水溶性phellinus多糖PS1的分离提取及免疫活性研究

目的：从Phellinus pini子实体中提取分离到一种水溶性多糖纽分PS1,并对其免疫活性进行初步研究。方法：先进行热水提取,DEAE-纤维素离子交换树脂,sepharose CL-4B凝胶树脂分离纯化PS1,并利用GC色谱、FT-1R光谱进行组成成分分析,然后通过刚果红吞噬实验、脾脏B淋巴细胞增殖实验及免疫器官指数评价其免疫活性。结果：PS1为一种β型杂多糖,总糖含量70．36％,蛋白质含量4．69％,分子量为230kDa。糖类构成有鼠李糖、阿拉伯糖、木糖、甘露糖、半乳糖、葡萄糖,其摩尔比为2．14：2．36：0．44：4．28：5．17：85,61。多糖PS1能显著提高正常小鼠的脾指数和胸腺指数（P〈0．01）,免疫力低下小鼠的肝指数、胸腺指数也有提高,但效果不明显．PS1均能提高正常和免疫低下小鼠的巨噬细胞吞噬能力。此外。PS1能显著促进脾细胞体外增殖能力（P〈0．01）。结论：多糖PS1能显著提高机体的免疫能力。可作为一种生物效应调节剂应用于医药或保健食品领域。     

C．shehatae TZ8耐乙醇菌株的筛选及发酵性能研究

以C.shehataeTZ8为出发茵株,利用1％溶壁酶和1％蜗牛酶酶解1．5h,制备成C.shehataeTZ8原生质体,并对原生质体进行紫外诱变,以含不同浓度乙醇的木糖液体培养基培养进行初筛和复筛,获得一株遗传性能稳定、耐乙醇能力达5．5％（v／v）的蕾株C．shehataeTZ8-4,比初始菌株耐乙醇能力提高了2％。对突变株C．shehataeTZ8-4发酵性能的研究结果表明：C．shehataeTZ8-4发酵糖能力从80g/L（葡糖糖和木糖比为2：1）提高到120g／L,最大乙醇产量从27．41g／L提高到43．12g／L。     

具有降胆固醇功能益生菌的筛选研究

目的通过体外实验从发酵制品及人体肠道内分离筛选出安全高效的降胆固醇乳酸菌,并研究其生理生化特性,为今后功能性乳制品的开发提供优良菌种。方法应用MRS．胆固醇培养基液体发酵法进行目的菌株筛选,并测定其耐酸及耐胆盐等能力。结果筛选出4株具有降胆固醇能力的乳酸菌,其降解率分别为DM8403163．1％、DM8403470．3％、DM850381．1％、DM8605663．1％;同时4株乳酸菌均表现出不同程度的耐酸及耐胆盐能力,其中DM86056能力最强,其他3株乳酸菌次之;经鉴定,DM84031为保加利亚乳杆菌、DM84034为嗜热链球菌、DM8503为詹氏乳杆菌、DN86056为屎肠球菌。结论经上述实验综合比较,DM86056降胆固醇能力比较强且耐酸及耐胆盐等能力也较强,因此有待于将其应用于动物体内进行深入研究。     

施钾时期对冬小麦旗叶光合特性和籽粒淀粉积累的影响

在相同施钾量的基础上。采用一次性基施,1／2基施、1／2于拔节期追施。研究施钾时期对小麦旗叶光合特性和籽粒淀粉积累的影响．结果表明。分期施钾比一次性施钾提高了小麦开花后旗叶的光合速率、旗叶中磷酸蔗糖合成酶(SPS)和籽粒中腺苷二磷酸葡萄糖焦磷酸化酶(ADPGPPase)的活性,提高了籽粒中蔗糖的供应强度和淀粉积累速率。增加了籽粒产量．研究还表明。两个施钾处理均提高了小麦叶片中蔗糖的合成能力和其在籽粒中转化为淀粉的能力,施钾提高产量的主要原因是施钾较好地协调了光合物质合成、运输与转化,即较好地协调了淀粉合成的源库关系．     

产赤藓糖醇菌种的诱变育种

以耐高渗酵母为出发菌株,采用紫外线诱变处理,得到了一株变异株C1。其摇瓶发酵产赤藓糖醇24．9g／L左右。通过摇瓶发酵试验,研究了菌株C1的遗传稳定性。研究结果表明,经多次传代实验,菌株C1的发酵产糖醇能力没有改变,表明其是稳定的变异株。赤藓糖醇的产量由诱变前的12、594g／L提高到24.943g／L,提高了98.1％。关键词：     

紫茎泽兰光合特性对生长环境光强的适应

测定了不同光强下生长的紫茎泽兰叶片最大净光合速率(Pmax)、叶绿素荧光参数、光合色素含量和比叶重(SLW),探讨了其光适应能力及生理生态学机制．强光下(100％相对光强)紫茎泽兰发生了轻度光抑制,Pmax、SLW、类胡萝卜素含量和日间热耗散升高,但热耗散能力没有提高．强光下紫茎泽兰通过：1)加强日间热耗散和活性氧清除能力以及光系统Ⅱ反应中心可逆失活来耗散过剩光能;2)增大P～以增加光能利用;3)提高SLW,降低单位干重叶绿素含量以减少光能吸收3个途径避免了光合机构光破坏．弱光下(36％、12．5％和4．5％相对光强)紫茎泽兰日间热耗散很小,SLW降低,但P～较高,这有利于其增加光能吸收和利用效率．紫茎泽兰能在很大的光强范围内有效地维持光合系统正常运转,这可能是其表现较强入侵性的原因之一．     

朝向和对比度同时快速变化条件下的分辨能力

在自然的视觉中,投射到视网膜上的视觉图像总是在不停地变化,而人类的感知系统依然可以准确高效地识别物体.因此,人类的感知系统有相应的快速处理机制以应对这种动态变化．然而,前人的实验都是在相对稳定的刺激条件下研究人类被试的感知系统对一个刺激参数的反应,比如在固定对比度下测试朝向分辨能力,或在固定朝向测定对比度分辨能力,而朝向和对比度同时变化时,人类对这两个参数的分辨能力仍然缺乏研究．因此,在本实验中,我们使用朝向和对比度同时变化的刺激,研究了人类被试对朝向和对比度的分辨能力．结果表明,在这种动态变化的条件下,被试对朝向和对比度的分辨阈值都有显著性的降低．而且,朝向分辨阈值降低的幅度与在固定对比度参数条件下的分辨阈值成负相关,即在固定对比度条件下朝向分辨阈值较高的被试,在朝向和对比度同时变化条件下,其朝向分辨阈值降低的幅度相对要大,朝向分辨能力也就相对地提高更大．对比度分辨能力也呈现同样的规律．这些结果说明,朝向和对比度的同时变化提高了被试对朝向和对比度的分辨能力,一个参数变化时其分辨能力越低的被试,两个参数变化时其分辨能力提高的幅度就越大．揭示了视觉系统处理这种多刺激参量信息变化的能力和机制,对人类视觉系统在真实的视觉过程中如何处理朝向和对比度信息提供了认识．     

鸟苷酸二钠体外抗氧化能力的研究

本文研究了鸟苷酸二钠（GMPNa2）对羟自由基和DPPH·自由基的清除效果,同时建立了H2O2氧化损伤体外培养脾细胞模型,用MTT法检测GMPN％的修复及增殖作用,并分析了GMPNa2对细胞抗氧化体系及抗氧化能力的影响,以评价其抗氧化活性。结果表明：GMPNa2具有剂量依赖性的体外抗氧化和清除活性氧能力,10mmol／LGMPNa2的羟自由基清除能力高达96．644％,但DPPH清除率为6．589％。GMPNa2清除羟自由基与同浓度Vc相近,而其清除DPPH自由基的能力很弱。添加0．5、1、5和10mmol／LGMPNa2均能显著修复H2O2诱导的脾细胞氧化损伤（P〈0．05）,提高总抗氧化能力和抗氧化酶类活力（P〈0．01）。GMPNa2添加量大于1mmol／L时,可显著降低MDA含量（P〈0．01）。说明GMPNa2具有显著的抗氧化作用。     

关于高三第1轮复习方法的探讨

在整个高三1年的备考复习中,我们进行了以夯实基础知识为教学目标的第1轮复习;以提高学生能力．拓宽学生视野为目标的题型专题练习、实验专题练习和热点专题练习;以查漏补缺,增强学生自信心和提高学生应试能力为目标的冲刺模拟训练等3轮复习,以帮助学生理解、掌握生物学的基础知识,提高学生分析问题和解决问题的能力等,收到了良好的教学效果。     

低温胁迫下钼对冬小麦抗氧化防御系统及膜脂过氧化的影响

研究了低温（0～5℃）胁迫下钼对冬小麦抗氧化系统和膜脂过氧化的影响。结果表明,低温胁迫下施钼植株电解质渗漏率和丙二醛含量显著降低。施用钼肥提高了冬小麦叶片中抗氧化酶类如超氧化物歧化酶（SOD,EC1．15．1．1）、过氧化物酶（POX,EC1．11．1．7）和过氧化氢酶（CAT,ECl．11．1．6）的活性。低温胁迫下施钼对抗氧化酶（SOD、POX和CAT）活性提高幅度比常温下高。不论常温还是低温下,施铝均提高了冬小麦叶片中抗坏血酸和脯氨酸含量,低温胁迫下提高幅度更大。常温下缺钼和施钼处理后,叶片中类胡萝卜素含量差异不显著;低温下施钼后,冬小麦叶片类胡萝卜素含量显著增加。因此,低温胁迫下施钼植株活性氧清除能力增强、细胞膜伤害减轻可能是冬小麦抗寒力提高的原因之一。     

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.