微量量热法筛选抑菌特效药的研究

用微量最热计连续测定细菌代谢过程中的热显变化，可获得反映细菌代谢规律的完整的热谱图以按指数生长模型对指数生长期进行处理，可计算出细菌正常代谢的生长速率常数L’．若在培养基中加入合成药物，使细菌在药物抑制作用下生长，也可获得完整的热谱图，从而计算出在药物抑制作用下细菌的生长速率常数．本义对福氏志贺氏Zb菌和金黄色葡萄球莉在四种合成药物抑制作用下的热谱进行了测定，并计算了生长速率常数，找出了细菌生长速率常数与所用药物浓度之间的定量关系，可为筛选抑菌药物和确定用药显提供定量依据’1基本原理设细菌在代谢过…     

Schiff碱药物对产气杆菌代谢抑制的热力学研究

用微量热法测定产气杆菌在不同温度条件下受到Schiff碱药物抑制的热谱曲线, 根据其指数生长期的热谱信息, 确定它在不同温度条件下的生长速率常数和反应活化能, 找出了该细菌的最佳生长温度。同时借用化学反应中的过渡态理论, 得到一系列热力学参数, 对细菌在受到抑制时的生长代谢进行了热力学分析。     

环境气氛对微量热安瓿法测定细菌生长速率常数的干扰

采用微量热安瓿法测定细菌生长时,发现细菌的代谢产热曲线在第一指数生长期内出现了停留法没有报导过的显著分阶段现象,且在不同的阶段生长速率常数有很大差异,对药物抗菌性能的评估造成极大干扰.为了寻找此现象的可能原因,以具有代表性的兼性细菌大肠杆菌为例,设计了微量热安瓿法实验,考察了不同环境气氛下大肠杆菌的生长代谢产热;并模拟了停留法条件下细菌的生长环境,通过安瓿法测定了大肠杆菌的生长代谢产热,重新解析了这些条件下细菌的生长速率常数.结果表明环境气氛是造成此现象的主要可能因素,并为在不同环境气氛下采用微量热安瓿法准确评估细菌的生长速率提供了一个可参考的标准.     

微量热法测定细菌的临界生长温度

应用微量热学的方法,我们已能成功地测得细菌生长过程的热谱,这种热谱包含着有关细菌生长代谢过程的丰富信息,例如对热谱曲线的指数生长段进行解析,可得出细菌生长的速率常数、激活能和有关的热力学参数。故采用微量热法测定细菌在不同培养温度下的生长速率常数,利用计算机拟合出相应k(速率常数)和T(培养温度)的线性关系式后,若把生长速率为零的温度定义为临界生长温度时,就可以根据由上述实验所得的k～T线性关系式求得细菌的临界生长温度。本工作仍采用微量热法对福氏志贺氏菌(S. flexneri)和大肠埃希氏菌(E. coli)进行实验测定。按文献的方法求出它们在不同温度下的生长速率常数;对于大肠埃希氏菌还用几种不同的培养基分别进行实验测定。     

药物对福氏志贺氏菌代谢抑制的微量热法研究

药物抑制细菌生长的热化学研究是当今热化学法研究的一个活跃领域．在这项研究中，Boling[1]、Nordmark[2]、屈松生[3]等人已做了不少有意义的工作．在前人工作的基础上，我们用热活性检测系统测定了福氏志贺氏菌属中五株细菌在药物抑制下生长的完整的热谱曲线．按指数生长模型计算出细菌代谢抑制下的生长速车常数，并用计算机拟会出生长速率常数与不同浓度药物之间的关系式，进一步得到生长速率常数为零（临界生长参数[4]）时的用药物浓度．此项研究工作的开展对于深入研究药物对细菌的抑制作用，筛选对某细菌抑制的特效药提供了一种新的…     

ABT-概念的应用

Kaiser提出的ABT-概念,其基本表示式和一些导出式如下:式中,b为组分谱峰的半峰宽,b_0为非滞留物的谱峰的半峰宽,a为直线的斜率或为组分的保留时间每增加t_m半峰宽所增加的宽度,k为组分的容量比,t_m为死时间,n为理论塔板数,n_(eff)为有效塔板数,n_(real)为真实塔板数,在一定实验条件下,a、b_0、t_m和n_(real)均为常数。本文根据上述各式说明n或n_(eff)随k的变化关系,半峰宽b与保留时间t_r的关系以及推导出新的色谱峰容量表示式。     

用微量热法研究左金丸及类方药的药性差异

采用微量热法测定了大肠杆菌在左金丸、甘露散、茱萸丸和反左金丸水煮液作用下的生长热谱曲线,获得相应的生物热动力学参数,经主成份分析并结合本草文献报道,综合分析左金丸及类方的药性差异,以从生物物理和生物化学的角度,探讨中医经典类方药性差异的客观真实性.实验发现,左金丸及类方的水煮液对大肠杆菌的生长代谢表现出不同的活性作用.寒凉药方左金丸和甘露散不同程度的抑制细菌的生长代谢.温热药方反左金丸和茱萸丸对细菌的生长代谢有不同程度的促进作用.类方之间存在较稳定的药性差异.类方药性主要受生物热动力学参数:第二指数生长期的生长速率常数k2和最大发热功率Pm2的影响.     

盐生盐杆菌生长过程热动力学研究

用 LKB2 2 77生物活性检测系统测定了盐生盐杆菌 R1、J7、S9以及 R1和 J7的融合子 F9生长的产热功率曲线 .根据曲线的特征 ,建立了古生菌生长过程的热动力学方程 :ln[P· ( 1 -P/Pm) r- 1 ]=ln[P0 · ( 1 -P0 /Pm) r- 1 ]+k· t.由此求得了盐生盐杆菌的生长速率常数 ,并对此模型和融合子 F9的生长进行了讨论 .该热动力学方程描述了一系列非理想的细菌生长过程的产热功率曲线 ,并将其与经典的指数式生长模型和 lo-gistic模型进行了比较 ,它具有更广泛的适用性 .首次报道了微量热技术在古生菌中的应用     

细胞动力学研究VI. 厌氧菌生长过程热化学特征

用LKB2277生物活性检测系统测定了三种厌氧菌---吉氏类杆菌、艰难梭状芽胞杆菌、黑色消化球菌的生长发热功率曲线。根据广义logistic方程, 建立了细菌生长过程的热动力学方程:ln[P/(Pm-P)^v^+^1]=ln[P0/(Pm-P0)^v^+^1]+k.t。由此热动力学方程, 求得了细菌的生长常数k, 根据Arrhenius公式求得吉氏菌的生长活化能Ea=59.7kj/mol, 应用过渡态理论得到吉氏菌在不同温度下的活化力学参数, 这个热动力学方程描述的是一系列不规则的细菌生长过程发热曲线, 将它与经典的指数模型和logistic模型进行比较, 它具有更广泛的适用性。     

细胞动力学研究VI. 厌氧菌生长过程热化学特征

用LKB2277生物活性检测系统测定了三种厌氧菌---吉氏类杆菌、艰难梭状芽胞杆菌、黑色消化球菌的生长发热功率曲线。根据广义logistic方程, 建立了细菌生长过程的热动力学方程:ln[P/(Pm-P)^v^+^1]=ln[P0/(Pm-P0)^v^+^1]+k.t。由此热动力学方程, 求得了细菌的生长常数k, 根据Arrhenius公式求得吉氏菌的生长活化能Ea=59.7kj/mol, 应用过渡态理论得到吉氏菌在不同温度下的活化力学参数, 这个热动力学方程描述的是一系列不规则的细菌生长过程发热曲线, 将它与经典的指数模型和logistic模型进行比较, 它具有更广泛的适用性。     

Microcalorimetric Study of Antibacterial Activity of Salicylaldehyde Glucosamine Copper(Ⅱ) Complex on E.coli

Since Schiff base and its metal complexes are of antibacterial and anticancer bioactivity, it has been a research subject of much interest. It is reported that Cu(Ⅱ)-SG could inhibite the synthesis of O₂^- markedly and could also combine with the salmn sperm DNA. The paper repored that by using microcalorimetric method The growth meloabolism of E.coli at different temperature and reacted upon by Cu(Ⅱ)-SG. The power-time curves of E.coli reacted with Cu(Ⅲ)-SG at different temperature has been determined by LKB2277 Microcalorimetric Monitor and the multiplication rate constant k, generation time G,bacterial growth inhibition ratio I,total thermogenetic quantity Q, the heat quantity of a single bacterium. Q₀ and the heat quantity of a single bacterium per minute Q₀ have also been calculated. On the basis of k~T data, the formula Lnk~1/T has graphically obtained and activation energy Ea and pre-exponential factor A have been calculated. According to the parameters of the growth metabolism of E.coli,some linear relationships have been derived. The paper provides a discussion about the growth metabolism of E.coli reacted upon by Cu(Ⅱ)-SG at different temperature, and it is found that、and t_r can be used to characterize bacterial growth metabolism and the antibacterial activity of Cu(Ⅱ)-SG at different temperature.     

微量热法测定细菌的临界生长温度

In this paper, we have determined the multiplication rate constanis (k) of Shigella flexneri and E. coli. at different temperatures and in different culture media by means of a microcalorimeter. From these results a linear equation as k~(1/2)=a+bT can be established for the bacterial growth. The corresponding linear equation for S. flexneri is k~(1/2)=-1.2823+0.0047122 T(r=0.971), so its eritica lgrowth temperature T_0 is equal to 272.1 K. The linear equation for E coli is k~(1/2)=-1.6390+0.005948 T (r=0.994), T_0=275.5 K. The experimental results indicate that the critial growth temperature of E. coli. is nearly a constant (T_0=273.9 K) in different culture media, which is very informative for the study on microorganism growth.     

细菌生长速率的测定及其热力学性质的研究

细菌生长是一系列非常复杂的生化反应的结果。为了使问题简化、便于采用物理化学的理论和方法对其进行处理,可假设细菌在培养基中的分裂、生长分为三个阶段进行。首先是底物进行扩散,并与细菌表面的活性物质进行作用(如输运过程);其次是细菌将底物吸收到细胞内形成细胞-底物复合物;然后是细胞-底物复合物在其内部一系列酶的作用下产生酶促反应,进行分裂生长和排出代谢产物。现用下式表示:     

细胞动力学研究IV.细菌非理想生长过程的热动力学

By using LKB2277 Bioactivity Monitor, we have determined the thermogenesis power curves of four kinds of bacteria: Brucella M5(55010), 83-980, 83-981 and E. coli. We have also derived the thermokinetic equation for the process of bacterial growth, which was untypical "S" , unideal growth, as:
Ln[P•(1-P/Pm)?-1]=ln[P0•(1-P0/Pm)?-1]+kt
From this equation, the rate constants of bacterial growth k wore obtained. This thermokinetic equation is very suitable for cell growth of separated culture, in which the thermogenesis curve is untypical. The model propoted by equationl(1) has been compared with the exponential and logistic models. This thermokinetic equation is very significant for the study of bacterial limited growth and their characteristics.     

Kinetics of the wurtzite-to-rock-salt phase transformation in ZnO at high pressure

Kinetics of the wurtzite-to-rock-salt transformation in ZnO has been studied in the 5-7 GPa pressure range at temperatures below the activation of diffusion processes. The detailed analysis of non-isothermal experimental data using the general evolution equation describing the kinetics of direct phase transformations in solids allowed us to study the kinetic particularities of both nucleation and growth of the rock-salt phase in parent wurtzite ZnO. The main rate-limiting processes are thermally activated nucleation (E(N) = 383 kJ mol(-1) at 6.9 GPa) and thermally nonactivated (most probably quasi-martensitic) growth (k(G) = 0.833 min(-1) at 6.9 GPa). The high impact of thermal deactivation of nucleation places has been evidenced in the case of slow heating, which indirectly indicates that the rs-ZnO nucleation places are mainly produced by pressure-induced stresses in the parent phase.     

Microcalorimetric Character of Inhibition of Salicylaldehyde Glucosamine Schiff Base SG on Bacterial Metabolism

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Determination of the cis-trans isomerization barrier of enalaprilat by dynamic capillary electrophoresis and computer simulation

Dynamic capillary electrophoresis (DCE) and computer simulation of the elution profiles with the stochastic model has been applied to determine the isomerization barriers of the angiotensin converting enzyme inhibitor enalaprilat. The separation of the rotational cis-trans isomeric drug has been performed in an aqueous 20 mM borate buffer at pH 9.3. Interconversion profiles featuring plateau formation and peak broadening were observed. To evaluate the rate constants k(cis-->trans) and k(trans-->cis) of the cis-trans isomerization from the experimental electropherograms obtained by dynamic capillary electrophoresis, elution profiles were analyzed by a simulation with iterative convergence to the experimental data using the ChromWin software which requires the total migration times of the individual isomers t(R), the electroosmotic break-through time t(0), the plateau height h(plateau), the peak widths at half height of the individual isomers w(h), as well as the peak ratio of the isomers as experimental data input. From temperature-dependent measurements between 0 degrees and 15 degrees C the thermodynamic parameters Delta G, Delta H and Delta S, the rate constants k(cis-->trans) and k(trans-->cis) and the kinetic activation parameters Delta G*, Delta H*, and Delta S* of the cis-trans isomerization of enalaprilat were obtained. From the activation parameters the isomerization barriers at 37 degrees C were calculated to be Delta G* (trans-->cis) = 87.2 kJ.mol(-1) and Delta G*(cis-->trans) = 91.9 kJ.mol(-1).     

Isopentenyl diphosphate isomerase catalyzed reactions in D2O: product release limits the rate of this sluggish enzyme-catalyzed reaction

The E. coli isopentenyl diphosphate isomerase (IDI) catalyzed reaction of isopentenyl diphosphate (IPP) in D(2)O gives a 66% yield of dimethylallyl diphosphate labeled with deuterium at the (E)-methyl group (d-DMAPP) and a 34% yield of IPP labeled with 1 mol of deuterium at C-2 (d-IPP). This shows that the release to D(2)O of the initial product of the IDI-catalyzed reaction (d-DMAPP) is slower than its conversion to d-IPP. Product dissociation is therefore rate determining for isomerization of IPP with a rate constant k(dis) ≈ k(cat) = 0.08 s(-1). The data provide an estimated rate constant of k(as) = 6 × 10(3) M(-1) s(-1) for binding of DMAPP to E. coli IDI that is similar to rate constants determined for the binding of N-protonated 2-amino ethyl diphosphate intermediate analogs to IDI from yeast [Reardon, J. E.; Abeles, R. H. Biochemistry1986, 25, 5609-5616]. We propose that ligand binding to IDI is relatively slow because there is a significant kinetic barrier to reorganization of the initial encounter complex between enzyme, substrate, and an essential Mg(2+) to form the Michaelis complex where the metal cation bridges the protein and the substrate diphosphate group.     

两种稀土卟啉配合物与大肠杆菌作用的微量热研究

用LKB-2277生物活性检测系统测定了新合成的阳离子型稀土卟啉配合物{[Re(TMP)(H2O)3]Cl, Re=Y、Yb, TMP=5, 10, 15, 20-四(4’-甲氧基苯基)卟啉}在37 ℃时对大肠杆菌作用的产热曲线,根据产热曲线求算了在稀土卟啉配合物作用下,大肠杆菌生长代谢的速率常数k,抑制率I,传代时间tG和半抑制浓度cI,50等热动力学参数.结果表明,稀土卟啉配合物在低浓度下对大肠杆菌有刺激作用,高浓度下为抑制作用,[Yb(TMP)(H2O)3]Cl的半抑制浓度cI,50为143 mg•L-1,其对大肠杆菌的抑制作用优于[Y(TMP)(H2O)3]Cl.