为75.58％;大叶丁香丙酮提取物在5.0、4.0、3.0、2.0、1.0 μg/mL的质量浓度下,对皮氏叶螨酯酶、羧酸酯酶、碱性磷酸酯酶的活性均有抑制作用,作用大小均随处理浓度的增加而增强,但大叶丁香丙酮提取物对酸性磷酸酯酶则有一定程度的激活作用。      

Large-scale Separation of Gliadins and their Bread-making quality

A separation procedure was developed using S-Sepharose cation exchange chromatography under mildly acidic conditions to establish the effect of 70% (v/v) ethanol extractable proteins on bread-making quality. The separation of a 70% (v/v) ethanol extract of gluten was scaled up successfully from 3 mg to 60 g protein. The use of denaturing and dissociating agents, such as urea or guanidine-HCl, was unnecessary. The pilot-scale fractionation yielded five fractions that were bound to, and eluted from, the column. The fractions differed in gliadin composition as evidenced by lactate-PAGE, SDS-PAGE and RP-HPLC. The fractions were virtually free of lipid. Isolated fractions were evaluated for their effects on bread-making quality using a pan loaf baking test. The unbound fraction (D) contained lipids, mainly mono- and digalactosyldiacylglycerols, and it increased (cv. Obelisk flour) or decreased (cv. Camp Rémy flour) loaf volume at additions of up to 0·5% on flour weight. At higher levels of addition it had a strong negative effect on loaf volume. The unfractionated extract (containing some fraction D) or the recombined fractions improved loaf volume. All individual fractions improved loaf volume, but to different extents. For four out of five fractions the improvement corresponded to the statistical prediction of loaf volume by RP-HPLC gliadin peak areas.