Principles of covalent binding of reactive metabolites and examples of activation of bis-electrophiles by conjugation

Mechanisms of toxicity continue to be important in developing rational strategies to deal with chemicals present in the environment. Understanding and predicting toxicity have also become a critical step in the process of drug development. Covalent binding of chemicals to macromolecules is one aspect of toxicity, and the principles and outcomes of the process are considered. Two examples of chemicals for which several aspects of metabolism and reactions are understood are aflatoxin B(1) and polyhalogenated olefins. Ethylene dibromide is a compound that is activated to genotoxic half-mustards by conjugation with glutathione or the DNA repair protein O(6)-alkylguanine DNA alkyltransferase (AGT). The AGT reaction is unusual, in that crosslinking of the protein to DNA increases mutagenicity. One of the involved mechanisms is formation of N(7)-guanyl crosslinks and depurination to produce G-->T transversions; other reactions appear to yield the additional mutagenic events. The phenomenon of thiol conjugation to increase mutagenicity is widespread among bis-electrophiles.     

Designation of Pathotypes of Plant Pathogens

For evaluation and communication of data on populations of plant pathogens a sensible code to name pathotypes can be extremely helpful. Starting from a coding system proposed by Habgood in 1970, a system, called “coded triplets” is developed which has the same advantages but is easier to understand and to use. This is especially useful as, in the meantime, pathotypes did become increasingly complex due to the increased number of genes conferring race specific resistance in the host. An important advantage of the coded triplets is that codes change only at one digit if, for example, a new differentia) is added or if the pathotype changes from avirulence to virulence or vice versa on a single differential. In this way evoluationary patterns and changes in the pathogen population can be visualized easily. The system is used to describe complex data on haplotypes of the barley mildew pathogen, but it is suited equally well for designation of pathotypes of other pathogens. Some basic principles of coded triplets are similar to octal notation, described by Gilmour in 1973, which has, however, not become widely known. Reasons for this are discussed. – There is a fourth system belonging to the same group of mathematical, condensing codes. As there is reason to believe that the evolution of condensing codes is drawing to an end, the systems are compared extensively, and the benefits of a generally accepted designation are outlined.     

The Significance of Non-vertical Transmission of Phenotype for the Evolution of Altruism

My aim in this paper is to demonstrate that a very simple learning rule based on imitation can help to sustain altruism as a culturally transmitted pattern or behaviour among agents playing a standard prisoner’s dilemma game. The point of this demonstration is not to prove that imitation is single-handedly responsible for existing levels of altruism (a thesis that is false), nor is the point to show that imitation is an important factor in explanations for the evolution of altruism (a thesis already prominent in the existing literature). The point is to show that imitation contributes to the evolution of altruism in a particular way that is not always fairly represented by evolutionary game theory models. Specifically, the paper uses a simple model to illustrate that cultural transmission includes mechanisms that do not transmit phenotype vertically (i.e. from parent to related offspring) and that these mechanisms can promote altruism in the absence of any direct biological propensity favouring such behaviour. This is a noteworthy result because it shows that evolutionary models can be built to explicitly reflect the contribution of non-vertical transmission in our explanations for the evolution of altruism among humans and other social species.     

Analysis of morphogenetic mutants of hydra

Summary A mutant ofHydra attenuata is analysed, theaberrant, which is distinct from the wild type in having a smaller head with fewer tentacles and only half the number of head-specific cells. The rate of head and foot regeneration and the doubling time are slower inaberrants than in normal hydra.The lower head-forming potential is paralleled by a reduced concentration of head-specific morphogens: compared to the wild type, in theaberrant the concentration of head activator is reduced to 70% in the head and to 50% in the body, the concentration of head inhibitor is reduced to 50% in the head and to 80% in the body. Theaberrant is more sensitive (3 times) to added head activator and less sensitive (>5 times) to added head inhibitor than the wild type.The slower rate of foot regeneration is paralleled by a lower content of foot-specific morphogens: compared to the wild type, in theaberrant the foot activator is reduced to 40% and the foot inhibitor to 70%.     

4种小鼠的寒、热体质研究

[目的]研究4种品系小鼠的寒、热体质。[方法]8~9周龄昆明、BALB/c、C57BL/6J、ICR小鼠,以及4~5周龄昆明小鼠,同步系统检测其生物学特性,然后以统一的评价标准评价4种品系小鼠的寒、热体质。并对BALB/c小鼠给予参桂理中丸和利血平做药物反证。[结果]①4~5周龄昆明小鼠与8~9周龄昆明小鼠比较体质明显偏热;②BALB/c小鼠与C57BL/6J小鼠比较体质偏寒;③8~9周龄雄性BALB/c小鼠、雄性和雌性C57BL/6J小鼠与8~9周龄相应性别昆明小鼠比较体质无明显差异;8~9周龄雌性BALB/c小鼠与8~9周龄雌性昆明小鼠比较体质偏寒;④8~9周龄ICR小鼠与8~9周龄BALB/c小鼠、C57BL/6J小鼠比较体质偏热;8~9周龄雄性ICR小鼠与8~9周龄雄性昆明小鼠比较体质偏热。[结论]4种品系小鼠存在寒、热体质差异。     

Mechanisms of loss of latency of lysosomal enzymes. Effects of incubation on the properties of lysosomal membranes.

1. The effects of sucrose and KCl on the loss of latency of lysosomal enzymes caused by incubation at 37 degrees C, pH 7.4, were examined by using Triton-filled lysosomes from rat liver and two fractions from livers of rats not injected with Triton. 2. After incubation, the percentage free activity of lysosomal enzymes was measured before and after cooling to 0 degrees C in order to determine the amount of latency lost at 37 degrees C without cooling and the additional amount lost on cooling the incubated lysosomes to 0 degrees C. 3. The latency that is lost without cooling is first decreased and then increased by increasing the osmotic strength of the incubation medium with KCl, or with sucrose in the presence of KCl. However, if the osmotic strength is increased with sucrose alone, loss of latency is decreased up to 0.25M-sucrose, but is increased only slightly at higher sucrose concentrations. Apparently the lysosome is permeated by hyperosmolar KCl but not by sucrose during incubation. 4. If the osmotic strength of the assay medium is increased with KCl, the loss of latency caused by incubation for 60 min in hyperosmolar KCl is repressed. Thus it appears that a KCl-permeated lysosome can be obtained which is relatively stable until exposure to lower osmolarities. 5. The loss of latency caused by cooling incubated lysosomes to 0 degrees C is largely eliminated if the osmotic strength of the medium in which the lysosomes are cooled is raised sufficiently with either sucrose or KCl. 6. Osmotic-fragility curves were obtained after incubation for 1 and 60 min at iso-osmoticity (0.2M-KCl or 0.25 M-sucrose). Although little loss of latency occurs at iso-osmoticity, lysosomes incubated for 60 min display greatly increased fragility on exposure to hypo-osmolar KCl, hypo-osmolar sucrose or hyperosmolar KCl. 7. It is suggested that permeability to KCl at 37 degrees C and the increase in fragility on exposure to hypo-osmolar conditions are both consequences of injury, probably from enzymic action, sustained by the lysosomal membrane during incubation at 37 degrees C.     

Simple derivation of the function of genetic information and correction of the proof

The problem of predicting time to extinction in stochastics population models is approached in two ways. First, a finite Markov chain approximation is used to give the distribution of time to extinction and shown to predict simulation results accurately. Second, an approximate numerical integration technique is found to give good relative predictions of persistence using much less computer time. The relevance of the two approaches to real problems is discussed.     

Consequences of the widespread use of antibiotics

The cancer problem is increasing as life expectancy increases and greater portions of the populace live to the age at which cancer is more likely. Early diagnosis still is difficult. Even with modern methods and with considerable public education with regard to cancer, the disease is often not diagnosed until it is beyond the stage at which cure might be effected. The need for a serodiagnostic test for general screening purposes for cancer detection is tremendous. The major objective of cancer serodiagnostic test methods is to discover a general test that will detect cancer in a high percentage of cases while it is in an early stage; that will give few "false positive" results; that can be done in any laboratory; and that is simple and inexpensive. Many serodiagnostic tests for cancer have been published but none has proven worthy of being a good general test to detect cancer. Yet unless some serodiagnostic test which will be suitable for general screening purposes is developed, it is difficult to see how there can be much improvement in the early diagnosis of cancer, particularly internal cancer. It is hoped that an open-minded attitude will be maintained by physicians on this subject. Recent reports of such a test being developed are encouraging and it is hoped that continued investigations will be confirmatory.     

马陆在森林生态系统物质转化中的功能研究

马陆是森林生态系统重要的分解者,在帽儿山林区,马陆摄食量随温度的升高而增加。据初步估算,马陆地对凋落物的分解量约占该地区年平均凋落物量的０．２１％。马陆对同一种、不同腐解程度的叶片摄食不同,对妆分解凋落物的摄食量大于对未分解凋落物的摄食量。在不同温度条件下,马陆的生态效率不同,其同化效率随温度升高而降低,而粪便率则随温度升高而增加。在不同林型下个体数量分布不均匀。通常、阔叶林＞针阔叶混交林＞针叶林。在土壤的垂直分布上,具有明显的表聚现象。马陆的个体数量季节变化明显,以夏末最多,冬末最少。     

Use of the integral parameter of dermatoglyphic differences for determining the type of zygosity of twins]

A method is described increasing the reliability of twin zygosity diagnosis in cases when the possibility of using a large number of mendelian markers is restricted. The method is based on the determination of generalized index of dermatoglyphic differences between members of twin pair for 18 characteris of finger and palm dermatoglyphics and on principles of multivariate genetic analysis, which is worked out to determine the degree of heritability of multifactorial character and to study the structure of hereditary predisposition to multifactorial diseases. The efficiency of the method with respect to determinating the type of twin zygosity is approximately equivalent to the efficiency of using 5--6 mendelian marker systems.     

Primary structure of the oligosaccharide chain of lipopeptidophosphoglycan of epimastigote forms of Trypanosoma cruzi

The lipopeptidophosphoglycan of epimastigote forms of Trypanosoma cruzi is composed of a glycan linked through a non-N-acetylated glucosamine residue to an inositol phosphorylceramide. Using conventional analysis techniques, including 1H, 13C, and 31P NMR spectroscopy and negative ion fast atom bombardment mass spectroscopy, the structure of the carbohydrate-containing part of the molecule is determined as: (Sequence: see text). There is uncertainty as to which 2-O-substituted alpha-D-Manp unit is attached the side chain or whether it is distributed between the two units. Some of the structures lack the Galf side chain. The inositol unit is linked to ceramide via a phosphodiester bridge. The major aliphatic components of the ceramide portion were lignoceric acid and sphinganine.     

The Influence of Temperature on the Effect of Bacteriostatic Concentrations of Phenol Against Escherichia coli

S ummary . During early exponential growth of Escherichia coli in the absence of phenol there is a natural death rate at 20, 30, and 44° but at the optimum temperature around 37° there is little if any significant death. The influence of a rise in temperature from 20 to 44° is to decrease the generation time and at 44° the lower generation time compensates for a reduced generation index. The main effect of sub-bacteriostatic concentrations of phenol is to increase the generation time but at 30, 37 and 44° there is a significant reduction in the generation index at the higher concentrations resulting in a dynamic bacteriostasis. At 20° bacteriostasis is due mainly to a large generation time but there is a little growth and so bacteriostasis is essentially dynamic. There is also evidence to suggest that the effect of a particular concentration of phenol on the generation index is not merely influenced by the temperature but by the generation time under the particular set of conditions. If phenol is added to rapidly growing cultures of E. coli the effect of a rise in temperature is to reduce the concentration required for bacteriostasis but if it is added during the lag phase there is a maximum in the bacteriostatic concentration between 20 and 37°.     

Quantitative relationships of specific adsorption of colicins

The decrease in the number of sensitive bacteria in the presence of an excess of colicin is proportionate to their initial concentration; the proportion of surviving cells is not entirely constant, but is to some extent directly correlated to the initial cell concentration. The percentage of surviving cells is in inverse proportion to the colicin titre. The amount of nonadsorbed colicin is directly proportionate to the initial colicin titre. In the presence of an excessive number of sensitive bacteria in the suspension, the free colicin titre is much more lowered than in the suspension of resistant bacteria, the decrease being directly correlated to the number of bacteria in the suspension. Resistant—and even heterologous— bacteria can also adsorb large amounts of colicin nonspecifically, however. The experiments provide evidence in support of the concept of the lethal unit of colicin the course of adsorption of which is apparently different from that of phage.     

An Analysis of the Response of Young Barley Seedlings to Time of Application of Nitrogen

The reasons for the sensitivity of young barley seedlings totime of application of nitrogen have been examined. It is shownthat the transfer of nitrogenous reserves from endosperm toembryo which begins at about 36 h from planting proceeds ata faster relative rate than that of dry matter as a whole. Inconsequence embryo and endosperm nitrogen contents become temporarilysimilar some 24–36 h earlier than is the case for dryweights. Addition of nitrate on day 2 does not affect ratesof transfer of endosperm reserves but leads to a significantlyhigher nitrogen content in the embryo of treated plants, particularlyin the shoots. This additional nitrogen is present as nitrateup to around day 5 when reduction of accumulated nitrate commencesin the first leaf in significant amounts. For plants up to 14 days old delay in application of nitrateleads to a lowering of total nitrogen level which is proportionalto the delay in treatment. This is so for all parts of the plantexcept the first leaf for which the evidence indicates thatlevels of total and organic nitrogen and of accumulated nitrateare much lower when treatment is made late. It is argued thatnitrate accumulation by the leaf becomes progressively lessas it reaches full expansion, but irrespective of time of nitrateapplication about 95 per cent of the additional nitrogen presentin the leaf is in organic form Significant increases in organic nitrogen are found from day6 for plants supplied with nitrate up to day 4; for plants suppliedon day 6, or day 8nitrateand nitrate reductase activity in leafextracts are found within 6 h of treatment. Peak levels of nitratereductase activity are found for all treatments around days8–10 when the first leaf is fully expanded and when photosyntheticactivity is maximal. However, late supply of nitrate leads toa lower level of enzyme activity. Nitrate reduction in the rootsystem is undetectably low, and it is concluded that a substantialamount of carbon translocated from leaf to roots is in the formof nitrogenous compounds. The effects of time of application are also found when ammoniumnitrogen is substituted for nitrate indicating that the responseis independent of effects on the nitrate reducing system inthe leaf. Some inhibition of growth, particularly of the roots,is found due to ammonium toxicity. Why plants supplied early with nitrate show superior growthand enhanced photosynthetic activity in the first leaves isexplained in terms of treatment alleviating the restrictiveeffects of declining endosperm reserves. This is only possibleif nitrogen is supplied while the first leaf is expanding andable to accumulateand utilise the available nitrogen. Late supplyis associated with failure to use the nitrogen provided leadingto a lower protein level in the leaf; this can be correlatedwith the smaller size of leaf and the lower rates of carbonfixation occurring there.     

Inhibition of the transport of citrate during ADP-ribosylation of inner membrane proteins of the mitochondria

The ability of rat liver submitochondrial particles to catalyze NAD+ hydrolysis with a transfer of ADP-ribose residues to protein membranes has been demonstrated ADP-ribosylation is directly dependent on NAD+ concentration upon saturation with 1 mM NAD+ and is inhibited by physiological compounds (e.g., ATP, 10 mM; nicotinamide, 10 mM); besides, it is an artificial acceptor of ADP-ribose, arginine methyl ester. It was found that ADP-ribose is accepted by inner mitochondrial membrane protein, whose molecular masses amount to 25-30 kDa. The fact that 5'-AMP is a product of ADP-ribose degradation by snake venom phosphodiesterase suggests that the inner membrane vesiculate proteins are modified by mono(ADP-ribose). Covalent modification of membrane proteins by ADP-ribose leads to citrate transport inhibition in inner membrane vesicles the [14C]citrate uptake is significantly decreased thereby. The ability of ADP-ribosylation inhibitors to restore the citrate transport rate is suggestive of a direct regulatory effect of NAD+-dependent ADP-ribosylation on the activity of citrate-translocating system of inner mitochondrial membranes.     

Note on a mechanism of the distribution of wealth

A population of individuals is considered to be characterized by a distribution of wealth which is the result of gain and loss from the outside as well as a result of exchange. The population is assumed to be uniform except for the variation in a parameter determining the manner of partition during exchange. The parameter is assumed to be normally distributed over the population. The resulting distribution of wealth is calculated for some special cases and it is found to be very asymmetric.     

Mode of Action of Streptolydigin

Streptolydigin and rifamycin inhibit the catalytic function of ribonucleic acid (RNA) polymerase. Streptolydigin can inhibit polymerization after the reaction has started, whereas rifamycin is effective only if it is preincubated with RNA polymerase prior to the addition of substrates. The same relationships are observed with respect to these two antibiotics if the nucleoside triphosphate-pyrophosphate exchange reaction is used in the assay system. The inhibitory effect of streptolydigin is reversible by further addition of RNA polymerase but not by addition of deoxyribonucleic acid to the assay system.     

The mechanism of N-terminal acetylation of proteins

N alpha-acetylation is almost exclusively restricted to eukaryotic structural proteins. As a rule it is a post-initiational process, requiring the presence of the enzyme N alpha-acetyltransferase and the acetyl donor acetylcoenzyme A. N alpha-acetyltransferases appear to have a narrow substrate specificity, which is very similar for enzymes from different tissues and species. Amino acids predominantly present at the N terminus of N alpha-acetylated proteins are alanine, serine, and methionine. The occurrence of these residues is apparently a prerequisite for acetylation. The region following these amino acids is also important. If methionine is at the N terminus, the second position is always occupied by a strongly hydrophilic amino acid. Two- and three-dimensional structural characteristics of the protein do not seem to play a major role in N alpha-acetylation. Up to now the exact function for N alpha-acetylation is not known.     

Study of the glycosylation of apolipoprotein H

Apolipoprotein H is a single chain polypeptide composed of 326 amino acids highly glycosylated. Its carbohydrate content is approximately 19% of the molecular weight. We show that it is rich in sialic acid linked alpha (2-6) to galactose or N-acetylgalactosamine. Sialic acid is not alpha (2-3) linked to galactose. Galactose is beta (1-4) linked to N-acetylglucosamine and beta (1-3) linked to N-acetylgalactosamine. Carbohydrate O-linked chains (mainly sialic acid) are alpha (2-6) linked to galactose or N-acetylgalactosamine. Galactose is also organised in O-linked chains and beta (1-4) linked to N-acetylglucosamine and beta (1-3) linked to acetylgalactosamine. Concanavalin A lectin was used to isolate two groups of apolipoprotein H molecules bearing biantennary and truncated hybrids and high mannose and hybrid oligosaccharides. Apolipoprotein H fails to bind lysine-Sepharose. Our results thus show that it presents truncated hybrid or hybrid-type carbohydrate chains which bear few unmasked mannose residues as a terminal sugar. Biochemical analysis of carbohydrate structures conducted on single isoforms separated through IEF revealed that no specific carbohydrate complex is bound to a single isoform.     

Possible mechanisms of implementation of toxic potential of lipopolysaccharides of pathogenic bacteria

The significance of variability of biological properties of lipopolysaccharides (LPS) is discussed in the paper within the pathogenesis of infectious process. On the basis of an analysis of published data and of results of independent research of two microorganisms (Yersinia pestis and Francisella tularensis) a conclusion is made on that a biologically inert LPS form (with a weak cytokine-inducing ability, apirogenicity and non-toxicity etc.) is typical of highly pathogenic bacteria. It is suggested that the above phenomenon is biologically expedient. Presumably, the inert LPS transforms to the active form inside a sensitive host and, according to an infection stage, each of them being functionally significant. It is the inert status of LPS that enables the pathogens, at the initial stages, to surmount freely the humoral and cell barriers of host. As the infection progressively aggravates and the proliferation of bacteria modifies itself due to LPS micro- and macroorganisms, its chemical structure and biopolymer conformation change. Both modification mechanisms enhance the LPS toxic potential. In case of a sensitive host, such variations transform the biologically inert LPS into a toxically active form with its function of endotoxin being realized. There is no LPS modification in a host insensitive to such infection, which entails either recovery or prolonged persistence of the pathogen inside the microorganism.