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At least 19 recordsLinked to original sources
PubMed1980

Exometabolites of Leishmania donovani promastigotes. II. Spontaneous changes of exometabolite after isolation.

The defined medium of Steiger and Teiger conditioned by growth oif Leishmania domovani strain 3S promastigotes served as the primary source of parasite exometabolites. Four fractions of the conditioned medium were recovered by Sephadex G-25 column chromatography. These fractions shared immunologic determinants, but differed in their molecular weights, affinity of Sephadex G-25, and absorption spectra. Degradation and/or aggregation of one of the fractions (Fraction IV) appeared to yield substances found in the remaining three fractions. Furthermore, by appropriate manipulations, Fraction IV could be transformed into substances resembling those described by previous workers, eg., excretory factor (EF) or antigenically active glycoproteins (AAGP). The present findings suggest that the primary exometabolite released by L. donovani is a samll glycopeptide-like molecule; however, in media conditioned by growth of promastigotes and during isolation procedures, aggregation and/or degradation processes yield higher molecular weight substances which vary in size and physico-chemical properties.

Animals↗
PubMedDate not supplied

[Multiple protective effect of an exometabolite (exometabolites) released by Escherichia coli during treatment with tetracycline].

Exponentially growing tetracycline-treated Escherichia coli cells release (an) as yet unidentified compound(s) into the medium. These compounds produce a protective effect on E. coli cells under conditions of heat, oxidative, and osmotic shocks, or in the presence of tetracycline. The protective effect is manifested as an acceleration of growth in the presence of tetracycline or under conditions of heat shock or as a shortening of the period of adaptation to other stresses.

Adaptation, Physiological↗
PubMed2026

Glutathione acts as an exometabolite that promotes growth recovery in fission yeast with defects in amino acid metabolism and cell polarity.

UNLABELLED: Microorganisms in nature form communities through diverse interactions, such as mutualism and competition, to adapt to their ecological environments. These interactions seem to be mediated by extracellular metabolites (exometabolites), yet the chemical and biological diversity underlying these processes remains largely unexplored. In this study, we examined the chemical basis of exometabolite-mediated interactions in the fission yeast Schizosaccharomyces pombe by a genome-wide screen employing 3,420 viable gene deletion mutants. We identified 37 strains that exhibited growth defects in monoculture on a minimal medium but exhibited growth recovery in the vicinity of wild-type colonies (co-culture), suggesting that exometabolites derived from wild-type cells compensated for the gene deletion. Both lipophilic and water-soluble fractions obtained by solvent partitioning of the wild-type culture supernatant promoted growth recovery. Among the 11 mutants rescued by the water-soluble fraction, 6 were cysteine auxotrophs, prompting analyses of thiol-containing metabolites by liquid chromatography-mass spectrometry (LC-MS), revealing the presence of glutathione (GSH) in the culture supernatant. GSH restored growth in most strains as a nutrient source. In contrast, GSH rescued cell morphology defects in the hob3∆ mutant, lacking the Bin/amphiphysin/Rvs (BAR) adaptor protein Hob3, through a mechanism independent of nutrition. This research advances understanding of exometabolite-mediated interactions in S. pombe by identifying GSH as an exometabolite that influences cellular processes and potentially shapes microbial communities. IMPORTANCE: Microorganisms secrete a wide range of metabolites that control microbial community behavior. These extracellular metabolites (exometabolites) include not only well-studied signaling molecules but also diverse primary and secondary metabolites, suggesting complex interactions among microbes. However, the molecular basis of these interactions remains poorly understood, partly due to challenges in detecting them experimentally. In this study, we surveyed exometabolites involved in cell-cell interactions in the model eukaryotic microorganism Schizosaccharomyces pombe. S. pombe releases a wide variety of metabolites outside the cells, including previously reported nitrogen signaling factors (NSFs) and glutathione (GSH) identified in this work. By analyzing gene deletion mutants whose growth is supported by extracellular GSH, we provide new insights into how secreted primary exometabolites compensate for specific genetic defects and influence cell physiology in microbial populations.

exometabolite↗
PubMedDate not supplied

[Comparative study of effects of Escherichia coli M-17 exometabolites and fructooligosaccharides on the growth and antagonistic activity of Lactobacilli].

Facts concerning the evaluation of the influence of E. coli M17 exometabolites and fructooligosaccharides (FOS) on the growth and antagonistic activity of lactobacilli are presented. As revealed by these facts, preparation "Aktoflor" accelerates the growth of lactobacillary cultures, increases the final yield of biomass and antagonistic activity. E. coli M17 exometabolites contained in "Aktoflor" have been shown to be more active in comparison with FOS. The character of their influence on lactobacilli is discussed and the conclusion is made that the restoration and maintenance of eubiosis is greatly determined by the pool of metabolites excreted by the bacteria.

Biological Factors↗
PubMedDate not supplied

[Dynamics and functions of exometabolites in the process of the growth of Escherichia coli M-17 periodical culture].

The concentrations of metabolites altered immediately after culture inoculation into fresh medium and depended on the their dilution (in small dilutions metabolites were released into the medium, and, on the contrary, in great dilutions they were adsorbed). Acetate was the main exometabolite. The growth of culture started only when the acetate concentration reached the threshold value. At the stage of growth deceleration an intensive release of acetate and other exometabolites occurred. The process had the explosive character of chemical chain reaction. It could be initiated by high local concentrations of metabolites around bacteria, most sensitive to changes in growth conditions. At a high concentration of such cells the signal could be transmitted from one bacteria to another, otherwise the reaction chain was quickly broken and no mass release of metabolites occurred. At the stationary phase succinate, valine and lactate were consumed by bacteria with lactate concentration dropping practically to 0. At the same time acetate and citrate concentrations oscillated about some constant value. The release of growth inhibitors, formiate and alanine, continued to the end of cultivation, which was, seemingly, one of the factors of growth cessation. The specific features of the dymamics of metabolites were indicative of the fact that they had their individual regulatory functions. The problem of the self-synchronization of the bacterial culture is discussed.

Acetates↗
PubMed1987

[Characteristics of the effect of exometabolites of the cysticerci of the cat tapeworm Hydatigera taeniaeformis on fibroblasts in organ cultures].

The influence of the cestode H. taeniaeformis cysticercus exometabolites on the fibroblasts of their capsule in organ culture was studied. Half of explants were cultured in the presence of cestodes (the ratio between the parasite body weight and the cultural medium volume being 1:10 g/ml). After 2-30 days of cultivation the explants were examined by histological, histoautoradiographic and electron microscopic methods. The influence of cysticercus exometabolites on the culture resembled that of the growth-stimulating factors. The young, actively proliferating fibroblasts were mainly observed in the explants of the capsules cultured in the presence of cysticerci. Among the mature cells, fibroblasts with the predominance of the fibroclastic function were noticed rather than with the function of collagen biosynthesis. It is suggested that the change in the differentiation ways of fibroblasts may be due to some biologically active substrates of the cysticercus to be directed on slowing down the maturation of the connective tissue capsule.

Animals↗
PubMedDate not supplied

[Participation of exometabolites in adaptation of Escherichia coli to stressors].

Escherichia coli cells exposed to heat (48 degrees C), cold (5-15 degrees C), oxidative (N-ethylmaleimide), and tetracycline-induced stresses secreted yet unidentified compounds (exometabolites) into the medium. These compounds protected E. coli cells against the same or other stresses. The activity spectra, i.e., the potency of protection against different stresses, varied depending on the origination conditions of the exometabolites.

Adaptation, Physiological↗
PubMedDate not supplied

[Dormant forms of Yersinia pseudotuberculosis during interaction with green algae and their exometabolites (population dynamics and ultrastructure)].

The dynamics of the transition of Y.pseudotuberculosis to the latent (noncultivable) state in sterile soil extraction and in soil extraction, containing Scenedesmus algae or their exometabolites, was evaluated by the bacteriological method and with the use of polymerase chain reaction. The formation of Y.pseudotuberculosis latent forms achieved its highest rate under the action of algal exometabolites (on day 11), while in the presence of algal cells such formation was delayed to 3-5 months. The partial reversion of Y.pseudotuberculosis nonculativable forms to vegetative, bacteriologically detectable forms occurred under the action of fetal serum, as well as live or killed infusoria. Transmission electron microscopy demonstrated that noncultivable Y.pseudotuberculosis had a round form, diminished cell size, denser cytoplasm and enlarged cytoplasmic space. The reversible transition of bacteria to the latent state is regarded as their adaptation to unfavorable factors during their existence in soils and water reservoirs.

Adaptation, Physiological↗
PubMed1991

Biochemical and immunological characterization of exometabolites from an Indian strain of Leishmania donovani promastigotes grown in a chemically defined medium.

Exometabolites (EXOM) of an Indian strain of Leishmania donovani promastigotes isolated from a chemically defined medium by ultrafiltration consisted of proteins, glycoproteins, lipid and lipophosphopolysaccharide (LPPS). LPPS of Mr 40-28 kDa in SDS-PAGE could be labelled metabolically with [32P]-phosphate and recovered in the aqueous phase of hot-phenol-water extraction of EXOM (PE-Aq) along with a glycoprotein of Mr 150-130 kDa (GP150-130). These two molecules could be eluted from DE-52 column with 200 mM NaCl (D2). The 300 mM NaCl (D3) and 400 mM NaCl (D4) eluates from DE-52 column contained one unsaturated polar lipid component. The LPPS had Rf value of 0.65-0.75 in Thin Layer Chromatography (TLC) using saturated phenol water solvent system. EXOM revealed 15 bands in SDS-PAGE of which proteins of Mr 84, 66, 56, 50 and 29 kDa were prominent. When EXOM were fractionated through Con A-Sepharose column, the fraction eluted with alpha-methyl-D-mannoside (Con A-E) had seven bands as revealed by SDS-PAGE of which 25, 16, 13 and 12 kDa glycoproteins were prominent. The antigens present in EXOM can be classified as slower anodic migrating and faster anodic migrating antigens as revealed by immunoelectrophoresis (IEP). The slower anodic migrating antigens, LPPS and GP150-130 recovered in PE-Aq and D2 did not cross-react with kala-azar patients' sera but cross-reacted with homologous anti-promastigote sera. Two faster anodic migrating antigens which could be recovered in organic phase of hot phenol extraction of EXOM (PE-O) and eluted in D3 and D4 and Con A-E, cross-reacted with kala-azar patients' sera. The antigens of both the classes were sensitive to periodic acid oxidation.

Animals↗
PubMedDate not supplied

[Identification of partially deuterated exometabolites during culture of tea fungi in heavy water].

Exometabolites of tea fungus during the cultivation on heavy water were studied by methods of high-resolution proton and deuterium exchange. Is was shown that, depending on the degree of exchange of proton for deuterium in the methyl group of acetate, three isotopomers exist: -CH3, -CH2D, and -CHD2. Ethanol is represented by six isotopomers: -CHD-CH3, -CD2-CH3, -CD2-CH2D, -CD2-CHD2, -CHD-CH2D, and -CHD-CHD2. Relative concentration of these isotopomers and the percent content of deuterium were determined. Based on these data, the kinetics of metabolism of the object cultivated on heavy water was analyzed. It was show that the efficiency of glucose utilization is the same as during cultivation on light water with the exception that the time of utilization is significantly greater. At the same time, the parameters of utilization of ethanol and its conversion into acetic acid in the life activity of the tea fungus in heavy and light water are very similar.

Deuterium↗
PubMedDate not supplied

[Effect of blue-green alga (Cyanobacteria) and their exometabolites on formation of resting forms and variability of Yersinia pseudotuberculosis].

Research, carried out with the use of bacteriological methods and polymerase chain reaction, revealed that the transformation of Y. pseudotuberculosis, associated with blue-green algae Anabaena variabilis, into resting (noncultivable) forms took shorter time than in soil extract containing no algae. The exometabolites of "old" cultures of these algae sharply accelerated the formation of resting Y. pseudotuberculosis forms. The influence of the algae and the products of their metabolism was manifested far more intensively at 22 degrees C than at 4 degrees C. After passage through infusoria resting Y. pseudotuberculosis forms, preserved in the mucous covering of cyanobacteria, partially reverted into vegetative forms, capable of growing on solid culture media. The revertants essentially differed from the initial vegetative forms by having lower enzymatic activity, agglutinability and cytopathogenicity, as well as by the loss of plasmid p45. The probable role of blue-green algae, widely spread in soils and water reservoirs, in the processes of reversible transformation of Y. pseudotuberculosis vegetative and resting forms, closely connected with seasonal changes of temperature conditions.

Biological Factors↗
PubMedDate not supplied

[The significance of exometabolites in the formation and operation of the soybean-rhizobium symbiosis].

The effect of various inoculates of the soybean-specific strain of nodule bacteria Bradyrhizobium japonicum 634b (unwashed cells, cells washed from the exopolysaccharide-protein complex, and cells combined with the complex) on the formation and operation of soybean-rhizobium symbiosis. It was shown that addition of the exopolysaccharide-protein complex doubled the ability of the microsymbiont to form nodules, nodule weight, and the nitrogenase activity of the nodules. Bradyrhizobium japonicum 634b cells washed from exometabolites had lower indices of symbiotic activity than their intact counterparts.

Bacterial Proteins↗
PubMed2005

Biological and physiochemical methods for utilization of plant wastes and human exometabolites for increasing internal cycling and closure of life support systems.

Wheat was cultivated on soil-like substrate (SLS) produced by the action of worms and microflora from the inedible biomass of wheat. After the growth of the wheat crop, the inedible biomass was restored in SLS and exposed to decomposition ("biological" combustion) and its mineral compounds were assimilated by plants. Grain was returned to the SLS in the amount equivalent to human solid waste produced by consumption of the grain. Human wastes (urine and feces) after physicochemical processing turned into mineralized form (mineralized urine and mineralized feces) and entered the plants' nutrient solution amounts equal to average daily production. Periodically (once every 60-70 days) the nutrient solution was partly (up to 50%) desalinated by electrodialysis. Due to this NaCl concentration in the nutrient solution was sustained at a fixed level of about 0.26%. The salt concentrate obtained could be used in the human nutrition through NaCl extraction and the residuary elements were returned through the mineralized human liquid wastes into matter turnover. The control wheat cultivation was carried out on peat with use of the Knop nutrient solution. Serial cultivation of several wheat vegetations within 280 days was conducted during the experiment. Grain output varied and yield/harvest depended, in large part, upon the amount of inedible biomass returned to SLS and the speed of its decomposition. After achieving a stationary regime, (when the quantity of wheat inedible biomass utilized during vegetation in SLS is equal to the quantity of biomass introduced into SLS before vegetation) grain harvest in comparison with the control was at most 30% less, and in some cases was comparable to the control harvest values. The investigations carried out on the wheat example demonstrated in principle the possibility of long-term functioning of the LSS photosynthesizing link based on optimizations of biological and physicochemical methods of utilization of the human and plants wastes. The possibilities for the use of these technologies for the creation integrated biological-physicochemical LSS with high closure degree of internal matter turnover are discussed in this paper.

Biodegradation, Environmental↗
PubMedDate not supplied

[Pathways of inclusion of isotopes 2H and 13C into exometabolites in course of glucose utilization by medusomycete].

The inclusion of 2H and 13C isotopes into the products of glucose utilization by medusomycete during its growth on deuterated media was studied by high-resolution NMR spectroscopy. Both unlabeled and 13C-labeled (in positions 1, 2, 6) glucose was used. It was shown that the glucose utilization proceeds by the classical Embden-Meyerhof-Parnas pathway. The incorporation of deuterium to the methyl group of ethanol can occur only during glucose-fructose-6-phosphate and phosphoenolpyruvate--pyruvate conversion. None of these stages by themselves is responsible for the existing distribution of deuterium atoms. The maximum inclusion of deuterium to the methyl group is no more than two atoms for the first glucose fragment (C1-C2-C3) and no more than one, for the second fragment (C4-C5-C6). The methylene group of ethanol is more accessible for deuterons because the proton surroundings of carbon atoms C2 and C5 completely changes. It was concluded that the maximum proton exchange occurs at positions C2 and C5; at positions C1, the proton exchange is lesser, and at position C6 it is the least. It was also shown that about 10% C1-C3 of triose leave the glycolysis cycle and are used in other processes.

Carbon Isotopes↗
PubMedDate not supplied

[Identification of minor components of medusomycete exometabolites. 1H-NMR spectra in 13C and deuterium substitutions].

High-resolution 1H-NMR experiments were performed on 2H/13C isotopically labelled metabolites of growing medusomycete culture. Some minor metabolites were identified and the degree of their deuterization was established. Some of these metabolites were shown to be present in isomeric forms. Our results demonstrated that glycerol was produced in the growth medium on the early stage of the system adaptation to the growth in D2O.

Carbon Isotopes↗