响应面优化伏毛铁棒锤总生物碱微波辅助提取工艺

目的：优化微波辅助提取伏毛铁棒锤总生物碱工艺，并比较不同产地伏毛铁棒锤中总生物碱含量。方法：以单因素试验为基础，结合响应面法，以总生物碱的含量为评价指标，考察温度、料液比、时间和体积分数对提取得率的影响。结果：最佳微波辅助提取工艺参数（条件）为：温度48℃，料液比1∶19(g/mL)，时间12 min，甲醇体积分数39%。结论：该提取方法稳定可靠，操作简便，可用于优化伏毛铁棒锤总生物碱提取工艺。比较不同地区伏毛铁棒锤中总生物碱含量，贵南县伏毛铁棒锤总生物碱含量最高，为0.290%。     

魔芋飞粉总生物碱的提取工艺研究

目的:研究魔芋飞粉总生物碱提取的最佳条件。方法:以盐酸小檗碱为对照,采用酸性染料比色法测定总生物碱含量;通过单因素试验,考察乙醇浓度、料液比、pH、温度、时间、提取次数等对总生物碱提取效果的影响;通过正交实验确定最佳工艺条件。结果:影响魔芋飞粉总生物碱提取效果的因素的主次顺序是:pH>乙醇浓度>料液比>提取温度,其中pH对魔芋飞粉总生物碱提取效果影响显著(P<0.05)。魔芋飞粉总生物碱最佳提取工艺条件为:料液比为1:15,温度为50℃,乙醇浓度为70%,pH值为1。在此工艺条件下,总生物碱提取量可达到89.79mg/100g。结论:本文建立的优化方法简单可行,可为魔芋飞粉的总生物碱提取工业提供理论依据。     

微波辅助提取荷叶总生物碱的工艺研究

本文通过采用单因素试验和正交试验考察不同因素对荷叶总生物碱提取量的影响,从而探讨微波辅助提取荷叶中总生物碱的最佳工艺.结果表明:微波辅助提取荷叶总生物碱的最佳条件为:pH 2.5 HCI、微波765W辐照2.5 min、固液比1:40、浸提3 h,荷叶总生物碱提取量为175.95μg/g,与热回流提取6 h、索氏提取10.5h的结果接近.因此微波辅助提取技术应用于荷叶总生物碱的提取,具有省时、高效、节能等优点.     

秦巴山区野生绞股蓝枝叶中多糖提取工艺的优化

采用微波辅助法提取秦巴山区野生绞股蓝枝叶中的多糖,用苯酚-硫酸法测定多糖含量。选取酸碱度、料液比、微波温度和微波时间作为提取因素,通过单因素实验和L9(34)正交试验来优化绞股蓝枝叶中的多糖提取工艺。结果表明,野生绞股蓝枝叶中多糖的最佳提取条件为pH 9,料液比1∶20,微波温度60℃,微波处理时间15min,在此工艺条件下提取量高达40.10mg.g-1。     

鹰嘴豆铁蛋白提取工艺优化研究

本研究以鹰嘴豆为原料,研究了缓冲液种类、缓冲液pH值、料液比、盐析盐种类、盐浓度等因素对鹰嘴豆铁蛋白提取率、总蛋白提取率及干重的影响。在单因素实验的基础上,以L9(34)正交实验方法优化鹰嘴豆铁蛋白提取工艺。结果表明:各因素对鹰嘴豆铁蛋白提取率的影响顺序依次为:料液比盐浓度温度pH。最优提取工艺为:料液比1∶4,浓度为70 mmol/L MgCl2盐析,温度50℃,KH2PO4-NaOH缓冲液pH 7.5,最优提取率为0.002643%。     

葡萄叶中总黄酮的提取工艺研究

目的：从葡萄叶中提取总黄酮。方法：采用正交试验法研究葡萄叶总黄酮的最佳提取工艺条件,考察了乙醇浓度、回流温度、回流时间及料液比四因素对葡萄叶总黄酮提取率的影响。结果：确立了葡萄叶总黄酮最佳提取条件为：45％的乙醇为溶剂、液料比为1：40、提取温度为60％、提取时间2h,在最佳工艺条件下葡萄叶总黄酮含量为5．329mg／g。     

正交试验法优选三七茎叶中总黄酮的提取工艺

目的：从三七茎叶中提取总黄酮。方法：采用正交试验法研究三七茎叶总黄酮的提取工艺,考察了浸提用水的pH值、浸提温度、浸提时间、浸提次数、液料比五个因素对三七茎叶总黄酮提取率的影响。结果：确立了三七茎叶总黄酮最佳提取条件为：用pH10的稀碱水作溶剂,液料比30：1,浸提温度为80℃,回流提取2次,提取时间为每次40min。     

微波辅助提取灰树花多糖工艺研究

采用提取时间、微波功率、液料比的单因素试验和正交试验法优化微波辅助提取灰树花多糖条件.结果表明,以净多糖得率为指标,影响微波辅助提取灰树花多糖的主次因素为:提取时间＞微波功率＞液料比,并且提取时间和微波功率的影响达到了极显著水平.灰树花多糖最佳提取工艺条件为:提取时间为10 min,微波功率为80%(全功率为800 W),液料比为25∶1.创立了一种用苯酚-硫酸法测定多糖时排除蛋白质干扰的方法.     

Box-Behnken响应面法优化超声波辅助提取辣木叶多酚工艺研究

采用超声波辅助提取辣木Moringa oleifera叶多酚,通过单因素试验考察乙醇浓度、料液比、提取时间和提取次数对辣木叶多酚得率的影响,进一步利用四因素三水平Box-Behnken组合设计响应面试验对提取工艺参数进行优化。结果表明,超声波辅助提取辣木叶多酚的最佳工艺条件为乙醇浓度62%、料液比1∶30(W/V)、提取时间30 min、提取3次,在此条件下辣木叶多酚得率为27.32 mg·g-1,所得回归模型拟合情况良好。     

正交设计优选橙皮苷提取工艺研究

采用碱-醇提酸沉法提取陈皮中橙皮苷,首先针对提取温度、提取时间、pH值、碱液料液比、醇液料液比、提取次数等因素对提取率的影响进行单因素实验考察,并进一步利用正交实验对橙皮苷的提取工艺进行优化。得到最优浸提条件为:陈皮粉与食用乙醇料液比为1:10、与0.5%NaOH溶液料液比1:10,浸提温度70℃,浸提时间4 h,提取率最高。     

六种藓类植物茎的比较解剖学研究

通过对6种藓类植物,即褶叶青藓(Brachythecium salebrosum(Web.et Mohr.)B.S.G.)、湿地匐灯藓(Plagiomnium acutum(Lindb.)Kop.)、侧枝匐灯藓(Plagiomnium maximoviczii(Lindb.)Kop.)、大凤尾藓(Fissidensnobilis Griff.)、大羽藓(Thuidium cymbifolium(Doz.et Molk.)B.S.G.)和大灰藓(Hypnum plumaeforme Wils.)嫩茎和老茎的石蜡切片和显微观察发现,同一藓类植株的嫩茎和老茎,茎结构稳定,不同种藓类植物茎横切面具有不同特征.植物体茎横切面形状、表层细胞的层数、细胞大小和细胞壁厚薄、皮层细胞大小和形状、中轴的有无以及比例等特征可以作为藓类植物的分科分类依据之一.     

Photoregulation of seed germination of wild-type and of an aurea-mutant of tomato

Seed germination of an aurea mutant of tomato ( Lycopersicon esculentum Mill.) is promoted by continuous irradiation with red, far-red or long-wavelength far-red (758 nm) light as well as by cyclic irradiations (5 min red or 5 min far-red/25 min darkness). Far-red light applied immediately after each red does not change the germination behaviour. Seed germination of the isogenic wild-type, cv. UC-105, is promoted by continuous and cyclic red light while it is inhibited by continuous and cyclic far-red light and by continious 758 nm irradiation. Far-red irradiation reverses almost completely the promoting effect of red light. The promoting effect (in the aurea mutant) and the inhibitory effect (in the wild-type) of continuous far-red light do not show photon fluence rate dependency above 20 nmol m⁻² s⁻¹. It is concluded that phytochrome controls tomato seed germination throgh low energy responses in both the wild type and the au mutant. The promoting effect of continuous and cyclic far-red light in the au mutant can be attributed to a greater sensitivity to P_fr.     

Cause of Senescence of Nine Sorts of Flowers

The levels of endogenous phytohormones and respiratory rate in nine sorts of flowers such as Cymbidium faberi Rolfe, Nopalxochia ackermannii Kunth and others were investigated both at full bloom and senescence and meanwhile the effect of exogenous phytohormones on prolonging the blossoms and promoting ethylene production were tested. There is a high content of endogenous ethylene in all the long-lived flowere, about 3–16 folds higer than the short-lived ones. There is a high level of ABA at full blooming flowers of short-lived flowers, in which there is no or only some cytokinins in it, but the ratio of CTK (6BA+zeatin)/ABA is smaller(l.7). The endogenous ABA reached a much higher level at senescence in all nine sorts of flowers, so it is reasonable to consider that it is ABA which plays an important role of regulation in controlling flower's senescence. There is a much higher level of GA3 and zeatin in the long-lived flowers which is not demonstrated in the shortlived ones. The respiratory rate is one of the factors controtling the longevity of flowers, but it does not play a decided role. Application of 6BA and zeatin prolongs distinctly orchid’s longevity, however exogenous IAA through the promotive action on ethylene production, evidently extends the longevity of the flowers of the Nopalxochia ackermannii Kunth.     

龙胆科药用植物化学成分的研究现状

龙胆科植物在我国的分布范围很广,且多数为药用植物,其多数种属的药用植物,至今其化学成分尚未被系统研究。综述了目前龙胆科药用植物的化学成分的研究现状及一般提取方法,对近年来发现的环烯醚萜及裂环烯醚萜类化合物进行了总结,为本科药用植物的更深入研究提供了参考。     

Interconnection of parameters of regulation system of lipid peroxidation and of morphophysiological parameters of mouse liver

A complex analysis of seasonal fluctuations of the mean group parameters of the system of regulation of lipid peroxidation has been performed in liver of Balb/c mice. Association of lipid characteristics and morphophysiological parameters is studied in the Balb/c mouse liver. An inter-connection is revealed between the liver index and the amount of lysoforms of phospholipids, the scale and character of the interconnection differing essentially depending on proportion of phos-phatidylcholine in mouse liver phospholipids.     

The effects of glutamine of the maintenance of embryogenic cultures of Cryptomeria japonica

Summary Embryogenic tissues of sugi (Cryptomeria japonica) were induced on a modified Campbell and Durzan (CD) medium containing 1 μM 2,4-dichlorophenoxyacetic acid (2,4-D) and 600 mg l⁻¹ glutamine, and subcultured in the medium of the same composition for over 1 yr. This resulted in a mixed culture of embryogenic and non-embryogenic cells. When embryogenic cells were isolated and cultured independently, their capacity to form embryogenic aggregates was lost. Thus, the non-embryogenic cells present within a mixed culture system were essential to the formation of embryogenic aggregates. When embryogenic tissues were isolated and cultured independently on a high glutamine-containing (2400 mg l⁻¹) medium, dry weights and endogenous levels of glutamine increased, and the tissue could generate a large number of embryogenic aggregates. Amino acid analysis of embryogenic and non-embryogenic cells from the maintenance culture indicated a higher level of glutamine was present in the latter. The high endogenous level of glutamine in the non-embryogenic portion of mixed cell masses may be the supplier of glutamine for maintaining the embryogenic property of the tissues.     

Specificity of action of piperidylcholine derivatives as substrates of cholinesterases of various origin

The review deals with study of enzymologic properties of a novel highly specific acetylcholinesterase substrate, N-(β-acetoxyethyl) piperidinium iodomethylate (“piperidylcholine”), and its 30 derivatives that were tested as effectors of cholinesterases of mammals and various species of Pacific squids. It was proven for the first time that responsible for specificity of action was structure of cyclic ammonium grouping of the alcohol part of molecule of the ester substrate. Analysis of specificity is performed based on enzymatic hydrolysis parameters—activity of catalytic center of cholinesterases and bimolecular constant of the reaction rate that are determined at optimal and low substrate concentrations. Among the specially synthesized group of thioester compounds there is revealed one more highly specific acetylcholinesterase substrate—N-(β-acetoxyethyl) piperidinium.     

Physiological characteristics of various species of strains of carboxydobacteria

Seven strains of aerobic carbon monoxide-oxidizing bacteria (carboxydebacteria) when growing on CO as sole source of carbon and energy had doubling times which ranged from 12–42 h. The activity profiles obtained after discontinuous sucrose density gradient centrifugation indicated that the CO-oxidizing enzymes are soluble and the hydrogenases are membrane-bound in all strains examined. The CO-oxidizing enzymes of Pseudomonas carboxydohydrogena, Pseudomonas carboxydoflava, Comamonas compransoris, and the so far unidentified strains OM2, OM3, and OM4 had a molecular weight of 230,000; that of Achromobacter carboxydus amounted to 170,000. The molecular weights of the CO-oxidizing and H₂-oxidizing enzymes turned out to be identical. The cell sonicates were shown to catalyze the oxidation of both CO and H₂ with methylene blue, thionine, phenazine methosulfate, toluylene blue, dichlorophenolindophenol, cytochrome c or ferricyanide as electron acceptors. Methyl viologen, benzyl viologen, FAD⁺, FMN⁺, and NAD(P)⁺ were not reduced. The spectrum of electron acceptors was identical for all strains tested. Neither free formate, hydrogen nor oxygen gas were involved in the CO-oxidation reaction. Methylene blue was reduced by CO at a 1:1 molar ratio. The results indicate that CO-oxidation by carboxydobacteria is catalyzed by identical or similar enzymes and that the reaction obeys the equation CO+H₂OCO₂+2H⁺+2e^- as previously shown for Pseudomonas carboxydovorans.Dedicated to Otto Kandler remembering almost three decades of enjoyable cooperation     

Modulation of allostery of pyruvate kinase by shifting of an ensemble of microstates

Since the introduction of the concepts of allostery about four decades ago, much advancement has been made in elucidating the structure-function correlation in allostery. However, there are still a number of issues that remain unresolved. In this review we used mammalian pyruvate kinase (PK) as a model system to understand the role of protein dynamics in modulating cooperativity. PK has a triosephosphate isomerase (TIM)(α/β)₈ barrel structural motif. PK is an ideal system to address basic questions regarding regulatory mechanisms about this common (α/β)₈ structural motif. The simplest model accounting for all of the solution thermodynamic and kinetic data on ligand-enzyme interactions involves two conformational states, inactive E^T and active E^R. These conformational states are represented by domain movements. Further studies provide the first evidence for a differential effect of ligand binding on the dynamics of the structural elements, not major secondary structural changes. These data are consistent with our model that allosteric regulation of PK is the consequence of perturbation of the distribution of an ensemble of states in which the inactive E^T and active E^R represent the two extreme end states. Sequence differences and ligands can modulate the distribution of states leading to alterations of functions. The future work includes: defining the network of functionally connected residues; elucidating the chemical principles governing the sequence differences which affect functions; and probing the nature of mutations on the stability of the secondary structural elements, which in turn modulate allostery.