一类被开发的捕食系统的定性分析

讨论了一类食饵种群被开发的两种群捕食系统: dx/dt=x(a0+a1x-a2x2-a3y3)-h0, dy/dt=y(x-1)其中a0>0,a2>0,a3>0,h0>0,a1不定号.文中主要讨论了系统平衡点的行为以及系统的稳定性.用Pioncare切性曲线法及Dulac函数法讨论闭轨不存在的充分条件;用Hopf分支方法及张芷芬唯一性定理证明了极限环的存在性与唯一性.同时对相应结论的生态学意义给予了说明.     

Willis环状脑动脉瘤的生物数学模型的周期解

本文运用扭转映射的不动点定理,通过Poincare'映射,在(μ/2)+((β~2)/(4a))<1的条件下,证明了Willis环状脑动脉瘤生物数学模型 +μ+αx-βx~2+γx~3=Fcosωt(其中μ,α,β,γ,F,ω都是正常数)至少存在一个(2π)/ω周期解。     

拟孔蜂巨柄啮小蜂对家蝇的寄生作用

拟孔蜂巨柄啮小蜂Melittobia acasta Walker是一种可以寄生家蝇Musca domestica L.的寄生蜂。首次报道食物对该蜂寿命的影响,以及该蜂日龄、家蝇蛹龄、寄生蜂密度和蝇蛹密度与寄生率的关系。以15%糖水饲养该小蜂寿命最长;单只啮小蜂最多可以寄生8只蝇蛹,最大出蜂总量达58只;单个蝇蛹最多出蜂22只;随着寄生蜂的日龄和蝇蛹日龄增加,该蜂对蝇蛹的寄生个数有下降的趋势,寄生率和寄生蜂日龄符合y=3.36-0.062x-0.045x2,寄生率和蝇蛹日龄符合y=2.50+0.91x-0.34x2;蝇蛹的密度对小蜂的寄生率的影响拟合Holling功能反应模型:Na=0.6165TrN0(1+0.6165×0.499N0);寄生蜂自身密度对寄生率的影响符合方程:a=0.4943P-0.306。     

一类KOLMOGOROV系统的极限环

关于两种群互相作用的Kolmogorov模型 x=xF_1(x,y), y=yF_2(x,y),文〔1〕根据生态意义对F_1、F_2给出较多限制条件下作过研究,由于现实中总结出的模型归结到F_1、F_2为x和y的多项式的形式不少〔2,3〕,本文讨论一类Kolmogorov系统x=x(a_0+a_1x-a_3x~2+a_2y+a_4xy),y=y(x-1) (1)极限环的存在性和唯一性,其中x和y分别表示两种群的密度,参数a_0>o,a_3>o,a_1、a_2、a_4不定号,它们各表示一定的生态意义,随不同的取值范围而反映两种群的不同作用〔1〕。     

苍白秤钩风(Diploclisia Glaucescens)中的木脂素——左旋丁香脂素的晶体结构研究

通过X 射线单晶衍射法测定了标题化合物的晶体结构。结果表明 :晶体属正交晶系 ,P2 12 12 1空间群 ,a =8 6 0 10 (3) ,b =13 0 830 (9) ,c =18 1130 (11) ,V =2 0 38 2 0 (2 0 ) 3 ,Z =4 ,Mr =4 18 4 9,Dx =1 36 9g/cm3 ,λ(MoKα) =0 710 73 ,μ(MoKα) =1 12cm-1,F(0 0 0 ) =888。在 0 <2θ <5 0°范围内共收集了 1988个独立衍射点 ,其中可观测衍射点 196 3个 [Ⅰ≥ 8σ(Ⅰ ) ]。晶体结构用直接法解出 ,经全矩阵最小二乘法修正 ,最终偏离因子Rf=0 0 6 2 ,Rw=0 0 5 5。     

气液双升式反应器动物细胞培养及批式生长动力学模型

初步研究了气液双升式动物细胞反应器微载体培养 Bowes细胞和悬浮培养 M4G3杂交瘤细胞的生长条件 ,在不加入消泡剂和保护剂的情况下 ,批式培养 Bowes细胞的最大密度为 2 .6×1 0 6/ml,批式培养 M4G3细胞的最大密度为 1 .5× 1 0 6/ml。基于细胞生长的密度效应 ,建立了动物细胞生长动力学模型 :　　 μ=0　　 t相似文献   

重组巴氏毕赤酵母高密度发酵表达rHSA

对基因工程菌Pichiapastoris的摇瓶发酵条件进行了试验 ,并根据摇瓶发酵的优化结果进行了补料分批高密度发酵。在摇瓶发酵时 ,甲醇诱导基因工程菌P .pastoris表达重组人血清白蛋白的发酵周期为 96h ;甲醇的最佳诱导浓度为 1 0g L ;发酵pH范围为 5 72～ 6 5 9;在摇瓶培养时 ,随着接种量的增加 ,虽然目的蛋白表达量缓慢增加 ,但单位细胞光密度的蛋白产率却明显下降 ,符合y =1 2 941x- 0 50 59方程 (线性相关系数r=0 9789) ,其限制性因子很可能为溶氧。在分批发酵 ,接种量为 1 0 %且种子细胞光密度 (OD60 0 )为 2 0左右时 ,细胞生长的延迟期为 2 1 1h左右 ,细胞生长光密度与培养时间的关系模型为 :y =0 7841e0 .2 3 19t(线性相关系数r=0 .993 6 ) ;在补料发酵时细胞干重浓度可达到 1 1 5g L— 1 6 0g L ,在 1 2 0h重组人血清白蛋白表达量最大达到 3 6g L。     

外源性Wnt3a持续作用对小鼠胚胎干细胞Wnt／β-catenin信号通路的调控作用

目的观察Wnt/β-catenin信号通路是否在体外以外源性Wnt3a持续作用小鼠胚胎干细胞后被激活,并进一步调控该通路下游基因的表达。方法应用外源性Wnt3a持续作用ES-E14TG2a小鼠胚胎干细胞21d,通过细胞免疫荧光及Western Blotting检测细胞内β-catenin蛋白,以观察该蛋白的胞内积聚情况;同时QRT-PCR检测WNT下游靶标基因的表达量,采用完全随机F检验并用LSD法进行两两比较,来确定经典WNT／β-catenin信号通路是否被激活。结果ES-E14TG2a小鼠胚胎干细胞经Wnt3a连续培养21d后,β-catenin蛋白的细胞荧光明显较强,而对照组中的荧光强度较弱,说明细胞内β-catenin蛋白没有被降解而是在胞内大量积累;Western Blotting检测结果显示Wnt3a连续培养21d后ES-E14TG2a细胞内β-catenin蛋白条带明显比空白对照的蛋白条带粗;ES—E14TG2a细胞经wnt3a培养后Pitx2、Frizzled、Sox17的表达量均持续上升,Pitx2在培养7d、14d、21d分别为4．17±0．20、7．27±0．35、8．59±0．21（F=222．757,P=0．000）;Frizzled在培养7d、14d、21d分别为1．01±0．06、2．93±0．22、5．44±0．30（F=302．703,P=0．000）;Sox17在培养7d、14d、21d分别为8．45±0．41、18．35±0．17、34．93±0．16（F=7217．083,P=0．000）;Oct4培养到7d、14d的表达量持续增加分别为1．22±0．21、1．56±0．04,而连续培养21d后Oct4基因的表达量下降为1．15±0．07（F=8．827,P=0．016）。结论Wnt3a持续作用可激活Wnt／β-catenin信号通路,并调控下游基因的表达。     

北京东灵山地区植物群落多样性研究——种-面积曲线的拟合与评价

本文选择了 1 0条曲线作为种 -面积曲线的拟合模型 ,它们分别是S=b a A (1 )S=b aln A (2 )S=(b aln A) c (3)S=aln(A 1 ) (4)S=aln(b A 1 ) (5)S=a Ab (6)S=a A/ (1 b A) (7)S=c/ (1 ae-b A ) (8)S=c - ae-b A (9)S=a(1 - e-b A ) (1 0 )对其中的 7个非线性模型给出了参数初值的计算方法 ,并用 Gauss- Newton或 Marquardt方法计算非线性最优解。又选择了剩余标准差 (RSE)、相关指数 (CRI)、偏差绝对值的平均值 (AAD)和相对偏差绝对值的平均值 (AARD)作为模型拟合优劣的 4个评价指标。研究结果表明 :1 ) 7个非线性模型中参数初值的计算方法是可行的。从 4个评价指标来看 ,它们的非线性最小二乘解都明显优于线性最小二乘解 ;2 ) 1 0个模型的拟合效果都相当好 ,对 5个样地及其各层拟合的共 2 0 0个 CRI中有 71 .5%大于 0 .9,89%大于0 .8,其中曲线 (3)和 (9)最好 ,其次是 (5)、(6)、(2 ) ,(1 )和 (1 0 )最差 ;3)秩相关分析表明 ,3个评价指标RSE、AAD和 AARD相互之间存在极强的正秩相关 ,因此在本研究中 ,它们的评价结果具很强的一致性。     

时滞Logistic型差分方程的振动及稳定性

本文获得了如下Xn 1=xnexp(a bxn-k^p-cxn-1^q）时滞Logistic型差分方程所有正解关于其平衡点振动的充要条件，同时还获得了一个正平衡点渐近稳定的充分条件，其中A∈（0，∞），B∈（-∞，O]，C∈（0，∞），K,l∈N。     

The Effect of Tetracycline upon Establishment of Escherichia coli of Bovine Origin in the Enteric Tract of Man

S ummary . Human volunteers were given orally 0, 50 or 1000 mg of tetracycline/day for the 4 days preceding and the 5 days following ingestion of 1–2 x 10⁶ cells of tetracycline resistant Escherichia coli strain x-314 of bovine origin. Of those receiving 0, 50 or 1000 mg of tetracycline/day, 9/13, 5/9 and 12/13, respectively, excreted the organism at least once during the 25-day sampling period. Significant differences were not observed between subjects receiving 0 or 50 mg of tetracycline/day with respect to the length of time the coliform was recovered from faeces, or the maximum proportion of the total coliforms found to be E. coli x-314. Those receiving 1000 mg of tetracycline/day shed E. coli x-314 for longer periods and the latter's contribution to the coliform population was greater than in those subjects receiving 0 or 50 mg of tetracycline/day. It was concluded that 1000, but not 50 mg, of tetracycline/day taken orally potentiates the establishment of a tetracycline resistant E. coli in the enteric tract of man.     

A comparison of performance of tetraploid progenies produced by diploid and their vegetatively doubled (tetraploid) counterpart parents

 Two diploid potato parents, W5295.7 and W5337.3, and their colchicine-doubled tetraploids were used as male to cross with three cultivars: ‘Raritan’, ‘Shepody’ and ‘Superior’. Both diploids produced 2n gametes via first division restitution (FDR) during meiosis. Field experiments were carried out on seedlings of the 12 hybrid progenies in 1991 and 1992. Six of the progenies represented the tetraploid-diploid (4x-2x) hybrids and the other six tetraploid-tetraploid (4x-4x) progenies. The genetic consequence of FDR gametes was examined by comparing the mean and genotypic variance of six tuber traits of 4x-2x and 4x-4x progenies. Tuber appearance, eye depth, specific gravity and tuber size showed significant differences between the means of 4x-2x and 4x-4x progenies from either both or one of the diploid parents. The genotypic variances of these traits in 4x-2x progenies were reduced in various degrees from those observed in 4x-4x progenies. Major genes responsible for the inheritance of these traits are probably located close to the centromere. The two diploid parents may also carry alleles of different size and direction of non-additive genic effects in their 2n gametes. The 4x-2x progenies also outperformed the 4x-4x progenies with respect to the means of total and marketable yield. There were thus heterotic gene loci for high yield located close to the centromere. No marked reduction of genotypic variance, however, was observed. The results suggest that genes for yield would be scattered between the centromere and the site for maximum recombination. Received: 24 April 1996 / Accepted: 26 July 1996     

人MCM7 N-端融合蛋白的原核表达、纯化及其与AR蛋白相互作用的研究

目的：制备人MCM7 N-端的GST融合蛋白（GST-MCM7N）,研究其是否和雄激素受体（AR）蛋白存在直接的相互作用。方法：利用RT-PCR获得长度为744 bp的人mcm7 基因N-端cDNA碱基片段,把该片段构建到原核表达载体pGEX-5x-3中,转化大肠杆菌BL-21菌株。经IPTG诱导菌株基因表达产生了GST-MCM7N融合蛋白;使用Glutathione Sepharose 4B球珠分离纯化。利用GST pull-down 技术把纯化的融合蛋白分别和前列腺癌细胞LNCaP细胞裂解液及基因工程获得的AR蛋白孵育,检测MCM7蛋白的 N-端是否和AR蛋白直接相互作用。结果：酶切鉴定及基因测序表明,mcm7 基因cDNA的 N-端片段被构建到表达载体pGEX-5x-3中;SDS-PAGE及Western blotting结果分别显示,本研究获得了GST和GST-MCM7N融合蛋白;GST pull-down 结果证实GST-MCM7N和AR蛋白存在相互作用。结论：MCM7蛋白的N-端和AR蛋白至少在体外可以发生直接的相互作用。     

Amyloid beta peptide ratio 42/40 but not A beta 42 correlates with phospho-Tau in patients with low- and high-CSF A beta 40 load

Neurochemical dementia diagnostics (NDD) can significantly improve the clinically based categorization of patients with early dementia disorders, and the cerebrospinal fluid (CSF) concentrations of amyloid beta peptides ending at the amino acid position of 42 (A beta x-42 and A beta 1-42) are widely accepted biomarkers of Alzheimer's disease (AD). However, in subjects with constitutively high- or low-CSF concentrations of total A beta peptides (tA beta), the NDD interpretation might lead to erroneous conclusions as these biomarkers seem to correlate better with the total A beta load than with the pathological status of a given patient in such cases. In this multicenter study, we found significantly increased CSF concentrations of phosphorylated Tau (pTau181) and total Tau in the group of subjects with high CSF A beta x-40 concentrations and decreased A beta x-42/x-40 concentration ratio compared with the group of subjects with low CSF A beta x-40 and normal A beta ratio (p<0.001 in both cases). Furthermore, we observed significantly decreased A beta ratio (p<0.01) in the group of subjects with APOE epsilon 4 allele compared with the group of subjects without this allele. Surprisingly, patients with low-A beta x-40 and the decreased A beta ratio characterized with decreased pTau181 (p<0.05), and unaltered total Tau compared with the subjects with high A beta x-40 and the A beta ratio in the normal range. We conclude that the amyloid beta concentration ratio should replace the 'raw' concentrations of corresponding A beta peptides to improve reliability of the neurochemical dementia diagnosis.     

污染区域大气环境质量生物监测的数学模式

以常规标准取样法、静态挂片吸收取样法分别测定了深圳南山区范围内大气二氧化硫、硫酸盐化速率和氟化物的含量,并同步测定了植物叶片的污染物含量。利用回归方法分析了3种测定结果的相互关系,并以植物叶片污染物含量为基础建立大气环境质量生物监测的数学模型,其中以叶片含硫量评价大气硫酸盐化速率的模型为夏季y=0.781x-0.754,冬季y=1.88x-2.283;以叶片含氟量评价大气氟化物的模型为夏季y=0.363x-7.511,冬季y=0.175x-3.461,这些模型均有很高的可信度(p<0.001)。     

Expression of HSV-1 ICP0 Antigen Peptide in Prokaryotic Cells and Preparation of Specific Antibody

As an immediate-early protein of herpes simplex virus, infected-cell polypeptide 0 (ICP0) exhibits complicated interactions with host cells, and its regulatory function on gene expression is of great importance. Since the ICP0 encoding sequence contains many rare codons which are absent in E.coli, and ICP0 is highly unstable in prokaryotic cells, expression of entire ICP0 in prokaryotic cells has never been reported. In order to further investigate the function of ICP0, a recombinant plasmid was constructed by subcloning a cDNA fragment encoding an amino-terminal of 105 residues of the ICP0 protein into pGEX-5x-1 vector. The resulting GST-105 fusion antigen peptide was expressed with high efficiency in E.coli. Antibodies prepared after the immunization of mice with purified fusion protein can recognize not only the denatured ICP0 protein, but also the native ICP0 protein with normal biological conformation.     

Presenilin 1 Mutations Linked to Familial Alzheimer's Disease Increase the Intracellular Levels of Amyloid β-Protein 1–42 and Its N-Terminally Truncated Variant(s) Which Are Generated at Distinct Sites

Abstract: Mutations in the presenilin genes PS1 and PS2 cause the most common form of early-onset familial Alzheimer's disease. The influence of PS1 mutations on the generation of endogenous intracellular amyloid β-protein (Aβ) species was assessed using a highly sensitive immunoblotting technique with inducible mouse neuro-blastoma (Neuro 2a) cell lines expressing the human wild-type (wt) or mutated PS1 (M146L or Δexon 10). The induction of mutated PS1 increased the intracellular levels of two distinct Aβ species ending at residue 42 that were likely to be Aβ1–42 and its N-terminally truncated variant(s) Aβx-42. The induction of mutated PS1 resulted in a higher level of intracellular Aβ1–42 than of intracellular Aβx-42, whereas extracellular levels of Aβ1–42 and Aβx-42 were increased proportionally. In addition, the intracellular generation of these Aβ42 species in wt and mutated PS1 -induced cells was completely blocked by brefeldin A, whereas it exhibited differential sensitivities to monensin: the increased accumulation of intracellular Aβx-42 versus inhibition of intracellular Aβ1–42 generation. These data strongly suggest that Aβx-42 is generated in a proximal Golgi, whereas Aβ1–42 is generated in a distal Golgi and/or a post-Golgi compartment. Thus, it appears that PS1 mutations enhance the degree of 42-specific γ-secretase cleavage that occurs in the normal β-amyloid precursor protein processing pathway (a) in the endoplasmic reticulum or the early Golgi apparatus prior to β-secretase cleavage or (b) in the distinct sites where Aβx-42 and Aβ1–42 are generated.     

Amino-caprolactam γ-secretase inhibitors showing potential for the treatment of Alzheimer's disease

Herein we describe the structure-activity relationship (SAR) of amino-caprolactam analogs derived from amino-caprolactam benzene sulfonamide 1, highlighting affects on the potency of γ-secretase inhibition, selectivity for the inhibition of APP versus Notch processing by γ-secretase and selected pharmakokinetic properties. Amino-caprolactams that are efficacious in reducing the cortical Aβ_x-40 levels in FVB mice via a single 100 mpk IP dose are highlighted.