茉莉酸甲酯和水杨酸对西洋参愈伤组织生长和皂苷形成的影响CSCD

本文旨在探究不同诱导子对西洋参愈伤组织生长、相关酶活性及其人参皂苷含量的影响,在西洋参愈伤组织中,应用HPLC检测了添加诱导子茉莉酸甲酯(methyl jasmonate,MeJA)和水杨酸(salicylic acid,SA)后西洋参愈伤组织皂苷生物合成的变化。结果显示,MeJA抑制生长,但SA对其生长影响较小;2种诱导子均可以显著激活西洋参愈伤组织中超氧化物歧化酶(superoxide dismutase,SOD)、过氧化氢酶(catalase,CAT)、过氧化物酶(peroxidase,POD)活性和丙二醛(malondialdehyde,MDA)含量;培养基中MeJA浓度为100μmol/L时,愈伤组织中总皂苷含量和产量均达到最大值,人参皂苷Rg_(1)、Re、Rb_(1)、Rc的含量最高,在SA诱导子试验组中,当SA浓度为300μmol/L时,西洋参愈伤组织中总皂苷含量和产量均达到最大值,人参皂苷Rb_(1)的含量最高。结果表明,在西洋参愈伤组织中添加适当浓度MeJA和SA诱导子会提高人参皂苷化合物含量,其中以MeJA诱导人参总皂苷的效果最好,同时也会影响西洋参愈伤组织的生长量。说明在培养过程中添加外源诱导子,有利于提高西洋参愈伤组织中皂苷含量。     

西洋参发根的诱导及不同外源物质对发根生长和皂苷含量的影响

利用发根农杆菌A4菌株在西洋参根外植体上直接诱导产生发根,并分析不同浓度的植物激素6-BA、NAA,前体物醋酸镁(Mg(Ac)2)、L-亮氨酸和诱导子茉莉酸甲酯(MJA)、水杨酸(SA)对西洋参(Panax quinquefolium L.)发根生长和皂苷含量的影响。同时,研究MJA与SA组合作用对皂苷含量的影响。采用高效液相色谱法测定发根中单体皂苷Rb1的含量。结果显示,适宜浓度的外源物质均可促进皂苷含量的增加,MJA尤其明显。     

小型生物反应器内人参不定根的人参皂苷累积

对小型生物反应器(3~10 L)培养人参不定根的生长和人参皂苷(Rg1、Re、Rb1)的累积规律,以及蔗糖浓度、初始接种量对其生长和人参皂苷累积的影响进行研究。结果表明:小型生物反应器内人参不定根的最佳收获周期为7周。初始接种量和蔗糖浓度影响生物反应器内人参不定根的生长和人参皂苷的累积,20或40 g/L蔗糖对人参不定根的生长和人参皂苷的累积优于60 g/L蔗糖;5和10 L生物反应器内最佳初始接种量分别为15和30g,其不定根的生长量分别为9.29和19.17 g,人参皂苷含量分别为5.16和4.58 mg/g。生物反应器内培养7周的人参与栽培4年的人参相比,人参皂苷Rg1和Re含量相差不大,但栽培人参中Rb1的含量远高于生物反应器中所培养的人参不定根。     

根施SA对番茄幼苗盐害损伤的修复效应

探讨根施水杨酸(SA)缓解番茄幼苗盐胁迫伤害的调节作用,为合理利用SA解决番茄栽培中的盐害问题和培育抗盐番茄品种提供科学依据。以"秦丰保冠"番茄品种幼苗为试材,在营养液栽培条件下,研究50-800μmol/L SA对100 mmol/L NaCl胁迫下番茄幼苗生长、叶绿素含量、气体交换参数、叶绿素荧光参数、膜脂过氧化及抗氧化酶活性的影响。结果显示,盐胁迫下,不同浓度SA处理的番茄幼苗生长抑制均能得到有效缓解,同时叶片叶绿素含量、光合速率(Pn)、气孔导度(Gs)、蒸腾速率(Tr)、最大荧光(Fm)、PSⅡ最大光化学效率(Fv/Fm)、实际光化学效率(ΦPSⅡ)和光化学淬灭系数(qP)不同程度升高,细胞间隙CO2浓度(Ci)、最小荧光(Fo)和非光化学淬灭系数(NPQ)显著降低,其中SA浓度为200μmol/L时,各指标变幅均达到最大;在盐胁迫下,番茄幼苗叶片超氧化物歧化酶(SOD)、过氧化物酶(POD)活性、丙二醛含量和电解质渗出率显著升高,过氧化氢酶(CAT)活性变化不显著,施加各浓度外源SA处理促进了上述3种酶活性的升高,同时使叶片丙二醛含量和电解质渗出率显著降低,并以200μmol/L SA处理时变化最显著。外源SA主要通过增强幼苗叶片的光合能力来缓解盐胁迫造成的氧化伤害,进而提高番茄植株的耐盐性。本试验条件下,以200μmol/L SA处理效果最好。     

人参皂苷Rb1、Rg1、Re对白血病细胞株KG1α增殖的影响

目的:探讨人参皂苷Rb1、Rg1、Re对急性髓系白血病细胞株(KG1α)增殖的影响.方法:取对数生长期KG1α细胞,分设人参皂苷Rb1、Rg1、Re组和常规培养组,以MTT比色法检测作用24h、48h、72h时对KG1α细胞增殖抑制作用,并计算Rb1的IC_(50)值,以此浓度为工作浓度,设常规培养组和处理组,台盼蓝计数法观察对KG1α细胞增殖的影响;流式细胞术测定细胞周期分布的变化.结果:MTT、台盼蓝计数显示人参皂苷单体Rb1、Rg1可抑制KG1α细胞增殖,呈浓度依赖性,以Rb1抑制效应最佳,于作用48h抑制率最高.台盼蓝计数显示人参皂苷单体Rb1-120μmol/L作用48h时抑制率达50.22%;流式细胞术结果提示,与对照组比较,Rb1-120μmol/L组G_2/M期KG1α细胞比例增加(P<0.05).结论:Rb1可抑制KG1α细胞体外增殖,其增殖抑制作用与将KG1α细胞阻滞于G_2/M期有关.     

Cd2+胁迫对石菖蒲生理生化特性的影响

通过水堵实验,研究了不同浓度(0、50、200、400μmol/L)下和不同时间内(3、7、11d)Cd2+对石菖蒲(Acorus ta-tarinowii Sehott)叶片抗氧酶活性、叶绿素含量、脂质过氧化程度以及脯氨酸含量的影响.结果表明:(1)超氧化物歧化酶(SOD)活性在3d时随着胁迫浓度的增大而增加,但7d和11d时都是在50 μmol/L浓度下达到峰值,然后降低,但都高于对照;除400μmol/L处理下SOD随胁迫时间延长呈先降后升的趋势外,其余浓度处理下均升高.(2)过氧化物酶(POD)活性在胁迫3d和7d时均随着胁迫浓度的增大而增加,11d时在200 μmol/L处理下达到峰值,然后降低;各浓度处理组均随着胁迫时间的延长POD活性呈下降趋势.(3)过氧化氢酶(CAT)活性在不同时间内随着胁迫浓度的增加呈先增后降趋势,并且各浓度处理组的CAT均随胁迫时间的延长而增加.(4)叶绿素含量在不同胁迫时间内均在200μmol/L处理下达到峰值,然后降低;除400μmol/L处理下的叶绿素随胁迫时间延长而增加外,其余浓度处理组均呈下降趋势.(5)丙二醛(MDA)含量和脯氨酸(Pro)含量均随着胁迫浓度的增加和胁迫时间的延长而增加.研究结果分析表明石菖蒲对Cd2+胁迫有一定的耐受性.     

从西洋参中提取分离纯化人参皂苷R_(b1)和人参皂苷R_e的研究

用大孔吸附树脂从西洋参提取物中富集西洋参总皂苷,再利用丙酮沉淀及重结晶方法获得高纯度的人参皂苷Rb1和Re.可以得到含量大于95%的人参皂苷Rb1(收率2.6%)和92%的人参皂苷Re(收率0.5%),以及纯度为98.5%的人参皂苷Rb1(收率2.0%)和97.8%的人参皂苷Re(收率0.25%).该方法简便、实用,适用于工业大生产,为进一步开发成新药奠定了基础.     

外源脱落酸对小麦幼苗抗镉胁迫能力的影响

以小麦(Triticum aestivum L.)为试材,采用水培法研究了100mg/L镉(Cd2+)胁迫条件下施用外源脱落酸(ABA)对小麦幼苗生长及某些生理生化指标的影响。结果表明:(1)100mg/L Cd2+胁迫下,小麦叶片膜脂过氧化产物丙二醛(MDA)含量显著提高,植株生长受到抑制;(2)外源ABA能够明显提高Cd2+胁迫小麦幼苗的根系活力,增加其叶片SOD、CAT和POD活性,促进其脯氨酸积累,降低MDA的含量,并以5.0μmol/L ABA的效果最明显;(3)1.0～5.0μmol/L外源ABA不同程度地缓解Cd2+胁迫对小麦幼苗生长的抑制作用,且5.0μmol/L时效果最明显,其株高、根长、总干重分别比单一Cd2+胁迫处理显著提高6.73%、149%和10.52%,而10.0μmol/LABA反而加重了Cd2+对小麦幼苗生长的伤害。因此,适宜浓度的外源ABA能够通过增加体内保护酶活性和脯氨酸含量来缓解Cd2+胁迫对小麦幼苗生长的抑制作用,增强小麦幼苗的抗Cd2+胁迫能力,并以5.0μmol/L ABA处理效果最好。     

膨大期果面喷施IAA对桃成熟期果实性状和相关基因表达的影响北大核心CSCD

为明确桃果实发育后期外源生长素对果实成熟的影响及更深入的认识生长素调控果实发育与成熟的机制,本研究以桃品种‘小白凤’为试材,采用不同浓度的外源IAA(200,10,0.1μmol/L)喷施第2次快速膨大期的桃果实,在处理后10,20,30 d分别取样,分析桃果实的硬度,糖组分(蔗糖、葡萄糖、果糖、山梨醇),果胶,纤维素含量以及乙烯释放量的变化,并对200μmol/LIAA处理后30 d及对照组的果实进行了转录组测序分析,深入认识生长素调控桃果实成熟的作用和机理。结果表明,(1)IAA处理后30 d时,200μmol/L处理组桃果实果肉硬度与对照组相比显著增加,成熟期平均延迟5 d,而10,0.1μmol/LIAA处理组与同期对照组间无显著差异。(2)果肉蔗糖含量在0.1,200μmol/LIAA处理后30 d显著低于同期对照组,在10μmol/LIAA处理后30 d时与对照组无显著差异;葡萄糖、果糖和山梨醇含量在各浓度IAA处理后30 d时多与对照组间无明显差异。(3)在处理30 d时,果肉中可溶性果胶含量在0.1μmol/L IAA处理组与对照组无显著差异,在10,200μmol/LIAA处理组均显著低于对照组,此时不同浓度IAA处理桃果肉中不可溶果胶和纤维素含量均与对照组之间无显著差异。(4)在IAA处理后10,20,30 d时,果实乙烯释放量均表现为0.1,10μmol/L处理与对照组无显著差异,200μmol/L处理组显著低于对照组。(5)转录组数据显示,200μmol/L IAA处理与对照组中共存在86个差异表达基因,KEGG分析发现其中有6个与果实发育成熟密切相关的代谢途径中多个基因的表达谱发生显著变化,且变化趋势与已测定的生理指标数据吻合。综合分析表明200μmol/L的外源IAA处理第2次快速膨大期的桃果实能够延缓果实成熟的进程。     

北柴胡不定根培养及茉莉酸甲酯处理对柴胡皂苷含量的影响

目的:建立北柴胡不定根培养体系,明确茉莉酸甲酯(MeJA)处理对北柴胡不定根中柴胡皂苷含量积累的影响。方法:利用固体和液体相结合的组织培养技术培养北柴胡不定根;分别以不同浓度的MeJA处理不定根不同时间,利用HPLC测定处理后不定根中柴胡皂苷含量的积累变化。结果:培养了北柴胡不定根;MeJA处理对北柴胡不定根中柴胡皂苷含量的积累有明显促进作用,当MeJA浓度为200μmol/L时,柴胡皂苷含量最高,为0.45%;以200μmol/L MeJA处理北柴胡不定根26 d时,柴胡皂苷含量最高,为0.51%。结论:北柴胡不定根培养结合MeJA诱导,可做为柴胡皂苷次生代谢合成途径及其积累规律研究的有效技术体系。     

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.     

真菌类遗传学分析的知识结构教学

本文以认知结构理论为指导,讨论了真菌类遗传分析与高等动植物遗传分析的内在联系,认为利用这种内在联系进行教学可收到好的效果并说明了作者的具体教学过程。 Abstract:In the paper, the relationship between genetic analysis of Fungi and genetic analysis of high animal and plant was discussed.A good results were obtained when we adopted this method in the teaching.     

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.     

Time of detection of recessive genes: effects of system of mating and number of examined individuals

Summary Anthers were cultured from two sets of seven lines of hexaploid wheat (Triticum aestivum L.) with different cytoplasms, the euplasmic nucleus donors, Siete Cerros 66 and Penjamo 62, as well as their six alloplasmic lines derived from wild relative species of the genera Triticum and Aegilops. Significant cytoplasmic and nuclear effects but no cytoplasmic-nuclear interaction were found for embryogenic anther response, with the best performance of Penjamo 62 in Ae. kotschyi cytoplasm. Plant regeneration was not affected significantly by the cytoplasmic background of the lines cultured. The possible genetic implications of the observed cytoplasmic and nuclear influences on the in vitro haploid induction of wheat are discussed.     

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。     

Scales of spatial patterns of distribution of intertidal invertebrates

Few comparative studies of spatial patterns at different scales have examined several species in the same habitat or the same species over a range of habitats. Therefore, variability in patterns among species or among habitats has seldom been documented. This study quantifies spatial patterns of a suite of intertidal snails and a species of barnacle using a range of statistical techniques. Variability in densities was quantified from the scale of adjacent quadrats (over a distance of centimeters) to tens of kilometers. Significant differences in abundances occurred primarily at two spatial scales. Small-scale differences were found at the scales of centimeters or 1–2 m and, for many species on many shores, these accounted for most of the variability in abundances from place to place. These are likely to be determined by behavioural responses to small-scale patches of microhabitat. Large-scale differences in abundance were also found in most species at the scale of hundreds of meters alongshore. These are likely to be due to variation in recruitment (and/or mortality) because of limited dispersal by adults of these species. There was little or no additional variation among shores, separated by tens of kilometers, than was shown among patches of shore separated by hundreds of meters. Identification of the scale(s) at which significant differences in abundance are found focus attention on the processes (and the scales at which these processes operate) that influence patterns of distribution and abundance. Some of the advantages and disadvantages of various procedures are discussed.     

Identification of the site of glycation of human insulin

This study evaluates the nature of glycated human insulin formed following exposure to hyperglycemic conditions in vitro. Glycated insulin was purified by RP-HPLC and its molecular mass (5971.3 Da) determined by plasma desorption mass spectrometry (MS). The difference in mass (163.7 Da) from nonglycated insulin (5807.6 Da) corresponds to a single reduced glucose (glucitol) residue. Following reduction of insulin disulfide bridges, MS confirmed that the B-chain was glycated. Enzymatic digestions with trypsin, endoproteinase Glu-C, and thermolysin, followed by RP-HPLC and identification of fragments by MS, localized glycation to the B-chain (1–5) region. Electrospray tandem MS identified the site of glycation as the B-chain NH₂-terminal Phe¹ residue. This was confirmed by automated Edman degradation with glycated human insulin.